Hostname: page-component-54dcc4c588-hp6zs Total loading time: 0 Render date: 2025-09-28T18:00:41.599Z Has data issue: false hasContentIssue false

Identifying the Big Questions in paleontology: a community-driven project

Published online by Cambridge University Press:  26 September 2025

Jansen A. Smith*
Affiliation:
GeoZentrum Nordbayern, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen 91054, Germany Department of Earth and Atmospheric Sciences, University of Minnesota Duluth, Duluth, Minnesota 55812, U.S.A.
Elizabeth M. Dowding
Affiliation:
GeoZentrum Nordbayern, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen 91054, Germany
Ahmed A. Abdelhady
Affiliation:
Geology Department, Minia University, Al Minya, Al Minya 61519, Egypt
Paolo Abondio
Affiliation:
IRCCS Istituto delle Scienze Neurologiche di Bologna, Bologna, Emilia-Romagna 40139, Italy
Ricardo Araújo
Affiliation:
Instituto de Plasmas e Fusão Nuclear & Centro de Recursos Naturais e Ambiente (CERENA), Instituto Superior Técnico, Universidade de Lisboa, Lisbon 1049-001, Portugal
Tracy Aze
Affiliation:
School of Biological and Marine Sciences, University of Plymouth, Plymouth, Devon PL4 8AA, U.K.
Mairin A. Balisi
Affiliation:
Raymond M. Alf Museum of Paleontology, Claremont, California 91711, U.S.A. La Brea Tar Pits and Museum, Natural History Museums of Los Angeles County, Los Angeles, California 90036, U.S.A. Department of Life and Environmental Sciences, University of California–Merced, Merced, California 95343, U.S.A.
Luis A. Buatois
Affiliation:
Department of Geological Sciences, University of Saskatchewan, Saskatoon, Saskatchewan S7N 5E2, Canada
Humberto Carvajal-Chitty
Affiliation:
Departamento de Estudios Ambientales, Universidad Simón Bolívar, Valle de Sartenejas, Baruta/Miranda 89000, Venezuela
Devapriya Chattopadhyay
Affiliation:
Department of Earth and Climate Science, IISER Pune, Pune, MH 411008, India
Mario Coiro
Affiliation:
Department of Paleontology and Historical Geology, Senckenberg Research Institute and Natural History Museum, Frankfurt am Main 60395, Germany Department of Palaeontology, University of Vienna, Vienna, Vienna 1090, Austria
Gregory P. Dietl
Affiliation:
Paleontological Research Institution, Ithaca, New York 14850, U.S.A. Department of Earth and Atmospheric Sciences, Cornell University, Ithaca, New York 14853, U.S.A.
Catalina González Arango
Affiliation:
Departamento de Ciencias Biológicas, Universidad de los Andes, Bogotá 111711, Colombia
Charalampos Kevrekidis
Affiliation:
Museum für Ur- und Ortsgeschichte, Museumszentrum Quadrat, Bottrop, 46236, Germany
Julien Kimmig
Affiliation:
Paläontologie und Evolutionsforschung, Abteilung Geowissenschaften, Staatliches Museum für Naturkunde Karlsruhe, 76133 Karlsruhe, Germany Harold Hamm School of Geology and Geological Engineering, University of North Dakota, Grand Forks, North Dakota 58202, U.S.A.
Alexis M. Mychajliw
Affiliation:
La Brea Tar Pits and Museum, Natural History Museums of Los Angeles County, Los Angeles, California 90036, U.S.A. Department of Biology & Program in Environmental Studies, Middlebury College, Middlebury, Vermont 05753, U.S.A.
Catalina Pimiento
Affiliation:
Department of Paleontology, University of Zurich, Zurich 8006, Switzerland Department of Biosciences, Swansea University, Swansea SA28PP, U.K.
Omar Rafael Regalado Fernández
Affiliation:
Curation, Senckenberg Naturmuseum Frankfurt, Frankfurt am Main, Hesse 60395, Germany
Katlin M. Schroeder
Affiliation:
Institute for Biospheric Studies, Yale University, New Haven, Connecticut 06520, U.S.A.
Rachel C. M. Warnock
Affiliation:
GeoZentrum Nordbayern, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen 91054, Germany
Tzu-Ruei Yang
Affiliation:
National Museum of Natural Science, Taichung 404023, Taiwan Department of Life Sciences, National Chung Hsing University, Taichung 402202, Taiwan Department of Earth Sciences, National Cheng Kung University, Tainan, 701401 Taiwan
Moriaki Yasuhara
Affiliation:
School of Biological Sciences, Area of Ecology and Biodiversity, Swire Institute of Marine Science, Institute for Climate and Carbon Neutrality, and Musketeers Foundation Institute of Data Science, https://ror.org/02zhqgq86The University of Hong Kong , Hong Kong SAR, China State Key Laboratory of Marine Pollution, City University of Hong Kong, Kowloon, Hong Kong SAR, China
Lailah Gifty Akita
Affiliation:
Department of Marine and Fisheries Sciences, University of Ghana, Legon-Campus, Greater-Accra, Ghana
Bethany J. Allen
Affiliation:
Department of Biosystems Science and Engineering, ETH Zurich, Basel, Basel-Stadt 4056, Switzerland Computational Evolution Group, Swiss Institute of Bioinformatics, Lausanne, Vaud 1015, Switzerland
Brendan M. Anderson
Affiliation:
Paleontological Research Institution, Ithaca, New York 14850, U.S.A.
Jérémy Andréoletti
Affiliation:
Institut de Biologie, École Normale Supérieure, Université PSL, CNRS, INSERM, Paris 75005, France
Fernando M. Archuby
Affiliation:
Centro de Estudios Integrales de la Dinámica Exógena, Universidad Nacional de La Plata, La Plata (1900), Provincia de Buenos Aires, Argentina Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Ciudad Autónoma de Buenos Aires, CABA C1425FQB, Argentina
Gustavo A. Ballen
Affiliation:
Instituto de Biociências, Universidade Estadual Paulista “Júlio de Mesquita Filho”, Botucatu SP 18618-689, Brazil
Md. Ibrahimul Bari
Affiliation:
Geology, Indian Institute of Technology Bhubaneswar, Bhubaneswar, Odisha 752050, India; and Geology, JIS University, Kolkata, West Bengal 700109, India
Michael J. Benton
Affiliation:
Palaeobiology, Research Group, School of Earth Sciences, University of Bristol, Wills Memorial Building, Queen’s Road, Bristol, BS8 1RJ, U.K.
Eugene W. Bergh
Affiliation:
Unit for Environmental Sciences and Management, North-West University, Potchefstroom 2531, South Africa
Luciano Brambilla
Affiliation:
Centro de Estudios Interdisciplinarios, Universidad Nacional de Rosario, Rosario, Santa Fe 2000, Argentina
Anieke Brombacher
Affiliation:
Department of Earth & Planetary Sciences, Yale University, New Haven, Connecticut 06511, U.S.A.
Yong Kit Samuel Chan
Affiliation:
Department of Biological Sciences, National University of Singapore, Singapore, 117558 Singapore
Alfio Alessandro Chiarenza
Affiliation:
Department of Earth Sciences, University College London, London WC1E 6BS, U.K.
Tsogtbaatar Chinzorig
Affiliation:
Department of Biological Sciences, North Carolina State University, Raleigh, North Carolina 27695, U.S.A. Division of Paleozoology, The Institute of Paleontology, Mongolian Academy of Sciences, Ulaanbaatar 15160, Mongolia North Carolina Museum of Natural Sciences, Raleigh, North Carolina 27601, U.S.A.
Kadane M. Coates
Affiliation:
Department of Chemistry, The University of the West Indies, Mona, Kingston JMAAW15, Jamaica
David R. Cordie
Affiliation:
Division of Biological Sciences, Edgewood University, Madison, Wisconsin 53711, U.S.A.
Miguel Cortés-Sánchez
Affiliation:
Department of Prehistory and Archaeology. University of Seville, Seville 41004, Spain
Eduardo J. Cruz-Vega
Affiliation:
Geology, The University of Puerto Rico, Mayagüez Campus, Mayagüez, Puerto Rico 00680, U.S.A.
Jonathan D. Cybulski
Affiliation:
Smithsonian Tropical Research Institute, Balboa 0843, Republic of Panamá Graduate School of Oceanography, University of Rhode Island, Narragansett, Rhode Island 02882, U.S.A.
Kenneth De Baets
Affiliation:
Institute of Evolutionary Biology, University of Warsaw, Faculty of Biology, Warsaw 02-089, Poland
Julia De Entrambasaguas
Affiliation:
Departamento de Ciencias de la Tierra, Universidad de Zaragoza, Zaragoza 50009, Spain Instituto Universitario de Investigación de Ciencias Ambientales de Aragón (IUCA), Zaragoza 50009, Spain
Erin M. Dillon
Affiliation:
Smithsonian Tropical Research Institute, Balboa 0843, Republic of Panamá Department of Ecology, Evolution, and Marine Biology, University of California, Santa Barbara, Santa Barbara, California 93106, U.S.A.
Andrew Du
Affiliation:
Department of Anthropology & Geography, Colorado State University, Fort Collins, Colorado 80523, U.S.A.
Alexander M. Dunhill
Affiliation:
School of Earth and Environment, University of Leeds, Leeds LS2 9JT, U.K.
Jon M. Erlandson
Affiliation:
Museum of Natural & Cultural History, University of Oregon, Eugene, Oregon 97403, U.S.A.
Marie-Béatrice Forel
Affiliation:
Muséum national d’Histoire naturelle, Centre de Recherche en Paléontologie–Paris (CR2P), 75005 Paris, France
William J. Foster
Affiliation:
Institute for Geology, Universität Hamburg, Hamburg 20146, Germany
Terry A. Gates
Affiliation:
Department of Biological Sciences, North Carolina State University, Raleigh, North Carolina 27695, U.S.A. North Carolina Museum of Natural Sciences, Raleigh, North Carolina 27601, U.S.A.
Alexandra Gavryushkina
Affiliation:
School of Computer and Mathematical Sciences, University of Adelaide, SA 5005, Australia
Molly K. Grace
Affiliation:
Department of Biology, University of Oxford, Oxford OX1 3SZ, U.K.
Hans-Peter Grossart
Affiliation:
Plankton and Microbial Ecology, Leibniz Institute of Freshwater Ecology and Inland Fisheries (IGB), 16775 Stechlin, Germany Institute of Biochemistry and Biology, Potsdam University, 14469 Potsdam, Germany
Patrick Hänsel
Affiliation:
GeoZentrum Nordbayern, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen 91054, Germany
Paul G. Harnik
Affiliation:
Department of Earth and Environmental Geosciences, Colgate University, Hamilton, New York 13346, U.S.A.
Melanie Jane Hopkins
Affiliation:
Division of Paleontology (Invertebrates), American Museum of Natural History, New York, New York 10024, U.S.A.
Samantha S. B. Hopkins
Affiliation:
Museum of Natural & Cultural History, University of Oregon, Eugene, Oregon 97403, U.S.A. Department of Earth Sciences, University of Oregon, Eugene, Oregon 97403, U.S.A.
Keyi Hu
Affiliation:
School of Earth Sciences and Engineering, Nanjing University, Nanjing, Jiangsu 210023, China
Huai-Hsuan M. Huang
Affiliation:
Department of Geosciences, Princeton University, Princeton, New Jersey 08545, U.S.A.
Randall B. Irmis
Affiliation:
Natural History Museum of Utah, University of Utah, Salt Lake City, Utah 84108-1214, U.S.A. Department of Geology & Geophysics, University of Utah, Salt Lake City, Utah 84112-0102, U.S.A.
Victory A. J. Jaques
Affiliation:
CTLab, Central European Institute of Technology–Brno University of Technology, Brno, Moravia 61200, Czech Republic Institute of Geology and Palaeontology, Charles University, Prague, Bohemia 128 43, Czech Republic
Xavier A. Jenkins
Affiliation:
Department of Biological Sciences, Idaho State University, Pocatello, Idaho 83201, U.S.A.
Advait M. Jukar
Affiliation:
Department of Natural History, Florida Museum of Natural History, University of Florida, Gainesville, FL 32611 USA Department of Paleobiology, National Museum of Natural History, Smithsonian Institution, Washington, D.C. 20013, U.S.A. Division of Vertebrate Paleontology, Yale Peabody Museum, New Haven, Connecticut 06520, U.S.A.
Patricia H. Kelley
Affiliation:
Earth and Ocean Sciences, University of North Carolina Wilmington, Wilmington, North Carolina 28461-5944, U.S.A.
Romina G. Kihn
Affiliation:
Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Santa Rosa, La Pampa 6300, Argentina Universidad Nacional de La Pampa (UNLPam), Santa Rosa, La Pampa 6300, Argentina
Adiël A. Klompmaker
Affiliation:
Department of Museum Research and Collections & Alabama Museum of Natural History, University of Alabama, Tuscaloosa, Alabama 35487, U.S.A.
Ádám T. Kocsis
Affiliation:
GeoZentrum Nordbayern, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen 91054, Germany
Jürgen Kriwet
Affiliation:
Department of Palaeontology, University of Vienna, Vienna, Vienna 1090, Austria
David Lazarus
Affiliation:
Retired, Berlin, Germany
Chun-Chi Liao
Affiliation:
Institute of Vertebrate Paleontology and Paleoanthropology, Chinese Academy of Sciences, Beijing 100044, China
Chien-Hsiang Lin
Affiliation:
Biodiversity Research Center, Academia Sinica, Taipei 11529, Taiwan
Julien Louys
Affiliation:
Australian Research Centre for Human Evolution, Griffith University, Brisbane, Queensland 4111, Australia
Jesus Lozano-Fernandez
Affiliation:
Department de Genètica, Microbiologia i Estadística, & Institut de Recerca de la Biodiversitat (IRBio), Facultat de Biologia, Universitat de Barcelona, Barcelona, Spain
María Carmen Lozano-Francisco
Affiliation:
Ecology and Geology, University of Málaga, Málaga 29010, Spain
Jessica A. Lueders-Dumont
Affiliation:
Earth and Environmental Sciences, Boston College, Chestnut Hill, Massachusetts 02467, U.S.A.
Mariano E. Malvé
Affiliation:
IBIOMAR-CONICET, Puerto Madryn, Chubut U9120, Argentina
Rowan C. Martindale
Affiliation:
Department of Earth and Planetary Sciences, The University of Texas at Austin, Austin, Texas 78712, U.S.A.
Ilaria Mazzini
Affiliation:
CNR - Institute of Environmental Geology and Geoengineering, Area della Ricerca di Roma 1, Via Salaria km 29,300, 00015 Montelibretti, RM, Italy
Giorgia Modenini
Affiliation:
BiGeA Department, University of Bologna, Bologna 40126, Italy
Subhronil Mondal
Affiliation:
Department of Earth Sciences, Indian Institute of Science Education and Research (IISER) Kolkata, Mohanpur, West Bengal 741246, India
Mariana Mondini
Affiliation:
Laboratorio de Zooarqueología y Tafonomía de Zonas Áridas (LaZTA), Instituto de Antropología de Córdoba (IDACOR), Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET)–Universidad Nacional de Córdoba, Córdoba 5000, Argentina Facultad de Filosofía y Letras, Universidad de Buenos Aires, Ciudad Autónoma de Buenos Aires 1406, Argentina
Mateo D. Monferran
Affiliation:
Ciencias de la Tierra, Centro de Ecologia Aplicada del Litoral–Universidad Nacional del Nordeste, Corrientes, Corrientes 3400, Argentina
Laura P. A. Mulvey
Affiliation:
GeoZentrum Nordbayern, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen 91054, Germany
Karma Nanglu
Affiliation:
Department of Earth and Planetary Sciences, University of California Riverside, California, 92521, U.S.A.
Jacqueline M. T. Nguyen
Affiliation:
Australian Museum, Sydney, New South Wales 2010, Australia Flinders University, Adelaide, South Australia 5042, Australia
Richard Norris
Affiliation:
Scripps Institution of Oceanography, University of California, La Jolla, California 92093-0244, U.S.A.
Aaron O’Dea
Affiliation:
Smithsonian Tropical Research Institute, Balboa 0843, Republic of Panamá Sistema Nacional de Investigación (SENACYT), Panamá, Republic of Panamá
Amy L. Ollendorf
Affiliation:
Paleontology Division, Applied EarthWorks, Inc., Pasadena, California 91107, U.S.A.
Johanset Orihuela
Affiliation:
Department of Earth and Environment, Florida International University, Miami, Florida 33199, U.S.A.
John M. Pandolfi
Affiliation:
School of the Environment, The University of Queensland, St. Lucia, Queensland 4072, Australia
Telmo Pereira
Affiliation:
Universidade Autónoma de Lisboa, Lisboa 1169-023, Portugal Instituto Politécnico de Tomar, Tomar 2300-313, Portugal Centro de Geociências da Universidade de Coimbra, Coimbra 3030-790, Portugal UNIARQ, Centro de Arqueologia da Universidade de Lisboa, Lisboa 1600-214, Portugal
Alejandra Piro
Affiliation:
Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Ciudad Autónoma de Buenos Aires, CABA C1425FQB, Argentina División Paleontología Vertebrados, Museo de La Plata, Facultad de Ciencias Naturales y Museo, Universidad Nacional de La Plata, Paseo del Bosque S/N, La Plata, Buenos Aires B1900, Argentina
Roy E. Plotnick
Affiliation:
Department of Earth and Environmental Sciences, University of Illinois Chicago, Chicago, Illinois 60607, U.S.A.
Stephanie M. Plaza-Torres
Affiliation:
Department of Geological Sciences, University of Colorado Boulder, Boulder, Colorado 80309, U.S.A.
Arthur Porto
Affiliation:
Florida Museum of Natural History, University of Florida, Gainesville, Florida 32605, U.S.A.
Albert Prieto-Márquez
Affiliation:
Institut Català de Paleontologia Miquel Crusafont (ICP-CERCA), Universitat Autònoma de Barcelona, c/ Escola Industrial 23, 08201 Sabadell, Barcelona, Spain
Surangi W. Punyasena
Affiliation:
Department of Plant Biology, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801, U.S.A.
Tiago B. Quental
Affiliation:
Departamento de Ecologia, Universidade de São Paulo, São Paulo, SP 05508-090, Brazil
Nussaïbah B. Raja
Affiliation:
GeoZentrum Nordbayern, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen 91054, Germany
Voajanahary Ranaivosoa
Affiliation:
Mention Bassins Sedimentaires Evolution Conservation, Université d’Antananarivo, Faculté des Sciences, Antananarivo101, Madagascar
Lauriane Ribas-Deulofeu
Affiliation:
Institute of Oceanography, National Taiwan University, Taipei 106, Taiwan
Florent Rivals
Affiliation:
ICREA, Pg. Lluis Companys 23, 08010 Barcelona, Spain Institut Català de Paleoecologia Humana i Evolució Social (IPHES-CERCA), Tarragona 43007, Spain Departament d’Història i Història de l’Art, Universitat Rovira i Virgili, 43002 Tarragona, Spain
Vanessa Julie Roden
Affiliation:
GeoZentrum Nordbayern, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen 91054, Germany
Antonietta Rosso
Affiliation:
Department of Biological, Geological and Environmental Sciences, University of Catania, 95129 Catania, Italy
Farid Saleh
Affiliation:
Institute of Earth Sciences, University of Lausanne, 1015, Lausanne, Switzerland
Rodrigo Brincalepe Salvador
Affiliation:
Finnish Museum of Natural History, University of Helsinki, Helsinki, Uusimaa 00100, Finland The Arctic University Museum of Norway, UiT–The Arctic University of Norway, Tromsø, Troms og Finnmark 9006, Norway
Erin E. Saupe
Affiliation:
Department of Earth Sciences, University of Oxford, Oxford OX1 3AN, U.K.
Simon Schneider
Affiliation:
CASP, Cambridge CB3 0UD, U.K.
Judith A. Sclafani
Affiliation:
Earth and Planetary Sciences, University of California Davis, Davis, California 95616, U.S.A.
Martin R. Smith
Affiliation:
Earth Sciences, University of Durham, Durham DH1 3LE, U.K.
Antoine Souron
Affiliation:
Université de Bordeaux, CNRS, Ministère de la Culture, PACEA, UMR 5199, F-33600 Pessac, France
Manuel J. Steinbauer
Affiliation:
Bayreuth Center of Ecology and Environmental Research (BayCEER) & Bayreuth Center of Sport Science (BaySpo), University of Bayreuth, Bayreuth 95448, Germany
Mathew Stewart
Affiliation:
Australian Research Centre for Human Evolution, Griffith University, Brisbane, Queensland 4111, Australia
Claudia P. Tambussi
Affiliation:
Centro de Investigaciones en Ciencias de la Tierra (CICTERRA), UNC, CONICET, X5016GCA Córdoba, Argentina
Ellen Thomas
Affiliation:
Department of Earth & Planetary Sciences, Yale University, New Haven, Connecticut 06511, U.S.A. Earth & Environmental Sciences, Wesleyan University, Middletown, Connecticut 06459, U.S.A.
Emanuel Tschopp
Affiliation:
Department of Animal Biodiversity, Universität Hamburg, Hamburg 20146, Germany Department of Vertebrate Paleontology, American Museum of Natural History, New York City, New York 10024, U.S.A. Freie Universität Berlin, Institute for Geological Sciences, 12249 Berlin, Germany
Thomas Tütken
Affiliation:
AG für Angewandte und Analytische Paläontologie, Institut für Geowissenschaften, Johannes Gutenberg-Universität Mainz, Mainz 55128, Germany
Sara Varela
Affiliation:
Department of Ecology and Animal Biology, Universidade de Vigo, Vigo, Galicia 36310, Spain
Raúl I. Vezzosi
Affiliation:
Laboratorio de Paleontología de Vertebrados, Centro de Investigaciones Científicas y Transferencia de Tecnología a la Producción (CONICET, Gob. E.R., UADER), España 149, Diamante E3105BWA, Argentina Cátedra de Paleontología, Facultad de Ciencia y Tecnología, Universidad Autónoma de Entre Ríos, Diamante, Entre Ríos E3105BWA, Argentina
Amelia Villaseñor
Affiliation:
Anthropology, University of Arkansas, Fayetteville, Arkansas 72764, U.S.A.
Manuel F. G. Weinkauf
Affiliation:
Institute of Geology and Palaeontology, Univerzita Karlova, Prague 128 43, Czech Republic
Lindsay E. Zanno
Affiliation:
Department of Biological Sciences, North Carolina State University, Raleigh, North Carolina 27695, U.S.A. North Carolina Museum of Natural Sciences, Raleigh, North Carolina 27601, U.S.A.
Chi Zhang
Affiliation:
Institute of Vertebrate Paleontology and Paleoanthropology, Chinese Academy of Sciences, Beijing 100044, China
Qi Zhao
Affiliation:
Institute of Vertebrate Paleontology and Paleoanthropology, Chinese Academy of Sciences, Beijing 100044, China
Wolfgang Kiessling
Affiliation:
GeoZentrum Nordbayern, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen 91054, Germany
*
Corresponding author: Jansen Smith; Email: smithja@d.umn.edu

Abstract

Paleontology provides insights into the history of the planet, from the origins of life billions of years ago to the biotic changes of the Recent. The scope of paleontological research is as vast as it is varied, and the field is constantly evolving. In an effort to identify “Big Questions” in paleontology, experts from around the world came together to build a list of priority questions the field can address in the years ahead. The 89 questions presented herein (grouped within 11 themes) represent contributions from nearly 200 international scientists. These questions touch on common themes including biodiversity drivers and patterns, integrating data types across spatiotemporal scales, applying paleontological data to contemporary biodiversity and climate issues, and effectively utilizing innovative methods and technology for new paleontological insights. In addition to these theoretical questions, discussions touch upon structural concerns within the field, advocating for an increased valuation of specimen-based research, protection of natural heritage sites, and the importance of collections infrastructure, along with a stronger emphasis on human diversity, equity, and inclusion. These questions offer a starting point—an initial nucleus of consensus that paleontologists can expand on—for engaging in discussions, securing funding, advocating for museums, and fostering continued growth in shared research directions.

Resumen

Resumen

La paleontología permite conocer la historia del planeta, desde los orígenes de la vida hace miles de millones de años hasta los cambios bióticos de épocas recientes. El ámbito de la investigación paleontológica es tan vasto como variado y está en constante evolución. En un esfuerzo por identificar las “grandes preguntas” de la paleontología, expertos de todo el mundo se reunieron para elaborar una lista de cuestiones prioritarias que el campo puede abordar en los próximos años. Las 89 preguntas aquí presentadas (agrupadas en 11 temas) representan las contribuciones de casi 200 científicos internacionales. Estas preguntas se refieren a temas comunes, entre los que se incluyen los motores y patrones de la biodiversidad, la integración de diferentes tipos de datos a lo largo de escalas espacio-temporales, la aplicación de datos paleontológicos para resolver cuestiones contemporáneas de biodiversidad y clima, y la utilización eficaz de métodos y tecnologías innovadoras para obtener nuevos conocimientos paleontológicos. Además de estos interrogantes teóricos, los debates abordan inquietudes estructurales dentro del campo, y abogan por una mayor valoración de la investigación basada en especímenes, la protección de los sitios del patrimonio natural y la importancia de la infraestructura de las colecciones; junto con un mayor énfasis en la diversidad humana, la equidad y la inclusión. Estas preguntas representan un punto de partida—un núcleo inicial de consenso que los paleontólogos pueden ampliar—para fomentar debates, obtener financiación, abogar por el apoyo a los museos y estimular el crecimiento continuo en direcciones de investigación compartidas.

Riassunto

Riassunto

La paleontologia offre spunti fondamentali per comprendere la storia del pianeta, dalle origini della vita miliardi di anni fa fino ai cambiamenti biotici più recenti. L’ambito della ricerca paleontologica è tanto vasto quanto diversificato e rappresenta un campo in continua evoluzione. In questo studio, esperti provenienti da tutto il mondo si sono riuniti per redigere un elenco di “Grandi Domande” prioritarie che la paleontologia potrà affrontare nei prossimi anni. Le 89 domande qui presentate, raggruppate in 11 temi, rappresentano il contributo di circa 200 scienziati internazionali. Queste domande riguardano tematiche come i meccanismi e i pattern di biodiversità, l’integrazione di varie tipologie di dati su scale spazio-temporali multiple, l’applicazione delle conoscenze paleontologiche ai problemi attuali della crisi climatica e della biodiversità, e l’uso efficace di metodi e tecnologie innovative per ottenere nuove intuizioni paleontologiche. Oltre a questi temi teorici, la discussione si focalizza su problematiche strutturali del campo, promuovendo una maggiore valorizzazione della ricerca basata sugli esemplari, la protezione dei siti di interesse culturale e paleontologico, e l’importanza delle infrastrutture per preservare le collezioni, insieme a una crescente enfasi su un apporto multiculturale, equo e inclusivo. Queste domande costituiscono un punto di partenza—un nucleo di consenso iniziale che i paleontologi possono espandere—per avviare discussioni, ottenere finanziamenti, promuovere i musei e favorire una crescita continua verso direzioni condivise di ricerca.

Information

Type
Review
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
Copyright
© The Author(s), 2025. Published by Cambridge University Press on behalf of Paleontological Society

Non-technical Summary

Paleontologists study the history of life on Earth, from its beginnings billions of years ago to the present day. To unify the discipline and develop a shared research agenda, nearly 200 scientists from more than 30 countries worked together to identify key questions for the future of paleontology. The resulting questions address topics including biodiversity, data integration, application of paleontology to societal issues, and utilizing new technology. Discussions also focus on topics related to improving the field, such as valuing specimen-based research, protecting fossil collecting sites, advocating for museums, and promoting diversity and inclusion among practitioners. These questions are a starting point for paleontologists for future developments of the discipline.

Introduction

Paleontology offers an important scientific contribution by asking questions about life throughout the billions of years of Earth’s history. The field itself has expanded from one based principally on collecting and documenting fossils to a hypothesis-driven, evidence-based field of inquiry using increasingly complex data, analytical approaches, and computational techniques. Paleontologists examine a range of topics about the history of life, including extinction, the evolution of organisms, biodiversity, the impact of climate changes, and the complex dynamics between life and other components of the Earth system. These comprehensive studies of life in the past provide critical context for understanding life on the planet today and the possible responses to ongoing environmental changes.

As in all scientific disciplines, the questions pursued by paleontologists fall on a spectrum, from large overarching questions that are central to the discipline to questions that are more specific and focus on smaller scales or pressing topics or contribute a component for addressing broader questions. The large overarching questions are likely to be persistent, but we can begin to address these grand themes by asking specific questions at various levels of resolution. For example, while a consensus exists on the principal features of the broad trajectory of life preserved in the fossil record, continued and closer examination of the record is required to resolve the details of evolutionary processes, environmental perturbations, and random effects that led to the modern configuration of life on Earth. As the resolution of studies becomes more specific, questions can range from “To which taxon does this specimen belong?” to questions such as “What is the role of abiotic and biotic interactions in driving biodiversity patterns?” Whereas “smaller” questions like the former are foundational to studying paleontology and merit support on their own, it is questions such as the latter (i.e., a “Big Question”) that are the scope of this paper, as they indicate the current state of the discipline and its aims for future scientific development.

Through the Big Questions project detailed herein, we seek to provide a road map for how paleontological research might develop in the coming years, as prioritized by members of the paleontological community. A Big Question (BQ) is defined here as an open-ended question of high scientific importance that can be answered within a reasonable time frame. Defined in this way, BQs become priority questions that can be used to emphasize the importance of the discipline to the larger research community, as well as to direct scientific effort and research funding (Sutherland et al. Reference Sutherland, Adams, Aronson, Aveling, Blackburn, Broad and Ceballos2009; Willis and Bhagwat Reference Willis and Bhagwat2010; Parsons et al. Reference Parsons, Favaro, Aguirre, Bauer, Blight, Cigliano and Coleman2014; Seddon et al. Reference Seddon, Mackay, Baker, Birks, Breman, Buck and Ellis2014). For our purposes, we considered a reasonable time frame to be several years, although some questions may require a longer duration to address (e.g., the duration of a career). The amount of time needed to answer a BQ with precision and accuracy is variable and dependent on many factors, including technological advances and available resources.

The answer to a BQ should represent a substantive leap forward in the community’s understanding of an issue or address a knowledge gap. “Scientific importance” requires examination of the perceived value of a BQ within the paleontological community, the broader scientific community, and its transference to society at large. Incorporating a diverse set of individuals engaged in paleontological research increases the confidence with which we can present research directions that can justifiably be defined as scientifically important to the international paleontological community. As such, the Big Questions project represents a democratic perspective of the paleontological discipline by individuals conducting germane research; we acknowledge that this effort was influenced by the opinions of those who participated, who represent a small percentage of the global paleontological community.

As the discipline of paleontology continues to grow in scope and application, paleontologists have a responsibility to routinely reflect on, criticize, discuss, and refine research directions, the best practices for conducting professional activities, and the cohesion of the discipline across geopolitical boundaries. Here we present the outputs of such an effort, providing an examination of the current state of paleontological research as expressed by the questions pursued in this discipline.

Methods

Project Contributors

The Big Questions project is a community initiative, coordinated through the PaleoSynthesis Project, that sought to engage a broad range of scientists working in paleontology and related disciplines (e.g., archaeology, biology, climate science, geology). Members of the Big Questions coordination team (J.A.S., W.K.) invited participation from the community through three solicitations requesting the submission of BQs in 2020 and 2021 (Fig. 1). The first solicitation was distributed in June 2020 using the PaleoNet listserver and to members of societies including the Palaeontological Association, Paleontological Society, and Paläontologische Gesellschaft. To reach a broader audience, the coordination team issued a second call in January 2021, again using PaleoNet, but expanding to include social media (Facebook; Twitter, now X) and listservers for the Ecological Society of America (Ecolog-L) and the Conservation Paleobiology Network (CPN-L).

Figure 1. The question pathway in the Big Questions project. Questions were submitted by the global community in one of three solicitations. Submitted questions were assigned to working groups (n = 12) composed of self-identified topic experts who chose to participate in the project. Working groups were guided by one to three leaders (larger icons) and refined their assigned questions to a preliminary list. These preliminary questions were assessed by the entire Big Questions team to improve question quality and reduce redundancies in questions from different groups. Using whole-team feedback, working groups (reduced to 11 due to overlaps; Table 2) produced a refined set of final big questions. Created with BioRender.com.

In March 2021, the first virtual, plenary meeting was held for those individuals who indicated they would like to contribute to the project. As an outcome, participants in the meeting recognized that the group was dominated by individuals from the United States and Europe (Table 1). Consequently, a third solicitation was distributed in late March 2021 using the same approach as the second solicitation, this time with versions in English, French, Italian, Chinese, and Spanish (reflecting widely spoken language proficiencies in the existing group of participants). Participants involved via the first two solicitations were encouraged to use their personal networks to invite participants from places and with backgrounds not already represented in the project.

Table 1. Countries and administrative regions represented in the Big Questions project by affiliations of the authorship team at the time of manuscript submission, with respect to when individuals joined the project. Note: as countries and administrative regions represented are derived from the institutional affiliations of the authors, this is likely an underestimate of the number of countries and administrative regions represented by individuals in this project

Working Group Assignments

As a part of the first two solicitations, participants were asked to submit questions they felt were outstanding in the field of paleontology (Table 2). The coordination team then created 12 themes that captured as much of the variation as possible from the submitted questions. Individuals who joined the Big Questions project during the third solicitation were asked to self-select the best category for their questions, as the 12 themes had already been established. All assignments (from all solicitations) were checked for consistency, and when a question pertained to multiple themes, it was assigned to each relevant theme (Fig. 2). Ten of the groups focused on scientific questions (one of which was dropped due to overlaps with questions in related groups; Table 2) and two groups centered on structural issues relating to how paleontology is practiced, as scientific questions and scientific practice are not distinct domains.

Table 2. Working group themes and numbers of questions related to these groups at three stages of the project. The number of individuals assigned to each group is also provided, with the number of group leaders in parentheses. *The theme “Ecosystems, Environments, and their Records” was included originally, but after the whole-team feedback phase (Fig. 1), considerable overlaps with questions from other groups were apparent, and all questions from this theme were ultimately distributed elsewhere or subsumed by questions in other groups. Total is greater than the number of submitted questions (n = 528), because a question that was relevant to more than one group was assigned to each group for consideration

Figure 2. Assignments of originally submitted questions to different working groups. Each question was assigned to at least one group, and many were also assigned to a second group with topic overlap. Width of the outer circle represents the number of questions assigned to each working group (counts also provided in parentheses). Bands connecting different working groups represent the questions assigned to each of the groups, with thicker bands indicating a larger number of questions shared between groups. Created in R Statistical Software (v. 4.3.1; R Core Team Reference Team2023) using the circlize package (Gu et al. Reference Gu, Gu, Eils, Schlesner and Brors2014) and the Paired palette from RColorBrewer (Neuwirth Reference Neuwirth2022).

All participating individuals were asked to rank their top five theme preferences (Table 2) and assigned to their highest available preference, while attempting to balance numbers and diverse group composition using inferences regarding aspects to participants’ identities (e.g., career stage, country, gender identity). Such inferences are undoubtedly flawed (e.g., institutional affiliation may not reflect a participant’s nationality), but were an attempt to form diverse groups using incomplete information. Participants were given the additional option to join one of the groups addressing structural issues (“Fundamental Issues,” “Looking Inward and Outward”). All participants were given the option to volunteer as a working group leader, and one to three leaders were selected for each group from those volunteers, with consideration for representation of the diverse backgrounds of individuals participating in the project.

Refinement of Big Questions

Under the direction of working group leaders, the working groups were tasked with refining the set of questions assigned to their themes (Supplementary Material 1) into a condensed set of 8–12 preliminary questions. As a guide for this process, all were asked to consider the following discrete criteria (from Sutherland et al. Reference Sutherland, Adams, Aronson, Aveling, Blackburn, Broad and Ceballos2009) for what a BQ entails:

  1. 1. Addresses an important gap in knowledge

  2. 2. More than just a general topic area (e.g., climate change)

  3. 3. Answerable through a realistic research design

  4. 4. Has a spatial and temporal scale that can be addressed by a research team

  5. 5. Has a factual answer that does not depend on value judgments

  6. 6. Tends not to be situationally dependent (i.e., answerable with “it all depends”)

  7. 7. Is not likely to be answerable with “yes” or “no”

Groups accomplished this goal through a combination of strategies, chosen by group leaders, including one or more of: (1) separating questions into subthemes and condensing on common ideas; (2) formation of subgroups to evaluate subsets of questions; (3) virtual meetings to discuss refinements; and (4) drafting of questions to combine those that existed or cover omitted topics.

Following refinement of the preliminary questions by each group, all questions were compiled for cross-group comments. Participants were asked to suggest revisions, evaluate the importance of each question, and identify overlaps. The coordination team then compiled and summarized responses according to the importance of questions and overlaps. Group leaders coordinated efforts within and among groups to refine the questions further on the basis of this compiled information (Tables 313). Finally, each working group drafted text to contextualize their questions, forming the first version of this article.

Table 3. Big Questions for the working group on “The Adequacy of the Fossil Record”

The Big Questions in Paleontology

The three solicitations for submission of Big Questions resulted in 528 contributed questions. (Supplementary Material 1: Raw Questions). The number of questions assigned to a given theme ranged from 14 to 76 (Table 2). Groups refined these questions (Supplementary Material 1: Preliminary Questions) to a preliminary list including 4 – 16 questions from each group (Table 2).

After feedback from all BQ participants, working groups again refined their questions, producing 5 – 10 final questions from each group (Table 2; Fig. 1). The BQs are available in Tables 313 (in non-ordered lists from each group), clustered in related themes, starting with questions pertaining to topics that might affect any paleontological study (e.g., preservation, scaling, taxonomy). In the eleven sections that follow, explanatory text accompanies the set of questions from each working group, with questions referred to in the text by working group acronyms (see section headers and tables for acronyms) and non-ordered, unranked numbering. Given the strong relationships among different areas of research in paleontology, there are overlaps in the topics of some questions, which can be taken to indicate important, cross-cutting themes within the discipline (Fig. 2).

The Adequacy of the Fossil Record (AFR; Table 3)

The fossil record is our primary window into the origin and evolution of life on Earth, providing the only direct line of evidence for these events. Yet, the fossil record is composed primarily of organisms with anatomical, behavioral, and ecological attributes that enhance their preservation potential (AFR1, Table 3; Kidwell and Flessa Reference Kidwell and Flessa1996; Behrensmeyer et al. Reference Behrensmeyer, Kidwell and Gastaldo2000; Sansom et al. Reference Sansom, Gabbott and Purnell2010; Klompmaker et al. Reference Klompmaker, Portell and Frick2017; Saleh et al. Reference Saleh, Antcliffe, Lefebvre, Pittet, Laibl, Peris, Lustri, Gueriau and Daley2020, Reference Saleh, Bath-Enright, Daley, Lefebvre, Pittet, Vite and Ma2021). Preservational biases are also often exacerbated by other biases introduced throughout the life of specimens (AFR2; e.g., Seilacher et al. Reference Seilacher, Reif and Westphal1985; Behrensmeyer et al. Reference Behrensmeyer, Kidwell and Gastaldo2000; Louys et al. Reference Louys, Kealy, O’Connor, Price, Hawkins, Aplin and Rizal2017; Krone et al. Reference Krone, Magoulick and Yohler2024)—for example, those relating to acquisition and curation, collecting, digitization, geography and geopolitics, publication, specimen preservation, storage, and transport (Flessa et al. Reference Flessa, Kowalewski and Walker1992; Whitaker and Kimmig Reference Whitaker and Kimmig2020; Raja et al. Reference Raja, Dunne, Matiwane, Khan, Nätscher, Ghilardi and Chattopadhyay2022; Johnson et al. Reference Johnson and Owens2023). Methods development for evaluating and mitigating these biases continues to be an important area of research (AFR1–AFR3; e.g., Dunhill et al. Reference Dunhill, Hannisdal and Benton2014; Stewart et al. Reference Stewart, Carleton and Groucutt2021; De Baets et al. Reference De Baets, Jarochowska, Buchwald, Klug and Korn2022; Na et al. Reference Na, Li, Krause, Zhu and Kiessling2023; Antell et al. Reference Antell, Benson and Saupe2024; Hohmann et al. Reference Hohmann, Koelewijn, Burgess and Jarochowska2024). Adding to the challenge presented by these biases, maintenance of existing collections and capacity for new collections are threatened by a lack of funding, curatorial staff, and adequate storage facilities, both physical and digital (AFR3; Allmon et al. Reference Allmon, Dietl, Hendricks, Ross, Rosenberg and Clary2018; Marshall et al. Reference Marshall, Finnegan, Clites, Holroyd, Bonuso, Cortez and Davis2018).

Differences in data collection and reporting methods can compound biases in paleontological studies, as researchers have specific purposes when they acquire data (AFR4), and these idiosyncrasies can limit future uses of the data. To reduce duplication of data, reduce research costs, and increase versatility, it is imperative to document and clearly communicate data acquisition and management practices (e.g., as through the extended specimen concept; Lendemer et al. Reference Lendemer, Thiers, Monfils, Zaspel, Ellwood, Bentley and LeVan2020; Hardisty et al. Reference Hardisty, Ellwood, Nelson, Zimkus, Buschbom, Addink and Rabeler2022; Monfils et al. Reference Monfils, Krimmel, Linton, Marsico, Morris and Ruhfel2022). Establishing best practices in these areas will benefit paleontology as we move toward a “big data” future (i.e., data characterized by great variety, volume, and/or velocity; Balazka and Rodighiero Reference Balazka and Rodighiero2020), and digitization of existing and new specimens is becoming increasingly common (AFR2; Berents et al. Reference Berents, Hamer and Chavan2010; Allmon et al. Reference Allmon, Dietl, Hendricks, Ross, Rosenberg and Clary2018).

Methodological, imaging, and analytical advances—geochemical approaches in particular (e.g., nontraditional stable isotopes, synchrotron, handheld XRF)—have created new opportunities for evaluating preservational processes (e.g., Gueriau et al. Reference Gueriau, Bernard and Bertrand2016; Teng et al. Reference Teng, Dauphas and Watkins2017). For example, advances in organic geochemistry have increased the capacity to extract biomolecules and biomarkers from fossil and sedimentary archives (e.g., Schweitzer et al. Reference Schweitzer, Avci, Collier and Goodwin2008; Briggs and Summons Reference Briggs and Summons2014; Vinther Reference Vinther2015; Falk and Wolkenstein Reference Falk and Wolkenstein2017; Demarchi Reference Demarchi2020; Wiemann et al. Reference Wiemann, Crawford and Briggs2020; McNamara et al. Reference McNamara, Rossi, Slater, Rogers, Ducrest, Dubey and Roulin2021). However, it remains to be seen how deep in time biomolecules can be found and with what accuracy and resolution the methods can be applied through geological time (AFR5). Inorganic geochemistry has also advanced fundamentally in the last decades, as stable isotope (traditional and nontraditional) and clumped isotope systems provide new insights in studies of pCO2, pH, paleophysiology, mass extinctions, and the paleobiology and paleoenvironment of fossil taxa (e.g., Casey and Post Reference Casey and Post2011; Cook et al. Reference Cook, Languille, Dufour, Mocuta, Tombret, Fortuna and Bertrand2015; Kimmig and Holmden Reference Kimmig and Holmden2017; Martin et al. Reference Martin, Tacail and Balter2017; Chen et al. Reference Chen, Montañez, Qi, Shen and Wang2018; Kral et al. Reference Kral, Lagos, Guagliardo, Tütken and Geisler2022; Jung et al., Reference Jung, Zoppe, Söte, Moretti, Duprey, Foreman and Wald2024). Geochemical advances and continuing improvements to technology and equipment also are expanding the scope of paleontology by enhancing our understanding of diagenesis, morphology, paleoecology, and paleoclimate (AFR6, AFR7; e.g., Smith et al. Reference Smith, Bevitt, Zaim, Rizal, Aswan and Trihascaryo2021; Abdelhady et al. Reference Abdelhady, Seuss, Jain, Abdel-Raheem, Elsheikh, Ahmed, Elewa and Hussain2024; Comans et al. Reference Comans, Smart, Kast, Lu, Lüdecke, Leichliter, Sigman, Ikejiri and Martínez‐García2024).

The changing global environment also presents new challenges and opportunities for sampling the fossil record (AFR8). For example, as sea level rises and extreme weather events become more common, some existing fossil collecting sites along the coasts may be submerged (e.g., chalk deposits in Europe), while the same processes might lead to the exposure of new sites (e.g., Reimann et al. Reference Reimann, Vafeidis, Brown, Hinkel and Tol2018; Vousdoukas et al. Reference Vousdoukas, Clarke, Ranasinghe, Reimann, Khalaf, Duong and Ouweneel2022). It is also likely that rising temperatures causing the loss of permafrost and glacial ice will expose previously inaccessible outcrops that offer new opportunities for research, even as the changing climate alters erosional processes that may influence fossil exposure and quality (AFR8; e.g., Clark et al. Reference Clark, Bayarsaikhan, Miller, Vanderwarf, Hart, Caspari and Taylor2021).

Scaling Ecological and Evolutionary Processes and Patterns (SEP; Table 4)

The scale of an investigation influences the observation and interpretation of ecological and evolutionary processes (SEP1–SEP4, Table 4). In paleontology, scale often relates to the temporal and spatial dimensions of taxa, patterns, or processes (SEP2, SEP3). Ecological and evolutionary processes occur at multiple spatiotemporal scales, but identifying or demonstrating their significance at all scales is challenging and rare (SEP4; Jablonski Reference Jablonski2008; Price and Schmitz Reference Price and Schmitz2016; Rapacciuolo and Blois Reference Rapacciuolo and Blois2019; Louys et al. Reference Louys, Price and Travouillon2021; Liow et al. Reference Liow, Uyeda and Hunt2023). Evaluating the effects of scaling in the fossil record is further complicated by the need to identify and address the incompleteness of the record (SEP3, SEP5; Peters and Heim Reference Peters and Heim2011; Benson et al. Reference Benson, Butler, Close, Saupe and Rabosky2021; and see “The Adequacy of the Fossil Record”). The data captured in the fossil record are imperfect and biased, providing only a glimpse of longer and shorter processes, patterns, and interactions (SEP3, SEP5–SEP7; Faith et al. Reference Faith, Du, Behrensmeyer, Davies, Patterson, Rowan and Wood2021; Flannery-Sutherland et al. Reference Flannery-Sutherland, Silvestro and Benton2022; Dunne et al. Reference Dunne, Thompson, Butler, Rosindell and Close2023).

Table 4. Big Questions for the working group on “Scaling Ecological and Evolutionary Processes and Patterns”

Paleontological research into the ecological and evolutionary drivers of observed patterns is flourishing, as emergent research areas—for example, conservation paleobiology (Dietl et al. Reference Dietl, Kidwell, Brenner, Burney, Flessa, Jackson and Koch2015; Dillon et al. Reference Dillon, Pier, Smith, Raja, Dimitrijević, Austin and Cybulski2022), geobiology (Knoll et al. Reference Knoll, Canfield and Konhauser2012), and phylogenetic paleoecology (Lamsdell et al. Reference Lamsdell, Congreve, Hopkins, Krug and Patzkowsky2017)—bridge subdisciplines and broach connections between the micro- and macroevolutionary scales (SEP2, SEP5 – 7; e.g., Machado et al. Reference Machado, Mongle, Slater, Penna, Wisniewski, Soffin, Dutra and Uyeda2023; Rolland et al. Reference Rolland, Henao-Diaz, Doebeli, Germain, Harmon, Knowles, Liow, Mank, Machac and Otto2023). Paleontologists must grapple with demonstrating links to the biology of modern organisms (i.e., neontology) in studies at various scales in the fossil record (Dietl et al. Reference Dietl, Smith and Durham2019; Rapacciuolo and Blois Reference Rapacciuolo and Blois2019). Unifying paleo- and neontological data can reveal more about the natural world than either could in isolation (e.g., Hlusko et al. Reference Hlusko, Schmitt, Monson, Brasil and Mahaney2016; Smith et al. Reference Smith, Rillo, Kocsis, Dornelas, Fastovich, Huang and Jonkers2023c); however, the efficacy of cross-scale analyses needs continued examination. Macroecology (Brown Reference Brown1995; McGill Reference McGill2019) may provide one option to incorporate a conceptual basis for this work as, for example, studies of the metacommunity concept—a set of local communities that are linked by dispersal of multiple, potentially interacting species (Leibold et al. Reference Leibold, Holyoak, Mouquet, Amarasekare, Chase, Hoopes and Holt2004)—provide a framework for examining scale-based problems. A tenet of this concept is that the study of local patterns and processes is not sufficient to understand the structure and dynamics of a metacommunity (Leibold et al. Reference Leibold, Holyoak, Mouquet, Amarasekare, Chase, Hoopes and Holt2004). Studying metacommunity composition and community assembly over space and time acknowledges the fluidity and connection of communities and seeks common patterns across metacommunities (SEP6; e.g., Muscente et al. Reference Muscente, Prabhu, Zhong, Eleish, Meyer, Fox, Hazen and Knoll2018, Reference Muscente, Martindale, Prabhu, Ma, Fox, Hazen and Knoll2022; Eden et al. Reference Eden, Manica and Mitchell2022; Gibert et al. Reference Gibert, Zacaï, Fluteau, Ramstein, Chavasseau, Thiery and Souron2022). The relationship between the processes on evolutionary scales, their relative influence, and fluctuations through time continue to be important topics (SEP2, SEP4, SEP8).

Over the course of Earth’s history, the biosphere has had a profound impact on the geosphere in ways that we are still working to fully comprehend (SEP9). Studying the interaction from an abiotic perspective highlights the feedback mechanisms and interactions within the Earth–life system, as traces of life are ubiquitous from Earth’s mantle to the atmosphere (Pawlik et al. Reference Pawlik, Buma, Šamonil, Kvaček, Galązka, Kohout and Malik2020; Giuliani et al. Reference Giuliani, Drysdale, Woodhead, Planavsky, Phillips, Hergt, Griffin, Oesch, Dalton and Davies2022).

Phylogenetics, Taxonomy, and Systematics (PTS; Table 5)

The fossil record contains unique information on the diversity of previous life-forms and their relationships to one another, which provides retrospective context for cataloging and understanding life on the planet today. Phylogenetics is often perceived simply as a tool for inferring evolutionary relationships or organizing biodiversity but also can be seen more broadly as a framework for hypothesis testing and reconstructing past events that are not directly observable in the fossil record (Bromham Reference Bromham2016). This can include estimating species divergence times, studying trait evolution, or quantifying diversification dynamics. Although speciation and extinction have a long history of study, these processes are complex, and some aspects require further study to improve our understanding (PTS1, PTS2, Table 5). By adopting new methodologies, improving data collection practices, and integrating various types of data centered around current, carefully constructed taxonomies, we can unlock the full potential of hypothesis testing using phylogenetic approaches (PTS3).

Table 5. Big Questions for the working group on “Phylogenetics, Taxonomy, and Systematics”

Phylogenies are often constructed using molecular data, but there are many benefits to including information from other sources, such as the fossil record (PTS4, PTS5; Parham et al. Reference Parham, Donoghue, Bell, Calway, Head, Holroyd and Inoue2012; Lee and Palci Reference Lee and Palci2015; Mongiardino Koch et al. Reference Mongiardino Koch, Garwood and Parry2021; Wright et al. Reference Wright, Bapst, Barido-Sottani and Warnock2022). Other data sources, such as developmental biology (Wright Reference Wright2015), may also prove useful in phylogenetic inference (PTS6). The field requires a multidisciplinary perspective informed by computer and data science, ecology, geology, geochronology, phylogenomics, and statistics (Parham et al. Reference Parham, Donoghue, Bell, Calway, Head, Holroyd and Inoue2012; Liow et al. Reference Liow, Uyeda and Hunt2023). Phylogenomics and deep learning can help to discern and organize biodiversity, but their accuracy will always depend on the quality of their input data, which necessitates reliable systematics and taxonomic identifications (e.g., Bortolus Reference Bortolus2008). The accuracy of phylogenetic analyses that include fossils relies on information about taxonomies and their associated uncertainties (Bortolus Reference Bortolus2008; Parham et al. Reference Parham, Donoghue, Bell, Calway, Head, Holroyd and Inoue2012; Soul and Friedman Reference Soul and Friedman2015; Barido-Sottani et al. Reference Barido-Sottani, Pohle, De Baets, Murdock and Warnock2023). Taxonomy and comparative anatomy are invaluable in understanding diversification history and character evolution, establishing homologies, quantifying variability, and generating testable hypotheses using phylogenetics and species delimitation methods (Barido-Sottani et al. Reference Barido-Sottani, Pohle, De Baets, Murdock and Warnock2023). These research fields must be supported in their own right (Agnarsson and Kuntner Reference Agnarsson and Kuntner2007; Löbl et al. Reference Löbl, Klausnitzer, Hartmann and Krell2023; Smith et al. Reference Smith, Raja, Clements, Dimitrijević, Dowding, Dunne and Gee2023b).

Integrating different data types requires explicit process-based models (PTS7, PTS8), such as the fossilized birth–death model, which models speciation, extinction, and fossilization simultaneously (Stadler Reference Stadler2010; Heath et al. Reference Heath, Huelsenbeck and Stadler2014). Combined with models of molecular and morphological evolution, this framework allows for statistical inference of dated phylogenies that include extant and fossil taxa. Most existing models treat speciation and character evolution as independent (Warnock and Wright Reference Warnock and Wright2020), but further refinement of this framework can illuminate the tempo and mechanisms of speciation (PTS1). Comprehensive analyses also require approaches that capture uncertainty and biases while concurrently allowing for varied approaches to weighting of molecular and morphological data (PTS9). We can construct explicit Bayesian hierarchical models to incorporate different data types while accounting for uncertainty in a principled and intuitive way (e.g., Höhna et al. Reference Höhna, Landis, Heath, Boussau, Lartillot, Moore, Huelsenbeck and Ronquist2016; Bouckaert et al. Reference Bouckaert, Vaughan, Barido-Sottani, Duchêne, Fourment, Gavryushkina and Heled2019; Ronquist et al. Reference Ronquist, Kudlicka, Senderov, Borgström, Lartillot, Lundén, Murray, Schön and Broman2021). It is also imperative to assess the trade-off between data availability, computational efficiency, and model complexity. Simulations play an important role in confronting this challenge and parameter identifiability issues associated with phylogenetic models by helping to explore the performance of available methods, potential limitations of data, and the expectations under null hypotheses (Barido-Sottani et al. Reference Barido-Sottani, Pett, O’Reilly and Warnock2019; Louca and Pennell Reference Louca and Pennell2020; Höhna et al. Reference Höhna, Kopperud and Magee2022; Mulvey et al. Reference Mulvey, May, Brown, Höhna, Wright and Warnock2024).

Environmental and geological processes influence the course of evolution (e.g., Arakaki et al. Reference Arakaki, Christin, Nyffeler, Lendel, Eggli, Ogburn, Spriggs, Moore and Edwards2011; Hannisdal and Peters Reference Hannisdal and Peters2011; De Baets et al. Reference De Baets, Antonelli and Donoghue2016; Kocsis et al. Reference Kocsis, Reddin, Scotese, Valdes and Kiessling2021). Incorporating these processes into phylogenetics will elucidate their interaction with biological events, linking large-scale processes, such as the extent and timing of climatic change, continental breakup, or changes in depositional rates through time with evolutionary phenomena (PTS10).

Biodiversity Dynamics in Space and Time (BST; Table 6)

Quantifying and interpreting biodiversity dynamics over time is a long-standing theme in paleontology (Phillips Reference Phillips1860; Sepkoski et al. Reference Sepkoski, Bambach, Raup and Valentine1981; Benson et al. Reference Benson, Butler, Close, Saupe and Rabosky2021), leading to questions such as whether there are constraints on global biodiversity (BST1, Table 6; Alroy et al. Reference Alroy, Aberhan, Bottjer, Foote, Fürsich, Harries and Hendy2008; Harmon and Harrison Reference Harmon and Harrison2015; Rabosky and Hurlbert Reference Rabosky and Hurlbert2015; Close et al. Reference Close, Benson, Saupe, Clapham and Butler2020). Given the challenge of fully documenting modern biodiversity (Mora et al. Reference Mora, Tittensor, Adl, Simpson and Worm2011), we cannot expect to know absolute biodiversity in the past, but we can estimate relative changes in biodiversity. Genuine trajectories of biodiversity through time can be uncovered only if we can account for spatial differences and temporal changes in preservation potential, as well as other biases particular to the fossil record (e.g., Smiley Reference Smiley2018; Krone et al. Reference Krone, Magoulick and Yohler2024; and see “The Adequacy of the Fossil Record”). By dissecting the components of these trajectories, we can identify drivers of originations and extinctions in deep time (BST5; and see “Adaptations, Innovations, Origins”). To fully understand biodiversity, we must first agree on the most effective methods for measuring biodiversity over different timescales (BST6; see “Scaling Ecological and Evolutionary Processes and Patterns”). Such a consensus can help address pressing questions, including whether modern biodiversity is an outlier in geological time (BST7).

Table 6. Big Questions for the working group on “Biodiversity Dynamics in Space and Time”

Spatial aspects of biodiversity, such as the latitudinal diversity gradient (Humboldt Reference Humboldt1808), are as important as temporal patterns. An extensive literature explores causes of the latitudinal diversity gradient, including its dynamics over geological timescales (Jablonski et al. Reference Jablonski, Roy and Valentine2006; Allen et al. Reference Allen, Wignall, Hill, Saupe and Dunhill2020, Reference Allen, Clapham, Saupe, Wignall, Hill and Dunhill2023; Zacaï et al. Reference Zacaï, Monnet, Pohl, Beaugrand, Mullins, Kroeck and Servais2021; Fenton et al. Reference Fenton, Aze, Farnsworth, Valdes and Saupe2023; Quintero et al. Reference Quintero, Landis, Jetz and Morlon2023). Evidence points to a close link between the intensity of the latitudinal diversity gradient and paleoclimate (Mannion et al. Reference Mannion, Upchurch, Benson and Goswami2014; Yasuhara et al. Reference Yasuhara, Wei, Kucera, Costello, Tittensor, Kiessling and Bonebrake2020; Yasuhara and Deutsch Reference Yasuhara and Deutsch2022), but exactly how the latitudinal diversity gradient changed over time remains an open question (BST2).

Biodiversity patterns are the result of extinctions, originations, and the intricate interactions between living organisms and their environment. Identifying the specific factors that drive global changes in biodiversity and disentangling the individual and combined effects of these factors require careful research and analysis (BST3; and see “Biodiversity Drivers”). Approaches leveraging new tools—including mechanistic models (e.g., Saupe et al. Reference Saupe, Myers, Peterson, Soberón, Singarayer, Valdes and Qiao2019), machine learning (e.g., Raja et al. Reference Raja, Lauchstedt, Pandolfi, Kim, Budd and Kiessling2021), and network analysis (e.g., Muscente et al. Reference Muscente, Prabhu, Zhong, Eleish, Meyer, Fox, Hazen and Knoll2018, Reference Muscente, Martindale, Prabhu, Ma, Fox, Hazen and Knoll2022; Woodhouse et al. Reference Woodhouse, Swain, Fagan, Fraass and Lowery2023)—can identify key drivers of global and regional biodiversity and biodiversity hotspots through time (Cermeño et al. Reference Cermeño, García-Comas, Pohl, Williams, Benton, Chaudhary and Le Gland2022) or at least provide testable hypotheses. We are only beginning to understand and quantify the role of biodiversity as a driver of ecosystem function in the paleontological record (BST4), underscoring the need for consistent units of measure across spatiotemporal scales (BST6; McGuire et al. Reference McGuire, Lawing, Díaz and Stenseth2023).

Biodiversity Drivers (BD; Table 7)

In paleontology, documenting patterns of biodiversity is a central theme, but understanding the factors that drive these patterns is a large task (Jablonski Reference Jablonski2008, Reference Jablonski2017; Ezard et al. Reference Ezard, Quental and Benton2016; Di Martino et al. Reference Di Martino, Jackson, Taylor and Johnson2018). We can, however, begin to address this challenge by decomposing the task into more manageable questions and hypotheses that extend across taxonomic levels. Comparing taxa with differing ecological characteristics (BD1, Table 7) may help disentangle prevailing drivers—including anthropogenic drivers—under shared and disparate environmental conditions or times of perturbation (BD2; Harnik Reference Harnik2011; Klompmaker et al. Reference Klompmaker, Schweitzer, Feldmann and Kowalewski2013; Hull et al. Reference Hull, Darroch and Erwin2015; Trubovitz et al. Reference Trubovitz, Renaudie, Lazarus and Noble2023). To compare the potential drivers across taxonomic groups and to do so on different spatial and temporal scales, it is crucial to standardize, harmonize, and clearly communicate study design and methods (Hayek et al. Reference Hayek, Buzas and Thomas2019). Doing so will help us establish broader principles that transcend specific taxonomic, spatial, and temporal contexts (BD3).

Table 7. Big Questions for the working group on “Biodiversity Drivers”

Abiotic and biotic conditions change through time at varying rates and magnitudes, and their effects on biodiversity and ecosystem dynamics warrant further study (BD4, BD7). It has been suggested that abiotic drivers act over broad spatiotemporal scales (e.g., Court Jester model; Barnosky Reference Barnosky2001), whereas biotic drivers are more applicable on local and shorter scales (e.g., Red Queen model; Benton Reference Benton2009; Vermeij and Roopnarine Reference Vermeij and Roopnarine2013; Wisz et al. Reference Wisz, Pottier, Kissling, Pellissier, Lenoir, Damgaard and Dormann2013). The relative significance of these sets of drivers remains uncertain (BD6; e.g., Eichenseer et al. Reference Eichenseer, Balthasar, Smart, Stander, Haaga and Kiessling2019; Bush and Payne Reference Bush and Payne2021; Spiridonov and Lovejoy Reference Spiridonov and Lovejoy2022), underscoring the importance of conceptual models for how biodiversity responds to them (Vrba Reference Vrba1985, Reference Vrba1992, Reference Vrba1993; Mancuso et al. Reference Mancuso, Irmis, Pedernera, Gaetano, Benavente and Breeden2022). There is evidence that diversification patterns observed at higher taxonomic levels (e.g., family) are not always replicated at lower levels (e.g., species; Jablonski Reference Jablonski2007; Hendricks et al. Reference Hendricks, Saupe, Myers, Hermsen and Allmon2014; Balisi and Van Valkenburgh Reference Balisi and Van Valkenburgh2020). Across each of these variables, the effects of scale on which hypothesis is supported (i.e., biotic or abiotic drivers) merit further consideration—in some instances, relationships may be reversed when comparing shorter ecological and longer evolutionary timescales (BD3; e.g., De Baets et al. Reference De Baets, Huntley, Scarponi, Klompmaker and Skawina2021). Further exploration with differing spatiotemporal scales, taxonomic groups, and ecologies is needed, as it remains a challenge to dissect the complex interplay between ecology, microevolution, and macroevolution on geological timescales (BD8, BD9; e.g., Liow and Taylor Reference Liow and Taylor2019; Liow et al. Reference Liow, Uyeda and Hunt2023). Examining the reciprocal effects of biological evolution as an actor, as well as in feedbacks and as a primary driver in other Earth systems, is a promising research direction (BD5).

Adaptations, Innovations, Origins (AIO; Table 8)

The evolutionary history of many species (and higher taxa) is demarcated by adaptive novelties and innovations along with repeated migration, dispersal, and colonization events as species have evolved and survived through morphological adaptation, ontogenetic shifts, and novel behaviors (AIO1, Table 8; e.g., Nylin et al. Reference Nylin, Agosta, Bensch, Boeger, Braga, Brooks and Forister2018; Stigall Reference Stigall2019). Colonizing regions in new environments and adapting to cope with the challenges induced by new environmental pressures has led to the development and emergence of advantageous novelties over time. These novelties increase the capacity of individuals to survive, thrive, and reproduce (AIO1, AIO2; e.g., Patton et al. Reference Patton, Harmon, del Rosario Castañeda, Frank, Donihue, Herrel and Losos2021; Tihelka et al. Reference Tihelka, Howard, Cai and Lozano-Fernandez2022; Woehle et al. Reference Woehle, Roy, Glock, Michels, Wein, Weissenbach and Romero2022). Observing modern species and their responses to stimuli provides paleontologists with a means to connect microevolutionary processes and patterns to those observed over evolutionary timescales in the fossil record (AIO6), which are obscured by taphonomic processes (AIO3). Improving data integration across scales, leveraging new methods, and better accounting for biases can help us answer long-standing questions on topics relating to phylogenomic conflict (Parins-Fukuchi et al. Reference Parins-Fukuchi, Stull and Smith2021), evolutionary patterns (e.g., phyletic gradualism vs. punctuated equilibrium; Gould and Eldredge Reference Gould and Eldredge1972; Hunt Reference Hunt2007; Hunt et al. Reference Hunt, Hopkins and Lidgard2015; Tsuboi et al. Reference Tsuboi, Sztepanacz, De Lisle, Voje, Grabowski, Hopkins and Porto2024), and phylogenetic relationships (Wright et al. Reference Wright, Bapst, Barido-Sottani and Warnock2022).

Table 8. Big Questions for the working group on “Adaptations, Innovations, Origins”

The interdependence among ecological determinants and biological features requires thorough examination to reveal the inextricable relationship between micro- and macroevolutionary processes, environmental change, and preservation (AIO4–AIO6; e.g., Lamsdell et al. Reference Lamsdell, McCoy, Perron-Feller and Hopkins2020; Almécija et al. Reference Almécija, Hammond, Thompson, Pugh, Moyà-Solà and Alba2021; and see “The Adequacy of the Fossil Record”). To develop these research directions (AIO5–AIO7), hypotheses on the emergence of major features (e.g., Naranjo-Ortiz and Gabaldón Reference Naranjo-Ortiz and Gabaldón2019; Murdock Reference Murdock2020), changes in morphology (e.g., Anderson and Ruxton Reference Anderson and Ruxton2020; Hopkins and To Reference Hopkins and To2022), ontogeny (e.g., Chevalier et al. Reference Chevalier, Colard, Colombo, Golovanova, Doronichev and Hublin2021; Friend et al. Reference Friend, Anderson and Allmon2021; Lanzetti et al. Reference Lanzetti, Portela-Miguez, Fernandez and Goswami2022), and behavior (e.g., Berbee et al. Reference Berbee, Strullu-Derrien, Delaux, Strother, Kenrick, Selosse and Taylor2020; Yamamoto and Caterino Reference Yamamoto and Caterino2023) require contextualization with spatiotemporal, taphonomic, and preservational constraints (AIO3, AIO4). Answering these questions can facilitate the examination of overarching patterns in biotic developmental and community responses to perturbation throughout the history of life and can possibly be projected to the future (AIO6). Studies on the emergence of adaptations, innovative features, ontogenetic strategies, behaviors, and the development of novelties can provide paleontology with crucial insights into the processes of evolution and extinction, as well as the interactions between individuals, species, and communities (AIO5–AIO7; Barido-Sottani et al. Reference Barido-Sottani, Van Tiel, Hopkins, Wright, Stadler and Warnock2020; Brocklehurst and Benson Reference Brocklehurst and Benson2021; Stansfield et al. Reference Stansfield, Mitteroecker, Vasilyev, Vasilyev and Butaric2021; Dunhill et al. Reference Dunhill, Zarzyczny, Shaw, Atkinson, Little and Beckerman2024).

Extinction Dynamics (ED; Table 9)

The understanding that species are ephemeral and will eventually become extinct is now a fundamental principle of paleontology (Cuvier Reference Cuvier1813; Darwin Reference Darwin1859; MacLeod Reference MacLeod2014; Marshall Reference Marshall2017)—and potentially scales up from species to faunas and paleocommunities (e.g., Muscente et al. Reference Muscente, Martindale, Prabhu, Ma, Fox, Hazen and Knoll2022). This concept is integral to the study of the history of life on Earth, as it helps to explain changes in biodiversity observed in the fossil record (Jablonski Reference Jablonski1991; McKinney Reference McKinney1997). At the same time, extinction is a major theme in modern bioscience relating to impacts of anthropogenic stressors (e.g., climate change, habitat change, pollution; McKinney Reference McKinney1997; Dirzo et al. Reference Dirzo, Young, Galetti, Ceballos, Isaac and Collen2014). As is usual for comparisons of the modern and fossil records, attempting to bridge the differences in study characteristics (e.g., evolutionary history of ecosystems; spatiotemporal completeness, extent, and resolution; taxonomic completeness; Foote Reference Foote2000; Eichenseer et al. Reference Eichenseer, Balthasar, Smart, Stander, Haaga and Kiessling2019; Foster et al. Reference Foster, Allen, Kitzmann, Münchmeyer, Rettelbach, Witts and Whittle2023; Pohl et al. Reference Pohl, Stockey, Dai, Yohler, Le Hir, Hülse, Brayard, Finnegan and Ridgwell2023; Finnegan et al. Reference Finnegan, Harnik, Lockwood, Lotze, McClenachan and Kahanamoku2024) over which extinction can be observed necessitates reflection on which data types are suitable to facilitate cross-scale studies and comparisons (ED1, Table 9; Lotze et al. Reference Lotze, Erlandson, Hardt, Norris, Roy, Smith, Whitcraft, Jackson, Alexander and Sala2011; Andréoletti and Morlon Reference Andréoletti, Morlon and Scheiner2024).

Table 9. Big questions for the working group on “Extinction Dynamics”

The “BigFive” mass extinctions originally were defined using the concept of statistical outliers (Raup and Sepkoski Reference Raup and Sepkoski1982) at a high taxonomic level, using a specific rate metric, and based on skeletonized marine organisms. An updated definition of mass extinction is long overdue, as is a dialogue on how pattern and process should be included in the definition (ED2; Marshall Reference Marshall2023). This definition would precipitate the reexamination of whether mass extinctions are associated with consistent vulnerabilities of specific morphological and ecological traits (ED3, ED4; Foster et al. Reference Foster, Allen, Kitzmann, Münchmeyer, Rettelbach, Witts and Whittle2023) and whether their phases and recovery patterns are comparable (ED6, ED7; Hull et al. Reference Hull, Darroch and Erwin2015).

Another aspect of extinction dynamics, pertaining to the ecological impact of the event, is whether functional diversity is maintained across mass extinction events (ED5; Bambach et al. Reference Bambach, Bush and Erwin2007; Foster and Twitchett Reference Foster and Twitchett2014; Aberhan and Kiessling Reference Aberhan and Kiessling2015; Dunhill et al. Reference Dunhill, Foster, Sciberras and Twitchett2018; Muscente et al. Reference Muscente, Prabhu, Zhong, Eleish, Meyer, Fox, Hazen and Knoll2018; Cribb et al. Reference Cribb, Formoso, Woolley, Beech, Brophy, Byrne and Cassady2023). Mass extinctions are often attributed to abiotic changes (e.g., changes in temperature, oxygen content, pH), and finding thresholds relating to magnitudes and rates of such changes remains a priority (ED8; Song et al. Reference Song, Kemp, Tian, Chu, Song and Dai2021). Species also are likely to experience secondary extinction cascades due to the loss of critical biotic interactions (e.g., predator–prey relationships) in trophic or other biological interaction networks (Roopnarine Reference Roopnarine2006; Dunne and Williams Reference Dunne and Williams2009). If we are to truly understand the dynamics of extinction events in the fossil record and use them to predict extinction risk in our human-dominated world (Barnosky et al. Reference Barnosky, Matzke, Tomiya, Wogan, Swartz, Quental and Marshall2011; Braje and Erlandson Reference Braje and Erlandson2013; Song et al. Reference Song, Kemp, Tian, Chu, Song and Dai2021; Vahdati et al. Reference Vahdati, Weissmann, Timmermann, de León and Zollikofer2022), we need to understand the interplay between primary and secondary extinction events via the inclusion of biotic interactions in studies of extinction selectivity (e.g., Sanders et al. Reference Sanders, Thébault, Kehoe and van Veen2018; Mulvey et al. Reference Mulvey, Warnock and De Baets2022; Dunhill et al. Reference Dunhill, Zarzyczny, Shaw, Atkinson, Little and Beckerman2024).

Climate Change Past and Present (CPP; Table 10)

Paleontologists often reconstruct past climates using fossils or geochemical proxies, and this remains a major theme in the biogeosciences (CPP1, Table 10). For example, examining stable oxygen isotopes in fossils can reveal climate change across temporal scales, from the life span of individual organisms (e.g., Nützel et al. Reference Nützel, Joachimski and Correa2010; Alberti et al. Reference Alberti, Fürsich and Pandey2013) to the eon scale (e.g., Song et al. Reference Song, Wignall, Song, Dai and Chu2019; Grossman and Joachimski Reference Grossman and Joachimski2022). However, smoothly integrating data across these temporal scales remains challenging (CPP1). Assessing biotic responses to changing climates is becoming a major theme in paleontology, with several pertinent questions (CPP2–CPP9; e.g., Rita et al. Reference Rita, Nätscher, Duarte, Weis and De Baets2019; Piazza et al. Reference Piazza, Ullmann and Aberhan2020; Nätscher et al. Reference Nätscher, Gliwa, De Baets, Ghaderi and Korn2023). Nevertheless, it is critical to avoid circular reasoning where climate reconstructions based on fossil proxies subsequently are used to interpret fossils.

Table 10. Big Questions for the working group on “Climate Change Past and Present”

A host of variables—including direct and indirect measures of nutrient levels, temperature, pCO2, precipitation, salinity, pH, and, oxygen and other isotopes—can be used to examine the influence of climate on biodiversity (Bijma et al. Reference Bijma, Pörtner, Yesson and Rogers2013; Saupe et al. Reference Saupe, Myers, Peterson, Soberón, Singarayer, Valdes and Qiao2019; Jane et al. Reference Jane, Hansen, Kraemer, Leavitt, Mincer, North and Pilla2021; Jackson and O’Dea Reference Jackson and O’Dea2023; Lin et al. Reference Lin, Wei, Ho and Lo2023; Yasuhara and Deutsch Reference Yasuhara and Deutsch2023; Malanoski et al. Reference Malanoski, Farnsworth, Lunt, Valdes and Saupe2024). Elucidating the relative importance of these variables on biodiversity can guide conservation efforts (CPP2, CPP8), although best practices for bridging the mismatch in temporal scales studied in paleontology and those of interest to policymakers remain elusive (CPP3; Smith et al. Reference Smith, Durham, Dietl, Tyler and Schneider2018; Pimiento and Antonelli Reference Pimiento and Antonelli2022; Groff et al. Reference Groff, MacKenzie, Pier, Shaffer and Dietl2023; Kiessling et al. Reference Kiessling, Smith and Raja2023; and see “Scaling Ecological and Evolutionary Processes and Patterns”). Bridging these gaps can benefit from studies leveraging conservatism of physiology (Reddin et al. Reference Reddin, Nätscher, Kocsis, Pörtner and Kiessling2020), simulations (e.g., Hunt Reference Hunt2012; Barido-Sottani et al. Reference Barido-Sottani, Pett, O’Reilly and Warnock2019; Raja et al. Reference Raja, Lauchstedt, Pandolfi, Kim, Budd and Kiessling2021; Smith et al. Reference Smith, Pruden, Handley, Durham and Dietl2023a), and the pursuit of higher-resolution paleontological datasets (Smith et al. Reference Smith, Rillo, Kocsis, Dornelas, Fastovich, Huang and Jonkers2023c). The application of paleontological observations to conservation practice remains primarily aspirational (Groff et al. Reference Groff, MacKenzie, Pier, Shaffer and Dietl2023); however, leveraging the need for temporal context to understand climate change is a promising avenue for integrating paleontological data (Smith et al. Reference Smith, Durham, Dietl, Tyler and Schneider2018; Dietl et al. Reference Dietl, Smith and Durham2019; Kiessling et al. Reference Kiessling, Raja, Roden, Turvey and Saupe2019, Reference Kiessling, Smith and Raja2023).

Climate sensitivity has been defined as the global mean temperature increase when atmospheric CO2 equivalent concentration is doubled (IPCC Reference Masson-Delmotte, Zhai, Pirani, Connors, Péan, Berger and Caud2021), and we can use this framework to define “ecosystem sensitivity” (CPP4). For example, how much will ecological structure—a concept challenging to objectively measure (e.g., Parrott Reference Parrott2010; LaRue et al. Reference LaRue, Fahey, Alveshere, Atkins, Bhatt, Buma and Chen2023)—change on average with a given increase in temperature? A more straightforward assessment of shifts in spatial distribution is also possible, as there is modern (Lenoir et al. Reference Lenoir, Bertrand, Comte, Bourgeaud, Hattab, Murienne and Grenouillet2020) and past (Wing et al. Reference Wing, Harrington, Smith, Bloch, Boyer and Freeman2005; McElwain Reference McElwain2018) evidence of species ranges tracking climate. Still, the signal is complex (Reddin et al. Reference Reddin, Kocsis and Kiessling2018, Reference Reddin, Nätscher, Kocsis, Pörtner and Kiessling2020), primarily due to sampling constraints and limited temporal resolution, and merits further examination (CPP5). In isolation from or in combination with range shifts, the degree to which species can adapt their niches over time is crucial to predicting how they will respond to ongoing climate change (CPP6). Fossil data support niche stability at low taxonomic levels (Hopkins et al. Reference Hopkins, Simpson and Kiessling2014; Saupe et al. Reference Saupe, Hendricks, Peterson and Lieberman2014; Stigall Reference Stigall2014; Antell et al. Reference Antell, Kiessling, Aberhan and Saupe2020); however, thermal tolerances have evolved across the domains of life (Storch et al. Reference Storch, Menzel, Frickenhaus and Pörtner2014), suggesting that the rate and relative frequency at which tolerances evolve are key features in niche evolution.

The impacts of climate change on biotic systems are numerous (Pörtner Reference Pörtner2021), but cascading effects are less well known (CPP7; e.g., Pecl et al. Reference Pecl, Araújo, Bell, Blanchard, Bonebrake, Chen and Clark2017; Słowiński et al. Reference Słowiński, Skubała, Zawiska, Kruk, Obremska, Milecka and Ott2018). For example, differential range shifts of species in response to climate may lead to novel communities, with new biotic interactions and elevated potential for secondary extinctions (ED9; Pecl et al. Reference Pecl, Araújo, Bell, Blanchard, Bonebrake, Chen and Clark2017; Chiarenza et al. Reference Chiarenza, Waterson, Schmidt, Valdes, Yesson, Holroyd and Collinson2023). Identifying cascading effects in the fossil record is likely difficult but important to reveal the interplay of abiotic and biotic drivers under climate change (O’Keefe et al. Reference O’Keefe, Dunn, Weitzel, Waters, Martinez, Binder and Southon2023).

Conservation Paleobiology (CPB; Table 11)

Conservation paleobiology, which seeks to apply the methods and theories of paleontology to the conservation and restoration of biodiversity and ecosystem services (Dietl et al. Reference Dietl, Kidwell, Brenner, Burney, Flessa, Jackson and Koch2015), has emerged as a pathway for paleontologists to engage with conservation issues. A key theme in these questions is the integration of multiple types of data and methods across scales (CPB2, CPB4, CPB6, Table 11) to provide insights about biodiversity change (CPB3–CPB5, CPB8). Questions in this section crosscut many of the other sections—especially “Climate Change Past and Present”—as conservation paleobiology is an emergent area of research in paleontology that is informed by the entire discipline.

Many paleontologists are seeking ways to more directly connect their science to practice (CPB1, CPB2, CPB8; Dillon et al. Reference Dillon, Pier, Smith, Raja, Dimitrijević, Austin and Cybulski2022). Although there are several success stories of paleontological data application (e.g., Everglades restoration; Marshall et al. Reference Marshall, Wingard and Pitts2014), only 10.8% of published conservation paleobiology studies have had a demonstrable effect on conservation practice (comparable to other areas of conservation science; see Groff et al. Reference Groff, MacKenzie, Pier, Shaffer and Dietl2023). A cultural shift in the norms and practices of the paleontological community is required to produce research results that more closely align with the needs and concerns of practitioners (Dietl et al. Reference Dietl, Durham, Clark and Prado2023). How to get there is a big question (CPB1). At the same time, questions that form the theoretical basis for conservation paleobiology (CPB3–CPB7) remain research priorities, offering opportunities for scientific progress while highlighting gaps in our understanding of biodiversity and ecosystem function and, by extension, ecosystem services (Dillon et al. Reference Dillon, Pier, Smith, Raja, Dimitrijević, Austin and Cybulski2022). For example, it remains a significant challenge to untangle the different drivers that push ecosystems beyond their natural limits and to understand the resulting responses over time (CPB5). The extent to which paleoecological records can be utilized to broaden the temporal perspective for detecting critical transitions in ecosystems and signals of changing resilience (CPB7) is also not fully understood. Nor is it known how, and under which circumstances, looking to the past can contribute productively to setting baselines for ecosystem recovery (CPB4) or anticipating a climate-changed future (CPB3). Such knowledge could support conservation management and planning efforts designed to help reduce the loss of biodiversity and ecosystem services (CPB8) in the face of environmental change. Theoretical development in these areas is foundational for paleontology and is essential for the discipline to grow as an applied area of research to provide insights about future changes in the human-dominated world (Dietl and Flessa Reference Dietl and Flessa2011; Dietl et al. Reference Dietl, Kidwell, Brenner, Burney, Flessa, Jackson and Koch2015, Reference Dietl, Smith and Durham2019; Barnosky et al. Reference Barnosky, Hadly, Gonzalez, Head, Polly, Lawing and Eronen2017; Dillon et al. Reference Dillon, Pier, Smith, Raja, Dimitrijević, Austin and Cybulski2022; Pimiento and Antonelli Reference Pimiento and Antonelli2022; Groff et al. Reference Groff, MacKenzie, Pier, Shaffer and Dietl2023; Kiessling et al. Reference Kiessling, Smith and Raja2023; Kowalewski et al. Reference Kowalewski, Nawrot, Scarponi, Tomašových and Zuschin2023; Zuschin Reference Zuschin2023).

Table 11. Big Questions for the working group on “Conservation Paleobiology”

Fundamental Issues (FI; Table 12)

Every scientific discipline relies on a dedicated community and supportive infrastructure. To protect paleontology’s foundational resources, infrastructure updates are needed (FI1, FI3, FI5, Table 12). Best practices for collecting, curating, and archiving paleontological data and heritage are developing, but a consensus remains a work in progress (FI1). Assigning specimens an accurate taxonomy in a sound systematic framework is critical for their utility and inclusion in a shareable resource (e.g., GBIF, iDigBio, the Paleobiology Database, FI3; Marshall et al. Reference Marshall, Finnegan, Clites, Holroyd, Bonuso, Cortez and Davis2018). The accuracy and resolution of taxonomic identifications strongly affect biodiversity measurements and interpretation, but this fundamental work is consistently undervalued in the current system for rewarding academics (FI3; Agnarsson and Kuntner Reference Agnarsson and Kuntner2007; Mabry et al. Reference Mabry, Zapata, Paul, O’Connor, Soltis, Blackburn and Simmons2022; Salvador et al. Reference Salvador, Cavallari, Rands and Tomotani2022; Smith et al. Reference Smith, Raja, Clements, Dimitrijević, Dowding, Dunne and Gee2023b). As a result, taxonomic expertise is under threat (e.g., Agnarsson and Kuntner Reference Agnarsson and Kuntner2007; Salvador et al. Reference Salvador, Cavallari, Rands and Tomotani2022). Even so, novel methods for taxonomic analysis (e.g., machine learning; Romero et al. Reference Romero, Kong, Fowlkes, Jaramillo, Urban, Oboh-Ikuenobe, D’Apolito and Punyasena2020; De Baets Reference De Baets2021; Punyasena et al. Reference Punyasena, Haselhorst, Kong, Fowlkes and Moreno2022; Abdelhady et al. Reference Abdelhady, Seuss, Jain, Abdel-Raheem, Elsheikh, Ahmed, Elewa and Hussain2024; Adaïmé et al. Reference Adaïmé, Kong and Punyasena2024) hold the potential to make taxonomic work more efficient, reproducible, and sustainable. Reliable taxonomic, locality, and stratigraphic information are essential for building physical (e.g., samples) and digital (e.g., metadata, imagery) storage infrastructure that allows comparison and integration among researchers and scientific disciplines (Löbl et al. Reference Löbl, Klausnitzer, Hartmann and Krell2023). These improvements require a community effort that is supported by sustainable long-term funding—particularly in the Global South (e.g., Valenzuela-Toro and Viglino Reference Valenzuela-Toro and Viglino2021; Raja et al. Reference Raja, Dunne, Matiwane, Khan, Nätscher, Ghilardi and Chattopadhyay2022). This funding can enable expanded accessibility, use, and combination of data, all of which are critical for facilitating interdisciplinary research (Allmon et al. Reference Allmon, Dietl, Hendricks, Ross, Rosenberg and Clary2018; Kaufman et al. Reference Kaufman2018; Smith et al. Reference Smith, Raja, Clements, Dimitrijević, Dowding, Dunne and Gee2023b). Through interdisciplinary research and study programs, the field can continue to expand (FI3). For example, studies of prehistory demonstrate long-standing human collection and use of fossils from the middle Pleistocene onward, creating new opportunities to understand human behavior through interactions with fossils (Cortés-Sánchez et al. Reference Cortés-Sánchez, Simón-Vallejo, Corral, Lozano-Francisco, Vera-Peláez, Jiménez-Espejo and García-Alix2020). Interdisciplinarity will continue to generate new creative approaches with valuable perspectives from other disciplines (e.g., archaeology, biology) while providing new insights on long-pursued questions in paleontology (FI2–FI4).

Table 12. Big Questions for the working group on “Fundamental Issues”

Paleontology is also economically and societally important (FI4, FI5). Economic contributions include resource exploration, regional tourism (Perini and Calvo Reference Perini and Calvo2008; Kibria et al. Reference Kibria, Akhundjanov and Oladi2019), and diverse products based on paleontological research (e.g., books, clothing, film and television works, theme parks, toys, video games). Aside from these outputs, paleontology requires greater valorization within the scientific community and broader public (FI4, FI5; Plotnick et al. Reference Plotnick, Anderson, Carlson, Jukar, Kimmig and Petsios2023). Geosites are non-renewable areas important for understanding Earth’s history through the observation of biological and geological phenomena. Protecting and conserving important outcrops (e.g., Atkinson et al. Reference Atkinson, Buta, Kopaska-Merkel, Buta, Rindsberg and Kopaska-Merkel2005; Maran Reference Maran2014; Mexicana Reference Mexicana2020; Neto De Carvalho et al. Reference Neto De Carvalho, Baucon, Bayet-Goll and Belo2021; Carvalho and Leonardi Reference Carvalho and Leonardi2022) and access to them necessitate transparent discussion among all who interact with and care about the sites (e.g., paleontologists, landowners, traditional custodians of the land, universities, industrial companies, museums, government). Additionally, collection spaces are the physical repositories of our geoheritage (e.g., museums, geological surveys) and require sustained support from governments, academics, and the public. The primary evidence that paleontologists rely on (physical specimens) is under threat due to restructuring in funding models and museum closures, which removes from the public a pathway for engagement with geoheritage. Public engagement provides a valuable means to increase the profile of paleontology. This work and the people involved in it require significant investment to draw together science, economy, and culture to care for Earth and life’s heritage (FI1, FI4, FI5).

As scientists, we have a responsibility to communicate with the public about our work, yet many researchers receive no formal training on how to perform this duty (e.g., Salvador et al. Reference Salvador, Tomotani, O’Donnell, Cavallari, Tomotani, Salmon and Kasper2021), and these activities are secondary in hiring and promotion decisions (FI2, FI4; e.g., Davies et al. Reference Davies, Putnam, Ainsworth, Baum, Bove, Crosby and Côté2021; Raja and Dunne Reference Raja and Dunne2022). Without an informed public, policymakers cannot craft legislation that benefits the greatest number of people, and individuals cannot make accurate data-driven decisions. The roles of paleontologists continue to diversify, with a large proportion of graduates working outside academia in settings with variable skill requirements (FI2; e.g., industry, conservation, education, government; Keane et al. Reference Keane, Gonzales and Robinson2021). Paleontologists need skills to make them academically, economically, and socially valuable so they can share information about the long-term changes and variability that life on Earth has experienced with increased proficiency.

Looking Inward and Outward (LIO; Table 13)

Whereas paleontologists are keenly aware of the taphonomic biases constraining our view of past biodiversity, we have not systematically studied the biases linked to the identities and practices shaping how we collect, analyze, and interpret the fossil record. Presently, socioeconomic factors disproportionately influence the sampling coverage of both modern ecosystems and past biodiversity (Cisneros et al. Reference Cisneros, Raja, Ghilardi, Dunne, Pinheiro, Fernández and Sales2022; Monarrez et al. Reference Monarrez, Zimmt, Clement, Gearty, Jacisin, Jenkins and Kusnerik2022; Raja et al. Reference Raja, Dunne, Matiwane, Khan, Nätscher, Ghilardi and Chattopadhyay2022). Many perspectives and data are missing, which contributes to an incomplete understanding of past and present global biodiversity and restricts the development of ecological and evolutionary theory (LIO1, Table 13; Mohammed et al. Reference Mohammed, Turner, Fowler, Pateman, Nieves-Colón, Fanovich and Cooke2022; Raja et al. Reference Raja, Dunne, Matiwane, Khan, Nätscher, Ghilardi and Chattopadhyay2022). Identifying and addressing these biases and challenges in paleontology (e.g., dominance of the English language; Cisneros et al. Reference Cisneros, Raja, Ghilardi, Dunne, Pinheiro, Fernández and Sales2022; Raja et al. Reference Raja, Dunne, Matiwane, Khan, Nätscher, Ghilardi and Chattopadhyay2022) and incorporating as many diverse perspectives as possible will lead to a better understanding of all aspects of life on Earth (LIO2, LIO3).

Table 13. Big Questions for the working group on “Looking Inward and Outward”

Though many people globally have undertaken the study of past life, including within Indigenous traditions and local communities (Mayor Reference Mayor2007; Benoit et al. Reference Benoit, Penn-Clarke, Rust, Groenewald, Vickers-Rich and Helm2024), the earliest data points of Western academic paleontology are tied to the expansion of colonial empires (Monarrez et al. Reference Monarrez, Zimmt, Clement, Gearty, Jacisin, Jenkins and Kusnerik2022; Scarlett Reference Scarlett2022). Current research infrastructure is often built on these colonial legacies, including specimens held in museum collections (LIO4; Bradley et al. Reference Bradley, Adgemis and Haralampou2014; Cisneros et al. Reference Cisneros, Raja, Ghilardi, Dunne, Pinheiro, Fernández and Sales2022; Mohammed et al. Reference Mohammed, Turner, Fowler, Pateman, Nieves-Colón, Fanovich and Cooke2022; Monarrez et al. Reference Monarrez, Zimmt, Clement, Gearty, Jacisin, Jenkins and Kusnerik2022; Raja et al. Reference Raja, Dunne, Matiwane, Khan, Nätscher, Ghilardi and Chattopadhyay2022). Digitization efforts are making museum collections and exhibits more accessible internationally to those with internet access, but digital representations do not necessarily provide the same research and engagement opportunities as physical specimens and have their own complications (e.g., compliance with sharing policies, digital quality and resolution, large file sizes, internet access and bandwidth; Falkingham Reference Falkingham2012; Lewis Reference Lewis2019). Natural history specimens and geosites are often considered to be natural heritage items (including status as UNESCO sites, https://whc.unesco.org/en/list), and calls for repatriation are growing in number (Bradley et al. Reference Bradley, Adgemis and Haralampou2014; Vogel Reference Vogel2019), making evaluating this issue in paleontology a priority (LIO4; see “Fundamental Issues”).

Researchers, institutions, and funding bodies must make proactive decisions to avoid contributing further to colonial legacies by evaluating the power dynamics of international collaborations while contending with the curation of specimens collected in the past (LIO5; e.g., Dunne et al. Reference Dunne, Raja, Stewens, Zin-Maung-Maung-Thein and Zaw2022). These decisions can run counter to incentives for publication on “novelty” and unique specimens, which are often gleaned from fieldwork in key geographic regions (e.g., Myanmar; LIO6; Dunne et al. Reference Dunne, Raja, Stewens, Zin-Maung-Maung-Thein and Zaw2022; Raja et al. Reference Raja, Dunne, Matiwane, Khan, Nätscher, Ghilardi and Chattopadhyay2022).

More broadly, fieldwork is not equally accessible to everyone despite its high value as a component of science education (e.g., Shinbrot et al. Reference Shinbrot, Treibergs, Hernández, Esparza, Ghezzi-Kopel, Goebel and Graham2022). As in all the sciences with fieldwork components, paleontologists must grapple with safety and equity considerations, including mechanisms for reporting sexual harassment and assault (Clancy et al. Reference Clancy, Nelson, Rutherford and Hinde2014), explicit discussions about the safety of people of marginalized identities in field conditions (Demery and Pipkin Reference Demery and Pipkin2021; Rudzki et al. Reference Rudzki, Kuebbing, Clark, Gharaibeh, Janecka, Kramp and Kohl2022), and accessibility and inclusive design of field experiences for people with disabilities (LIO6; Stokes et al. Reference Stokes, Feig, Atchison and Gilley2019).

The exclusion and attrition of groups of people with particular identities and affinities (i.e., minoritized or marginalized groups) from academia have previously been described as a passive, leaky pipeline; however, this metaphor downplays the challenges posed by racism, colonial legacies, and systemic bias at institutional levels, which are now more accurately described as a “hostile obstacle course” (e.g., Bernard and Cooperdock Reference Bernard and Cooperdock2018; Valenzuela-Toro and Viglino Reference Valenzuela-Toro and Viglino2021; Berhe et al. Reference Berhe, Barnes, Hastings, Mattheis, Schneider, Williams and Marín-Spiotta2022; Carter et al. Reference Carter, Johnson and Schroeter2022). Recognizing that these challenges exist, paleontologists must identify and embrace practices that create a more inclusive and equitable culture (LIO7; Valenzuela-Toro and Viglino Reference Valenzuela-Toro and Viglino2021; Carter et al. Reference Carter, Johnson and Schroeter2022; Cisneros et al. Reference Cisneros, Raja, Ghilardi, Dunne, Pinheiro, Fernández and Sales2022; Raja et al. Reference Raja, Dunne, Matiwane, Khan, Nätscher, Ghilardi and Chattopadhyay2022). Current diversity, equity, and inclusion tasks fall disproportionately on minoritized individuals, yet often are not considered in tenure and promotion assessments (LIO8; Jimenez et al. Reference Jimenez, Laverty, Bombaci, Wilkins, Bennett and Pejchar2019). Although individual actions are important, support for diversity, equity, and inclusion must come from the highest levels of leadership (e.g., those making funding decisions) to signal their value (Dutt Reference Dutt2021; Chen et al. Reference Chen, Kahanamoku, Tripati, Alegado, Morris, Andrade and Hosbey2022). In implementing these changes, we can iteratively add to our dataset of changing outcomes in paleontology to evaluate whether such actions are effective (LIO2) and how this affects our understanding of both past and future worlds (LIO1).

Concluding Remarks

The present state of paleontological research is complex and constantly changing. Considering the limited number of paleontologists employed professionally in comparison to other scientific fields (e.g., Keane et al. Reference Keane, Gonzales and Robinson2021; Plotnick et al. Reference Plotnick, Anderson, Carlson, Jukar, Kimmig and Petsios2025), it is prudent to develop a shared research agenda that the paleontological community can jointly address (Fig. 3). The questions presented here are unavoidably influenced by the perspectives of those participating and by the initial set of questions submitted. However, we have attempted to minimize this influence through our strategy for an inclusive approach to question submission, project participation, and authorship. Doing so gives us confidence that these BQs faithfully represent a forward-looking agenda for the discipline of paleontology.

Figure 3. The Big Questions project can be used as a tool to guide research in paleontology and to advocate for the importance of funding paleontological research.

Whether this list of questions is taken as a whole, separated by theme, or examined piecemeal as individual questions, we encourage all in the paleontological community to use these BQs as a tool for communicating the importance of paleontology and securing research funding. Indeed, as the questions presented here have emerged from a community-wide effort, they likely are more representative of the state of the field than if the exercise was conducted with a top-down approach by a select few individuals, and this element may add credibility and power to arguments for funding in paleontology, broadly. As in other endeavors to define priority questions (e.g., Sutherland et al. Reference Sutherland, Adams, Aronson, Aveling, Blackburn, Broad and Ceballos2009; Seddon et al. Reference Seddon, Mackay, Baker, Birks, Breman, Buck and Ellis2014), we expect a variety of uses (e.g., development of research projects, spurring discussion on the importance of different BQs) and audiences (e.g., other scientists, funding bodies, students, the general public). We anticipate these BQs will be used by researchers as framing and inspiration for new research directions and as a tool they can use to justify paleontological research to funding organizations (Fig. 3). The BQs reiterate the substantive contributions of museums and physical collection spaces, making clear a need for sustained funding of the repositories of our geoheritage. The BQs highlight the breadth and vitality of paleontology and the important and substantive role the discipline will continue to play in pushing the frontiers of understanding throughout the life sciences.

Many of the questions included here are directed at pursuing long-standing hypotheses on how life has evolved and responded to environmental change. A large portion also pertains to the application of paleontological data to the biodiversity and environmental crises that permeate the modern world. Questions in each of these areas share common considerations, including the effects of scale on observations and the ever-present challenge of assessing the adequacy of the fossil record to address these questions. Reflecting larger ongoing discussions in science and society, there is also an emphasis on conducting paleontological research more inclusively and equitably as a community. Through efforts like this Big Questions project that bring together groups of people with many backgrounds, expertises, and motivations, we aspire to grow and strengthen the global paleontological community. Our collective understanding of the history and future of life on Earth will only be improved by creating a cohesive discipline where all interested individuals can contribute.

Acknowledgments

The Big Questions in Paleontology project was possible because of the participation of many members of the global paleontology community, and we thank all who contributed at any stage of the project. The project was coordinated through the PaleoSynthesis Project hosted at Friedrich-Alexander Universität Erlangen-Nürnberg, with funding from the Volkswagen Foundation (Az 96 796). We thank the editor (J. Crampton) and two anonymous reviewers for their comments on a previous version of this article.

Competing Interests

The authors declare no competing interests.

Data Availability Statement

Supplementary Material is available on Zenodo at: https://doi.org/10.5281/zenodo.14278550.

Footnotes

*

Authors are listed alphabetically in two groups: working group leaders and group members.

Indicates leadership role in a working group.

Handling Editor: James Crampton

References

Literature Cited

Abdelhady, A. A., Seuss, B., Jain, S., Abdel-Raheem, K. H., Elsheikh, A., Ahmed, M. S., Elewa, A. M., and Hussain, A. M.. 2024. New and emerging technologies in paleontology and paleobiology: a horizon scanning review. Journal of African Earth Sciences 210:105155.CrossRefGoogle Scholar
Aberhan, M., and Kiessling, W.. 2015. Persistent ecological shifts in marine molluscan assemblages across the end-Cretaceous mass extinction. Proceedings of the National Academy of Sciences USA 112:72077212.CrossRefGoogle ScholarPubMed
Adaïmé, M.-É., Kong, S., and Punyasena, S. W.. 2024. Deep learning approaches to the phylogenetic placement of extinct pollen morphotypes. PNAS Nexus 3:pgad419.CrossRefGoogle Scholar
Agnarsson, I., and Kuntner, M.. 2007. Taxonomy in a changing world: seeking solutions for a science in crisis. Systematic Biology 56:531539.CrossRefGoogle Scholar
Alberti, M., Fürsich, F. T., and Pandey, D. K.. 2013. Seasonality in low latitudes during the Oxfordian (Late Jurassic) reconstructed via high-resolution stable isotope analysis of the oyster Actinostreon marshi (J. Sowerby, 1814) from the Kachchh Basin, western India. International Journal of Earth Sciences 102:13211336.CrossRefGoogle Scholar
Allen, B. J., Wignall, P. B., Hill, D. J., Saupe, E. E., and Dunhill, A. M.. 2020. The latitudinal diversity gradient of tetrapods across the Permo-Triassic mass extinction and recovery interval. Proceedings of the Royal Society B 287:20201125.CrossRefGoogle ScholarPubMed
Allen, B. J., Clapham, M. E., Saupe, E. E., Wignall, P. B., Hill, D. J., and Dunhill, A. M.. 2023. Estimating spatial variation in origination and extinction in deep time: a case study using the Permian–Triassic marine invertebrate fossil record. Paleobiology 49:509526.CrossRefGoogle Scholar
Allmon, W. A., Dietl, G. P., Hendricks, J. R., and Ross, R. M.. 2018. Bridging the two fossil records: paleontology’s “big data” future resides in museum collections. Pp. 3544 in Rosenberg, G. D. and Clary, R. M., eds. Museums at the forefront of the history and philosophy of geology: history made, history in the making. Geological Society of America, Boulder, Colo.Google Scholar
Almécija, S., Hammond, A. S., Thompson, N. E., Pugh, K. D., Moyà-Solà, S., and Alba, D. M.. 2021. Fossil apes and human evolution. Science 372:eabb4363.CrossRefGoogle ScholarPubMed
Alroy, J., Aberhan, M., Bottjer, D. J., Foote, M., Fürsich, F. T., Harries, P. J., Hendy, A. J., et al. 2008. Phanerozoic trends in the global diversity of marine invertebrates. Science 321:97100.CrossRefGoogle ScholarPubMed
Anderson, S. C., and Ruxton, G. D.. 2020. The evolution of flight in bats: a novel hypothesis. Mammal Review 50:426439.CrossRefGoogle Scholar
Andréoletti, J., and Morlon, H.. 2024. Comparing extinction rates: past, present, and future. Pp. 348365 in Scheiner, S. M., ed. Encyclopedia of biodiversity, 3rd ed. Academic Press, Oxford.CrossRefGoogle Scholar
Antell, G. S., Kiessling, W., Aberhan, M., and Saupe, E. E.. 2020. Marine biodiversity and geographic distributions are independent on large scales. Current Biology 30:115121.CrossRefGoogle ScholarPubMed
Antell, G. T., Benson, R. B. J., and Saupe, E. E.. 2024. Spatial standardization of taxon occurrence data—a call to action. Paleobiology 50:177193.CrossRefGoogle Scholar
Arakaki, M., Christin, P.-A., Nyffeler, R., Lendel, A., Eggli, U., Ogburn, R. M., Spriggs, E., Moore, M. J., and Edwards, E. J.. 2011. Contemporaneous and recent radiations of the world’s major succulent plant lineages. Proceedings of the National Academy of Sciences USA 108:83798384.CrossRefGoogle ScholarPubMed
Atkinson, T. P., Buta, R. J., and Kopaska-Merkel, D. C.. 2005. Saving the Union Chapel Mine: how a group of determined amateurs teamed up with professionals to save a world-class trackway site in Alabama. Pp. 191200 in Buta, R. J., Rindsberg, A. K., and Kopaska-Merkel, D. C., eds. Pennsylvanian footprints in the Black Warrior Basin of Alabama. Alabama Paleontological Society Monograph 1. Alabama Paleontological Society, Birmingham.Google Scholar
Balazka, D., and Rodighiero, D.. 2020. Big data and the Little Big Bang: an epistemological (R)evolution. Frontiers in Big Data 3:131.CrossRefGoogle Scholar
Balisi, M. A., and Van Valkenburgh, B.. 2020. Iterative evolution of large-bodied hypercarnivory in canids benefits species but not clades. Communications Biology 3:19.CrossRefGoogle Scholar
Bambach, R. K., Bush, A. M., and Erwin, D. H.. 2007. Autecology and the filling of ecospace: key metazoan radiations. Palaeontology 50:122.CrossRefGoogle Scholar
Barido-Sottani, J., Pett, W., O’Reilly, J. E., and Warnock, R. C.. 2019. FossilSim: an R package for simulating fossil occurrence data under mechanistic models of preservation and recovery. Methods in Ecology and Evolution 10:835840.CrossRefGoogle Scholar
Barido-Sottani, J., Van Tiel, N. M., Hopkins, M. J., Wright, D. F., Stadler, T., and Warnock, R. C.. 2020. Ignoring fossil age uncertainty leads to inaccurate topology and divergence time estimates in time calibrated tree inference. Frontiers in Ecology and Evolution 8:fevo.2020.00183.CrossRefGoogle Scholar
Barido-Sottani, J., Pohle, A., De Baets, K., Murdock, D., and Warnock, R. C.. 2023. Putting the F into FBD analysis: tree constraints or morphological data? Palaeontology 66:e12679.CrossRefGoogle Scholar
Barnosky, A. D. 2001. Distinguishing the effects of the Red Queen and Court Jester on Miocene mammal evolution in the northern Rocky Mountains. Journal of Vertebrate Paleontology 21:172185.CrossRefGoogle Scholar
Barnosky, A. D., Matzke, N., Tomiya, S., Wogan, G. O., Swartz, B., Quental, T. B., Marshall, C., et al. 2011. Has the Earth’s sixth mass extinction already arrived? Nature 471:51.CrossRefGoogle ScholarPubMed
Barnosky, A. D., Hadly, E. A., Gonzalez, P., Head, J., Polly, P. D., Lawing, A. M., Eronen, J. T., et al. 2017. Merging paleobiology with conservation biology to guide the future of terrestrial ecosystems. Science 355:eaah4787.CrossRefGoogle ScholarPubMed
Behrensmeyer, A. K., Kidwell, S. M., and Gastaldo, R. A.. 2000. Taphonomy and paleobiology. Paleobiology 26:103147.CrossRefGoogle Scholar
Benoit, J., Penn-Clarke, C. R., Rust, R., Groenewald, D. P., Vickers-Rich, P., and Helm, C. W.. 2024. Indigenous knowledge of palaeontology in Africa. Geological Society of London Special Publication 543:SP543-2022–2236.CrossRefGoogle Scholar
Benson, R. B., Butler, R., Close, R. A., Saupe, E., and Rabosky, D. L.. 2021. Biodiversity across space and time in the fossil record. Current Biology 31:R1225R1236.CrossRefGoogle ScholarPubMed
Benton, M. J. 2009. The Red Queen and the Court Jester: species diversity and the role of biotic and abiotic factors through time. Science 323:728732.CrossRefGoogle ScholarPubMed
Berbee, M. L., Strullu-Derrien, C., Delaux, P.-M., Strother, P. K., Kenrick, P., Selosse, M.-A., and Taylor, J. W.. 2020. Genomic and fossil windows into the secret lives of the most ancient fungi. Nature Reviews Microbiology 18:717730.CrossRefGoogle ScholarPubMed
Berents, P., Hamer, M., and Chavan, V.. 2010. Towards demand driven publishing: approaches to the prioritization of digitization of natural history collections data. Biodiversity Informatics 7:113119.Google Scholar
Berhe, A. A., Barnes, R. T., Hastings, M. G., Mattheis, A., Schneider, B., Williams, B. M., and Marín-Spiotta, E.. 2022. Scientists from historically excluded groups face a hostile obstacle course. Nature Geoscience 15:24.CrossRefGoogle Scholar
Bernard, R. E., and Cooperdock, E. H. G.. 2018. No progress on diversity in 40 years. Nature Geoscience 11:292295.CrossRefGoogle Scholar
Bijma, J., Pörtner, H.-O., Yesson, C., and Rogers, A. D.. 2013. Climate change and the oceans–What does the future hold? Marine Pollution Bulletin 74:495505.CrossRefGoogle ScholarPubMed
Bortolus, A. 2008. Error cascades in the biological sciences: the unwanted consequences of using bad taxonomy in ecology. AMBIO: A Journal of the Human Environment 37:114118.CrossRefGoogle ScholarPubMed
Bouckaert, R., Vaughan, T. G., Barido-Sottani, J., Duchêne, S., Fourment, M., Gavryushkina, A., Heled, J., et al. 2019. BEAST 2.5: an advanced software platform for Bayesian evolutionary analysis. PLoS Computational Biology 15:e1006650.CrossRefGoogle ScholarPubMed
Bradley, J., Adgemis, P., and Haralampou, L.. 2014. “Why can’t they put their names?”: colonial photography, repatriation and social memory. History and Anthropology 25:4771.CrossRefGoogle Scholar
Braje, T. J., and Erlandson, J. M.. 2013. Human acceleration of animal and plant extinctions: a Late Pleistocene, Holocene, and Anthropocene continuum. Anthropocene 4:1423.Google Scholar
Briggs, D. E., and Summons, R. E.. 2014. Ancient biomolecules: their origins, fossilization, and role in revealing the history of life. BioEssays 36:482490.CrossRefGoogle ScholarPubMed
Brocklehurst, N., and Benson, R. J.. 2021. Multiple paths to morphological diversification during the origin of amniotes. Nature Ecology and Evolution 5:12431249.CrossRefGoogle ScholarPubMed
Bromham, L. 2016. Testing hypotheses in macroevolution. Studies in History and Philosophy of Science A 55:4759.CrossRefGoogle ScholarPubMed
Brown, J. H. 1995. Macroecology. University of Chicago Press, Chicago.Google Scholar
Bush, A. M., and Payne, J. L.. 2021. Biotic and abiotic controls on the Phanerozoic history of marine animal biodiversity. Annual Review of Ecology, Evolution, and Systematics 52:269289.CrossRefGoogle Scholar
Carter, A. M., Johnson, E. H., and Schroeter, E. R.. 2022. Long-term retention of diverse paleontologists requires increasing accessibility. Frontiers in Ecology and Evolution 10. https://doi.org/10.3389/fevo.2022.876906.CrossRefGoogle Scholar
Carvalho, I. de S., and Leonardi, G.. 2022. The invisibles of science and the paleontological heritage: the Brazilian study case. Geoheritage 14:107.CrossRefGoogle Scholar
Casey, M. M., and Post, D. M.. 2011. The problem of isotopic baseline: reconstructing the diet and trophic position of fossil animals. Earth-Science Reviews 106:131148.CrossRefGoogle Scholar
Cermeño, P., García-Comas, C., Pohl, A., Williams, S., Benton, M. J., Chaudhary, C., Le Gland, G., et al. 2022. Post-extinction recovery of the Phanerozoic oceans and biodiversity hotspots. Nature 607:507511.CrossRefGoogle ScholarPubMed
Chen, C. Y., Kahanamoku, S. S., Tripati, A., Alegado, R. A., Morris, V. R., Andrade, K., and Hosbey, J.. 2022. Systemic racial disparities in funding rates at the National Science Foundation. eLife 11:e83071.CrossRefGoogle ScholarPubMed
Chen, J., Montañez, I. P., Qi, Y., Shen, S., and Wang, X.. 2018. Strontium and carbon isotopic evidence for decoupling of pCO2 from continental weathering at the apex of the late Paleozoic glaciation. Geology 46:395398.CrossRefGoogle Scholar
Chevalier, T., Colard, T., Colombo, A., Golovanova, L., Doronichev, V., and Hublin, J.-J.. 2021. Early ontogeny of humeral trabecular bone in Neandertals and recent modern humans. Journal of Human Evolution 154:102968.CrossRefGoogle ScholarPubMed
Chiarenza, A. A., Waterson, A. M., Schmidt, D. N., Valdes, P. J., Yesson, C., Holroyd, P. A., Collinson, M. E., et al. 2023. 100 million years of turtle paleoniche dynamics enable the prediction of latitudinal range shifts in a warming world. Current Biology 33:109121.e3.CrossRefGoogle Scholar
Cisneros, J. C., Raja, N. B., Ghilardi, A. M., Dunne, E. M., Pinheiro, F. L., Fernández, O. R. Regalado, Sales, M. A. F., et al. 2022. Digging deeper into colonial palaeontological practices in modern day Mexico and Brazil. Royal Society Open Science 9:210898.CrossRefGoogle ScholarPubMed
Clancy, K. B., Nelson, R. G., Rutherford, J. N., and Hinde, K.. 2014. Survey of academic field experiences (SAFE): trainees report harassment and assault. PLoS ONE 9:e102172.CrossRefGoogle ScholarPubMed
Clark, J., Bayarsaikhan, J., Miller, A. V., Vanderwarf, S., Hart, I., Caspari, G., and Taylor, W. T. T.. 2021. Mongolia’s frozen heritage: a summary of the archaeology of the cultural cryosphere. Journal of Glacial Archaeology 5:103120.CrossRefGoogle Scholar
Close, R. A., Benson, R. B., Saupe, E. E., Clapham, M. E., and Butler, R. J.. 2020. The spatial structure of Phanerozoic marine animal diversity. Science 368:420424.CrossRefGoogle ScholarPubMed
Comans, C. M., Smart, S. M., Kast, E. R., Lu, Y., Lüdecke, T., Leichliter, J. N., Sigman, D. M., Ikejiri, T., and Martínez‐García, A.. 2024. Enameloid‐bound δ15N reveals large trophic separation among Late Cretaceous sharks in the northern Gulf of Mexico. Geobiology 22:e12585.CrossRefGoogle Scholar
Cook, P. K., Languille, M.-A., Dufour, E., Mocuta, C., Tombret, O., Fortuna, F., and Bertrand, L.. 2015. Biogenic and diagenetic indicators in archaeological and modern otoliths: potential and limits of high definition synchrotron micro-XRF elemental mapping. Chemical Geology 414:115.CrossRefGoogle Scholar
Cortés-Sánchez, M., Simón-Vallejo, M. D., Corral, J.-C., Lozano-Francisco, M. del C., Vera-Peláez, J. L., Jiménez-Espejo, F. J., García-Alix, A., et al. 2020. Fossils in Iberian prehistory: a review of the palaeozoological evidence. Quaternary Science Reviews 250:106676.CrossRefGoogle Scholar
Cribb, A. T., Formoso, K. K., Woolley, C. H., Beech, J., Brophy, S., Byrne, P., Cassady, V. C., et al. 2023. Contrasting terrestrial and marine ecospace dynamics after the end-Triassic mass extinction event. Proceedings of the Royal Society B 290:20232232.CrossRefGoogle ScholarPubMed
Cuvier, G. 1813. Essay on the theory of the Earth. Routledge, Oxford, U.K.Google Scholar
Darwin, C. 1859. On the origin of species by means of natural selection, or, the preservation of favoured races in the struggle for life. Appleton and Company, New York.CrossRefGoogle Scholar
Davies, S. W., Putnam, H. M., Ainsworth, T., Baum, J. K., Bove, C. B., Crosby, S. C., Côté, I. M., et al. 2021. Promoting inclusive metrics of success and impact to dismantle a discriminatory reward system in science. PLoS Biology 19:e3001282.CrossRefGoogle ScholarPubMed
De Baets, K. 2021. Performance of machine-learning approaches in identifying ammonoid species based on conch properties. Peer Community in Paleontology 1:100010.CrossRefGoogle Scholar
De Baets, K., Antonelli, A., and Donoghue, P. C.. 2016. Tectonic blocks and molecular clocks. Philosophical Transactions of the Royal Society B 371:20160098.CrossRefGoogle ScholarPubMed
De Baets, K., Huntley, J. W., Scarponi, D., Klompmaker, A. A., and Skawina, A.. 2021. Phanerozoic parasitism and marine metazoan diversity: dilution versus amplification. Philosophical Transactions of the Royal Society B 376:20200366.CrossRefGoogle ScholarPubMed
De Baets, K., Jarochowska, E., Buchwald, S. Z., Klug, C., and Korn, D.. 2022. Lithology controls ammonoid size distributions. Palaios 37:744754.CrossRefGoogle Scholar
Demarchi, B. 2020. Amino acids and proteins in fossil biominerals: an introduction for archaeologists and palaeontologists. Wiley, Hoboken, N.J.CrossRefGoogle Scholar
Demery, A.-J. C., and Pipkin, M. A.. 2021. Safe fieldwork strategies for at-risk individuals, their supervisors and institutions. Nature Ecology and Evolution 5:59.CrossRefGoogle ScholarPubMed
Dietl, G. P., and Flessa, K. W.. 2011. Conservation paleobiology: putting the dead to work. Trends in Ecology and Evolution 26:3037.CrossRefGoogle ScholarPubMed
Dietl, G. P., Kidwell, S. M., Brenner, M., Burney, D. A., Flessa, K. W., Jackson, S. T., and Koch, P. L.. 2015. Conservation paleobiology: leveraging knowledge of the past to inform conservation and restoration. Annual Review of Earth and Planetary Sciences 43:79103.CrossRefGoogle Scholar
Dietl, G. P., Smith, J. A., and Durham, S. R.. 2019. Discounting the past: the undervaluing of paleontological data in conservation science. Frontiers in Ecology and Evolution 7:108.CrossRefGoogle Scholar
Dietl, G. P., Durham, S. R., Clark, C., and Prado, R.. 2023. Better together: building an engaged conservation paleobiology science for the future. Ecological Solutions and Evidence 4:e12246.CrossRefGoogle Scholar
Dillon, E. M., Pier, J. Q., Smith, J. A., Raja, N. B., Dimitrijević, D., Austin, E. L., Cybulski, J. D., et al. 2022. What is conservation paleobiology? Tracking 20 years of research and development. Frontiers in Ecology and Evolution 10:1117.CrossRefGoogle Scholar
Di Martino, E., Jackson, J. B. C., Taylor, P. D., and Johnson, K. G.. 2018. Differences in extinction rates drove modern biogeographic patterns of tropical marine biodiversity. Science Advances 4:eaaq1508.CrossRefGoogle ScholarPubMed
Dirzo, R., Young, H. S., Galetti, M., Ceballos, G., Isaac, N. J., and Collen, B.. 2014. Defaunation in the Anthropocene. Science 345:401406.CrossRefGoogle ScholarPubMed
Dunhill, A. M., Hannisdal, B., and Benton, M. J.. 2014. Disentangling rock record bias and common-cause from redundancy in the British fossil record. Nature Communications 5:4818.CrossRefGoogle ScholarPubMed
Dunhill, A. M., Foster, W. J., Sciberras, J., and Twitchett, R. J.. 2018. Impact of the Late Triassic mass extinction on functional diversity and composition of marine ecosystems. Palaeontology 61:133148.CrossRefGoogle Scholar
Dunhill, A. M., Zarzyczny, K., Shaw, J. O., Atkinson, J. W., Little, C. T., and Beckerman, A. P.. 2024. Extinction cascades, community collapse, and recovery across a Mesozoic hyperthermal event. Nature Communications 15:8599.CrossRefGoogle ScholarPubMed
Dunne, E. M., Raja, N. B., Stewens, P. P., Zin-Maung-Maung-Thein, , and Zaw, K.. 2022. Ethics, law, and politics in palaeontological research: the case of Myanmar amber. Communications Biology 5:110.CrossRefGoogle ScholarPubMed
Dunne, E. M., Thompson, S. E., Butler, R. J., Rosindell, J., and Close, R. A.. 2023. Mechanistic neutral models show that sampling biases drive the apparent explosion of early tetrapod diversity. Nature Ecology and Evolution 7:14801489.CrossRefGoogle ScholarPubMed
Dunne, J. A., and Williams, R. J.. 2009. Cascading extinctions and community collapse in model food webs. Philosophical Transactions of the Royal Society B 364:17111723.CrossRefGoogle ScholarPubMed
Dutt, K. 2021. Addressing racism through ownership. Nature Geoscience 14:5858.CrossRefGoogle Scholar
Eden, R., Manica, A., and Mitchell, E. G.. 2022. Metacommunity analyses show an increase in ecological specialisation throughout the Ediacaran period. PLoS Biology 20:e3001289.CrossRefGoogle ScholarPubMed
Eichenseer, K., Balthasar, U., Smart, C. W., Stander, J., Haaga, K. A., and Kiessling, W.. 2019. Jurassic shift from abiotic to biotic control on marine ecological success. Nature Geoscience 12:638642.CrossRefGoogle Scholar
Ezard, T. H. G., Quental, T. B., and Benton, M. J.. 2016. The challenges to inferring the regulators of biodiversity in deep time. Philosophical Transactions of the Royal Society B 371:20150216.CrossRefGoogle ScholarPubMed
Faith, J. T., Du, A., Behrensmeyer, A. K., Davies, B., Patterson, D. B., Rowan, J., and Wood, B.. 2021. Rethinking the ecological drivers of hominin evolution. Trends in Ecology and Evolution 36:797807.CrossRefGoogle ScholarPubMed
Falk, H., and Wolkenstein, K.. 2017. Natural product molecular fossils. Progress in the Chemistry of Organic Natural Products 104:1126.CrossRefGoogle ScholarPubMed
Falkingham, P. 2012. Acquisition of high resolution three-dimensional models using free, open-source, photogrammetric software. Palaeontologia Electronica 15:1T:15p.Google Scholar
Fenton, I. S., Aze, T., Farnsworth, A., Valdes, P., and Saupe, E. E.. 2023. Origination of the modern-style diversity gradient 15 million years ago. Nature 614:708712.CrossRefGoogle ScholarPubMed
Finnegan, S., Harnik, P. G., Lockwood, R., Lotze, H. K., McClenachan, L., and Kahanamoku, S. S.. 2024. Using the fossil record to understand extinction risk and inform marine conservation in a changing world. Annual Review of Marine Science 16:307333.CrossRefGoogle Scholar
Flannery-Sutherland, J. T., Silvestro, D., and Benton, M. J.. 2022. Global diversity dynamics in the fossil record are regionally heterogeneous. Nature Communications 13:2751.CrossRefGoogle ScholarPubMed
Flessa, K., Kowalewski, M., and Walker, S. E.. 1992. Post-collection taphonomy: shell destruction and the Chevrolet. Palaios 7:553554.CrossRefGoogle Scholar
Foote, M. 2000. Origination and extinction components of taxonomic diversity: Paleozoic and post-Paleozoic dynamics. Paleobiology 26:578605.2.0.CO;2>CrossRefGoogle Scholar
Foster, W. J., and Twitchett, R. J.. 2014. Functional diversity of marine ecosystems after the Late Permian mass extinction event. Nature Geoscience 7:233238.CrossRefGoogle Scholar
Foster, W. J., Allen, B. J., Kitzmann, N. H., Münchmeyer, J., Rettelbach, T., Witts, J. D., Whittle, R. J., et al. 2023. How predictable are mass extinction events? Royal Society Open Science 10:221507.CrossRefGoogle ScholarPubMed
Friend, D. S., Anderson, B. M., and Allmon, W. D.. 2021. Geographic contingency, not species sorting, dominates macroevolutionary dynamics in an extinct clade of neogastropods (Volutospina; Volutidae). Paleobiology 47:236250.CrossRefGoogle Scholar
Gibert, C., Zacaï, A., Fluteau, F., Ramstein, G., Chavasseau, O., Thiery, G., Souron, A., et al. 2022. A coherent biogeographical framework for Old World Neogene and Pleistocene mammals. Palaeontology 65:e12594.CrossRefGoogle Scholar
Giuliani, A., Drysdale, R. N., Woodhead, J. D., Planavsky, N. J., Phillips, D., Hergt, J., Griffin, W. L., Oesch, S., Dalton, H., and Davies, G. R.. 2022. Perturbation of the deep-Earth carbon cycle in response to the Cambrian Explosion. Science Advances 8:eabj1325.CrossRefGoogle Scholar
Gould, S. J., and Eldredge, N.. 1972. Punctuated equilibria: an alternative to phyletic gradualism. Models in Paleobiology 1972:82115.Google Scholar
Groff, D. V., MacKenzie, C. M., Pier, J. Q., Shaffer, A. B., and Dietl, G. P.. 2023. Knowing but not doing: quantifying the research-implementation gap in conservation paleobiology. Frontiers in Ecology and Evolution 11:1058992.CrossRefGoogle Scholar
Grossman, E. L., and Joachimski, M. M.. 2022. Ocean temperatures through the Phanerozoic reassessed. Scientific Reports 12:113.CrossRefGoogle ScholarPubMed
Gu, Z., Gu, L., Eils, R., Schlesner, M., and Brors, B.. 2014. Circlize implements and enhances circular visualization in R. Bioinformatics 30:28112812.CrossRefGoogle ScholarPubMed
Gueriau, P., Bernard, S., and Bertrand, L.. 2016. Advanced synchrotron characterization of paleontological specimens. Elements 12:4550.CrossRefGoogle Scholar
Hannisdal, B., and Peters, S. E.. 2011. Phanerozoic Earth system evolution and marine biodiversity. Science 334:11211124.CrossRefGoogle ScholarPubMed
Hardisty, A. R., Ellwood, E. R., Nelson, G., Zimkus, B., Buschbom, J., Addink, W., Rabeler, R. K., et al. 2022. Digital extended specimens: enabling an extensible network of biodiversity data records as integrated digital objects on the Internet. BioScience 72:978987.CrossRefGoogle ScholarPubMed
Harmon, L. J., and Harrison, S.. 2015. Species diversity is dynamic and unbounded at local and continental scales. American Naturalist 185:584593.CrossRefGoogle ScholarPubMed
Harnik, P. G. 2011. Direct and indirect effects of biological factors on extinction risk in fossil bivalves. Proceedings of the National Academy of Sciences USA 108:1359413599.CrossRefGoogle ScholarPubMed
Hayek, L.-A. C., Buzas, M. A., and Thomas, E.. 2019. Identifying disruptions to the ecological balance of nature: a foraminiferal example across the initiation of the Paleocene–Eocene thermal maximum. Paleobiology 45:98113.CrossRefGoogle Scholar
Heath, T. A., Huelsenbeck, J. P., and Stadler, T.. 2014. The fossilized birth–death process for coherent calibration of divergence-time estimates. Proceedings of the National Academy of Sciences USA 111:E2957E2966.CrossRefGoogle ScholarPubMed
Hendricks, J. R., Saupe, E. E., Myers, C. E., Hermsen, E. J., and Allmon, W. D.. 2014. The generification of the fossil record. Paleobiology 40:511528.CrossRefGoogle Scholar
Hlusko, L. J., Schmitt, C. A., Monson, T. A., Brasil, M. F., and Mahaney, M. C.. 2016. The integration of quantitative genetics, paleontology, and neontology reveals genetic underpinnings of primate dental evolution. Proceedings of the National Academy of Sciences USA 113:92629267.CrossRefGoogle ScholarPubMed
Hohmann, N., Koelewijn, J. R., Burgess, P., and Jarochowska, E.. 2024. Identification of the mode of evolution in incomplete carbonate successions. BMC Ecology and Evolution 24:113.CrossRefGoogle ScholarPubMed
Höhna, S., Landis, M. J., Heath, T. A., Boussau, B., Lartillot, N., Moore, B. R., Huelsenbeck, J. P., and Ronquist, F.. 2016. RevBayes: Bayesian phylogenetic inference using graphical models and an interactive model-specification language. Systematic Biology 65:726736.CrossRefGoogle Scholar
Höhna, S., Kopperud, B. T., and Magee, A. F.. 2022. CRABS: congruent rate analyses in birth–death scenarios. Methods in Ecology and Evolution 13:27092718.CrossRefGoogle Scholar
Hopkins, M. J., and To, R.. 2022. Long-term clade-wide shifts in trilobite segment number and allocation during the Palaeozoic. Proceedings of the Royal Society B 289:20221765.CrossRefGoogle ScholarPubMed
Hopkins, M. J., Simpson, C., and Kiessling, W.. 2014. Differential niche dynamics among major marine invertebrate clades. Ecology Letters 17:314323.CrossRefGoogle ScholarPubMed
Hull, P. M., Darroch, S. A. F., and Erwin, D. H.. 2015. Rarity in mass extinctions and the future of ecosystems. Nature 528:345351.CrossRefGoogle ScholarPubMed
Humboldt, A. v. 1808. Ansichten der Natur. Cotta, Tübingen, Germany.Google Scholar
Hunt, G. 2007. The relative importance of directional change, random walks, and stasis in the evolution of fossil lineages. Proceedings of the National Academy of Sciences USA 104:1840418408.CrossRefGoogle ScholarPubMed
Hunt, G. 2012. Measuring rates of phenotypic evolution and the inseparability of tempo and mode. Paleobiology 38:351373.CrossRefGoogle Scholar
Hunt, G., Hopkins, M. J., and Lidgard, S.. 2015. Simple versus complex models of trait evolution and stasis as a response to environmental change. Proceedings of the National Academy of Sciences USA 112:48854890.CrossRefGoogle ScholarPubMed
[IPCC] Intergovernmental Panel on Climate Change. 2021. Climate Change 2021: the physical science basis. Contribution of Working Group I to the Sixth Assessment Report of the Intergovernmental Panel on Climate Change. P. 2391 in Masson-Delmotte, V., Zhai, P., Pirani, A., Connors, S. L., Péan, C., Berger, S., Caud, N., et al., eds. Cambridge University Press, Cambridge.Google Scholar
Jablonski, D. 1991. Extinctions: a paleontological perspective. Science 253:754757.CrossRefGoogle ScholarPubMed
Jablonski, D. 2007. Scale and hierarchy in macroevolution. Palaeontology 50:87109.CrossRefGoogle Scholar
Jablonski, D. 2008. Biotic interactions and macroevolution: extensions and mismatches across scales and levels. Evolution: International Journal of Organic Evolution 62:715739.CrossRefGoogle ScholarPubMed
Jablonski, D. 2017. Approaches to macroevolution: 2. Sorting of variation, some overarching issues, and general conclusions. Evolutionary Biology 44:451475.CrossRefGoogle ScholarPubMed
Jablonski, D., Roy, K., and Valentine, J. W.. 2006. Out of the tropics: evolutionary dynamics of the latitudinal diversity gradient. Science 314:102106.CrossRefGoogle ScholarPubMed
Jackson, J. B. C., and O’Dea, A.. 2023. Evolution and environment of Caribbean coastal ecosystems. Proceedings of the National Academy of Sciences USA 120:e2307520120.CrossRefGoogle ScholarPubMed
Jane, S. F., Hansen, G. J. A., Kraemer, B. M., Leavitt, P. R., Mincer, J. L., North, R. L., Pilla, R. M., et al. 2021. Widespread deoxygenation of temperate lakes. Nature 594:6670.CrossRefGoogle ScholarPubMed
Jimenez, M. F., Laverty, T. M., Bombaci, S. P., Wilkins, K., Bennett, D. E., and Pejchar, L.. 2019. Underrepresented faculty play a disproportionate role in advancing diversity and inclusion. Nature Ecology and Evolution 3:10301033.CrossRefGoogle ScholarPubMed
Johnson, K. R., Owens, I. F. P., and the Global Collection Group. 2023. A global approach for natural history museum collections. Science 379:11921194.CrossRefGoogle ScholarPubMed
Jung, J., Zoppe, S. F., Söte, T., Moretti, S., Duprey, N. N., Foreman, A. D., Wald, T., et al. 2024. Coral photosymbiosis on Mid-Devonian reefs. Nature 636:647653.CrossRefGoogle ScholarPubMed
Kaufman, D. S. and PAGES 2k special-issue editorial team. 2018. Technical note: open-paleo-data implementation pilot—the PAGES 2k special issue. Climate of the Past 14:593600. https://doi.org/10.5194/cp-14-593-2018CrossRefGoogle Scholar
Keane, C., Gonzales, L., and Robinson, D.. 2021. Status of recent geoscience graduates. American Geosciences Institute, Alexandria, Va.Google Scholar
Kibria, A., Akhundjanov, S. B., and Oladi, R.. 2019. Fossil fuel share in the energy mix and economic growth. International Review of Economics and Finance 59:253264.CrossRefGoogle Scholar
Kidwell, S. M., and Flessa, K. W.. 1996. The quality of the fossil record: populations, species, and communities. Annual Review of Ecology and Systematics 24:433464.Google Scholar
Kiessling, W., Raja, N. B., Roden, V. J., Turvey, S. T., and Saupe, E. E.. 2019. Addressing priority questions of conservation science with palaeontological data. Philosophical Transactions of the Royal Society B 374:20190222.CrossRefGoogle ScholarPubMed
Kiessling, W., Smith, J. A., and Raja, N. B.. 2023. Improving the relevance of paleontology to climate change policy. Proceedings of the National Academy of Sciences USA 120:e2201926119.CrossRefGoogle ScholarPubMed
Kimmig, S. R., and Holmden, C.. 2017. Multi-proxy geochemical evidence for primary aragonite precipitation in a tropical-shelf “calcite sea” during the Hirnantian glaciation. Geochimica et Cosmochimica Acta 206:254272.CrossRefGoogle Scholar
Klompmaker, A. A., Schweitzer, C. E., Feldmann, R. M., and Kowalewski, M.. 2013. The influence of reefs on the rise of Mesozoic marine crustaceans. Geology 41:11791182.CrossRefGoogle Scholar
Klompmaker, A. A., Portell, R. W., and Frick, M. G.. 2017. Comparative experimental taphonomy of eight marine arthropods indicates distinct differences in preservation potential. Palaeontology 60:773794.CrossRefGoogle Scholar
Knoll, A. H., Canfield, D. E., and Konhauser, K. O.. 2012. Fundamentals of geobiology. Wiley, Hoboken, N.J.CrossRefGoogle Scholar
Kocsis, Á. T., Reddin, C. J., Scotese, C. R., Valdes, P. J., and Kiessling, W.. 2021. Increase in marine provinciality over the last 250 million years governed more by climate change than plate tectonics. Proceedings of the Royal Society B 288:20211342.CrossRefGoogle ScholarPubMed
Kowalewski, M., Nawrot, R., Scarponi, D., Tomašových, A., and Zuschin, M.. 2023. Marine conservation palaeobiology: what does the late Quaternary fossil record tell us about modern-day extinctions and biodiversity threats? Cambridge Prisms: Extinction 1:e24.Google ScholarPubMed
Kral, A. G., Lagos, M., Guagliardo, P., Tütken, T., and Geisler, T.. 2022. Rapid alteration of cortical bone in fresh- and seawater solutions visualized and quantified from the millimeter down to the atomic scale. Chemical Geology 609:121060.CrossRefGoogle Scholar
Krone, I. W., Magoulick, K. M., and Yohler, R. M.. 2024. All the Earth will not remember: how geographic gaps structure the record of diversity and extinction. Paleobiology 50:214225.CrossRefGoogle Scholar
Lamsdell, J. C., Congreve, C. R., Hopkins, M. J., Krug, A. Z., and Patzkowsky, M. E.. 2017. Phylogenetic paleoecology: tree-thinking and ecology in deep time. Trends in Ecology and Evolution 32:452463.CrossRefGoogle ScholarPubMed
Lamsdell, J. C., McCoy, V. E., Perron-Feller, O. A., and Hopkins, M. J.. 2020. Air breathing in an exceptionally preserved 340-million-year-old sea scorpion. Current Biology 30:43164321.CrossRefGoogle ScholarPubMed
Lanzetti, A., Portela-Miguez, R., Fernandez, V., and Goswami, A.. 2022. Testing heterochrony: connecting skull shape ontogeny and evolution of feeding adaptations in baleen whales. Evolution and Development 25:257273.CrossRefGoogle Scholar
LaRue, E. A., Fahey, R. T., Alveshere, B. C., Atkins, J. W., Bhatt, P., Buma, B., Chen, A., et al. 2023. A theoretical framework for the ecological role of three‐dimensional structural diversity. Frontiers in Ecology and the Environment 21:413.CrossRefGoogle Scholar
Lee, M. S., and Palci, A.. 2015. Morphological phylogenetics in the genomic age. Current Biology 25:R922R929.CrossRefGoogle ScholarPubMed
Leibold, M. A., Holyoak, M., Mouquet, N., Amarasekare, P., Chase, J. M., Hoopes, M. F., Holt, R. D., et al. 2004. The metacommunity concept: a framework for multi-scale community ecology. Ecology Letters 7:601613.CrossRefGoogle Scholar
Lendemer, J., Thiers, B., Monfils, A. K., Zaspel, J., Ellwood, E. R., Bentley, A., LeVan, K., et al. 2020. The Extended Specimen Network: a strategy to enhance US biodiversity collections, promote research and education. BioScience 70:2330.CrossRefGoogle ScholarPubMed
Lenoir, J., Bertrand, R., Comte, L., Bourgeaud, L., Hattab, T., Murienne, J., and Grenouillet, G.. 2020. Species better track climate warming in the oceans than on land. Nature Ecology and Evolution 4:10441059.CrossRefGoogle ScholarPubMed
Lewis, D. 2019. The fight for control over virtual fossils. Nature 567:2023.CrossRefGoogle ScholarPubMed
Lin, C.-H., Wei, C.-L., Ho, S. L., and Lo, L.. 2023. Ocean temperature drove changes in the mesopelagic fish community at the edge of the Pacific Warm Pool over the past 460,000 years. Science Advances 9:eadf0656.CrossRefGoogle ScholarPubMed
Liow, L. H., and Taylor, P. D.. 2019. Cope’s Rule in a modular organism: directional evolution without an overarching macroevolutionary trend. Evolution 73:18631872.CrossRefGoogle Scholar
Liow, L. H., Uyeda, J., and Hunt, G.. 2023. Cross-disciplinary information for understanding macroevolution. Trends in Ecology and Evolution 38:250260.CrossRefGoogle ScholarPubMed
Löbl, I., Klausnitzer, B., Hartmann, M., and Krell, F.-T.. 2023. The silent extinction of species and taxonomists—an appeal to science policymakers and legislators. Diversity 15:1053.CrossRefGoogle Scholar
Lotze, H. K., Erlandson, J. M., Hardt, M. J., Norris, R. D., Roy, K., Smith, T. D., and Whitcraft, C. R.. 2011. How do we know about the past. Pp. 137161 in Jackson, J. B. C., Alexander, K. E., and Sala, E., eds. Shifting baselines: the past and the future of ocean fisheries. Island Press, Washington, D.C.CrossRefGoogle Scholar
Louca, S., and Pennell, M. W.. 2020. Extant timetrees are consistent with a myriad of diversification histories. Nature 580:502505.CrossRefGoogle ScholarPubMed
Louys, J., Kealy, S., O’Connor, S., Price, G., Hawkins, S., Aplin, K. P., Rizal, Y., et al. 2017. Differential preservation of vertebrates in Southeast Asian caves. International Journal of Speleology 46:379408.CrossRefGoogle Scholar
Louys, J., Price, G. J., and Travouillon, K. J.. 2021. Space-time equivalence in the fossil record, with a case study from Pleistocene Australia. Quaternary Science Reviews 253:106764.CrossRefGoogle Scholar
Mabry, M. E., Zapata, F., Paul, D. L., O’Connor, P. M., Soltis, P. S., Blackburn, D. C., and Simmons, N. B.. 2022. Monographs as a nexus for building extended specimen networks using persistent identifiers. Bulletin of the Society of Systematic Biologists 1. https://doi.org/10.18061/bssb.v1i1.8323.CrossRefGoogle Scholar
Machado, F. A., Mongle, C. S., Slater, G., Penna, A., Wisniewski, A., Soffin, A., Dutra, V., and Uyeda, J. C.. 2023. Rules of teeth development align microevolution with macroevolution in extant and extinct primates. Nature Ecology and Evolution 7:17291739.CrossRefGoogle ScholarPubMed
MacLeod, N. 2014. The geological extinction record: history, data, biases, and testing. Geological Society of America Special Paper 505:128.Google Scholar
Malanoski, C. M., Farnsworth, A., Lunt, D. J., Valdes, P. J., and Saupe, E. E.. 2024. Climate change is an important predictor of extinction risk on macroevolutionary timescales. Science 383:11301134.CrossRefGoogle Scholar
Mancuso, A. C., Irmis, R. B., Pedernera, T. E., Gaetano, L. C., Benavente, C. A., and Breeden, B. T. III. 2022. Paleoenvironmental and biotic changes in the Late Triassic of Argentina: testing hypotheses of abiotic forcing at the basin scale. Frontiers in Earth Science 10. https://doi.org/10.3389/feart.2022.883788.CrossRefGoogle Scholar
Mannion, P. D., Upchurch, P., Benson, R. B., and Goswami, A.. 2014. The latitudinal biodiversity gradient through deep time. Trends in Ecology and Evolution 29:4250.CrossRefGoogle ScholarPubMed
Maran, S. A. 2014. Conservation of paleontological heritage in Serbia: from philosophy to practice. Bulletin of the Natural History Museum 7:728.CrossRefGoogle Scholar
Marshall, C. R. 2017. Five palaeobiological laws needed to understand the evolution of the living biota. Nature Ecology and Evolution 1:0165.CrossRefGoogle ScholarPubMed
Marshall, C. R. 2023. Forty years later: the status of the “Big Five” mass extinctions. Cambridge Prisms: Extinction 1:e5.Google ScholarPubMed
Marshall, C. R., Finnegan, S., Clites, E. C., Holroyd, P. A., Bonuso, N., Cortez, C., Davis, E., et al. 2018. Quantifying the dark data in museum fossil collections as palaeontology undergoes a second digital revolution. Biology Letters 14:20180431.CrossRefGoogle ScholarPubMed
Marshall, F. E., Wingard, G. L., and Pitts, P. A.. 2014. Estimates of natural salinity and hydrology in a subtropical estuarine ecosystem: implications for greater everglades restoration. Estuaries and Coasts 37:14491466.CrossRefGoogle Scholar
Martin, J. E., Tacail, T., and Balter, V.. 2017. Non-traditional isotope perspectives in vertebrate palaeobiology. Palaeontology 60:485502.CrossRefGoogle Scholar
Mayor, A. 2007. Place names describing fossils in oral traditions. Geological Society of London Special Publication 273:245261.CrossRefGoogle Scholar
McElwain, J. C. 2018. Paleobotany and global change: important lessons for species to biomes from vegetation responses to past global change. Annual Review of Plant Biology 69:761787.CrossRefGoogle ScholarPubMed
McGill, B. J. 2019. The what, how and why of doing macroecology. Global Ecology and Biogeography 28:617.CrossRefGoogle Scholar
McGuire, J. L., Lawing, A. M., Díaz, S., and Stenseth, N. Chr. 2023. The past as a lens for biodiversity conservation on a dynamically changing planet. Proceedings of the National Academy of Sciences USA 120:e2201950120.CrossRefGoogle ScholarPubMed
McKinney, M. L. 1997. Extinction vulnerability and selectivity: combining ecological and paleontological views. Annual Review of Ecology and Systematics 28:495516.CrossRefGoogle Scholar
McNamara, M. E., Rossi, V., Slater, T. S., Rogers, C. S., Ducrest, A.-L., Dubey, S., and Roulin, A.. 2021. Decoding the evolution of melanin in vertebrates. Trends in Ecology and Evolution 36:430443.CrossRefGoogle ScholarPubMed
Mexicana, P. 2020. How is the paleontological heritage of Mexico and other Latin American countries protected? Paleontología Mexicana 9:8390.Google Scholar
Mohammed, R. S., Turner, G., Fowler, K., Pateman, M., Nieves-Colón, M. A., Fanovich, L., Cooke, S. B., et al. 2022. Colonial legacies influence biodiversity lessons: how past trade routes and power dynamics shape present-day scientific research and professional opportunities for Caribbean scientists. American Naturalist 200:140155.CrossRefGoogle ScholarPubMed
Monarrez, P. M., Zimmt, J. B., Clement, A. M., Gearty, W., Jacisin, J. J., Jenkins, K. M., Kusnerik, K. M., et al. 2022. Our past creates our present: a brief overview of racism and colonialism in Western paleontology. Paleobiology 48:173185.CrossRefGoogle Scholar
Monfils, A. K., Krimmel, E. R., Linton, D. L., Marsico, T. D., Morris, A. B., and Ruhfel, B. R.. 2022. Collections education: the extended specimen and data acumen. BioScience 72:177188.CrossRefGoogle ScholarPubMed
Mongiardino Koch, N., Garwood, R. J., and Parry, L. A.. 2021. Fossils improve phylogenetic analyses of morphological characters. Proceedings of the Royal Society B 288:20210044.CrossRefGoogle ScholarPubMed
Mora, C., Tittensor, D. P., Adl, S., Simpson, A. G., and Worm, B.. 2011. How many species are there on Earth and in the ocean? PLoS Biology 9:e1001127.CrossRefGoogle ScholarPubMed
Mulvey, L. P., Warnock, R. C., and De Baets, K.. 2022. Where traditional extinction estimates fall flat: using novel cophylogenetic methods to estimate extinction risk in platyhelminths. Proceedings of the Royal Society B 289:20220432.CrossRefGoogle ScholarPubMed
Mulvey, L. P., May, M. R., Brown, J. M., Höhna, S., Wright, A. M., and Warnock, R. C.. 2024. Assessing the adequacy of morphological models using posterior predictive simulations. Systematic Biology 74:3452.CrossRefGoogle Scholar
Murdock, D. J. 2020. The “biomineralization toolkit” and the origin of animal skeletons. Biological Reviews 95:13721392.CrossRefGoogle Scholar
Muscente, A. D., Prabhu, A., Zhong, H., Eleish, A., Meyer, M. B., Fox, P., Hazen, R. M., and Knoll, A. H.. 2018. Quantifying ecological impacts of mass extinctions with network analysis of fossil communities. Proceedings of the National Academy of Sciences USA 115:52175222.CrossRefGoogle ScholarPubMed
Muscente, A. D., Martindale, R. C., Prabhu, A., Ma, X., Fox, P., Hazen, R. M., and Knoll, A. H.. 2022. Appearance and disappearance rates of Phanerozoic marine animal paleocommunities. Geology 50:341345.CrossRefGoogle Scholar
Na, L., Li, Q., Krause, C., Zhu, M., and Kiessling, W.. 2023. Revisiting the Phanerozoic rock–diversity relationship. Geological Magazine 160:18531862.CrossRefGoogle Scholar
Naranjo-Ortiz, M. A., and Gabaldón, T.. 2019. Fungal evolution: major ecological adaptations and evolutionary transitions. Biological Reviews 94:14431476.CrossRefGoogle ScholarPubMed
Nätscher, P. S., Gliwa, J., De Baets, K., Ghaderi, A., and Korn, D.. 2023. Exceptions to the temperature–size rule: no Lilliput Effect in end-Permian ostracods (Crustacea) from Aras Valley (northwest Iran). Palaeontology 66:e12667.CrossRefGoogle Scholar
Neto De Carvalho, C., Baucon, A. N., Bayet-Goll, A. N., and Belo, J. N.. 2021. The Penha Garcia Ichnological Park at Naturtejo UNESCO Global Geopark (Portugal): a geotourism destination in the footprint of the Great Ordovician Biodiversification Event. Geoconservation Research 4:7079.Google Scholar
Neuwirth, E. 2022. RColorBrewer: ColorBrewer Palettes, R package version 1.1-3. https://cran.r-project.org/web/packages/RColorBrewer/index.htmlGoogle Scholar
Nützel, A., Joachimski, M., and Correa, M. L.. 2010. Seasonal climatic fluctuations in the Late Triassic tropics—high-resolution oxygen isotope records from aragonitic bivalve shells (Cassian Formation, northern Italy). Palaeogeography, Palaeoclimatology, Palaeoecology 285:194204.CrossRefGoogle Scholar
Nylin, S., Agosta, S., Bensch, S., Boeger, W. A., Braga, M. P., Brooks, D. R., Forister, M. L., et al. 2018. Embracing colonizations: a new paradigm for species association dynamics. Trends in Ecology and Evolution 33:414.CrossRefGoogle ScholarPubMed
O’Keefe, F. R., Dunn, R. E., Weitzel, E. M., Waters, M. R., Martinez, L. N., Binder, W. J., Southon, J. R., et al. 2023. Pre–Younger Dryas megafaunal extirpation at Rancho La Brea linked to fire-driven state shift. Science 381:eabo3594.CrossRefGoogle ScholarPubMed
Parham, J. F., Donoghue, P. C. J., Bell, C. J., Calway, T. D., Head, J. J., Holroyd, P. A., Inoue, J. G., et al. 2012. Best practices for justifying fossil calibrations. Systematic Biology 61:346359.CrossRefGoogle ScholarPubMed
Parins-Fukuchi, C., Stull, G. W., and Smith, S. A.. 2021. Phylogenomic conflict coincides with rapid morphological innovation. Proceedings of the National Academy of Sciences USA 118:e2023058118.CrossRefGoogle ScholarPubMed
Parrott, L. 2010. Measuring ecological complexity. Ecological Indicators 10:10691076.CrossRefGoogle Scholar
Parsons, E. C. M., Favaro, B., Aguirre, A. A., Bauer, A. L., Blight, L. K., Cigliano, J. A., Coleman, M. A., et al. 2014. Seventy-one important questions for the conservation of marine biodiversity. Conservation Biology 28:12061214.CrossRefGoogle ScholarPubMed
Patton, A. H., Harmon, L. J., del Rosario Castañeda, M., Frank, H. K., Donihue, C. M., Herrel, A., and Losos, J. B.. 2021. When adaptive radiations collide: different evolutionary trajectories between and within island and mainland lizard clades. Proceedings of the National Academy of Sciences USA 118:e2024451118.CrossRefGoogle ScholarPubMed
Pawlik, L., Buma, B., Šamonil, P., Kvaček, J., Galązka, A., Kohout, P., and Malik, I.. 2020. Impact of trees and forests on the Devonian landscape and weathering processes with implications to the global Earth’s system properties—a critical review. Earth-Science Reviews 205:103200.CrossRefGoogle Scholar
Pecl, G. T., Araújo, M. B., Bell, J. D., Blanchard, J., Bonebrake, T. C., Chen, I.-C., Clark, T. D., et al. 2017. Biodiversity redistribution under climate change: impacts on ecosystems and human well-being. Science 355:eaai9214.CrossRefGoogle ScholarPubMed
Perini, M. M., and Calvo, J. O.. 2008. Paleontological tourism: an alternative income to vertebrate paleontology. Arquivos do Museu Nacional 66:285289.Google Scholar
Peters, S. E., and Heim, N. A.. 2011. Macrostratigraphy and macroevolution in marine environments: testing the common-cause hypothesis. Geological Society of London Special Publication 358:95104.CrossRefGoogle Scholar
Phillips, J. 1860. Life on the Earth: its origin and succession. Macmillan and Company, London and Cambridge.Google Scholar
Piazza, V., Ullmann, C. V., and Aberhan, M.. 2020. Temperature-related body size change of marine benthic macroinvertebrates across the Early Toarcian Anoxic Event. Scientific Reports 10:4675.CrossRefGoogle ScholarPubMed
Pimiento, C., and Antonelli, A.. 2022. Integrating deep-time palaeontology in conservation prioritisation. Frontiers in Ecology and Evolution 10:959364.CrossRefGoogle Scholar
Plotnick, R. E., Anderson, B. M., Carlson, S. J., Jukar, A. M., Kimmig, J., and Petsios, E.. 2023. Paleontology is far more than new fossil discoveries. Scientific American, August 30.Google Scholar
Plotnick, R. E., Anderson, B. A., Carlson, S. J., Jukar, A., Kimmig, J. and Petsios, E.. 2025. Employment in paleontology: status and trends in the United States. Paleobiology, 1–11.CrossRefGoogle Scholar
Pohl, A., Stockey, R. G., Dai, X., Yohler, R., Le Hir, G., Hülse, D., Brayard, A., Finnegan, S., and Ridgwell, A.. 2023. Why the Early Paleozoic was intrinsically prone to marine extinction. Science Advances 9:eadg7679.CrossRefGoogle ScholarPubMed
Pörtner, H.-O. 2021. Climate impacts on organisms, ecosystems and human societies: integrating OCLTT into a wider context. Journal of Experimental Biology 224:jeb238360.CrossRefGoogle ScholarPubMed
Price, S. A., and Schmitz, L.. 2016. A promising future for integrative biodiversity research: an increased role of scale-dependency and functional biology. Philosophical Transactions of the Royal Society B 371:20150228.CrossRefGoogle ScholarPubMed
Punyasena, S. W., Haselhorst, D. S., Kong, S., Fowlkes, C. C., and Moreno, J. E.. 2022. Automated identification of diverse Neotropical pollen samples using convolutional neural networks. Methods in Ecology and Evolution 13:20492064.CrossRefGoogle Scholar
Quintero, I., Landis, M. J., Jetz, W., and Morlon, H.. 2023. The build-up of the present-day tropical diversity of tetrapods. Proceedings of the National Academy of Sciences USA 120:e2220672120.CrossRefGoogle ScholarPubMed
Rabosky, D. L., and Hurlbert, A. H.. 2015. Species richness at continental scales is dominated by ecological limits. American Naturalist 185:572583.CrossRefGoogle ScholarPubMed
Raja, N. B., and Dunne, E. M.. 2022. Publication pressure threatens the integrity of palaeontological research. Geological Curator 11:407418.CrossRefGoogle Scholar
Raja, N. B., Lauchstedt, A., Pandolfi, J. M., Kim, S. W., Budd, A. F., and Kiessling, W.. 2021. Morphological traits of reef corals predict extinction risk but not conservation status. Global Ecology and Biogeography 30:15971608.CrossRefGoogle Scholar
Raja, N. B., Dunne, E. M., Matiwane, A., Khan, T. M., Nätscher, P. S., Ghilardi, A. M., and Chattopadhyay, D.. 2022. Colonial history and global economics distort our understanding of deep-time biodiversity. Nature Ecology and Evolution 6:145154.CrossRefGoogle ScholarPubMed
Rapacciuolo, G., and Blois, J. L.. 2019. Understanding ecological change across large spatial, temporal and taxonomic scales: integrating data and methods in light of theory. Ecography 42:12471266.CrossRefGoogle Scholar
Raup, D. M., and Sepkoski, J. J. Jr. 1982. Mass extinctions in the marine fossil record. Science 215:15011503.CrossRefGoogle ScholarPubMed
Team, R Core. 2023. R: a language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria. http://www.R-project.org.Google Scholar
Reddin, C. J., Kocsis, Á. T., and Kiessling, W.. 2018. Marine invertebrate migrations trace climate change over 450 million years. Global Ecology and Biogeography 27:704713.CrossRefGoogle Scholar
Reddin, C. J., Nätscher, P. S., Kocsis, Á. T., Pörtner, H.-O., and Kiessling, W.. 2020. Marine clade sensitivities to climate change conform across timescales. Nature Climate Change 10:249253.CrossRefGoogle Scholar
Reimann, L., Vafeidis, A. T., Brown, S., Hinkel, J., and Tol, R. S. J.. 2018. Mediterranean UNESCO World Heritage at risk from coastal flooding and erosion due to sea-level rise. Nature Communications 9:4161.CrossRefGoogle ScholarPubMed
Rita, P., Nätscher, P., Duarte, L. V., Weis, R., and De Baets, K.. 2019. Mechanisms and drivers of belemnite body-size dynamics across the Pliensbachian–Toarcian crisis. Royal Society Open Science 6:190494.CrossRefGoogle ScholarPubMed
Rolland, J., Henao-Diaz, L. F., Doebeli, M., Germain, R., Harmon, L. J., Knowles, L. L., Liow, L. H., Mank, J. E., Machac, A., and Otto, S. P.. 2023. Conceptual and empirical bridges between micro-and macroevolution. Nature Ecology and Evolution 7:11811193.CrossRefGoogle ScholarPubMed
Romero, I. C., Kong, S., Fowlkes, C. C., Jaramillo, C., Urban, M. A., Oboh-Ikuenobe, F., D’Apolito, C., and Punyasena, S. W.. 2020. Improving the taxonomy of fossil pollen using convolutional neural networks and superresolution microscopy. Proceedings of the National Academy of Sciences USA 117:2849628505.CrossRefGoogle ScholarPubMed
Ronquist, F., Kudlicka, J., Senderov, V., Borgström, J., Lartillot, N., Lundén, D., Murray, L., Schön, T. B., and Broman, D.. 2021. Universal probabilistic programming offers a powerful approach to statistical phylogenetics. Communications Biology 4:110.Google ScholarPubMed
Roopnarine, P. D. 2006. Extinction cascades and catastrophe in ancient food webs. Paleobiology 32:119.CrossRefGoogle Scholar
Rudzki, E. N., Kuebbing, S. E., Clark, D. R., Gharaibeh, B., Janecka, M. J., Kramp, R., Kohl, K. D., et al. 2022. A guide for developing a field research safety manual that explicitly considers risks for marginalized identities in the sciences. Methods in Ecology and Evolution 13:23182330.CrossRefGoogle Scholar
Saleh, F., Antcliffe, J. B., Lefebvre, B., Pittet, B., Laibl, L., Peris, F. P., Lustri, L., Gueriau, P., and Daley, A. C.. 2020. Taphonomic bias in exceptionally preserved biotas. Earth and Planetary Science Letters 529:115873.CrossRefGoogle Scholar
Saleh, F., Bath-Enright, O. G., Daley, A. C., Lefebvre, B., Pittet, B., Vite, A., Ma, X., et al. 2021. A novel tool to untangle the ecology and fossil preservation knot in exceptionally preserved biotas. Earth and Planetary Science Letters 569:117061.CrossRefGoogle Scholar
Salvador, R. B., Tomotani, B. M., O’Donnell, K. L., Cavallari, D. C., Tomotani, J. V., Salmon, R. A., and Kasper, J.. 2021. Invertebrates in science communication: confronting scientists’ practices and the public’s expectations. Frontiers in Environmental Science 9. https://doi.org/10.3389/fenvs.2021.606416.CrossRefGoogle Scholar
Salvador, R. B., Cavallari, D. C., Rands, D., and Tomotani, B. M.. 2022. Publication practice in taxonomy: global inequalities and potential bias against negative results. PLoS ONE 17:e0269246.CrossRefGoogle ScholarPubMed
Sanders, D., Thébault, E., Kehoe, R., and van Veen, F. J. Frank. 2018. Trophic redundancy reduces vulnerability to extinction cascades. Proceedings of the National Academy of Sciences USA 115:24192424.CrossRefGoogle ScholarPubMed
Sansom, R. S., Gabbott, S. E., and Purnell, M. A.. 2010. Decay of vertebrate characters in hagfish and lamprey (Cyclostomata) and the implications for the vertebrate fossil record. Proceedings of the Royal Society B 278:11501157.CrossRefGoogle ScholarPubMed
Saupe, E. E., Hendricks, J. R., Peterson, A. T., and Lieberman, B. S.. 2014. Climate change and marine molluscs of the western North Atlantic: future prospects and perils. Journal of Biogeography 41:13521366.CrossRefGoogle Scholar
Saupe, E. E., Myers, C. E., Peterson, A. Townsend, Soberón, J., Singarayer, J., Valdes, P., and Qiao, H.. 2019. Spatio-temporal climate change contributes to latitudinal diversity gradients. Nature Ecology and Evolution 3:14191429.CrossRefGoogle ScholarPubMed
Scarlett, J. P. 2022. The harmful legacy of colonialism in natural hazard risk. Nature Communications 13:6945.CrossRefGoogle ScholarPubMed
Schweitzer, M. H., Avci, R., Collier, T., and Goodwin, M. B.. 2008. Microscopic, chemical and molecular methods for examining fossil preservation. Comptes Rendus Palevol 7:159184.CrossRefGoogle Scholar
Seddon, A. W. R., Mackay, A. W., Baker, A. G., Birks, H. J. B., Breman, E., Buck, C. E., Ellis, E. C., et al. 2014. Looking forward through the past: identification of 50 priority research questions in palaeoecology. Journal of Ecology 102:256267.CrossRefGoogle Scholar
Seilacher, A., Reif, W. E., and Westphal, F.. 1985. Sedimentological, ecological and temporal patterns of fossil Lagerstätten. Philosophical Transactions of the Royal Society B 311:523.Google Scholar
Sepkoski, J. J., Bambach, R. K., Raup, D. M., and Valentine, J. W.. 1981. Phanerozoic marine diversity and the fossil record. Nature 293:435437.CrossRefGoogle Scholar
Shinbrot, X. A., Treibergs, K., Hernández, L. M. A., Esparza, D., Ghezzi-Kopel, K., Goebel, M., Graham, O. J., et al. 2022. The impact of field courses on undergraduate knowledge, affect, behavior, and skills: a scoping review. BioScience 72:10071017.CrossRefGoogle ScholarPubMed
Słowiński, M., Skubała, P., Zawiska, I., Kruk, A., Obremska, M., Milecka, K., and Ott, F.. 2018. Cascading effects between climate, vegetation, and macroinvertebrate fauna in 14,000-year palaeoecological investigations of a shallow lake in eastern Poland. Ecological Indicators 85:329341.CrossRefGoogle Scholar
Smiley, T. M. 2018. Detecting diversification rates in relation to preservation and tectonic history from simulated fossil records. Paleobiology 44:124.CrossRefGoogle Scholar
Smith, H. E., Bevitt, J. J., Zaim, J., Rizal, Y., Aswan, M. R. Puspaningrum, Trihascaryo, A., et al. 2021. High-resolution high-throughput thermal neutron tomographic imaging of fossiliferous cave breccias from Sumatra. Scientific Reports 11:19953.CrossRefGoogle ScholarPubMed
Smith, J. A., Durham, S. R., and Dietl, G. P.. 2018. Conceptions of long-term data among marine conservation biologists and what conservation paleobiologists need to know. Pp. 2354 in Tyler, C. L. and Schneider, C. L., eds. Marine conservation paleobiology. Springer International, Cham.CrossRefGoogle Scholar
Smith, J. A., Pruden, M. J., Handley, J. C., Durham, S. R., and Dietl, G. P.. 2023a. Assessing the utility of death assemblages as reference conditions in a common benthic index (M-AMBI) with simulations. Geological Society of London Special Publication 529:131151.CrossRefGoogle Scholar
Smith, J. A., Raja, N. B., Clements, T., Dimitrijević, D., Dowding, E. M., Dunne, E. M., Gee, B. M., et al. 2023b. Increasing the equitability of data citation in paleontology: capacity building for the big data future. Paleobiology 50:165176.CrossRefGoogle Scholar
Smith, J. A., Rillo, M. C., Kocsis, Á. T., Dornelas, M., Fastovich, D., Huang, H.-H. M., Jonkers, L., et al. 2023c. BioDeepTime: a database of biodiversity time series for modern and fossil assemblages. Global Ecology and Biogeography 32:16801689.CrossRefGoogle Scholar
Song, H., Wignall, P. B., Song, H., Dai, X., and Chu, D.. 2019. Seawater temperature and dissolved oxygen over the past 500 million years. Journal of Earth Science 30:236243.CrossRefGoogle Scholar
Song, H., Kemp, D. B., Tian, L., Chu, D., Song, H., and Dai, X.. 2021. Thresholds of temperature change for mass extinctions. Nature Communications 12:4694.CrossRefGoogle ScholarPubMed
Soul, L. C., and Friedman, M.. 2015. Taxonomy and phylogeny can yield comparable results in comparative paleontological analyses. Systematic Biology 64:608620.CrossRefGoogle ScholarPubMed
Spiridonov, A., and Lovejoy, S.. 2022. Life rather than climate influences diversity at scales greater than 40 million years. Nature 607:307312.CrossRefGoogle Scholar
Stadler, T. 2010. Sampling-through-time in birth–death trees. Journal of Theoretical Biology 267:396404.CrossRefGoogle ScholarPubMed
Stansfield, E., Mitteroecker, P., Vasilyev, S. Y., Vasilyev, S., and Butaric, L. N.. 2021. Respiratory adaptation to climate in modern humans and Upper Palaeolithic individuals from Sungir and Mladeč. Scientific Reports 11:7997.CrossRefGoogle ScholarPubMed
Stewart, M., Carleton, W. C., and Groucutt, H. S.. 2021. Climate change, not human population growth, correlates with Late Quaternary megafauna declines in North America. Nature Communications 12:965.CrossRefGoogle ScholarPubMed
Stigall, A. L. 2014. When and how do species achieve niche stability over long time scales? Ecography 37:11231132.CrossRefGoogle Scholar
Stigall, A. L. 2019. The invasion hierarchy: ecological and evolutionary consequences of invasions in the fossil record. Annual Review of Ecology, Evolution, and Systematics 50:355380.CrossRefGoogle Scholar
Stokes, A., Feig, A. D., Atchison, C. L., and Gilley, B.. 2019. Making geoscience fieldwork inclusive and accessible for students with disabilities. Geosphere 15:18091825.CrossRefGoogle Scholar
Storch, D., Menzel, L., Frickenhaus, S., and Pörtner, H.-O.. 2014. Climate sensitivity across marine domains of life: limits to evolutionary adaptation shape species interactions. Global Change Biology 20:30593067.CrossRefGoogle ScholarPubMed
Sutherland, W. J., Adams, W. M., Aronson, R. B., Aveling, R., Blackburn, T. M., Broad, S., Ceballos, G., et al. 2009. One hundred questions of importance to the conservation of global biological diversity. Conservation Biology 23:557567.CrossRefGoogle Scholar
Teng, F.-Z., Dauphas, N., and Watkins, J. M.. 2017. Non-traditional stable isotopes: retrospective and prospective. Reviews in Mineralogy and Geochemistry 82:126.CrossRefGoogle Scholar
Tihelka, E., Howard, R. J., Cai, C., and Lozano-Fernandez, J.. 2022. Was there a Cambrian explosion on land? The case of arthropod terrestrialization. Biology 11:1516.CrossRefGoogle Scholar
Trubovitz, S., Renaudie, J., Lazarus, D., and Noble, P. J.. 2023. Abundance does not predict extinction risk in the fossil record of marine plankton. Communications Biology 6:110.CrossRefGoogle Scholar
Tsuboi, M., Sztepanacz, J., De Lisle, S., Voje, K. L., Grabowski, M., Hopkins, M. J., Porto, A., et al. 2024. The paradox of predictability provides a bridge between micro- and macroevolution. Journal of Evolutionary Biology 37:14131432.CrossRefGoogle ScholarPubMed
Vahdati, A. R., Weissmann, J. D., Timmermann, A., de León, M. P., and Zollikofer, C. P.. 2022. Exploring Late Pleistocene hominin dispersals, coexistence and extinction with agent-based multi-factor models. Quaternary Science Reviews 279:107391.CrossRefGoogle Scholar
Valenzuela-Toro, A. M., and Viglino, M.. 2021. Latin American challenges. Nature 598:374375.CrossRefGoogle Scholar
Vermeij, G. J., and Roopnarine, P. D.. 2013. Reining in the Red Queen: the dynamics of adaptation and extinction reexamined. Paleobiology 39:560575.CrossRefGoogle Scholar
Vinther, J. 2015. A guide to the field of palaeo colour: melanin and other pigments can fossilise: reconstructing colour patterns from ancient organisms can give new insights to ecology and behaviour. BioEssays 37:643656.CrossRefGoogle Scholar
Vogel, G. 2019. Natural history museums face their own past. Science 363:13711372.CrossRefGoogle ScholarPubMed
Vousdoukas, M. I., Clarke, J., Ranasinghe, R., Reimann, L., Khalaf, N., Duong, T. M., Ouweneel, B., et al. 2022. African heritage sites threatened as sea-level rise accelerates. Nature Climate Change 12:256262.CrossRefGoogle Scholar
Vrba, E. S. 1985. Environment and evolution: alternative causes of the temporal distribution of evolutionary events. South African Journal of Science 81:229236.Google Scholar
Vrba, E. S. 1992. Mammals as a key to evolutionary theory. Journal of Mammalogy 73:128.CrossRefGoogle Scholar
Vrba, E. S. 1993. Turnover-pulses, the Red Queen, and related topics. American Journal of Science 293:418.CrossRefGoogle Scholar
Warnock, R. C., and Wright, A. M.. 2020. Understanding the tripartite approach to Bayesian divergence time estimation. Cambridge University Press, Cambridge.CrossRefGoogle Scholar
Whitaker, A. F., and Kimmig, J.. 2020. Anthropologically introduced biases in natural history collections, with a case study on the invertebrate paleontology collections from the middle Cambrian Spence Shale Lagerstätte. Palaeontologia Electronica 23:a58.Google Scholar
Wiemann, J., Crawford, J. M., and Briggs, D. E.. 2020. Phylogenetic and physiological signals in metazoan fossil biomolecules. Science Advances 6:eaba6883.CrossRefGoogle ScholarPubMed
Willis, K. J., and Bhagwat, S. A.. 2010. Questions of importance to the conservation of biological diversity: answers from the past. Climate of the Past 6:759769.CrossRefGoogle Scholar
Wing, S. L., Harrington, G. J., Smith, F. A., Bloch, J. I., Boyer, D. M., and Freeman, K. H.. 2005. Transient floral change and rapid global warming at the Paleocene-Eocene boundary. Science 310:993996.CrossRefGoogle ScholarPubMed
Wisz, M. S., Pottier, J., Kissling, W. D., Pellissier, L., Lenoir, J., Damgaard, C. F., Dormann, C. F., et al. 2013. The role of biotic interactions in shaping distributions and realised assemblages of species: implications for species distribution modelling. Biological Reviews 88:1530.CrossRefGoogle ScholarPubMed
Woehle, C., Roy, A.-S., Glock, N., Michels, J., Wein, T., Weissenbach, J., Romero, D., et al. 2022. Denitrification in foraminifera has an ancient origin and is complemented by associated bacteria. Proceedings of the National Academy of Sciences USA 119:e2200198119.CrossRefGoogle ScholarPubMed
Woodhouse, A., Swain, A., Fagan, W. F., Fraass, A. J., and Lowery, C. M.. 2023. Late Cenozoic cooling restructured global marine plankton communities. Nature 614:713718.CrossRefGoogle ScholarPubMed
Wright, D. F. 2015. Fossils, homology, and “Phylogenetic Paleo-ontogeny”: a reassessment of primary posterior plate homologies among fossil and living crinoids with insights from developmental biology. Paleobiology 41:570591.CrossRefGoogle Scholar
Wright, A. M., Bapst, D. W., Barido-Sottani, J., and Warnock, R. C. M.. 2022. Integrating fossil observations into phylogenetics using the fossilized birth–death model. Annual Review of Ecology, Evolution, and Systematics 53:251273.CrossRefGoogle Scholar
Yamamoto, S., and Caterino, M. S.. 2023. A remarkable new fossil species of Amplectister with peculiar hindleg modifications (Coleoptera: Histeridae): further evidence for myrmecophily in Cretaceous clown beetles. Palaeoworld 32:481489.CrossRefGoogle Scholar
Yasuhara, M., and Deutsch, C. A.. 2022. Paleobiology provides glimpses of future ocean: fossil records from tropical oceans predict biodiversity loss in a warmer world. Science 375:2526.CrossRefGoogle Scholar
Yasuhara, M., and Deutsch, C. A.. 2023. Tropical biodiversity linked to polar climate. Nature 614:626628.CrossRefGoogle ScholarPubMed
Yasuhara, M., Wei, C.-L., Kucera, M., Costello, M. J., Tittensor, D. P., Kiessling, W., Bonebrake, T. C., et al. 2020. Past and future decline of tropical pelagic biodiversity. Proceedings of the National Academy of Sciences USA 117:1289112896.CrossRefGoogle ScholarPubMed
Zacaï, A., Monnet, C., Pohl, A., Beaugrand, G., Mullins, G., Kroeck, D. M., and Servais, T.. 2021. Truncated bimodal latitudinal diversity gradient in early Paleozoic phytoplankton. Science Advances 7:eabd6709.CrossRefGoogle ScholarPubMed
Zuschin, M. 2023. Challenges of conservation paleobiology: from baselines to novel communities to the necessity for granting rights to nature. Palaios 38:259263.CrossRefGoogle Scholar
Figure 0

Figure 1. The question pathway in the Big Questions project. Questions were submitted by the global community in one of three solicitations. Submitted questions were assigned to working groups (n = 12) composed of self-identified topic experts who chose to participate in the project. Working groups were guided by one to three leaders (larger icons) and refined their assigned questions to a preliminary list. These preliminary questions were assessed by the entire Big Questions team to improve question quality and reduce redundancies in questions from different groups. Using whole-team feedback, working groups (reduced to 11 due to overlaps; Table 2) produced a refined set of final big questions. Created with BioRender.com.

Figure 1

Table 1. Countries and administrative regions represented in the Big Questions project by affiliations of the authorship team at the time of manuscript submission, with respect to when individuals joined the project. Note: as countries and administrative regions represented are derived from the institutional affiliations of the authors, this is likely an underestimate of the number of countries and administrative regions represented by individuals in this project

Figure 2

Table 2. Working group themes and numbers of questions related to these groups at three stages of the project. The number of individuals assigned to each group is also provided, with the number of group leaders in parentheses. *The theme “Ecosystems, Environments, and their Records” was included originally, but after the whole-team feedback phase (Fig. 1), considerable overlaps with questions from other groups were apparent, and all questions from this theme were ultimately distributed elsewhere or subsumed by questions in other groups. Total is greater than the number of submitted questions (n = 528), because a question that was relevant to more than one group was assigned to each group for consideration

Figure 3

Figure 2. Assignments of originally submitted questions to different working groups. Each question was assigned to at least one group, and many were also assigned to a second group with topic overlap. Width of the outer circle represents the number of questions assigned to each working group (counts also provided in parentheses). Bands connecting different working groups represent the questions assigned to each of the groups, with thicker bands indicating a larger number of questions shared between groups. Created in R Statistical Software (v. 4.3.1; R Core Team 2023) using the circlize package (Gu et al. 2014) and the Paired palette from RColorBrewer (Neuwirth 2022).

Figure 4

Table 3. Big Questions for the working group on “The Adequacy of the Fossil Record”

Figure 5

Table 4. Big Questions for the working group on “Scaling Ecological and Evolutionary Processes and Patterns”

Figure 6

Table 5. Big Questions for the working group on “Phylogenetics, Taxonomy, and Systematics”

Figure 7

Table 6. Big Questions for the working group on “Biodiversity Dynamics in Space and Time”

Figure 8

Table 7. Big Questions for the working group on “Biodiversity Drivers”

Figure 9

Table 8. Big Questions for the working group on “Adaptations, Innovations, Origins”

Figure 10

Table 9. Big questions for the working group on “Extinction Dynamics”

Figure 11

Table 10. Big Questions for the working group on “Climate Change Past and Present”

Figure 12

Table 11. Big Questions for the working group on “Conservation Paleobiology”

Figure 13

Table 12. Big Questions for the working group on “Fundamental Issues”

Figure 14

Table 13. Big Questions for the working group on “Looking Inward and Outward”

Figure 15

Figure 3. The Big Questions project can be used as a tool to guide research in paleontology and to advocate for the importance of funding paleontological research.