Hostname: page-component-78c5997874-j824f Total loading time: 0 Render date: 2024-11-13T02:09:47.678Z Has data issue: false hasContentIssue false

In search of the ice age tropics, a tribute to Prof. Daniel Livingstone and Prof. Paul Colinvaux

Published online by Cambridge University Press:  17 January 2018

Mark B. Bush*
Affiliation:
Department of Biological Sciences, Florida Institute of Technology, Melbourne, Florida 32901, USA
William D. Gosling
Affiliation:
Institute for Biodiversity and Ecosystem Dynamics, University of Amsterdam, 1090 GE Amsterdam, the Netherlands School of Environmental, Earth and Ecosystem Sciences, The Open University, Milton Keynes MK7 6AA, United Kingdom
*
*Corresponding author at: Department of Biological Sciences, Florida Institute of Technology, 150 W. University Blvd., Melbourne, Florida 32901, USA. E-mail address: mbush@fit.edu (M.B. Bush).
Rights & Permissions [Opens in a new window]

Abstract

Type
Tribute to Daniel Livingstone and Paul Colinvaux
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 (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
Copyright
Copyright © University of Washington. Published by Cambridge University Press, 2018

PIONEERS OF TROPICAL PALEOECOLOGY

Daniel Livingstone and Paul Colinvaux (Fig. 1a and b) were intellectual pioneers who helped to shape modern tropical paleoecology. Linked in life by bonds of friendship, they shared a common philosophy of challenging conventional wisdom and exploring remote areas to seek answers. Dan and Paul both had common starts to their research careers with PhD’s focused on the arctic (Livingstone, Reference Livingstone1955a) and strong early influence and guidance from Prof. Ed Deevey at Yale; he was Dan’s PhD advisor and Paul’s postdoctoral mentor. At Deevey’s urging, both men turned their attention to the tropics. In his 2007 book, Paul summed up their division of labor: “Dan was already doing Africa; I chose the Amazon” (Colinvaux, Reference Colinvaux2007, p. 11). Both Livingstone and Colinvaux were first and foremost ecologists, who used paleoecology to answer ecological questions. Dan and Paul both died in the spring of 2016, and this special issue is a tribute to the inspiring enthusiasm and energy they brought to research and education.

Figure 1 (color online) (a) Dan Livingstone (photo courtesy of Duke University). (b) Paul Colinvaux at El Junco Crater Lake, Galapagos Islands (photo courtesy of Miriam Steinitz-Kannan).

Members of every generation can argue that they live in interesting times, but for budding ecologists, the late 1950s and 1960s, when Dan and Paul were in graduate school, were especially formative. Geology, climatology, and ecology were being revolutionized by new ideas and technologies. In this period, plate tectonics went from being a fringe idea to being widely accepted (Dietz, Reference Dietz1961). Gone was the insistence that organisms must have dispersed across oceans or migrated across lost land bridges. Vicariance was now a far more plausible means of speciation than previously thought (Wilson, Reference Wilson1963). A welter of new information based on isotopic chemistry was reshaping paleoecology and paleoclimatology. Radiocarbon dating, first developed by Libby (Reference Libby1960), allowed fist-sized sections of organic-rich material to be dated. This development transformed the study of lake sedimentary sequences, allowing real chronologies to be developed and to set aside assumptions that similar looking vegetation changes were coeval. Emiliani’s (Reference Emiliani1955) isotopic record of marine sediment provided the first strong record of the changes of global temperature within the Quaternary.

That Quaternary ice ages were relatively slow to develop, stair-stepping down toward a maximum cooling, before rapidly bouncing out into interglacial conditions, was of tremendous significance to anyone contemplating species migrations. For decades ecologists had been debating whether communities were relatively fixed or fluid in composition (Clements, Reference Clements1916; Gleason, Reference Gleason1926), and a pivotal moment was reached in that discussion in the early 1960s. Plant phytosociologists whose views had held sway since the 1920s tended to see the world as tightly coevolved communities that would migrate as a unit. When viewed through time, vegetation zones of temperate forest, boreal forest, and tundra were depicted being driven north and south (Braun, Reference Braun1955) or up- and downslope (Gonzalez et al., Reference Gonzalez, Van der Hammen and Flint1966). Whittaker’s demonstration that species did not turn over in unison along ecological gradients in the Smoky and Siskyou Mountains (Whittaker, Reference Whittaker1956, Reference Whittaker1960) signaled a paradigm shift in how ecologists viewed species occurrence in communities. As paleoecologists started to champion the individuality of species’ responses to past climate change, Livingstone in Africa and Colinvaux in South America became advocates of this new view.

Livingstone and Colinvaux combined developments in geology, climatology, and ecology and used these advances to tackle great questions of species distributions, endemicity, and richness. When they started their careers in the 1960s, fossil pollen records existed for Europe and much of North America, but areas of more extreme climate were virtually unknown. At the time of their deaths, in 2016, hundreds of records of past ecological change existed from the tropics (Flantua et al., Reference Flantua, Hooghiemstra, Grimm, Behling, Bush, González-Arango, Gosling, Ledru, Lozano-García and Maldonado2015). Today, the pursuit of the origins of tropical diversity goes on, but this is now guided by a framework of knowledge that both Dan and Paul helped establish. In their search for the ice age tropics, both Dan and Paul came to realize the rarity of ancient lakes in the tropical lowlands and the potential importance of any such archive. Consequently, they were at the forefront of multiproxy analysis, actively seeking collaborators to maximize data extraction from sediments using X-radiography, geochemistry, diatoms, charcoal, wood, phytoliths, and cuticles (e.g., Livingstone and Fleischer, Reference Livingstone and Fleischer1963; Steinitz-Kannan et al., Reference Steinitz-Kannan, De Oliveira, Miller and Colinvaux1986; Maley et al., Reference Maley, Livingstone, Giresse, Thouveny, Brenac, Kelts and Kling1990; Bush et al., Reference Bush, Piperno, Colinvaux, de Oliveira, Krissek, Miller and Rowe1992).

Dan Livingstone will be remembered for his seminal studies of the paleoecology of African lake systems that revealed the history of African glaciations (Livingstone, Reference Livingstone1962, Reference Livingstone1965, Reference Livingstone1967, Reference Livingstone1971a, Reference Livingstone1975; Talbot et al., Reference Talbot, Livingstone, Palmer, Maley, Melack, Delibrias and Gulliksen1984), the history of the African rift lakes (Livingstone, Reference Livingstone1965), and the invention of the Livingstone piston corer (Livingstone, Reference Livingstone1955b). Dan’s first publication had been on fish populations in four lakes in northern Alaska (Livingstone, 1950/Reference Livingstone1951). Although his career moved away from fish biology, he maintained a deep connection to limnology, and his graduate students were often engaged in studying the limnology of tropical systems (Stager et al., Reference Stager, Reinthal and Livingstone1986; Haberyan and Hecky, Reference Haberyan and Hecky1987; Kling, Reference Kling1988). Dan built an extensive pollen collection, describing the pollen of many African species for the first time. The pollen collection supported analysis of fossil pollen from African lake sediments. Although obtaining long histories of African climate and vegetation change was a passion, his laboratory at Duke University was an incubator of ideas where ecological questions, not geography, drove inquiry. Indeed, Dan’s first doctoral student, Paul Colinvaux, never worked in Africa, but undertook a study of Alaskan systems, and Dan’s last student, Eric Kjellmark, worked on blue holes in the Bahamas (Kjellmark, Reference Kjellmark1995). It was this breadth of knowledge that made Dan such an engaging colleague and effective mentor. In today’s world of H-indexes and academic metrics, Dan stood out by not claiming authorship on papers resulting from his PhD students’ endeavors. He contributed to those papers but believed the body of work was that of the students and that they deserved full, sole-author recognition.

Paul Colinvaux loved the challenge of big ideas. Unlike Livingstone, who was naturally retiring, Colinvaux was energized by a crowd and thrived at Ohio State University where he taught ecology classes to as many as a thousand students. He advanced newly burgeoning ideas in ecology and attempted to popularize the discipline through textbooks (Colinvaux, Reference Colinvaux1973), social commentary (Colinvaux, Reference Colinvaux1980), and short essays (Colinvaux, Reference Colinvaux1979). As a researcher, the driving question behind much of his work was, why are there so many tropical species? Haffer (Reference Haffer1969) revolutionized the discussion over the origin of Amazonian diversity by hypothesizing that during glacial periods, arid conditions forced a contraction of rain forests into isolated islands separated by seas of savanna, with forests expanding to their present limits during the interglacial periods. He argued that such glacial-interglacial changes in rainfall served as a pumping mechanism creating the isolation necessary for allopatric speciation. After at first accepting this idea, Colinvaux went on to challenge it. Indeed, the quest to refute the refugial hypothesis propelled him to search for ancient lakes across Central and tropical South America.

Colinvaux’s first foray into South American ecology was to investigate the paleoecology of the Galapagos Islands (Colinvaux, Reference Colinvaux1968, Reference Colinvaux1972). His efforts spread to mainland Ecuador, Peru, Panama, and Brazil (Steinitz-Kannan et al., Reference Steinitz-Kannan, Colinvaux and Kannan1983; Colinvaux et al., Reference Colinvaux, Miller, Liu, Steinitz-Kannan and Frost1985, Reference Colinvaux, Frost, Frost, Liu and Steinitz-Kannan1988; Liu and Colinvaux, Reference Liu and Colinvaux1985; De Oliveira et al., Reference De Oliveira, Steinitz-Kannan, Miller and Colinvaux1986; Bush and Colinvaux, Reference Bush and Colinvaux1990; Piperno et al., Reference Piperno, Bush and Colinvaux1990) and still pursued long records in the Arctic (Eisner and Colinvaux, Reference Eisner and Colinvaux1990; Lozhkin et al., Reference Lozhkin, Anderson, Eisner, Ravako, Hopkins, Brubaker, Colinvaux and Miller1993). To facilitate his exploration of remote areas, Paul developed the lake sediment corer invented by Dan into a lightweight “backpackable” design (Fig. 2) that has become the standard kit for many tropical paleoecologists (Colinvaux et al., Reference Colinvaux, de Oliveira and Moreno1999). Both Paul and Dan recruited and trained graduate students from the countries where they worked, creating an international legacy of ecologists and paleoecologists.

Figure 2 (color online) A core being raised using a Colinvaux-Vohnout piston sampler from a raft of inflatable boats at Lake Llaviucu (also called Surucucho) in June 2010. This lake had previously been cored by Colinvaux’s team in 1988 (Colinvaux et al., Reference Colinvaux, Bush, Steinitz-Kannan and Miller1997).

CLIMATE, VEGETATION, AND BIODIVERSITY

In this issue, we present 10 articles that build on the legacy of Livingstone and Colinvaux, contributing to the key themes of climate, vegetation, and biodiversity within the tropics that can be found throughout their work. Inferences about the magnitude of past human influence and climatic change in the tropics have been based on inferences drawn from the fossil record, including seminal work by Livingstone in Africa (Livingstone, Reference Livingstone1971b, Reference Livingstone1975, Reference Livingstone1982, Reference Livingstone1984) and Colinvaux in South America (Colinvaux, Reference Colinvaux1989, Reference Colinvaux1996; Colinvaux et al., Reference Colinvaux, Irion, Räsänen, Bush and De Mello2001). In the 10 articles in this issue, 9 new tropical fossil records are presented to provide new insights into past climate change and help to expand our knowledge of spatial variation in tropical vegetation change.

From Africa, new data from three sites, Lakes Edward, Ejagham, and Ishiba Ngandu, are presented (Haberyan, Reference Haberyan2018; Ivory and Russell, Reference Ivory and Russell2018; Stager et al., Reference Stager, Alton, Martin, King, Petruny, Wiltse and Livingstone2018). Ivory and Russell present new fossil pollen and charcoal data from Lake Edward (Democratic Republic of Congo and Uganda) that indicate an expansion of forests during the early Holocene under warm, wet climates. Subsequent oscillations in forest cover reflect a combination of change in precipitation and human land-use practices. Stager et al. (Reference Stager, Alton, Martin, King, Petruny, Wiltse and Livingstone2018) report a 14C-dated paleoecological record from Lake Ejagham in Cameroon. Originally cored by Dan Livingstone, the sediments from this lake define the age of the lake and constrain the evolutionary window that allowed five cichlid fish to speciate. Haberyan provides fossil diatom data from Lake Ishiba Ngandu, Zambia; Livingstone raised the sediments in the early 1960s and described the fossil pollen (Livingstone, Reference Livingstone1971a). The diatom data provide a limnological history of the site and suggest unusually stable conditions for the last 30,000 yr compared with systems such as the Okavango to the west and the great rift lakes to the east.

Vegetation reconstructions from five previously unstudied South American lakes (one in Peru and four in Brazil) are presented here and give new insights into past climate. The data presented by Schiferl et al. (Reference Schiferl, Bush, Silman and Urrego2018) provide a 3800 yr paleoclimatic history from midelevation forests in the Peruvian Andes. The fossil pollen data relate changes in forest composition to changes in North Atlantic sea-surface temperature. The record from Lake Acarabixi (Rodriguez-Zorro et al., Reference Rodriguez-Zorro, Turqu, Cordeiro, Moreira, McMichael and Behling2018) lends weight to inferences that Amazonia was already forested at the onset of the Holocene (following Colinvaux et al., Reference Colinvaux, De Oliveira, Moreno, Miller and Bush1996), although the composition of the fossil pollen shows marked differences between the early Holocene and modern times. The Serra do Tabuleiro peat bog record, presented by Behling and de Oliveira (Reference Behling and de Oliveira2018) is from the Atlantic rain forest and captures the transition from open woodland to Atlantic rain forest at the onset of the Holocene. Raczka et al. (Reference Raczka, Bush and de Oliveira2018) present the first study from the lowland Neotropics on fossil pollen and Sporormiella to reconstruct the history of megafaunal loss from two sites in southeastern Brazil. The 25,000 yr sequences provide new insights about the timing of nonanalog plant communities relative to megafaunal population collapse.

Loughlin et al. (Reference Loughlin, Gosling and Montoya2018) studied an area that had yielded one of Colinvaux’s most important paleoecological records, that of Mera Ecuador (Liu and Colinvaux, Reference Liu and Colinvaux1985; Bush et al., Reference Bush, Colinvaux, Wiemann, Piperno and Liu1990). Loughlin et al.’s work explores an understudied source of potential paleoecological data by analyzing nonpollen palynomorphs. Habitat fidelity is revealed among spores that had never previously been described.

With the ever-increasing number of studies from the tropics, collating and synthesizing information is an ongoing challenge. This special issue includes two synthetic analyses of fossil pollen data—one from Africa, led by Jean Maley, a longtime collaborator of Livingstone (Maley et al., Reference Maley, Doumenge, Giresse, Mahe, Philippon, Hubau, Lokonda, Tshibamba and Chepstow-Lusty2018), and one from South America by Smith and Mayle (Reference Smith and Mayle2018). The manuscript by Maley et al. centers on the equatorial east African region and provides insights on regional vegetation prior to widespread agricultural expansion. Smith and Mayle provide a synthesis of vegetation change for the last 6000 yr, drawn from 153 Southern Hemisphere Neotropical sites. The 83 citations that underpin this study reflect how rapidly this field is changing, insofar as just 13 of those citations predate the year 2000.

LEGACY AND FUTURE PERSPECTIVES

Dan Livingstone and Paul Colinvaux advanced their science and provided a platform of knowledge from which the current generation of paleoecological researchers is able to delve deeper into tropical ecological and biogeographic questions. They would have been the first to recognize that, although making significant discoveries, some of those big questions that they strove to address remain as topics for future research. Such an admission lies at the heart of science, for as we gain knowledge of a system, the questions become more sharply focused. When Livingstone and Colinvaux started their research, the lowland tropics were seen as climatically stable over the long term or, in the case of refugial hypothesis, a very simple dichotomy between wet and dry (with constant temperature). It was their efforts that revealed ice age cooling in the tropical lowlands and indicated that there was also considerable variation in precipitation.

Throughout the tropics, paleoecology is a lake-limited science. Livingstone and Colinvaux knew the disappointment of coring many promising sites only to find pollen was not preserved, the coring was stopped by ash, or the site was simply too young to provide a glacial-aged record. However, they were motivated to keep searching by the sheer delight of the rare find, an ancient lake with a story to tell. Over the coming years, paleoecologists working in the tropics must continue the quest for further records to improve our understanding of spatial variance within these complex systems. The heterogeneity of the tropics to climatic forcing is becoming ever more apparent from modern studies (Marengo et al., Reference Marengo, Tomasella, Soares, Alves and Nobre2012), so it is unlikely that vast tropical regions, such as Amazonia, responded in a spatially uniform fashion to past global climate changes.

The sheer diversity of lowland tropical systems is both a curse and a boon. Nowhere else is there the potential sensitivity to investigate ecosystem responses to human or natural forcing. The challenge, however, is in recognizing the host of rare taxa that form the long distributional tail of tropical pollen data. Again, Livingstone and Colinvaux led the way in establishing significant modern pollen reference collections, some of which were captured in pollen atlases (Colinvaux et al., Reference Colinvaux, de Oliveira and Moreno1999; Bush and Weng, Reference Bush and Weng2007; Gosling et al., Reference Gosling, Miller and Livingstone2013), but there is a huge potential for improvement in this aspect of our discipline.

Ancient lakes suitable for paleoecological reconstruction are treasures, especially in the lowland tropics where they are so rare. Extracting the maximum amount of information from those records is an obligation for all tropical paleoecologists and should foster new collaborations to broaden the range of analytical techniques applied to each record. As truly multiproxy records emerge from the tropics, we can move from linking vegetation change and climate to understanding the function of ecosystems and landscapes. Such understandings improve our ability to relate ecosystem resilience and sensitivity to habitat and species complexity and, ultimately, to conserving biodiversity. This observation brings us back to that most fundamental question inherent to, but not answered by, Livingstone’s and Colinvaux’s research: Why are there so many tropical species?

References

REFERENCES

Behling, H., de Oliveira, M.A.T., 2018. Evidence of a late glacial warming event and early Holocene cooling in the southern Brazilian coastal highlands. Quaternary Research (in press). https://doi.org/10.1017/qua.2017.87.Google Scholar
Braun, E.L., 1955. The phytogeography of unglaciated eastern United States and its interpretation. Botanical Review 21, 297.Google Scholar
Bush, M.B., Colinvaux, P.A., 1990. A pollen record of a complete glacial cycle from lowland Panama. Journal of Vegetation Science 1, 105118.Google Scholar
Bush, M.B., Colinvaux, P.A., Wiemann, M.C., Piperno, D.R., Liu, K.-B., 1990. Late Pleistocene temperature depression and vegetation change in Ecuadorian Amazonia. Quaternary Research 34, 330345.Google Scholar
Bush, M.B., Piperno, D.R., Colinvaux, P.A., de Oliveira, P.E., Krissek, L.A., Miller, M.C., Rowe, W.E., 1992. A 14 300-yr paleoecological profile of a lowland tropical lake in Panama. Ecological Monographs 62, 251275.Google Scholar
Bush, M.B., Weng, C., 2007. Introducing a new (freeware) tool for palynology. Journal of Biogeography 34, 377380.Google Scholar
Clements, F.E., 1916. Plant Succession. Cargnegie Institution of Washington, Washington, DC.Google Scholar
Colinvaux, P., de Oliveira, P.E., Moreno, P.J.E., 1999. Amazon Pollen Manual and Atlas. Harwood Academic, Amsterdam.Google Scholar
Colinvaux, P., Irion, G., Räsänen, M., Bush, M., De Mello, J.N., 2001. A paradigm to be discarded: geological and paleoecological data falsify the Haffer & Prance refuge hypothesis of Amazonian speciation. Amazoniana 16, 609646.Google Scholar
Colinvaux, P., Miller, M., Liu, K.-b., Steinitz-Kannan, M., Frost, I., 1985. Discovery of permanent Amazon lakes and hydraulic disturbance in the upper Amazon basin. Nature 313, 4245.Google Scholar
Colinvaux, P.A., 1968. Reconaissance and chemistry of the lakes and bogs of the Galapagos Islands. Nature 219, 590594.Google Scholar
Colinvaux, P.A., 1972. Climate and the Galapagos Islands. Nature 240, 1720.Google Scholar
Colinvaux, P.A., 1973. Introduction to Ecology. Wiley, New York.Google Scholar
Colinvaux, P.A., 1979. Why Big Fierce Animals Are Rare: An Ecologist’s Perspective. Princeton University Press, Princeton, NJ.Google Scholar
Colinvaux, P.A., 1980. The Fates of Nations. Simon and Schuster, New York.Google Scholar
Colinvaux, P.A., 1989. The past and future Amazon. Scientific American 260, 101108.Google Scholar
Colinvaux, P.A., 1996. Quaternary environmental history and forest diversity in the Neotropics. In: Jackson, J.B.C., Budd, A.F., Coates, A.G. (Eds.), Evolution and Environment in Tropical America. University of Chicago Press, Chicago, pp. 359405.Google Scholar
Colinvaux, P.A., 2007. Amazon Expeditions: My Quest for the Ice-Age Equator. Yale University Press, New Haven, CT.Google Scholar
Colinvaux, P.A., Bush, M.B., Steinitz-Kannan, M., Miller, M.C., 1997. Glacial and postglacial pollen records from the Ecuadorian Andes and Amazon. Quaternary Research 48, 6978.Google Scholar
Colinvaux, P.A., De Oliveira, P.E., Moreno, J.E., Miller, M.C., Bush, M.B., 1996. A long pollen record from lowland Amazonia: forest and cooling in glacial times. Science 274, 8588.Google Scholar
Colinvaux, P.A., Frost, M., Frost, I., Liu, K.-B., Steinitz-Kannan, M., 1988. Three pollen diagrams of forest disturbance in the western Amazon basin. Review of Palaeobotany and Palynology 55, 7381.Google Scholar
Correa-Metrio, A., Urrego, D.H., Cabrera, K.R., Bush, M.B., 2010. paleoMAS: Paleoecological analysis. R package version 2.0 (accessed). The R Project for Statistical Computing, Vienna http://cran.r-project.org/package=paleoMAS.Google Scholar
De Oliveira, P.E., Steinitz-Kannan, M., Miller, M.A.C., Colinvaux, P.A., 1986. Las diatomeas del Ecuador III. Diatomeas fosiles de la Laguna de Kumpaka. Revista Geografica 24, 4160.Google Scholar
Dietz, R.S., 1961. Continent and ocean basin evolution by spreading of the sea floor. Nature 190, 854857.Google Scholar
Eisner, W.R., Colinvaux, P.A., 1990. A long pollen record from Ahaliorak Lake, arctic Alaska. Review of Palaeobotany and Palynology 63, 3552.Google Scholar
Emiliani, C., 1955. Pleistocene temperatures. Journal of Geology 63, 538578.Google Scholar
Flantua, S.G., Hooghiemstra, H., Grimm, E.C., Behling, H., Bush, M.B., González-Arango, C., Gosling, W.D., Ledru, M.-P., Lozano-García, S., Maldonado, A., 2015. Updated site compilation of the Latin American Pollen Database. Review of Palaeobotany and Palynology 223, 104115.Google Scholar
Gleason, H.A., 1926. The individualistic concept of the plant association. Bulletin of the Torrey Botanical Club 53, 726.Google Scholar
Gonzalez, E., Van der Hammen, T., Flint, R.F., 1966. Late Quaternary glacial and vegetational sequence in Valle de Lagunillas, Sierra Nevada del Cocuy, Colombia. Leidse Geologische Mededelingen 32, 157182.Google Scholar
Gosling, W.D., Miller, C.S., Livingstone, D.A., 2013. Atlas of the tropical West African pollen flora. Review of Palaeobotany and Palynology 199, 1135.Google Scholar
Haberyan, K.A., Hecky, R.E., 1987. The late Pleistocene and Holocene stratigraphy and paleolimnology of Lakes Kivu and Tanganyika. Palaeogeography, Palaeoclimatology, Palaeoecology 61, 169197.Google Scholar
Haffer, J., 1969. Speciation in Amazonian forest birds. Science 165, 131137.Google Scholar
Ivory, S.J., Russell, J., 2018. Lowland forest collapse and early human impacts at the end of the African Humid Period at Lake Edward, equatorial East Africa. Quaternary Research (in press). https://doi.org/10.1017/qua.2017.48.Google Scholar
Kjellmark, E.W., 1995. The Effects of Late Holocene Climate Change and Human Disturbance on the Vegetation and Fire History of Andros Island, Bahamas. Duke University, Durham, NC.Google Scholar
Kling, G.W., 1988. Comparative transparency, depth of mixing, and stability of stratification in lakes of Cameroon, West Africa. Limnology and Oceanography 33, 2740.Google Scholar
Libby, W.F., 1960. Radiocarbon Dating. Nobel lecture.Google Scholar
Liu, K., Colinvaux, P.A., 1985. Forest changes in the Amazon Basin during the last glacial maximum. Nature 318, 556557.Google Scholar
Livingstone, D., 1955a. Some pollen profiles from arctic Alaska. Ecology 36, 587600.Google Scholar
Livingstone, D.A., 1950/1951. The freshwater fishes on Nova Scotia. Proceedings of the Nova Scotia Institute of Science 23, 190.Google Scholar
Livingstone, D.A., 1955b. A lightweight piston sampler for lake deposits. Ecology 36, 137139.Google Scholar
Livingstone, D.A., 1962. Age of deglaciation in the Ruwenzori Range, Uganda. Nature 194, 859860.Google Scholar
Livingstone, D.A., 1965. Sedimentation and the history of water level change in Lake Tanganyika. Limnology and Oceanography 10, 607610.Google Scholar
Livingstone, D.A., 1967. Postglacial vegetation of the Ruwenzori Mountains in equatorial Africa. Ecological Monographs 37, 2552.Google Scholar
Livingstone, D.A., 1971a. A 22,000-year pollen record from the plateau of Zambia. Limnology and Oceanography 16, 349356.Google Scholar
Livingstone, D.A., 1971b. Speculations on the climatic history of mankind: inference from the fossil record of lake deposits suggests how climate may have controlled the distribution and abundance of man over the ages. American Scientist 59, 332337.Google Scholar
Livingstone, D.A., 1975. Late Quaternary climate change in Africa. Annual Review of Ecology and Systematics 6, 249280.Google Scholar
Livingstone, D.A., 1982. Quaternary geography of Africa and the refuge theory. In: Prance, G.T. (Ed.), Biological Diversification in the Tropics. Columbia University Press, New York, pp. 523536.Google Scholar
Livingstone, D.A., 1984. Interactions of food production and changing vegetation in Africa. In: Clark, J.D., Brandt, S.A. (Eds.), From Hunters to Farmers: The Causes and Consequences of Food Production in Africa. University of California Press, Berkeley, pp. 2225.Google Scholar
Livingstone, D.A., Fleischer, M., 1963. Data of Geochemistry. U.S. Government Printing Office, Washington, DC.Google Scholar
Loughlin, N.J.D., Gosling, W.D., Montoya, E., 2018. Identifying environmental drivers of fungal non-pollen palynomorphs in the montane forest of the eastern Andean flank, Ecuador. Quaternary Research (in press). https://doi.org/10.1017/qua.2017.73.Google Scholar
Lozhkin, A.V., Anderson, P.M., Eisner, W.R., Ravako, L.G., Hopkins, D.M., Brubaker, L.B., Colinvaux, P.A., Miller, M.C., 1993. Late Quaternary lacustrine pollen records from southwestern Beringia. Quaternary Research 39, 314324.Google Scholar
Maley, J., Doumenge, C., Giresse, P., Mahe, G., Philippon, N., Hubau, W., Lokonda, M., Tshibamba, J., Chepstow-Lusty, A., 2018. Late Holocene forest contraction and fragmentation in Central Africa. Quaternary Research (in press).Google Scholar
Maley, J., Livingstone, D.A., Giresse, P., Thouveny, N., Brenac, P., Kelts, K., Kling, G., et al., 1990. Lithostratigraphy, volcanism, palaeomagnetism and palynology of Quaternary lacustrine deposits from Barombi Mbo (West Cameroon): preliminary results. Journal of Volcanology and Geothermal Research 42, 319335.Google Scholar
Marengo, J., Tomasella, J., Soares, W., Alves, L., Nobre, C., 2012. Extreme climatic events in the Amazon basin. Theoretical and Applied Climatology 107, 7385.Google Scholar
Piperno, D.R., Bush, M.B., Colinvaux, P.A., 1990. Paleoenvironments and human settlement in late-glacial Panama. Quaternary Research 33, 108116.Google Scholar
Raczka, M.F., Bush, M.B., de Oliveira, P.D., 2018. The collapse of megafaunal populations in southeastern Brazil. Quaternary Research (in press). https://doi.org/10.1017/qua.2017.60.Google Scholar
Rodriguez-Zorro, P.A., Turqu, B., Cordeiro, R.C., Moreira, L.S., McMichael, C.H., Behling, H., 2018. Forest stability during the early and late Holocene in the igapo floodplans of the Rio Negro, northwestern Brazil. Quaternary Research (in press).Google Scholar
Schiferl, J.D., Bush, M.B., Silman, M.R., Urrego, D.H., 2018. Vegetation responses to late-Holocene climate changes in an Andean forest. Quaternary Research (in press). https://doi.org/10.1017/qua.2017.64.Google Scholar
Smith, R.J., Mayle, F.E., 2018. Impact of mid- to late Holocene precipitation changes on vegetation across lowland tropical South America: a paleo-data synthesis. Quaternary Research (in press). https://doi.org/10.1017/qua.2017.89.Google Scholar
Stager, J.C., Alton, K., Martin, C.H., King, D.T., Petruny, L.W., Wiltse, B., Livingstone, D.A., 2018. On the age and origin of Lake Ejagham, Cameroon, and its endemic fishes. Quaternary Research (in press). https://doi.org/10.1017/qua.2017.37.Google Scholar
Stager, J.C., Reinthal, P.N., Livingstone, D.A., 1986. A 25,000-year history for Lake Victoria, East Africa, and some comments on its significance for the evolution of cichlid fishes. Freshwater Biology 16, 1519.Google Scholar
Steinitz-Kannan, M., Colinvaux, P., Kannan, R., 1983. Limnological studies in Ecuador: 1. A survey of chemical and physical properties of Ecuadorian lakes. Archiv für Hydrobiologie Supplement 65, 61105.Google Scholar
Steinitz-Kannan, M., De Oliveira, P.E., Miller, M.C., Colinvaux, P.A., 1986. Las diatomeas del Ecuador I. Diatomeas Fosiles de la Laguna de Cunro, Provincia de Imbabura. Revista del Museo Ecuatoriano de Cencias Naturales, Quito, Ecuador.Google Scholar
Talbot, M.R., Livingstone, D.A., Palmer, P.G., Maley, J., Melack, J.M., Delibrias, G., Gulliksen, S., 1984. Preliminary results from sediment cores from Lake Bosumtwi, Ghana. Palaeoecology of Africa. 16, 173192.Google Scholar
Whittaker, R.H., 1956. Vegetation of the Great Smoky Mountains. Ecological Monographs 26, 180.Google Scholar
Whittaker, R.H., 1960. Vegetation of the Siskiyou Mountains, Oregon and California. Ecological Monographs 30, 279338.Google Scholar
Wilson, J.T., 1963. A possible origin of the Hawaiian Islands. Canadian Journal of Physics 41, 863870.Google Scholar
Figure 0

Figure 1 (color online) (a) Dan Livingstone (photo courtesy of Duke University). (b) Paul Colinvaux at El Junco Crater Lake, Galapagos Islands (photo courtesy of Miriam Steinitz-Kannan).

Figure 1

Figure 2 (color online) A core being raised using a Colinvaux-Vohnout piston sampler from a raft of inflatable boats at Lake Llaviucu (also called Surucucho) in June 2010. This lake had previously been cored by Colinvaux’s team in 1988 (Colinvaux et al., 1997).