Hostname: page-component-78c5997874-94fs2 Total loading time: 0 Render date: 2024-11-10T20:52:03.022Z Has data issue: false hasContentIssue false

Climate-driven animal mass mortality events: is there a role for scavengers?

Published online by Cambridge University Press:  24 October 2022

Philip S Barton*
Affiliation:
Future Regions Research Centre, Federation University Australia, Mount Helen, VIC 3350, Australia
Anna Reboldi
Affiliation:
Future Regions Research Centre, Federation University Australia, Mount Helen, VIC 3350, Australia Research School of Biology, The Australian National University, Canberra, ACT 2602, Australia
Stefanie Bonat
Affiliation:
School of Life and Environmental Sciences, The University of Sydney, Sydney, NSW 2006, Australia
Patricia Mateo-Tomás
Affiliation:
Biodiversity Research Institute, University of Oviedo – CSIC – Principality of Asturias, Mieres, E-33600, Spain
Thomas M Newsome
Affiliation:
School of Life and Environmental Sciences, The University of Sydney, Sydney, NSW 2006, Australia
*
Author for correspondence: Dr Philip S Barton, Email: ps.barton@federation.edu.au
Rights & Permissions [Opens in a new window]

Summary

Animal mass mortality events (MMEs) will increase with weather and climate extremes. MMEs can add significant stress to ecosystems through extraordinary nutrient pulses or contribute to potential disease transmission risks. Given their efficient removal of carrion biomass from landscapes, we argue here for the potential of scavenger guilds to be a key nature-based solution to mitigating MME effects. However, we caution that scavenger guilds alone will not be a silver bullet. It is critical for further research to identify how the composition of scavenger guilds and the magnitude of MMEs will determine when scavengers will buffer the impacts of such events on ecosystems and when intervention might be required. Some MMEs are too large for scavengers to remove efficiently, and there is a risk of MMEs subsidizing pest species, altering nutrient cycling or leading to disease spread. Prioritizing native scavenger taxa in conservation management policies may help to boost ecosystem resilience through preserving their key ecological services. This should be part of a multi-pronged approach to MME mitigation that combines scavenger conservation with practices such as carcass dispersal or removal when exceeding a threshold quantity. Policymakers are urged to identify such thresholds and to recognize both the insects and the vertebrate scavengers that could act as allies for mitigating the emerging problem of climate-driven MMEs.

Type
Perspectives
Copyright
© The Author(s), 2022. Published by Cambridge University Press on behalf of Foundation for Environmental Conservation

An emerging global problem of mass mortalities

Mass mortality events (MMEs) involve the rare, sudden death of large numbers of animals (Fey et al. Reference Fey, Siepielski, Nussle, Cervantes-Yoshida, Hwan and Huber2015). They affect all age groups in a population and so differ from natural events such as seasonal migration (Subalusky et al. Reference Subalusky, Dutton, Rosi and Post2017) or mass emergence events (Yang Reference Yang2004), and they are increasingly attributed to extreme climate- and weather-related phenomena (Seneviratne et al. Reference Seneviratne, Zhang, Adnan, Badi, Dereczynski, Di Luca, Masson-Delmotte, Zhai, Pirani, Connors, Péan and Berger2021) such as droughts, floods or wildfires and cause mortality via heat stress, asphyxiation, disease or starvation (Fey et al. Reference Fey, Siepielski, Nussle, Cervantes-Yoshida, Hwan and Huber2015). In our view, MMEs represent an emerging but overlooked problem that extends beyond species conservation into ecosystem functioning, and our aim in this paper is to highlight the potential of scavenger guilds to be a key nature-based solution to mitigating the effects of MMEs.

In the last decade, many MMEs have occurred across a global range of biomes and animal taxa (Fig. 1), and the proximate causes of death are mostly linked to climate and weather extremes (Table 1). MMEs range in magnitude from a few hundred elephants in Botswana (Wang et al. Reference Wang, Xu, Liu, Jeppesen, Svenning and Wu2021) or reindeer in Norway (Hansen et al. Reference Hansen, Isaksen, Benestad, Kohler, Pedersen and Loe2014) through to many millions of mussels in the English Channel (Seuront et al. Reference Seuront, Nicastro, Zardi and Goberville2019) and perhaps billions of mammals and birds following Australia’s catastrophic megafires in 2019/2020 (Dickman et al. Reference Dickman, Driscoll, Garnett, Keith, Legge and Lindenmayer2020). The resulting quantities of carcass biomass through MMEs are therefore staggering (e.g., 700 million tonnes in a single event; Fey et al. Reference Fey, Siepielski, Nussle, Cervantes-Yoshida, Hwan and Huber2015). As the magnitude of climate variability worsens and extreme weather events increase in frequency and intensity (Field et al. Reference Field, Barros, Stocker, Qin, Dokken, Ebi and Mastrandrea2012, Seneviratne et al. Reference Seneviratne, Zhang, Adnan, Badi, Dereczynski, Di Luca, Masson-Delmotte, Zhai, Pirani, Connors, Péan and Berger2021), the world will probably witness more frequent and severe MMEs (Fey et al. Reference Fey, Siepielski, Nussle, Cervantes-Yoshida, Hwan and Huber2015, Lamberti et al. Reference Lamberti, Levesque, Brueseke, Chaloner and Benbow2020).

Fig. 1. Selected animal mass mortality events (MMEs) showcasing links to extremes in weather that have occurred across multiple biomes and animal taxa, involving hundreds to billions of individuals over periods of days to weeks. Examples are numbered 1–14 with details provided in Table 1.

Table 1. Details of example mass mortality events (MMEs) as illustrated in Fig. 1 and grouped by cause of death and link to climate change.

HAB = harmful algal bloom.

MMEs can affect ecosystem equilibria through rapid and large shifts in numbers of the affected species, but they also cause changes to species interactions and energy flows through food webs (Fey et al. Reference Fey, Gibert and Siepielski2019, Lamberti et al. Reference Lamberti, Levesque, Brueseke, Chaloner and Benbow2020). In nature, background inputs of carrion are continuously provided by countless species of animals across a large body-size spectrum that die from natural causes such as predation and disease (Barton et al. Reference Barton, Evans, Foster, Pechal, Bump, Quaggiotto and Benbow2019a). Regular inputs of animal carcasses are important for maintaining the ecological and evolutionary processes that enhance biodiversity (DeVault et al. Reference DeVault, Rhodes, Olin and Shivik2003, Barton et al. Reference Barton, Cunningham, Lindenmayer and Manning2013, Benbow et al. Reference Benbow, Barton, Ulyshen, Beasley, DeVault and Strickland2019), and they contribute to the dynamics of ecosystem productivity, structure and function through, for example, scavenging by well-adapted species (Wilson & Wolkovich Reference Wilson and Wolkovich2011, Subalusky et al. Reference Subalusky, Dutton, Rosi and Post2017, Barton et al. Reference Barton, Evans, Foster, Pechal, Bump, Quaggiotto and Benbow2019a). But MMEs are a risk to ecological equilibria and human well-being where such events are not the result of millennia of evolution and adaptation (Oro et al. Reference Oro, Genovart, Tavecchia, Fowler and Martínez-Abraín2013, Fey et al. Reference Fey, Siepielski, Nussle, Cervantes-Yoshida, Hwan and Huber2015, Reference Fey, Gibert and Siepielski2019, Lamberti et al. Reference Lamberti, Levesque, Brueseke, Chaloner and Benbow2020) and where scavenging food webs have become severely altered due to landscape modification or direct persecution by humans (Pain et al. Reference Pain, Cunningham, Donald, Duckworth, Houston and Katzner2003, Ogada et al. Reference Ogada, Shaw, Beyers, Buij, Murn and Thiollay2016, Sebastian-Gonzalez et al. Reference Sebastian-Gonzalez, Morales-Reyes, Botella, Naves-Alegre, Perez-Garcia and Mateo-Tomas2020). For example, increasing occurrences of MMEs could lead to nutrient pollution in soils or waterways, subsidies of pest species populations or promote disease transmission among wildlife. Among the most frequently threatened scavengers, vultures and top predators are functionally dominant species that are able to rapidly consume large amounts of carrion in some ecosystems (Supplementary Table S1, available online). Accordingly, their removal from those ecosystems could result in dysfunctional scavenger guilds and lead to longer carcass persistence in landscapes (Cunningham et al. Reference Cunningham, Johnson, Barmuta, Hollings, Woehler and Jones2018, Hill et al. Reference Hill, DeVault, Beasley, Rhodes and Belant2018). This has also been demonstrated in Asia and Africa, where vultures have undergone significant declines (Pain et al. Reference Pain, Cunningham, Donald, Duckworth, Houston and Katzner2003, Sebastian-Gonzalez et al. Reference Sebastian-Gonzalez, Morales-Reyes, Botella, Naves-Alegre, Perez-Garcia and Mateo-Tomas2020). An overlooked but ubiquitous group of scavengers is made up of blowflies (Calliphoridae), which can also contribute significantly to carrion removal (Barton & Evans Reference Barton and Evans2017, Lashley et al. Reference Lashley, Jordan, Tomberlin and Barton2018). The absence of dominant scavenger groups may lead to altered pathways of nutrient flow or elevated risks of disease transmission to wildlife, livestock or people (Ogada et al. Reference Ogada, Torchin, Kinnaird and Ezenwa2012, O’Bryan et al. Reference O’Bryan, Braczkowski, Magalhães and McDonald-Madden2020, Sanderson & Alexander Reference Sanderson and Alexander2020, Barbier Reference Barbier2021, Bloom et al. Reference Bloom, Chan, Baric, Bjorkman, Cobey and Deverman2021). Thus, conserving scavenger communities should be considered as part of the solution to mitigating the effects of MMEs on both ecosystems and human well-being.

Native scavenger guilds as a nature-based solution to mitigating MMEs

Although scavengers cannot prevent MMEs from occurring, they can help buffer ecosystems against the impacts of MMEs on species interactions and nutrient flows through their consumption and dispersal of carrion biomass. A diverse range of scavenger species contribute to carcass consumption and removal from landscapes (Mateo-Tomás et al. Reference Mateo-Tomás, Olea, Moleón, Selva and Sánchez-Zapata2017, Anderson et al. Reference Anderson, Archer, Barton, Wallace, Olea, Mateo-Tomas and Sanchez-Zapata2019, Sebastian-Gonzalez et al. Reference Sebastian-Gonzalez, Morales-Reyes, Botella, Naves-Alegre, Perez-Garcia and Mateo-Tomas2020). Vertebrate scavengers include a range of mammalian, bird and reptile taxa (DeVault et al. Reference DeVault, Rhodes, Olin and Shivik2003, Mateo-Tomás et al. Reference Mateo-Tomás, Olea, Moleón, Vicente, Botella and Selva2015, Selva et al. Reference Selva, Moleon, Sebastián-González, DeVault, Quaggiotto, Bailey, Olea, Mateo-Tomas and Sanchez-Zapata2019), as well as invertebrates such as flies, beetles and ants (Anderson et al. Reference Anderson, Archer, Barton, Wallace, Olea, Mateo-Tomas and Sanchez-Zapata2019, Barton & Bump Reference Barton, Bump, Olea, Mateo-Tomas and Sanchez-Zapata2019). These different taxa combine to form scavenging guilds that are unique to different biogeographical regions, land uses and habitat types (Anderson et al. Reference Anderson, Archer, Barton, Wallace, Olea, Mateo-Tomas and Sanchez-Zapata2019, Beasley et al. Reference Beasley, Olson, Selva, DeVault, Olea, Mateo-Tomas and Sanchez-Zapata2019, Sebastian-Gonzalez et al. Reference Sebastian-Gonzalez, Barbosa, Perez-Garcia, Morales-Reyes, Botella and Olea2019, Selva et al. Reference Selva, Moleon, Sebastián-González, DeVault, Quaggiotto, Bailey, Olea, Mateo-Tomas and Sanchez-Zapata2019). Where data are available for carrion consumption, they show that removal of carcasses can be up to 100% for some scavenger species and groups (Table S1). However, consumption rates are still poorly understood for many taxa and locations, and increasing knowledge in this regard is critical to improving our understanding of the extent to which scavengers can assist with MME mitigation. Consumption capacity (as quantities per unit time or proportions of carcasses visited or biomass consumed) is particularly well known for keystone and native scavengers such as vultures, which dominate carcass consumption in many ecosystems across Asia, Africa and Europe (e.g., Mateo-Tomás et al. Reference Mateo-Tomás, Olea, Moleón, Selva and Sánchez-Zapata2017, Gutierrez-Canovas et al. Reference Gutierrez-Canovas, Moleon, Mateo-Tomas, Olea, Sebastian-Gonzalez and Sanchez-Zapata2020, Buechley et al. Reference Buechley, Murgatroyd, Ruffo, Bishop, Christensen and Marra2022). Large native predators such as eagles, lions, wolves and bears are also able to rapidly consume large quantities of carrion in some African, European and North American ecosystems (Wilmers et al. Reference Wilmers, Stahler, Crabtree, Smith and Getz2003, Mateo-Tomás et al. Reference Mateo-Tomás, Olea, Moleón, Selva and Sánchez-Zapata2017). The contributions of many less dominant species, including ‘meso-scavengers’ such as foxes, corvids and suids, may also be important in some contexts (Beasley et al. Reference Beasley, Olson, Selva, DeVault, Olea, Mateo-Tomas and Sanchez-Zapata2019, O’Bryan et al. Reference O’Bryan, Holden and Watson2019).

Despite the impressive quantity of carrion that many scavengers can consume (Table S1) in a few hours or days (e.g., >15 kg/day for Gyps vultures in Mediterranean and African ecosystems; Mateo-Tomás et al. Reference Mateo-Tomás, Olea, Moleón, Selva and Sánchez-Zapata2017), there could be a threshold over which scavengers will be overwhelmed and cannot assist with the rapid consumption and dispersal of carrion resulting from MMEs without further affecting ecosystem integrity (Oro et al. Reference Oro, Genovart, Tavecchia, Fowler and Martínez-Abraín2013). In these instances, additional intervention (e.g., disposing of carcasses via burial, burning or composting) may be required to reduce the impacts of MMEs on altered species interactions, pest species, nutrient pollution or disease risk. It is important to recognize this limitation, but research is needed to develop our knowledge regarding the ecological functions of scavenger guilds in different ecosystems and their capacity to consume very large and irregular influxes of carrion biomass, as well as other ecological and evolutionary consequences of such consumption (e.g., population and community alterations; Oro et al. Reference Oro, Genovart, Tavecchia, Fowler and Martínez-Abraín2013).

Dominant scavenger species play an important role in the rapid consumption of large quantities of carrion across ecosystems (Mateo-Tomás et al. Reference Mateo-Tomás, Olea, Moleón, Selva and Sánchez-Zapata2017, Buechley et al. Reference Buechley, Murgatroyd, Ruffo, Bishop, Christensen and Marra2022), but it is the combined effect of the entire scavenger guild that often results in the complete recycling of carcass biomass and will be important to their response to MMEs. Research has identified behavioural plasticity among social vultures (black vultures, Coragyps atratus) that resulted in higher consumption rates when presented with larger carrion inputs (Baruzzi et al. Reference Baruzzi, Barton, Cove and Lashley2022). Furthermore, the rapid development times and voracious appetite of blowflies (Calliphoridae; Barton et al. Reference Barton, Evans, Higgins, Strong and Quaggiotto2019b) suggest that they also have the capacity to rapidly colonize and consume excess carrion biomass (Lashley et al. Reference Lashley, Jordan, Tomberlin and Barton2018). Yet scavenger guilds may also include pest or invasive species that opportunistically consume carrion, such as wasps (Vespula germanica) or pigs (Sus scrofa) in south-east Australia (Spencer et al. Reference Spencer, Dickman, Greenville, Crowther, Kutt and Newsome2021), or rats (Rattus sp.) and dogs (Canis familiaris) where vultures (Gyps sp.) have been extirpated in Southeast Asia (Pain et al. Reference Pain, Cunningham, Donald, Duckworth, Houston and Katzner2003). These pest species have been shown to alter species interactions at carcasses or change disease transmission risk, respectively. Thus, although scavenger guilds are a part of the solution to mitigating MMEs through the rapid consumption and dispersal of carrion, consideration must be given to those vertebrate and invertebrate scavengers that are able to maintain ecosystem resilience after climate-driven MMEs.

How can scavengers be incorporated into climate change mitigation strategies?

The UNEP Adaptation Gap Report 2020 (United Nations Environment Programme 2021) stresses the importance of identifying ecosystem-based solutions to mitigating the effects of climate change on people and nature. This should extend to the conservation and management of scavengers and scavenging food webs in order to boost ecosystem resilience to shocks and pressures stemming from MMEs. We suggest that this can be achieved in three ways: (1) improving knowledge of the roles of different vertebrate and invertebrate scavengers as providers of nutrient cycling services across ecosystems; (2) the protection and conservation of extant scavenger species known to be dominant carrion consumers and the reintroduction of locally extinct ones; and (3) planning mitigation actions to assist scavenger communities that are not able to deal with MMEs, particularly in vulnerable ecosystems already experiencing multiple threatening processes (Tulloch et al. Reference Tulloch, Mortelliti, Kay, Florance and Lindenmayer2016).

Globally, there is also a need for greater awareness of MMEs and their link to extreme weather and climate events, as well as raised awareness of scavengers as ecosystem service providers (Mateo-Tomás et al. Reference Mateo-Tomás, Olea, Moleón, Selva and Sánchez-Zapata2017, Olea et al. Reference Olea, Mateo-Tomas and Barton2019). Such knowledge should be integrated into international policies and agreements dealing with climate change, but also with the conservation and management of biodiversity in general and of scavengers in particular (Mateo-Tomas & Olea Reference Mateo-Tomas and Olea2018). For example, the action plan for vultures in Africa and Europe (Botha et al. Reference Botha, Andevski, Bowden, Gudka, Safford, Tavares and Williams2017) highlights the potential impacts of climate change on these species but does not mention vultures as potential key actors for resilient ecosystems through rapid carcass consumption over large areas (Ogada et al. Reference Ogada, Torchin, Kinnaird and Ezenwa2012, Mateo-Tomás et al. Reference Mateo-Tomás, Olea, Moleón, Selva and Sánchez-Zapata2017).

At regional and local scales, conservation management plans should include concrete actions for handling MMEs, acknowledging the key role that scavengers could play as providers of both supporting and regulating ecosystem services in this regard. Assessments of the status and health of ecosystems for adaptation to global change should include the assessment of scavenger biodiversity and the identification of dominant scavenger species, their conservation status and their contribution to carcass removal.

We also emphasize that species conservation is biased towards vertebrates (Clark & May Reference Clark and May2002), but equal emphasis on both vertebrate and invertebrate scavenger guilds (Olea et al. Reference Olea, Mateo-Tomas and Barton2019) should be promoted in conservation policy to encourage resilience to perturbations resulting from MMEs.

In light of the recently started United Nations Decade on Ecosystem Restoration (www.decadeonrestoration.org), conservation actions should also consider reintroductions of previously extirpated scavengers that clearly play a major role in carrion consumption and removal from landscapes. Scavengers should be part of a multi-pronged approach to MME mitigation that combines their conservation with practices such as carcass dispersal or removal when exceeding a threshold quantity. Scavengers may not be a silver bullet to solve all problems associated with MMEs, but it is important to recognize that they are one of the few nature-based solutions available to mitigate the effects of mass mortalities on ecosystems and human well-being.

Supplementary material

To view supplementary material for this article, please visit https://doi.org/10.1017/S0376892922000388.

Data accessibility

All data are available in the main text or Supplementary Material.

Acknowledgments

None.

Author contributions

Conceptualization: PSB, AR, SB, PM-T, TMN. Writing – original draft: PSB, AR. Writing – review and editing: PSB, AR, SB, PM-T, TMN. Visualization: PSB, AR, SB, PM-T, TMN. Project administration: PSB, AR. Supervision: PSB, TMN.

Financial support

We thank the Hermon Slade Foundation for supporting this work (HSF19069). AR was supported by an Australian Government Research Training Program (RTP) Fee-Offset Scholarship through Federation University Australia. SB is supported by an Australian Government Research Training Program (RTP) Stipend and RTP Fee-Offset Scholarship through The University of Sydney. PM-T is supported by a GRUPIN research grant from the Regional Government of Asturias (IDI/2021/000075).

Competing interests

The authors declare none.

Ethical standards

None.

References

Anderson, GJ, Archer, MS, Barton, PS, Wallace, J (2019) Invertebrate scavenging communities. In: Olea, PP, Mateo-Tomas, P, Sanchez-Zapata, JA (eds), Carrion Ecology and Management (pp. 4569). Berlin, Germany: Springer.CrossRefGoogle Scholar
Barbier, EB (2021) Habitat loss and the risk of disease outbreak. Journal of Environmental Economics and Management 108: 102451.CrossRefGoogle ScholarPubMed
Barton, PS, Bump, JK (2019) Carrion decomposition. In: Olea, PP, Mateo-Tomas, P, Sanchez-Zapata, JA (eds), Carrion Ecology and Management (pp. 101124). Berlin, Germany: Springer.CrossRefGoogle Scholar
Barton, PS, Cunningham, SA, Lindenmayer, DB, Manning, AD (2013) The role of carrion in maintaining biodiversity and ecological processes in terrestrial ecosystems. Oecologia 171: 761772.CrossRefGoogle ScholarPubMed
Barton, PS, Evans, MJ (2017) Insect biodiversity meets ecosystem function: differential effects of habitat and insects on carrion decomposition. Ecological Entomology 42: 364374.CrossRefGoogle Scholar
Barton, PS, Evans, MJ, Foster, CN, Pechal, JL, Bump, JK, Quaggiotto, MM, Benbow, ME (2019a) Towards quantifying carrion biomass in ecosystems. Trends in Ecology & Evolution 34: 950961.CrossRefGoogle ScholarPubMed
Barton, PS, Evans, MJ, Higgins, A, Strong, C, Quaggiotto, MM (2019b) Nutrient and moisture transfer to insect consumers and soil during vertebrate decomposition. Food Webs 18: e00110.CrossRefGoogle Scholar
Baruzzi, C, Barton, BT, Cove, MV, Lashley, MA (2022) Mass mortality events and declining obligate scavengers in the Anthropocene: social feeders may be critical. Biological Conservation 269: 109527.CrossRefGoogle Scholar
Beasley, JC, Olson, ZH, Selva, N, DeVault, TL (2019) Ecological functions of vertebrate scavenging. In: Olea, PP, Mateo-Tomas, P, Sanchez-Zapata, JA (eds), Carrion Ecology and Management (pp. 125157). Berlin, Germany: Springer.CrossRefGoogle Scholar
Benbow, ME, Barton, PS, Ulyshen, MD, Beasley, JC, DeVault, TL, Strickland, MS et al. (2019) Necrobiome framework for bridging decomposition ecology of autotrophically- and heterotrophically-derived organic matter. Ecological Monographs 89: e01331.CrossRefGoogle Scholar
Bergstrom, DM, Wienecke, BC, van den Hoff, J, Hughes, L, Lindenmayer, DB, Ainsworth, TD et al. (2021) Combating ecosystem collapse from the tropics to the Antarctic. Global Change Biology 27: 16921703.CrossRefGoogle ScholarPubMed
Bloom, JD, Chan, YA, Baric, RS, Bjorkman, PJ, Cobey, S, Deverman, BE et al. (2021) Investigate the origins of COVID-19. Science 372: 694.CrossRefGoogle ScholarPubMed
Botha, AJ, Andevski, J, Bowden, CGR, Gudka, M, Safford, RJ, Tavares, J, Williams, NP (2017) Multi-Species Action Plan to Conserve African-Eurasian Vultures. CMS Raptors MOU Technical Publication No. 5. CMS Technical Series No. 35. Abu Dhabi, United Arab Emirates: Coordinating Unit of the CMS Raptors MOU.Google Scholar
Buechley, ER, Murgatroyd, M, Ruffo, AD, Bishop, RC, Christensen, T, Marra, PP et al. (2022) Declines in scavenging by endangered vultures in the Horn of Africa. Journal of Wildlife Management 86: e22194.Google Scholar
Clark, JA, May, RM (2002) Taxonomic bias in conservation research. Science 297: 191192.CrossRefGoogle ScholarPubMed
Cunningham, CX, Johnson, CN, Barmuta, LA, Hollings, T, Woehler, EJ, Jones, ME (2018) Top carnivore decline has cascading effects on scavengers and carrion persistence. Proceedings of the Royal Society B – Biological Sciences 285: 20181582.CrossRefGoogle ScholarPubMed
DeVault, TL, Beasley, JC, Olson, ZH, Moleón, M, Carrete, M, Margalida, A, Sánchez-Zapata, JA (2016) Ecosystem services provided by avian scavengers. In: Sekercioglu, ÇH, Wenny, DG, Whelan, CJ (eds), Ecosystem Services Provided by Birds (pp. 235270). Chicago, IL, USA, and London, UK: University of Chicago Press.Google Scholar
DeVault, TL, Rhodes, J, Olin, E, Shivik, JA (2003) Scavenging by vertebrates: behavioral, ecological, and evolutionary perspectives on an important energy transfer pathway in terrestrial ecosystems. Oikos 102: 225234.Google Scholar
Dickman, C, Driscoll, D, Garnett, S, Keith, D, Legge, S, Lindenmayer, D et al. (2020) After the Catastrophe: A Blueprint for a Conservation Response to Large-Scale Ecological Disaster. Canberra, Australia: Threatened Species Recovery Hub, National Environmental Science Program.Google Scholar
Fey, SB, Gibert, JP, Siepielski, AM (2019) The consequences of mass mortality events for the structure and dynamics of biological communities. Oikos 128: 16791690.CrossRefGoogle Scholar
Fey, SB, Siepielski, AM, Nussle, S, Cervantes-Yoshida, K, Hwan, JL, Huber, ER et al. (2015) Recent shifts in the occurrence, cause, and magnitude of animal mass mortality events. Proceedings of the National Academy of Sciences of the United States of America 112: 10831088.CrossRefGoogle ScholarPubMed
Field, CB, Barros, V, Stocker, TF, Qin, D, Dokken, DJ, Ebi, KL, Mastrandrea, MD, et al. (2012) Managing the Risks of Extreme Events and Disasters to Advance Climate Change Adaptation: Special Report of the Intergovernmental Panel on Climate Change. Cambridge, UK: Cambridge University Press.CrossRefGoogle Scholar
Forbes, BC, Kumpula, T, Meschtyb, N, Laptander, R, Macias-Fauria, M, Zetterberg, P, Verdonen, M, et al. (2016) Sea ice, rain-on-snow and tundra reindeer nomadism in Arctic Russia. Biology Letters 12: 20160466.CrossRefGoogle ScholarPubMed
Genin, A, Levy, L, Sharon, G, Raitsos, DE, Diamant, A (2020) Rapid onsets of warming events trigger mass mortality of coral reef fish. Proceedings of the National Academy of Sciences of the United States of America 117: 2537825385.CrossRefGoogle ScholarPubMed
Gobler, CJ (2020) Climate change and harmful algal blooms: insights and perspective. Harmful Algae 91: 101731.CrossRefGoogle ScholarPubMed
Goss, M, Swain, DL, Abatzoglou, JT, Sarhadi, A, Kolden, CA, Williams, AP, Diffenbaugh, NS (2020) Climate change is increasing the likelihood of extreme autumn wildfire conditions across California. Environmental Research Letters 15: 094016.CrossRefGoogle Scholar
Gutierrez-Canovas, C, Moleon, M, Mateo-Tomas, P, Olea, PP, Sebastian-Gonzalez, E, Sanchez-Zapata, JA (2020) Large home range scavengers support higher rates of carcass removal. Functional Ecology 34: 19211932.CrossRefGoogle Scholar
Hansen, BB, Isaksen, K, Benestad, RE, Kohler, J, Pedersen, AO, Loe, LE et al. (2014) Warmer and wetter winters: characteristics and implications of an extreme weather event in the High Arctic. Environmental Research Letters 9: 114021.CrossRefGoogle Scholar
Haussermann, V, Gutstein, CS, Bedington, M, Cassis, D, Olavarria, C, Dale, AC, et al. (2017) Largest baleen whale mass mortality during strong El Nino event is likely related to harmful toxic algal bloom. Peerj 5: e3123.CrossRefGoogle ScholarPubMed
Hill, JE, DeVault, TL, Beasley, JC, Rhodes, OE Jr, Belant, JL (2018) Effects of vulture exclusion on carrion consumption by facultative scavengers. Ecology and Evolution 8: 25182526.CrossRefGoogle ScholarPubMed
Ho, JC, Michalak, AM, Pahlevan, N (2019) Widespread global increase in intense lake phytoplankton blooms since the 1980s. Nature 574: 667670.CrossRefGoogle ScholarPubMed
Jackson, S, Head, L (2020) Australia’s mass fish kills as a crisis of modern water: understanding hydrosocial change in the Murray–Darling Basin. Geoforum 109: 4456.CrossRefGoogle Scholar
Jones, T, Parrish, JK, Peterson, WT, Bjorkstedt, EP, Bond, NA, Ballance, LT et al. (2018) Massive mortality of a planktivorous seabird in response to a marine heatwave. Geophysical Research Letters 45: 31933202.CrossRefGoogle Scholar
Kock, RA, Orynbayev, M, Robinson, S, Zuther, S, Singh, NJ, Beauvais, W et al. (2018) Saigas on the brink: multidisciplinary analysis of the factors influencing mass mortality events. Science Advances 4: eaao2314.CrossRefGoogle ScholarPubMed
Lamberti, GA, Levesque, NM, Brueseke, MA, Chaloner, DT, Benbow, ME (2020) Editorial: animal mass mortalities in aquatic ecosystems: how common and influential? Frontiers in Ecology and Evolution 8: 17.CrossRefGoogle Scholar
Lashley, MA, Jordan, HR, Tomberlin, JK, Barton, BT (2018) Indirect effects of larval dispersal following mass mortality events. Ecology 99: 491493.Google ScholarPubMed
Lauber, CL, Metcalf, JL, Keepers, K, Ackermann, G, Carter, DO, Knight, R (2014) Vertebrate decomposition is accelerated by soil microbes. Applied and Environmental Microbiology 80: 49204929.CrossRefGoogle ScholarPubMed
Louzao, M, Gallagher, R, Garcia-Baron, I, Chust, G, Intxausti, I, Albisu, J et al. (2019) Threshold responses in bird mortality driven by extreme wind events. Ecological Indicators 99: 183192.CrossRefGoogle Scholar
Mateo-Tomas, P, Olea, PP (2018) Scavengers need help from IPBES. Nature 558: 520520.Google Scholar
Mateo-Tomás, P, Olea, PP, Moleón, M, Selva, N, Sánchez-Zapata, JA (2017) Both rare and common species support ecosystem services in scavenger communities. Global Ecology and Biogeography 26: 14591470.CrossRefGoogle Scholar
Mateo-Tomás, P, Olea, PP, Moleón, M, Vicente, J, Botella, F, Selva, N et al. (2015) From regional to global patterns in vertebrate scavenger communities subsidized by big game hunting. Diversity and Distributions 21: 913924.CrossRefGoogle Scholar
Mazdiyasni, O, AghaKouchak A (2015) Substantial increase in concurrent droughts and heatwaves in the United States. Proceedings of the National Academy of Sciences of the United States of America 112: 1148411489.CrossRefGoogle ScholarPubMed
Mo, M, Roache, M, Davies, J, Hopper, J, Pitty, H, Foster, N, et al. (2021) Estimating flying-fox mortality associated with abandonments of pups and extreme heat events during the austral summer of 2019–20. Pacific Conservation Biology 28: 124139.CrossRefGoogle Scholar
Moleón, M, Selva, N, Quaggiotto, MM, Bailey, DM, Cortés-Avizanda, A, DeVault, TL (2019) Carrion availability in space and time. In: Olea, PP, Mateo-Tomas, P, Sanchez-Zapata, JA (eds), Carrion Ecology and Management (pp. 2344). Berlin, Germany: Springer.CrossRefGoogle Scholar
Moreno-Opo, R, Margalida, A (2013) Carcasses provide resources not exclusively to scavengers: patterns of carrion exploitation by passerine birds. Ecosphere 4: 115.CrossRefGoogle Scholar
Normile, D (2019) Massive fish die-off sparks outcry in Australia. Science 363: 331.CrossRefGoogle ScholarPubMed
O’Bryan, CJ, Braczkowski, AR, Magalhães, RJS, McDonald-Madden, E (2020) Conservation epidemiology of predators and scavengers to reduce zoonotic risk. Lancet Planetary Health 4: e304e305.CrossRefGoogle ScholarPubMed
O’Bryan, CJ, Holden, MH, Watson, JEM (2019) The mesoscavenger release hypothesis and implications for ecosystem and human well-being. Ecology Letters 22: 13401348.CrossRefGoogle ScholarPubMed
Ogada, DL, Shaw, P, Beyers, RL, Buij, R, Murn, C, Thiollay, JM et al. (2016) Another continental vulture crisis: Africa’s vultures collapsing toward extinction. Conservation Letters 9: 8997.CrossRefGoogle Scholar
Ogada, DL, Torchin, ME, Kinnaird, MF, Ezenwa, VO (2012) Effects of vulture declines on facultative scavengers and potential implications for mammalian disease transmission. Conservation Biology 26: 453460.CrossRefGoogle ScholarPubMed
Olea, PP, Mateo-Tomas, P, Barton, PS (2019) Invertebrate scavengers matter. Science 363: 1162.CrossRefGoogle ScholarPubMed
Oro, D, Genovart, M, Tavecchia, G, Fowler, MS, Martínez-Abraín, A (2013) Ecological and evolutionary implications of food subsidies from humans. Ecology Letters 16: 15011514.CrossRefGoogle ScholarPubMed
Paerl, HW, Paul, VJ (2012) Climate change: links to global expansion of harmful cyanobacteria. Water Research 46: 13491363.CrossRefGoogle ScholarPubMed
Pain, DJ, Cunningham, AA, Donald, PF, Duckworth, JW, Houston, DC, Katzner, T et al. (2003) Causes and effects of temporospatial declines of Gyps vultures in Asia. Conservation Biology 17: 661671.CrossRefGoogle Scholar
Peisley, RK, Saunders, ME, Robinson, WA, Luck, GW (2017) The role of avian scavengers in the breakdown of carcasses in pastoral landscapes. Emu 117: 6877.CrossRefGoogle Scholar
Piatt, JF, Parrish, JK, Renner, HM, Schoen, SK, Jones, TT, Arimitsu, ML, et al. (2020) Extreme mortality and reproductive failure of common murres resulting from the northeast Pacific marine heatwave of 2014–2016. PLoS ONE 15: e0226087.CrossRefGoogle ScholarPubMed
Pruvot, M, Cappelle, J, Furey, N, Hul, V, Heng, HS, Duong, V et al. (2019) Extreme temperature event and mass mortality of insectivorous bats. European Journal of Wildlife Research 65: 41.CrossRefGoogle ScholarPubMed
Ratnayake, HU, Kearney, MR, Govekar, P, Karoly, D, Welbergen, JA (2019) Forecasting wildlife die-offs from extreme heat events. Animal Conservation 22: 386395.CrossRefGoogle Scholar
Reguera, R, Bresnan, E (2015) High sea surface temperature, the potential trigger of mass mortality of fish, exceptional toxin producing HABs, and other socio-economic impacts in Uruguay. UNESCO Harmful Algae News 51: 2.Google Scholar
Roberts, SD, Van Ruth, PD, Wilkinson, C, Bastianello, SS, Bansemer, MS (2019) Marine heatwave, harmful algae blooms and an extensive fish kill event during 2013 in South Australia. Frontiers in Marine Science 6: 120.CrossRefGoogle Scholar
Robinson, S, Milner-Gulland, EJ, Grachev, Y, Salemgareyev, A, Orynbayev, M, Lushchekina, A et al. (2019) Opportunistic bacteria and mass mortality in ungulates: lessons from an extreme event. Ecosphere 10: e02671.CrossRefGoogle Scholar
Ropert-Coudert, Y, Kato, A, Shiomi, K, Barbraud, C, Angelier, F, Delord, K et al. (2018) Two recent massive breeding failures in an adelie penguin colony call for the creation of a marine protected area in D’Urville Sea/Mertz. Frontiers in Marine Science 5: 264.CrossRefGoogle Scholar
Sanderson, CE, Alexander, KA (2020) Unchartered waters: climate change likely to intensify infectious disease outbreaks causing mass mortality events in marine mammals. Global Change Biology 26: 42844301.CrossRefGoogle ScholarPubMed
Schwingshackl, C, Sillmann, J, Vicedo-Cabrera, AM, Sandstad, M, Aunan, K (2021) Heat stress indicators in CMIP6: estimating future trends and exceedances of impact-relevant thresholds. Earth’s Future 9: e2020EF001885.CrossRefGoogle Scholar
Sebastian-Gonzalez, E, Barbosa, JM, Perez-Garcia, JM, Morales-Reyes, Z, Botella, F, Olea, PP et al. (2019) Scavenging in the Anthropocene: human impact drives vertebrate scavenger species richness at a global scale. Global Change Biology 25: 30053017.CrossRefGoogle ScholarPubMed
Sebastian-Gonzalez, E, Morales-Reyes, Z, Botella, F, Naves-Alegre, L, Perez-Garcia, JM, Mateo-Tomas, P et al. (2020) Network structure of vertebrate scavenger assemblages at the global scale: drivers and ecosystem functioning implications. Ecography 43: 11431155.CrossRefGoogle Scholar
Selva, N, Moleon, M, Sebastián-González, E, DeVault, TL, Quaggiotto, MM, Bailey, DM et al. (2019) Vertebrate scavenging communities. In: Olea, PP, Mateo-Tomas, P, Sanchez-Zapata, JA (eds), Carrion Ecology and Management (pp. 71100). Berlin, Germany: Springer.CrossRefGoogle Scholar
Seneviratne, S, Zhang, X, Adnan, M, Badi, W, Dereczynski, C, Di Luca, A et al. (2021) Weather and climate extreme events in a changing climate. In: Masson-Delmotte, V, Zhai, P, Pirani, A, Connors, S, Péan, C, Berger, S et al. (eds), Climate Change 2021: The Physical Science Basis. Contribution of Working Group to the Sixth Assessment Report of the Intergovernmental Panel on Climate Change (pp. 15131766). Cambridge, UK: Cambridge University Press.Google Scholar
Seuront, L, Nicastro, KR, Zardi, GI, Goberville, E (2019) Decreased thermal tolerance under recurrent heat stress conditions explains summer mass mortality of the blue mussel Mytilus edulis . Scientific Reports 9: 17498.CrossRefGoogle ScholarPubMed
Siberian Times (2021) Mass deaths of reindeer on Yamal peninsula might be linked to climate change, scientists believe [www document]. URL https://siberiantimes.com/other/others/news/mass-deaths-of-reindeer-on-yamal-peninsula-might-be-linked-to-climate-change-scientists-believe/ Google Scholar
Smith, WO, Barber, DG (2007) Polynyas and climate change: a view to the future. In: Smith, WO, Barber, DG (eds), Elsevier Oceanography Series (pp. 411419). Amsterdam, The Netherlands: Elsevier.Google Scholar
Spencer, EE, Dickman, CR, Greenville, A, Crowther, MS, Kutt, A, Newsome, TM (2021) Carcasses attract invasive species and increase artificial nest predation in a desert environment. Global Ecology and Conservation 27: e01588.CrossRefGoogle Scholar
Subalusky, AL, Dutton, CL, Rosi, EJ, Post, DM (2017) Annual mass drownings of the Serengeti wildebeest migration influence nutrient cycling and storage in the Mara River. Proceedings of the National Academy of Sciences of the United States of America 114: 76477652.CrossRefGoogle ScholarPubMed
Tamura, T, Williams, GD, Fraser, AD, Ohshima, KI (2012) Potential regime shift in decreased sea ice production after the Mertz Glacier calving. Nature Communications 3: 826.CrossRefGoogle ScholarPubMed
Till, A, Rypel, AL, Bray, A, Fey, SB (2019) Fish die-offs are concurrent with thermal extremes in north temperate lakes. Nature Climate Change 9: 637641.CrossRefGoogle Scholar
Tulloch, AIT, Mortelliti, A, Kay, GM, Florance, D, Lindenmayer, D (2016) Using empirical models of species colonization under multiple threatening processes to identify complementary threat-mitigation strategies. Conservation Biology 30: 867882.CrossRefGoogle ScholarPubMed
Tuohy, E, Wade, C, Weil, E (2020) Lack of recovery of the long-spined sea urchin Diadema antillarum Philippi in Puerto Rico 33 years after the Caribbean-wide mass mortality. PeerJ 8: e8428.CrossRefGoogle ScholarPubMed
United Nations Environment Programme (2021) Adaptation Gap Report 2020. Nairobi, Kenya: UNEP.Google Scholar
Wang, H, Xu, C, Liu, Y, Jeppesen, E, Svenning, J-C, Wu, J et al. (2021) From unusual suspect to serial killer: cyanotoxins boosted by climate change may jeopardize megafauna. The Innovation 2: 100092.CrossRefGoogle ScholarPubMed
Wenting, E, Rinzema, SCY, van Langevelde, F (2022) Functional differences in scavenger communities and the speed of carcass decomposition. Ecology and Evolution 12: e8576.CrossRefGoogle ScholarPubMed
Williams, AP, Abatzoglou, JT, Gershunov, A, Guzman-Morales, J, Bishop, DA, Balch, JK, Lettenmaier, DP (2019) Observed impacts of anthropogenic climate change on wildfire in California. Earth’s Future 7: 892910.CrossRefGoogle Scholar
Wilmers, CC, Stahler, DR, Crabtree, RL, Smith, DW, Getz, WM (2003) Resource dispersion and consumer dominance: scavenging at wolf- and hunter-killed carcasses in Greater Yellowstone, USA. Ecology Letters 6: 9961003.CrossRefGoogle Scholar
Wilson, EE, Wolkovich, EM (2011) Scavenging: how carnivores and carrion structure communities. Trends in Ecology & Evolution 26: 129135.CrossRefGoogle ScholarPubMed
Yang, LH (2004) Periodical cicadas as resource pulses in North American forests. Science 306: 15651567.CrossRefGoogle ScholarPubMed
Young, EJ, Bannister, J, Buller, NB, Vaughan-Higgins, RJ, Stephens, NS, Whiting, SD et al. (2020) Streptococcus iniae associated mass marine fish kill off Western Australia. Diseases of Aquatic Organisms 142: 197201.CrossRefGoogle ScholarPubMed
Figure 0

Fig. 1. Selected animal mass mortality events (MMEs) showcasing links to extremes in weather that have occurred across multiple biomes and animal taxa, involving hundreds to billions of individuals over periods of days to weeks. Examples are numbered 1–14 with details provided in Table 1.

Figure 1

Table 1. Details of example mass mortality events (MMEs) as illustrated in Fig. 1 and grouped by cause of death and link to climate change.

Supplementary material: File

Barton et al. supplementary material

Table S1

Download Barton et al. supplementary material(File)
File 171.6 KB