Category Archives: General Ecology

On Conservation Complexities

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It is too often the case that biodiversity problems are managed by single species solutions. If you have too many deer in your parks or conservation areas, start a culling program. If your salmon fishing stocks are declining, cull seals and sea lions. The overall issue confounding these kinds of ‘solutions’ are now being recognized as a failure to appreciate the food web of the community and ecosystem in which the problem is embedded. Much of conservation action is directed at heading back to the “good old days” without very much data about what the ecosystem was like in the “good old days”.

Problems with introduced species top the list of conservation dilemmas, and nowhere are these problems more clearly illustrated than by the conservation dilemmas of New Zealand and Australia. If we concentrate our management efforts on introduced predators or herbivores, we face a large set of conservation issues, well-illustrated by the current New Zealand situation (Leathwick and Byrom 2023, Parkes and Murphy 2003).

New Zealand is a particularly strong case history because we have a good knowledge of its indigenous biodiversity from the time that people colonized these islands, as well as reasonable information about how things have changed since Europeans colonized the country (Thomson 1922). It is in some respects the classic case of biodiversity impacts from introduced species. The introduced species list is large and I can talk only about part of these species introduced mostly in the late 1800s. Seven species of deer were released in New Zealand, along with chamois, hares, rabbits, cats, hedgehogs, three mustelid species, brushtail possums, rats, house mice, along with all the usual farm animals like cattle, horses, and dogs (King & Forsyth 2021). The first concerns began about 100 years ago over ungulate browsing in forests and grasslands. Deer control began about 1930, and over 3 million deer were shot between 1932 and 1954. Caughley (1983) showed that this amount of control did not reduce the impact of browsing and grazing by ungulates in native ecosystems. Control and harvesting efforts decreased in recent years partly from a lack of government funding with the result that deer numbers have rebounded. The recognition of the impact of other pests like rabbits, weasels, and rats led to a focus on poison campaigns. Brushtail possum control with poisons was started to reduce tree browsing damage by the 1970s and gradually increased to reduce TB transmission to domestic livestock by the 1990s. Large scale predator control began in the late 1990s with a focus on rats, stoats (weasels, Mustela erminea), and possums with good success in preventing declines in threatened bird species. All this history is covered in detail in Leathwick and Byrom (2023).

These efforts led to a declaration in 2016 of “Predator Free New Zealand 2050” (PF2050) a compelling promise that would alleviate biodiversity problems by making New Zealand free of possums, mustelids, and rats by 2050, and predator control has thus became the focus of recent conservation action. The 2050 part of the promise was always a worry, since governments in general promise much in advances by that year, but the optimistic view is that predator control will achieve this objective if careful planning is made, adequate funding is available (c.f. Department of Conservation 2021), and well-articulated guidelines for eradication of invasive species are followed (Bomford & O’Brien 1995). The message is that biodiversity goals can be achieved if we move from single species management to a stable system of ecosystem management in the broad sense, including strong research, good public participation and support toward these goals, and that biodiversity conservation will be greatly boosted by thorough consultation with (if not leadership by) the indigenous groups involved.

The New Zealand specific situation cannot be applied directly to all biodiversity concerns, but the New Zealand conservation story and the 12 recommendations given in Leathwick and Byrom (2023) show the necessity of goal definition and coordination between the public, government, and private foundations if we are to maximize the effectiveness of our approach to the biodiversity crisis. Not every conservation issue involves introduced species, but the principle must be: What do we want to achieve, and how are we going to get there?

Bomford, M, & O’Brien, P 1995. Eradication or control for vertebrate pests? Wildlife Society Bulletin 23, 249–255.

Caughley, G. (1983) The Deer Wars: The Story of Deer in New Zealand. Heinemann, Auckland. ISBN: 0868633895.

Department of Conservation (2020). Annual Report. Available at: https://www.doc.govt. nz/nature/pests-and-threats/predator-free-2050/goal-tactics-and-new-technology/tools-to-market/.    See also: PF2050-Limited-Annual-Report-2022.pdf

King, C.M. & Forsyth, D.M. (2021). eds. The Handbook of New Zealand Mammals. 3rd edition. CSIRO Publishing, Canberra. ISBN 978-1988592589.

Leathwick, J.R. & Byrom, A.E. (2023) The rise and rise of predator control: a panacea, or a distraction from conservation goals? New Zealand Journal of Ecology, 47, 3515. doi: 10.20417/nzjecol.47.3515.

Parkes, J. & Murphy, E. (2003) Management of introduced mammals in New Zealand. New Zealand Journal of Zoology, 30, 335-359. doi:10.1080/03014223.2003.9518346.

Thomson, G.M. (1922) The Naturalisation of Animals and Plants in New Zealand. The University Press, Cambridge, England. doi: 10.5962/bhl.title.28093.

On Ecological Imperialism

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It is well known among ecologists that there are more species of almost everything in the tropical regions, and it is also well known that there is rather much more research in the ecosystems of the temperate zone. A recent note in Science 379 (6632) – 8 Feb. 2023 highlights the problems faced by ornithologists in Latin America and the Caribbean trying to carry out research on their local birds. The details are in two papers now published (Soares et al. 2023, Ruelas Inzunza et al. 2023). Both of these papers are a response to a review paper published in 2020 (Lees et al. 2020) which discussed how much was not known about birds in Latin America, but which ignored most of the contributions of Latin American scientists. The red flag arose in part because all the authors of the 2020 paper were based at universities either in the United States or in the United Kingdom. The central criticisms were that the 2020 paper perpetuated an elitist, exclusionary, “northern” approach that has overlooked the knowledge produced by Latin American experts and Indigenous people, partly because these papers were not in English.

    Their case is certainly important and should be a call-to-arms but it should be read with a few minor qualifications. It is certainly not valid to ignore local knowledge both of scientists and indigenous peoples. But this has been going on now for more than 200 years in all areas of biological science, not that history justifies these barriers. Alas Charles Darwin would fall under the knife of this criticism. The funding for ecological research is higher in most European countries as well as North America compared with tropical countries. So we are dealing with economic issues that underlie the scientific funding that is less in Latin America in addition to the global problem that too many governments prefer guns to butter. We recognize these problems, but we can do nothing immediately about them.

    The language issue is much more difficult because it is so clear. There is a long history of this conflict in scientific papers as well as in literature in general. French scientists years ago refused to publish in English, that has changed. Chinese scientists were all educated in Russian but when the tide turned they learned English and started to write scientific papers in English. The problem revolves back to the education system of North American schools that seem to operate on the assumption that to learn a foreign language is very close to being a traitor. Alas students hardly learn to speak and write English but that is another social issue. I think many northern scientists have helped Latin America scientists to assist them in English usage, so it is to me quite obscene to think that someone has a business charging people $600 for a translation. So much of the complaint in the predominance of English scientific papers arises from social issues that are difficult to overcome.

    In the end I am very sympathetic with the inequities raised in these papers and the desire to move forward on all these issues. Ironically the skeleton of the Lees et al. (2020) paper is an excellent roadmap for the analysis of any taxonomic group anywhere is the world, and these papers should be a reminder that similar reviews should be more inclusive of all published literature. Remember always that European or American knowledge is not the only or the best knowledge.

Lees, A.C., Rosenberg, K.V., Ruiz-Gutierrez, V., Marsden, S., Schulenberg, T.S. & Rodewald, A.D. (2020) A roadmap to identifying and filling shortfalls in Neotropical ornithology. Auk, 137, 1-17. doi: 10.1093/auk/ukaa048.

Ruelas Inzunza, E., Cockle, K.L., Núñez Montellano, M.G., Fontana, C.S., Cuatianquiz Lima, C., Echeverry-Galvis, M.A., Fernández-Gómez, R.A., Montaño-Centellas, F.A., Bonaccorso, E., Lambertucci, S.A., Cornelius, C., Bosque, C., Bugoni, L., Salinas-Melgoza, A., Renton, K., Freile, J.F., Angulo, F., Mugica Valdés, L., Velarde, E., Cuadros, S. & Miño, C.I. (2023) How to include and recognize the work of ornithologists based in the Neotropics: Fourteen actions for Ornithological Applications, Ornithology, and other global-scope journals. Ornithological Applications, 125, duac047. doi: 10.1093/ornithapp/duac047.

Soares, L., Cockle, K.L., Ruelas Inzunza, E., Ibarra, J.T., Miño, C.I., Zuluaga, S., Bonaccorso, E., Ríos-Orjuela, J.C., Montaño-Centellas, F.A., Freile, J.F., Echeverry-Galvis, M.A., Bonaparte, E.B., Diele-Viegas, L.M., Speziale, K., Cabrera-Cruz, S.A., Acevedo-Charry, O., Velarde, E., Cuatianquiz Lima, C., Ojeda, V.S., Fontana, C.S., Echeverri, A., Lambertucci, S.A., Macedo, R.H., Esquivel, A., Latta, S.C., Ruvalcaba-Ortega, I., Alves, M.A.S., Santiago-Alarcon, D., Bodrati, A., González-García, F., Fariña, N., Martínez-Gómez, J.E., Ortega-Álvarez, R., Núñez Montellano, M.G., Ribas, C.C., Bosque, C., Di Giacomo, A.S., Areta, J.I., Emer, C., Mugica Valdés, L., González, C., Rebollo, M.E., Mangini, G., Lara, C., Pizarro, J.C., Cueto, V.R., Bolaños-Sittler, P.R., Ornelas, J.F., Acosta, M., Cenizo, M., Marini, M.Â., Vázquez-Reyes, L.D., González-Oreja, J.A., Bugoni, L., Quiroga, M., Ferretti, V., Manica, L.T., Grande, J.M., Rodríguez-Gómez, F., Diaz, S., Büttner, N., Mentesana, L., Campos-Cerqueira, M., López, F.G., Guaraldo, A.C., MacGregor-Fors, I., Aguiar-Silva, F.H., Miyaki, C.Y., Ippi, S., Mérida, E., Kopuchian, C., Cornelius, C., Enríquez, P.L., Ocampo-Peñuela, N., Renton, K., Salazar, J.C., Sandoval, L., Correa Sandoval, J., Astudillo, P.X., Davis, A.O., Cantero, N., Ocampo, D., Marin Gomez, O.H., Borges, S.H., Cordoba-Cordoba, S., Pietrek, A.G., de Araújo, C.B., Fernández, G., de la Cueva, H., Guimarães Capurucho, J.M., Gutiérrez-Ramos, N.A., Ferreira, A., Costa, L.M., Soldatini, C., Madden, H.M., Santillán, M.A., Jiménez-Uzcátegui, G., Jordan, E.A., Freitas, G.H.S., Pulgarin-R, P.C., Almazán-Núñez, R.C., Altamirano, T., Gomez, M.R., Velazquez, M.C., Irala, R., Gandoy, F.A., Trigueros, A.C., Ferreyra, C.A., Albores-Barajas, Y.V., Tellkamp, M., Oliveira, C.D., Weiler, A., Arizmendi, M.d.C., Tossas, A.G., Zarza, R., Serra, G., Villegas-Patraca, R., Di Sallo, F.G., Valentim, C., Noriega, J.I., Alayon García, G., de la Peña, M.R., Fraga, R.M. & Martins, P.V.R. (2023) Neotropical ornithology: Reckoning with historical assumptions, removing systemic barriers, and reimagining the future. Ornithological Applications, 125, duac046. doi: 10.1093/ornithapp/duac046.

Belief vs. Evidence

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There is an interesting game you could enter into if you classified the statements you hear or read in the media or in ecological papers. The initial dichotomy is whether or not a statement is a BELIEF or EVIDENCE BASED. There is a continuum between these polar opposites so there can easily be disagreements based on a person’s background. If I say “I believe that the earth is round” you will recognize that this is not a simple belief but a physical fact that is evidence-based. Consequently we use the word ‘belief’ in many different ways. If I say that “Aliens from outer space are firing ray guns to cause flooding in California and Australia”, it is unlikely that you will be convinced because there is no evidence of how this process could work.

If we listen to the media or read the news, you will hear many statements that I or we ‘believe’ that speed limits on streets should be reduced, or that certain types of firearms should be prohibited. The natural response of a scientist to such statements is to ask for what evidence is available that such actions will solve problems, and if there is no evidence, we deal only with opinions or beliefs. If  you lived several hundred years ago, you would be told that “malaria” was a disease caused by “bad air” coming from swamps and rivers, since there was no evidence at the time about microorganisms causing disease. So in a broad sense historical progress was made by people looking for ‘evidence’ to temper and test ‘beliefs’.

How does all this relate to ecological science? I would add the requirement to papers that state some conclusions in ecology journals to also state the beliefs the paper rely on to reach its conclusions, in addition to stating clear hypotheses and alternative hypotheses. Consider the simple case of random sampling, a basic requirement in all statistical methods. But almost no paper states what statistical population is being sampled, and if it does often the study plots are not placed randomly. The standard excuse to this is that our results apply to a large biome, and it is not physically possible to sample randomly, or that we get the same results whether we sample randomly or not. Whatever the excuse, we need to recognize this as a belief or an assumption, a less damning scientific term. And if this assumption is not accepted it is possible to sample other areas or with other methods to test if the evidence validates the assumption. Evidence can always be improved with enough funding, and this replication is exactly what many scientists are doing daily.

Until recently most scientists believed that CO2 was good for plants, and so the more CO2 the better. But the evidence provided was based on simple theory and short term lab experiments. Reich et al. (2018) and Zhu et al. (2018) pointed out that this was not correct when long-term studies were done on C3 plants like rice. So this is a good illustration of the progress of science from belief to evidence. And over the past 50 years it has become very clear that increased CO2 increases atmospheric temperature with drastic climatic and biodiversity consequences (Ripple et al. 2021). The result of these scientific advances is that now there is an extensive amount of scientific research giving the empirical evidence of climate change and CO2 effects on plants and animals. Most people agree with these broad conclusions, but there are people in large corporations and governments around the world who deny these scientific conclusions because they believe that climate change is not happening and is of little consequence to biodiversity or to daily life.

It is quite possible to ignore all the scientific literature about the consequences of climate change, CO2 increase, and biodiversity loss but the end result of passing over these problems now will fall heavily onto your children and grandchildren. The biosphere is screaming the message that ignorance will not necessarily lead to bliss.

Reich, P.B., Hobbie, S.E., Lee, T.D. & Pastore, M.A. (2018) Unexpected reversal of C3 versus C4 grass response to elevated CO2 during a 20-year field experiment. Science, 360, 317-320.doi: 10.1126/science.aas9313.

Ripple, W.J., Wolf, C., Newsome, T.M., Gregg, J.W., Lenton, T.M., Palomo, I., Eikelboom, J.A.J., Law, B.E., Huq, S., Duffy, P.B. & Rockström, J. (2021) World Scientists’ Warning of a Climate Emergency 2021. BioScience, 71, 894-898.doi: 10.1093/biosci/biab079.

Shivanna, K.R. (2022) Climate change and its impact on biodiversity and human welfare. Proceedings of the Indian National Science Academy, 88, 160-171.doi: 10.1007/s43538-022-00073-6.

Watson, R., Kundzewicz, Z.W. & Borrell-Damián, L. (2022) Covid-19, and the climate change and biodiversity emergencies. Science of The Total Environment, 844, 157188.doi: 10.1016/j.scitotenv.2022.157188.

Williams, S.E., Williams, S.E. & de la Fuente, A. (2021) Long-term changes in populations of rainforest birds in the Australia Wet Tropics bioregion: A climate-driven biodiversity emergency. PLoS ONE, 16.doi: 10.1371/journal.pone.0254307.

Zhu, C., Kobayashi, K., Loladze, I., Zhu, J. & Jiang, Q. (2018) Carbon dioxide (CO2) levels this century will alter the protein, micronutrients, and vitamin content of rice grains with potential health consequences for the poorest rice-dependent countries. Science Advances, 4, eaaq1012 doi: 10.1126/sciadv.aaq1012.

Should Empirical Ecology be all Long-term?

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The majority of empirical ecology research published in our journals is short-term with the time span dictated by the need for 1–2-year Master’s degree studies and 3-4-year PhD research. This has been an excellent model when there was little of a framework for researching the critical questions ecologists ought to answer. Much of ecology in the good old days was based on equilibrium models of populations, communities, and ecosystems, an assumption we know to be irrelevant to a world with a changing climate. Perhaps we should have listened to the paleoecologists who kept reminding us that there was monumental change going on in the eras of glaciation and much earlier in the time of continental drift (Birks 2019). All of this argues that we need to change direction from short-term studies to long-term studies and long-term thinking.

There are many short-term ecological studies that are useful and should be done. It is necessary for management agencies to know if the spraying of forest insect pests this year reduces damage next year, and many similar problems exist that can be used for student projects. But the big issues of our day are long term problems, defined in the first place by longer than the research lifespan of the average ecologist, about 40 years. These big issues are insufficiently studied for two reasons. First, there is little funding for long term research. We can find a few exemptions to this statement, but they are few and many of them are flawed. Second, we as research scientists want to do something new that no one has done before. This approach leads to individual fame and sometimes fortune and is the social model behind many of the research prizes that we hear about in the media, the Nobel Prize, the MacArthur Awards, the National Medal of Science, the Kyoto Prize and many more. The point here is not that we should stop giving these awards (because they are socially useful), but that we should take a broader perspective on how research really works. Many have recognized that scientific advances are made by groups of scientists standing on the shoulders of an earlier generation. Perhaps some of the awards in medicine recognize this more frequently than other areas of science. My point is that large problems in ecology require a group effort by scientists that is too often unrecognized in favour of the individual fame model of science prizes.

A few examples may exemplify the need in ecology to support group studies of long-term problems. The simplest cases are in the media every day. The overharvesting of trees continues with little research into the long-term recovery of the harvested area and exactly how the forest community changes as it recovers. We mine areas for minerals and drill and mine tar sands for oil and gas with little long-term view of the recovery path which may stretch to hundreds or thousands of years while our current research program is long-term if it goes for 10 years. Canada has enough of these disturbance problems to fill the leger. The Giant Gold Mine in the Northwest Territories of Canada mined 220,000 kg of gold from 1948 to 2004 when it closed. It left 237 tonnes of arsenic trioxide dust, a by-product for extracting gold. The long-term ecosystem problems from this toxic compound will last for centuries but you might expect it will be much sooner forgotten than subjected to long-term study.

So where are we ecologists with respect to these large problems? We bewail biodiversity loss and when you look at the available data and the long-term studies you would expect to measure biodiversity and, if possible, manage this biodiversity loss. But you will find only piecemeal short-term studies of populations, communities, and ecosystems that are affected. We tolerate this unsatisfactory scientific situation even for ecosystems as iconic as the Great Barrier Reef of eastern Australia where we have a small number of scientists monitoring the collapse of the reef from climate change. The only justification we can give is that “Mother Nature will heal itself” or in the scientific lingo, “the organisms involved will adapt to environmental change”. All the earth’s ecosystems have been filtered through a million years of geological change, so we should not worry, and all will be well for the future, or so the story goes.

I think few ecologists would agree with such nonsense as the statements above, but what can we do about it? My main emphasis here is long-term monitoring. No matter what you do, this should be part of your research program. If possible, do not count birds on a plot for 3 years and then stop. Do not live trap mice for one season and think you are done. If you have any control over funding recommendations, think continuity of monitoring. Long-term monitoring is a necessary but not a sufficient condition for managing biodiversity change.

There are many obstacles interfering with achieving this goal. Money is clearly one. If your research council requests innovation in all research proposals, they are probably driven by Apple iPhone producers who want a new model every year. For the past 50 years we have been able to fund monitoring in our Yukon studies without ever using the forbidden word monitor because it was not considered science by the government granting agencies. In one sense it is not whether you consider science = innovation or not, but part of the discussion about long term studies might be shifted to consider the model of weather stations, and to discuss why we continue to report temperatures and CO2 levels daily when we have so much past data. No one would dream of shutting down weather monitoring now after the near fiasco around whether or not to measure CO2 in the atmosphere (Harris, 2010, Marx et al. 2017).

Another obstacle has been the destruction of research sites by human developments. Anyone with a long history of doing field research can tell you of past study areas that have been destroyed by fire or are now parking lots, or roads, or suburbia. This problem could be partly alleviated by the current proposals to maintain 30% of the landscape in protected areas. We should however avoid designating areas like the toxic waste site of the Giant Gold Mine as a “protected area” for ecological research.

Where does this all lead? Consider long-term monitoring if you can do the research as part of your overall program. Read the recent contributions of Hjeljord, and Loe (2022) and Wegge et al. (2022) as indicators of the direction in which we need to move, and if you need more inspiration about monitoring read Lindenmayer (2018).

Birks, H.J.B. (2019) Contributions of Quaternary botany to modern ecology and biogeography. Plant Ecology & Diversity, 12, 189-385.doi: 10.1080/17550874.2019.1646831.

Harris, D.C. (2010) Charles David Keeling and the story of atmospheric CO2 measurements. Analytical Chemistry, 82, 7865-7870.doi: 10.1021/ac1001492.

Hjeljord, O. & Loe, L.E. (2022) The roles of climate and alternative prey in explaining 142 years of declining willow ptarmigan hunting yield. Wildlife Biology, 2022, e01058.doi: 10.1002/wlb3.01058.

Lindenmayer, D. (2018) Why is long-term ecological research and monitoring so hard to do? (And what can be done about it). Australian Zoologist, 39, 576-580.doi: 10.7882/az.2017.018.

Marx, W., Haunschild, R., French, B. & Bornmann, L. (2017) Slow reception and under-citedness in climate change research: A case study of Charles David Keeling, discoverer of the risk of global warming. Scientometrics, 112, 1079-1092.doi: 10.1007/s11192-017-2405-z.

Wegge, P., Moss, R. & Rolstad, J. (2022) Annual variation in breeding success in boreal forest grouse: Four decades of monitoring reveals bottom-up drivers to be more important than predation. Ecology and Evolution.12, e9327. doi: 10.1002/ece3.9327.

Is Ecology Becoming a Correlation Science?

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One of the first lessons in Logic 101 is classically called “Post hoc, ergo propter hoc” or in plain English, “After that, therefore because of that”. The simplest example of many you can see in the newspapers might be: “The ocean is warming up, salmon populations are going down, it must be another effect of climate change. There is a great deal of literature on the problems associated with these kinds of simple inferences, going back to classics like Romesburg (1981), Cox and Wermuth (2004), Sugihara et al. (2012), and Nichols et al. (2019). My purpose here is only to remind you to examine cause and effect when you make ecological conclusions.

My concern is partly related to news articles on ecological problems. A recent example is the collapse of the snow crab fishery in the Gulf of Alaska which in the last 5 years has gone from a very large and profitable fishery interacting with a very large crab population to, at present, a closed fishery with very few snow crabs. What has happened? Where did the snow crabs go? No one really knows but there are perhaps half a dozen ideas put forward to explain what has happened. Meanwhile the fishery and the local economy are in chaos. Without very many critical data on this oceanic ecosystem we can list several factors that might be involved – climate change warming of the Bering Sea, predators, overfishing, diseases, habitat disturbances because of bottom trawl fishing, natural cycles, and then recognizing that we have no simple way for deciding cause and effect and therefore making management choices.

The simplest solution is to say that many interacting factors are involved and many papers indicate the complexity of populations, communities and ecosystems (e,g, Lidicker 1991, Holmes 1995, Howarth et al. 2014). Everyone would agree with this general idea, “the world is complex”, but the arguments have always been “how do we proceed to investigate ecological processes and solve ecological problems given this complexity?” The search for generality has led mostly into replications in which ‘identical’ populations or communities behave very differently. How can we resolve this problem? A simple answer to all this is to go back to the correlation coefficient and avoid complexity.

Having some idea of what is driving changes in ecological systems is certainly better than having no idea, but it is a problem when only one explanation is pushed without a careful consideration of alternative possibilities. The media and particularly the social media are encumbered with oversimplified views of the causes of ecological problems which receive wide approbation with little detailed consideration of alternative views. Perhaps we will always be exposed to these oversimplified views of complex problems but as scientists we should not follow in these footsteps without hard data.

What kind of data do we need in science? We must embrace the rules of causal inference, and a good start might be the books of Popper (1963) and Pearl and Mackenzie (2018) and for ecologists in particular the review of the use of surrogate variables in ecology by Barton et al. (2015). Ecologists are not going to win public respect for their science until they can avoid weak inference, minimize hand waving, and follow the accepted rules of causal inference. We cannot build a science on the simple hypothesis that the world is complicated or by listing multiple possible causes for changes. Correlation coefficients can be a start to unravelling complexity but only a weak one. We need better methods for resolving complex issues in ecology.

Barton, P.S., Pierson, J.C., Westgate, M.J., Lane, P.W. & Lindenmayer, D.B. (2015) Learning from clinical medicine to improve the use of surrogates in ecology. Oikos, 124, 391-398.doi: 10.1111/oik.02007.

Cox, D.R. and Wermuth, N. (2004). Causality: a statistical view. International Statistical Reviews 72: 285-305.

Holmes, J.C. (1995) Population regulation: a dynamic complex of interactions. Wildlife Research, 22, 11-19.

Howarth, L.M., Roberts, C.M., Thurstan, R.H. & Stewart, B.D. (2014) The unintended consequences of simplifying the sea: making the case for complexity. Fish and Fisheries, 15, 690-711.doi: 10.1111/faf.12041

Lidicker, W.Z., Jr. (1991) In defense of a multifactor perspective in population ecology. Journal of Mammalogy, 72, 631-635.

Nichols, J.D., Kendall, W.L. & Boomer, G.S. (2019) Accumulating evidence in ecology: Once is not enough. Ecology and Evolution, 9, 13991-14004.doi: 10.1002/ece3.5836.

Pearl, J., and Mackenzie, D. 2018. The Book of Why. The New Science of Cause and Effect. Penguin, London, U.K. 432 pp. ISBN: 978-1541698963

Popper, K.R. 1963. Conjectures and Refutations: The Growth of Scientific Knowledge. Routledge and Kegan Paul, London. 608 pp. ISBN: 978-1541698963

Romesburg, H.C. (1981) Wildlife science: gaining reliable knowledge. Journal of Wildlife Management, 45, 293-313.

Sugihara, G., et al. (2012) Detecting causality in complex ecosystems. Science, 338, 496-500.doi: 10.1126/science.1227079.

On the Meaning of ‘Food Limitation’ in Population Ecology

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There are many different ecological constraints that are collected in the literature under the umbrella of ‘food limitation’ when ecologists try to explain the causes of population changes or conservation problems. ‘Sockeye salmon in British Columbia are declining in abundance because of food limitation in the ocean’. ’Jackrabbits in some states in the western US are increasing because climate change has increased plant growth and thus removed the limitation of their plant food supplies.’ ‘Moose numbers in western Canada are declining because their food plants have shifted their chemistry to cope with the changing climate and now suffer food limitation”. My suggestion here is that ecologists should be careful in defining the meaning of ‘limitation’ in discussing these kinds of population changes in both rare and abundant species.

Perhaps the first principle is that it is the definition of life that food is always limiting. One does not need to do an experiment to demonstrate this truism. So to start we must agree that modern agriculture is built on the foundation that food can be improved and that this form of ‘food limitation’ is not what ecologists who are interested in population changes in the real world are trying to test. The key to explain population differences must come from resource differences in the broad sense, not food alone but a host of other ecological causal factors that may produce changes in birth and death rates in populations.

‘Limitation’ can be used in a spatial or a temporal context. Population density of deer mice can differ in average density in 2 different forest types, and this spatial problem would have to be investigated as a search for the several possible mechanisms that could be behind this observation. Often this is passed off too easily by saying that “resources” are limiting in the poorer habitat, but this statement takes us no closer to understanding what the exact food resources are. If food resources carefully defined are limiting density in the ‘poorer’ habitat, this would be a good example of food limitation in a spatial sense. By contrast if a single population is increasing in one year and declining in the next year, this could be an example of food limitation in a temporal sense.

The more difficult issue now becomes what evidence you have that food is limiting in either time or space. Growth in body size in vertebrates is one clear indirect indicator but we need to know exactly what food resources are limiting. The temptation is to use feeding experiments to test for food limitation (reviewed in Boutin 1990). Feeding experiments in the lab are simple, in the field not simple. Feeding an open population can lead to immigration and if your response variable is population density, you have an indirect effect of feeding. If animals in the experimentally fed area grow faster or have a higher reproductive output, you have evidence of the positive effect of the feeding treatment. You can then claim ‘food limitation’ for these specific variables. If population density increases on your feeding area relative to unfed controls, you can also claim ‘food limitation of density’. The problems then come when you consider the temporal dimension due to seasonal or annual effects. If the population density falls and you are still feeding in season 2 or year 2, then food limitation of density is absent, and the change must have been produced by higher mortality in season 2 or higher emigration.

Food resources could be limiting because of predator avoidance (Brown and Kotler 2007). The ecology of fear from predation has blossomed into a very large literature that explores the non-consumptive effects of predators on prey foraging that can lead to food limitation without food resources being in short supply (e.g., Peers et al. 2018, Allen et al. 2022).

All of this seems to be terribly obvious but the key point is that if you examine the literature about “food limitation” look at the evidence and the experimental design. Ecologists like medical doctors at times have a long list of explanations designed to sooth the soul without providing good evidence of what exact mechanism is operating. Economists are near the top with this distinguished approach, exceeded only by politicians, who have an even greater art in explaining changes after the fact with limited evidence.

As a footnote to defining this problem of food limitation, you should read Boutin (1990). I have also raved on about this topic in Chapter 8 of my 2013 book on rodent populations if you wish more details.

Allen, M.C., Clinchy, M. & Zanette, L.Y. (2022) Fear of predators in free-living wildlife reduces population growth over generations. Proceedings of the National Academy of Sciences (PNAS), 119, e2112404119. doi: 10.1073/pnas.2112404119.

Boutin, S. (1990). Food supplementation experiments with terrestrial vertebrates: patterns, problems, and the future. Canadian Journal of Zoology 68(2): 203-220. doi: 10.1139/z90-031.

Brown, J.S. & Kotler, B.P. (2007) Foraging and the ecology of fear. Foraging: Behaviour and Ecology (eds. D.W. Stephens, J.S. Brown & R.C. Ydenberg), pp. 437-448.University of Chicago Press, Chicago. ISBN: 9780226772646

Krebs, C.J. (2013) Chapter 8, The Food Hypothesis. In Population Fluctuations in Rodents. University of Chicago Press, Chicago. ISBN: 978-0-226-01035-9

Five Stages of Ecological Research

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Ecological research falls into five broad classes or stages. Each stage has its strengths and its limitations, and it is important to recognize these since no one stage is more or less important than any other. I suggest a classification of these five stages as follows:

  1. Natural History
  2. Behavioural Ecology
  3. Applied Ecology
  4. Conservation Ecology
  5. Ecosystem Ecology

The Natural History stage is the most popular with the public and in some sense the simplest type of ecological research while at the same time the critical foundation of all subsequent research. Both Bartholomew (1986) and Dayton (2003) made impassioned pleas for the study of natural history as a basis of understanding all the biological sciences. In some sense this stage of biological science has now come into its own in popularity, partly because of influential TV shows like those of David Attenborough but also because of the ability of talented wildlife photographers to capture amazing moments of animals in the natural world. Many scientists still look upon natural history as “stamp-collecting” unworthy of a serious ecologist, but this stage is the foundational element of all ecological research.

Behavioural ecology became popular as one of the early outcomes of natural history observations within the broad framework of asking questions about how individuals in a population behave, and what the ecological and evolutionary consequences of these behaviours are to adaptation and possible future evolution. One great advantage of studying behavioural ecology has been that it is quick, perfectly suited to asking simple questions, devising experimental tests, and then being able to write a report, or a thesis on these results (Davies et al. 2012). Behavioural ecology is one of the strongest research areas of ecological science and provides entertainment for students of natural history and excellent science to understand individual behaviour and how it fits into population studies. It is perhaps the strongest of the ecological approaches for drawing the public into an interest in biodiversity.

Applied ecology is one of the oldest fields of ecology since it arose more than 100 years ago from local problems of how organisms affected human livelihoods. It has subdivided into three important sub-fields – pest management, wildlife management, and fisheries management. Applied ecology relies heavily on the principles of population ecology, one level above the individual studies of behavioural and natural history research. These fields are concerned with population changes, whether to reduce populations to stop damage to crops, or to understand why some species populations become pests. All applied ecology heavily interreacts with human usage of the environment and the economics of farming, fisheries, and wildlife harvesting. In a general sense applied ecology is a step more difficult than behavioural ecology because answering the applied problems or management has a longer time frame than the typical three-year thesis project. Applied ecology has a broad interface with evolutionary ecology because human actions can disrupt natural selection and pest evolution can complicate every management problem.

Conservation ecology is the new kid on the block. It was part of wildlife and fisheries management until about 1985 when it was clear to all that some populations were endangered by human changes to the ecosystems of fisheries, forestry, and agriculture. The essential problems of conservation ecology were described elegantly by Caughley (1994). Conservation issues are the most visible of all issues in population and community ecology, and they are often the most difficult to resolve when science dictates one conservation solution that interferes with the dominant economic view of human society. If species of interest are rare the problem is further confounded by the difficulty of studying rare species in the field. What will become of the earth’s ecosystems in the future depends in large part as to how these conservation conflicts can be resolved.

Ecosystem ecology and community ecology are the important focus at present but are hampered by a lack of a clear vision of what needs to be done and what can be done. The problem is partly that there is much poor theory, coupled with much poor data. The critical questions in ecosystem ecology are currently too vague to be studied in a realistic time period of less than 50 years. Climate change is impacting all our current ideas about community stability and resilience, and what predictions we can make for whole ecosystems in the light of a poor database. Ironically experimental manipulations are being done by companies with an economic focus such as forestry but there are few funds to make use of these large-scale landscape changes. In the long term, ecosystem ecology is the most significant aspect of ecology for humans, but it is the weakest in terms of understanding ecosystem processes. We can all see the negative effects of human changes on landscapes, but we have little in the way of scientific guidance to predict the long-term consequences of these changes and how they can be successfully ameliorated.

All of this is distressing to practical ecologists who wish to make a difference and be able to counteract undesirable changes in populations and ecosystems. It is important for all of us not to give up on reversing negative trends in conservation and land management and we need to do all we can to influence the public in general and politicians in particular to change negative trends to positive ones in our world. An array of good books points this out very forcefully (e.g., Monbiot 2018, Klein 2021). It is the job of every ecologist to gather the data and present ecological science to the community at large so we can contribute to decision making about the future of the Earth.

Bartholomew, G. A. (1986). The role of natural history in contemporary biology. BioScience 36, 324-329. doi: 10.2307/1310237

Caughley, G. (1994). Directions in conservation biology. Journal of Animal Ecology 63, 215-244. doi: 10.2307/5542

Davies, N.B., Krebs, J.R., and West, S.A. (2012) ‘An Introduction to Behavioural Ecology.‘ 4th edn. (Wiley-Blackwell: Oxford.). 520 pp.

Dayton, P.K. (2003). The importance of the natural sciences to conservation. American Naturalist 162, 1-13. doi: 10.1086/376572

Klein, Naomi (2021) ‘How to Change Everything: The Young Human’s Guide to Protecting the Planet and Each Other ‘ (Simon and Schuster: New York.) 336 pp. ISBN: 978-1534474529

Monbiot, George. (2018) ‘Out of the Wreckage: A New Politics for an Age of Crisis.’ (Verso.). 224 pp. ISBN: 1786632896

What is the Ratio of Thought to Action in Biodiversity Conservation?

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Many ecologists who peruse the conservation literature will come away with a general concern about the amount of effort that goes into thoughts about how conservation should be done and how much action is currently being carried out to achieve these goals in the field. My premise here is that currently the person-power given to thought greatly exceeds the person-power devoted to actually achieving the broad conservation goal of protecting biodiversity. Let me illustrate this with one dilemma in conservation: should we be concerned predominately with the loss of threatened and endangered species, or should we concentrate on the major dominant species in our ecosystems? Of course, this is not a black-or-white dichotomy, and the first answer is that we should do both. But the economist would suggest that resources are limited, and you cannot do both, so the question should be reworded as to what fraction of resources should go to one or the other of these two activities.

Consider the example of threatened and endangered species. Many of these species are rare numerically at present. In the past they may have been abundant but that is not always the case. The ecologist will know as a universal constant that most species in ecosystems are rare, and because they are rare, they are most difficult to study to answer the simple question why are they rare? Pick your favourite rare species and try to answer this question. For some species under persecution by humans the answer is simple; for most it is not, and ecologists fall back on explanations like the resources they require are not abundant, or their niche is specialized, meaningless statements that can be called panchrestons unless we have infinite time and funds to find out exactly what the limiting resources are, or why their niche is specialized. Now let us make a simple thought experiment that asks: what would happen if all these rare and endangered species disappeared from the world’s ecosystems? The first response would be total outrage that anyone would ask such a terrible question, so it is best not to talk about it. The second would be that we would be outraged if our favorite bird or frog disappeared like the passenger pigeon. The third might be that we should consider this question seriously.

Some community and ecosystem ecologists might wager that nothing would happen to ecosystem dynamics if all the rare and endangered species disappeared. No one of course would admit to such a point of view since it would end their career. At the moment we are in the unenviable state of doing the opposite experiment on the world’s coral reefs which are suffering in an ocean that is acidifying and heating up, pollution that is increasing, and overfishing that is common (Fraser et al. 2019, Lebrec et al. 2019, Romero-Torres et al. 2020). Coral reefs are an extreme example of human impacts on areas of high conservation and economic value such that the entire ecosystem will have to reconstruct itself with corals of greater tolerance to current and future conditions, a future with no clear guess of what positive effects will transpire.

Perhaps the message of both coral reef conservation and terrestrial ecosystem conservation is that you cannot destroy the major species without major consequences. Australia provides a good example of the consequences of altering predator abundance in an ecosystem. The dingo (Canis familaris) has been persecuted because of predation on sheep, and at the same time domestic cats (Felis catus) and red foxes (Vulpes vulpes) have been introduced to the continent. The ecological question is whether the reintroduction of the dingo to places where it has been exterminated will reduce the abundance of cats and foxes, and thus save naïve prey species from local extinction (Newsome et al. 2015). The answer to this question is far from clear (Morgan et al. 2017, Hunter and Letnic 2022) and may differ in different ecosystems within Australia.  

The bottom line is that our original question about rare species cannot be answered. There is much literature on introduced predators affecting food webs, following from Estes et al. (2011) important paper. and now there is much research effort on the roles of apex predators and consumers on ecosystem dynamics (Serrouya et al. 2021). Much of this effort concentrates on the common animals rather than the rare ones with which we began this discussion. Much more action in the field is needed on all conservation fronts since in my opinion the amount of thought we have available now will last field workers for the rest of the century.

Estes, J.A., Terborgh, J., Brashares, J.S., Power, M.E., Berger, J., et al. (2011). Trophic downgrading of Planet Earth. Science 333, 301-306. doi: 10.1126/science.1205106.

Fraser, K.A., Adams, V.M., Pressey, R.L., and Pandolfi, J.M. (2019). Impact evaluation and conservation outcomes in marine protected areas: A case study of the Great Barrier Reef Marine Park. Biological Conservation 238, 108185. doi: 10.1016/j.biocon.2019.07.030

Hunter, D.O. and Letnic, M. (2022). Dingoes have greater suppressive effect on fox populations than poisoning campaigns. Australian Mammalogy 44. doi: 10.1071/AM21036.

Lebrec, M., Stefanski, S., Gates, R., Acar, S., Golbuu, Y., Claudel-Rusin, A., Kurihara, H., Rehdanz, K., Paugam-Baudoin, D., Tsunoda, T., and Swarzenski, P.W. (2019). Ocean acidification impacts in select Pacific Basin coral reef ecosystems. Regional Studies in Marine Science 28, 100584. doi: 10.1016/j.rsma.2019.100584.

Morgan, H.R., Hunter, J.T., Ballard, G., Reid, N.C.H., and Fleming, P.J.S. (2017). Trophic cascades and dingoes in Australia: Does the Yellowstone wolf–elk–willow model apply? Food Webs 12, 76-87. doi: 10.1016/j.fooweb.2016.09.003.

Newsome, TM., Ballard, G.-A., Crowther, M.S., Dellinger, J.A., Fleming, P.J.S., et al. (2015). Resolving the value of the dingo in ecological restoration. Restoration Ecology 23, 201-208.  doi: 10.1111/rec.12186.

Romero-Torres, M., Acosta, A., Palacio-Castro, A.M., Treml, E.A., Zapata, F.A., Paz-García, D.A., and Porter, J.W. (2020). Coral reef resilience to thermal stress in the Eastern Tropical Pacific. Global Change Biology 26, 3880-3890. doi: 10.1111/gcb.15126

Serrouya, R., Dickie, M., Lamb, C., Oort, H. van, Kelly, A.P., DeMars, C., et al. (2021). Trophic consequences of terrestrial eutrophication for a threatened ungulate. Proceedings of the Royal Society B: Biological Sciences 288, 20202811. doi: 10.1098/rspb.2020.2811.

How Do We Decide Controversial Issues in Conservation?

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While almost everyone favours conservation of plants and animals around the globe, it is far from clear how this broad goal can be disarticulated into smaller issues. Once we have done this the solution of the conservation problem should be simple. But it is not (Sutherland et al, 2021). Take an example of the koala in Australia, cute mid-size marsupials that live in trees and eat leaves. If koalas are to be protected, you must protect forests, but if you protect forests the companies that survive by logging on both private and crown land will be adversely affected. We have an immediate conflict, so how do we decide what to do. One response which we can label have-your-cake-and-eat-it-too suggests that we use some of our forests for logging and protect some forests for ecological reserves. Everyone is now happy, but things unravel. As the human population grows, we need more wood, so over time we would have to log more and more of the forested areas that could support koalas. Conflict now, jobs for loggers vs. conservation of koalas. The simplest solution is to decide all this in economic terms. Logging produces much money; conservation is largely a drain on the taxpayers. To propose that conservation should win, ecologists will pull out David Attenborough to show all the beauties of the forest and to point out that the forest contains many other animals and plants and not just trees for lumber. Stalemate, and social and economic goals begin to override the ecological issue until some compromise is suggested and accepted.

While this kind of oversimplified scenario is common, the whole issue of conservation decision making is fraught with problems and who is going to decide these issues (Christie et al. 2022)? In a democracy in the good old days, you took a vote or a poll and decided to win/lose at >50% of the vote. But this cannot work for critical problems. We have a good example of this problem now with Covid vaccination requirements, and a vocal minority opposed to vaccinations. This now spills over into the issue of whether to wear a face mask or not. In all these kinds of scenarios science delivers a simple decision about the consequences of decision A vs decision B, but the problem is that society can refuse to recognize the scientific results or just prefer decision B with little visible justification. Science is not always perfect, adding further complications. And in the case of the covid virus, the virus can mutate in unexpected ways, complicating prognoses. In the case of protected conservation areas, we can suffer fires, floods, insect outbreaks and any number of events that affect the balance of decision making.

There is a large literature on decision making in conservation (e.g., Bower et al. 2018) and even good advice from the field of psychology about this problem of making decisions (Papworth 2017). The best systematic decision tree I have found is that in Sutherland et al. 2021). Sutherland et al. (2021) compiled a framework that can be used profitably in deciding on the level of evidence assessment (see Table 1 and Figure 1 below from their paper).

Table 1 and Figure 1 from Sutherland et al. (2021)

The Strategic Evidence Assessment Framework. Seven levels of evidence assessment, how to apply them.

Assessment LevelApproach UsedGeneral Database ApplicationApproximate Time to reflect on the evidence
1 No consideration of evidenceContinue with existing practice or make decisions without considering scientific evidencenone
2 Assertion but no independent consideration of evidenceConsultation with others (including experts) that affect decision but are not verified e.g. “we normally do this”, “accepted best practice is to do this”minutes
3Papers reviewed, looking at: Read the title and/or summary points to determine whether action described in the paper is likely to be effective or not. Review effectiveness category e.g. “likely to be beneficial” on action page to decide whether action is likely to be effective or notminutes
4 Read abstract to assess the evidence described in the paper in relation to the local problemTens of minutes- hours
5  Read abstract, key results and conclusion assessing each paper in relation to the decision being madeHours
6 Read the full underlying paper/s. This is likely to affect decisions on study quality, relevance and modificationsHours to days
7Comprehensive assessmentA systematic review of all available literature. Assessed papers summarised as part of new reviewMonths to a year

Figure 1. A framework for considering the appropriate level of effort in decision making. Numbers refer to assessment level (Table 1). For a given decision about an action identify the column with the relevant level of consequence, start at the lowest level (1) and decide whether it would benefit from examining higher levels of evidence. Keep moving up until either the uncertainty in the effectiveness of the action is resolved from examining the evidence (from any platform) or the arrows end. This final number is the level at which the evidence assessment should occur. (From Sutherland et al. 2021 with permission).

Clearly conservation ecologists cannot use the highest assessment level for all issues that arise and must result to triage in many cases (Hayward and Castley 2018). But triage and assessment levels 1 and 2 should be rare in making judgement on what program to adopt. We need to get the science right for all conservation problems.

But this is not enough to get thoughtful political decisions. Some native species can be pests, yet nothing is done to reduce their damage (e.g. horses in North America and Australia, camels and goats in Australia, feral pigs in North America) and the list goes on. Nothing is done because of budget limitations or political concerns about “cute species”. The science of conservation is difficult enough, the social science of conservation is too often out of our control.

Bower, S.D., Brownscombe, J.W., Birnie-Gauvin, K. Ford, M.I. et al. (2018). Making Tough Choices: Picking the appropriate conservation decision-making tool. Conservation Letters 11, e12418. doi: 10.1111/conl.12418.

Christie, A.P., Downey, H., Bretagnolle, V., Brick, C., Bulman, C.R., et al. (2022). Principles for the production of evidence-based guidance for conservation actions. Conservation Science and Practice 4, e579. doi: 10.1111/csp2.12663.

Hayward, M.W. and Castley, J.G. (2018). Triage in Conservation. Frontiers in Ecology and Evolution 5, 168. doi: 10.3389/fevo.2017.00168.

Papworth, Sarah (2017). Decision-making psychology can bolster conservation. Nature Ecology & Evolution 1, 1217-1218. doi: 10.1038/s41559-017-0281-9.

Sutherland, W.J., Downey, H., Frick, W.F., Tinsley-Marshall, P., and McPherson, T. (2021). Planning practical evidence-based decision making in conservation within time constraints: the Strategic Evidence Assessment Framework. Journal for Nature Conservation 60, 125975. doi: 10.1016/j.jnc.2021.125975.

On How Genomics will not solve Ecological Problems

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I am responding to this statement in an article in the Conversation by Anne Murgai on April 19, 2022 (https://phys.org/news/2022-04-african-scientists-genes-species.html#google_vignette) : The opening sentence of her article on genomics encapsulates one of the problems of conservation biology today:

“DNA is the blueprint of life. All the information that an organism needs to survive, reproduce, adapt to environments or survive a disease is in its DNA. That is why genomics is so important.”

If this is literally correct, almost all of ecological science should disappear, and our efforts to analyse changes in geographic distributions, abundance, survival and reproductive rates, competition with other organisms, wildlife diseases, conservation of rare species and all things that we discuss in our ecology journals are epiphenomena, and thus our slow progress in sorting out these ecological issues is solely because we have not yet sequenced all our species to find the answers to everything in their DNA.

This is of course not correct, and the statement quoted above is a great exaggeration. But, if it is believed to be correct, it has some important consequences for scientific funding. I will confine my remarks to the fields of conservation and ecology. The first and most important is that belief in this view of genetic determinism is having large effects on where conservation funding is going. Genomics has been a rising star in biological science for the past 2 decades because of technological advances in sequencing DNA. As such, given a fixed budget, it is taking money away from the more traditional approaches to conservation such as setting up protected areas and understanding the demography of declining populations. Hausdorf (2021) explores these conflicting problems in an excellent review, and he concludes that often more cost-effective methods of conservation should be prioritized over genomic analyses. Examples abound of conservation problems that are immediate and typically underfunded (e.g., Turner et al. 2021, Silva et al, 2021).   

What is the resolution of these issues? I can recommend only that those in charge of dispensing funding for conservation science examine the hypotheses being tested and avoid endless funding for descriptive genomics that claim to have a potential and immediate outcome that will forward the main objectives of conservation. Certainly, some genomic projects will fit into this desirable science category, but many will not, and the money should be directed elsewhere.  

The Genomics Paradigm listed above is used in the literature on medicine and social science, and a good critique of this view from a human perspective is given in a review by Feldman and Riskin (2022). Scientists dealing with human breast cancer or schizophrenia show the partial but limited importance of DNA in determining the cause or onset of these complex conditions (e.g., Hilker et al 2018, Manobharathi et al. 2021). Conservation problems are equally complex, and in the climate emergency have a short time frame for action. I suspect that genomics for all its strengths will have only a minor part to play in the resolution of ecological problems and conservation crises in the coming years.

Feldman, Marcus W. and Riskin, Jessica (2022). Why Biology is not Destiny. The New York Review of Books 69 (April 21, 2022), 43-46.

Hausdorf, Bernhard (2021). A holistic perspective on species conservation. Biological Conservation 264, 109375. doi: 10.1016/j.biocon.2021.109375.

Hilker, R., Helenius, D., Fagerlund, B., Skytthe, A., Christensen, K., Werge, T.M., Nordentoft, M., and Glenthøj, B. (2018). Heritability of Schizophrenia and Schizophrenia Spectrum based on the Nationwide Danish Twin Register. Biological Psychiatry 83, 492-498. doi: 10.1016/j.biopsych.2017.08.017.

Manobharathi, V., Kalaiyarasi, D., and Mirunalini, S. (2021). A concise critique on breast cancer: A historical and scientific perspective. Research Journal of Biotechnology 16, 220-230.

Samuel, G. N. and Farsides, B. (2018). Public trust and ‘ethics review’ as a commodity: the case of Genomics England Limited and the UK’s 100,000 genomes project. Medicine, Health Care, and Philosophy 21, 159-168. doi: 10.1007/s11019-017-9810-1.

Silva, F., Kalapothakis, E., Silva, L., and Pelicice, F. (2021). The sum of multiple human stressors and weak management as a threat for migratory fish. Biological Conservation 264, 109392. doi: 10.1016/j.biocon.2021.109392.

Turner, A., Wassens, S., and Heard, G. (2021). Chytrid infection dynamics in frog populations from climatically disparate regions. Biological Conservation 264, 109391. doi: 10.1016/j.biocon.2021.109391.