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Latest recommendations
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31 Oct 2022
Ten simple rules for working with high resolution remote sensing dataAdam L. Mahood, Maxwell Benjamin Joseph, Anna Spiers, Michael J. Koontz, Nayani Ilangakoon, Kylen Solvik, Nathan Quarderer, Joe McGlinchy, Victoria Scholl, Lise St. Denis, Chelsea Nagy, Anna Braswell, Matthew W. Rossi, Lauren Herwehe, Leah wasser, Megan Elizabeth Cattau, Virginia Iglesias, Fangfang Yao, Stefan Leyk, Jennifer Balch https://doi.org/10.31219/osf.io/kehqzPreventing misuse of high-resolution remote sensing dataRecommended by Eric Goberville based on reviews by Jane Wyngaard and 1 anonymous reviewerTo observe, characterise, identify, understand, predict... This is the approach that researchers follow every day. This sequence is tirelessly repeated as the biological model, the targeted ecosystem and/or the experimental, environmental or modelling conditions change. This way of proceeding is essential in a world of rapid change in response to the frenetic pace of intensifying pressures and forcings that impact ecosystems. To better understand our Earth and the dynamics of its components, to map ecosystems and diversity patterns, and to identify changes, humanity had to demonstrate inventiveness and defy gravity. Gustave Hermite and Georges Besançon were the first to launch aloft balloons equipped with radio transmitters, making possible the transmission of meteorological data to observers in real time [1]. The development of aviation in the middle of the 20th century constituted a real leap forward for the frequent acquisition of aerial observations, leading to a significant improvement in weather forecasting models. The need for systematic collection of data as holistic as possible – an essential component for the observation of complex biological systems - has resulted in pushing the limits of technological prowess. The conquest of space and the concurrent development of satellite observations has largely contributed to the collection of a considerable mass of data, placing our Earth under the "macroscope" - a concept introduced to ecology in the early 1970s by Howard T. Odum (see [2]), and therefore allowing researchers to move towards a better understanding of ecological systems, deterministic and stochastic patterns … with the ultimate goal of improving management actions [2,3]. Satellite observations have been carried out for nearly five decades now [3] and have greatly contributed to a better qualitative and quantitative understanding of the functioning of our planet, its diversity, its climate... and to a better anticipation of possible future changes (e.g., [4-7]). This access to rich and complex sources of information, for which both spatial and temporal resolutions are increasingly fine, results in the implementation of increasingly complex computation-based analyses, in order to meet the need for a better understanding of ecological mechanisms and processes, and their possible changes. Steven Levitt stated that "Data is one of the most powerful mechanisms for telling stories". This is so true … Data should not be used as a guide to thinking and a critical judgment at each stage of the data exploitation process should not be neglected. This is what Mahood et al. [8] rightly remind us in their article "Ten simple rules for working with high-resolution remote sensing data" in which they provide the fundamentals to consider when working with data of this nature, a still underutilized resource in several topics, such as conservation biology [3]. In this unconventional article, presented in a pedagogical way, the authors remind different generations of readers how satellite data should be handled and processed. The authors aim to make the readers aware of the most frequent pitfalls encouraging them to use data adapted to their original question, the most suitable tools/methods/procedures, to avoid methodological overkill, and to ensure both ethical use of data and transparency in the research process. While access to high-resolution data is increasingly easy thanks to the implementation of dedicated platforms [4], and because of the development of easy-to-use processing software and pipelines, it is important to take the time to recall some of the essential rules and guidelines for managing them, from new users with little or no experience who will find in this article the recommendations, resources and advice necessary to start exploiting remote sensing data, to more experienced researchers. References [1] Jeannet P, Philipona R, and Richner H (2016). 8 Swiss upper-air balloon soundings since 1902. In: Willemse S, Furger M (2016) From weather observations to atmospheric and climate sciences in Switzerland: Celebrating 100 years of the Swiss Society for Meteorology. vdf Hochschulverlag AG. [2] Odum HT (2007) Environment, Power, and Society for the Twenty-First Century: The Hierarchy of Energy. Columbia University Press. [3] Boyle SA, Kennedy CM, Torres J, Colman K, Pérez-Estigarribia PE, Sancha NU de la (2014) High-Resolution Satellite Imagery Is an Important yet Underutilized Resource in Conservation Biology. PLOS ONE, 9, e86908. https://doi.org/10.1371/journal.pone.0086908 [4] Le Traon P-Y, Antoine D, Bentamy A, Bonekamp H, Breivik LA, Chapron B, Corlett G, Dibarboure G, DiGiacomo P, Donlon C, Faugère Y, Font J, Girard-Ardhuin F, Gohin F, Johannessen JA, Kamachi M, Lagerloef G, Lambin J, Larnicol G, Le Borgne P, Leuliette E, Lindstrom E, Martin MJ, Maturi E, Miller L, Mingsen L, Morrow R, Reul N, Rio MH, Roquet H, Santoleri R, Wilkin J (2015) Use of satellite observations for operational oceanography: recent achievements and future prospects. Journal of Operational Oceanography, 8, s12–s27. https://doi.org/10.1080/1755876X.2015.1022050 [5] Turner W, Rondinini C, Pettorelli N, Mora B, Leidner AK, Szantoi Z, Buchanan G, Dech S, Dwyer J, Herold M, Koh LP, Leimgruber P, Taubenboeck H, Wegmann M, Wikelski M, Woodcock C (2015) Free and open-access satellite data are key to biodiversity conservation. Biological Conservation, 182, 173–176. https://doi.org/10.1016/j.biocon.2014.11.048 [6] Melet A, Teatini P, Le Cozannet G, Jamet C, Conversi A, Benveniste J, Almar R (2020) Earth Observations for Monitoring Marine Coastal Hazards and Their Drivers. Surveys in Geophysics, 41, 1489–1534. https://doi.org/10.1007/s10712-020-09594-5 [7] Zhao Q, Yu L, Du Z, Peng D, Hao P, Zhang Y, Gong P (2022) An Overview of the Applications of Earth Observation Satellite Data: Impacts and Future Trends. Remote Sensing, 14, 1863. https://doi.org/10.3390/rs14081863 [8] Mahood AL, Joseph MB, Spiers A, Koontz MJ, Ilangakoon N, Solvik K, Quarderer N, McGlinchy J, Scholl V, Denis LS, Nagy C, Braswell A, Rossi MW, Herwehe L, Wasser L, Cattau ME, Iglesias V, Yao F, Leyk S, Balch J (2021) Ten simple rules for working with high resolution remote sensing data. OSFpreprints, ver. 6 peer-reviewed and recommended by Peer Community in Ecology. https://doi.org/10.31219/osf.io/kehqz | Ten simple rules for working with high resolution remote sensing data | Adam L. Mahood, Maxwell Benjamin Joseph, Anna Spiers, Michael J. Koontz, Nayani Ilangakoon, Kylen Solvik, Nathan Quarderer, Joe McGlinchy, Victoria Scholl, Lise St. Denis, Chelsea Nagy, Anna Braswell, Matthew W. Rossi, Lauren Herwehe, Leah wasser,... | <p>Researchers in Earth and environmental science can extract incredible value from high-resolution (sub-meter, sub-hourly or hyper-spectral) remote sensing data, but these data can be difficult to use. Correct, appropriate and competent use of su... | Biogeography, Landscape ecology, Macroecology, Spatial ecology, Metacommunities & Metapopulations, Terrestrial ecology | Eric Goberville | 2021-10-19 21:41:22 | View | ||
03 Jan 2024
Efficient sampling designs to assess biodiversity spatial autocorrelation : should we go fractal?Fabien Laroche https://doi.org/10.1101/2022.07.29.501974Spatial patterns and autocorrelation challenges in ecological conservationRecommended by Eric Goberville based on reviews by Nigel Yoccoz and Charles J Marsh“Pattern, like beauty, is to some extent in the eye of the beholder” (Grant 1977 in Wiens, 1989) Ecologists are immersed in unraveling the complex spatial patterns that govern species diversity, driven by both practical and theoretical imperatives (Rahbek, 2005; Wang et al., 2019). This dual focus necessitates a practical imperative for strategic biodiversity conservation, requiring a nuanced understanding of locations with peak species richness and dynamic shifts in species assemblages (Chase et al., 2020). Simultaneously, there is a theoretical interest in using diversity patterns as empirical testing grounds for theories explaining factors influencing diversity disparities and the associated increase in species turnover correlated with inter-site distance (Condit et al., 2002).
McGill (2010), in his paper "Matters of Scale", highlights the scale-dependent nature of ecology, aligning with the recognition that spatial autocorrelation is inherent in biogeographical data and often correlated with sample size (Rahbek, 2005). Spatial autocorrelation, often underestimated in ecological studies (Dormann, 2007), occurs when proximate locations exhibit similarities in ecological attributes (Tobler, 1970; Getis, 2010), introducing a latent bias that compromises the robustness of ecological findings (Dormann, 2007; Dormann et al., 2007). This phenomenon serves as both an asset, providing valuable information for inferring processes from patterns (Palma et al. 1999), and a challenge, imposing limitations on hypothesis testing and prediction (Dormann et al., 2007 and references therein). Various factors contribute to spatial autocorrelation, with three primary contributors (Dormann et al., 2007; Legendre, 1993; Legendre and Fortin, 1989; Legendre and Legendre, 2012): (i) distance-related effects in biological processes, (ii) misrepresentation of non-linear relationships between the environment and species as linear and (iii) the oversight of a crucial spatially structured environmental determinant in the statistical model, leading to spatial structuring in the response (Dormann et al., 2007).
Recognising the pivotal role of spatial heterogeneity in ecological theories (Wang et al., 2019), it becomes imperative to discern and address the limitations introduced by spatial autocorrelation (Legendre, 1993). McGill (2011) emphasises that the ultimate goal of biodiversity pattern studies should be to develop a quantitative predictive theory useful for conservation. The spatial dimension's importance in study planning, determining the system's scale, appropriate quadrat size, and spacing between sampling stations, is paramount (Fortin, 1999a,b). Responses to these considerations are intricately linked with study objectives and insights from pre-sampling campaigns, underscoring the need for a nuanced and rigorous approach (Delmelle, 2021).
Understanding statistical techniques and nested sampling designs is crucial to answering fundamental ecological questions (Dormann et al., 2007; McDonald, 2012). In addressing spatial autocorrelation challenges, ecologists must recognize the limitations of many standard statistical methods in ecological studies (Dale and Fortin, 2002; Legendre and Fortin, 1989; Steel et al., 2013). In the initial phases of description or hypothesis generation, ecologists should proactively acknowledge the spatial structure in their data and conduct tests for spatial autocorrelation (for a comprehensive description, see Legendre and Fortin, 1989): various tools, including correlograms, spectral analysis, the Mantel test, and clustering methods, facilitate the assessment and description of spatial structures. The partial Mantel test enables the study of causal models with space as an explanatory variable. Techniques for mapping ecological variables, such as interpolation, trend surface analysis, and constrained clustering, yield maps providing valuable insights into the spatial dynamics of ecological systems.
This refined consideration of spatial autocorrelation emerges as an imperative in ecological research, fostering a deeper and more precise understanding of the intricate interplay between species diversity, spatial patterns, and the inherent limitations imposed by spatial autocorrelation (Legendre et al., 2002). This not only contributes significantly to the scientific discourse in ecology but also aligns with McGill's vision of developing predictive theories for effective conservation (Bacaro et al., 2016; McGill, 2011).
In this study by Fabien Laroche (2023), titled “Efficient sampling designs to assess biodiversity spatial autocorrelation: should we go fractal?” the primary focus was on addressing the challenges associated with estimating the autocorrelation range of species distribution across spatial scales. The study aimed to explore alternative sampling designs, with a particular focus on the application of fractal designs—self-similar designs with well-identified scales. The overarching goal was to evaluate whether fractal designs could offer a more efficient compromise compared to traditional hybrid designs, which involve mixing random sampling points with a systematic grid.
Virtual ecology provides a way to test whether sampling designs can accurately detect or quantify effects of interest before implementing them in the field. Beyond the question of assessing the power of empirical designs, a virtual ecology analysis contributes to clearly formulating the set of questions associated with a design. However, only a few virtual studies have focused on efficient designs to accurately estimate the autocorrelation range of biodiversity variables. In this study, the statistical framework of optimal design of experiments was employed—a methodology often used in building and comparing designs of temporal or spatiotemporal biodiversity surveys but rarely applied to the specific problem of quantifying spatial autocorrelation.
Key findings from the study shed light on optimal sampling strategies, with a notable dependence on the feasible grid mesh size over the study area in relation to expected autocorrelation range values. The results demonstrated that the efficiency of designs varied based on the specific effect under study. Fractal designs, however, exhibited superior performance, particularly when assessing the effect of a monotonic environmental gradient across space.
In conclusion, the study provides valuable insights into the potential benefits of incorporating fractal designs in biodiversity studies, offering a nuanced and efficient approach to estimate spatial autocorrelation. These findings contribute significantly to the ongoing scientific discourse in ecology, providing practical considerations for improving sampling designs in biodiversity assessments.
References
Bacaro, G., Altobelli, A., Cameletti, M., Ciccarelli, D., Martellos, S., Palmer, M.W., Ricotta, C., Rocchini, D., Scheiner, S.M., Tordoni, E., Chiarucci, A., 2016. Incorporating spatial autocorrelation in rarefaction methods: Implications for ecologists and conservation biologists. Ecological Indicators 69, 233-238. https://doi.org/10.1016/j.ecolind.2016.04.026
Chase, J.M., Jeliazkov, A., Ladouceur, E., Viana, D.S., 2020. Biodiversity conservation through the lens of metacommunity ecology. Annals of the New York Academy of Sciences 1469, 86-104. https://doi.org/10.1111/nyas.14378
Condit, R., Pitman, N., Leigh, E.G., Chave, J., Terborgh, J., Foster, R.B., Núñez, P., Aguilar, S., Valencia, R., Villa, G., Muller-Landau, H.C., Losos, E., Hubbell, S.P., 2002. Beta-Diversity in Tropical Forest Trees. Science 295, 666-669. https://doi.org/10.1126/science.1066854
Dale, M.R.T., Fortin, M.-J., 2002. Spatial autocorrelation and statistical tests in ecology. Écoscience 9, 162-167. https://doi.org/10.1080/11956860.2002.11682702
Delmelle, E.M., 2021. Spatial Sampling, in: Fischer, M.M., Nijkamp, P. (Eds.), Handbook of Regional Science. Springer Berlin Heidelberg, Berlin, Heidelberg, pp. 1829-1844.
Dormann, C.F., 2007. Effects of incorporating spatial autocorrelation into the analysis of species distribution data. Global Ecology & Biogeography 16, 129-128. https://doi.org/10.1111/j.1466-8238.2006.00279.x
Dormann, C.F., McPherson, J.M., Araújo, M.B., Bivand, R., Bolliger, J., Carl, G., Davies, R.G., Hirzel, A., Jetz, W., Kissling, W.D., Kühn, I., Ohlemüler, R., Peres-Neto, P.R., Reineking, B., Schröder, B., Schurr, F.M., Wilson, R., 2007. Methods to account for spatial autocorrelation in the analysis of species distributional data: a review. Ecography 33, 609-628. https://doi.org/10.1111/j.2007.0906-7590.05171.x
Fortin, M.-J., 1999a. Effects of quadrat size and data measurement on the detection of boundaries. Journal of Vegetation Science 10, 43-50. https://doi.org/10.2307/3237159
Fortin, M.-J., 1999b. Effects of sampling unit resolution on the estimation of spatial autocorrelation. Écoscience 6, 636-641. https://doi.org/10.1080/11956860.1999.11682547
Getis, A., 2010. Spatial Autocorrelation, in: Fischer, M.M., Getis, A. (Eds.), Handbook of Applied Spatial Analysis: Software Tools, Methods and Applications. Springer Berlin Heidelberg, Berlin, Heidelberg, pp. 255-278.
Laroche, F., 2023. Efficient sampling designs to assess biodiversity spatial autocorrelation: should we go fractal? bioRxiv, 2022.07.29.501974, ver. 4 peer-reviewed and recommended by Peer Community in Ecology. https://doi.org/10.1101/2022.07.29.501974
Legendre, P., 1993. Spatial Autocorrelation: Trouble or New Paradigm? Ecology 74, 1659-1673. https://doi.org/10.2307/1939924
Legendre, P., Dale, M.R.T., Fortin, M.-J., Gurevitch, J., Hohn, M., Myers, D., 2002. The consequences of spatial structure for the design and analysis of ecological field surveys. Ecography 25, 601-615. https://doi.org/10.1034/j.1600-0587.2002.250508.x
Legendre, P., Fortin, M.J., 1989. Spatial pattern and ecological analysis. Vegetatio 80, 107-138. https://doi.org/10.1007/BF00048036
Legendre, P., Legendre, L., 2012. Numerical Ecology, Third Edition ed. Elsevier, The Netherlands.
McDonald, T., 2012. Spatial sampling designs for long-term ecological monitoring, in: Cooper, A.B., Gitzen, R.A., Licht, D.S., Millspaugh, J.J. (Eds.), Design and Analysis of Long-term Ecological Monitoring Studies. Cambridge University Press, Cambridge, pp. 101-125.
McGill, B.J., 2010. Matters of Scale. Science 328, 575-576. https://doi.org/10.1126/science.1188528
McGill, B.J., 2011. Linking biodiversity patterns by autocorrelated random sampling. American Journal of Botany 98, 481-502. https://doi.org/10.3732/ajb.1000509
Rahbek, C., 2005. The role of spatial scale and the perception of large-scale species-richness patterns. Ecology Letters 8, 224-239. https://doi.org/10.1111/j.1461-0248.2004.00701.x
Steel, E.A., Kennedy, M.C., Cunningham, P.G., Stanovick, J.S., 2013. Applied statistics in ecology: common pitfalls and simple solutions. Ecosphere 4, art115. https://doi.org/10.1890/ES13-00160.1
Tobler, W.R., 1970. A Computer Movie Simulating Urban Growth in the Detroit Region. Economic Geography 46, 234-240. https://doi.org/10.2307/143141
Wang, S., Lamy, T., Hallett, L.M., Loreau, M., 2019. Stability and synchrony across ecological hierarchies in heterogeneous metacommunities: linking theory to data. Ecography 42, 1200-1211. https://doi.org/10.1111/ecog.04290
Wiens, J.A., 1989. The ecology of bird communities. Cambridge University Press.
| Efficient sampling designs to assess biodiversity spatial autocorrelation : should we go fractal? | Fabien Laroche | <p>Quantifying the autocorrelation range of species distribution in space is necessary for applied ecological questions, like implementing protected area networks or monitoring programs. However, the power of spatial sampling designs to estimate t... | Biodiversity, Landscape ecology, Spatial ecology, Metacommunities & Metapopulations, Statistical ecology | Eric Goberville | 2023-04-21 10:54:29 | View | ||
10 Oct 2024
Large-scale spatio-temporal variation in vital rates and population dynamics of an alpine birdChloé R. Nater, Francesco Frassinelli, James A. Martin, Erlend B. Nilsen https://doi.org/10.32942/X2VP6JDo look up: building a comprehensive view of population dynamics from small scale observation through citizen scienceRecommended by Aidan Jonathan Mark Hewison based on reviews by Todd Arnold and 1 anonymous reviewerPopulation ecologists are in the business of decrypting the drivers of variation in the abundance of organisms across space and time (Begon et al. 1986). Comprehensive studies of wild vertebrate populations which provide the necessary information on variations in vital rates in relation to environmental conditions to construct informative models of large-scale population dynamics are rare, ostensibly because of the huge effort required to monitor individuals across ecological contexts and over generations. In this current aim, Nater et al. (2024) are leading the way forward by combining distance sampling data collected through a large-scale citizen science (Fraisl et al. 2022) programme in Norway with state-of-the-art modelling approaches to build a comprehensive overview of the population dynamics of willow ptarmigan. Their work enhances our fundamental understanding of this system and provides evidence-based tools to improve its management (Williams et al. 2002). Even better, they are working for the common good, by providing an open-source workflow that should enable ecologists and managers together to predict what will happen to their favourite model organism when the planet throws its next curve ball. In the case of the ptarmigan, for example, it seems that the impact of climate change on their population dynamics will differ across the species’ distributional range, with a slower pace of life (sensu Stearns 1983) at higher latitudes and altitudes. On a personal note, I have often mused whether citizen science, with its inherent limits and biases, was just another sticking plaster over the ever-deeper cuts in the research budgets to finance long-term ecological research. Here, Nater et al. are doing well to convince me that we would be foolish to ignore such opportunities, particularly when citizens are engaged, motivated, with an inherent capacity for the necessary discipline to employ common protocols in a standardised fashion. A key challenge for us professional ecologists is to inculcate the next generation of citizens with a sense of their opportunity to contribute to a better understanding of the natural world. References Begon, Michael, John L Harper, and Colin R Townsend. 1986. Ecology: individuals, populations and communities. Blackwell Science. Fraisl, Dilek, Gerid Hager, Baptiste Bedessem, Margaret Gold, Pen-Yuan Hsing, Finn Danielsen, Colleen B Hitchcock, et al. 2022. Citizen Science in Environmental and Ecological Sciences. Nature Reviews Methods Primers 2 (1): 64. https://doi.org/10.1038/s43586-022-00144-4 Chloé R. Nater, Francesco Frassinelli, James A. Martin, Erlend B. Nilsen (2024) Large-scale spatio-temporal variation in vital rates and population dynamics of an alpine bird. EcoEvoRxiv, ver.4 peer-reviewed and recommended by PCI Ecology https://doi.org/10.32942/X2VP6J Stearns, S.C. 1983. The influence of size and phylogeny of covariation among life-history traits in the mammals. Oikos, 41, 173–187. https://doi.org/10.2307/3544261 Williams, Byron K, James D Nichols, and Michael J Conroy. 2002. Analysis and Management of Animal Populations. Academic Press. | Large-scale spatio-temporal variation in vital rates and population dynamics of an alpine bird | Chloé R. Nater, Francesco Frassinelli, James A. Martin, Erlend B. Nilsen | <p>Quantifying temporal and spatial variation in animal population size and demography is a central theme in ecological research and important for directing management and policy. However, this requires field sampling at large spatial extents and ... | Biodiversity, Biogeography, Conservation biology, Demography, Euring Conference, Landscape ecology, Life history, Population ecology, Spatial ecology, Metacommunities & Metapopulations, Statistical ecology, Terrestrial ecology | Aidan Jonathan Mark Hewison | 2024-02-02 08:54:06 | View | ||
14 Dec 2018
Recommendations to address uncertainties in environmental risk assessment using toxicokinetics-toxicodynamics modelsVirgile Baudrot and Sandrine Charles https://doi.org/10.1101/356469Addressing uncertainty in Environmental Risk Assessment using mechanistic toxicological models coupled with Bayesian inferenceRecommended by Luis Schiesari based on reviews by Andreas Focks and 2 anonymous reviewersEnvironmental Risk Assessment (ERA) is a strategic conceptual framework to characterize the nature and magnitude of risks, to humans and biodiversity, of the release of chemical contaminants in the environment. Several measures have been suggested to enhance the science and application of ERA, including the identification and acknowledgment of uncertainties that potentially influence the outcome of risk assessments, and the appropriate consideration of temporal scale and its linkage to assessment endpoints [1]. References [1] Dale, V. H., Biddinger, G. R., Newman, M. C., Oris, J. T., Suter, G. W., Thompson, T., ... & Chapman, P. M. (2008). Enhancing the ecological risk assessment process. Integrated environmental assessment and management, 4(3), 306-313. doi: 10.1897/IEAM_2007-066.1 | Recommendations to address uncertainties in environmental risk assessment using toxicokinetics-toxicodynamics models | Virgile Baudrot and Sandrine Charles | <p>Providing reliable environmental quality standards (EQS) is a challenging issue for environmental risk assessment (ERA). These EQS are derived from toxicity endpoints estimated from dose-response models to identify and characterize the environm... | Chemical ecology, Ecotoxicology, Experimental ecology, Statistical ecology | Luis Schiesari | 2018-06-27 21:33:30 | View | ||
05 Apr 2019
Using a large-scale biodiversity monitoring dataset to test the effectiveness of protected areas at conserving North-American breeding birdsVictor Cazalis, Soumaya Belghali, Ana S.L. Rodrigues https://doi.org/10.1101/433037Protected Areas effects on biodiversity: a test using bird data that hopefully will give ideas for much more studies to comeRecommended by Paul Caplat based on reviews by Willson Gaul and 1 anonymous reviewerIn the face of worldwide declines in biodiversity, evaluating the effectiveness of conservation practices is an absolute necessity. Protected Areas (PA) are a key tool for conservation, and the question “Are PA effective” has been on many a research agenda, as the introduction to this preprint will no doubt convince you. A challenge we face is that, until now, few studies have been explicitly designed to evaluate PA, and despite the rise of meta-analyses on the topic, our capacity to quantify their effect on biodiversity remains limited. References [1] Cazalis, V., Belghali, S., & Rodrigues, A. S. (2019). Using a large-scale biodiversity monitoring dataset to test the effectiveness of protected areas at conserving North-American breeding birds. bioRxiv, 433037, ver. 4 peer-reviewed and recommended by PCI Ecology. doi: 10.1101/433037 | Using a large-scale biodiversity monitoring dataset to test the effectiveness of protected areas at conserving North-American breeding birds | Victor Cazalis, Soumaya Belghali, Ana S.L. Rodrigues | <p>Protected areas currently cover about 15% of the global land area, and constitute one of the main tools in biodiversity conservation. Quantifying their effectiveness at protecting species from local decline or extinction involves comparing prot... | Biodiversity, Conservation biology, Human impact, Landscape ecology, Macroecology | Paul Caplat | 2018-10-04 08:43:34 | View | ||
03 Apr 2020
A macro-ecological approach to predators' functional responseMatthieu Barbier, Laurie Wojcik, Michel Loreau https://doi.org/10.1101/832220A meta-analysis to infer generic predator functional responseRecommended by Samir Simon Suweis based on reviews by Ludek Berec and gyorgy barabasSpecies interactions are classically derived from the law of mass action: the probability that, for example, a predation event occurs is proportional to the product of the density of the prey and predator species. In order to describe how predator and prey species populations grow, is then necessary to introduce functional response, describing the intake rate of a consumer as a function of food (e.g. prey) density. References [1] Volterra, V. (1928). Variations and Fluctuations of the Number of Individuals in Animal Species living together. ICES Journal of Marine Science, 3(1), 3–51. doi: 10.1093/icesjms/3.1.3 | A macro-ecological approach to predators' functional response | Matthieu Barbier, Laurie Wojcik, Michel Loreau | <p>Predation often deviates from the law of mass action: many micro- and meso-scale experiments have shown that consumption saturates with resource abundance, and decreases due to interference between consumers. But does this observation hold at m... | Community ecology, Food webs, Meta-analyses, Theoretical ecology | Samir Simon Suweis | 2019-11-08 15:42:16 | View | ||
15 Feb 2024
Sources of confusion in global biodiversity trendsMaelys Boennec, Vasilis Dakos, Vincent Devictor https://doi.org/10.32942/X29W3HUnraveling the Complexity of Global Biodiversity Dynamics: Insights and ImperativesRecommended by Paulo Borges based on reviews by Pedro Cardoso and 1 anonymous reviewerBiodiversity loss is occurring at an alarming rate across terrestrial and marine ecosystems, driven by various processes that degrade habitats and threaten species with extinction. Despite the urgency of this issue, empirical studies present a mixed picture, with some indicating declining trends while others show more complex patterns. In a recent effort to better understand global biodiversity dynamics, Boennec et al. (2024) conducted a comprehensive literature review examining temporal trends in biodiversity. Their analysis reveals that reviews and meta-analyses, coupled with the use of global indicators, tend to report declining trends more frequently. Additionally, the study underscores a critical gap in research: the scarcity of investigations into the combined impact of multiple pressures on biodiversity at a global scale. This lack of understanding complicates efforts to identify the root causes of biodiversity changes and develop effective conservation strategies. This study serves as a crucial reminder of the pressing need for long-term biodiversity monitoring and large-scale conservation studies. By filling these gaps in knowledge, researchers can provide policymakers and conservation practitioners with the insights necessary to mitigate biodiversity loss and safeguard ecosystems for future generations. References Boennec, M., Dakos, V. & Devictor, V. (2023). Sources of confusion in global biodiversity trend. bioRxiv, ver. 4 peer-reviewed and recommended by Peer Community in Ecology. https://doi.org/10.32942/X29W3H
| Sources of confusion in global biodiversity trends | Maelys Boennec, Vasilis Dakos, Vincent Devictor | <p>Populations and ecological communities are changing worldwide, and empirical studies exhibit a mixture of either declining or mixed trends. Confusion in global biodiversity trends thus remains while assessing such changes is of major social, po... | Biodiversity, Conservation biology, Meta-analyses | Paulo Borges | 2023-09-20 11:10:25 | View | ||
11 May 2020
Interplay between historical and current features of the cityscape in shaping the genetic structure of the house mouse (Mus musculus domesticus) in Dakar (Senegal, West Africa)Claire Stragier, Sylvain Piry, Anne Loiseau, Mamadou Kane, Aliou Sow, Youssoupha Niang, Mamoudou Diallo, Arame Ndiaye, Philippe Gauthier, Marion Borderon, Laurent Granjon, Carine Brouat, Karine Berthier https://doi.org/10.1101/557066Urban past predicts contemporary genetic structure in city ratsRecommended by Michelle DiLeo based on reviews by Torsti Schulz, ? and 1 anonymous reviewerUrban areas are expanding worldwide, and have become a dominant part of the landscape for many species. Urbanization can fragment pre-existing populations of vulnerable species leading to population declines and the loss of connectivity. On the other hand, expansion of urban areas can also facilitate the spread of human commensals including pests. Knowledge of the features of cityscapes that facilitate gene flow and maintain diversity of pests is thus key to their management and eradication. References [1] Rivkin, L. R., Santangelo, J. S., Alberti, M. et al. (2019). A roadmap for urban evolutionary ecology. Evolutionary Applications, 12(3), 384-398. doi: 10.1111/eva.12734 | Interplay between historical and current features of the cityscape in shaping the genetic structure of the house mouse (Mus musculus domesticus) in Dakar (Senegal, West Africa) | Claire Stragier, Sylvain Piry, Anne Loiseau, Mamadou Kane, Aliou Sow, Youssoupha Niang, Mamoudou Diallo, Arame Ndiaye, Philippe Gauthier, Marion Borderon, Laurent Granjon, Carine Brouat, Karine Berthier | <p>Population genetic approaches may be used to investigate dispersal patterns of species living in highly urbanized environment in order to improve management strategies for biodiversity conservation or pest control. However, in such environment,... | Biological invasions, Landscape ecology, Molecular ecology | Michelle DiLeo | 2019-02-22 08:36:13 | View | ||
30 Mar 2020
Environmental variables determining the distribution of an avian parasite: the case of the Philornis torquans complex (Diptera: Muscidae) in South AmericaPablo F. Cuervo, Alejandro Percara, Lucas Monje, Pablo M. Beldomenico, Martín A. Quiroga https://doi.org/10.1101/839589Catching the fly in dystopian timesRecommended by Rodrigo Medel based on reviews by 4 anonymous reviewersHost-parasite interactions are ubiquitous on Earth. They are present in almost every conceivable ecosystem and often result from a long history of antagonist coevolution [1,2]. Recent studies on climate change have revealed, however, that modification of abiotic variables are often accompanied by shifts in the distributional range of parasites to habitats far beyond their original geographical distribution, creating new interactions in novel habitats with unpredictable consequences for host community structure and organization [3,4]. This situation may be especially critical for endangered host species having small population abundance and restricted distribution range. The infestation of bird species with larvae of the muscid fly genus Philornis is a case in point. At least 250 bird species inhabiting mostly Central and South America are infected by Philornis flies [5,6]. Fly larval development occurs in bird faeces, nesting material, or inside nestlings, affecting the development and nestling survival. References [1] Thompson JN (1994) The Coevolutionary Process. University of Chicago Press. | Environmental variables determining the distribution of an avian parasite: the case of the Philornis torquans complex (Diptera: Muscidae) in South America | Pablo F. Cuervo, Alejandro Percara, Lucas Monje, Pablo M. Beldomenico, Martín A. Quiroga | <p>*Philornis* flies are the major cause of myasis in altricial nestlings of neotropical birds. Its impact ranges from subtle to lethal, being of major concern in endangered bird species with geographically-restricted, fragmented and small-sized p... | Biogeography, Macroecology, Parasitology, Species distributions | Rodrigo Medel | 2019-11-26 21:31:33 | View | ||
13 Jul 2023
Parasites make hosts more profitable but less available to predatorsLoïc Prosnier, Nicolas Loeuille, Florence D. Hulot, David Renault, Christophe Piscart, Baptiste Bicocchi, Muriel Deparis, Matthieu Lam, Vincent Médoc https://doi.org/10.1101/2022.02.08.479552Indirect effects of parasitism include increased profitability of prey to optimal foragersRecommended by Luis Schiesari based on reviews by Thierry DE MEEUS and Eglantine Mathieu-BégnéEven though all living organisms are, at the same time, involved in host-parasite interactions and embedded in complex food webs, the indirect effects of parasitism are only beginning to be unveiled. Prosnier et al. investigated the direct and indirect effects of parasitism making use of a very interesting biological system comprising the freshwater zooplankton Daphnia magna and its highly specific parasite, the iridovirus DIV-1 (Daphnia-iridescent virus 1). Daphnia are typically semitransparent, but once infected develop a white phenotype with a characteristic iridescent shine due to the enlargement of white fat cells. In a combination of infection trials and comparison of white and non-white phenotypes collected in natural ponds, the authors demonstrated increased mortality and reduced lifetime fitness in infected Daphnia. Furthermore, white phenotypes had lower mobility, increased reflectance, larger body sizes and higher protein content than non-white phenotypes. As a consequence, total energy content was effectively doubled in white Daphnia when compared to non-white broodless Daphnia. Next the authors conducted foraging trials with Daphnia predators Notonecta (the backswimmer) and Phoxinus (the European minnow). Focusing on Notonecta, unchanged search time and increased handling time were more than compensated by the increased energy content of white Daphnia. White Daphnia were 24% more profitable and consistently preferred by Notonecta, as the optimal foraging theory would predict. The authors argue that menu decisions of optimal foragers in the field might be different, however, as the prevalence – and therefore availability - of white phenotypes in natural populations is very low. The study therefore contributes to our understanding of the trophic context of parasitism. One shortcoming of the study is that the authors rely exclusively on phenotypic signs for determining infection. On their side, DIV-1 is currently known to be highly specific to Daphnia, their study site is well within DIV-1 distributional range, and the symptoms of infection are very conspicuous. Furthermore, the infection trial – in which non-white Daphnia were exposed to white Daphnia homogenates - effectively caused several lethal and sublethal effects associated with DIV-1 infection, including iridescence. However, the infection trial also demonstrated that part of the exposed individuals developed intermediate traits while still keeping the non-white, non-iridescent phenotype. Thus, there may be more subtleties to the association of DIV-1 infection of Daphnia with ecological and evolutionary consequences, such as costs to resistance or covert infection, that the authors acknowledge, and that would be benefitted by coupling experimental and observational studies with the determination of actual infection and viral loads. References Prosnier L., N. Loeuille, F.D. Hulot, D. Renault, C. Piscart, B. Bicocchi, M, Deparis, M. Lam, & V. Médoc. (2023). Parasites make hosts more profitable but less available to predators. BioRxiv, ver. 4 peer-reviewed and recommended by Peer Community in Ecology. https://doi.org/10.1101/2022.02.08.479552 | Parasites make hosts more profitable but less available to predators | Loïc Prosnier, Nicolas Loeuille, Florence D. Hulot, David Renault, Christophe Piscart, Baptiste Bicocchi, Muriel Deparis, Matthieu Lam, Vincent Médoc | <p>Parasites are omnipresent, and their eco-evolutionary significance has aroused much interest from scientists. Parasites may affect their hosts in many ways by altering host density, vulnerability to predation, and energy content, thus modifying... | Community ecology, Eco-evolutionary dynamics, Epidemiology, Experimental ecology, Food webs, Foraging, Freshwater ecology, Host-parasite interactions, Life history, Parasitology, Statistical ecology | Luis Schiesari | 2022-05-20 10:15:41 | View |
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