Coral reefs in the Florida Keys are severely degraded with a reported 38% loss between 1996 and 2000, yet the causes of these devastating declines remain largely unknown. Our long-term studies in the Upper Keys and Biscayne National Park indicate acute stress events affecting physiological condition in species representing different trophic levels in the reef community, one of which was white grunt (Haemulon plumieri; Lacepede, 1801). We initiated a preliminary investigation describing cellular physiological stress effects and the possible causes of these stress events using cellular diagnostic profiling coupled with a cursory body-load contaminant chemistry analysis. The cellular biomarker profiles from fish taken from Alina's Reef indicated a toxic response profile that was suggestive of a suicide reaction of the cytochrome P450 2-class as a result of an interaction with a xenobiotic that adversely affects heme metabolism. Elevated levels of damaged porphyrin products were also found in fish from Alina's Reef. Liver loads of anthropogenic contaminants ( e. g., pesticides, PCBs) were measured and provided further evidence for possible causative agents. Evaluation and synthesis of each type of data were used to establish a biological effect, develop a mechanism of pathogenicity, and build a profile for possible causative agent(s).
Coral reefs within the Florida Keys are disappearing at an alarming rate. Coral cover in the Florida Keys National Marine Sanctuary declined by 38% from 1996 to 2000. In 2000, populations of Montastraea annularis at four sites near Molasses Reef within the Florida Keys National Marine Sanctuary and one reef within Biscayne National Park were sampled on a quarterly basis. Anecdotal observations showed corals at Alina’s Reef in Biscayne National Park appeared healthy in March, but experienced an acute loss of coral cover by August. Cellular Diagnostic analysis indicated that Alina’s Reef corals were in distress: they had been afflicted with a severe oxidative damaging and protein-denaturing stress that affected both the corals and their symbiotic zooxanthellae. This condition was associated with a significant xenobiotic detoxification response in both species, reflecting probable chemical contaminant exposure. These results demonstrate that applying a Cellular Diagnostic approach can be effective in helping to identify stress and its underlying causes, providing diagnostic and prognostic biomarkers of coral health.
Size-specific interactions between predators can affect both species population dynamics and the structure and biodiversity of communities they inhabit. Interactions between size-structured populations of predators, especially those with complex life-cycles, often change with resource-use changes driven by ontogenetic niche shifts. However, if resource use is determined largely by prey size, generalist predators may compete across a wider range of body sizes and life stages resulting in diffuse intra- and interspecific competition. We examined size- and stage-specific interactions between juvenile sirens (Siren i. intermedia) and adult newts (Notophthalmus viridescens dorsalis) in the context of previous experiments demonstrating competitive equality of larvae and strong effects of adult S. intermedia on adult N. viridescens. Competition between juvenile siren and adult newts was mutually negative and roughly symmetrical. Two S. intermedia reduced growth of three N. viridescens by 21%, while three N. viridescens reduced growth of two S. intermedia by 29%. Together with previous work, this implicates diffuse competition as a critical feature in the ecology of these species across the range of body sizes and suggests that intensity of competition varies more with size than species identity. Competition that varies incrementally with body size expands the realm of possibilities for continuous niche changes and diffuse competition across large size gradients. For generalist predators such as S. intermedia and N. viridescens, body size, except at the extremes, is not an adequate niche difference either intra- or interspecifically.
Conservation BiologyVolume 18, Issue 4 p. 1156-1159 Fire as Friend and Foe of Amphibians: a Reply JAMIE M. SCHURBON, JAMIE M. SCHURBON Anoka Conservation District, 16015 Central Ave NE, Suite 103, Ham Lake, MN 55304–5618, U.S.A.Search for more papers by this authorJOHN E. FAUTH, Corresponding Author JOHN E. FAUTH Department of Biology, University of Central Florida, 4000 Central Florida Boulevard, Orlando, FL 32816–2368, U.S.A., email [email protected]‡Address correspondence to J. E. Fauth.Search for more papers by this author JAMIE M. SCHURBON, JAMIE M. SCHURBON Anoka Conservation District, 16015 Central Ave NE, Suite 103, Ham Lake, MN 55304–5618, U.S.A.Search for more papers by this authorJOHN E. FAUTH, Corresponding Author JOHN E. FAUTH Department of Biology, University of Central Florida, 4000 Central Florida Boulevard, Orlando, FL 32816–2368, U.S.A., email [email protected]‡Address correspondence to J. E. Fauth.Search for more papers by this author First published: 23 July 2004 https://doi.org/10.1111/j.1523-1739.2004.00215.xCitations: 9Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat Literature Cited Brennan, L. A., R. T. Engstrom, W. E. Palmer, S. M. Hermann, G. A. Hurst, L. W. Burger, and C. L. Hardy. 1998. Whither wildlife without fire Transactions of the North American Wildlife and Natural Resources Conference 63 : 402–414. Web of Science®Google Scholar Chapin, F. S., III, E. S. Zavaleta, V. T. Eviners, R. L. Naylor, P. M. Vitousek, H. L. Reynolds, D. U. Hooper, S. Lavorel, O. E. Sala, S. E. Hobbie, M. C. Mack, and S. Diaz. 2000. Consequences of changing biodiversity. Nature 405 : 234–242. 10.1038/35012241 CASPubMedWeb of Science®Google Scholar Connell, J. H. 1978. Diversity in tropical rain forests and coral reefs. Science 199 : 1302–1310. 10.1126/science.199.4335.1302 CASPubMedWeb of Science®Google Scholar Conner, R. N., D. C. Rudolph, and J. R. Walters. 2001. The Red-Cockaded Woodpecker: surviving in a fire-maintained ecosystem. University of Texas Press, Austin . 10.7560/712348 Google Scholar Eason, G. E., Jr., and J. E. Fauth. 2001. Ecological correlates of anuran diversity in temporary ponds: a field study in South Carolina, USA. Israel Journal of Zoology 47 : 347–365. 10.1560/4GQM-E0MV-NRCX-EP4A Web of Science®Google Scholar Fauth, J. E. 1999. Identifying potential keystone species from field data: an example from temporary ponds. Ecology Letters 2 : 36–43. 10.1046/j.1461-0248.1999.21046.x Web of Science®Google Scholar Frost, C. C. 1995. Presettlement fire regimes in southeastern marshes, peatlands, and swamps. Pages 39–60 in S. Cerulean and R. Engstrom, editors. Proceedings of the 19th Tall Timbers fire ecology conference. Tall Timbers Research Station , Tallahassee , Florida . Google Scholar Hurlbert, S. H. 1971. The nonconcept of species diversity: a critique and alternative parameters. Ecology 52 : 577–586. 10.2307/1934145 PubMedWeb of Science®Google Scholar Hurlbert, S. H. 1984. Pseudoreplication and the design of ecological field experiments. Ecological Monographs 54 : 187–211. 10.2307/1942661 Web of Science®Google Scholar Means, D. B., C. K. Dodd, Jr., S. A. Johnson, and J. G. Palis. 2004. Amphibians and fire in longleaf pine ecosystems: response to Shurbon and Fauth. Conservation Biology 18 : 1149–1153. 10.1111/j.1523-1739.2004.00017.x Web of Science®Google Scholar Morin, P. J. 1995. Functional redundancy, non-additive interactions, and supply-side dynamics in experimental pond communities. Ecology 76 : 133–149. 10.2307/1940637 Web of Science®Google Scholar Mushinsky, H. R. 1985. Fire and the Florida sandhill herpetofaunal community. Herpetologica 41 : 333–342. Web of Science®Google Scholar Mushinsky, H. R. 1986. Fire, vegetation structure, and herpetofaunal communities. Pages 383–388 in Z. Rocek, editor. Studies in herpetology: proceedings of the 3rd European herpetological meeting, Charles University , Prague . Google Scholar Pilliod, D. S., R. B. Bury, E. J. Hyde, C. A. Pearl, and P. S. Corn. 2003. Fire and amphibians in North America. Forest Ecology and Management 178 : 163–181. 10.1016/S0378-1127(03)00060-4 Web of Science®Google Scholar Resetarits, W. J., Jr., and J. E. Fauth. 1998. From cattle tanks to Carolina bays: the utility of model systems for understanding natural communities. Pages 133–151 in : W. J. Resetarits and J. Bernardo, editors. Experimental ecology: issues and perspectives. Oxford University Press, New York . Google Scholar Robertson, K. M., and T. E. Ostertag. 2004. Problems with Shurbon and Fauth's test of effects of prescribed burning on amphibian diversity. Conservation Biology 18 : 1154–1155. 10.1111/j.1523-1739.2004.581_1.x Web of Science®Google Scholar Roxburgh, S. H., K. Shea, and J. B. Wilson. 2004. The intermediate disturbance hypothesis: patch dynamics and mechanisms of species coexistence. Ecology 85 : 359–371. 10.1890/03-0266 Web of Science®Google Scholar Schurbon, J. M. 2000. Effects of prescribed burning on amphibian diversity in the Francis Marion National Forest, South Carolina. M.S. thesis. University of Charleston , Charleston , South Carolina . Google Scholar Schurbon, J. M., and J. E. Fauth. 2003. Effects of prescribed burning on amphibian diversity in a southeastern U.S. national forest. Conservation Biology 17 : 1338–1349. 10.1046/j.1523-1739.2003.01514.x Web of Science®Google Scholar Streng, D. R., J. S. Glitzenstein, and W. J. Platt. 1993. Evaluating effects of season of burn in longleaf pine forests: a critical literature review and some results from an ongoing long-term study. Pages 227–263 in S. M. Hermann, editor. Proceedings of 18th Tall Timbers fire ecology conference. Tall Timbers Research Station , Tallahassee , Florida . Google Scholar Sokal, R. R., and F. J. Rohlf. 1995. Biometry. 3rd edition. H. Freeman, New York . 10.1577/1548-8659(1986)115<149:LOPDOR>2.0.CO;2 Google Scholar Citing Literature Volume18, Issue4August 2004Pages 1156-1159 ReferencesRelatedInformation
Abstract: Fire alters the abundance and diversity of many species, but its effects on amphibians are poorly known. We tested whether prescribed burning affected amphibian abundance and diversity within the Francis Marion National Forest, South Carolina, by monitoring assemblages at 15 temporary ponds with five different burn histories: 0, 1, 3, 5, and 12 years after burns. We also monitored terrestrial and aquatic environmental variables likely to influence amphibian diversity, such as leaf‐litter depth, pond water chemistry, and distance to neighboring ponds. Fire had significant negative effects. Immediate effects ( burning during the study ) explained 12.8% and 10.8% of the variation in anuran and amphibian abundance, respectively, whereas short‐term effects explained 31.8% and 24.6% of variation in amphibian species richness and evenness, respectively. Species richness increased and evenness decreased with time since burn, primarily because salamanders were rarely encountered at sites burned within 2 years. These sites had the shallowest leaf litter and highest soil temperature variances. Environmental factors unrelated to burning also significantly influenced amphibian diversity. Water chemistry explained 31.1% of variation in species richness, 32.2% of evenness, and>25% of anuran, salamander, and total amphibian abundances. Salamanders were most sensitive to water chemistry factors, particularly pH. Our results suggest that decreasing the frequency of prescribed burns from the current 2–3 years to 3–7 years will better maintain diverse amphibian and plant assemblages. Substituting growing‐season burns for the current practice of winter and spring burns would avoid repeatedly interrupting amphibian breeding and would maintain the desired longleaf pine community.
During the past two decades, coral reefs have experienced extensive degradation worldwide. One etiology for this global degradation is a syndrome known as coral bleaching. Mass coral bleaching events are correlated with increased sea-surface temperatures, however, the cellular mechanism underlying this phenomenon is uncertain. To determine if oxidative stress plays a mechanistic role in the process of sea-surface temperature-related coral bleaching, we examined corals along a depth transect in the Florida Keys over a single season that was characterized by unusually high sea-surface temperatures. We observed strong positive correlations between accumulation of oxidative damage products and bleaching in corals over a year of sampling. High levels of antioxidant enzymes and small heat-shock proteins were negatively correlated with levels of oxidative damage products. Corals that experienced oxidative stress had higher chaperonin levels and protein turnover activity. Our results indicate that coral bleaching is tightly coupled to the antioxidant and cellular stress capacity of the symbiotic coral, supporting the mechanistic model that coral bleaching (zooxanthellae loss) may be a final strategy to defend corals from oxidative stress.
The objective of this study was to determine the cellular physiological status of the bivalves Mya arenaria and Mytilus trossulus in an area experiencing a 10-yr chronic exposure of spilled Exxon Valdez crude oil in Prince William Sound Bivalves were collected from.,well-characterized oiled and unoiled sites. We used a novel biotechnology (Environmental Cellular Diagnostic S stem) to determine (i) if bivalves Were Physiologically stressed, (ii) the nature of the altered physiological state, and (iii) whether the bivalves were responding to an exposure of polyaromatic hydrocarbons (PAH). Molecular diagnostic analysis indicated that bivalve's at the oiled site were experiencing both oxidative and xenobiotic stress, resulting in increased. protein turnover and chaperone activity. Bivalves from the impacted area were responding specifically to a PAH-xenobiotic exposure and accumulating protein-PAH adducts. Finally, species-specific responses were observed that could be related to the habitat preferences of each species We conclude that bivalves inhabiting a site impacted by crude oil from. the 1989 Exxon Valdez spill showed clear indications,of cellular physiological stress.
Identifying the factors that limit species distributions and maintain patterns of diversity is a major goal of temporary pond ecologists, and an important pursuit for conservation biologists. We used multiple regression analysis to identify ecological correlates of anuran species richness in twenty-one temporary pools within the Francis Marion National Forest, South Carolina. Analysis of data collected in 1996-1997 revealed that anuran richness was limited by the multiplicative effects of pool acidity, hydroperiod, and fish species richness. Anuran species richness declined with decreasing pH and hydroperiod, and with colonization by more species-rich assemblages of predatory fish. Two species of frog (Hyla cinerea and Rana grylio) and a newt (Notophthalmus viridescens) were excluded from the most acidic pools, and three anurans (Bufo quercicus, Pseudacris ornata, and R. capito) were limited by fish. Two large-bodied frogs with tadpoles that overwinter prior to metamorphosis (R. catesbeiana and R. virgatipes) were restricted to pools with longer hydroperiods, and R. capito was more likely to breed in large than in small ponds. The results suggest that anuran richness at our study site is controlled by different factors than in similar ponds in North Carolina, where hydroperiod and the densities of tadpoles and two species of salamander were important, Identifying mechanisms likely to affect local anuran species richness allowed us to predict how subtle anthropogenic stresses could cause declines in amphibians to begin, in a region where few have been reported.
Using field sampling and experiments in natural and artificial ponds, I studied interactions between branchiate adult mole salamanders (Ambystoma talpoideum) and lesser sirens (Siren intermedia), two top predators in temporary ponds of the southeastern United States. The abundance and distribution of these two salamanders were independent among ponds, with A. talpoideum more numerous and widespread than S. intermedia. Both species were more likely to be found in ponds near other intermittent wetlands. Within a pond, captures of these two species were negatively correlated, and a field experiment showed that paedomorphic A. talpoideum avoided traps containing S. intermedia. An experiment in artificial ponds confirmed that interactions between these two species were highly asymmetrical; S. intermedia reduced the growth and recruitment of A. talpoideum without experiencing reciprocal. positive or negative effects. These results suggest that S. intermedia competes with and is an intraguild predator of A. talpoideum, limiting its growth and controlling its recruitment.
In salamanders, biting serves three potential purposes: subduing prey (e.g., Reilly and Lauder, 1990), repelling competitors and predators (e.g., Jaeger, 1981; Brodie et al., 1989), and stimulating the opposite sex during courtship (Arnold, 1977). In Siren intermedia, nonpredatory biting was first reported by Gehlbach and Walker (1970), who observed it while recording underwater vocalizations. Bitten individuals often fled
Previous articleNext article No AccessNotes and CommentsSimplifying the Jargon of Community Ecology: A Conceptual ApproachJ. E. Fauth, J. Bernardo, M. Camara, W. J. Resetarits, Jr., J. Van Buskirk, and S. A. McCollumJ. E. Fauth Search for more articles by this author , J. Bernardo Search for more articles by this author , M. Camara Search for more articles by this author , W. J. Resetarits, Jr. Search for more articles by this author , J. Van Buskirk Search for more articles by this author , and S. A. McCollum Search for more articles by this author PDFPDF PLUS Add to favoritesDownload CitationTrack CitationsPermissionsReprints Share onFacebookTwitterLinkedInRedditEmail SectionsMoreDetailsFiguresReferencesCited by The American Naturalist Volume 147, Number 2Feb., 1996 Published for The American Society of Naturalists Article DOIhttps://doi.org/10.1086/285850 Views: 242Total views on this site Citations: 250Citations are reported from Crossref Copyright 1996 The University of ChicagoPDF download Crossref reports the following articles citing this article:Anne Strack, Lukas Jonkers, Marina C. Rillo, Helmut Hillebrand, Michal Kucera Plankton response to global warming is characterized by non-uniform shifts in assemblage composition since the last ice age, Nature Ecology & Evolution 13 (Oct 2022).https://doi.org/10.1038/s41559-022-01888-8Andrés Felipe Suárez‐Castro, Martine Maron, Matthew G. E. Mitchell, Jonathan R. Rhodes Disentangling direct and indirect effects of landscape structure on urban bird richness and functional diversity, Ecological Applications 24 (Oct 2022).https://doi.org/10.1002/eap.2713Matthew P. Peters, Steve N. Matthews, Anantha M. Prasad, Louis R. Iverson Defining landscape-level forest types: application of latent Dirichlet allocation to species distribution models, Landscape Ecology 37, no.77 (Apr 2022): 1819–1837.https://doi.org/10.1007/s10980-022-01436-6Rafaela Bastos‐Pereira, Tássia Rayane Ferreira Chagas, Débora Reis de Carvalho, Ananza Mara Rabello, Wallace Beiroz, Karla Palmieri Tavares, Karen Cristina Braga Lima, Lucas Mendes Rabelo, Silvia Valenzuela, César M. A. Correa, Paulo Santos Pompeu, Carla Rodrigues Ribas Are the functional diversity terms functional? The hindrances of functional diversity understanding in the Brazilian scientific community, Ecological Research 37, no.44 (Apr 2022): 505–521.https://doi.org/10.1111/1440-1703.12306Lauren M. Gibson, K. C. Busch, Kathryn T. Stevenson, Bethany B. Cutts, Elizabeth A. DeMattia, Olivia M. Aguilar, Nicole M. Ardoin, Sarah J. Carrier, Charlotte R. Clark, Caren B. Cooper, Noah Weeth Feinstein, Jean Goodwin, M. Nils Peterson, Mele Wheaton What is community-level environmental literacy, and how can we measure it? A report of a convening to conceptualize and operationalize CLEL, Environmental Education Research 5 (May 2022): 1–29.https://doi.org/10.1080/13504622.2022.2067325Jörg Müller, Roland Brandl, Marc W. Cadotte, Christoph Heibl, Claus Bässler, Ingmar Weiß, Klaus Birkhofer, Simon Thorn, Sebastian Seibold A replicated study on the response of spider assemblages to regional and local processes, Ecological Monographs 334 (Apr 2022).https://doi.org/10.1002/ecm.1511Mateo D. M. Ruiz, José Luis Rangel Salazar Guild‐level response to Hurricane Carlotta among birds in a Mexican wetland, Ibis 164, no.22 (Dec 2021): 587–595.https://doi.org/10.1111/ibi.13028Antoine C. Dussault Does the study of facilitation require a revision of the Hutchinsonian niche concept?, Biology & Philosophy 37, no.22 (Apr 2022).https://doi.org/10.1007/s10539-022-09844-3Annette E. Evans, Marketa Zimova, Sean T. Giery, Heidi E. Golden, Amanda L. Pastore, Christopher P. Nadeau, Mark C. Urban An eco‐evolutionary perspective on the humpty‐dumpty effect and community restoration, Oikos 1982 (Mar 2022).https://doi.org/10.1111/oik.08978Zachery D. Zbinden A needle in the haystack? Applying species co‐occurrence frameworks with fish assemblage data to identify species associations and sharpen ecological hypotheses, Journal of Fish Biology 100, no.22 (Apr 2021): 339–351.https://doi.org/10.1111/jfb.14752Ángel Gálvez, Anne E. Magurran, Xavier Armengol, Sukonthip Savatenalinton, Francesc Mesquita-Joanes Metacommunity structure and dynamics, (Jan 2022): 549–586.https://doi.org/10.1016/B978-0-12-822362-8.00011-6Benoît Vincent What has become of our cenosis? For a renewed cenology, Plant Sociology 58, no.22 (Dec 2021): 29–40.https://doi.org/10.3897/pls2021582/03María L. Miranda-García, Andrés Muñoz-Pedreros, Heraldo V. Norambuena Waterbird assemblages of inland wetlands in Chile: A meta-analysis, Nature Conservation 45 (Dec 2021): 41–61.https://doi.org/10.3897/natureconservation.45.74062Manuel E. Lequerica Tamara, Tanya Latty, Caragh G. Threlfall, Dieter F. Hochuli Major insect groups show distinct responses to local and regional attributes of urban green spaces, Landscape and Urban Planning 216 (Dec 2021): 104238.https://doi.org/10.1016/j.landurbplan.2021.104238Patil Tawidian, Kerri L. Coon, Ari Jumpponen, Lee W. Cohnstaedt, Kristin Michel, Vincent B. Young Host-Environment Interplay Shapes Fungal Diversity in Mosquitoes, mSphere 6, no.55 (Oct 2021).https://doi.org/10.1128/mSphere.00646-21Galo Buitrón-Jurado, Virginia Sanz Specialization increases in a frugivorous bird–plant network from an isolated montane forest remnant, Community Ecology 22, no.33 (Apr 2020): 261–274.https://doi.org/10.1007/s42974-020-00010-xSébastien Descamps, Hallvard Strøm As the Arctic becomes boreal: ongoing shifts in a high‐Arctic seabird community, Ecology 75 (Aug 2021).https://doi.org/10.1002/ecy.3485Sonia Llorente-Culebras, Rafael Molina-Venegas, A. Márcia Barbosa, Silvia B. Carvalho, Miguel Á. Rodríguez, Ana M. C. Santos Iberian Protected Areas Capture Regional Functional, Phylogenetic and Taxonomic Diversity of Most Tetrapod Groups, Frontiers in Ecology and Evolution 9 (Jul 2021).https://doi.org/10.3389/fevo.2021.634653Analía L. Giménez, Guillermo H. Omad, Óscar De Paz, Norberto P. Giannini Diet and resource partitioning in Patagonian bats (Chiroptera: Vespertilionidae and Molossidae), Mammal Research 66, no.33 (Jun 2021): 467–480.https://doi.org/10.1007/s13364-021-00574-7José L. Reyes-Hernández, José L. Navarrete-Heredia Composition and Seasonality of Staphylinidae (Coleoptera) Collected with Carrion Traps in a Cloud Forest in Jalisco, Mexico, Proceedings of the Entomological Society of Washington 123, no.33 (Jul 2021).https://doi.org/10.4289/0013-8797.123.3.595Jonathan Syme, Jeremy J. Kiszka, Guido J. Parra Dynamics of Cetacean Mixed-Species Groups: A Review and Conceptual Framework for Assessing Their Functional Significance, Frontiers in Marine Science 8 (Jun 2021).https://doi.org/10.3389/fmars.2021.678173Qingqing Chen Evolutionary responses of a dominant plant along a successional gradient in a salt-marsh system, Plant Ecology 222, no.66 (Apr 2021): 681–691.https://doi.org/10.1007/s11258-021-01137-1Nerea Abrego, Tomas Roslin, Tea Huotari, Yinqiu Ji, Niels Martin Schmidt, Jiaxin Wang, Douglas W. Yu, Otso Ovaskainen Accounting for species interactions is necessary for predicting how arctic arthropod communities respond to climate change, Ecography 44, no.66 (Mar 2021): 885–896.https://doi.org/10.1111/ecog.05547Victor Moctezuma Spatial autocorrelation in a Mexican dung beetle ensemble: Implications for biodiversity assessment and monitoring, Ecological Indicators 125 (Jun 2021): 107548.https://doi.org/10.1016/j.ecolind.2021.107548Natalia B. Naumova, Tatiana Y. Alikina, Natalia S. Zolotova, Alexey V. Konev, Valentina I. Pleshakova, Nadezhda A. Lescheva, Marsel R. Kabilov Bacillus-Based Probiotic Treatment Modified Bacteriobiome Diversity in Duck Feces, Agriculture 11, no.55 (May 2021): 406.https://doi.org/10.3390/agriculture11050406Ina Falfán, Ian MacGregor-Fors Mismatching streetscapes: Woody plant composition across a Neotropical city, Urban Ecosystems 24, no.22 (Jul 2020): 265–274.https://doi.org/10.1007/s11252-020-01033-yMiriam Mariana Morales, Norberto Pedro Giannini Pleistocene extinction and geographic singularity explain differences in global felid ensemble structure, Evolutionary Ecology 35, no.22 (Feb 2021): 271–289.https://doi.org/10.1007/s10682-021-10103-2Natalia B. Naumova, Ivan P. Belanov, Tatiana Y. Alikina, Marsel R. Kabilov Undisturbed Soil Pedon under Birch Forest: Characterization of Microbiome in Genetic Horizons, Soil Systems 5, no.11 (Feb 2021): 14.https://doi.org/10.3390/soilsystems5010014Gilberto M. de M. Santos, Emanuelle L. S. Brito, Marcos Aragão Community Ecology of Social Wasps in Brazil: Forty Years of Studies, (Nov 2020): 373–394.https://doi.org/10.1007/978-3-030-53510-0_20Madina Kozhieva, Natalia Naumova, Tatiana Alikina, Alexey Boyko, Valentin Vlassov, Marsel R. Kabilov The Core of Gut Life: Firmicutes Profile in Patients with Relapsing-Remitting Multiple Sclerosis, Life 11, no.11 (Jan 2021): 55.https://doi.org/10.3390/life11010055Eliot Graeff, Nicolas Maranzana, Améziane Aoussat Biological Practices and Fields, Missing Pieces of the Biomimetics’ Methodological Puzzle, Biomimetics 5, no.44 (Nov 2020): 62.https://doi.org/10.3390/biomimetics5040062Emily Khazan, Jelena Bujan, Brett R. Scheffers Patterns of ant activity and nesting ecology depend on flooding intensity in a Neotropical floodplain, International Journal of Tropical Insect Science 40, no.44 (May 2020): 909–917.https://doi.org/10.1007/s42690-020-00149-0Scott D. Peacor, Brandon T. Barton, David L. Kimbro, Andrew Sih, Michael J Sheriff A framework and standardized terminology to facilitate the study of predation‐risk effects, Ecology 101, no.1212 (Oct 2020).https://doi.org/10.1002/ecy.3152Diego J. Elías, Caleb D. McMahan, Wilfredo A. Matamoros, Adan E. Gómez‐González, Kyle R. Piller, Prosanta Chakrabarty Scale(s) matter: Deconstructing an area of endemism for Middle American freshwater fishes, Journal of Biogeography 47, no.1111 (Aug 2020): 2483–2501.https://doi.org/10.1111/jbi.13941Yiping Niu, Guodong Ren, Giulia Lin, Letizia Di Biase, Simone Fattorini Fine-Scale Vegetation Characteristics Drive Insect Ensemble Structures in a Desert Ecosystem: The Tenebrionid Beetles (Coleoptera: Tenebrionidae) Inhabiting the Ulan Buh Desert (Inner Mongolia, China), Insects 11, no.77 (Jul 2020): 410.https://doi.org/10.3390/insects11070410Michelle H. Busch, Katie H. Costigan, Ken M. Fritz, Thibault Datry, Corey A. Krabbenhoft, John C. Hammond, Margaret Zimmer, Julian D. Olden, Ryan M. Burrows, Walter K. Dodds, Kate S. Boersma, Margaret Shanafield, Stephanie K. Kampf, Meryl C. Mims, Michael T. Bogan, Adam S. Ward, Mariana Perez Rocha, Sarah Godsey, George H. Allen, Joanna R. Blaszczak, C. Nathan Jones, Daniel C. Allen What’s in a Name? Patterns, Trends, and Suggestions for Defining Non-Perennial Rivers and Streams, Water 12, no.77 (Jul 2020): 1980.https://doi.org/10.3390/w12071980Owen S. Middleton, Jörn P. W. Scharlemann, Christopher J. Sandom Homogenization of carnivorous mammal ensembles caused by global range reductions of large-bodied hypercarnivores during the late Quaternary, Proceedings of the Royal Society B: Biological Sciences 287, no.19291929 (Jun 2020): 20200804.https://doi.org/10.1098/rspb.2020.0804Otso Ovaskainen, Nerea Abrego Joint Species Distribution Modelling, 14 (May 2020).https://doi.org/10.1017/9781108591720D Morales-de-Anda, AL Cupul-Magaña, FA Rodríguez-Zaragoza, C Aguilar-Betancourt, G González-Sansón, AP Rodríguez-Troncoso Reef fish functional composition and metrics reveal spatial differences in three protected islands in the Eastern Pacific, Marine Ecology Progress Series 635 (Feb 2020): 139–150.https://doi.org/10.3354/meps13186Cecilia De Dios Arcos, Maribel Badillo-Alemán, Daniel Arceo-Carranza, Xavier Chiappa-Carrara Feeding ecology of the waterbirds in a tropical mangrove in the southeast Gulf of Mexico, Studies on Neotropical Fauna and Environment 55, no.11 (Oct 2019): 1–9.https://doi.org/10.1080/01650521.2019.1682232DIEGO O. DI PIETRO, JORGE D. WILLIAMS, MARIO R. CABRERA, LEANDRO ALCALDE, RODRIGO CAJADE, FEDERICO P. KACOLIRIS Resource partitioning in a snake assemblage from east-central Argentina, Anais da Academia Brasileira de Ciências 92, no.22 (Jan 2020).https://doi.org/10.1590/0001-3765202020180766Natalia B. Naumova, Ivan P. Belanov, Tatiana Yu. Alikina Taxonomic diversity of bacterial assemblage in technosol of the revegetating fly ash dump, Почвы и окружающая среда 2, no.33 (Dec 2019).https://doi.org/10.31251/pos.v2i3.84Fereshteh Lagzi, Fatihcan M. Atay, Stefan Rotter Bifurcation analysis of the dynamics of interacting subnetworks of a spiking network, Scientific Reports 9, no.11 (Aug 2019).https://doi.org/10.1038/s41598-019-47190-9Natalia B. Naumova, Oleg A. Savenkov, Tatiana Y. Alikina, Marsel R. Kabilov Rhizosphere Bacteriobiome of the Husk Tomato Grown in the Open Field in West Siberia, Agriculture (Pol'nohospodárstvo) 65, no.44 (Dec 2019): 147–154.https://doi.org/10.2478/agri-2019-0015Pedro F Quintana-ascencio, Ian N Biazzo Ecological Terms Strongly Impact Research and its Implications, BioScience 69, no.1010 (Aug 2019): 769–770.https://doi.org/10.1093/biosci/biz099Phillip J. Oelbaum, M. Brock Fenton, Nancy B. Simmons, Hugh G. Broders Community structure of a Neotropical bat fauna as revealed by stable isotope analysis: Not all species fit neatly into predicted guilds, Biotropica 346 (Sep 2019).https://doi.org/10.1111/btp.12700Elizabeth S. Forbes, J. Hall Cushman, Deron E. Burkepile, Truman P. Young, Maggie Klope, Hillary S. Young, Alison Brody Synthesizing the effects of large, wild herbivore exclusion on ecosystem function, Functional Ecology 33, no.99 (Jun 2019): 1597–1610.https://doi.org/10.1111/1365-2435.13376Mateo D. M. Ruiz, Jorge L. León-Cortés, Paula L. Enríquez, Carlos García-Estrada, José Luis Rangel Salazar Habitat-Use Patterns among Migrant and Resident Landbirds of Contrasting Dietary Habits in a Southern Mexican Wetland, Ardeola 66, no.22 (Jul 2019): 291.https://doi.org/10.13157/arla.66.2.2019.ra3Rebecca de Araújo Fiore, José Barbosa dos Santos, Evander Alves Ferreira, Cássia Michelle Cabral, Marcelo Laia, Daniel Valadão Silva, Matheus de Freitas Souza Selection of arboreal species to compose and remedy riparian forests next to agricultural areas, Ecological Engineering 131 (Jun 2019): 9–15.https://doi.org/10.1016/j.ecoleng.2019.02.023H. John B. Birks Contributions of Quaternary botany to modern ecology and biogeography, Plant Ecology & Diversity 12, no.3-43-4 (Dec 2019): 189–385.https://doi.org/10.1080/17550874.2019.1646831N. L. McKenzie, R. D. Bullen, L. A. Gibson Habitat associations of zoophagic bat ensembles in north-western Australia, Australian Journal of Zoology 67, no.66 (Jan 2019): 243.https://doi.org/10.1071/ZO19049Juan Francisco Fuentes-Pérez, Mario Eckert, Jeffrey A. Tuhtan, Maria Teresa Ferreira, Maarja Kruusmaa, Paulo Branco Spatial preferences of Iberian barbel in a vertical slot fishway under variable hydrodynamic scenarios, Ecological Engineering 125 (Dec 2018): 131–142.https://doi.org/10.1016/j.ecoleng.2018.10.014Marguerite Tibbles, Martin D. Robards Critical trophic links in southern Chukchi Sea lagoons, Food Webs 17 (Dec 2018): e00099.https://doi.org/10.1016/j.fooweb.2018.e00099L. D. Mason, G. Wardell-Johnson, S. J. Luxton, P. W. Bateman Predators Show Seasonal Predilections for Model Clay Spiders in an Urban Environment, Scientific Reports 8, no.11 (Aug 2018).https://doi.org/10.1038/s41598-018-30778-yFranciele Parreira Peixoto, Pedro Henrique Pereira Braga, Poliana Mendes A synthesis of ecological and evolutionary determinants of bat diversity across spatial scales, BMC Ecology 18, no.11 (Jun 2018).https://doi.org/10.1186/s12898-018-0174-zConor Waldock, Maria Dornelas, Amanda E Bates Temperature-Driven Biodiversity Change: Disentangling Space and Time, BioScience 525 (Sep 2018).https://doi.org/10.1093/biosci/biy096Manuel Roeleke, Lilith Johannsen, Christian C. Voigt How Bats Escape the Competitive Exclusion Principle—Seasonal Shift From Intraspecific to Interspecific Competition Drives Space Use in a Bat Ensemble, Frontiers in Ecology and Evolution 6 (Jul 2018).https://doi.org/10.3389/fevo.2018.00101Brian J. Armitage, Steven C. Harris The Trichoptera of Panama IX. Preliminary comparison of caddisfly assemblages for two proximate watersheds in western Panama, Aquatic Insects 39, no.2-32-3 (Sep 2018): 275–295.https://doi.org/10.1080/01650424.2018.1481217Chiara Lelli, Juri Nascimbene, Alessandro Chiarucci Are available vegetation data suitable for assessing plant diversity? A study case in the Foreste Casentinesi National Park (Italy), Rendiconti Lincei. Scienze Fisiche e Naturali 29, no.22 (Mar 2018): 355–362.https://doi.org/10.1007/s12210-018-0681-zShobit Thapa, Radha Prasanna Prospecting the characteristics and significance of the phyllosphere microbiome, Annals of Microbiology 68, no.55 (Mar 2018): 229–245.https://doi.org/10.1007/s13213-018-1331-5C.M. Steinbeiser, C.A. Wawrzynowski, X. Ramos, Z.H. Olson Scavenging and the ecology of fear: do animal carcasses create islands of risk on the landscape?, Canadian Journal of Zoology 96, no.33 (Mar 2018): 229–236.https://doi.org/10.1139/cjz-2016-0268Anne E. Magurran, Amy E. Deacon, Faye Moyes, Hideyasu Shimadzu, Maria Dornelas, Dawn A. T. Phillip, Indar W. Ramnarine Divergent biodiversity change within ecosystems, Proceedings of the National Academy of Sciences 115, no.88 (Feb 2018): 1843–1847.https://doi.org/10.1073/pnas.1712594115Markus Arne Kjaer Sydenham, Katrine Eldegard, Stein Joar Hegland, Anders Nielsen, Ørjan Totland, Siri Fjellheim, Stein R. Moe Community level niche overlap and broad scale biogeographic patterns of bee communities are driven by phylogenetic history, Journal of Biogeography 45, no.22 (Nov 2017): 461–472.https://doi.org/10.1111/jbi.13103Jenna E. Dorey, James C. Lendemer, Robert F. C. Naczi Patterns of biodiverse, understudied groups do not mirror those of the surrogate groups that set conservation priorities: a case study from the Mid-Atlantic Coastal Plain of eastern North America, Biodiversity and Conservation 27, no.11 (Aug 2017): 31–51.https://doi.org/10.1007/s10531-017-1420-yMathieu Doray, Camille Hervy, Martin Huret, Pierre Petitgas , Progress in Oceanography 166 ( 2018): 88.https://doi.org/10.1016/j.pocean.2017.11.003Renan Maestri, Leandro Rabello Monteiro, Rodrigo Fornel, Thales Renato Ochotorena de Freitas, Bruce D. Patterson Geometric morphometrics meets metacommunity ecology: environment and lineage distribution affects spatial variation in shape, Ecography 41, no.11 (Aug 2017): 90–100.https://doi.org/10.1111/ecog.03001Fabiana Fedatto Bernardon, Carolina S. Mascarenhas, Joaber Pereira Jr, Gertrud Müller Host-Parasite relationships and co-infection of nasal mites of Chrysomus ruficapillus (Passeriformes: Icteridae) in southern Brazil, Iheringia. Série Zoologia 108, no.00 (Jun 2018).https://doi.org/10.1590/1678-4766e2018025Matthew T Milholland, Iván Castro-Arellano, Elizabeth Arellano, Elizabeth Nava-García, Guadalupe Rangel-Altamirano, Francisco X Gonzalez-Cozatl, Gerardo Suzán, Tony Schountz, Shiara González-Padrón, Ana Vigueras, André V Rubio, Troy J Maikis, Bradford J Westrich, Jose A Martinez, Maria D Esteve-Gassent, Madison Torres, Erick R Rodriguez-Ruiz, Dittmar Hahn, Thomas E Lacher Species Identity Supersedes the Dilution Effect Concerning Hantavirus Prevalence at Sites across Texas and México, ILAR Journal 58, no.33 (Apr 2018): 401–412.https://doi.org/10.1093/ilar/ily001David A. Steen, Kyle Barrett, Ellen Clarke, Craig Guyer Conceptualizing communities as natural entities: a philosophical argument with basic and applied implications, Biology & Philosophy 32, no.66 (Sep 2017): 1019–1034.https://doi.org/10.1007/s10539-017-9589-8Nenibarini Zabbey, Francis O. Arimoro Environmental forcing of intertidal benthic macrofauna of Bodo Creek, Nigeria: Preliminary index to evaluate cleanup of Ogoniland, Regional Studies in Marine Science 16 (Nov 2017): 89–97.https://doi.org/10.1016/j.rsma.2017.08.004Ken J. Wallace, Mark Jago Category mistakes: A barrier to effective environmental management, Journal of Environmental Management 199 (Sep 2017): 13–20.https://doi.org/10.1016/j.jenvman.2017.05.029Sanderson T. P. de Sousa, Lucélia Cabral, Gileno Vieira Lacerda Júnior, Valéria M. Oliveira Diversity of aromatic hydroxylating dioxygenase genes in mangrove microbiome and their biogeographic patterns across global sites, MicrobiologyOpen 6, no.44 (May 2017): e00490.https://doi.org/10.1002/mbo3.490Craig J. Plante Defining Disturbance for Microbial Ecology, Microbial Ecology 74, no.22 (Mar 2017): 259–263.https://doi.org/10.1007/s00248-017-0956-4Mariana Griotti, Christian Muñoz-Escobar, Nelson E. Ferretti Linking Vegetation Structure and Spider Diversity in Riparian and Adjacent Habitats in Two Rivers of Central Argentina: An Analysis at Two Conceptual Levels, Environmental Entomology 46, no.44 (May 2017): 794–803.https://doi.org/10.1093/ee/nvx094Nicholas J. Gotelli, Hideyasu Shimadzu, Maria Dornelas, Brian McGill, Faye Moyes, Anne E. Magurran Community-level regulation of temporal trends in biodiversity, Science Advances 3, no.77 (Jul 2017).https://doi.org/10.1126/sciadv.1700315David G. Jenkins, Simon Pierce, Hans Cornelissen General allometric scaling of net primary production agrees with plant adaptive strategy theory and has tipping points, Journal of Ecology 105, no.44 (Jan 2017): 1094–1104.https://doi.org/10.1111/1365-2745.12726Thomas W. Davies, Jonathan Bennie, Dave Cruse, Dan Blumgart, Richard Inger, Kevin J. Gaston Multiple night-time light-emitting diode lighting strategies impact grassland invertebrate assemblages, Global Change Biology 23, no.77 (Jan 2017): 2641–2648.https://doi.org/10.1111/gcb.13615Mark Sagoff On the Definition of Ecology, Biological Theory 12, no.22 (Apr 2017): 85–98.https://doi.org/10.1007/s13752-017-0263-9Cristian Kraker-Casta?eda, Antonio Santos-Moreno, Consuelo Lorenzo, Anna Horv?th, M. Cristina MacSwiney G., Dar?o Navarrete-Guti?rrez Responses of phyllostomid bats to forest cover in upland landscapes in Chiapas, southeast Mexico, Studies on Neotropical Fauna and Environment 52, no.22 (Mar 2017): 112–121.https://doi.org/10.1080/01650521.2017.1297559Ratha Sor, Pieter Boets, Ratha Chea, Peter L.M. Goethals, Sovan Lek Spatial organization of macroinvertebrate assemblages in the Lower Mekong Basin, Limnologica 64 (May 2017): 20–30.https://doi.org/10.1016/j.limno.2017.04.001Paulo Branco, Susana D. Amaral, Maria T. Ferreira, José M. Santos Do small barriers affect the movement of freshwater fish by increasing residency?, Science of The Total Environment 581-582 (Mar 2017): 486–494.https://doi.org/10.1016/j.scitotenv.2016.12.156Daniel Escoriza, Jihène Ben Hassine, Benedikt R. Schmidt Diversity of Guilds of Amphibian Larvae in North-Western Africa, PLOS ONE 12, no.11 (Jan 2017): e0170763.https://doi.org/10.1371/journal.pone.0170763F.X. Palacio, M. Valoy, F. Bernacki, M.S. Sánchez, M.G. Núñez-Montellano, O. Varela, M. Ordano Bird fruit consumption results from the interaction between fruit-handling behaviour and fruit crop size, Ethology Ecology & Evolution 29, no.11 (Sep 2015): 24–37.https://doi.org/10.1080/03949370.2015.1080195Ian MacGregor-Fors, Michelle García-Arroyo Who Is Who in the City? Bird Species Richness and Composition in Urban Latin America, (Nov 2017): 33–55.https://doi.org/10.1007/978-3-319-63475-3_3M. D’Amen, R.G. Mateo, A. Guisan Species Assemblages, Macroecology, and Global Change ☆, (Jan 2017).https://doi.org/10.1016/B978-0-12-809633-8.02351-7Sun-Joong Kim, Ji-Hyun Lee A study on metadata structure and recommenders of biological systems to support bio-inspired design, Engineering Applications of Artificial Intelligence 57 (Jan 2017): 16–37.https://doi.org/10.1016/j.engappai.2016.10.003Mariana Zarazúa-Carbajal, Luis Daniel Avila-Cabadilla, Mariana Yólotl Alvarez-Añorve, Julieta Benítez-Malvido, Kathryn E. Stoner Importance of riparian habitat for frugivorous bats in a tropical dry forest in western Mexico, Journal of Tropical Ecology 33, no.11 (Dec 2016): 74–82.https://doi.org/10.1017/S0266467416000572Robert S. Voss, David W. Fleck, Richard E. Strauss, Paúl M. Velazco, Nancy B. Simmons Roosting Ecology of Amazonian Bats: Evidence for Guild Structure in Hyperdiverse Mammalian Communities, American Museum Novitates 3870, no.38703870 (Dec 2016): 1–43.https://doi.org/10.1206/3870.1Gustavo Fonseca, Fabiane Gallucci The need of hypothesis-driven designs and conceptual models in impact assessment studies: An example from the free-living marine nematodes, Ecological Indicators 71 (Dec 2016): 79–86.https://doi.org/10.1016/j.ecolind.2016.06.051Virginia Capmourteres, Madhur Anand “Conservation value”: a review of the concept and its quantification, Ecosphere 7, no.1010 (Oct 2016).https://doi.org/10.1002/ecs2.1476A Bourg, F Escobar, I MacGregor-Fors, C E Moreno Got Dung? Resource Selection by Dung Beetles in Neotropical Forest Fragments and Cattle Pastures, Neotropical Entomology 45, no.55 (May 2016): 490–498.https://doi.org/10.1007/s13744-016-0397-7Brody Sandel, Anne-Christine Monnet, Maria Vorontsova, Zoltán Botta-Dukát Multidimensional structure of grass functional traits among species and assemblages, Journal of Vegetation Science 27, no.55 (Jun 2016): 1047–1060.https://doi.org/10.1111/jvs.12422David C. Deane, Damien A. Fordham, Fangliang He, Corey J. A. Bradshaw Diversity patterns of seasonal wetland plant communities mainly driven by rare terrestrial species, Biodiversity and Conservation 25, no.88 (May 2016): 1569–1585.https://doi.org/10.1007/s10531-016-1139-1S. Purusothaman, N. Jayaprabha, P. Murugesan Diversity and seasonal variation of fish assemblages associated with trawl catches from southeast coast of India, Regional Studies in Marine Science 6 (Jul 2016): 29–36.https://doi.org/10.1016/j.rsma.2016.03.012Neil M. Furey, Paul A. Racey Can wing morphology inform conservation priorities for Southeast Asian cave bats?, Biotropica 48, no.44 (Mar 2016): 545–556.https://doi.org/10.1111/btp.12322Juliano André Bogoni, Jorge José Cherem, Eduardo Luís Hettwer Giehl, Luiz Gustavo Oliveira-Santos, Pedro Volkmer de Castilho, Vilmar Picinatto Filho, Felipe Moreli Fantacini, Marcos Adriano Tortato, Micheli Ribeiro Luiz, Renato Rizzaro, Maurício Eduardo Graipel Landscape features lead to shifts in communities of medium- to large-bodied mammals in subtropical Atlantic Forest, Journal of Mammalogy 97, no.33 (Jan 2016): 713–725.https://doi.org/10.1093/jmammal/gyv215Matheus G. Reis, Carolline Z. Fieker, Manoel M. Dias The influence of fire on the assemblage structure of foraging birds in grasslands of the Serra da Canastra National Park, Brazil, Anais da Academia Brasileira de Ciências 88, no.22 (May 2016): 891–901.https://doi.org/10.1590/0001-3765201620150177D. Escoriza, A. Ruhí, David Green Functional distance to recipient communities may favour invasiveness: insights from two invasive frogs, Diversity and Distributions 22, no.55 (Jan 2016): 519–533.https://doi.org/10.1111/ddi.12421 Organisation at the community scale, (Feb 2016): 131–160.https://doi.org/10.1002/9781118905982.ch10Zachary H. Olson, James C. Beasley, Olin E. Rhodes, Antoni Margalida Carcass Type Affects Local Scavenger Guilds More than Habitat Connectivity, PLOS ONE 11, no.22 (Feb 2016): e0147798.https://doi.org/10.1371/journal.pone.0147798Brody Sandel, Constantinos Tsirogiannis Species introductions and the phylogenetic and functional structure of California's grasses, Ecology 97, no.22 (Mar 2016): 472–483.https://doi.org/10.1890/15-0220.1Markus A. K. Sydenham, Lise D. Häusler, Stein R. Moe, Katrine Eldegard Inter‐assemblage facilitation: the functional diversity of cavity‐producing beetles drives the size diversity of cavity‐nesting bees, Ecology and Evolution 6, no.22 (Jan 2016): 412–425.https://doi.org/10.1002/ece3.1871Kim A. Medley, Elizabeth H. Boughton, David G. Jenkins, John E. Fauth, Patrick J. Bohlen, Pedro F. Quintana-Ascencio Intense ranchland management tips the balance of regional and local factors affecting wetland community structure, Agriculture, Ecosystems & Environment 212 (Dec 2015): 207–244.https://doi.org/10.1016/j.agee.2015.06.024James T. Stroud, Michael R. Bush, Mark C. Ladd, Robert J. Nowicki, Andrew A. Shantz, Jennifer Sweatman Is a community still a community? Reviewing definitions of key terms in community ecology, Ecology and Evolution 5, no.2121 (Oct 2015): 4757–4765.https://doi.org/10.1002/ece3.1651Christopher M. Schalk, Carmen G. Montaña, Laura Springer Morphological diversity and community organization of desert anurans, Journal of Arid Environments 122 (Nov 2015): 132–140.https://doi.org/10.1016/j.jaridenv.2015.06.019Sandi Wong, W. Zac Stephens, Adam R. Burns, Keaton Stagaman, Lawrence A. David, Brendan J. M. Bohannan, Karen Guillemin, John F. Rawls, Ana Maldonado, Maria Gloria Dominguez Bello Ontogenetic Differences in Dietary Fat Influence Microbiota Assembly in the Zebrafish Gut, mBio 6, no.55 (Oct 2015).https://doi.org/10.1128/mBio.00687-15Julie Backus-Freer, Mark Pyron Concordance among fish and macroinvertebrate assemblages in streams of Indiana, USA, Hydrobiologia 758, no.11 (Apr 2015): 141–150.https://doi.org/10.1007/s10750-015-2281-6Ricardo Rocha, Tarmo Virtanen, Mar Cabeza Bird Assemblages in a Malagasy Forest-Agricultural Frontier: Effects of Habitat Structure and Forest Cover, Tropical Conservation Science 8, no.33 (Sep 2015): 681–710.https://doi.org/10.1177/194008291500800307Marco Aurelio Ribeiro Mello, Francisco Aparecido Rodrigues, Luciano da Fontoura Costa, W. Daniel Kissling, Çağan H. Şekercioğlu, Flavia Maria Darcie Marquitti, Elisabeth Klara Viktoria Kalko Keystone species in seed dispersal networks are mainly determined by dietary specialization, Oikos
Is the ability to function as a keystone predator a property of a species or an emergent property of the community? We discussed this question in a temporary—pond community where the broken—striped newt Notophthalmus viridescens dorsalis is known to act as a keystone predator on larval anurans. We independently manipulated the initial density of adult Notophthalmus (two or four) and the presence or absence of one adult Siren intermedia in a set of 20 artificial ponds to determine if this additional predator affected the ability of Notophthalmus to function as a keystone predator. Each pond received a diverse assemblage of larval anuran prey: a spring—breeding assemblage of 275 Rana utricularia, 100 Pseudacris crucifer and 25 Bufo americanus tadpoles, and a summer assemblage of 200 Hyla chrysoscelis and 150 Gastrophryne carolinensis tadpoles. Two additional pond received neither predator, to assay the outcome of competition among the tadpoles. The effect of the salamander Siren on Notophthalmus survival and fecundity depended on the density of Notophthalmus. At low newt density Siren had no effect on survival, but at high newt density competition reduced the survival and growth rates of Notophthalmus. The density of Notophthalmus and the presence of Siren interacted to determine the fecundity of Notophthalmus. At low newt density Siren reduced Notophthalmus reproductive success by preying on larvae. At high newt density Siren indirectly enhanced reproductive success by reducing survival of adults, thus releasing larvae from intraspecific competition and cannibalism. Notophthalmus density had no effect on adult Siren survival or growth rate in this experiment, but other evidence indicates that competition with Notophthalmus reduces the growth rates of Siren. Notophthalmus acted as a keystone predator on the assemblage of spring—breeding anurans; it increased the number of metamorphs of the weak competitor Pseudacris crucifer by releasing them from interspecific competition. Siren preyed on tadpoles in a nonselective manner. An additive model was sufficient to describe the effects of Siren and initial density of Notophthalmus on the structure of the tadpole assemblage. In our system of experimental ponds, the strong interaction between Siren and Notophthalmus density did not extend its effects to lower trophic levels, and the direct and indirect effects of Siren did not alter the role of Notophthalmus as a keystone predator.
The hypothesis that local isolated populations differed in the genetic basis for life-history traits was tested in the salamander Ambystoma talpoideum. Genetic basis was defined as the specific genetic architecture (additive and nonadditive) that contributes, along with maternal and environmental factors, to the phenotype. All crosses within and between three populations were made to produce nine F1 populations. Nine within-population crosses produced the F2 generation. This design does not permit an estimation of the exact nature of the genetic basis (e.g., additive, nonadditive) for any trait within populations. However, hybrid dissimilarity in the F2 generation was taken as evidence of a different genetic basis for a trait in each population. The genetic basis of life-history pathway (metamorphosis vs. paedomorphosis) and per capita fecundity differed between two populations. The genetic basis of life-history pathway, per capita fecundity, survival, and growth rate was similar between the remaining sets of populations. This study and related ones (Semlitsch and Wilbur, 1989; Semlitsch et al., 1990) suggest that a heterochronic shift that causes rapid morphological evolution between metamorphosis and paedomorphosis (a macroevolutionary pattern) can evolve independently and does not require a macromutation or other nonmicroevolutionary mechanisms.
We used a replicated field experiment to determine the relative intensity of intraspecific and interspecific competition between larvae of Siren intermedia and Notophthalmus viridescens. These two salamanders possess markedly different morphologies and life histories and belong to distantly related salamander families, but feed on similar prey. Each species was raised in artificial ponds, alone at either low density (3 larvae per pond, 1.95 m-2) or high density (6 larvae per pond, 3.90 m-2) or together in a 3:3 ratio for a combined density of 6 larvae per pond. These 5 treatments were each replicated 4 times in a total of 20 ponds. The experimental design allowed us to explicitly compare the relative intensities of intra- and interspecific competition under realistic conditions. Competition affected different components of fitness in each species. Both intraspecific and interspecific competition caused a decline in survival of Notophthalmus, but had no detectable effect on body size or length of larval period. Negative densitydependent mortality may regulate Notophthalmus populations in the larval stage of their complex life cycle. Intraspecific competition caused a decline in both the survival and growth of larval Siren, but interspecific competition caused only growth to decline. Decreased growth rates may increase the vulnerability of larval Siren to desiccation and to predation. We found no evidence to reject the null hypothesis that larvae of these two species are equal competitors at the densities we employed. Our results indicate that, despite dissimilarities in life history and morphology, and a distant phylogenetic relationship, larval Siren and larval Notophthalmus compete as equals. J.E. Fauth, W.J. Resetarits, Jr. and H.M. Wilbur, Dept of Zoology, Duke Univ., Durham, NC 27706, USA.
Ecologists need to determine the frequency and nature of higher order interactions and to predict when such interactions will be important to understand community dynamics. I experimentally tested for higher order interactions in a freshwater food web by independently manipulating the presence and absence of two predators (the salamander Notophthalmus viridescens and the crayfish Cambarus bartonii) and their tadpole prey (Hyla chrysoscelis) in a series of artificial ponds. By destructively sampling selected ponds early in the larval period (days 5 and 6), I hoped to predict whether the predators would have an interactive effect on tadpole survival and growth on day 30. Early destructive samples adequately predicted subsequent influences of interactions on the survival, but not on the size of Hyla. Early samples predicted that the predators would interact to determine tadpole survival and size. The two predators did not act additively to determine tadpole abundance: more survived in the presence of both predators than was predicted. This higher order interaction was most likely caused by physical interference between the predators and predator avoidance by the tadpoles. Early samples correctly predicted higher order interactions would be seen on tadpole growth, but completely failed to predict their direction because the biological interactions changed over time. Early in their larval period, tadpoles behaviorally avoided predators, which caused slower growth, but later, tadpoles in predator treatments grew faster due to diminished intraspecific competition. These results suggest that higher order interactions may be important in nature. Short—term experiments may prove useful in predicting when higher order interactions will occur, but detailed models may be required to predict their outcome accurately.
The abundance, species richness, and evenness of the Costa Rican leaf-litter herpetofauna was estimated during the late wet season of 1985 by quantitative sampling of replicate plots at ten sites encompassing an elevation range of 3 to 1670 m. Species richness was positively correlated with leaf-litter depth, and negatively correlated with elevation. Herpetofaunal density also tended to increase with litter depth and decline with elevation. A strong positive correlation existed between species richness and herpetofaunal density. Evenness was highly variable and independent of both leaf-litter depth and elevation. Analysis of a subset of the data, representing an elevational transect from Tortuguero to the Braulio Carrillo National Park Extension, yielded similar results. Tropical leaf-litter reptiles and amphibians appear to be both more diverse and more abundant at lower elevations. Sites with deep leaf litter generally sustain dense and diverse reptile and amphibian populations. Local herpetofaunas typically consist of a few very common species along with a large number of comparatively rare species. REPTILES AND AMPHIBIANS are a major constituent of the fauna inhabiting tropical forest litter. Studies of tropical leaf-litter herpetofaunas have emphasized patterns of abundance and distribution among geographic regions (Lloyd et al. 1968; Heyer & Berven 1973; Scott 1976, 1982; Inger 1980a, b; Heatwole 1982), vegetational zones (Brown & Alcala 1961, Heatwole & Sexton 1966, Heyer 1967), and elevational gradients (Brown & Alcala 1961, Scott 1976) as well as seasonal changes (Lieberman 1982, 1986). It has become generally accepted that leaf-litter reptiles and amphibians are more abundant in the New World Tropics than in Southeast Asia (Scott 1976, Inger 1980b, Duellman & Trueb 1986) although the exact reason remains a subject of debate (May 1980). Similarly, the general consensus is that the abundance of tropical leaf-litter herpetofaunas increases with increasing elevation, while species richness and equitability both decline (Brown & Alcala 1961, Scott 1976, Heatwole 1982, Duellman & Trueb 1986). Scott (1976) attributed this pattern to greater overall forest productivity at intermediate elevations, coupled with increased densities of the most common species at higher elevations. Before attempting to determine the mechanisms responsible for observed patterns of tropical leaf-litter herpetofaunal abundance and diversity, we must document the phenomenon conclusively. Previous quantitative studies have sampled few sites, have been unable to provide replicated samples (Brown & Alcala 1961), or may have confounded site and year effects by sampling different sites in different years (Scott 1976). We surveyed the Costa Rican leaf-litter herpetofauna by quantitatively sampling replicate plots at ten sites, ranging from 3 to 1670 m in elevation, during the late wet season of July-September 1985. Our sampling strategy permitted statistical analyses to determine the relationship between litter depth and elevation, and leaf-litter herpetofaunal richness, evenness and abundance. The results of our study contradict several of the generally accepted patterns of tropical leaf-litter herpetofaunal abundance and diversity.