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      Environmental and Host Effects on Skin Bacterial Community Composition in Panamanian Frogs

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          Abstract

          Research on the amphibian skin microbiota has focused on identifying bacterial taxa that deter a pathogenic chytrid fungus, and on describing patterns of microbiota variation. However, it remains unclear how environmental variation affects amphibian skin bacterial communities, and whether the overall functional diversity of the amphibian skin microbiota is associated to such variation. We sampled skin microbial communities from one dendrobatoid frog species across an environmental gradient along the Panama Canal, and from three dendrobatoid frog species before and after the onset of the wet season in one site. We found frog skin microbial alpha diversity to be highest in frogs from sites with low soil pH, but no clear effect of the onset of the wet season. However, we found frog skin microbial community structure to be affected by soil pH and the onset of the wet season, which also resulted in a decrease in between-sample variation. Across the sampled frog species, bacterial functional groups changed with the onset of the wet season, with certain bacterial functional groups entirely disappearing and others differing in their relative abundances. In particular, we found the proportion of Bd-inhibitory bacteria to correlate with mean soil pH, and to increase in two of the frog species with the onset of the wet season. Taken together, our results suggest that structure and predicted function of amphibian bacterial skin communities may be influenced by environmental variables such as pH and precipitation, site effects, and host effects.

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          The diversity and biogeography of soil bacterial communities.

          For centuries, biologists have studied patterns of plant and animal diversity at continental scales. Until recently, similar studies were impossible for microorganisms, arguably the most diverse and abundant group of organisms on Earth. Here, we present a continental-scale description of soil bacterial communities and the environmental factors influencing their biodiversity. We collected 98 soil samples from across North and South America and used a ribosomal DNA-fingerprinting method to compare bacterial community composition and diversity quantitatively across sites. Bacterial diversity was unrelated to site temperature, latitude, and other variables that typically predict plant and animal diversity, and community composition was largely independent of geographic distance. The diversity and richness of soil bacterial communities differed by ecosystem type, and these differences could largely be explained by soil pH (r(2) = 0.70 and r(2) = 0.58, respectively; P < 0.0001 in both cases). Bacterial diversity was highest in neutral soils and lower in acidic soils, with soils from the Peruvian Amazon the most acidic and least diverse in our study. Our results suggest that microbial biogeography is controlled primarily by edaphic variables and differs fundamentally from the biogeography of "macro" organisms.
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            Emerging infectious disease and the loss of biodiversity in a Neotropical amphibian community.

            Pathogens rarely cause extinctions of host species, and there are few examples of a pathogen changing species richness and diversity of an ecological community by causing local extinctions across a wide range of species. We report the link between the rapid appearance of a pathogenic chytrid fungus Batrachochytrium dendrobatidis in an amphibian community at El Copé, Panama, and subsequent mass mortality and loss of amphibian biodiversity across eight families of frogs and salamanders. We describe an outbreak of chytridiomycosis in Panama and argue that this infectious disease has played an important role in amphibian population declines. The high virulence and large number of potential hosts of this emerging infectious disease threaten global amphibian diversity.
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              Drought sensitivity shapes species distribution patterns in tropical forests.

              Although patterns of tree species distributions along environmental gradients have been amply documented in tropical forests, mechanisms causing these patterns are seldom known. Efforts to evaluate proposed mechanisms have been hampered by a lack of comparative data on species' reactions to relevant axes of environmental variation. Here we show that differential drought sensitivity shapes plant distributions in tropical forests at both regional and local scales. Our analyses are based on experimental field assessments of drought sensitivity of 48 species of trees and shrubs, and on their local and regional distributions within a network of 122 inventory sites spanning a rainfall gradient across the Isthmus of Panama. Our results suggest that niche differentiation with respect to soil water availability is a direct determinant of both local- and regional-scale distributions of tropical trees. Changes in soil moisture availability caused by global climate change and forest fragmentation are therefore likely to alter tropical species distributions, community composition and diversity.
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                Author and article information

                Contributors
                Journal
                Front Microbiol
                Front Microbiol
                Front. Microbiol.
                Frontiers in Microbiology
                Frontiers Media S.A.
                1664-302X
                22 February 2018
                2018
                : 9
                : 298
                Affiliations
                [1] 1Department of Biology, McGill University , Montreal, QC, Canada
                [2] 2Redpath Museum, McGill University , Montreal, QC, Canada
                [3] 3Smithsonian Tropical Research Institute , Panama City, Panama
                [4] 4Department of Biology, Laurentian University , Sudbury, ON, Canada
                [5] 5Departamento de Zoología, Universidad de Panamá , Panama City, Panama
                Author notes

                Edited by: Eria Alaide Rebollar, James Madison University, United States

                Reviewed by: Sandra V. Flechas, Alexander von Humboldt Biological Resources Research Institute, Colombia; Ana E. Escalante, National Autonomous University of Mexico, Mexico

                *Correspondence: Brandon J. Varela, varelabjv@ 123456gmail.com

                This article was submitted to Microbial Symbioses, a section of the journal Frontiers in Microbiology

                Article
                10.3389/fmicb.2018.00298
                5826957
                29520260
                1a44ae90-dd7d-4cc8-8638-fecf06eb6921
                Copyright © 2018 Varela, Lesbarrères, Ibáñez and Green.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 01 May 2017
                : 08 February 2018
                Page count
                Figures: 5, Tables: 3, Equations: 0, References: 82, Pages: 13, Words: 0
                Funding
                Funded by: Natural Sciences and Engineering Research Council of Canada 10.13039/501100000038
                Award ID: CGS-M-481960-2015
                Funded by: Natural Sciences and Engineering Research Council of Canada 10.13039/501100000038
                Award ID: CSM-MSFSS-488268
                Funded by: Natural Sciences and Engineering Research Council of Canada 10.13039/501100000038
                Award ID: 312126-2012
                Funded by: Natural Sciences and Engineering Research Council of Canada 10.13039/501100000038
                Award ID: 106154-2013
                Categories
                Microbiology
                Original Research

                Microbiology & Virology
                frog skin microbiota,metabarcoding,abiotic factors,dendrobates auratus,silverstoneia flotator,allobates talamancae,chytrid,batrachochytrium dendrobatidis

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