<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Thapa‐Magar, Khum B.</style></author><author><style face="normal" font="default" size="100%">Eric R. Sokol</style></author><author><style face="normal" font="default" size="100%">Michael N. Gooseff</style></author><author><style face="normal" font="default" size="100%">Salvatore, Mark R.</style></author><author><style face="normal" font="default" size="100%">John E. Barrett</style></author><author><style face="normal" font="default" size="100%">Joseph S. Levy</style></author><author><style face="normal" font="default" size="100%">Knightly, J. Paul</style></author><author><style face="normal" font="default" size="100%">Power, Sarah N.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Remote sensing for species distribution models: An illustration from a sentinel taxon of the world's driest ecosystem</style></title><secondary-title><style face="normal" font="default" size="100%">Ecology</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antarctica</style></keyword><keyword><style  face="normal" font="default" size="100%">McMurdo Dry Valleys</style></keyword><keyword><style  face="normal" font="default" size="100%">microbial mats</style></keyword><keyword><style  face="normal" font="default" size="100%">remote sensing</style></keyword><keyword><style  face="normal" font="default" size="100%">species distribution modeling</style></keyword><keyword><style  face="normal" font="default" size="100%">species occurrence</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style  face="normal" font="default" size="100%">02/2025</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://esajournals.onlinelibrary.wiley.com/doi/full/10.1002/ecy.70035</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">106</style></volume><pages><style face="normal" font="default" size="100%">e70035</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;In situ observed data are commonly used as species occurrence response variables in species distribution models. However, the use of remotely observed data from high-resolution multispectral remote-sensing images as a source of presence/absence data for species distribution models remains under-developed. Here, we describe an ensemble species distribution model of black microbial mats (Nostoc spp.) using presence/absence points derived from the unmixing of 4-m resolution WorldView-2 and WorldView-3 images in the Lake Fryxell basin region of Taylor Valley, Antarctica. Environmental and topographical characteristics such as soil moisture, snow, elevation, slope, and aspect were used as predictor variables in our models. We demonstrate that we can build and run ensemble species distribution models using both dependent and independent variables derived from remote-sensing data to generate spatially explicit habitat suitability maps. Snow and soil moisture were found to be the most important variables accounting for about 80% of the variation in the distribution of black mats throughout the Fryxell basin. This study highlights the potential contribution of high-resolution remote-sensing to species distribution modeling and informs new studies incorporating remotely derived species occurrences in species distribution models, especially in remote areas where access to in situ data is often limited.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Snyder, Meredith D.</style></author><author><style face="normal" font="default" size="100%">Adams, Byron J.</style></author><author><style face="normal" font="default" size="100%">Borgmeier, Abigail</style></author><author><style face="normal" font="default" size="100%">Jorna, Jesse</style></author><author><style face="normal" font="default" size="100%">Power, Sarah N.</style></author><author><style face="normal" font="default" size="100%">Salvatore, Mark R.</style></author><author><style face="normal" font="default" size="100%">John E. Barrett</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Soil biota sensitivity to hydroclimate variability in a polar desert ecosystem</style></title><secondary-title><style face="normal" font="default" size="100%">Arctic, Antarctic, and Alpine Research</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">climate variation</style></keyword><keyword><style  face="normal" font="default" size="100%">extreme weather</style></keyword><keyword><style  face="normal" font="default" size="100%">McMurdo Dry Valleys</style></keyword><keyword><style  face="normal" font="default" size="100%">microbial community</style></keyword><keyword><style  face="normal" font="default" size="100%">soil invertebrates</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style  face="normal" font="default" size="100%">05/2025</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://www.tandfonline.com/doi/full/10.1080/15230430.2025.2485283</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">57</style></volume><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;An anomalous warm weather event in the Antarctic McMurdo Dry Valleys on 18 March 2022 created an opportunity to characterize soil biota communities most sensitive to freeze&amp;ndash;thaw stress. This event caused unseasonal melt within Taylor Valley, activating stream water and microbial mats around Canada Stream. Liquid water availability in this polar desert is a driver of soil biota distribution and activity. Because climate change impacts hydrological regimes, we aimed to determine the effect on soil communities. We sampled soils identified from this event that experienced thaw, nearby hyper-arid areas, and wetted areas that did not experience thaw to compare soil bacterial and invertebrate communities. Areas that exhibited evidence of freeze&amp;ndash;thaw supported the highest live and dead nematode counts and were composed of soil taxa from hyper-arid landscapes and wetted areas. They received water inputs from snowpacks, hyporheic water, or glacial melt, contributing to community differences associated with organic matter and salinity gradients. Inundated soils had higher organic matter and lower conductivity (p &amp;lt;&amp;nbsp;.02) and hosted the most diverse microbial and invertebrate communities on average. Our findings suggest that as liquid water becomes more available under predicted climate change, soil communities adapted to the hyper-arid landscape will shift toward diverse, wetted soil communities.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Gutterman, William S.</style></author><author><style face="normal" font="default" size="100%">Peter T. Doran</style></author><author><style face="normal" font="default" size="100%">Ross A. Virginia</style></author><author><style face="normal" font="default" size="100%">John E. Barrett</style></author><author><style face="normal" font="default" size="100%">Myers, Krista F.</style></author><author><style face="normal" font="default" size="100%">Tulaczyk, Slawek M.</style></author><author><style face="normal" font="default" size="100%">Foley, Neil T.</style></author><author><style face="normal" font="default" size="100%">Jill A. Mikucki</style></author><author><style face="normal" font="default" size="100%">Hilary A. Dugan</style></author><author><style face="normal" font="default" size="100%">Grombacher, Denys</style></author><author><style face="normal" font="default" size="100%">Bording, Thue S.</style></author><author><style face="normal" font="default" size="100%">Auken, E.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Causes and characteristics of electrical resistivity variability in shallow (&lt;4 m) soils in Taylor Valley, East Antarctica</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Geophysical Research: Earth Surface</style></secondary-title><short-title><style face="normal" font="default" size="100%">JGR Earth Surface</style></short-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">active layer</style></keyword><keyword><style  face="normal" font="default" size="100%">airborne electromagnetic surveys</style></keyword><keyword><style  face="normal" font="default" size="100%">McMurdo Dry Valleys</style></keyword><keyword><style  face="normal" font="default" size="100%">permafrost dynamics</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">02/2023</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://onlinelibrary.wiley.com/doi/10.1029/2022JF006696</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">128</style></volume><pages><style face="normal" font="default" size="100%">e2022JF006696</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Airborne electromagnetic surveys collected in December 2011 and November 2018 and three soil sampling transects were used to analyze the spatial heterogeneity of shallow (&amp;lt;4 m) soil properties in lower Taylor Valley (TV), East Antarctica. Soil resistivities from 2011 to 2018 ranged from &amp;sim;33 Ωm to &amp;sim;3,500 Ωm with 200 Ωm assigned as an upper boundary for brine-saturated sediments. Elevations below &amp;sim;50 m above sea level (masl) typically exhibit the lowest resistivities with resistivity increasing at high elevations on steeper slopes. Soil water content was empirically estimated from electrical resistivities using Archie&amp;#39;s Law and range from &amp;sim;&amp;lt;1% to &amp;sim;68% by volume. An increase in silt- and clay-sized particles at low elevations increases soil porosity but decreases hydraulic conductivity, promoting greater residence times of soil water at low elevations near Lake Fryxell. Soil resistivity variability between 2011 and 2018 shows soils at different stages of soil freeze-thaw cycles, which are caused predominantly by solar warming of soils as opposed to air temperature. This study furthers the understanding of the hydrogeologic structure of the shallow subsurface in TV and identifies locations of soils that are potentially prone to greater rates of thaw and resulting ecosystem homogenization of soil properties from projected increases in hydrological connectivity across the region over the coming decades.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Salvatore, Mark R.</style></author><author><style face="normal" font="default" size="100%">Borges, Schuyler R.</style></author><author><style face="normal" font="default" size="100%">John E. Barrett</style></author><author><style face="normal" font="default" size="100%">Eric R. Sokol</style></author><author><style face="normal" font="default" size="100%">Lee F. Stanish</style></author><author><style face="normal" font="default" size="100%">Power, Sarah N.</style></author><author><style face="normal" font="default" size="100%">Morin, Paul</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Remote characterization of photosynthetic communities in the Fryxell basin of Taylor Valley, Antarctica</style></title><secondary-title><style face="normal" font="default" size="100%">Antarctic Science</style></secondary-title><short-title><style face="normal" font="default" size="100%">Antarctic Science</style></short-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">ecology</style></keyword><keyword><style  face="normal" font="default" size="100%">hydrology</style></keyword><keyword><style  face="normal" font="default" size="100%">McMurdo Dry Valleys</style></keyword><keyword><style  face="normal" font="default" size="100%">microbiology</style></keyword><keyword><style  face="normal" font="default" size="100%">remote sensing</style></keyword><keyword><style  face="normal" font="default" size="100%">spectroscopy</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">03/2020</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://www.cambridge.org/core/journals/antarctic-science/article/remote-characterization-of-photosynthetic-communities-in-the-fryxell-basin-of-taylor-valley-antarctica/8576F6BB1BCFDCA8409F5EA96CA00C6F</style></url></web-urls></urls><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;We investigate the spatial distribution, spectral properties and temporal variability of primary producers (e.g. communities of microbial mats and mosses) throughout the Fryxell basin of Taylor Valley, Antarctica, using high-resolution multispectral remote-sensing data. Our results suggest that photosynthetic communities can be readily detected throughout the Fryxell basin based on their unique near-infrared spectral signatures. Observed intra- and inter-annual variability in spectral signatures are consistent with short-term variations in mat distribution, hydration and photosynthetic activity. Spectral unmixing is also implemented in order to estimate mat abundance, with the most densely vegetated regions observed from orbit correlating spatially with some of the most productive regions of the Fryxell basin. Our work establishes remote sensing as a valuable tool in the study of these ecological communities in the McMurdo Dry Valleys and demonstrates how future scientific investigations and the management of specially protected areas could benefit from these tools and techniques.&lt;/p&gt;</style></abstract></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Aanderud, Zachary T.</style></author><author><style face="normal" font="default" size="100%">Saurey, Sabrina D.</style></author><author><style face="normal" font="default" size="100%">Ball, Becky</style></author><author><style face="normal" font="default" size="100%">Diana H. Wall</style></author><author><style face="normal" font="default" size="100%">John E. Barrett</style></author><author><style face="normal" font="default" size="100%">Muscarella, Mario E.</style></author><author><style face="normal" font="default" size="100%">Griffin, Natasha A.</style></author><author><style face="normal" font="default" size="100%">Ross A. Virginia</style></author><author><style face="normal" font="default" size="100%">Byron Adams</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Stoichiometric Shifts in Soil C:N:P Promote Bacterial Taxa Dominance, Maintain Biodiversity, and Deconstruct Community Assemblages</style></title><secondary-title><style face="normal" font="default" size="100%">Frontiers in Microbiology</style></secondary-title><short-title><style face="normal" font="default" size="100%">Front. Microbiol.</style></short-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">ecological stoichiometry</style></keyword><keyword><style  face="normal" font="default" size="100%">Lake Fryxell Basin</style></keyword><keyword><style  face="normal" font="default" size="100%">McMurdo Dry Valleys</style></keyword><keyword><style  face="normal" font="default" size="100%">network community modeling</style></keyword><keyword><style  face="normal" font="default" size="100%">nutrient colimitation</style></keyword><keyword><style  face="normal" font="default" size="100%">Solirubrobacteriaceae</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">07/2018</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://www.frontiersin.org/article/10.3389/fmicb.2018.01401/full</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Imbalances in C:N:P supply ratios may cause bacterial resource limitations and constrain biogeochemical processes, but the importance of shifts in soil stoichiometry are complicated by the nearly limitless interactions between an immensely rich species pool and a multiple chemical resource forms. To more clearly identify the impact of soil C:N:P on bacteria, we evaluated the cumulative effects of single and coupled long-term nutrient additions (i.e., C as mannitol, N as equal concentrations NH4 + and NO3 &amp;minus; , and P as Na3PO4) and water on communities in an Antarctic polar desert, Taylor Valley. Untreated soils possessed relatively low bacterial diversity, simplified organic C sources due to the absence of plants, limited inorganic N, and excess soil P potentially attenuating links between C:N:P. After 6 years of adding resources, an alleviation of C and N colimitation allowed one rare Micrococcaceae, an Arthrobacter species, to dominate, comprising 47% of the total community abundance and elevating soil respiration by 136% relative to untreated soils. The addition of N alone reduced C:N ratios, elevated bacterial richness and diversity, and allowed rare taxa relying on ammonium and nitrite for metabolism to become more abundant [e.g., nitrite oxidizing Nitrospira species (Nitrosomonadaceae), denitrifiers utilizing nitrite (Gemmatimonadaceae) and members of Rhodobacteraceae with a high affinity for ammonium]. Based on community co-occurrence networks, lower C:P ratios in soils following P and CP additions created more diffuse and less connected communities by disrupting 73% of species interactions and selecting for taxa potentially exploiting abundant P. Unlike amended nutrients, water additions alone elicited no lasting impact on communities. Our results suggest that as soils become nutrient rich a wide array of outcomes are possible from species dominance and the deconstruction of species interconnectedness to the maintenance of biodiversity.&lt;/p&gt;</style></abstract></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>32</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Kevin M. Geyer</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">John E. Barrett</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">Environmental Controls Over the Distribution and Function of Antarctic Soil Bacterial Communities</style></title><secondary-title><style face="normal" font="default" size="100%">Biological Sciences</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">biogeochemistry</style></keyword><keyword><style  face="normal" font="default" size="100%">biogeography</style></keyword><keyword><style  face="normal" font="default" size="100%">McMurdo Dry Valleys</style></keyword><keyword><style  face="normal" font="default" size="100%">microbial ecology</style></keyword><keyword><style  face="normal" font="default" size="100%">productivity/diversity theory</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2014</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://hdl.handle.net/10919/64417</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">Virginia Tech</style></publisher><pub-location><style face="normal" font="default" size="100%">Blacksburg, VA</style></pub-location><volume><style face="normal" font="default" size="100%">Ph.D.</style></volume><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;div title=&quot;Page 2&quot;&gt;&lt;div&gt;&lt;div&gt;&lt;p&gt;Microbial community composition plays a vital role in soil biogeochemical cycling. Information that explains the biogeography of microorganisms is consequently necessary for predicting the timing and magnitude of important ecosystem services mediated by soil biota, such as decomposition and nutrient cycling. Theory developed to explain patterns in plant and animal distributions such as the prevalent relationship between ecosystem productivity and diversity may be successfully extended to microbial systems and accelerate an emerging ecological understanding of the &amp;quot;unseen majority.&amp;quot; These considerations suggest a need to define the important mechanisms which affect microbial biogeography as well as the sensitivity of community structure/function to changing climatic or environmental conditions. To this end, my dissertation covers three data chapters in which I have 1) examined patterns in bacterial biogeography using gradients of environmental severity and productivity to identify changes in community diversity (e.g. taxonomic richness) and structure (e.g. similarity); 2) detected potential bacterial ecotypes associated with distinct soil habitats such as those of high alkalinity or electrical conductivity and; 3) measured environmental controls over the function (e.g. primary production, exoenzyme activity) of soil organisms in an environment of severe environmental limitations. Sampling was performed in the polar desert of Antarctica&amp;#39;s McMurdo Dry Valleys, a model ecosystem which hosts microbially-dominated soil foodwebs and displays heterogeneously distributed soil properties across the landscape. Results for Chapter 2 indicate differential effects of resource availability and geochemical severity on bacterial communities,&amp;nbsp;&lt;span style=&quot;font-size: 0.923em;&quot;&gt;with a significant productivity-diversity relationship that plateaus near the highest observed concentrations of the limiting resource organic carbon (0.30mg C/g soil). Geochemical severity (e.g. pH, electrical conductivity) primarily affected bacterial community similarity and successfully explained the divergent structure of a subset of samples. 16S rRNA amplicon pyrosequencing further revealed in Chapter 3 the identity of specific phyla that preferentially exist within certain habitats (i.e.&amp;nbsp;Acidobacteria&amp;nbsp;in alkaline soils,&amp;nbsp;Nitrospira&amp;nbsp;in mesic soils) suggesting the presence of niche specialists and spatial heterogeneity of taxa-specific functions (i.e. nitrite oxidation). Additionally, environmental parameters had different explanatory power towards predicting bacterial richness at varying taxonomic scales, from 57% of phylum-level richness with pH to 91% of order- and genus-level richness with moisture. Finally, Chapter 4 details a simultaneous sampling of soil communities and their associated ecosystem functions (primary productivity, enzymatic decomposition) and indicates that the overall organic substrate diversity may be greater in mesic soils where bacterial diversity is also highest, thus a potentially unforeseen driver of community dynamics. I also quantified annual rates of soil production which range between 0.7 - 18.1g C/m2/yr from the more arid to productive soils, respectively. In conclusion, the extension of biogeographical theory for macroorganisms has proven successful and both environmental severity and resource availability have obvious (although different) effects on the diversity and composition of soil microbial communities.&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;</style></abstract><work-type><style face="normal" font="default" size="100%">doctoral</style></work-type></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>32</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Adam E. Altrichter</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">John E. Barrett</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">Landscape history and contemporary environmental drivers of microbial community structure and function</style></title><secondary-title><style face="normal" font="default" size="100%">Biological Sciences</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">community similarity</style></keyword><keyword><style  face="normal" font="default" size="100%">extracellular enzyme activity</style></keyword><keyword><style  face="normal" font="default" size="100%">McMurdo Dry Valleys</style></keyword><keyword><style  face="normal" font="default" size="100%">microbial biogeography</style></keyword><keyword><style  face="normal" font="default" size="100%">soil geochemistry</style></keyword><keyword><style  face="normal" font="default" size="100%">T-RFLP</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2010</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://hdl.handle.net/10919/31883</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">Virginia Tech</style></publisher><pub-location><style face="normal" font="default" size="100%">Blacksburg, VA</style></pub-location><volume><style face="normal" font="default" size="100%">MS</style></volume><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Recent work in microbial ecology has focused on elucidating controls over biogeographic patterns and connecting microbial community composition to ecosystem function. My objective was to investigate the relative influences of landscape legacies and contemporary environmental factors on the distribution of soil microbial communities and their contribution to ecosystem processes across a glacial till sequence in Taylor Valley, Antarctica. Within each till unit, I sampled from dry areas and areas with visible evidence of recent surface water movement generated by seasonal melting of ephemeral snow packs and hillslope ground ice. Using T-RFLP 16S rRNA gene profiles of microbial communities, I analyzed the contribution of till and environmental factors to community similarity, and assessed the functional potential of the microbial community using extracellular enzyme activity assays. Microbial communities were influenced by geochemical differences among both tills and local environments, but especially organized by variables associated with water availability as the first axis of an NMDS ordination was strongly related to shifts in soil moisture content. CCA revealed that tills explained only 3.4% of the variability in community similarity among sites, while geochemical variables explained 18.5%. Extracellular enzyme activity was correlated with relevant geochemical variables reflecting the influence of nutrient limitation on microbial activity. In addition, enzyme activity was related to changes in community similarity, particularly in wet environments with a partial Mantel correlation of 0.32. These results demonstrate how landscape history and environmental conditions can shape the functional potential of a microbial community mediated through shifts in microbial community composition.&lt;/p&gt;</style></abstract><work-type><style face="normal" font="default" size="100%">masters</style></work-type></record></records></xml>