<?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%">Power, Sarah N.</style></author><author><style face="normal" font="default" size="100%">Osburn, Ernest D.</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%">Microbial mat activity and soil biogeochemistry across variable phosphorus availability in Taylor Valley, Antarctica</style></title><secondary-title><style face="normal" font="default" size="100%">Antarctic Science</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">carbon</style></keyword><keyword><style  face="normal" font="default" size="100%">cyanobacteria</style></keyword><keyword><style  face="normal" font="default" size="100%">nitrogen fixation</style></keyword><keyword><style  face="normal" font="default" size="100%">phosphorus</style></keyword><keyword><style  face="normal" font="default" size="100%">pigments</style></keyword><keyword><style  face="normal" font="default" size="100%">soil ecology</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.cambridge.org/core/journals/antarctic-science/article/microbial-mat-activity-and-soil-biogeochemistry-across-variable-phosphorus-availability-in-taylor-valley-antarctica/0655E2F09B8D6961618B8F396BA692F2</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;Primary production is fundamental to ecosystems, and in many extreme environments production is facilitated by microbial mats. Microbial mats are complex assemblages of photo- and heterotrophic microorganisms colonizing sediment and soil surfaces. These communities are the dominant producers of the McMurdo Dry Valleys, Antarctica, where they occupy lentic and lotic environments as well as intermittently wet soils. While the influence of microbial mats on stream nutrient dynamics and lake organic matter cycling is well documented, the influence of microbial mats on underlying soil is less well understood, particularly the effects of microbial mat nitrogen and carbon fixation. Taylor Valley soils occur across variable levels of inorganic phosphorus availability, with the Ross Sea drift containing four times that of the Taylor drifts, providing opportunities to examine how soil geochemistry influences microbial mats and the ecological functions they regulate. We found that inorganic phosphorus availability is positively correlated with microbial mat biomass, pigment concentration and nitrogen fixation potential. Additionally, our results demonstrate that dense microbial mats influence the ecological functioning of underlying soils by enriching organic carbon and total nitrogen stocks (two times higher). This work contributes to ongoing questions regarding the sources of energy fuelling soil food webs and the regional carbon balance in the McMurdo Dry Valleys.&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%">Power, Sarah N.</style></author><author><style face="normal" font="default" size="100%">Thomas, Valerie A.</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%">Habitat suitability of biocrust communities in a cold desert ecosystem</style></title><secondary-title><style face="normal" font="default" size="100%">Ecology and Evolution</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">biocrust</style></keyword><keyword><style  face="normal" font="default" size="100%">carbon</style></keyword><keyword><style  face="normal" font="default" size="100%">dryland</style></keyword><keyword><style  face="normal" font="default" size="100%">habitat suitability</style></keyword><keyword><style  face="normal" font="default" size="100%">remote sensing</style></keyword><keyword><style  face="normal" font="default" size="100%">soil ecology</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">07/2024</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://onlinelibrary.wiley.com/toc/20457758/14/7</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">14</style></volume><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Drylands are unique among terrestrial ecosystems in that they have a significant proportion of primary production facilitated by non-vascular plants such as colonial cyanobacteria, moss, and lichens, i.e., biocrusts, which occur on and in the surface soil. Biocrusts inhabit all continents, including Antarctica, an increasingly dynamic continent on the precipice of change. Here, we describe in-situ field surveying and sampling, remote sensing, and modeling approaches to assess the habitat suitability of biocrusts in the Lake Fryxell basin of Taylor Valley, Antarctica, which is the main site of the McMurdo Dry Valleys Long-Term Ecological Research Program. Soils suitable for the development of biocrusts are typically wetter, less alkaline, and less saline compared to unvegetated soils. Using random forest models, we show that gravimetric water content, electrical conductivity, and snow frequency are the top predictors of biocrust presence and biomass. Areas most suitable for the growth of dense biocrusts are soils associated with seasonal snow patches. Using geospatial data to extrapolate our habitat suitability model to the whole basin predicts that biocrusts are present in 2.7 &amp;times; 10&lt;sup&gt;5&lt;/sup&gt;&amp;nbsp;m&lt;sup&gt;2&lt;/sup&gt; and contain 11&amp;ndash;72 Mg of aboveground carbon, based on the 90% probability of occurrence. Our study illustrates the synergistic effect of combining field and remote sensing data for understanding the distribution and biomass of biocrusts, a foundational community in the carbon balance of this region. Extreme weather events and changing climate conditions in this region, especially those influencing snow accumulation and persistence, could have significant effects on the future distribution and abundance of biocrusts and therefore soil organic carbon storage in the McMurdo Dry Valleys.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">7</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%">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%">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%">Borges, Schuyler R.</style></author><author><style face="normal" font="default" size="100%">Byron Adams</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%">Remotely characterizing photosynthetic biocrust in snowpack-fed microhabitats of Taylor Valley, Antarctica</style></title><secondary-title><style face="normal" font="default" size="100%">Science of Remote Sensing</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antarctica</style></keyword><keyword><style  face="normal" font="default" size="100%">biocrust</style></keyword><keyword><style  face="normal" font="default" size="100%">carbon</style></keyword><keyword><style  face="normal" font="default" size="100%">reflectance spectroscopy</style></keyword><keyword><style  face="normal" font="default" size="100%">snow</style></keyword><keyword><style  face="normal" font="default" size="100%">soil ecology</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">02/2024</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://www.sciencedirect.com/science/article/pii/S266601722400004X</style></url></web-urls></urls><pages><style face="normal" font="default" size="100%">100120</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Microbial communities are the primary drivers of carbon cycling in the McMurdo Dry Valleys of Antarctica. Dense microbial mats, consisting mainly of photosynthetic cyanobacteria, occupy aquatic areas associated with streams and lakes. Other microbial communities also occur at lower densities as patchy surface biological soil crusts (hereafter, biocrusts) across the terrestrial landscape. Multispectral satellite data have been used to model microbial mat abundance in high-density areas like stream and lake margins, but no previous studies have investigated the lower detection limits of biocrusts. Here, we describe remote sensing and field-based survey and sampling approaches to study the detectability and distribution of biocrusts in the McMurdo Dry Valleys. Using a combination of multi- and hyperspectral tools and spectral linear unmixing, we modeled the abundances of biocrust in eastern Taylor Valley. Our spectral approaches can detect low masses of biocrust material in laboratory microcosms down to biocrust concentrations of 1% by mass. These techniques also distinguish the spectra of biocrust from both surface rock and mineral signatures from orbit. We found that biocrusts are present throughout the soils of eastern Taylor Valley and are associated with diverse underlying soil communities. The densest biocrust communities identified in this study had total organic carbon 5x greater than the content of typical arid soils. The most productive biocrusts were located downslope of melting snowpacks in unique soil ecosystems that are distinct from the surrounding arid landscape. There are similarities between the snowpack and stream sediment communities (high diversity of soil invertebrates) as well as their ecosystem properties (e.g., persistence of liquid water, high transfer of available nutrients, lower salinity from flushing) compared to the typical arid terrestrial ecosystem of the dry valleys. Our approach extends the capability of orbital remote sensing of photosynthetic communities out of the aquatic margins and into the drier soils which comprise most of this landscape. This interdisciplinary work is critical for measuring and monitoring terrestrial carbon stocks and predicting future ecosystem dynamics in this currently water-limited but increasingly dynamic Antarctic landscape, which is particularly climate-sensitive and difficult to access.&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%">Saurey, Sabrina D.</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Aanderud, Zachary T.</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">Resource Legacies and Priming Regulate Microbial Communities in Antarctica's Dry Valleys</style></title><secondary-title><style face="normal" font="default" size="100%">Department of Plant and Wildlife Sciences</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">454 pyrosequencing</style></keyword><keyword><style  face="normal" font="default" size="100%">Antarctica</style></keyword><keyword><style  face="normal" font="default" size="100%">bacteria</style></keyword><keyword><style  face="normal" font="default" size="100%">microbial ecology</style></keyword><keyword><style  face="normal" font="default" size="100%">soil</style></keyword><keyword><style  face="normal" font="default" size="100%">soil ecology</style></keyword><keyword><style  face="normal" font="default" size="100%">stable isotope probing</style></keyword><keyword><style  face="normal" font="default" size="100%">target metagenomics</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2013</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://hdl.lib.byu.edu/1877/etd6229</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">Brigham Young University</style></publisher><pub-location><style face="normal" font="default" size="100%">Provo, UT</style></pub-location><volume><style face="normal" font="default" size="100%">M.S.</style></volume><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Multiple mechanisms control bacterial community structure but two in particular, the &amp;quot;legacy&amp;quot; of past environmental conditions, and the &amp;quot;priming&amp;quot; of bacteria to respond to seasonal or reoccurring fluctuations in resources, have the potential to determine both bacterial communities, as well as, temporal shifts in active bacterial taxa. To begin to evaluate the legacy effects of resources on microbial communities, we added four limiting resources annually (i.e., water only; C-mannitol + water; N-NH4NO3 + water; and C, N + water) and measured shifts in bacterial community composition after seven years in a cold desert ecosystem in the McMurdo Dry Valleys, Antarctica. Further, to investigate the ecological significance of priming, we conducted a series of stable isotope probing experiments (i.e., 18O-DNA SIP with 18O-labeled water, 13C-DNA SIP with 13C-labeled mannitol, 15N-DNA with 15N- NH4NO3, and a combined C and N SIP) and characterized the responding (i.e., isotopically labeled) and seed bank (i.e., unlabeled) bacterial communities. We performed each of the SIPs in soil microcosms corresponding to a single resource manipulation (e.g., 13C-labeled mannitol in C addition soils). We hypothesized that all long-term additions of nutrients and water will lead to a distinct bacterial community&amp;mdash;a legacy effect due to the nutrient and water impoverished state of Antarctica soils. We also hypothesized that the stronger the legacy effects demonstrated by a specific community the more adapted or primed bacterial species will be to take advantage of the resource and respond. As hypothesized, resource additions created distinct bacterial legacy but to different degrees among the treatments. The extent of the resource legacy effects was greatest in the CN, intermediate in water and N, and lowest in C communities relative to the control communities, suggesting that C induced changes in communities were intensified by tandem N additions and that water alone created a more distinct legacy than water and C additions combined. Contrary to our hypothesis, the stronger the legacy effects, the less adapted or primed the community was to take advantage of resource additions. For example, the CN treatment that induced the greatest effect on bacterial communities had the lowest number of species (20.9%) in common between the responding and seed bank communities. This inverse relationship may be due to only two species (i.e., Arthrobacter, Actinobacteria and Massilia, Betaproteobacteria) really being primed to take advantage of CN and these species constituting over 75% of the seed bank community. Water, N, and C additions had similar levels of priming with 38.4%, 41.4%, and 36.3% of the responding species being present in the seed bank community, respectively. But of these three treatments, only the priming with water resulted in a unique responding community, suggesting that water, a universal bacterial resource, was enough to prime bacteria. Furthermore, water generates the most diverse responding community of all the resources with stemming from all of the fourteen dominant phyla. We did find patterns of ecological coherence among the responders, especially in the major responders (i.e., responders that increased in relative recovery by at least ten-fold). These responders were predominantly found in only three phyla (i.e., Actinobacteria, Bacteriodetes, and Gammaproteobacteria) regardless of resource addition. Alternatively minor responders (i.e., responders that increased in relative recovery at least two-fold) were contained in fourteen different phyla with specific taxa stimulated by CN (i.e., Betaproteobacteria) and N and water (i.e., Deltaproteobacteria). Further, resource additions elicited responses from 37% of bacterial species with species specializing on a specific resource (e.g., Chloroflexi) or being a generalist (e.g., Planctomycetes and Gammaproteobacteria). Our results offer the first direct links between legacy and priming effects on bacterial community composition and demonstrate that these mechanisms are not always complimentary leading to the formation of similar communities but may both be essential to maintain the high levels of bacterial diversity. Further, all resources produced elicited responders that were either specialists of generalists demonstrating that even bacteria in the extreme environment of Antarctica respond to pulses of resources.&lt;/p&gt;</style></abstract><work-type><style face="normal" font="default" size="100%">masters</style></work-type></record></records></xml>