<?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%">Lee F. Stanish</style></author><author><style face="normal" font="default" size="100%">Tyler J. Kohler</style></author><author><style face="normal" font="default" size="100%">Darling, Joshua P.</style></author><author><style face="normal" font="default" size="100%">Diane M. McKnight</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Drifting along: Using diatoms to track the contribution of microbial mats to particulate organic matter transport in a glacial meltwater stream in the McMurdo Dry Valleys, Antarctica</style></title><secondary-title><style face="normal" font="default" size="100%">Frontiers in Microbiology</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">cyanobacteria</style></keyword><keyword><style  face="normal" font="default" size="100%">diatom</style></keyword><keyword><style  face="normal" font="default" size="100%">flow regime</style></keyword><keyword><style  face="normal" font="default" size="100%">hydrology</style></keyword><keyword><style  face="normal" font="default" size="100%">microbial mat</style></keyword><keyword><style  face="normal" font="default" size="100%">Nostoc</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%">05/2024</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://www.frontiersin.org/journals/microbiology/articles/10.3389/fmicb.2024.1352666/full</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">15</style></volume><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Flow pulses mobilize particulate organic matter (POM) in streams from the surrounding landscape and streambed. This POM serves as a source of energy and nutrients, as well as a means for organismal dispersal, to downstream communities. In the barren terrestrial landscape of the McMurdo Dry Valleys (MDV) of Antarctica, benthic microbial mats occupying different in-stream habitat types are the dominant POM source in the many glacier-fed streams. Many of these streams experience daily flow peaks that mobilize POM, and diatoms recovered from underlying stream sediments suggest that mat-derived diatoms in the POM are retained there through hyporheic exchange. Yet, &amp;lsquo;how much&amp;rsquo; and &amp;lsquo;when&amp;rsquo; different in-stream habitat types contribute to POM diatom assemblages is unknown. To quantify the contribution of different in-stream habitat types to POM diatom assemblages, we collected time-integrated POM samples over four diel experiments, which spanned a gradient of flow conditions over three summers. Diatoms from POM samples were identified, quantified, and compared with dominant habitat types (i.e., benthic &amp;lsquo;orange&amp;rsquo; mats, marginal &amp;lsquo;black&amp;rsquo; mats, and bare sediments). Like bulk POM, diatom cell concentrations followed a clockwise hysteresis pattern with stream discharge over the daily flow cycles, indicating supply limitation. Diatom community analyses showed that different habitat types harbor distinct diatom communities, and mixing models revealed that a substantial proportion of POM diatoms originated from bare sediments during baseflow conditions. Meanwhile, orange and black mats contribute diatoms to POM primarily during daily flow peaks when both cell concentrations and discharge are highest, making mats the most important contributors to POM diatom assemblages at high flows. These observations may help explain the presence of mat-derived diatoms in hyporheic sediments. Our results thus indicate a varying importance of different in-stream habitats to POM generation and export on daily to seasonal timescales, with implications for biogeochemical cycling and the local diatom metacommunity.&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%">Tyler J. Kohler</style></author><author><style face="normal" font="default" size="100%">Singley, Joel G.</style></author><author><style face="normal" font="default" size="100%">Wlostowski, Adam</style></author><author><style face="normal" font="default" size="100%">Diane M. McKnight</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Nitrogen fixation facilitates stream microbial mat biomass across the McMurdo Dry Valleys, Antarctica</style></title><secondary-title><style face="normal" font="default" size="100%">Biogeochemistry</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">biofilm</style></keyword><keyword><style  face="normal" font="default" size="100%">C</style></keyword><keyword><style  face="normal" font="default" size="100%">cyanobacteria</style></keyword><keyword><style  face="normal" font="default" size="100%">hyporheic zone</style></keyword><keyword><style  face="normal" font="default" size="100%">MCM LTER</style></keyword><keyword><style  face="normal" font="default" size="100%">mineralization</style></keyword><keyword><style  face="normal" font="default" size="100%">N</style></keyword><keyword><style  face="normal" font="default" size="100%">P biogeochemistry</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%">07/2023</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://link.springer.com/article/10.1007/s10533-023-01069-0</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;Nitrogen (N) fixation is a fundamental mechanism by which N enters streams. Yet, because of modern N saturation, it is difficult to study the importance of N-fixation to stream nutrient budgets. Here, we utilized relatively simple and pristine McMurdo Dry Valley streams to investigate the role of N-fixing &lt;i&gt;Nostoc&lt;/i&gt; abundance, streamwater dissolved inorganic N (DIN) concentration, and distance from the source glacier in regulating the elemental and isotopic composition of three microbial mat types (black, orange, and green) at the landscape scale. We found &lt;i&gt;Nostoc&lt;/i&gt;-based black mats were the most enriched in δ15N, and δ15N signatures of mats increased where &lt;i&gt;Nostoc&lt;/i&gt; was abundant, but did not surpass the atmospheric standard (δ15N &amp;asymp; 0&amp;permil;). Furthermore, green and orange mat δ15N signatures became more depleted with increasing DIN, indicating that mats utilize glacial meltwater-sourced N when available. The distance from the source glacier explained limited variability in mat δ15N across sites, indicating the influence of individual stream characteristics on N spiraling. To further explore longitudinal N spiraling processes generating observed δ15Ν patterns, we developed a simple steady-state mathematical model. Analysis of plausible scenarios with this model confirmed that streams both have the capacity to remove allochthonous DIN over the plausible range of inputs, and that internal N sources are required to account for δ15N signatures and observed DIN concentrations at stream outlets. Collectively, these data and modeling results demonstrate that N-fixation exerts substantial influence within and across these streams, and is presumably dependent upon interconnected organic matter reserves, mineralization rates, and geomorphology.&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%">Evans, Thomas W.</style></author><author><style face="normal" font="default" size="100%">Kalambokidis, Maria J.</style></author><author><style face="normal" font="default" size="100%">Jungblut, Anne D.</style></author><author><style face="normal" font="default" size="100%">Millar, Jasmin L.</style></author><author><style face="normal" font="default" size="100%">Bauersachs, Thorsten</style></author><author><style face="normal" font="default" size="100%">Grotheer, Hendrik</style></author><author><style face="normal" font="default" size="100%">Mackey, Tyler J.</style></author><author><style face="normal" font="default" size="100%">Ian Hawes</style></author><author><style face="normal" font="default" size="100%">Summons, Roger E.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Lipid biomarkers from microbial mats on the McMurdo Ice Shelf, Antarctica: Signatures for life in the cryosphere</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%">Antarctica</style></keyword><keyword><style  face="normal" font="default" size="100%">bacteriohopanepolyol</style></keyword><keyword><style  face="normal" font="default" size="100%">cyanobacteria</style></keyword><keyword><style  face="normal" font="default" size="100%">heterocyte glycolipids</style></keyword><keyword><style  face="normal" font="default" size="100%">homeoviscous adaptation</style></keyword><keyword><style  face="normal" font="default" size="100%">intact polar lipid</style></keyword><keyword><style  face="normal" font="default" size="100%">microbial mats</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">06/2022</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://www.frontiersin.org/articles/10.3389/fmicb.2022.903621/full</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">13</style></volume><pages><style face="normal" font="default" size="100%">903621</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Persistent cold temperatures, a paucity of nutrients, freeze-thaw cycles, and the strongly seasonal light regime make Antarctica one of Earth&amp;rsquo;s least hospitable surface environments for complex life. Cyanobacteria, however, are well-adapted to such conditions and are often the dominant primary producers in Antarctic inland water environments. In particular, the network of meltwater ponds on the &amp;lsquo;dirty ice&amp;rsquo; of the McMurdo Ice Shelf is an ecosystem with extensive cyanobacteria-dominated microbial mat accumulations. This study investigated intact polar lipids (IPLs), heterocyte glycolipids (HGs), and bacteriohopanepolyols (BHPs) in combination with 16S and 18S rRNA gene diversity in microbial mats of twelve ponds in this unique polar ecosystem. To constrain the effects of nutrient availability, temperature and freeze-thaw cycles on the lipid membrane composition, lipids were compared to stromatolite-forming cyanobacterial mats from ice-covered lakes in the McMurdo Dry Valleys as well as from (sub)tropical regions and hot springs. The 16S rRNA gene compositions of the McMurdo Ice Shelf mats confirm the dominance of Cyanobacteria and Proteobacteria while the 18S rRNA gene composition indicates the presence of Ochrophyta, Chlorophyta, Ciliophora, and other microfauna. IPL analyses revealed a predominantly bacterial community in the meltwater ponds, with archaeal lipids being barely detectable. IPLs are dominated by glycolipids and phospholipids, followed by aminolipids. The high abundance of sugar-bound lipids accords with a predominance of cyanobacterial primary producers. The phosphate-limited samples from the (sub)tropical, hot spring, and Lake Vanda sites revealed a higher abundance of aminolipids compared to those of the nitrogen-limited meltwater ponds, affirming the direct affects that N and P availability have on IPL compositions. The high abundance of polyunsaturated IPLs in the Antarctic microbial mats suggests that these lipids provide an important mechanism to maintain membrane fluidity in cold environments. High abundances of HG keto-ols and HG keto-diols, produced by heterocytous cyanobacteria, further support these findings and reveal a unique distribution compared to those from warmer climates.&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%">Chrismas, Nathan A. M.</style></author><author><style face="normal" font="default" size="100%">Williamson, Christopher J.</style></author><author><style face="normal" font="default" size="100%">Yallop, Marian L.</style></author><author><style face="normal" font="default" size="100%">Alexandre M. Anesio</style></author><author><style face="normal" font="default" size="100%">Sánchez-Baracaldo, Patricia</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Photoecology of the Antarctic cyanobacterium &lt;i&gt;Leptolyngbya&lt;/i&gt;               sp. BC1307 brought to light through community analysis, comparative genomics and in vitro photophysiology</style></title><secondary-title><style face="normal" font="default" size="100%">Molecular Ecology</style></secondary-title><short-title><style face="normal" font="default" size="100%">Mol Ecol</style></short-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antarctica</style></keyword><keyword><style  face="normal" font="default" size="100%">cyanobacteria</style></keyword><keyword><style  face="normal" font="default" size="100%">genomics</style></keyword><keyword><style  face="normal" font="default" size="100%">photoecology</style></keyword><keyword><style  face="normal" font="default" size="100%">photophysiology</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%">11/2018</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://onlinelibrary.wiley.com/doi/full/10.1111/mec.14953</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">27</style></volume><pages><style face="normal" font="default" size="100%">5279 - 5293</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Cyanobacteria are important photoautotrophs in extreme environments such as the McMurdo Dry Valleys, Antarctica. Terrestrial Antarctic cyanobacteria experience constant darkness during the winter and constant light during the summer which influences the ability of these organisms to fix carbon over the course of an annual cycle. Here, we present a unique approach combining community structure, genomic and photophysiological analyses to understand adaptation to Antarctic light regimes in the cyanobacterium &lt;em&gt;Leptolyngbya&lt;/em&gt; sp. BC1307. We show that &lt;em&gt;Leptolyngbya&lt;/em&gt; sp. BC1307 belongs to a clade of cyanobacteria that inhabits near‐surface environments in the McMurdo Dry Valleys. Genomic analyses reveal that, unlike close relatives, &lt;em&gt;Leptolyngbya&lt;/em&gt; sp. BC1307 lacks the genes necessary for production of the pigment phycoerythrin and is incapable of complimentary chromatic acclimation, while containing several genes responsible for known photoprotective pigments. Photophysiology experiments confirmed &lt;em&gt;Leptolyngbya&lt;/em&gt; sp. BC1307 to be tolerant of short‐term exposure to high levels of photosynthetically active radiation, while sustained exposure reduced its capacity for photoprotection. As such, &lt;em&gt;Leptolyngbya&lt;/em&gt; sp. BC1307 likely exploits low‐light microenvironments within cyanobacterial mats in the McMurdo Dry Valleys.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">24</style></issue></record></records></xml>