<?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%">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%">Castendyk, Devin</style></author><author><style face="normal" font="default" size="100%">Maciek K. Obryk</style></author><author><style face="normal" font="default" size="100%">Leidman, Sasha Z.</style></author><author><style face="normal" font="default" size="100%">Michael N. Gooseff</style></author><author><style face="normal" font="default" size="100%">Ian Hawes</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Lake Vanda: A sentinel for climate change in the McMurdo Sound Region of Antarctica</style></title><secondary-title><style face="normal" font="default" size="100%">Global and Planetary Change</style></secondary-title><short-title><style face="normal" font="default" size="100%">Global and Planetary Change</style></short-title></titles><dates><year><style  face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style  face="normal" font="default" size="100%">Jan-09-2016</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.sciencedirect.com/science/article/pii/S092181811530014X</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">144</style></volume><pages><style face="normal" font="default" size="100%">213 - 227</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Lake Vanda is a perennially ice-covered, meromictic, endorheic lake located in the McMurdo Dry Valleys of Antarctica, and an exceptional sentinel of climate change within the region. Lake levels rose 15 m over the past 68 years in response to climate-driven variability in ice-cover sublimation, meltwater production, and annual discharge of the Onyx River, the main source of water to the lake. Evidence from a new bathymetric map and water balance model combined with annual growth laminations in benthic mats suggest that the most recent filling trend began abruptly 80 years ago, in the early 1930s. This change increased lake volume by &amp;gt; 50%, triggered the formation of a new, upper, thermohaline convection cell, and cooled the lower convection cell by at least 2 &amp;deg;C and the bottom-most waters by at &amp;gt; 4 &amp;deg;C. Additionally, the depth of the deep chlorophyll a maximum rose by &amp;gt; 2 m, and deep-growing benthic algal mats declined while shallow benthic mats colonized freshly inundated areas. We attribute changes in hydrology to regional variations in air flow related to the strength and position of the Amundsen Sea Low (ASL) pressure system which have increased the frequency of down-valley, föhn winds associated with surface air temperature warming in the McMurdo Dry Valleys. The ASL has also been implicated in the recent warming of the Antarctic Peninsula, and provides a common link for climate-related change on opposite sides of the continent. If this trend persists, Lake Vanda should continue to rise and cool over the next 200 years until a new equilibrium lake level is achieved. Most likely, future lake rise will lead to isothermal conditions not conducive to thermohaline convection, resulting in a drastically different physical, biogeochemical, and biological structure than observed today.&lt;/p&gt;</style></abstract></record></records></xml>