<?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%">Jorna, Jesse</style></author><author><style face="normal" font="default" size="100%">Adams, Byron J.</style></author><author><style face="normal" font="default" size="100%">Aanderud, Zachary T.</style></author><author><style face="normal" font="default" size="100%">Frandsen, Paul B.</style></author><author><style face="normal" font="default" size="100%">Cristina D. Takacs-Vesbach</style></author><author><style face="normal" font="default" size="100%">Kéfi, Sonia</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">The underground network: Facilitation in soil bacteria</style></title><secondary-title><style face="normal" font="default" size="100%">Oikos</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">bacteria</style></keyword><keyword><style  face="normal" font="default" size="100%">climate change</style></keyword><keyword><style  face="normal" font="default" size="100%">facilitation</style></keyword><keyword><style  face="normal" font="default" size="100%">resilience</style></keyword><keyword><style  face="normal" font="default" size="100%">stress-gradient hypothesis</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%">06/2024</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://nsojournals.onlinelibrary.wiley.com/doi/10.1111/oik.10299</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;Our understanding of the fundamental role that soil bacteria play in the structure and functioning of Earth&amp;#39;s ecosystems is ever expanding, but insight into the nature of interactions within these bacterial communities remains rudimentary. Bacterial facilitation may enhance the establishment, growth, and succession of eukaryotic biota, elevating the complexity and diversity of the entire soil community and thereby modulating multiple ecosystem functions. Global climate change often alters soil bacterial community composition, which, in turn, impacts other dependent biota. However, the impact of climate change on facilitation within bacterial communities remains poorly understood even though it may have important cascading consequences for entire ecosystems. The wealth of metagenomic data currently being generated gives community ecologists the ability to investigate bacterial facilitation in the natural world and how it affects ecological systems responses to climate change. Here, we review current evidence demonstrating the importance of facilitation in promoting emergent properties such as community diversity, ecosystem functioning, and resilience to climate change in soil bacterial communities. We show that a synthesis is currently missing between the abundant data, newly developed models and a coherent ecological framework that addresses these emergent properties. We highlight that including phylogenetic information, the physicochemical environment, and species-specific ecologies can improve our ability to infer interactions in natural soil communities. Following these recommendations, studies on bacterial facilitation will be an important piece of the puzzle to understand the consequences of global change on ecological communities and a model to advance our understanding of facilitation in complex communities more generally.&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%">Melisa A. Diaz</style></author><author><style face="normal" font="default" size="100%">Christopher B. Gardner</style></author><author><style face="normal" font="default" size="100%">Elliot, David H.</style></author><author><style face="normal" font="default" size="100%">Byron Adams</style></author><author><style face="normal" font="default" size="100%">W. Berry Lyons</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Change at 85 degrees south: Shackleton Glacier region proglacial lakes from 1960 to 2020</style></title><secondary-title><style face="normal" font="default" size="100%">Annals of Glaciology</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antarctic glaciology</style></keyword><keyword><style  face="normal" font="default" size="100%">climate change</style></keyword><keyword><style  face="normal" font="default" size="100%">meltwater chemistry</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%">05/2023</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://www.cambridge.org/core/journals/annals-of-glaciology/article/change-at-85-degrees-south-shackleton-glacier-region-proglacial-lakes-from-1960-to-2020/565D96AD7AE72BD22C49CCB772867AC4</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;Over the last two decades, anomalous warming events have been observed in coastal Antarctic regions. While these events have been documented in the Ross Sea sector, the Antarctic interior is believed to have been buffered from warming. In this work, we present data from lakes located near Mt. Heekin and Thanksgiving Valley (~85&amp;deg; S) along the Shackleton Glacier, which are believed to be the southern-most Antarctic dry valley lakes. In 2018, the lakes were characterized, repeat satellite images were examined, and lake water chemistry was measured. Our analysis shows that lake areas recently increased, and the water-soluble ion chemistry indicates a flushing of salts from periglacial soils, likely from increased glacial melt as illustrated by water isotope data. Our results show that high southern latitude ice-free areas have likely been affected by warm pulses over the past 60 years and these pulses may be quasi-synchronous throughout the Transantarctic Mountains.&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%">Robinson, Colin Michael</style></author><author><style face="normal" font="default" size="100%">Hansen, Lee D.</style></author><author><style face="normal" font="default" size="100%">Xue, Xia</style></author><author><style face="normal" font="default" size="100%">Adams, Byron J.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Temperature response of metabolic activity of an Antarctic nematode</style></title><secondary-title><style face="normal" font="default" size="100%">Biology</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antarctica</style></keyword><keyword><style  face="normal" font="default" size="100%">carbon cycling</style></keyword><keyword><style  face="normal" font="default" size="100%">climate change</style></keyword><keyword><style  face="normal" font="default" size="100%">nematode</style></keyword><keyword><style  face="normal" font="default" size="100%">respiration rates</style></keyword><keyword><style  face="normal" font="default" size="100%">soil temperature</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%">01/2023</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://www.mdpi.com/2079-7737/12/1/109</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">109</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Because of climate change, the McMurdo Dry Valleys of Antarctica (MCM) have experienced an increase in the frequency and magnitude of summer pulse warming and surface ice and snow melting events. In response to these environmental changes, some nematode species in the MCM have experienced steady population declines over the last three decades, but &lt;i&gt;Plectus murrayi&lt;/i&gt;, a mesophilic nematode species, has responded with a steady increase in range and abundance. To determine how &lt;i&gt;P. murrayi&lt;/i&gt; responds to increasing temperatures, we measured metabolic heat and CO&lt;sub&gt;2&lt;/sub&gt; production rates and calculated O&lt;sub&gt;2&lt;/sub&gt; consumption rates as a function of temperature at 5 &amp;deg;C intervals from 5 to 50 &amp;deg;C. Heat, CO&lt;sub&gt;2&lt;/sub&gt; production, and O&lt;sub&gt;2&lt;/sub&gt; consumption rates increase approximately exponentially up to 40 &amp;deg;C, a temperature never experienced in their polar habitat. Metabolic rates decline rapidly above 40 &amp;deg;C and are irreversibly lost at 50 &amp;deg;C due to thermal stress and mortality. &lt;i&gt;Caenorhabditis elegans&lt;/i&gt;, a much more widespread nematode that is found in more temperate environments reaches peak metabolic heat rate at just 27 &amp;deg;C, above which it experiences high mortality due to thermal stress. At temperatures from 10 to 40 &amp;deg;C, &lt;i&gt;P. murrayi&lt;/i&gt; produces about 6 times more CO&lt;sub&gt;2&lt;/sub&gt; than the O&lt;sub&gt;2&lt;/sub&gt; it consumes, a respiratory quotient indicative of either acetogenesis or de novo lipogenesis. No potential acetogenic microbes were identified in the &lt;i&gt;P. murrayi&lt;/i&gt; microbiome, suggesting that &lt;i&gt;P. murrayi&lt;/i&gt; is producing increased CO&lt;sub&gt;2&lt;/sub&gt; as a byproduct of de novo lipogenesis. This phenomenon, in conjunction with increased summer temperatures in their polar habitat, will likely lead to increased demand for carbon and subsequent increases in CO&lt;sub&gt;2&lt;/sub&gt; production, population abundance, and range expansion. If such changes are not concomitant with increased carbon inputs, we predict the MCM soil ecosystems will experience dramatic declines in functional and taxonomic diversity.&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%">Pothula, Satyendra K.</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%">Community assembly in the wake of glacial retreat: A meta‐analysis</style></title><secondary-title><style face="normal" font="default" size="100%">Global Change Biology</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">chronosequence</style></keyword><keyword><style  face="normal" font="default" size="100%">climate change</style></keyword><keyword><style  face="normal" font="default" size="100%">community assembly</style></keyword><keyword><style  face="normal" font="default" size="100%">deglaciation</style></keyword><keyword><style  face="normal" font="default" size="100%">ecological succession</style></keyword><keyword><style  face="normal" font="default" size="100%">glacial forefields</style></keyword><keyword><style  face="normal" font="default" size="100%">soil ecosystems</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%">09/2022</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://onlinelibrary.wiley.com/doi/10.1111/gcb.16427</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;Antarctic biodiversity faces an unknown future with a changing climate. Most terrestrial biota is restricted to limited patches of ice-free land in a sea of ice, where they are adapted to the continent&amp;#39;s extreme cold and wind and exploit microhabitats of suitable conditions. As temperatures rise, ice-free areas are predicted to expand, more rapidly in some areas than others. There is high uncertainty as to how species&amp;#39; distributions, physiology, abundance, and survivorship will be affected as their habitats transform. Here we use current knowledge to propose hypotheses that ice-free area expansion (i) will increase habitat availability, though the quality of habitat will vary; (ii) will increase structural connectivity, although not necessarily increase opportunities for species establishment; (iii) combined with milder climates will increase likelihood of non-native species establishment, but may also lengthen activity windows for all species; and (iv) will benefit some species and not others, possibly resulting in increased homogeneity of biodiversity. We anticipate considerable spatial, temporal, and taxonomic variation in species responses, and a heightened need for interdisciplinary research to understand the factors associated with ecosystem resilience under future scenarios. Such research will help identify at-risk species or vulnerable localities and is crucial for informing environmental management and policymaking into the future.&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%">Hudson, Amy R.</style></author><author><style face="normal" font="default" size="100%">Debra P. C. Peters</style></author><author><style face="normal" font="default" size="100%">J.M. Blair</style></author><author><style face="normal" font="default" size="100%">Childers, Daniel L.</style></author><author><style face="normal" font="default" size="100%">Peter T. Doran</style></author><author><style face="normal" font="default" size="100%">Geil, Kerrie</style></author><author><style face="normal" font="default" size="100%">Michael N. Gooseff</style></author><author><style face="normal" font="default" size="100%">Gross, Katherine L.</style></author><author><style face="normal" font="default" size="100%">Haddad, Nick M.</style></author><author><style face="normal" font="default" size="100%">Pastore, Melissa A.</style></author><author><style face="normal" font="default" size="100%">Rudgers, Jennifer A.</style></author><author><style face="normal" font="default" size="100%">Osvaldo E. Sala</style></author><author><style face="normal" font="default" size="100%">Seabloom, Eric W.</style></author><author><style face="normal" font="default" size="100%">Shaver, Gaius</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Cross-site comparisons of dryland ecosystem response to climate change in the US Long-Term Ecological Research Network</style></title><secondary-title><style face="normal" font="default" size="100%">BioScience</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">ANPP</style></keyword><keyword><style  face="normal" font="default" size="100%">climate change</style></keyword><keyword><style  face="normal" font="default" size="100%">Disturbance</style></keyword><keyword><style  face="normal" font="default" size="100%">drought</style></keyword><keyword><style  face="normal" font="default" size="100%">LTER</style></keyword><keyword><style  face="normal" font="default" size="100%">wildfire</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%">08/2022</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://academic.oup.com/bioscience/advance-article/doi/10.1093/biosci/biab134/6654840</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;Long-term observations and experiments in diverse drylands reveal how ecosystems and services are responding to climate change. To develop generalities about climate change impacts at dryland sites, we compared broadscale patterns in climate and synthesized primary production responses among the eight terrestrial, nonforested sites of the United States Long-Term Ecological Research (US LTER) Network located in temperate (Southwest and Midwest) and polar (Arctic and Antarctic) regions. All sites experienced warming in recent decades, whereas drought varied regionally with multidecadal phases. Multiple years of wet or dry conditions had larger effects than single years on primary production. Droughts, floods, and wildfires altered resource availability and restructured plant communities, with greater impacts on primary production than warming alone. During severe regional droughts, air pollution from wildfire and dust events peaked. Studies at US LTER drylands over more than 40 years demonstrate reciprocal links and feedbacks among dryland ecosystems, climate-driven disturbance events, and climate change.&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, Jasmine R.</style></author><author><style face="normal" font="default" size="100%">Waterman, Melinda J.</style></author><author><style face="normal" font="default" size="100%">Shaw, Justine D.</style></author><author><style face="normal" font="default" size="100%">Bergstrom, Dana M.</style></author><author><style face="normal" font="default" size="100%">Lynch, Heather J.</style></author><author><style face="normal" font="default" size="100%">Diana H. Wall</style></author><author><style face="normal" font="default" size="100%">Robinson, Sharon A.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Islands in the ice: Potential impacts of habitat transformation on Antarctic biodiversity</style></title><secondary-title><style face="normal" font="default" size="100%">Global Change Biology</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antarctica</style></keyword><keyword><style  face="normal" font="default" size="100%">biodiversity</style></keyword><keyword><style  face="normal" font="default" size="100%">biotic homogenization</style></keyword><keyword><style  face="normal" font="default" size="100%">climate change</style></keyword><keyword><style  face="normal" font="default" size="100%">connectivity</style></keyword><keyword><style  face="normal" font="default" size="100%">ice-free</style></keyword><keyword><style  face="normal" font="default" size="100%">non-native species</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%">07/2022</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://onlinelibrary.wiley.com/doi/10.1111/gcb.16331</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;Antarctic biodiversity faces an unknown future with a changing climate. Most terrestrial biota is restricted to limited patches of ice-free land in a sea of ice, where they are adapted to the continent&amp;#39;s extreme cold and wind and exploit microhabitats of suitable conditions. As temperatures rise, ice-free areas are predicted to expand, more rapidly in some areas than others. There is high uncertainty as to how species&amp;#39; distributions, physiology, abundance, and survivorship will be affected as their habitats transform. Here we use current knowledge to propose hypotheses that ice-free area expansion (i) will increase habitat availability, though the quality of habitat will vary; (ii) will increase structural connectivity, although not necessarily increase opportunities for species establishment; (iii) combined with milder climates will increase likelihood of non-native species establishment, but may also lengthen activity windows for all species; and (iv) will benefit some species and not others, possibly resulting in increased homogeneity of biodiversity. We anticipate considerable spatial, temporal, and taxonomic variation in species responses, and a heightened need for interdisciplinary research to understand the factors associated with ecosystem resilience under future scenarios. Such research will help identify at-risk species or vulnerable localities and is crucial for informing environmental management and policymaking into the future.&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%">Franco, André L. C.</style></author><author><style face="normal" font="default" size="100%">Byron Adams</style></author><author><style face="normal" font="default" size="100%">Melisa A. Diaz</style></author><author><style face="normal" font="default" size="100%">Lemoine, Nathan P.</style></author><author><style face="normal" font="default" size="100%">Dragone, Nicholas B.</style></author><author><style face="normal" font="default" size="100%">Noah Fierer</style></author><author><style face="normal" font="default" size="100%">W. Berry Lyons</style></author><author><style face="normal" font="default" size="100%">Hogg, Ian D.</style></author><author><style face="normal" font="default" size="100%">Diana H. Wall</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Response of Antarctic soil fauna to climate‐driven changes since the Last Glacial Maximum</style></title><secondary-title><style face="normal" font="default" size="100%">Global Change Biology</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">biodiversity</style></keyword><keyword><style  face="normal" font="default" size="100%">climate change</style></keyword><keyword><style  face="normal" font="default" size="100%">glacial retreat</style></keyword><keyword><style  face="normal" font="default" size="100%">nematodes</style></keyword><keyword><style  face="normal" font="default" size="100%">Shackleton Glacier</style></keyword><keyword><style  face="normal" font="default" size="100%">soil invertebrates</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%">01/2022</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://onlinelibrary.wiley.com/doi/10.1111/gcb.15940</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">28</style></volume><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Understanding how terrestrial biotic communities have responded to glacial recession since the Last Glacial Maximum (LGM) can inform present and future responses of biota to climate change. In Antarctica, the Transantarctic Mountains (TAM) have experienced massive environmental changes associated with glacial retreat since the LGM, yet we have few clues as to how its soil invertebrate-dominated animal communities have responded. Here, we surveyed soil invertebrate fauna from above and below proposed LGM elevations along transects located at 12 features across the Shackleton Glacier region. Our transects captured gradients of surface ages possibly up to 4.5 million years and the soils have been free from human disturbance for their entire history. Our data support the hypothesis that soils exposed during the LGM are now less suitable habitats for invertebrates than those that have been exposed by deglaciation following the LGM. Our results show that faunal abundance, community composition, and diversity were all strongly affected by climate-driven changes since the LGM. Soils more recently exposed by glacial recession (as indicated by distances from present ice surfaces) had higher faunal abundances and species richness than older exposed soils. Higher abundances of the dominant nematode &lt;i&gt;Scottnema&lt;/i&gt; were found in older exposed soils, while &lt;i&gt;Eudorylaimus&lt;/i&gt;, &lt;i&gt;Plectus&lt;/i&gt;, tardigrades, and rotifers preferentially occurred in more recently exposed soils. Approximately 30% of the soils from which invertebrates could be extracted had only &lt;i&gt;Scottnema&lt;/i&gt;, and these single-taxon communities occurred more frequently in soils exposed for longer periods of time. Our structural equation modeling of abiotic drivers highlighted soil salinity as a key mediator of &lt;i&gt;Scottnema&lt;/i&gt; responses to soil exposure age. These changes in soil habitat suitability and biotic communities since the LGM indicate that Antarctic terrestrial biodiversity throughout the TAM will be highly altered by climate warming.&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%">Gutt, Julian</style></author><author><style face="normal" font="default" size="100%">Isla, Enrique</style></author><author><style face="normal" font="default" size="100%">Xavier, José C.</style></author><author><style face="normal" font="default" size="100%">Adams, Byron J.</style></author><author><style face="normal" font="default" size="100%">Ahn, In‐Young</style></author><author><style face="normal" font="default" size="100%">Cheng, C.‐H. Christina</style></author><author><style face="normal" font="default" size="100%">Colesie, Claudia</style></author><author><style face="normal" font="default" size="100%">Cummings, Vonda J.</style></author><author><style face="normal" font="default" size="100%">di Prisco, Guido</style></author><author><style face="normal" font="default" size="100%">Griffiths, Huw J.</style></author><author><style face="normal" font="default" size="100%">Ian Hawes</style></author><author><style face="normal" font="default" size="100%">Hogg, Ian D.</style></author><author><style face="normal" font="default" size="100%">McIntyre, Trevor</style></author><author><style face="normal" font="default" size="100%">Meiners, Klaus M.</style></author><author><style face="normal" font="default" size="100%">Pearce, David A.</style></author><author><style face="normal" font="default" size="100%">Lloyd S. Peck</style></author><author><style face="normal" font="default" size="100%">Piepenburg, Dieter</style></author><author><style face="normal" font="default" size="100%">Reisinger, Ryan R.</style></author><author><style face="normal" font="default" size="100%">Saba, Grace</style></author><author><style face="normal" font="default" size="100%">Schloss, Irene R.</style></author><author><style face="normal" font="default" size="100%">Signori, Camila N.</style></author><author><style face="normal" font="default" size="100%">Smith, Craig R.</style></author><author><style face="normal" font="default" size="100%">Vacchi, Marino</style></author><author><style face="normal" font="default" size="100%">Verde, Cinzia</style></author><author><style face="normal" font="default" size="100%">Diana H. Wall</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Antarctic ecosystems in transition – life between stresses and opportunities</style></title><secondary-title><style face="normal" font="default" size="100%">Biological Reviews</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">adaptation</style></keyword><keyword><style  face="normal" font="default" size="100%">benthic dynamism</style></keyword><keyword><style  face="normal" font="default" size="100%">biogeochemical cycles</style></keyword><keyword><style  face="normal" font="default" size="100%">climate change</style></keyword><keyword><style  face="normal" font="default" size="100%">invasion</style></keyword><keyword><style  face="normal" font="default" size="100%">new habitats</style></keyword><keyword><style  face="normal" font="default" size="100%">ocean acidification</style></keyword><keyword><style  face="normal" font="default" size="100%">Primary production</style></keyword><keyword><style  face="normal" font="default" size="100%">range shifts</style></keyword><keyword><style  face="normal" font="default" size="100%">sea ice</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">06/2021</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://onlinelibrary.wiley.com/doi/full/10.1111/brv.12679</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;Important findings from the second decade of the 21st century on the impact of environmental change on biological processes in the Antarctic were synthesised by 26 international experts. Ten key messages emerged that have stakeholder‐relevance and/or a high impact for the scientific community. They address (i) altered biogeochemical cycles, (ii) ocean acidification, (iii) climate change hotspots, (iv) unexpected dynamism in seabed‐dwelling populations, (v) spatial range shifts, (vi) adaptation and thermal resilience, (vii) sea ice related biological fluctuations, (viii) pollution, (ix) endangered terrestrial endemism and (x) the discovery of unknown habitats. Most Antarctic biotas are exposed to multiple stresses and considered vulnerable to environmental change due to narrow tolerance ranges, rapid change, projected circumpolar impacts, low potential for timely genetic adaptation, and migration barriers. Important ecosystem functions, such as primary production and energy transfer between trophic levels, have already changed, and biodiversity patterns have shifted. A confidence assessment of the degree of &amp;lsquo;scientific understanding&amp;rsquo; revealed an intermediate level for most of the more detailed sub‐messages, indicating that process‐oriented research has been successful in the past decade. Additional efforts are necessary, however, to achieve the level of robustness in scientific knowledge that is required to inform protection measures of the unique Antarctic terrestrial and marine ecosystems, and their contributions to global biodiversity and ecosystem services.&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%">Gemma E. Collins</style></author><author><style face="normal" font="default" size="100%">Hogg, Ian D.</style></author><author><style face="normal" font="default" size="100%">Convey, Peter</style></author><author><style face="normal" font="default" size="100%">Sancho, Leopoldo G.</style></author><author><style face="normal" font="default" size="100%">Cowan, Don A.</style></author><author><style face="normal" font="default" size="100%">W. Berry Lyons</style></author><author><style face="normal" font="default" size="100%">Byron Adams</style></author><author><style face="normal" font="default" size="100%">Diana H. Wall</style></author><author><style face="normal" font="default" size="100%">Allan Green, T. G.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Genetic diversity of soil invertebrates corroborates timing estimates for past collapses of the West Antarctic Ice Sheet</style></title><secondary-title><style face="normal" font="default" size="100%">Proceedings of the National Academy of Sciences</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">climate change</style></keyword><keyword><style  face="normal" font="default" size="100%">microarthropods</style></keyword><keyword><style  face="normal" font="default" size="100%">molecular clock</style></keyword><keyword><style  face="normal" font="default" size="100%">phylogeography</style></keyword><keyword><style  face="normal" font="default" size="100%">terrestrial biodiversity</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%">08/2020</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://www.pnas.org/content/early/2020/08/19/2007925117</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;During austral summer field seasons between 1999 and 2018, we sampled at 91 locations throughout southern Victoria Land and along the Transantarctic Mountains for six species of endemic microarthropods (Collembola), covering a latitudinal range from 76.0&amp;deg;S to 87.3&amp;deg;S. We assembled individual mitochondrial cyto-chrome &lt;em&gt;c&lt;/em&gt; oxidase subunit 1 (COI) sequences (&lt;em&gt;n&lt;/em&gt; = 866) and found high levels of sequence divergence at both small (&amp;lt;10 km) and large (&amp;gt;600 km) spatial scales for four of the six Collembola species. We applied molecular clock estimates and assessed genetic divergences relative to the timing of past glacial cycles, including collapses of the West Antarctic Ice Sheet (WAIS). We found that genetically distinct lineages within three species have likely been isolated for at least 5.54 My to 3.52 My, while the other three species diverged more recently (&amp;lt;2 My). We suggest that Collembola had greater dispersal opportunities under past warmer climates, via flotation along coastal margins. Similarly increased opportunities for dispersal may occur under contemporary climate warming scenarios, which could influence the genetic structure of extant populations. As Collembola are a living record of past landscape evolution within Antarctica, these findings provide biological evidence to support geological and glaciological estimates of historical WAIS dynamics over the last ca. 5 My.&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%">Echeverría, Sebastián</style></author><author><style face="normal" font="default" size="100%">Hausner, Mark B.</style></author><author><style face="normal" font="default" size="100%">Bambach, Nicolás</style></author><author><style face="normal" font="default" size="100%">Vicuña, Sebastián</style></author><author><style face="normal" font="default" size="100%">Suárez, Francisco</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Modeling present and future ice covers in two Antarctic lakes</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Glaciology</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">climate change</style></keyword><keyword><style  face="normal" font="default" size="100%">energy balance</style></keyword><keyword><style  face="normal" font="default" size="100%">ice and climate</style></keyword><keyword><style  face="normal" font="default" size="100%">ice-sheet modeling</style></keyword><keyword><style  face="normal" font="default" size="100%">lake ice</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%">02/2020</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://www.cambridge.org/core/journals/journal-of-glaciology/article/modeling-present-and-future-ice-covers-in-two-antarctic-lakes/9306439ADD5492BC05F3BAF0E076B1C3</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">66</style></volume><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Antarctic lakes with perennial ice covers provide the opportunity to investigate in-lake processes without direct atmospheric interaction, and to study their ice-cover sensitivity to climate condi- tions. In this study, a numerical model &amp;ndash; driven by radiative, atmospheric and turbulent heat fluxes from the water body beneath the ice cover &amp;ndash; was implemented to investigate the impact of climate change on the ice covers from two Antarctic lakes: west lobe of Lake Bonney (WLB) and Crooked Lake. Model results agreed well with measured ice thicknesses of both lakes (WLB &amp;ndash; RMSE= 0.11 m over 16 years of data; Crooked Lake &amp;ndash; RMSE= 0.07 m over 1 year of data), and had acceptable results with measured ablation data at WLB (RMSE= 0.28 m over 6 years). The differences between measured and modeled ablation occurred because the model does not consider interannual variability of the ice optical properties and seasonal changes of the lake&amp;rsquo;s thermal structure. Results indicate that projected summer air temperatures will increase the ice-cover annual melting in WLB by 2050, but that the ice cover will remain peren- nial through the end of this century. Contrarily, at Crooked Lake the ice cover becomes ephem- eral most likely due to the increase in air temperatures.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">255</style></issue></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%">Sherwell, Shasten S.</style></author><author><style face="normal" font="default" size="100%">Rachael M. Morgan-Kiss</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Response of microbial communities to climatic disturbances in Lake Bonney, McMurdo Dry Valleys, Antarctica</style></title></titles><keywords><keyword><style  face="normal" font="default" size="100%">climate change</style></keyword><keyword><style  face="normal" font="default" size="100%">McMurdo Dry Valleys</style></keyword><keyword><style  face="normal" font="default" size="100%">microbial communities</style></keyword><keyword><style  face="normal" font="default" size="100%">phytoplankton</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%">2020</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://rave.ohiolink.edu/etdc/view?acc_num=miami1595958688364877</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">Miami University</style></publisher><pub-location><style face="normal" font="default" size="100%">Oxford, OH</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;The McMurdo Dry Valleys is a polar desert ecosystem which composes the largest ice-free area in Antarctica, with the exception of perennially ice-covered lakes and ponds. The lakes in the valleys are the only landscape unit that support metabolic activity year-round. Recent increases in air temperature and solar radiation have led to a chain of disturbances altering the environmental conditions of these lakes. In this study, we test the impact of climatic disturbances on microbial communities in Lake Bonney, one of the lakes in the MDV. Through an integrated approach of combining field studies on natural communities in the lake (in situ) and laboratory experiments on algal isolates (ex situ), this study will attempt to understand how phytoplankton, eukaryal and bacterial communities respond to simulated disturbances. Results from the in situ experiments showed that the moat is a unique and stressful environment for under-ice communities and that under-ice shallow communities are highly sensitive to climatic disturbances. The ex situ experiments showed that certain phytoplankton species, like the chlorophytes, are more resistant to environmental alterations and thus will outcompete other phytoplankton species.&lt;/p&gt;</style></abstract><work-type><style face="normal" font="default" size="100%">masters</style></work-type></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%">Teufel, Amber G.</style></author><author><style face="normal" font="default" size="100%">Li, Wei</style></author><author><style face="normal" font="default" size="100%">Kiss, Andor J.</style></author><author><style face="normal" font="default" size="100%">Rachael M. Morgan-Kiss</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Impact of nitrogen and phosphorus on phytoplankton production and bacterial community structure in two stratified Antarctic lakes: a bioassay approach</style></title><secondary-title><style face="normal" font="default" size="100%">Polar Biology</style></secondary-title><short-title><style face="normal" font="default" size="100%">Polar Biol</style></short-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Algal–bacteria interactions</style></keyword><keyword><style  face="normal" font="default" size="100%">climate change</style></keyword><keyword><style  face="normal" font="default" size="100%">McMurdo Dry Valleys</style></keyword><keyword><style  face="normal" font="default" size="100%">Nutrient bioassay</style></keyword><keyword><style  face="normal" font="default" size="100%">Primary production</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">05/2017</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://link.springer.com/article/10.1007/s00300-016-2025-8</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">40</style></volume><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Arctic, Antarctic, and alpine ecosystems are recognized as sensors and sentinels of global change. As a consequence of their high sensitivity to minor climatic perturbations, permanently ice-covered lakes located in the McMurdo Dry Valleys (MDV), Antarctica, represent end members in the global network of inland bodies of water. Episodic climatic events in the form of increased summer glacial melt result in inputs of organic sediment and nutrients from glacial streams to these closed basins. Phytoplankton communities residing in the oligotrophic water columns are highly responsive to pulses in nutrient availability; however, there is a lack of understanding on whether specific phytoplankton groups are more competitive during a summer flood event and how shifts in the phytoplankton community may influence heterotrophic bacteria. A bioassay approach in 3-l bottles was used to investigate the influence of inorganic nitrogen and phosphorus availability on planktonic communities from the oligotrophic upper waters of two chemically distinct MDV lakes (Lakes Bonney and Fryxell) which differ in their external inputs and water column N/P stoichiometry. While microbial community responses varied between lakes and were nutrient-dependent, stimulation of phytoplankton biomass and productivity across all treatments was strongly linked with increased abundance of a single phytoplankton phylum (Chlorophyta). Despite stimulation of phytoplankton growth, primary and bacterial productivity was generally uncoupled; however, shifts in bacterial community diversity were observed in bioassays amended with either P or NP. We suggest that climate-associated increases in phytoplankton production and concomitant shifts in diversity will influence MDV bacterial community structure by altering the availability and composition of autochthonous carbon for heterotrophic production.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><section><style face="normal" font="default" size="100%">1007</style></section></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%">Teufel, Amber G.</style></author><author><style face="normal" font="default" size="100%">Rachael M. Morgan-Kiss</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Influence of abiotic drivers (light and nutrients) on photobiology and diversity of Antarctic lake phytoplankton communities</style></title><secondary-title><style face="normal" font="default" size="100%">Department of Microbiology</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antarctica</style></keyword><keyword><style  face="normal" font="default" size="100%">bacterial production</style></keyword><keyword><style  face="normal" font="default" size="100%">Chlamydomonas sp ICE MDV</style></keyword><keyword><style  face="normal" font="default" size="100%">Chlorophyll fluorescence</style></keyword><keyword><style  face="normal" font="default" size="100%">circadian rhythm</style></keyword><keyword><style  face="normal" font="default" size="100%">climate change</style></keyword><keyword><style  face="normal" font="default" size="100%">McMurdo Dry Valleys</style></keyword><keyword><style  face="normal" font="default" size="100%">nutrient amendment</style></keyword><keyword><style  face="normal" font="default" size="100%">photobiology</style></keyword><keyword><style  face="normal" font="default" size="100%">Primary production</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2016</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://rave.ohiolink.edu/etdc/view?acc_num=miami1468411564</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">Miami University</style></publisher><pub-location><style face="normal" font="default" size="100%">Oxford, OH</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;p&gt;Arctic, Antarctic, and alpine ecosystems are recognized as sensors and sentinels of global climate change. As a consequence of their high sensitivity to minor climatic perturbations, permanently ice-covered lakes located in the McMurdo Dry Valleys (MCM), Antarctica, represent end members in the global network of inland bodies of water. Episodic climatic events in the form of increased summer glacial melt result in inputs of organic sediment and nutrients from glacial streams to these closed basins. By better understanding how Antarctic lake communities respond to mimicked climate change, we can more accurately predict how they will react to further temperature changes in the future. We began by investigating the influence of inorganic nitrogen and phosphorus availability on planktonic communities residing in the oligotrophic upper waters of two chemically distinct MCM lakes (Lakes Bonney and Fryxell) which differ in their external inputs as well as water column N:P stoichiometry. Although microbial community responses varied between the lakes and were nutrient-dependent, stimulation of phytoplankton biomass and productivity across all treatments was strongly linked with increased abundance of a single phytoplankton phylum (Chlorophyta). Despite stimulation of phytoplankton growth, primary and bacterial productivity were largely uncoupled across all enrichments. We suggest that climate-associated shifts in phytoplankton diversity influence the bacterial community structure by altering the availability and composition of autochthonous carbon for heterotrophic production. To monitor the physiological adaptations that occur over time and depth, we then transplanted two dominant phytoplankton, &lt;em&gt;Chlamydomonas&lt;/em&gt; sp. ICE- MDV and &lt;em&gt;Isochrysis&lt;/em&gt; sp. MDV back into the Lake Bonney water column. Our results demonstrated that both organisms are specialists for surviving specific depths of the water column and are capable of acclimating to their native environment within a short period of time, and that the chlorophyte &lt;em&gt;Chlamydomonas&lt;/em&gt; sp. ICE-MDV most likely makes this adjustment via photoacclimation and accumulating chlorophyll-a per cell. The final study presented here investigated whether or not the dominant chlorophyte, &lt;em&gt;Chlamydomonas&lt;/em&gt; sp. ICE-MDV has retained the ability to respond to a diel 12-hour day/night cycle. Although light levels in MCM lakes remain low during the austral summers, daily irradiation varies by as much as tenfold during the course of the day, resulting in a circadian-like light cycle for organisms residing there. With decreased ice coverage on the lakes due to climate change and increased melt, it is likely that these light variations will become amplified over time. This study tested for the presence of a circadian rhythm under various light quality, light quantity, and temperature conditions and demonstrated that although a diel rhythm was maintained in terms of growth and several photochemical parameters, a true circadian rhythm was not identified. Although it is predicted that photosynthetic communities in polar regions will be more responsive to climate warming and episodic events, the complexity of these systems provides numerous challenges to understanding how these organism will adapt in the future.&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%">Tyler J. Kohler</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Diane M. McKnight</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">Physical and chemical controls on the abundance and composition of stream microbial mats from the McMurdo Dry Valleys, Antarctica</style></title><secondary-title><style face="normal" font="default" size="100%">Environmental Studies</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">algae</style></keyword><keyword><style  face="normal" font="default" size="100%">Antarctica</style></keyword><keyword><style  face="normal" font="default" size="100%">biological sciences</style></keyword><keyword><style  face="normal" font="default" size="100%">climate change</style></keyword><keyword><style  face="normal" font="default" size="100%">Disturbance</style></keyword><keyword><style  face="normal" font="default" size="100%">earth sciences</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></keywords><dates><year><style  face="normal" font="default" size="100%">2015</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://search.proquest.com/docview/1690497718?accountid=14503</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">University of Colorado</style></publisher><pub-location><style face="normal" font="default" size="100%">Boulder, CO</style></pub-location><volume><style face="normal" font="default" size="100%">Ph.D.</style></volume><pages><style face="normal" font="default" size="100%">272</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;div title=&quot;Page 4&quot;&gt;&lt;div&gt;&lt;div&gt;&lt;p&gt;The McMurdo Dry Valleys of Antarctica are a cold, dry desert, yet perennial microbial mats are abundant in the ephemeral glacial meltwater streams that flow during austral summers. Three types of mats are present (orange, black, and green), and are primarily comprised of filamentous cyanobacteria,&amp;nbsp;Nostoc, and chlorophytes, respectively. Mat types furthermore occupy distinct habitats within streams, utilizing the benthos, hyporheic zone, and water column, which expose them to different environmental conditions. Due to a lack of lateral inflows, allochthonous organic inputs, and negligible grazing activity, these streams are ideal for the controlled ecological study of microbial mats. Here, I investigated how mats will respond to physical disturbance, alterations in the hydrologic regime, and nutrient liberation from permafrost melt in the future. Specifically, I: 1) quantified and characterized the regrowth of mat biomass, community structure, and elemental stoichiometry after a scouring disturbance, 2) investigated how geomorphology and taxonomic identity influences the response of mat biomass to hydrologic regime in transects monitored over two decades, and 3) evaluated relationships between water chemistry and the elemental and isotopic composition of mat types over longitudinal and valley-wide gradients in Taylor Valley. I found that mats recovered ~20-50% of their biomass over the course of an austral summer following scour. Algal communities were significantly different in composition between disturbed and control treatments, but all samples naturally varied in species and elemental stoichiometry over the study period. When the long- term record of mat biomass was compared with hydrologic variables, stream channel mats (orange and green) had the greatest correlations, while marginal mats (black) showed weaker relationships with flow regime. Relationships also differed as a function of stream geomorphology, indicating the importance of substrata and gradient in conjunction with discharge. Lastly, mats showed unique elemental and isotopic compositions. Green and orange mats within the stream channel most reflected water column nutrient concentrations, while black mats showed significant nitrogen fixation. These results highlight the importance of taxonomic identity and habitat to modeling primary production here and elsewhere, and provide insight to how stream microbial mat communities are formed, maintained, and ultimately persist in an isolated polar desert.&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></records></xml>