<?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%">Rachael M. Morgan-Kiss</style></author><author><style face="normal" font="default" size="100%">Popson, Devon</style></author><author><style face="normal" font="default" size="100%">Pereira, Rochelle</style></author><author><style face="normal" font="default" size="100%">Dolhi-Binder, J</style></author><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%">Kalra, Isha</style></author><author><style face="normal" font="default" size="100%">Sherwell, Shasten S.</style></author><author><style face="normal" font="default" size="100%">Reynebeau, Emily</style></author><author><style face="normal" font="default" size="100%">Cristina D. Takacs-Vesbach</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Sentinel protist taxa of the McMurdo Dry Valley lakes, Antarctica: A review</style></title><secondary-title><style face="normal" font="default" size="100%">Frontiers in Ecology and Evolution</style></secondary-title><short-title><style face="normal" font="default" size="100%">Front. Ecol. Evol.</style></short-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antarctica</style></keyword><keyword><style  face="normal" font="default" size="100%">Disturbance</style></keyword><keyword><style  face="normal" font="default" size="100%">McMurdo Dry Valley lakes</style></keyword><keyword><style  face="normal" font="default" size="100%">phytoplankton</style></keyword><keyword><style  face="normal" font="default" size="100%">protist</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%">03/2024</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://www.frontiersin.org/articles/10.3389/fevo.2024.1323472</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">1323472</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;High-latitude meromictic lakes such as those in the Antarctic McMurdo Dry Valleys (MDV) harbor aquatic ecosystems dominated by the microbial loop. Within this habitat, which is limited year-round by light and nutrients, protists, or single celled eukaryotes, play outsized roles in the food web as the dominant primary producers and the apex predators. Thus, the MDV lake ecosystem represents an ideal system to study the role of sentinel protist taxa in carbon and nutrient cycling. The perennially ice-covered lakes are part of the McMurdo Long Term Ecological Research (McM LTER; mcmlter.org) established in 1993. In this review we will highlight the diversity and trophic roles of the MDV lake protist community and compare environmental factors driving spatiotemporal patterns in key protist taxa in two lakes within the McM LTER, Lakes Bonney and Fryxell. We will then discuss lessons learned from manipulated experiments on the impact of current and future climate-driven environmental change on sensitive protist taxa. Last, we will integrate knowledge gained from 25 years of lab-controlled experiments on key photosynthetic protists to extend our understanding of the function of these extremophiles within the MDV aquatic food webs. Our research group has studied the distribution and function of the MDV microbial community for nearly two decades, training the next generation of scientists to tackle future problems of these globally significant microbes. This review article will also highlight early career scientists who have contributed to this body of work and represent the future of scientific understanding in the Anthropocene.&lt;/p&gt;</style></abstract></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>5</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%">Physiological and Biochemical Adaptations of Psychrophiles</style></title><secondary-title><style face="normal" font="default" size="100%">Extremophiles</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2018</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://www.taylorfrancis.com/books/e/9781498774932/chapters/10.1201%2F9781315154695-9</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">CRC Press</style></publisher><pub-location><style face="normal" font="default" size="100%">Boca Raton</style></pub-location><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;The cold biosphere encompasses many microorganism-dominated habitats that rely on light-dependent primary production. Within these environments, there are numerous physical and chemical factors limiting metabolism and growth that the microorganisms must overcome. The psychrophilic microorganisms discussed herein integrate a complex spectrum of adaptive strategies to survive these physiological challenges, including genome evolution, enzyme structure and catalysis rate changes, cryoprotectant formation, and a multitude of photosynthetic adaptations. Psychrophilic organisms also hold the key to biotechnical advances and the future, such that psychrophilic enzymes are used for everything from laboratory reagents and industrial work to medical research and environmental sustainability. Researchers have learned to exploit psychrophiles&amp;rsquo; efficiency at low temperatures (i.e., cooler washing machines and energy-saving, cost-effective enzyme production), their higher energy activity (thus allowing lower concentrations of needed catalysts, reducing costs and procedure time), and their ability to contribute to hydrocarbon bioremediation. Although psychrophilic microbes exist in numerous habitats and undergo various adaptive strategies, an understanding of what makes an organism psychrophilic is still unknown in a large majority of cold-adapted organisms, and thus future investigations are needed regarding cold adaptation and their biotechnological potential. Even as research has increased over the last decade, new technological advances and high-throughput DNA sequencing will continue to provide information about cold adaptation or the mechanisms needed for survival in a changing world.&lt;/p&gt;</style></abstract><section><style face="normal" font="default" size="100%">9</style></section></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></records></xml>