21 results on '"Dolores Deregibus"'
Search Results
2. Different feeding strategies in Antarctic scavenging amphipods and their implications for colonisation success in times of retreating glaciers
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Meike Anna Seefeldt, Gabriela Laura Campana, Dolores Deregibus, María Liliana Quartino, Doris Abele, Ralph Tollrian, and Christoph Held
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Southern Ocean ,King George Island/ Isla 25 de Mayo ,Potter Cove ,Succession ,Carrion-feeding ,Food web ,Zoology ,QL1-991 - Abstract
Abstract Background Scavenger guilds are composed of a variety of species, co-existing in the same habitat and sharing the same niche in the food web. Niche partitioning among them can manifest in different feeding strategies, e.g. during carcass feeding. In the bentho-pelagic realm of the Southern Ocean, scavenging amphipods (Lysianassoidea) are ubiquitous and occupy a central role in decomposition processes. Here we address the question whether scavenging lysianassoid amphipods employ different feeding strategies during carcass feeding, and whether synergistic feeding activities may influence carcass decomposition. To this end, we compared the relatively large species Waldeckia obesa with the small species Cheirimedon femoratus, Hippomedon kergueleni, and Orchomenella rotundifrons during fish carcass feeding (Notothenia spp.). The experimental approach combined ex situ feeding experiments, behavioural observations, and scanning electron microscopic analyses of mandibles. Furthermore, we aimed to detect ecological drivers for distribution patterns of scavenging amphipods in the Antarctic coastal ecosystems of Potter Cove. In Potter Cove, the climate-driven rapid retreat of the Fourcade Glacier is causing various environmental changes including the provision of new marine habitats to colonise. While in the newly ice-free areas fish are rare, macroalgae have already colonised hard substrates. Assuming that a temporal dietary switch may increase the colonisation success of the most abundant lysianassoids C. femoratus and H. kergueleni, we aimed to determine their consumption rates (g food x g amphipods−1 x day−1) and preferences of macroalgae and fish. Results We detected two functional groups with different feeding strategies among scavenging amphipods during carcass feeding: carcass ‘opener’ and ‘squeezer’. Synergistic effects between these groups were not statistically verified under the conditions tested. C. femoratus switched its diet when fish was not available by consuming macroalgae (about 0.2 day−1) but preferred fish by feeding up to 80% of its own mass daily. Contrary, H. kergueleni rejected macroalgae entirely and consumed fish with a maximal rate of 0.8 day−1. Conclusion This study reveals functional groups in scavenging shallow-water amphipods and provides new information on coastal intraguild niche partitioning. We conclude that the dietary flexibility of C. femoratus is a potential ecological driver and central to its success in the colonisation of newly available ice-free Antarctic coastal habitats.
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- 2017
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3. Implications of Glacial Melt-Related Processes on the Potential Primary Production of a Microphytobenthic Community in Potter Cove (Antarctica)
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Ralf Hoffmann, Adil Yousif Al-Handal, Angela Wulff, Dolores Deregibus, Katharina Zacher, María Liliana Quartino, Frank Wenzhöfer, and Ulrike Braeckman
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Antarctic benthic diatoms ,effects of sedimentation ,environmental photosynthetic active radiation ,primary production efficiency ,Southern Ocean ,oxygen flux ,Science ,General. Including nature conservation, geographical distribution ,QH1-199.5 - Abstract
The Antarctic Peninsula experiences a fast retreat of glaciers, which results in an increased release of particles and sedimentation and, thus, a decrease in the available photosynthetic active radiation (PAR, 400–700 nm) for benthic primary production. In this study, we investigated how changes in the general sedimentation and shading patterns affect the primary production by benthic microalgae, the microphytobenthos. In order to determine potential net primary production and respiration of the microphytobenthic community, sediment cores from locations exposed to different sedimentation rates and shading were exposed to PAR of 0–70 μmol photons m–2 s–1. Total oxygen exchange rates and microphytobenthic diatom community structure, density, and biomass were determined. Our study revealed that while the microphytobenthic diatom density and composition remained similar, the net primary production of the microphytobenthos decreased with increasing sedimentation and shading. By comparing our experimental results with in situ measured PAR intensities, we furthermore identified microphytobenthic primary production as an important carbon source within Potter Cove’s benthic ecosystem. We propose that the microphytobenthic contribution to the total primary production may drop drastically due to Antarctic glacial retreat and related sedimentation and shading, with yet unknown consequences for the benthic heterotrophic community, its structure, and diversity.
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- 2019
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4. Ensemble Modeling of Antarctic Macroalgal Habitats Exposed to Glacial Melt in a Polar Fjord
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Kerstin Jerosch, Frauke K. Scharf, Dolores Deregibus, Gabriela L. Campana, Katharina Zacher, Hendrik Pehlke, Ulrike Falk, H. Christian Hass, Maria L. Quartino, and Doris Abele
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seaweed distribution modeling ,bioclimatic ecosystem change ,distribution shift ,macroalgae summer production ,South Shetland Islands ,Antarctica ,Evolution ,QH359-425 ,Ecology ,QH540-549.5 - Abstract
Macroalgae are the main primary producers in polar coastal regions and of major importance for the associated heterotrophic communities. On King George Island/Isla 25 de Mayo, West Antarctic Peninsula (WAP) several fjords undergo rapid glacial retreat in response to increasing atmospheric temperatures. Hence, extended meltwater plumes laden with suspended particulate matter (SPM) are generated that hamper primary production during the austral summer season. We used ensemble modeling to approximate changes in the benthic productivity of an Antarctic fjord as a function of SPM discharge. A set of environmental variables was statistically selected and an ensemble of correlative species-distribution models was devised to project scattered georeferenced observation data to a spatial distribution of macroalgae for a “time of measurement” (“tom”) scenario (2008–2015). The model achieved statistically reliable validation results (true scale statistics 0.833, relative operating characteristics 0.975) and explained more than 60% of the modeled macroalgae distribution with the variables “hard substrate” and “SPM.” This “tom” scenario depicts a macroalgae cover of ~8% (63 ha) for the total study area (8 km2) and a summer production of ~350 t dry weight. Assuming a linear increase of meltwater SPM load over time, two past (1991 and 1998), and two future (2019 and 2026) simulations with varying SPM intensities were applied. The simulation using only 50% of the “tom” scenario SPM amount (simulating 1991) resulted in increased macroalgal distribution (143 ha) and a higher summer production (792 t) compared to the “tom” status and could be validated using historical data. Forecasting the year 2019 from the “tom” status, an increase of 25% SPM results in a predicted reduction of macroalgae summer production to ~60% (141 t). We present a first quantitative model for changing fjordic macroalgal production under continued melt conditions at WAP. As meltwater influenced habitats are extending under climate change conditions, our approach can serve to approximate future productivity shifts for WAP fjord systems. The reduction of macroalgal productivity as predicted for Potter Cove may have significant consequences for polar coastal ecosystems under continuing climate change.
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- 2019
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5. Evidence of macroalgal colonization on newly ice-free areas following glacial retreat in Potter Cove (South Shetland Islands), Antarctica.
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María Liliana Quartino, Dolores Deregibus, Gabriela Laura Campana, Gustavo Edgar Juan Latorre, and Fernando Roberto Momo
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Medicine ,Science - Abstract
Climate warming has been related to glacial retreat along the Western Antarctic Peninsula. Over the last years, a visible melting of Fourcade Glacier (Potter Cove, South Shetland Islands) has exposed newly ice-free hard bottom areas available for benthic colonization. However, ice melting produces a reduction of light penetration due to an increase of sediment input and higher ice impact. Seventeen years ago, the coastal sites close to the glacier cliffs were devoid of macroalgae. Are the newly ice-free areas suitable for macroalgal colonization? To tackle this question, underwater video transects were performed at six newly ice-free areas with different degree of glacial influence. Macroalgae were found in all sites, even in close proximity to the retreating glacier. We can show that: 1. The complexity of the macroalgal community is positively correlated to the elapsed time from the ice retreat, 2. Algae development depends on the optical conditions and the sediment input in the water column; some species are limited by light availability, 3. Macroalgal colonization is negatively affected by the ice disturbance, 4. The colonization is determined by the size and type of substrate and by the slope of the bottom. As macroalgae are probably one of the main energy sources for the benthos, an expansion of the macroalgal distribution can be expected to affect the matter and energy fluxes in Potter Cove ecosystem.
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- 2013
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6. Detection of the phycotoxin pectenotoxin-2 in waters around King George Island, Antarctica
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Gaston Osvaldo Almandoz, Dolores Deregibus, Irene R. Schloss, Nicole Trefault, Urban Tillmann, Bernd Krock, Marcelo Pablo Hernando, Mona Hoppenrath, and Julieta Antoni
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0106 biological sciences ,SOLID PHASE ADSORPTION TOXINS TRACKING (SPATT) ,HARMFUL ALGAE BLOOM (HAB) ,Harmful algae bloom (HAB) ,010504 meteorology & atmospheric sciences ,Biología ,01 natural sciences ,purl.org/becyt/ford/1 [https] ,Water column ,Abundance (ecology) ,LIQUID CHROMATOGRAPHY-TANDEM MASS SPECTROMETRY (LC–MS/MS) ,Ciencias Naturales ,14. Life underwater ,PROTISTAN PLANKTON COMMUNITY ,purl.org/becyt/ford/1.6 [https] ,Cove ,0105 earth and related environmental sciences ,DINOFLAGELLATES ,Phycotoxin ,geography ,geography.geographical_feature_category ,biology ,Solid phase adsorption toxins tracking (SPATT) ,010604 marine biology & hydrobiology ,Dinoflagellate ,Plankton ,biology.organism_classification ,Dinoflagellates ,Background level ,Protistan plankton community ,PHYCOTOXIN ,Oceanography ,Liquid chromatography-tandem mass spectrometry (LC–MS/MS) ,General Agricultural and Biological Sciences ,Dinophysis - Abstract
In order to set a base line for the observation of planktonic community changes due to global change, protistan plankton sampling in combination with phycotoxin measurements and solid phase adsorption toxin tracking (SPATT) was performed in two bays of King George Island (KGI) in January 2013 and 2014. In addition, SPATT sampling was performed in Potter Cove during a one-year period from January 2014 until January 2015. Known toxigenic taxa were not firmly identified in plankton samples but there was microscopical evidence for background level presence of Dinophysis spp. in the area. This was consistent with environmental conditions during the sampling periods, especially strong mixing of the water column and low water temperatures that do not favor dinoflagellate proliferations. Due to the lack of significant abundance of thecate toxigenic dinoflagellate species in microplankton samples, no phycotoxins were found in net tow samples. In contrast, SPATT sampling revealed the presence of dissolved pectenotoxin-2 (PTX-2) and its hydrolyzed form PTX-2 seco acid in both bays and during the entire one-year sampling period. The presence of dissolved PTX in coastal waters of KGI is strong new evidence for the presence of PTX-producing species, i.e., dinoflagellates of the genus Dinophysis in the area. The presence of phycotoxins and their respective producers, even at the low background concentrations found in this study, may be the seed of possible proliferations of these species under changing environmental conditions. Furthermore, phycotoxins can be used as chemotaxonomic markers for a very specific group of plankton thus allowing to track the presence of this group over time., Este artículo tiene una corrección (ver "Documentos relacionados")., Facultad de Ciencias Naturales y Museo
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- 2020
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7. Glacial melt disturbance shifts community metabolism of an Antarctic seafloor ecosystem from net autotrophy to heterotrophy
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Ann Vanreusel, Adil Y. Al-Handal, Francesca Pasotti, Dolores Deregibus, Ulrike Falk, Ralf Hoffmann, Nene Lefaible, Angela Wulff, Frank Wenzhöfer, Irene R. Schloss, Ulrike Braeckman, Anders Torstensson, and Susana Vázquez
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0106 biological sciences ,Food Chain ,010504 meteorology & atmospheric sciences ,QH301-705.5 ,Ecosystem ecology ,Oceans and Seas ,CLIMATE CHANGE ,Antarctic Regions ,Medicine (miscellaneous) ,Climate change ,Global Warming ,01 natural sciences ,Article ,General Biochemistry, Genetics and Molecular Biology ,Carbon cycle ,purl.org/becyt/ford/1 [https] ,Water column ,Microalgae ,Ecosystem ,14. Life underwater ,Glacial period ,Biology (General) ,purl.org/becyt/ford/1.6 [https] ,0105 earth and related environmental sciences ,Autotrophic Processes ,010604 marine biology & hydrobiology ,Climate-change ecology ,Ice ,Biology and Life Sciences ,Biogeochemistry ,Heterotrophic Processes ,15. Life on land ,POTTER COVE ,Biota ,CARBON BALANCE ,ANTARCTICA ,Oceanography ,13. Climate action ,Benthic zone ,Environmental science ,Seasons ,General Agricultural and Biological Sciences ,Environmental Monitoring - Abstract
Climate change-induced glacial melt affects benthic ecosystems along the West Antarctic Peninsula, but current understanding of the effects on benthic primary production and respiration is limited. Here we demonstrate with a series of in situ community metabolism measurements that climate-related glacial melt disturbance shifts benthic communities from net autotrophy to heterotrophy. With little glacial melt disturbance (during cold El Niño spring 2015), clear waters enabled high benthic microalgal production, resulting in net autotrophic benthic communities. In contrast, water column turbidity caused by increased glacial melt run-off (summer 2015 and warm La Niña spring 2016) limited benthic microalgal production and turned the benthic communities net heterotrophic. Ongoing accelerations in glacial melt and run-off may steer shallow Antarctic seafloor ecosystems towards net heterotrophy, altering the metabolic balance of benthic communities and potentially impacting the carbon balance and food webs at the Antarctic seafloor., Ulrike Braeckman et al. use in situ benthic community and benthic biogeochemistry measurements in Potter Cove on the Antarctic Peninsula to show that climate-related glacial melt disturbance shifts benthic communities from net autotrophy to heterotrophy. This study sheds light on how future glacial melt and run-off may affect the metabolic balance of Antarctic benthic communities.
- Published
- 2021
8. Antarctic harpacticoids exploit different trophic niches: a summer snapshot using fatty acid trophic markers (Potter Cove, King George Island)
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Marleen De Troch, Ann Vanreusel, Eva Werbrouck, Dirk Van Gansbeke, and Dolores Deregibus
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DYNAMICS ,0106 biological sciences ,PHYTOPLANKTON COMMUNITY ,Storage lipids ,Aquatic Science ,010603 evolutionary biology ,01 natural sciences ,Copepods ,HERBIVOROUS COPEPODS ,ALGAE ,Water column ,Copepoda [copepods] ,Ecosystem ,Harpacticoida ,Ecology, Evolution, Behavior and Systematics ,Trophic level ,Ecological niche ,STABLE-ISOTOPE ANALYSIS ,SOUTH SHETLAND ,CLIMATE-CHANGE ,Ecology ,biology ,010604 marine biology & hydrobiology ,fungi ,Biology and Life Sciences ,Epiphytic ,biology.organism_classification ,Food web ,Diet ,Benthic zone ,Earth and Environmental Sciences ,Polar ,FOOD-WEB ,PENINSULA ,Copepod ,LIPIDS - Abstract
Unraveling food webs is a first step toward understanding of ecosystem functioning and a requirement to forecast climate-induced ecosystem responses. In this study, the organisms under examination were benthic copepods (order Harpacticoida) inhabiting a fjord-like environment on the southern coastline of King George Island at the northwestern tip of the Antarctic Peninsula, one of the most rapidly warming regions on Earth. Despite increased understanding of Antarctic food web structures, little is known about the feeding ecology of benthic copepods in these systems. A fatty acid trophic marker strategy was used to unravel the diet composition of Antarctic harpacticoid copepod species or assemblages collected from distinct habitats in summer. Their diverse storage fatty acid composition revealed the occupation of different trophic niches associated with their specific lifestyles, i. e. endobenthic or epiphytic with (Alteutha spp.) or without (Harpacticus sp.) frequent water column excursions. Moreover, the prevalence of biosynthesized.7 long-chain monounsaturated fatty acids in Harpacticus sp. and.9 fatty acids in Alteutha spp. further suggested adaptations to particular habitats in polar ecosystems, as different dietary precursors-16: 1 omega 7 (microphytobenthos, epiphytic diatoms) or 18: 1.9 (flagellates)-fuel these elongation pathways.
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- 2017
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9. Life between tides: Spatial and temporal variations of an intertidal macroalgal community at Potter Peninsula, South Shetland Islands, Antarctica
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Maria Liliana Quartino, Leonardo A. Saravia, Gabriela Laura Campana, Dolores Deregibus, and María Laura Marcías
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0106 biological sciences ,Shetland ,010504 meteorology & atmospheric sciences ,Ecology ,010604 marine biology & hydrobiology ,Community structure ,Intertidal zone ,Aquatic Science ,Intertidal ecology ,Oceanography ,01 natural sciences ,Geography ,Habitat ,Benthos ,Species richness ,Transect ,0105 earth and related environmental sciences - Abstract
Intertidal zones are one of the most studied habitats in the world. However, in Antarctica, further studies are needed for a more complete understanding of these systems. When conspicuous Antarctic intertidal communities occur, macroalgae are a key component. Given that intertidal communities have a fast response to variations in environmental conditions and could reflect climate fluctuations, we conducted a non-destructive study with photographic transects in an intertidal zone at Potter Peninsula, Isla 25 de Mayo/King George Island, over four years and during five months of the warm season. We tested the general hypothesis that macroalgal intertidal communities are mainly structured by the vertical stress gradient and that changes in temperature between seasons and between years have a great influence in the macroalgal community structure. Spatial, seasonal and inter-annual variations were studied using GLM, quantile regression and NMDS ordinations. The vertical stress gradient was the main factor that explained macroalgal cover. The Low and the Middle level shared similarities, but the latter was more variable. The High level had the lowest cover, richness and diversity. The dominant species here was the endemic red alga Pyropia endiviifolia , which is strongly adapted to extreme conditions. At the Middle level, there was a significant increase in macroalgal cover during spring months, and it stabilized in summer. Inter-annual variations showed that there is a strong variation in the total macroalgal cover and community structure over the studied years. Environmental conditions have a significant effect in shaping the studied intertidal community, which is very sensitive to climate oscillations. An increase in temperature produced a decrease of annual ice foot cover, number of snow days and - as a result - an increase in macroalgal cover. In a global climate-change scenario, a shift in species composition could also occur. Species with wide physiological tolerance that grow in warmer conditions, like Palmaria decipiens , could benefit, while other species will be discriminated. More detailed studies are necessary to predict future changes in Antarctic intertidal communities.
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- 2017
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10. Carbon Balance Under a Changing Light Environment
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Fernando Momo, Katharina Zacher, Inka Bartsch, Gabriela Laura Campana, Iván Gómez, Christian Wiencke, Dolores Deregibus, and Maria Liliana Quartino
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0106 biological sciences ,chemistry.chemical_classification ,010504 meteorology & atmospheric sciences ,010604 marine biology & hydrobiology ,chemistry.chemical_element ,Biomass ,Atmospheric sciences ,Photosynthesis ,01 natural sciences ,Water column ,chemistry ,13. Climate action ,Photosynthetically active radiation ,Photosynthetic acclimation ,Environmental science ,Compounds of carbon ,14. Life underwater ,Turbidity ,Carbon ,0105 earth and related environmental sciences - Abstract
The natural environment of Antarctic seaweeds is characterized by changing seasonal light conditions. The ability to adapt to this light regime is one of the most important prerequisites for their ecological success. Thus, the persistence of seaweeds depends on their capacity to maintain a positive carbon balance (CB) for buildup of biomass over the course of the year. A positive CB in Antarctica occurs only during the ice-free period in spring and summer, when photosynthetically active radiation (PAR, 400–700 nm) penetrates deeply into the water column. The accumulated carbon compounds during this period are stored and remobilized to support metabolism for the rest of the year.
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- 2020
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11. Production and Biomass of Seaweeds in Newly Ice-Free Areas: Implications for Coastal Processes in a Changing Antarctic Environment
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Fernando Momo, Alicia L. Boraso, Leonardo A. Saravia, Carolina Veronica Matula, Dolores Deregibus, Maria Liliana Quartino, and Gabriela Laura Campana
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Biomass (ecology) ,Benthos ,Benthic zone ,Ecology ,Environmental science ,Marine ecosystem ,Ecosystem ,Pelagic zone ,Energy source ,Trophic level - Abstract
The Antarctic rocky coasts are mainly colonized by extensive seaweed communities, which play key roles as food resource, habitat, and refuge for many benthic and pelagic organisms. Due to climate warming, Antarctic marine ecosystems are being affected by glacier retreat opening new habitats, e.g., newly ice-free areas that can be colonized by macroalgae. As a consequence, primary production and fate of macroalgae are changing in these new polar environments. In these ecosystems, the carbon production, especially from large brown algae, is an important food source to the benthic invertebrate communities mainly when other resources are scarce. Thus, in new areas colonized by seaweeds, the trophic structure and biogeochemical fluxes can vary considerably. Moreover, when seaweeds die or are removed by water movement, ice scouring, or storms, they are detached, fragmented, and degraded, incorporating and releasing particulate and dissolved organic matter to the coastal food webs, i.e., they support a large fraction of the secondary production of the benthos. The present chapter is a review of the knowledge on seaweed biomass and production in the coastal Antarctic ecosystem opening a discussion on the role of these organisms as main energy sources in, e.g., small fjords and glacier-influenced sites, impacted by recent climatic change.
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- 2020
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12. Correction to: Detection of the phycotoxin pectenotoxin-2 in waters around King George Island, Antarctica
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Urban Tillmann, Nicole Trefault, Bernd Krock, Irene R. Schloss, Mona Hoppenrath, Julieta Antoni, Marcelo Pablo Hernando, Gaston Osvaldo Almandoz, and Dolores Deregibus
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Phycotoxin ,Oceanography ,Ecology (disciplines) ,George (robot) ,Biology ,General Agricultural and Biological Sciences - Abstract
A correction to this paper has been published: https://doi.org/10.1007/s00300-021-02834-3
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- 2021
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13. Implications of glacial melt-related processes on the potential primary production of a microphytobenthic community in Potter Cove (Antarctica)
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Ulrike Braeckman, Frank Wenzhöfer, Angela Wulff, Adil Y. Al-Handal, Dolores Deregibus, Ralf Hoffmann, Maria Liliana Quartino, and Katharina Zacher
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0106 biological sciences ,BIOVOLUME ,lcsh:QH1-199.5 ,primary production efficiency ,Antarctic benthic diatoms ,Ocean Engineering ,Aquatic Science ,lcsh:General. Including nature conservation, geographical distribution ,Oceanography ,SEDIMENT ,010603 evolutionary biology ,01 natural sciences ,MICROALGAE ,Ecosystem ,MACROALGAE ,lcsh:Science ,Southern Ocean ,Cove ,TEMPERATURE ,Water Science and Technology ,Global and Planetary Change ,geography ,geography.geographical_feature_category ,biology ,010604 marine biology & hydrobiology ,PHOTOSYNTHESIS ,fungi ,ICE ,Community structure ,Primary production ,Biology and Life Sciences ,environmental photosynthetic active radiation ,15. Life on land ,BENTHIC DIATOMS ,biology.organism_classification ,humanities ,carbon flux ,Diatom ,Photosynthetically active radiation ,Benthic zone ,Earth and Environmental Sciences ,Environmental science ,lcsh:Q ,effects of sedimentation ,Shading ,oxygen flux ,KING-GEORGE-ISLAND ,ASSEMBLAGE - Abstract
The Antarctic Peninsula experiences a fast retreat of glaciers, which results in an increased release of particles and sedimentation and, thus, a decrease in the available photosynthetic active radiation (PAR, 400-700 nm) for benthic primary production. In this study, we investigated how changes in the general sedimentation and shading patterns affect the primary production by benthic microalgae, the microphytobenthos. In order to determine potential net primary production and respiration of the microphytobenthic community, sediment cores from locations exposed to different sedimentation rates and shading were exposed to PAR of 0-70 mu.mol photons m(-2)s(-1). Total oxygen exchange rates and microphytobenthic diatom community structure, density, and biomass were determined. Our study revealed that while the microphytobenthic diatom density and composition remained similar, the net primary production of the microphytobenthos decreased with increasing sedimentation and shading. By comparing our experimental results with in situ measured PAR intensities, we furthermore identified microphytobenthic primary production as an important carbon source within Potter Cove's benthic ecosystem. We propose that the microphytobenthic contribution to the total primary production may drop drastically due to Antarctic glacial retreat and related sedimentation and shading, with yet unknown consequences for the benthic heterotrophic community, its structure, and diversity.
- Published
- 2019
14. Icebergs, sea ice, blue carbon and Antarctic climate feedbacks
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Maria Liliana Quartino, Dolores Deregibus, Andrew Fleming, Chester J. Sands, and David K. A. Barnes
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0106 biological sciences ,010504 meteorology & atmospheric sciences ,General Mathematics ,General Physics and Astronomy ,chemistry.chemical_element ,Climate change ,iceberg A68 ,7. Clean energy ,01 natural sciences ,Blue carbon ,Benthos ,Phytoplankton ,Sea ice ,14. Life underwater ,Southern Ocean ,blue carbon sink ,0105 earth and related environmental sciences ,geography ,geography.geographical_feature_category ,Continental shelf ,010604 marine biology & hydrobiology ,General Engineering ,benthos ,Articles ,15. Life on land ,Iceberg ,Oceanography ,climate change ,chemistry ,13. Climate action ,phytoplankton ,Environmental science ,Carbon ,Research Article - Abstract
Sea ice, including icebergs, has a complex relationship with the carbon held within animals (blue carbon) in the polar regions. Sea-ice losses around West Antarctica's continental shelf generate longer phytoplankton blooms but also make it a hotspot for coastal iceberg disturbance. This matters because in polar regions ice scour limits blue carbon storage ecosystem services, which work as a powerful negative feedback on climate change (less sea ice increases phytoplankton blooms, benthic growth, seabed carbon and sequestration). This resets benthic biota succession (maintaining regional biodiversity) and also fertilizes the ocean with nutrients, generating phytoplankton blooms, which cascade carbon capture into seabed storage and burial by benthos. Small icebergs scour coastal shallows, whereas giant icebergs ground deeper, offshore. Significant benthic communities establish where ice shelves have disintegrated (giant icebergs calving), and rapidly grow to accumulate blue carbon storage. When 5000 km2giant icebergs calve, we estimate that they generate approximately 106tonnes of immobilized zoobenthic carbon per year (t C yr−1). However, their collisions with the seabed crush and recycle vast benthic communities, costing an estimated 4 × 104 t C yr−1. We calculate that giant iceberg formation (ice shelf disintegration) has a net potential of approximately 106 t C yr−1sequestration benefits as well as more widely known negative impacts.This article is part of the theme issue ‘The marine system of the West Antarctic Peninsula: status and strategy for progress in a region of rapid change’.
- Published
- 2018
15. Different feeding strategies in Antarctic scavenging amphipods and their implications for colonisation success in times of retreating glaciers
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Maria Liliana Quartino, Meike Anna Seefeldt, Dolores Deregibus, Gabriela Laura Campana, Ralph Tollrian, Doris Abele, and Christoph Held
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0106 biological sciences ,Niche ,Carrion-feeding ,Notothenia coriiceps ,010603 evolutionary biology ,01 natural sciences ,Palmaria decipiens ,lcsh:Zoology ,King George Island/ Isla 25 de Mayo ,Desmarestia menziesii ,lcsh:QL1-991 ,14. Life underwater ,Southern Ocean ,Notothenia rossii ,Cove ,Succession ,Ecology, Evolution, Behavior and Systematics ,geography ,geography.geographical_feature_category ,biology ,Ecology ,010604 marine biology & hydrobiology ,Research ,Marine habitats ,Niche differentiation ,Food web ,biology.organism_classification ,Colonisation ,Notothenia ,Habitat ,Potter Cove ,Animal Science and Zoology - Abstract
Background: Scavenger guilds are composed of a variety of species, co-existing in the same habitat and sharing the same niche in the food web. Niche partitioning among them can manifest in different feeding strategies, e.g. during carcass feeding. In the bentho-pelagic realm of the Southern Ocean, scavenging amphipods (Lysianassoidea) are ubiquitous and occupy a central role in decomposition processes. Here we address the question whether scavenging lysianassoid amphipods employ different feeding strategies during carcass feeding, and whether synergistic feeding activities may influence carcass decomposition. To this end, we compared the relatively large species Waldeckia obesa with the small species Cheirimedon femoratus, Hippomedon kergueleni, and Orchomenella rotundifrons during fish carcass feeding (Notothenia spp.). The experimental approach combined ex situ feeding experiments, behavioural observations, and scanning electron microscopic analyses of mandibles. Furthermore, we aimed to detect ecological drivers for distribution patterns of scavenging amphipods in the Antarctic coastal ecosystems of Potter Cove. In Potter Cove, the climate-driven rapid retreat of the Fourcade Glacier is causing various environmental changes including the provision of new marine habitats to colonise. While in the newly ice-free areas fish are rare, macroalgae have already colonised hard substrates. Assuming that a temporal dietary switch may increase the colonisation success of the most abundant lysianassoids C. femoratus and H. kergueleni, we aimed to determine their consumption rates (g food x g amphipods−1 x day−1) and preferences of macroalgae and fish.Results: We detected two functional groups with different feeding strategies among scavenging amphipods during carcass feeding: carcass 'opener' and 'squeezer'. Synergistic effects between these groups were not statistically verified under the conditions tested. C. femoratus switched its diet when fish was not available by consuming macroalgae (about 0.2 day−1) but preferred fish by feeding up to 80% of its own mass daily. Contrary, H. kergueleni rejected macroalgae entirely and consumed fish with a maximal rate of 0.8 day−1.Conclusion: This study reveals functional groups in scavenging shallow-water amphipods and provides new information on coastal intraguild niche partitioning. We conclude that the dietary flexibility of C. femoratus is a potential ecological driver and central to its success in the colonisation of newly available ice-free Antarctic coastal habitats.
- Published
- 2017
16. Understanding the link between sea ice, ice scour and Antarctic benthic biodiversity; the need for cross station and nation collaboration
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Dolores Deregibus, Katharina Zacher, Gabriela Laura Campana, David K. A. Barnes, and Maria Liliana Quartino
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0106 biological sciences ,geography ,geography.geographical_feature_category ,010504 meteorology & atmospheric sciences ,Ecology ,010604 marine biology & hydrobiology ,Geography, Planning and Development ,Climate change ,Antarctic sea ice ,01 natural sciences ,Arctic ice pack ,Scuba diving ,Oceanography ,13. Climate action ,Benthic zone ,Sea ice ,General Earth and Planetary Sciences ,Environmental science ,Cryosphere ,14. Life underwater ,Seabed gouging by ice ,0105 earth and related environmental sciences - Abstract
The western Antarctic Peninsula (WAP) is a hotspot of rapid recent regional ‘climate change’. This has resulted in a 0.4°C rise in sea temperature in the last 50 years, five days of sea ice lost per decade and increased ice scouring in the shallows. The WAP shallows are ideal for studying the biological response to physical change because most known Antarctic species are benthic, physical change occurs mainly in the shallows and most research stations are coastal. Studies at Rothera Station have found increased benthic disturbance with losses of winter sea ice and assemblage-level changes coincident with this ice scouring. Such studies are difficult to scale up as they depend on SCUBA diving – a very spatially limited technique. Here we report attempts to broaden the understanding of benthic ecosystem responses to physical change by replicating the Rothera experimental grids at Carlini Station through collaboration between the UK, Argentina and Germany across Signy, Rothera and Carlini stations. We argue that such collaborations are the way forward towards understanding the big picture of biota responses to physical climate changes at a regional scale.
- Published
- 2017
17. Habitat modeling as a predictive tool for analyzing spatial shifts in Antarctic benthic communities due to global climate change
- Author
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Kerstin Jerosch, Gabriela Laura Campana, Hendrik Pehlke, Frauke Katharina Scharf, Ulrike Falk, Doris Abele, Maria Liliana Quartino, Dolores Deregibus, Christian Hass, and Katharina Zacher
- Subjects
Biomass (ecology) ,Ensemble forecasting ,Species distribution ,Environmental science ,Climate change ,Global change ,Spatial variability ,Physical geography ,Spatial distribution ,Environmental niche modelling - Abstract
Ensemble habitat modeling is a tool in the multivariate analysis of arbitrary species or community distribution which combines models of best fit to an optimized model (ensemble model, EM). To simulate spatial variation of communities and predict the impact of climate change, it is essential to identify the distribution-controlling factors. Macroalgae biomass production in polar regions is determined by environmental factors such as irradiance, which are modified under climate change impact. In coastal fjords of King George Island/Isla 25 de Mayo, Antarctica, suspended particulate matter (SPM) from glacial melting causes shading of algal communities during summer. Ten different species distribution models (SDMs) were applied to predict macroalgae distribution based on their statistical relationships with environmental variables. The suitability of the SDMs was assessed by two different evaluation methods. Those SDMs based on a multitude of decision trees such as Random Forest and Classification Tree Analysis reached the highest predictive ability followed by generalized boosted models and maximum-entropy approaches. We achieved excellent results for the current status EM (true scale statistics 0.833 and relative operating characteristics 0.975). The environmental variables hard substrate and SPM were identified as the best predictors explaining more than 60 % of the modelled distribution. Additional variables distance to glacier, total organic carbon, bathymetry and slope increased the explanatory power proved by cross-validation. Presumably, the SPM load of the meltwater streams on the Potter Peninsula will continue to increase at least linearly. We therefore coupled the EM with changing SPM conditions representing enhanced or reduced melt water input. Increasing SPM by 25% decreased predicted macroalgal coverage by approximately 38%. The ensemble species distribution modelling helps to identify the important factors controlling spatial distribution and can be used to link causes to effects in (Antarctic) coastal community change.
- Published
- 2017
- Full Text
- View/download PDF
18. Oxidative balance in macroalgae from Antarctic waters. Possible role of Fe
- Author
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Gabriela Fabiana Malanga, Paula Mariela González, Dolores Deregibus, Susana Puntarulo, Gabriela Laura Campana, Maria Liliana Quartino, and Katharina Zacher
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0106 biological sciences ,0301 basic medicine ,Ecology ,010604 marine biology & hydrobiology ,Otras Ciencias Biológicas ,Aquatic Science ,Biology ,01 natural sciences ,Fe ,Antioxidants ,Ciencias Biológicas ,03 medical and health sciences ,030104 developmental biology ,Macroalgae ,13. Climate action ,Oxidative stress ,Botany ,Lipid Radicals ,Antarctica ,Ecology, Evolution, Behavior and Systematics ,CIENCIAS NATURALES Y EXACTAS - Abstract
The hypothesis of this work was that exposure to diverse abiotic factors in two sites with different sediment and iron input (Peñón de Pesca: low impact; Island D: high impact, both areas in Potter Cove, King George Island, Antarctica) affects the physiological and oxidative profile of Gigartina skottsbergii and Himantothallus grandifolius. Daily metabolic carbon balance was significantly lower in both macroalgae from Island D compared to Peñón de Pesca. Lipid radical (LR) content was significantly higher in G. skottsbergii collected from Island D compared to Peñón de Pesca. In contrast, H. grandifolius showed significantly lower values in Island D compared to Peñón de Pesca. The β-carotene (β-C) content was significantly lower in G. skottsbergii from Island D compared to Peñón de Pesca, and the ratio LR/β-C showed a 6-fold increase in Island D samples compared to Peñón de Pesca. On the other hand, β-C content in H. grandifolius showed no significant differences between both areas. The LR/β-C content ratio in this alga was significantly lower (26%) in Island D as compared to Peñón de Pesca. Total iron content was significantly higher in both macroalgae from Island D compared to samples from Peñón de Pesca. Results with G. skottsbergii suggested changes in the oxidative cellular balance, probably related to the higher environmental iron in Island D as compared to Peñón de Pesca. The species H. grandifolius seems to be better adapted to the environmental conditions especially through a higher antioxidant capacity to cope with oxidative stress. Fil: González, Paula Mariela. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Bioquímica y Medicina Molecular. Universidad de Buenos Aires. Facultad Medicina. Instituto de Bioquímica y Medicina Molecular; Argentina Fil: Deregibus, Dolores. Ministerio de Relaciones Exteriores, Comercio Interno y Culto. Dirección Nacional del Antártico. Instituto Antártico Argentino; Argentina Fil: Malanga, Gabriela Fabiana. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Bioquímica y Medicina Molecular. Universidad de Buenos Aires. Facultad Medicina. Instituto de Bioquímica y Medicina Molecular; Argentina Fil: Campana, Gabriela Laura. Ministerio de Relaciones Exteriores, Comercio Interno y Culto. Dirección Nacional del Antártico. Instituto Antártico Argentino; Argentina. Universidad Nacional de Luján; Argentina Fil: Zacher, Katharina. Alfred Wegener Institute Helmholtz Centre for Polar and Marine Research; Alemania Fil: Quartino, Maria Liliana. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Museo Argentino de Ciencias Naturales ; Argentina. Ministerio de Relaciones Exteriores, Comercio Interno y Culto. Dirección Nacional del Antártico. Instituto Antártico Argentino; Argentina Fil: Puntarulo, Susana Ángela. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Bioquímica y Medicina Molecular. Universidad de Buenos Aires. Facultad Medicina. Instituto de Bioquímica y Medicina Molecular; Argentina
- Published
- 2017
19. Succession of Antarctic benthic algae (Potter Cove, South Shetland Islands): structural patterns and glacial impact over a four year period
- Author
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Fernando Momo, Christian Wiencke, Katharina Zacher, Dolores Deregibus, Maria Liliana Quartino, and Gabriela Laura Campana
- Subjects
0106 biological sciences ,Shetland ,geography ,geography.geographical_feature_category ,biology ,Ecology ,010604 marine biology & hydrobiology ,Sediment ,Glacier ,Ecological succession ,15. Life on land ,biology.organism_classification ,010603 evolutionary biology ,01 natural sciences ,Diatom ,Oceanography ,Photosynthetically active radiation ,14. Life underwater ,Glacial period ,General Agricultural and Biological Sciences ,Cove - Abstract
There is a general lack of information on the succession of marine benthic algae in Antarctica. We performed two colonization experiments in the upper subtidal (3 and 5 metres depth) using artificial substrates in Potter Cove (South Shetland Islands): in the outer cove, an area mainly unaffected by sedimentation, and in the inner cove, in close proximity to a retreating glacier, with high sediment inflow particularly during the melting season. Seasonal and interannual changes in total, diatom and macroalgal cover, species composition and ecological indexes were assessed over four years. Tiles were analysed in spring and summer in the laboratory and by year-round photographic monitoring. Irradiance (photosynthetically active radiation and ultraviolet radiation), salinity and temperature were monitored on a monthly basis. Benthic algae dominated the assemblages, with macroalgae reaching ~70% cover after two years. There were site and temporal differences in the contribution of diatom mats (mainly pennate forms) and macroalgal cover. Diatom cover was higher at the glacier-influenced site, particularly at the early stages, and decreased significantly with time. Between years, macroalgal assemblages changed significantly in a site-specific manner. Assemblages mainly comprised annual and pseudoperennial species at both sites, with absence of adult large Desmarestiales. Although a year separated the establishment of the two experiments, there were convergence patterns in the changes of cover over time - that seemed to be controlled by competitive interactions - and in the patterns of species replacement. However, the inner cove site exhibited lower number of macroalgal taxa and a tendency to decreased diversity over time that could be related to higher the level of stress and disturbance caused by glacial influence.
- Published
- 2017
20. Photosynthetic light requirements and vertical distribution of macroalgae in newly ice-free areas in Potter Cove, South Shetland Islands, Antarctica
- Author
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Katharina Zacher, Gabriela Laura Campana, Maria Liliana Quartino, Dolores Deregibus, Christian Wiencke, and Fernando Momo
- Subjects
0106 biological sciences ,geography ,geography.geographical_feature_category ,010504 meteorology & atmospheric sciences ,biology ,010604 marine biology & hydrobiology ,Glacier ,biology.organism_classification ,Spatial distribution ,01 natural sciences ,Salinity ,Oceanography ,Algae ,13. Climate action ,Photosynthetically active radiation ,Aquatic plant ,14. Life underwater ,Glacial period ,General Agricultural and Biological Sciences ,Cove ,0105 earth and related environmental sciences - Abstract
In Potter Cove, Antarctica, newly ice-free areas appeared due to glacial retreat. Simultaneously, the inflow of sediment increased, reducing underwater photosynthetically active radiation (PAR, 400–700 nm). The aim of this study was to determine the photosynthetic characteristics of two macroalgal species colonizing three newly ice-free areas, A1, A2 and A3, with increasing degree of glacial influence from A1 to A3. Turbidity, salinity and temperature were measured, and light attenuation coefficients (K d) calculated and considered as a proxy for glacial sediment input. The lower depth distribution of the red alga Palmaria decipiens and the brown alga Himantothallus grandifolius was 10 m in A3, 20 m in A2 and 30 m in A1. Both species were then collected, at 5 and 10 m at all areas. Photosynthetic parameters and the daily metabolic carbon balance (CB) were determined. K d was significantly higher in A3 compared with A1 and A2. The CB of P. decipiens was significantly higher in A1 followed by A2 and A3, and significantly higher at shallower than at greater depth. For H. grandifolius CB was significantly lower in A3 and in A2 at deeper depths compared with the rest of areas and depths. The lower distribution limit of the algae was positively correlated to the light penetration. An increase in the sediment run-off due to global warming might lead to an elevation of the lower depth distribution limit but retreating glaciers can open new space for macroalgal colonization. These changes will probably affect macroalgal primary productivity in Potter Cove with consequences for the coastal ecosystem.
- Published
- 2016
21. Evidence of macroalgal colonization on newly ice-free areas following glacial retreat in Potter Cove (South Shetland Islands), Antarctica
- Author
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Gustavo Edgar Juan Latorre, Gabriela Laura Campana, Maria Liliana Quartino, Fernando Momo, and Dolores Deregibus
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Geographic Mapping ,lcsh:Medicine ,Plant Science ,Global Change Ecology ,Oceans ,Desmarestia menziesii ,Geología ,Ice Cover ,Glacial period ,Photosynthesis ,lcsh:Science ,Multidisciplinary ,geography.geographical_feature_category ,Ecology ,Marine Ecology ,Biodiversity ,Plants ,Antarctic Ocean ,climate change ,Oceanography ,Community Ecology ,Benthic zone ,Energy source ,Research Article ,microbial colonization ,glacier ,Regiones Antárticas ,Algae ,Climate Change ,Antarctic Regions ,Climate change ,Marine Biology ,Biology ,Benthos ,Desmarestia anceps ,Water Movements ,Ciencias Naturales ,Community Structure ,Cove ,Demography ,Shetland ,Analysis of Variance ,geography ,lcsh:R ,greenhouse effect ,Glacier ,macroalga ,Seaweed ,Marine Environments ,Marine and aquatic sciences ,Earth sciences ,lcsh:Q ,Ecological Environments - Abstract
Climate warming has been related to glacial retreat along the Western Antarctic Peninsula. Over the last years, a visible melting of Fourcade Glacier (Potter Cove, South Shetland Islands) has exposed newly ice-free hard bottom areas available for benthic colonization. However, ice melting produces a reduction of light penetration due to an increase of sediment input and higher ice impact. Seventeen years ago, the coastal sites close to the glacier cliffs were devoid of macroalgae. Are the newly ice-free areas suitable for macroalgal colonization? To tackle this question, underwater video transects were performed at six newly ice-free areas with different degree of glacial influence. Macroalgae were found in all sites, even in close proximity to the retreating glacier. We can show that: 1. The complexity of the macroalgal community is positively correlated to the elapsed time from the ice retreat, 2. Algae development depends on the optical conditions and the sediment input in the water column; some species are limited by light availability, 3. Macroalgal colonization is negatively affected by the ice disturbance, 4. The colonization is determined by the size and type of substrate and by the slope of the bottom. As macroalgae are probably one of the main energy sources for the benthos, an expansion of the macroalgal distribution can be expected to affect the matter and energy fluxes in Potter Cove ecosystem., Facultad de Ciencias Naturales y Museo
- Published
- 2013
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