Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “Ice Cover”

Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 55 records · Page 3Linked to original sources

Paleolakes on Mars.

Observational evidence such as outflow channels and valley networks suggest that in the past there was flowing water on Mars. The images of fluvial features on Mars logically suggest that there must exist downstream locations in which the water pooled and the sediment load deposited (i.e. lakes). Sediments and morphological features associated with the martian paleolakes are believed to occur in Valles Marineris, and several large basins including Amazonis, Chryse and Elysium planitia. As Mars became progressively colder over geological time, any lakes on its surface would have become seasonally, and eventually perennially ice-covered. We know from polar lakes on Earth that ice-covered lakes can persist even when the mean annual temperature falls below freezing. Thus, the most recent lacustrine sediments on Mars were probably deposited in ice-covered lakes. While life outside of the Earth's atmosphere has yet to be observed, there is a general consensus among exobiologists that the search for extraterrestrial life should be based upon liquid water. The inference that there was liquid water on Mars during an earlier epoch is the primary motivation for considering the possibility of life during this time. It would be of enormous interest from both an exobiological and paleolimnological perspective to discover lakes or the evidence of former lakes on another planet such as Mars. Limnology would then become an interplanetary science.

Atmosphere↗

The structure and stability of the bacterioplankton community in Antarctic freshwater lakes, subject to extremely rapid environmental change.

In this study, variation in the bacterioplankton community structure of three Antarctic lakes of different nutrient status, was determined in relation to physical and chemical gradients at depth and at time intervals, across the seasonal transition from winter ice-cover to the summer ice-free period. The three lakes studied were: Moss Lake (low nutrient, with typical nutrient concentrations of 80 microg l(-1) nitrate and 10 microg l(-1) dissolved reactive phosphate), Sombre Lake (low nutrient, but becoming progressively enriched, with typical nutrient concentrations of 185 microg l(-1) nitrate and 7 microg l(-1) dissolved reactive phosphate) and Heywood Lake (enriched, with typical nutrient concentrations of 1180 microg l(-1) nitrate and 124 microg l(-1) dissolved reactive phosphate). Bacterioplankton community structure was determined using a combination of PCR amplification of 16S rRNA gene fragments and denaturing gradient gel electrophoresis (DGGE). Results indicated marked changes in this bacterioplankton community structure, which were particularly associated with the transition period. However, significant changes also occurred during the period of holomixis. Comparison of the results from lakes of different nutrient status suggest that increased levels of nutrient input, and in the timing and duration of ice cover will lead to marked changes in the structure and stability of the bacterioplankton community at existing levels of environmental change.

Antarctic Regions↗

Duration of liquid water habitats on early Mars.

We have employed a simple climate model of early Mars in order to estimate the duration of ice-covered lakes after the onset of freezing conditions on Mars. The critical parameter determining the existence of ice-covered lakes is the existence of peak seasonal temperatures above freezing. The peak temperature occurs at the subsolar point at perihelion. We use the weathering model of Pollack et al. (Icarus 71, 203-224, 1987) to compute the pressure and temperature evolution of the atmosphere. We have included the variability of the solar luminosity. We find that if there was a source of ice to provide meltwater, liquid water habitats could have been maintained under relatively thin ice covers for up to 700 million years after mean global temperatures fell below the freezing point. At this point, the mean annual temperature is 227 K, and the pressure of atmospheric CO2 is about 0.5 bar. Without the presence of stable bodies of liquid water, it is not clear what mechanisms were responsible for the removal of this remaining CO2. From a biological point of view, we find that the duration of liquid water habitats on early Mars exceeds the upper limit on the time required for the origin of life on Mars.

Atmosphere↗

Influence of ice and snow covers on the UV exposure of terrestrial microbial communities: dosimetric studies.

Bacillus subtilis spore biological dosimeters and electronic dosimeters were used to investigate the exposure of terrestrial microbial communities in micro-habitats covered by snow and ice in Antarctica. The melting of snow covers of between 5- and 15-cm thickness, depending on age and heterogeneity, could increase B. subtilis spore inactivation by up to an order of magnitude, a relative increase twice that caused by a 50% ozone depletion. Within the snow-pack at depths of less than approximately 3 cm snow algae could receive two to three times the DNA-weighted irradiance they would receive on bare ground. At the edge of the snow-pack, warming of low albedo soils resulted in the formation of overhangs that provided transient UV protection to thawed and growing microbial communities on the soils underneath. In shallow aquatic habitats, thin layers of heterogeneous ice of a few millimetres thickness were found to reduce DNA-weighted irradiances by up to 55% compared to full-sky values with equivalent DNA-weighted diffuse attenuation coefficients (K(DNA)) of >200 m(-1). A 2-mm snow-encrusted ice cover on a pond was equivalent to 10 cm of ice on a perennially ice covered lake. Ice covers also had the effect of stabilizing the UV exposure, which was often subject to rapid variations of up to 33% of the mean value caused by wind-rippling of the water surface. These data show that changing ice and snow covers cause relative changes in microbial UV exposure at least as great as those caused by changing ozone column abundance.

Antarctic Regions↗

Granular flow in the marginal ice zone.

The region of sea ice near the edge of the sea ice pack is known as the marginal ice zone (MIZ), and its dynamics are complicated by ocean wave interaction with the ice cover, strong gradients in the atmosphere and ocean and variations in sea ice rheology. This paper focuses on the role of sea ice rheology in determining the dynamics of the MIZ. Here, sea ice is treated as a granular material with a composite rheology describing collisional ice floe interaction and plastic interaction. The collisional component of sea ice rheology depends upon the granular temperature, a measure of the kinetic energy of flow fluctuations. A simplified model of the MIZ is introduced consisting of the along and across momentum balance of the sea ice and the balance equation of fluctuation kinetic energy. The steady solution of these equations is found to leading order using elementary methods. This reveals a concentrated region of rapid ice flow parallel to the ice edge, which is in accordance with field observations, and previously called the ice jet. Previous explanations of the ice jet relied upon the existence of ocean currents beneath the ice cover. We show that an ice jet results as a natural consequence of the granular nature of sea ice.

Complex Mixtures↗

Sediment oxygen profiles in a super-oxygenated antarctic lake.

Perennially ice-covered lakes are found in the McMurdo Dry Valleys of southern Victoria Land, Antarctica. In contrast to temperate lakes that have diurnal photic periods, antarctic (and arctic) lakes have a yearly photic period. An unusual feature of the antarctic lakes is the occurrence of O2 at supersaturated levels in certain portions of the water column. Here we report the first sediment O2 profiles obtained using a microelectrode from a perennially ice-covered antarctic lake. Sediment cores collected in January and October 1987 from Lake Hoare in Taylor Valley show oxygenation down to 15, and in some cases, 25 cm. The oxygenation of sediments several centimeters below the sediment-water interface is atypical for lake sediments and may be characteristic of perennially ice-covered lakes. There is a significant difference between the observed January and October sediment O2 profiles. Several explanations may account for the difference, including seasonality. A time-dependent model is presented which tests the feasibility of a seasonal cycle resulting from the long photoperiod and benthic primary production in sediments overlain by a highly oxygenated water column.

Antarctic Regions↗

Perennial N2 supersaturation in an Antarctic lake.

The dry valleys of southern Victoria Land in Antarctica contain several closed basins in which perennially ice-covered lakes are found. One of the most unusual features of these lakes is the occurrence of high O2 concentrations in the water column; values ranging from slightly more than saturation to more than four times saturation have been reported. Recently, we considered a bulk O2 budget for Lake Hoare, Antarctica, which led us to suggest that biological processes alone were not sufficient to explain the observed elevated oxygen levels. Consequently, there must be a non-biological source of O2. We suggested that this source results from the exclusion of O2 during the freezing of aerated meltstream water at the bottom of the ice cover, and predicted that this physical mechanism should also enhance the other atmospheric gases. Here we report the results of a study which, for the first time, documents the supersaturation of N2 in a lake. Dissolved N2 levels of 145% and 163% were determined from samples taken just below the ice cover and at a depth of 12 m, respectively. The relatively importance of biological and abiological sources is reflected in the ratio of N2 concentration to O2 concentration. In Lake Hoare this ratio was 1.20 at ice/water interface and 1.05 at 12 m; considerably different from the ratio in equilibrium with air (approximately 1.8). Based on these results, we have determined that about half of the net O2 production in the lake is the result of biological processes.

Antarctic Regions↗

Recent climate change in the Arctic and its impact on contaminant pathways and interpretation of temporal trend data.

The Arctic has undergone dramatic change during the past decade. The observed changes include atmospheric sea-level pressure, wind fields, sea-ice drift, ice cover, length of melt season, change in precipitation patterns, change in hydrology and change in ocean currents and watermass distribution. It is likely that these primary changes have altered the carbon cycle and biological systems, but the difficulty of observing these together with sporadic, incomplete time series makes it difficult to evaluate what the changes have been. Because contaminants enter global systems and transport through air and water, the changes listed above will clearly alter contaminant pathways. Here, we review what is known about recent changes using the Arctic Oscillation as a proxy to help us understand the forms under which global change will be manifest in the Arctic. For Pb, Cd and Zn, the Arctic is likely to become a more effective trap because precipitation is likely to increase. In the case of Cd, the natural cycle in the ocean appears to have a much greater potential to alter exposure than do human releases of this metal. Mercury has an especially complex cycle in the Arctic including a unique scavenging process (mercury depletion events), biomagnifying foodwebs, and chemical transformations such as methylation. The observation that mercury seems to be increasing in a number of aquatic species whereas atmospheric gaseous mercury shows little sign of change suggests that factors related to change in the physical system (ice cover, permafrost degradation, organic carbon cycling) may be more important than human activities. Organochlorine contaminants offer a surprising array of possibilities for changed pathways. To change in precipitation patterns can be added change in ice cover (air-water exchange), change in food webs either from the top down or from the bottom up (biomagnification), change in the organic carbon cycle and change in diets. Perhaps the most interesting possibility, presently difficult to predict, is combination of immune suppression together with expanding ranges of disease vectors. Finally, biotransport through migratory species is exceptionally vulnerable to changes in migration strength or in migration pathway-in the Arctic, change in the distribution of ice and temperature may already have caused such changes. Hydrocarbons, which tend to impact surfaces, will be mostly affected by change in the ice climate (distribution and drift tracks). Perhaps the most dramatic changes will occur because our view of the Arctic Ocean will change as it becomes more amenable to transport, tourism and mineral exploration on the shelves. Radionuclides have tended not to produce a radiological problem in the Arctic; nevertheless one pathway, the ice, remains a risk because it can accrue, concentrate and transport radio-contaminated sediments. This pathway is sensitive to where ice is produced, what the transport pathways of ice are, and where ice is finally melted-all strong candidates for change during the coming century. The changes that have already occurred in the Arctic and those that are projected to occur have an effect on contaminant time series including direct measurements (air, water, biota) or proxies (sediment cores, ice cores, archive material). Although these 'system' changes can alter the flux and concentrations at given sites in a number of obvious ways, they have been all but ignored in the interpretation of such time series. To understand properly what trends mean, especially in complex 'recorders' such as seals, walrus and polar bears, demands a more thorough approach to time series by collecting data in a number of media coherently. Presently, a major reservoir for contaminants and the one most directly connected to biological uptake in species at greatest risk-the ocean-practically lacks such time series.

Air Movements↗

Labile aluminium chemistry downstream a limestone treated lake and an acid tributary: effects of warm winters and extreme rainstorms.

The outlet from the limestone treated Lake Terjevann consisted mainly of well-mixed lake water (mean pH 6.1) during the ice-free seasons including the unusually warm winters of 1992 and 1993. However, during the ice-covered period acidic water (mean pH 4.8, mean inorganic aluminium (Al(i)) about 160 microg/l) from the catchment draining under the lake ice dominated. A downstream tributary was generally acid and rich in aluminium (mean pH 4.6, Al(i) about 230 microg/l). After an extreme rainstorm loaded with sea-salts cation exchange in the soil resulted in more than a doubling of the Al(i) concentration (reaching about 500 microg/l). It took 3-4 months until the Al(i) concentration returned to pre-event levels. During the ice-covered period, the acidic outlet and tributary waters resulted in acidic conditions below the confluence (pH<4.8, Al(i) about 150 microg/l) while during the ice-free periods the more neutral outlet water resulted in higher pH and lower Al(i) concentrations (pH>5.2, Al(i) about 95 microg/l). However, during the latter climatic conditions the water was most probably more harmful to fish due to hydrolysing and polymerizing aluminium. After the sea-salt event, the increased Al(i) concentration in the tributary made the zone below the confluence potentially more toxic (pH approximately 5, Al(i) approximately 250 microg/l). Expected global warming resulting in winter mean temperatures above 0 degrees C may eliminate the seasonal acidification of the outlet from limestone-treated lakes creating permanent toxic mixing zones in the confluence below acidic aluminium-rich tributaries. Besides, more frequent rainstorms as a consequence of global warming may increase the frequency of sea-salt events and the Al(i) concentrations in the mixing zones.

Aluminum↗

Contribution of winter to the annual CH4 emission from a eutrophied boreal lake.

The springtime methane (CH4) emission from a small, eutrophied boreal lake was assessed during the winter ice-cover by measurement of gas ebullition and CH4 accumulation in the water column in association with the development of oxygen depletion after ice formation. The winter CH4 production was estimated to result in a loss of 3.6-7.9 g CH4 m(-2) from the lake to the atmosphere during the short period of ice melt. This could account for 22-48% of the annual CH4 emission from the pelagic zone of the lake. The contribution of winter to the annual CH4 release can be similar or even higher in seasonally ice-covered northern aquatic ecosystems than in northern terrestrial wetlands, thus winter must be considered in any studies into the aquatic CH4 emissions. The trophic state and wintertime oxygen conditions, linked to the changes in land-use in the catchments and climate, are important factors controlling the springtime lake CH4 emissions.

Eutrophication↗

Sea-ice switches and abrupt climate change.

We propose that past abrupt climate changes were probably a result of rapid and extensive variations in sea-ice cover. We explain why this seems a perhaps more likely explanation than a purely thermohaline circulation mechanism. We emphasize that because of the significant influence of sea ice on the climate system, it seems that high priority should be given to developing ways for reconstructing high-resolution (in space and time) sea-ice extent for past climate-change events. If proxy data can confirm that sea ice was indeed the major player in past abrupt climate-change events, it seems less likely that such dramatic abrupt changes will occur due to global warming, when extensive sea-ice cover will not be present.

Climate↗

Perennial Antarctic lake ice: an oasis for life in a polar desert.

The permanent ice covers of Antarctic lakes in the McMurdo Dry Valleys develop liquid water inclusions in response to solar heating of internal aeolian-derived sediments. The ice sediment particles serve as nutrient (inorganic and organic)-enriched microzones for the establishment of a physiologically and ecologically complex microbial consortium capable of contemporaneous photosynthesis, nitrogen fixation, and decomposition. The consortium is capable of physically and chemically establishing and modifying a relatively nutrient- and organic matter-enriched microbial "oasis" embedded in the lake ice cover.

Antarctic Regions↗

Thickness of ice on perennially frozen lakes.

The dry valleys of southern Victoria Land, constituting the largest ice-free expanse in the Antarctic, contain numerous lakes whose perennial ice cover is the cause of some unique physical and biological properties. Although the depth, temperature and salinity of the liquid water varies considerably from lake to lake, the thickness of the ice cover is remarkably consistent, ranging from 3.5 to 6 m, which is determined primarily by the balance between conduction of energy out of the ice and the release of latent heat at the ice-water interface and is also affected by the transmission and absorption of sunlight. In the steady state, the release of latent heat at the ice bottom is controlled by ablation from the ice surface. Here we present a simple energy-balance model, using the measured ablation rate of 30 cm yr-1, which can explain the observed ice thickness.

Antarctic Regions↗

Modelling of temperature effects on removal efficiency and dissolved oxygen concentrations in stormwater ponds.

The performance of stormwater ponds, operated under winter conditions, was modelled using the commercial software Mike21 and MOUSE. Direct and indirect effects of changing temperature were investigated. The most important effect of winter conditions is the changed hydrology, characterised by long periods with no runoff followed by snowmelt events with large runoff volumes during several days. This gives lower removal efficiencies than during a period with the same precipitation but without winter conditions. For the concentration of dissolved oxygen, wind is an important factor. Consequently the most important effect of an ice cover on the pond is that it prevents the oxygenation effects of the wind. The direct temperature effects on the removal processes are negligible compared to the indirect effects in changed hydrology and forming of ice cover.

Climate↗

Ectoenzymatic ratios in relation to particulate organic matter distribution (Ross Sea, Antarctica).

The results of a study on ectoenzymatic activity (the enzyme activity bound to particles larger than 0.2 micro m) and its relation to organic particle concentration are reported here. The sampling was carried out during the 1994 Antarctic spring, at a fixed station (Station 11) in the polynya of the Ross Sea, an area characterized by quick changes in sea ice cover. The sampling was repeated 4 times over a 20-day time period. The particulate organic matter distribution followed the physical structure of the water column, which depends on ice dynamics and is mainly determined by salinity. In the mixed-water surface layer (0-50 m) the concentrations were higher (on average 65.6 micro gC/L) than in the deeper water layer (50 m-bottom) (on average 19.1 micro gC/L). This distribution and quality, expressed by the protein:carbohydrate ratio, linked the particulate organic matter to the phytoplanktonic bloom which was in progress in the area. We determined the kinetic parameters of the glycolytic and proteolytic ectoenzymes and also the total activity for the proteolytic enzyme, in order to evaluate the contribution of the particle-bound activity. We observed higher values in the surface layer than in the deeper layer. b-Glucosidase activity ranged between 0.03 and 0.92 nmol L(-1) h(-1); b-N-acetylglucosaminidase activity was in the range of 0.04-0.58 nmol (L-1) (h-1). The total proteolytic activity (leucine aminopeptidase) ranged between 0.85 and 33.71 nmol L(-1) (h-1). The ectoproteolytic activity was about 35-60% of the total. The Km values were slightly higher for the proteolytic activity (on average 0.43 micro M for ectoproteolytic activity and 0.58 micro M for total proteolytic activity) than for the b-glucosidase (on average 0.36 micro M) and b-N-acetylglucosaminidase (on average 0.17 micro M), showing no remarkable variations in the water column. The ectoenzymatic ratios and their relationship with particulate organic substrates confirm the close link between organic substrate availability and degradation system response. The significant and positive correlations are not specific and suggest a prompt and efficient systemic response to the input of trophic resources. Nevertheless, changes in ectoenzyme activity and synthesis may act as adaptive responses to changing features of the ecosystem. In particular, variations in the proteolysis:glycolysis ratio depend on the functional features of the ecological system. In our study area this ratio is higher (about 10 or more) during production (particularly autotrophic) and lower (about 5 or less) during degradation/consumption events. The analysis of previous data, collected over a larger area characterized by different environmental conditions due to the changes of the pack ice cover, during the same cruise, confirms the existence of a significant relationship. Furthermore, the analysis of enzyme-uptake systems, expressed as Vmax:Km ratio, suggests that glycolytic ectoenzymes, although poorly expressed, may encourage microconsumers to grow rapidly on a wide range of organic substrates, including the refractory ones such as cellulose and chitin. However, low ectoenzyme potential exploitation rates of available organic substrates (on average about 5% for glycolytic and 12% for proteolytic ectoenzymes) would suggest that, during spring, zooplankton grazing or vertical and lateral transport are likely to play an important role in the removal of organic materials from the system.

Antarctic Regions↗

Competition among penguins and cetaceans reveals trophic cascades in the western Ross Sea, Antarctica.

An apparent trophic cascade that appears during summer in the western Ross Sea, Antarctica, explains why the Antarctic silverfish (Pleuragramma antarcticum) there becomes cannibalistic; its principal prey, crystal krill (Euphausia crystallorophias) becomes scarce; and the diatom community is minimally grazed compared to adjacent areas. The krill is the major grazer of diatoms. On the basis of fieldwork at Ross Island, we suggest that the cascade results from foraging by unusually numerous Adélie Penguins (Pygoscelis adeliae), minke whales (Balaenoptera bonaerensis), and fish-eating killer whales (Orcinus orca). These species and other top predators apparently deplete the krill and silverfish. In drawing our conclusions, we were aided by two "natural experiments." In one "experiment," large, grounded icebergs altered the seasonal pattern of change in regional sea-ice cover, but not the seasonal change in penguin diet and foraging behavior that was also detected during the pre-iceberg era. In the other "experiment," a short-term polynya (opening in the ice) brought penguins and whales together in a confined area, this time altering both penguin diet and foraging behavior. We conclude that the foraging of penguins and whales, and not a formerly hypothesized seasonal decrease in sea-ice cover, explains (1) the annual switch in the penguins' prey from krill to silverfish, (2) the subsequent lengthening of penguin foraging trips, and (3) a marked decline of cetaceans in the area later in the season. Reduction in the middle-trophic-level prey is expressed in the relaxed grazing pressure on phytoplankton.

Animals↗