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Antarctica is a highly interesting region for ecologists because of its extreme climatic conditions and the uniqueness of its species. In this article, we describe the trends in Antarctic ecological research participation by Latin American countries. In a survey of articles indexed by the ISI Web of Science, we searched under the categories ‘‘Ecology,’’ ‘‘Biodiversity Conservation’’ and ‘‘Evolutionary Biology’’ and found a total of 254 research articles published by Latin American countries. We classified these articles according to the country of affiliation, kingdom of the study species, level of biological organization and environment. Our main finding is that there is a steady increase in the relative contribution of Latin American countries to Antarctic ecological research. Within each category, we found that marine studies are more common than terrestrial studies. Between the different kingdoms, most studies focus on animals and most studies use a community approach. The leading countries in terms of productivity were Argentina, Chile and Brazil, with Argentina showing the highest rate of increase. Keywords: Antarctica; Argentina; Brazil; Chile; research trends; scientific productivity.

King George Island is the largest island and the principal area used for research bases in Antarctica. Argentina, Brazil, Chile, China, Poland, Russia, South Korea and Uruguay have permanent open bases on this island. Other countries have seasonal summer stations on different parts of this island, which demonstrates that human impact is strong on King George Island relative to other areas in the maritime and continental Antarctica. The objective of this work was to present a phytosociological approach for ice-free areas of Hennequin Point, eastern coast of Admiralty Bay, King George Island. The study started with the classification and description of the plant communities based primarily on phytosociological and biodiversity data. The area was mapped using an Astech Promark II® DGPS, yielding sub-metric precision after post-processing with software. The plant communities were described as follows: (1) lichen and moss cushion formation; (2) moss carpet formation; (3) fellfield formation; (4) grass and cushion chamaephyte formation; and (5) Deschampsia Antarctica–lichen formation. Characterizations and distributions of the plant communities are presented on a map at a scale of 1:5000. The plant communities found at Hennequin Point, in general, differ from those found in other areas of the Admiralty Bay region, probably because of the concentration of skua nests in the area and the relief singularities. We conclude by highlighting the importance of the study of plant species found in the ice-free areas of the Antarctic with respect to environmental monitoring and for evaluating global climate and environmental changes. Keywords: Plant communities mapping; lichens; mosses; flowering plants; Antarctic

The Antarctic terrestrial environment is under increasing pressure from human activities. The Fildes Region is characterized by high biodiversity, but is also a major logistic centre for the northern Antarctic Peninsula. Different interests, from scientific research, nature conservation, protection of geological and historical values, station operations, transport logistics and tourism, regularly overlap in space and time. This has led to increasing conflict among the multiple uses of the region and breaches of the legal requirements for environmental protection that apply in the area. The aim of this study was to assess the impacts of human activities in the Fildes Region by monitoring the distribution of bird and seal breeding sites and recording human activities and their associated environmental impacts. Data from an initial monitoring period 200306 were compared with data from 200810. We observed similar or increased levels of air, land and ship traffic, but fewer violations of overflight limits near Antarctic Specially Protected Area No. 150 Ardley Island. Open waste dumping and oil contamination are still major environmental impacts. Scientific and outdoor leisure activities undertaken by station personnel are more frequent than tourist activities and are likely to have a commensurate level of environmental impact. Despite the initial success of some existing management measures, it is essential that scientific and environmental values continue to be safeguarded, otherwise environmental impacts will increase and the habitat will be further degraded. We argue that the Fildes Region should be considered for designation as an Antarctic Specially Managed Area, a measure that has proven effective for environmental management of vulnerable areas of the Antarctic.

Affiliations of the dominant culturable bacteria isolated from Potter Cove, South Shetland Islands, Antarctica, were investigated together with their production of cold-active hydrolytic enzymes. A total of 189 aerobic heterotrophic bacterial isolates were obtained at 4°C and sorted into 63 phylotypes based on their amplified ribosomal DNA restriction analysis profiles. The sequencing of the 16S rRNA genes of representatives from each phylotype showed that the isolates belong to the phyla Proteobacteria (classes Alpha- and Gamma-proteobacteria), Bacteroidetes (class Flavobacteria), Actinobacteria (class Actinobacteria) and Firmicutes (class Bacilli). The predominant culturable group in the site studied belongs to the class Gammaproteobacteria, with 65 isolates affiliated to the genus Pseudoalteromonas and 58 to Psychrobacter. Among the 189 isolates screened, producers of amylases (9.5%), pectinases (22.8%), cellulases (14.8%), CM-cellulases (25.4%), xylanases (20.1%) and proteases (44.4%) were detected. More than 25% of the isolates produced at least one extracellular enzyme, with some of them producing up to six of the tested extracellular enzymatic activities. These results suggest that a high culturable bacterial diversity is present in Potter Cove and that this place represents a promising source of biomolecules. Keywords: Microbial enzymes; Antarctic bacteria; marine bacteria; cold enzymes; psychrophiles.

Bioremediation in cold climates is frequently regarded with skepticism. Owners of polluted sites and regulatory agencies may doubt the effectiveness of biological degradation at near freezing temperatures. While it is true that biodegradation rates decrease with decreasing temperatures, this does not mean that bioremediation is inappropriate for cold regions. Microbial degradation of hydrocarbons occurs even around 0 °C (Chapter 4). In remote alpine, Arctic, and Antarctic locations, excavation and shipping of contaminated soil may be prohibitively expensive. Bioremediation may be the most cost-effective alternative. This chapter discusses microbial adaptation to cold temperatures as well as results of laboratory and field studies of bioremediation at low temperatures.Microorganisms can grow at temperatures ranging from subzero to more than 100 °C. Microbes are divided into four groups based on the range of temperature at which they can grow. The psychrophiles grows at temperatures below 20 °C, the mesophiles between 20 °C and 44 °C, the thermophiles between 45 °C and 70 °C, and the hyperthermophiles require growth temperatures above 70 °C to over 110 °C. The term “cold-adapted microorganisms” (CAMs) is frequently used for describing bacteria growing at or close to zero degrees Celsius. Depending on the cardinal temperatures (the minimal, the optimal, and the maximum growth temperature), CAMs can be classified as psychrophiles or psychrotrophs. Morita's (1975) definition, which holds that psychrophiles have a maximum growth temperature of less than 20 °C and an optimal growth temperature of less than 15 °C, while psychrotrophs have a maximum temperature of 40 °C and an optimal growth temperature higher than 15 °C, is widely accepted.

Oil and fuel spills are among the most extensive and environmentally damaging pollution problems in cold regions and are recognized as potential threats to human and ecosystem health. It is generally thought that spills are more damaging in cold regions, and that ecosystem recovery is slower than in warmer climates (AMAP 1998; Det Norske Veritas 2003). Slow natural attenuation rates mean that petroleum concentrations remain high for many years, and site managers are therefore often forced to select among a range of more active remediation options, each of which involves a trade-off between cost and treatment time (Figure 11). The acceptable treatment timeline is usually dictated by financial circumstance, perceived risks, regulatory pressure, or transfer of land ownership.In situations where remediation and site closure are not urgent, natural attenuation is often considered an option. However, for many cold region sites, contaminants rapidly migrate off-site (Gore et al. 1999; Snape et al. 2006a). In seasonally frozen ground, especially in wetlands, a pulse of contamination is often released with each summer thaw (AMAP 1998; Snape et al. 2002). In these circumstances natural attenuation is likely not a satisfactory option. Simply excavating contaminants and removing them for off-site treatment may not be viable either, because the costs are often prohibitive and the environmental consequences of bulk extraction can equal or exceed the damage caused by the initial spill (Filler et al. 2006; Riser-Roberts 1998).

We examined deep-sea benthic data on polychaetes, isopods and bivalves from the Atlantic sector of the Southern Ocean. Samples were taken during the expeditions EASIZ II (1998), ANDEEP I and II (2002) (depth: 742-6,348 m). The range between sites varies from 3 to 1,900 km. Polychaetes (175 species in total) and isopods (383 species) had a high proportion of species restricted to one or two sites (72 and 70%, respectively). Bivalves (46 species) had a higher proportion of species represented at more sites. Beta diversity (Whittaker and Jaccard) was higher for polychaetes and isopods than for bivalves. The impact of depth on species richness was not consistent among groups; polychaetes showed a negative relationship to depth, isopods displayed highest richness in the middle depth range (2,000-4,000 m), whereas bivalves showed no clear relationship to depth. Species richness was not related to latitude (58-74 degrees S) or longitude (22-60 degrees W) for any group.

Our knowledge of the biodiversity of the Southern Ocean (SO) deep benthos is scarce. In this review, we describe the general biodiversity patterns of meio-, macro- and megafaunal taxa, based on historical and recent expeditions, and against the background of the geological events and phylogenetic relationships that have influenced the biodiversity and evolution of the investigated taxa. The relationship of the fauna to environmental parameters, such as water depth, sediment type, food availability and carbonate solubility, as well as species interrelationships, probably have shaped present-day biodiversity patterns as much as evolution. However, different taxa exhibit different large-scale biodiversity and biogeographic patterns. Moreover, there is rarely any clear relationship of biodiversity pattern with depth, latitude or environmental parameters, such as sediment composition or grain size. Similarities and differences between the SO biodiversity and biodiversity of global oceans are outlined. The high percentage (often more than 90%) of new species in almost all taxa, as well as the high degree of endemism of many groups, may reflect undersampling of the area, and it is likely to decrease as more information is gathered about SO deep-sea biodiversity by future expeditions. Indeed, among certain taxa such as the Foraminifera, close links at the species level are already apparent between deep Weddell Sea faunas and those from similar depths in the North Atlantic and Arctic. With regard to the vertical zonation from the shelf edge into deep water, biodiversity patterns among some taxa in the SO might differ from those in other deep-sea areas, due to the deep Antarctic shelf and the evolution of eurybathy in many species, as well as to deep-water production that can fuel the SO deep sea with freshly produced organic matter derived not only from phytoplankton, but also from ice algae.

We examined deep-sea epibenthic sledge isopod data from the Atlantic sector of the Southern Ocean (SO) (depth range=742–5,191 m). Samples were taken during the expeditions EASIZ II (ANT XV-3) in 1998 and ANDEEP I and II (ANT XIX3/4) in 2002. A total of 471 isopod species were recorded from 28 sites. The species richness of the epibenthic sledge samples was highly variable (6–82 species). Species richness was highest at site 131-3 in 3,053 m depth in the north-eastern Weddell Sea. The highest numbers of species were sampled in the middle depth range and lower species richness was found in the shallower and deeper parts of the study area. Depth is suggested to explain isopod species richness better than both latitude and longitude. Between 58°S and 65°S, the number of species ranged from 9 to 82 (mean=35.9). Further south in the Weddell Sea, between 73°S and 74°S, species richness was lower and the number of species ranged from 6 to 35 (mean=19.2). With regard to longitude, the highest species richness (up to 82 species) was found between 50°W and 60°W in the area of the South Shetland Islands and around the Antarctic Peninsula, while numbers did not exceed 50 species in the eastern Weddell Sea. The haul length, ranging from 807 to 6,464 m, was positively correlated with depth; however, there was no linear relationship between haul length and species richness. We therefore suggest that depth was the most important factor explaining isopod species richness. However, only 28 sites were visited and the statistical power is thus limited. Sampling in the deep sea is expensive and time consuming and as yet this is the best isopod data set available from the Atlantic sector of the SO. Future expeditions are therefore important to better explain the current patterns of benthic diversity in Antarctica.

Marine soft sediments comprise one of the largest and oldest habitats in the world, yet remarkably little is known about patterns of species richness. Here I present a short review of patterns of species richness and possible factors that influence such patterns. Species richness in general is remarkably high in both shallow coastal areas and the deep sea. However, there are clear differences the deep-sea has higher number of species for a given number of individuals than the coast. This can be explained by the larger amounts of primary production that reach coastal compared with deep-sea sediments, leading to higher numbers of individuals per unit area. Species density (the number of species per unit area) is also higher in the deep-sea than in coastal areas, but it is not obvious why this is so. Most studies of the broad patterns of species richness have used samples taken at small scales only. The problem with such analyses is that unless a large number of samples are taken, the true underlying pattern (or lack of it) may be wrongly interpreted. Recent studies have analysed species richness at larger scales. In general there seems to be a cline of increasing species richness from the Arctic to the tropics, but this is not the case in the southern hemisphere, where Antarctic species richness is high. However, it is not known whether high species richness in the Antarctic occurs at all spatial scales. To what extent these patterns are determined by evolutionary factors remains to be determined by the application of molecular methods. The available evidence suggests that environmental factors such as productivity, temperature, and sediment grain-size diversity play dominant roles in determining patterns of regional-scale species richness and patterns in species turnover, and it is probably the regional scale that primarily determines local species richness. KEYWORDS: Diversity · Deep sea · Coasts · Patterns · Scales

In the 1950s and 1960s, the first data sets were assembled to examine whether or not there was a latitudinal gradient of species richness in the sea. These data comprised very few species and were from very small areas. However, recent data from large species lists covering broad geographical ranges suggest strongly that there is a gradient of increasing species richness from the Arctic to the tropics. However, the Southern Ocean has high species richness and in the southern hemisphere there is no clear evidence of a cline of increasing richness from pole to tropic. The great richness of the Southern Ocean compared with the Arctic is probably due to its great age, the fact that it covers a much larger area and that it has higher structural heterogeneity formed by living organisms. The importance of area as a determinant of species richness needs to be studied in more detail since most studies have been confined to small areas. A number of hypotheses have been proposed to explain the species:area relationship and these are discussed. An alternative explanation for the latitudinal cline in the northern hemisphere is the energy-input hypothesis, but again this has not been adequately tested. Two studies on the relationship between local and regional species richness show a significant positive correlation. These findings suggest that local assemblages are not tightly organised and saturated with species but are open to recruitment from the regional species pool. Whether or not such a relationship holds in Antarctica is unknown. It is concluded that further studies of the Southern Ocean are likely to provide new findings fundamental to the "new" discipline of macroecology, which examines patterns and processes at the geographic scale.

Environmental seasonality is a critical factor in structuring polar marine ecosystems. The extensive data now available on the lipids of Arctic and Antarctic euphausiids show that all species are characterised by a seasonally high lipid content, and neutral lipids, whether wax esters or triacylglycerols, are primarily accumulated for reproduction. The Arctic Thysanoessa inermis and the Antarctic Euphausia crystallorophias contain high levels of wax esters and higher concentrations of 18:4(n-3) and 20:5(n-3) and a lower ratio of 18:1(n-9)/(n-7) fatty acids in their neutral lipids than the Arctic Thysanoessa raschii and the Antarctic Thysanoessa macrura and Euphausia superba. Large amounts of phytol in the lipids of T. raschii and E. crystallorophias during winter suggest the ingestion of decaying algae originating in sedimenting material or in sea ice. Thysanoessa raschii, T. macrura, and E. superba have a high ratio of 18:1(n-9)/ (n-7) fatty acids, indicating animal carnivory. We conclude that T. inermis and E. crystallorophias are true high polar herbivores, while T. raschii, T. macrura, and E. superba are omnivores with a more boreal distribution. The Arctic species Thysanoessa longicaudata and Meganyctiphanes norvegica are carnivores feeding on Calanus, as indicated by high amounts of 20:1(n-9) and 22:1(n-11) fatty acids.

Zooplankton samples were collected in January 1993 off Dronning Maud Land along a transect from open waters to the marginal ice zone close to the Antarctic ice shelf. Thysanoessa macrura was caught in open waters while Calanoides acutus and Calanus propinquus were mainly sampled between ice floes in the marginal ice zone. The “ice-krill”Euphausia crystallorophias was found over the shelf directly associated with ice floes. T. macrura had a lipid content up to 36% of its dry weight with the dominant lipid class, wax ester, accounting for 45–50% of the total lipid. The predominance of 18:1 fatty alcohols is the striking characteristic of the wax esters. Small specimens of E. crystallorophias had lipid levels up to 26% of their dry weight with, unexpectedly, triacylglycerols being the dominant lipid (up to 41% of total lipid). The small levels of wax esters in these animals (3–6% of total lipid) had phytol as a major constituent. Large specimens of E. crystallorophias had up to 34% of their dry weight as lipid, with wax esters (47% of total lipid) dominated by 16:0 and 14:0 fatty alcohols as the major lipid. Calanus propinquus had lipid levels of up to 34% of their dry weight, with triacylglycerols (up to 63% of total lipid) being the dominant lipid. High levels of 22:1 (n-9) fatty acid were present in the triacylglycerols. Calanoides acutus had lipid levels up to 35% of the dry weight with wax esters accounting for up to 83% of total lipid. High levels of (n-3) polyunsaturated fatty acids were recorded with 20:5(n-3), 22:6(n-3) and 18:4(n-3) being the dominant moieties. On the basis of their lipid compositions we deduce that: (1) Calanoides acutus is the strictest herbivore among the four species studied, heavily utilizing the typical spring bloom; (2) T. macrura is essentially omnivorous, probably utilizing the less defined bloom situations found in oceanic waters; (3) E. crystallorophias is an omnivore well adapted to utilize both a bloom situation and to feed on ice algae and micro-zooplankton associated with the ice; (4) Calanus propinquus seems to be the most opportunistic feeder of the four species studied, probably grazing heavily on phytoplankton during a bloom and, during the rest of the year, feeding on whatever material is available, including particulates, flagellates and other ice-associated algae. We conclude that the different biochemical pathways generating large oil reserves of different compositions, enabling species to utilize different ecological niches, are major determinants of biodiversity in polar zooplankton.

The growing salience of interactions between the functionally broad but geographically narrow regimes for the polar regions and the geographically broad but functionally specific regimes emerging to deal with global environmental changes directs attention to the issue of institutional interplay. Interplay among regimes can cause mutual interference or foster synergy. Adopting a pragmatic stance that assumes no fundamental changes in international society, this essay suggests ways to: (1) adapt global regimes dealing with ozone depletion, climate change and biodiversity to the conditions prevailing in the polar regions; and (2) ensure that concerns arising in the polar regions receive serious consideration in global forums. Specific suggestions range from modest initiatives involving monitoring and assessment to more ambitious initiatives, such as the establishment of a chamber of regions in global regimes.

Eight crabeater seals (Lobodon carcinophagus) (three females, five males), ranging in body mass between 125 and 220 kg, were captured off Queen Maud Land (70-72 degrees S, 7-16 degrees W) during the last week of February, just after moulting, and tagged with Argos satellite-linked dive recorders to provide data on location and diving depth and duration. During the first few weeks of March the seals were moving in the pack ice along the continental shelf edge, close to the coast of Queen Maud Land. In April and May, when the pack ice extended northwards, most of the seals moved north, one reaching 63 degrees S in late May. In the first half of June the two remaining seals turned south and moved back deep into the pack ice. The seals made about 150 dives per day each throughout the study period. Ninety percent of these were made to depths of less than 52 m. Individual maximum diving depths varied between 288 and 528 m. In March the seals were most active at night, when the dive depth was shallower than during the day. In April and May the seals were more active during day-time, with an absence of any diurnal change in diving depth. These results support the notion that crabeater seals predominantly feed on krill in Antarctic pack ice, even when winter returns to the waters off Queen Maud Land.

We present data on sexual dimorphism in some morphological measurements (wing length, head length, bill depth and bill length) in the Antarctic Petrel Thalassoica antarctica. Males were on average larger than females for all measurements. Sexual dimorphism was on average largest for bill depths whereas wing lengths discriminated least between the sexes. A discriminant function including bill depth, head length and wing length correctly sexed 92% of the sample. Due to between-measurer variation it is recommended that morphometric measurements obtained by others on sexed birds are compared with ours before proceeding with the use of the discriminant function on unsexed individuals.

Eleven fish species from the Weddell Sea (Antarctic) were examined for infestation with anisakid nematodes. Two species of the genus Contracaecum and the sealworm Pseudoterranova decipiens were isolated from the liver and the body cavity of fish affected. Only two specimens of P. decipiens (1.4%) partly invaded the belly flaps. The following fish species were infested by P. decipiens at the given prevalences: Cygnodraco mawsoni (74.4%), Trematomus scotti (23.2%), Pagetopsis maculatus (10.0%), Cryodraco antarcticus (7.1%), Trematomus lepidorhinus (3.0%), and Dolloidraco longedorsalis (2.7%). All of these, except Trematomus scotti, are new host records. Chaenodraco wilsoni, Chionodraco myersi, Gerlachea australis, Racovitzia glacialis and T. eulepidotus were not infested. The reasons for low prevalence and intensity of infestation are seen in the difficulties of P. decipiens in completing its benthic life cycle in the Weddell Sea environment, in the absence of shallow coastal waters due to the floating shelf-ice. Cygnodraco mawsoni is a crucial intermediate host, without which completion of the parasite life cycle might not be possible. In order to clarify the taxonomical position of Antarctic Pseudoterranova, morphological comparisons with specimens of P. decipiens from the German and Norwegian coast were made using scanning electron microscopy. Results revealed no differences; hence, all specimens studied belong to the same species P. decipiens.

Polar regions are covered by extensive sea ice that is inhabited by a variety of plants and animals. The environments where the organisms live vary depending on the structure and age of the ice. Many terms have been used to describe the habitats and the organisms. We here characterize the habitats and communities and suggest some standard terms for them. We also suggest routine sampling methods and reporting units for measurements of biological and chemical variables.