Abstract:Cadmium toxicity to 3 marine and brackish-water nematodes (Monhystera microphthalma, M. disjuncta, Pellioditis marina) was estimated under static tests. These nematodes are very resistant to cadmium poisoning. LC 50 values are extremely time-dependent; an exposure time of 96 h underestimates the degree of toxicity. For M. rnicrophthalrna LC 50 values decreased from 23.6 ppm after 96 h to 5.4 ppm after 312 h. For M. disjuncta LC 50 values were 21.2 and 18.4 ppm after 192 and 264 h respectively. P. marina was mu… Show more
“…It has been suggested that marine nematodes do not accumulate lipids for energy storage [27] indicating that nematode fatty acid composition reflects membrane fatty acid composition, however, information remains scant. In this study we will focus on the marine free-living nematode Halomonhystera disjuncta (formerly known as Geomonhystera disjuncta), which is known for its high resistance to environmental stress, especially to heavy metals and temperature changes [25,[75][76][77]. H. disjuncta and sister species has been reported both in shallow-water [15,47,74] and in deep-sea environments [53,71].…”
The deep-sea free-living nematode Halomonhystera hermesi, dominant in the sulphidic sediments of the Håkon Mosby mud volcano (1280 m, Barent sea slope), is part of the mainly estuarine Halomonhystera disjuncta species complex consisting of five cryptic species (GD1-GD5). Cryptic species have a very similar morphology raising questions on their specific environmental differences. This study analyzed total fatty acid (FA) compositions of H. hermesi and GD1, one of H. hermesi's closest relatives. Additionally, we experimentally investigated the effect of a temperature reduction, salinity increase and sulphide concentrations on GD1's FA composition. Because nematodes are expected to have low amounts of storage FA, total FA compositions most likely reflect FA contents of cellular membranes. The deep-sea nematode H. hermesi had significantly lower saturation levels and increased highly unsaturated fatty acid (HUFAs) proportions due to the presence of docosahexanoic acid (DHA-22:6ω3) and higher eicosapentaenoic acid (EPA-20:5ω3) proportions. HUFAs were absent in H. hermesi's food source indicating the ability and need for this nematode to synthesize HUFAs in a deep-sea environment. Our experimental data revealed that only a decrease in temperature resulted in lower saturated fatty acids proportions, indicating that the FA content of H. hermesi is most likely a response to temperature but not to sulphide concentrations or salinity differences. In experimental nematodes, EPA proportions were low and DHA was absent indicating that other factors than temperature, salinity and sulphides mediate the presence of these HUFAs in H. hermesi.
“…It has been suggested that marine nematodes do not accumulate lipids for energy storage [27] indicating that nematode fatty acid composition reflects membrane fatty acid composition, however, information remains scant. In this study we will focus on the marine free-living nematode Halomonhystera disjuncta (formerly known as Geomonhystera disjuncta), which is known for its high resistance to environmental stress, especially to heavy metals and temperature changes [25,[75][76][77]. H. disjuncta and sister species has been reported both in shallow-water [15,47,74] and in deep-sea environments [53,71].…”
The deep-sea free-living nematode Halomonhystera hermesi, dominant in the sulphidic sediments of the Håkon Mosby mud volcano (1280 m, Barent sea slope), is part of the mainly estuarine Halomonhystera disjuncta species complex consisting of five cryptic species (GD1-GD5). Cryptic species have a very similar morphology raising questions on their specific environmental differences. This study analyzed total fatty acid (FA) compositions of H. hermesi and GD1, one of H. hermesi's closest relatives. Additionally, we experimentally investigated the effect of a temperature reduction, salinity increase and sulphide concentrations on GD1's FA composition. Because nematodes are expected to have low amounts of storage FA, total FA compositions most likely reflect FA contents of cellular membranes. The deep-sea nematode H. hermesi had significantly lower saturation levels and increased highly unsaturated fatty acid (HUFAs) proportions due to the presence of docosahexanoic acid (DHA-22:6ω3) and higher eicosapentaenoic acid (EPA-20:5ω3) proportions. HUFAs were absent in H. hermesi's food source indicating the ability and need for this nematode to synthesize HUFAs in a deep-sea environment. Our experimental data revealed that only a decrease in temperature resulted in lower saturated fatty acids proportions, indicating that the FA content of H. hermesi is most likely a response to temperature but not to sulphide concentrations or salinity differences. In experimental nematodes, EPA proportions were low and DHA was absent indicating that other factors than temperature, salinity and sulphides mediate the presence of these HUFAs in H. hermesi.
“…Nonselective deposit-feeders and omnivores are extremely nonsensitive, they can rapidly increase their density by completely changing the trophic structure of the nematocene. Such structural alteration has been reported for heavily polluted areas of the North Sea where bottom sediments are inhabited by impoverished communities of nematodes composed almost entirely of nonselective deposit-feeding and omnivorous species [30], in ports of the Sea of Japan [16,17], and in microcosm experiments [14,24].…”
Section: Resultsmentioning
confidence: 97%
“…Cuticular adsorption and the absorption of heavy metals cause increased metal contents in the hypoderm [19]. The external part of the three-layer cuticle consists of collagenlike material secreted by nematodes, which contains disulfide bonds that support its tertiary structure and sulfhydric groups ensuring heavy metal binding and detoxification [10,19,21,30].…”
Municipal and anthropogenic inputs into the ports of Peter the Great Bay have led to foci of local-and regional-scale pollution where the natural course of biological processes is disturbed [3]. Here, the content of heavy metals in the bottom sediments, pore water, and near-bottom water is far higher than in the water column [17,28]. High environmental levels of heavy metals cause metal accumulation by aquatic organisms [13].Study of heavy metal accumulation by bottom organisms and metal toxicity in the biota is part of the study of pollution effects on aquatic ecosystems. Up to now, the interaction of bottom biota and pollutants (particularly heavy metals) has largely been examined for microorganisms [12,15], phyto-and zooplankton [7], and seston-feeding [8,15] and fouling organisms [4,5]. Small representatives of the infauna have not been investigated [1,28] in this respect. Polychaetes and round worms are the major functional components of the biota in the bottom sediments. They can build up a significant biomass and play an important role in the transformation of organic compounds of the sea bottom [7,18]. However, the mechanism of the effect of pollution on the metabolism and numbers of marine bottom communities is inadequately known.The aim of this study was to determine the heavy metals contents in the tissues of dominant species of the benthos and in the bottom sediments of chronically polluted areas.
MATERIALS AND METHODSSamples of silt sediments were collected in 2000-2003 in Zolotoi Rog Bay (Sea of Japan) near the port of Vladivostok from the 13 m depth at Wharf no. 44. Animals were collected from samples in Zolotoi Rog Bay and Vostok Bay in 2003.Sediment samples were washed with seawater through gauze (mesh size 0.1 × 0.1 mm). Sediment was placed in petri dishes and examined, by parts, under a stereomicroscope for the presence of bottom worm. Worms were isolated and sorted into species. Two to 100 specimens (lengths of 9-100 mm) of each species were taken for heavy metal analyses. To remove sediment particles, the worms were washed with seawater and then placed for 1-4 days in separate vessels with filtered seawater to purge the intestine.For each species, the measurements of the heavy metal concentrations were made in three samples with the number of worms depending on their size. For atomic absorption analysis, worm samples were prepared using the method of acid mineralization according to standard procedure GOST 26929-94 [2]. Wet tis-ECOLOGY Abstract -Data on heavy metal contents in polychaetes and free-living nematodes inhabiting the bottom sediments of Zolotoi Rog Bay near the port of Vladivostok are reported. Chronically high contents of heavy metals (Fe, Cu, Zn, and Cd) were found in the bottom sediments and in the infauna. The levels of some toxic elements in tissues of the polychaete Dorvillea (Schistomeringos) japonica inhabiting polluted sediments of Zolotoi Rog Bay were higher than in worms of this species from relatively clean areas of the Sea of Japan. Similar high concentrations of Fe w...
“…The type species H. disjuncta (Bastian 1865) is one of the most well-known marine nematodes. As a model species, H. disjuncta (then under generic names Monhystera and Geomonhystera) has been subject of previous studies on morphology and ultrastructure (Geraert et al 1981; Van de Velde and Coomans 1987, 1991, 1992, demography, physiology and energetics (Chitwood and Murphy 1964;Vranken et al 1988;Herman and Vranken 1988;Herman et al 1984), impact of temperature and salinity on life cycle (Gerlach and Schrage 1971;Vranken and Heip 1986), and toxicology (Vranken et al , 1985(Vranken et al , 1989. Data on geographical records of H. disjuncta and related species have been summarized by Gerlach and Riemann (1973), Jacobs (1987) and in some subsequent publications thereafter.…”
Morphological descriptions of two Halomonhystera species (Nematoda, Monhysterida) are presented (Halomonhystera hermesi and Halomonhystera socialis). Halomonhystera hermesi sp. n. occurs in a dense monospecific and homogeneous population on bacterial mats in the Håkon Mosby mud volcano in the Barents Sea at a depth of 1,280 m. The species is an endemic lineage distinctly separated from other shallow-water cryptotaxa of the Halomonhystera disjucta species complex on the base of the mitochondrial gene cytochrome oxidase subunit I (genetic divergence 19.6-23.8 %) and nuclear genetic markers, and on the base of morphometrics by Van Campenhout et al.
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