Degradation of bacteria by Mytilus edulis

The uptake of several species of bacteria by the common mussel Mytilus edulis (L.) and the subsequent fate of some polymers of the bacteria have been investigated in a study carried out during 1981. Bacteria (Escherichia coli, Micrococcus luteus, M. roseus, Bacillus cereus, Staphylococcus aureus and a marine pseudomonad, 1-1-1) were radiolabelled by growth in medium containing ³H-thymidine and the uptake of bacteria by Mytilus edulis was monitored. Labelled and unlabelled bacteria, at initial concentrations of 0.5 to 1x10⁷ bacteria ml^-1, were cleared at similar, exponential rates with no significant difference in the rates for different bacteria: 90% of bacteria were cleared in a mean time of 1.93±0.12 h (SEM, n=63). Those bacteria with cell walls which were sensitive to M. edulis lysozyme were rapidly degraded by the mussel and ³H-labelled DNA was released in a form not precipitable by 10% trichloroacetic acid. Lysozyme-resistant bacteria (Micrococcus roseus and S. aureus) were cleared from suspension by Mytilus edulis but most were rejected intact. By measuring the rate of release of ³H-thymidine-labelled material from the mussel the rate of degradation of lysozyme-sensitive bacteria by M. edulis was found. For different bacteria the degradation rate varied from approx 2x10⁸ to 27x10⁸ bacteria h^-1 with an overall mean of 10x10⁸ bacteria h^-1. A thymidine- and diaminopimelicacid-requiring auxotroph of E. coli was radiolabelled with ³H-thymidine, ³H-diaminopimelic acid or ¹⁴C-glucose and fed to M. edulis. Bacteria were cleared and degraded by the mussel; ³H-diaminopimelic acid-labelled or ¹⁴C-glucose-labelled polymers were retained, whereas ³H-thymidine-labelled polymers were released into the surrounding water. Extracts of the digestive gland of M. edulis degraded lysozyme-sensitive bacteria to release ³H-thymidine-labelled material, but did not release ³H-thymidine-labelled material from lysozyme-resistant bacteria. It is concluded that M. edulis can select lysozymesensitive bacteria for subsequent processing and discriminate between bacterial polymers to reject DNA. Also, bacteria could provide a substantial fraction of the carbon requirement of the mussel.     

Evaluation of the relationship of picoplankton and viruses to environmental variables in a lagoon system (Çakalburnu Lagoon,Turkey)

Lagoons are defined as wetlands separated from the sea coasts on which they are located and sit between continental and marine aquatic ecosystems. Çakalburnu Lagoon is a coastal wetland on the southern side of the Bay of ?zmir. Microorganisms, which are quite sensitive to changes occurring in environmental factors, are commonly used to determine the impact of environmental effects on the functioning of the ecosystem. In this study, variations in the abundance and biomass of picoplankton (Synechococcus spp. and bacteria) and the abundance of viruses, which identify the ecological productivity of the food chain, were seasonally examined by epifluorescence microscopy. Moreover, the microbial abundance and biomass relation over time between the physical and chemical parameters was evaluated. According to our results, the maximum abundance of Synechococcus spp. and viruses was 6.7?×?10⁴ cell/ml and 9.9?×?10⁸?cell/ml in the summer, respectively. Otherwise, the highest level of bacteria was measured at 3.6?×?10⁷ cell/ml in the spring. Based on the principal component analysis and Pearson correlation analysis results, we concluded that total suspended solids, Chl-a, particulate organic carbon and particulate organic nitrogen were the major parameters influencing the observed variability of the lagoon system. Overall, to protect and improve the ecological and microbiological quality of aquatic systems such as lagoons, the necessary monitoring and measurement studies should be conducted in these sensitive areas.     

Toxicity evaluation of a complex metal mixture to the softshell clam Mya arenaria

Adults of the softshell clam Mya arenaria were continuously subjected to a flowing raw seawater solution containing a mixture of salts of manganese, zinc, lead, nickel, copper, and cadmium. Final calculated concentrations, in g l^-1, of the toxicant solution were 7200 Mn, 2500 Zn, 70 Pb, 50 Ni, 50 Cu and 1 Cd; these concentrations approximated highest measured levels within surficial interstitial sediment waters from mid-Narragansett Bay, Rhode Island. M. arenaria were also subjected to a 20% solution, i.e., 1440 Mn, 500 Zn, 14 Pb, 10 Ni, 10 Cu, and 0.2 g l^-1 Cd. One study was conducted for 112 days in winter at 0° to 10°C and another for 16 days in summer at 16° to 22°C. In the winter study, all clams exposed to a 100% solution died between the 4th and 10th week; soft parts of survivors at 6 weeks contained about 19 times more Pb, 15 x more Zn, 12 x more Cu, 10 x more Mn, 3 x more Ni and 0.1 x more Cd than controls; relatively minor changes in whole body elemental content of Ca, Cr, Fe, K, Mg, Na, Sr, and V were observed. Clams exposed to a 20% solution during winter survived the 112 day study; at that time these contained about 5 x more Cu, 4 x more Mn, 3 x more Zn and about 2 x more Pb than controls; comparatively minor changes were observed in other elements examined. In the summer study, all M. arenaria subjected to the 100% solution died between 6 and 14 days; survivors from this group at 7 days contained about 25 x more Pb, 13 x more Cu, 11 x more Zn, 7 x more Mn, and 3 x more Ni than controls; other changes in elemental content were not as pronounced. Mortality in the 20% group during summer was slightly higher than controls during the 16 day study; at 14 days survivors from this group contained about 12 x more Mn, 7 x more Pb, 7 x more Zn, 4 x more Cu, and 3 x more Ni than controls. Survival and bioaccumulation patterns were not altered through feeding a supplemental diet of algae. The significance of these findings are discussed in terms of potential environmental perturbations, especially local dredging practices.     

Temporal and spatial variation in bacterial production in the water column over a coral reef

Production and doubling times of the bacterial populations in the water around and over the reefs at Lizard Island, Great Barrier Reef were measured during summer and winter, 1982 and 1983. Bacterial productivity, determined from the rate of tritiated thymidine incorporation into DNA, was high over the reef flats and a Thalassia hemprichii sand flat (28 to 58 g Cl^-1 d^-1). Bacterial growth rates increased during the day and fell at night over the reef flats and seagrass bed. Growth rates were slower over the reef front and in open water. Doubling times ranged from about 2 d in the open water to about 3 h over the reef flat in summer. As numbers did not increase, grazing was probably intense on the reef flats. Growth rates were much slower in winter. The main source of organic nutrient used by the bacteria was probably mucus released following photosynthesis in the corals. The cyanobacterium Synechococcus sp. was sometimes very numerous, especially in summer when 2×10⁸ cells l^-1 were recorded in one water mass. The number of bacteria was also very high in summer, with values ranging from 1×10⁹ to 2.5×10⁹l^-1.     

Productivity of bacteria and microalgae and the effect of grazing by holothurians in sediments on a coral reef flat

Bacterial productivity in sandy sediments on reef flats at Lizard Island, Great Barrier Reef was determined from the rate of incorporation of tritiated thymidine into DNA. The study was conducted during January 1982 and July 1983. A small diurnal increase occurred in sediments having a dense population of microalgae. Bacterial production was 120 to 370 mg C m^-2 d^-1 in summer on reef flats, which was equivalent to 30–40% of primary production by benthic microalgae. In winter, rates of primary production by benthic microalgae and secondary production by bacteria were about one-half to one-fifth of those in summer. There was much variation in production, due to patchiness in the distribution of benthic microbes, especially microalgae. Doubling times for the bacteria in surface sediment were 1 to 2 d in summer and 4 to 16 d in winter on the reef flats. These high productivity values for bacteria indicated that a net input of organic matter to the sediment was needed to support the growth of bacteria. Sediment bacteria thus have a very important role in transforming organic matter on the reef flats. Grazing by Holothuria atra depressed both primary production and bacterial production. It was estimated that these holothurians ate about 10 to 40% of bacterial carbon produced each day in summer, and thus have an important role in the carbon cycle. Harpacticoid copepods were numerically important components of the benthic meiofaunal community and probably had a significant impact on bacterial density as grazers.     

Studies on short-term variations of heterotrophic activity in the Kiel Fjord

In summer, 1973, a short-term study with frequent sampling was performed in the Kiel Fjord (FRG). Temperature, salinity, number of viable bacteria, maximum uptakevelocity of glucose and acetate, concentrations of chlorophyll a, labile organic substances and ammonia and phosphate were measured. Strong variations in all parameters during short periods of time could be demonstrated. The number of viable bacteria fluctuated between 26x10⁶ and 195x10⁶ bacteria/l. Changes in the maximum uptake-velocity (V _m ) of glucose between 0.23 and 0.85 μg C l^-1 h^-1 and in the V _m of acetate between 0.36 and 2.40 μg C l^-1 h^-1 were recorded. A highly significant correlation between the number of viable bacteria and the maximum uptake-velocity of the two solutes was found. It is assumed that, at least for this area, at certain times the plate counts represent a major part of the active bacteria flora.     

The biological degradation of arginine and glutamic acid in seawater in relation to the growth of phytoplankton

The responses of natural summer coastal plankton communities to low-level additions (10^-5 to 10^-7 M) of arginine and glutamic acid has been followed by in vivo measurement of chlorophyll fluorescence. This technique is capable of detecting a response to a 10^-6 M enrichment under most conditions. The time sequence of the response varied with the amino acid used and with the enantiomeric form of the amino acid. Ammonia and carbon dioxide were liberated before the increase in chlorophyll fluorescence occurred. Liberation of ammonia in a dark bottle from L-arginine was from 75 to 85% of the theoretical yield. Microautoradiography using ¹⁴C L-arginine or L-glutamic acid at 10^-7 M showed heavy labeling associated with fecal pellets and detrital aggregates. Phytoplankton cells were not appreciably labeled. The evidence suggests that bacteria are important in the cycling of these compunds.     

Production and respiration of overall plankton and ultraplankton communities at the entrance to the Gulf of Finland in the Baltic Sea

Primary productivity and respiration of the overall plankton community and of ultraplankton (organisms passing through a 3-m Nuclepore filter) were studied at the entrance to the Gulf of Finland during the growth season in 1982. Data of the respiration measurements from previous years are also presented. During the development of a diatom spring bloom, the algal component could be successfully separated from the bacterial component by size fractionation with a 3-m Nuclepore filter and thus the algal respiration could be approximated, being on the order of 10 to 20% of the gross production. After the phytoplankton spring maximum, bacteria played an important role in mediating the energy flow from phytoplankton exudates to higher trophic levels. Maximum values of 1 230 and 740 mg O₂ m^-2 d^-1 were recorded for overall and for ultraplankton respiration, respectively, during late July. High productivity values coupled with low phytoplankton biomass and low inorganic nutrient values were also recorded in late July, indicating effective nutrient regeneration and rapid turnover of the plankton community. During late summer, a considerable fraction (over 30%) of phytoplankton production was released as exudates, suggesting that much of the energy is channeled to higher trophic levels via bacterial pathways rather than by direct herbivorous grazing during this season. The summer development of phytoplankton community structure and functioning is strongly controlled by hydrographic conditions, i.e. by nutrient inputs via upwelling and by water temperature. A carbon budget for late summer indicated that bacteria may contribute only up to 50% of the overall respiration of the plankton community, which suggests that heterotrophs other than bacteria play an important role in nutrient regeneration. The present study stresses the importance of energy flow via the phytoplankton exudatebacteria-micrograzer pathway in relatively oligotrophic, brackish water ecosystems.     

Symbiosis between bacteria and oceanic clonal sea star larvae in the western North Atlantic Ocean

Bacteria were present in the majority of clonal sea star bipinnariae (Luidia sp.) collected between June 1987 and August 1990 from oceanic populations in the subtropical western North Atlantic Ocean. Light and electron microscopy revealed dense aggregations of bacteria within lobes of the epidermal cuticle in the gastric region of larvae. Gram-negative rods and less-common elongate spiral bacteria were observed, always in close association with branching epidermal microvilli. Intact and partially digested bacteria occurred in vesicles and phagosomes within epidermal cells, a probable indication of phagocytotic activity by the host. The association of larvae of Luidia sp. and bacteria ranged widely on both geographical and temporal scales. During July and August 1988, larvae were abundant (1.6 to 11.1 m³) in the mixed surface layer (<10 to 100 m) of stations in the Gulf Stream, the Sargasso Sea and the North Equatorial Drift, and 96% (mean of 5 stations, n=8 to 10 larvae in each station) of the individuals surveyed harbored bacteria beneath their cuticle. In a single station on the Florida Current sampled during winter, spring, and summer months between 1989 and 1991, 79 to 90% of the larvae harbored bacteria. The incidence of symbiosis was higher in actively cloning larvae than in non-cloning larvae. This is the first documentation of a symbiosis in field populations of echinoderm larvae.     

Omnivorous feeding behavior of the Antarctic krill Euphausia superba

Feeding experiments were conducted at Palmer Station from December 1985 to February 1986 to examine the potential role of copepod prey as an alternative food source for Euphausia superba. Copepod concentration, copepod size, phytoplankton concentration, the duration of krill starvation and the volume of experimental vessels were altered to determine effects on ingestion and clearance rates. Krill allowed to feed on phytoplankton and copepods in 50-litre tubs showed greatly increased feeding rates relative to animals feeding in the much smaller volumes of water traditionally used for krill-feeding studies. Clearance rates on copepods remained constant over the range of concentrations offered, but clearance rates on phytoplankton increased linearly with phytoplankton concentration. Feeding rates increased when larger copepods were offered and when krill were starved for two weeks prior to experiments. Clearance rates of krill feeding on copepods were higher than, but not correlated with, their clearance rates on phytoplankton in the same vessel. E. superba may have a distinct mechanism for capturing copepods, perhaps through mechanoreception. Although our observed clearance rate of 1055 ml krill^-1 h^-1 indicates that krill can feed very efficiently on copepod prey, such feeding would meet less than 10% of their minimum metabolic requirements at the typical copepod concentrations reported for Antarctic waters. However, substantial energy could be gained if krill fed on the patches of high copepod concentrations occasionally reported during the austral summer, or if krill and copepods were concentrated beneath the sea ice during the winter or spring months. Our results, indicating efficient feeding on zooplankton and higher clearance rates on phytoplankton than previously believed, represent a step towards balancing the energy budget of E. superba in Antarctic waters.     

Luminous bacteria of a monocentrid fish (Monocentris japonicus) and two anomalopid fishes (Photoblepharon palpebratus and Kryptophanaron alfredi): population sizes and growth within the light organs,and rates of release into the seawater

The light organs of monocentrid and anomalopid fishes consist of bacteria-filled tubular invaginations of the epidermis which are connected to the surrounding seawater by ducts. We used the release of bacteria from the light organs to estimate bacterial rates of growth in the light organs. For one monocentrid fish (4 specimens of Monocentris japonicus collected at Jogashima, Japan in 1980) and for two anomalopid fishes (2 specimens each of Photoblepharon palpebratus collected at Sebu, Phillipines in 1981 and Grand Comore Island in 1975 and Kryptophanaron alfredi collected at Parguera, Puerto Rico in 1982) we measured rates of release of bacteria into the surrounding seawater and the bacterial population sizes in the light organs; from this information we calculated doubling times of bacteria in the light organs. In addition, we determined the luminescence of bacteria after their release into the seawater. For M. japonicus, two specimens released 1.1 to 6×10⁶ and 2×10⁷ bacteria h^–1, respectively; the light organs contained about 1.5×10⁸ bacteria. For P. palpebratus, one specimen released 2.2×10⁸ bacteria h^–1; a second specimen had light organs containing 5.2×10⁹ bacteria. For K. alfredi, one specimen released 7×10⁷ bacteria h^–1 and had light organs containing 5.6×10⁸ bacteria; a second specimen released 3.6×10⁷ bacteria h^–1 and had light organs containing 7.3×10⁸ bacteria. Bacterial doubling times in the light organs of these three fishes were variable and ranged from 7.5 to 135 h in M. japonicus and 8 to 23 h in the anomalopids. Bacteria released from M. japonicus into the seawater remained viable, but bacteria from all of the fishes soon ceased to emit light.     

Bacteriological quality assessment of drinking water available at the flood affected areas of Peshawar

Monsoon flooding occurred in the main areas of the Khyber Pakhtunkhwa, Punjab, and Balochistan as well as parts of Gilgit Baltistan of Pakistan and Azad Jammu Kashmir in July 2010. Water-borne diseases such as cholera, enteric fever, and dysentery were common among the inhabitants of flood-affected areas which were selected for sample collection. In the present study, 10 sites in District Peshawar were selected and drinking water samples collected. These samples were analyzed for the total plate count (TPC), total coliform bacteria (TCB), total fecal coliform bacteria (TFCB), Escherichia coli (EC), Pseudomonas aeruginosa (PA), Vibrio cholerae (VB), Salmonella Shigella, and Staphylococcus aureus. The TPC ranged from 8 × 10¹ to 7 × 10⁴ CFU/ml. The TCB ranged from <1.1 to 280 MPN/100 ml. Twenty percent of the samples were contaminated with TFCB, EC, Salmonella, Shigella, and Staphylococcus aureus, while only one sample contaminated with PA. Forty percent of the samples were contaminated with VB. The surface and well water was greatly contaminated by flooding and major improvements on priority basis are essential.     

Role of bacteria in decomposition of faecal pellets egested by the epiphyte-grazing gastropod Gibbula umbilicaris

The significance of the microheterotrophic utilization of faecal pellets derived from Gibbula umbilicaris — one of the most important gastropod species in the Posidonia oceanica ecosystem around the Isle of Ischia (Italy) — was investigated by means of microcosm-experiments. Initial total organic carbon (TOC) content of faecal pellets was 32 gC (mg faeces dry wt)^-1 and declined continuously over a 2-month incubation period. The low values of TOC coincided with SEM observations of pellets which were found to consist mainly of diatom frustules and other slowly utilizable material. In a long-term experiment freshly egested faecal pellets were rapidly colonized by bacteria, which reached densities of up to 14x10⁵ cells (mg faeces dry wt)^-1 within 12 h. Thereafter bacterial numbers declined and fluctuated in a very narrow range between 2 and 3.5x10⁵ cells (mg faeces dry wt)^-1 during the two months of the investigation period. In short-term experiments (over 5 d) similar trends were observed. Peak densities of attached bacteria were followed by a decline of this population. Concurrently the number of free-living bacteria increased. This observation was confirmed by O₂ consumption measurements of freshly egested faecal pellets over 24 h, where the highest O₂ consumption rates were obtained after 12 h, followed by a rapid decline, thus supporting the view that detachment of bacteria may occur. Moreover, the respiration data indicate that about 4% of faecal TOC are remineralized within the first day.     

Ecology and characteristics of bdellovibrios from three tropical marine habitats

Marine bdellovibrios have not previously been reported from the southern hemisphere, and knowledge of their occurrence in marine ecosystems is rudimentary. This study examined quantitative and qualitative aspects of bdellovibrios parasitic to the bacterium Vibrio alginolyticus at each of three representative tropical marine habitats of the Great Barrier Reef. Bdellovibrios were found in the water column throughout a 12 mo period from May 1992 at a sandy beach, a mangrove and a fringing coral reef. Their abundance was correlated with water temperature (P<0.001) and was highest in summer, lowest in winter and intermediate in spring and autumn. Over the sampling period, bdellovibrios were most abundant at the mangrove habitat (36.6 ml^-1) and least abundant at the reef (9.5 ml^-1), but there was substantial variability in numbers at all habitats among seasons and months of the year. On some occasions no bdellovibrios were found in replicate samples from the beach and reef habitats, while on others the maximum detectable by the method used (180 ml^-1) was sometimes found at the beach and mangrove habitats. Bdellovibrios within each habitat were uniformly distributed among sampling sites (P>0.05). They were more abundant in sub-surface than bottom waters in summer, but the reverse occurred in winter. Midwater samples usually had least bdellovibrios. Bdellovibrio numbers were significantly correlated with those of potential host bacteria—colony-forming bacteria at all habitats and total bacteria at the beach and reef habitats. Strain characteristics, primarily based on host range, indicated qualitative differences in bdellovibrio populations among habitats. Pseudomonas atlantica, P. aeruginosa, P. marina, Cytophaga marinoflava, Vibrio gazogenes, V. mimicus and a Spirillum-like bacterium were not parasitised by bdellovibrios from any habitat. Of the other 25 Vibrio spp. tested, most were parasitised by the majority of bdellovibrio strains from each habitat. Strain differences were principally with respect to parasitism of non-Vibrio bacteria. All strains required Na⁺ and grew at 35°C, but some failed to grow at 15°C.     

Development and metamorphosis of the planktotrophic larvae of Rostanga pulchra (Mollusca: Nudibranchia)

Rostanga pulchra MacFarland, a small (1 to 2 cm) dorid nudibranch, lays an average of 7000 eggs in the laboratory during a period of 30 days in the summer. The veligers hatch 15 to 16 days after oviposition and it takes another 35 to 40 days to become competent for metamorphosis at a temperature of 10° to 15°C. Larval cultures were maintained initially at a concentration of 500 veligers per 100 ml of filtered sea water (antibiotics added). During the planktotrophic phase of development, the veliger grows from 150 to 300 m in shell length. Although the veligers are generalists in their food preference, the best result (faster growth) was achieved by feeding them with a combination of Monochrysis lutheri and Isochrysis galbana. The concentration of food cells was kept at 10⁴ cells per ml of culture media and was supplied every 2 to 3 days. A veliger which is competent to metamorphose is identifiable morphologically by its propodium, eyespots, rhinophores, and spiculated dorsal papillae. The entire metamorphic process lasts 24 h when a suitable substrate such as the food sponge Ophlitaspongia pennata is provided. The competent veliger is able to delay metamorphosis for at least 3 weeks. Juveniles were kept in the laboratory for 70 days and, during this period, grew to a length of 4.5 mm.     

Seasonal changes of benthic bacteria in a seagrass bed (Posidonia oceanica) of the Ligurian Sea in relation to origin,composition and fate of the sediment organic matter

Variations in number and biomass of benthic bacteria were examined in the surface sediments of a Mediterranean seagrass bed [Posidonia oceanica (L.) Delile] in the Gulf of Marconi (northwestern Mediterranean Sea) from 1990 to 1991. The annual dynamics of benthic bacterial density and biomass were compared to changes in elemental (organic C and total N) and biochemical (lipids, proteins, carbohydrates) composition of sediment organic matter, as well as to microphytobenthic biomass, dissolved inorganic nutrients and ATP. Bacterial densities exhibited marked seasonal variations (5.12 to 322.7x10⁸ cells g^-1 sediment dry wt) with highest values in late spring. Bacterial standing stocks (15.8 to 882.33 g C g^-1 of sediment dry wt) were high. Bacterial biomass did not correlate with organic C, total N or to specific biochemical components, but correlated significantly with chlorophyll a, ATP and porewater phosphate concentrations. There is evidence that benthic bacteria were responding to variations of algal biomass. Bacterial biomass accounted, on average, for 30% of total living carbon (calculated on the basis of the ATP concentrations) and 8.4% of total organic carbon.     

Effects of algal and larval densities on development and survival of asteroid larvae

Effects of larval and algal culture density and diet composition on development and survival of temperate asteroid larvae were studied in the laboratory at Santa Cruz, California, USA, during summer and fall of 1990. Larvae of Asterina miniata were reared at two densities, 0.5 or 1.0 ml^-1, and fed one or two species of cultured phytoflagellates — Dunaliella tertiolecta alone or mixed with Rhodomonas sp. — at three concentrations of 5x10², 5x10³, and 5x10⁴ total cells ml^-1. Algal concentration strongly influenced larval development; however, larval density also had a marked effect. Development progressed further with increasing algal concentration. Larval growth and differentiation were sometimes uncoupled; i.e., growth measures were directly related to food level, while differentiation indicators were less so. At the lowest food level, growth was negative and differentiation was arrested at early precompetent stages; these larvae never formed juvenile rudiments or brachiolar attachment structures. Development times of larvae given more food ranged from 26 to 50 d and depended directly on food availability. Development time to metamorphosis at the highest food concentration was similar for siblings fed D. tertiolecta alone or mixed with Rhodomonas sp. In contrast, when food level was an order of magnitude lower, larvae fed the algal mixture metamorphosed significantly earlier than larvae fed the unialgal diet. This suggests interactive effects of food quantity and food quality. Survival was little affected by larval or food density, except at the lowest ration. Feeding experiments in well-controlled laboratory conditions are useful to predict and compare the physiological or developmental scope of response of larvae to defined environmental factors; however, results from such studies should not be extrapolated to predict rates and processes of larval development in nature.     

Untersuchungen über die heterotrophe Aktivität in der zentralen Ostsee

The distribution of some microbial parameters was studied at 3 stations in the Central Baltic Sea (Bornholm Basin, BB; Danzig Deep, DD; and Gotland Deep, GD) during May 1976. The following analyses were performed: total bacterial numbers and biomass, viable counts and maximum uptake velocity (V _max) of glucose. The values found for thesurface, samples were, total bacterial counts: 0.6x10⁶ (BB); 1.7x10⁶ (DD); 0.4x10⁶ (GD) cells/ml; bacterial biomass: 1.9 g C/l (BB); 6.9 g C/l (DD); 1.6 g C/l (GD); viable counts: 0.37x10³ (BB); 17x10³ (DD); 0.4x10³ (GD) counts/ml; V _max: 0.01 g glucose-C/l (BB), 0.06 g glucose-C/l (DD); 0.01 g glucose-C/l (GD). The relatively high microbial numbers and activities of the Danzig Deep may be associated with the fertilization of the area by the River Vistula. The vertical distribution of the microbial parameters in the Bornholm Basin and Danzig Deep showed high values both in the top layer (0 to 20 m) and in the deep layer (>40 m). In the intermediate layer, however, the values decreased significantly. It is suggested that the high values of the microbial parameters at depth are caused by at least two major processes during the inflow of North Sea water into the deep layers of the Baltic Sea: (1) the North Sea water may already have contained high numbers of bacteria; (2) during the inflow, the high concentrations of bacteria normally located at the sediment-water interface are distributed throughout the whole deep layer by mixing.

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Beitrag Nr. 143 aus dem Sonderforschungsbereich 95 Wechselwirkung Meer-Meeresboden, Universität Kiel.     

不同补给水源的城市人工湖中异养菌耐药性及耐药菌种属分布研究

为了阐明不同补给水源的城市人工湖中异养菌耐药状况和耐药菌种属分布特征,选取分别以地表水和再生水为补水来源的XQ湖和FQ湖为代表进行研究。从2018年4—11月逐月采集水样,考察了各水样中对氨苄西林(AMP)、磺胺甲恶唑(SMZ)和四环素(TET)这3种不同种类抗生素具有耐药性的异养菌含量,并对分离菌株的耐药表型、耐药菌株的种属分布以及水质理化指标进行了分析。结果表明,2处人工湖中的AMP耐药菌和SMZ耐药菌含量约为10~2～10~4CFU·(100 m L)~(-1),而TET耐药菌含量则约10~1～10~3CFU·(100 m L)~(-1)。分离出的84株耐药菌归属于19个种,其中蜡状芽孢杆菌、大肠埃希氏菌、维氏气单胞菌、豚鼠气单胞菌和鸟氨酸拉乌尔菌为2个湖共有耐药菌。71.4%的耐药菌都是对AMP单一耐药,以蜡状芽孢杆菌为主。由于具有固有耐药性的细菌在分离出的耐药菌中占比很低,获得性耐药很可能在城市人工湖中异养菌耐药性的发展上发挥了主要贡献作用。地表水补水的XQ湖和再生水补水的FQ湖在总异养菌含量、耐药菌含量和检出率上均无显著差异。分离来源对16株耐药性气单胞菌的聚类无明显影响。     

Enhancement of chlorophyll a production in Gulf Stream surface seawater by synthetic versus natural rain

Rainwater concentrations of either ammonium or nitrate were sufficient to stimulate chlorophyll a (chl a) production in bioassay experiments using Gulf Stream surface water collected off North Carolina during the summer of 1991. Previous studies primarily examined inshore waters and did not address the impact of rainwater ammonium. An increase in chl a occurred within 1 d of the addition of synthetic rainwater (2 or 5% rainwater, 98 or 95% seawater) containing up to 10 M ammonium; this increase was followed by a decrease in chl a the following day. A similar response to nitrate addition (5% addition of 20 M nitrate rain) was observed. In separate experiments, natural rainwater having nitrate and ammonium concentrations less than those in the experimental synthetic rain yielded a greater chl a response than synthetic rain when added at similar dilutions (0.5 to 5.0% rain). The maximum dissolved inorganic nitrogen concentration in the enriched seawater in these bioassays was 1.8 M; prior to enrichment the maximum was < 0.4 M. Bioassay experiments begun 2 d after a major storm event (sustained NE winds with gusts to 13 m s^-1 and ca. 390 mol m^-2 inorganic nitrogen deposition from rain) showed a chl a increase in response to addition of natural rainwater, but not to synthetic rainwater with similar dissolved inorganic nitrogen concentration. These results suggest that phytoplankton stimulants, in addition to nitrate and ammonium, exist in natural rain but not in the synthetic rain used in these experiments.