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1.
South Africa lacks a commercial oyster hatchery. To inform the sourcing of seed for future hatchery establishments, we compared half-sib Pacific oyster Crassostrea gigas cohorts from hatcheries in Namibia and Chile. We measured oyster growth, mortality, condition and feeding organ morphology in Algoa Bay (AB, Eastern Cape) and Saldanha Bay (SB, Western Cape), South Africa, from July 2011 to June 2012. Within SB, 14.3% of mean daily sea temperatures exceeded this species’ thermal optimum of 19 °C, compared to 50.5% in AB. Food abundance (mean daily chlorophyll a concentration) in SB (7.8 mg m–3) was double that in AB (3.9 mg m–3) where, presumably to increase particle clearance rates in a relatively phytoplankton-poor environment, oysters had larger gill:palp surface area ratios. Plankton fatty acid profiles (indicators of food quality) differed between locations. In AB, instantaneous growth rates differed between cohorts, and trends varied seasonally. Within both locations, condition index was usually higher in Chilean oysters, whereas shell density was higher in Namibian oysters. In AB only, Chilean seed suffered substantially higher summer mortalities than Namibian seed, suggesting that the latter are more suited to temperatures in AB. AB should also be assessed for culture of the indigenous oyster species that occur there.  相似文献   

2.
It is well known that temporal changes in bivalve body mass are strongly correlated with temporal variations in water temperature and food supply. In order to study the influence of the year-to-year variability of environmental factors on oyster growth, we coupled a biogeochemical sub-model, which simulates trophic resources of oysters (i.e. phytoplankton biomass via chlorophyll a), and an ecophysiological sub-model, which simulates growth and reproduction (i.e. gametogenesis and spawning), using mechanistic bases. The biogeochemical sub-model successfully simulated phytoplankton dynamics using river nutrient inputs and meteorological factors as forcing functions. Adequate simulation of oyster growth dynamics requires a relevant food quantifier compatible with outputs of the biogeochemical sub-model (i.e. chlorophyll a concentration). We decided to use the phytoplankton carbon concentration as quantifier for food, as it is a better estimator of the energy really available to oysters. The transformation of chlorophyll a concentration into carbon concentration using a variable chlorophyll a to carbon ratio enabled us to improve the simulation of oyster growth especially during the starvation period (i.e. autumn and winter). Once validated, the coupled model was a suitable tool to study the influence of the year-to-year variability of phytoplankton dynamics and water temperature on the gonado-somatic growth of the Pacific oyster. Four years with highly contrasted meteorological conditions (river inputs, water temperature and light) 2000, 2001, 2002 and 2003, were simulated. The years were split into two groups, wet years (2000 and 2001) and dry years (2002 and 2003). Significant variability of the response of oysters to environmental conditions was highlighted between the four scenarios. In the wet years, an increase in loadings of river nutrients and suspended particulate matter led to a shift in the initiation and the magnitude of the phytoplanktonic spring bloom, and consequently to a shift in oyster growth patterns. In contrast, in the dry years, an increase in water temperature—especially during summer—resulted in early spawning. Thus, the gonado-somatic growth pattern of oysters was shown to be sensitive to variations in river loadings and water temperature. In this context, the physiological status of oysters is discussed using a relevant indicator of energy needs.  相似文献   

3.
A bio-energetic model, based on the DEB theory exists for the Pacific oyster Crassostrea gigas. Pouvreau et al. [Pouvreau, S., Bourles, Y., Lefebvre, S., Gangnery, A., Alunno-Bruscia, M., 2006. Application of a dynamic energy budget model to the Pacific oyster, C. gigas, reared under various environmental conditions. J. Sea Res. 56, 156–167.] successfully applied this model to oysters reared in three environments with no tide and low turbidity, using chlorophyll a concentration as food quantifier. However, the robustness of the oyster-DEB model needs to be validated in varying environments where different food quantifiers reflect the food available for oysters, as is the case in estuaries and most coastal ecosystems. We therefore tested the oyster-DEB model on C. gigas reared in an Atlantic coastal pond from January 2006 to January 2007. The model relies on two forcing variables: seawater temperature and food density monitored through various food quantifiers. Based on the high temperature range measured in this oyster pond (3–30 °C), new boundary values of the temperature tolerance range were estimated both for ingestion and respiration rates. Several food quantifiers were then tested to select the most suitable for explaining the observed growth and reproduction of C. gigas reared in an oyster pond. These were: particulate organic matter and carbon, chlorophyll a concentration and phytoplankton enumeration (expressed in cell number per litre or in cumulative cell biovolume). We conclude that when phytoplankton enumeration was used as food quantifier, the new version of oyster-DEB model presented here reproduced the growth and reproduction of C. gigas very accurately. The next step will be to validate the model under contrasting coastal environmental conditions so as to confirm the accuracy of phytoplankton enumeration as a way of representing the available food that sustains oyster growth.  相似文献   

4.
Abundance of picoplanktonic chroococcoid marine cyanobacteria Synechococcus was monitored weekly over the year 1998 in shallow coastal waters of the northern Levantine Basin. The ambient physical, chemical and biological variables (temperature, salinity, Secchi disk depth, total suspended sediment, nitrate, phosphate, Chl a and phytoplankton) were also measured. Synechococcus was found to be more abundant during summer and early autumn and less during winter and early spring. At the surface and 15 m depth, cell concentrations were in the range 6.4 × 103–1.5 × 105 and 3.2 × 103–1.6 × 105 cells·ml−1, respectively. Based on the Pearson product–moment correlation analysis, a highly significant correlation between Synechococcus abundance and ambient temperature was observed (n = 40, r = 0.558, P < 0.01). As Synechococcus forms blooms that usually do not last more than a week, the short time‐scale survey achieved in this study was appropriate to reveal its abundance dynamics. Several factors such as rapid changes in nutrient concentration (especially nitrate), phytoplankton, light availability, temperature, salinity, freshwater input and vertical mixing played a relevant role on the abundance of Synechococcus over the year in the highly dynamic shallow coastal waters of the Levantine Basin.  相似文献   

5.
北部湾北部海域水体异养细菌的时空分布特征研究   总被引：2，自引：1，他引：1  
贺成  徐沙  宋书群  李才文 《海洋学报》2019,41(4):94-108
为探讨环境因素对异养细菌丰度的影响，2016年9月至2017年8月通过月度航次调查对北部湾北部海域异养细菌丰度的时空分布特征进行了系统研究。结果表明，调查海区异养细菌丰度介于（2.75~56.86）×105 cell/mL，平均值为（11.01±6.31）×105 cell/mL。各季节细菌丰度从高至低依次为:夏季、春季、冬季、秋季。异养细菌丰度由近岸海域向西南深水区方向逐渐降低，在近岸浅水区垂直分布均匀，在水深大于20 m的海区出现季节性分层现象:表层细菌丰度较高，底层细菌丰度较低。主成分分析显示温度对异养细菌时空分布有重要影响，秋、冬季异养细菌丰度与温度呈显著负相关，在春、夏季呈显著正相关。细菌丰度与盐度呈显著负相关，说明海水盐度变化是细菌时空分布重要影响因素。异养细菌丰度与叶绿素a和溶解氧含量呈显著正相关，表明浮游植物初级生产过程影响了异养细菌的时空分布。在秋、冬和春3季异养细菌丰度与营养盐水平呈显著负相关，二者关系受浮游植物生物量间接影响。异养细菌时空分布差异取决于环境条件的变化，温度、盐度、叶绿素a和溶解氧含量是影响异养细菌丰度分布的主要因素。  相似文献   

6.
Alterations in sea ice and primary production are expected to have cascading influences on the food web in high Arctic marine ecosystems. This study spanned four years and examined the spring phytoplankton production bloom in Disko Bay, West Greenland (69°N, 53°W) (using chlorophyll a concentrations as a proxy) under contrasting sea ice conditions in 2001 and 2003 (heavy sea ice) and 2002 and 2004 (light sea ice). Satellite-based observations of chlorophyll a, sea ice and sea surface temperature were used together with in situ depth profiles of chlorophyll a fluorescence collected at 24 sampling stations along the south coast of Disko Island (5-30 km offshore) in May 2003 and 2004. Chlorophyll a and sea surface temperatures were also obtained from the Moderate Resolution Imaging Spectroradiometer (MODIS: EOS-Terra and AQUA satellites) between March 2001 and July 2004. Daily SMMR/SSMI sea ice data were obtained in the same years. An empirical regional algorithm was developed to calibrate ratios of remotely sensed measurements of water leaving radiance with in situ chlorophyll a fluorescence. The optimal integration depth was 0-4 m, explaining between 70% and 91% of the variance. The spatial development of the phytoplankton bloom showed that the southwestern corner of the study area had the earliest and the largest spring phytoplankton bloom. The eastern part of Disko Bay, influenced by meltwater outflow from the glaciers, shows no signs of an early phytoplankton bloom and followed the general pattern of an accelerated bloom soon after the disappearance of sea ice. In all four years the coupling between phytoplankton and sea ice was bounded by average open water between 50% and 80%, likely due to the combined availability of light and stable open water. The daily incremental growth in both mean chlorophyll a density (chlorophyll a per volume water, μg l−1) and abundance (density of chlorophyll a extrapolated to ice free areas, tons) estimated by linear regression (chlorophyll a vs. day) between 1 April and 15 May was highest in 2002 and 2004 (light ice years) and lowest in 2001 and 2003 (heavy ice years). In years with late sea ice retreat the chlorophyll a attained only slightly lower densities than in years with early sea ice retreat. However, the abundance of chlorophyll a in light ice years was considerably larger than in heavy ice years, and there was an obvious effect of more open water for light-induced stimulation of primary production. This observation demonstrates the importance of estimating chlorophyll a abundance rather than density in sea ice covered areas. This study also presents the first regional calibration of MODIS chlorophyll a data for Arctic waters.  相似文献   

7.
Abstract

Bacterial numbers and production were measured in the upper water column in the winter and spring of 1993 in five water masses surrounding the South Island of New Zealand. Average bacterial numbers and production were found to be higher in spring (8.5 × 105 cells ml?1 and 0.20 mg m3 h?1, respectively) than winter (5.5 × 105 cells ml?1 and 0.05 mg C m3 h?1 respectively). Bacterial production was strongly correlated with chlorophyll a and primary production (P < 0.001) in spring but not in winter. Spring bacterial production and at 10 m depth averaged across 28 stations was 23% of primary production, and with a growth efficency of 40%, may have consumed up to 57% of primary production. Bacterial biomass was greater than phytoplankton biomass for 75% of the 10 m depth comparisons during winter sampling and 44% during the spring sampling. The bacterial biomass was found to represent 24.6–33.5% of the nitrogen in particulate organic matter (<200 μm) supporting the concept that in New Zealand oceanic water masses bacteria are of significant biogeochemical importance.  相似文献   

8.
Biogenic reefs built by oysters and other suspension feeders are vital components of estuarine ecosystems. By consuming phytoplankton, suspension feeders act to suppress accumulation of organic matter in the water column. Nutrient loading increases the rate of primary production, thereby causing eutrophication. As suspension feeders consume more organic matter from increasing abundance of phytoplankton, their rate of growth should also increase if they are food limited. We show here that the eastern oyster, Crassostrea virginica (Gmelin), from St. Mary's and Patuxent rivers, Chesapeake Bay, grew faster during anthropogenic eutrophication relative to C. virginica before eutrophication. Growth of shell height, shell thickness and adductor muscle increased after eutrophication began in the late 18th century. After 1860, growth decreased, perhaps reflecting the negative effects of hypoxia, harmful algal blooms, disease and fishing on oyster growth. These results are consistent with the view that an increasing supply of phytoplankton resulting from eutrophication enhanced growth of C. virginica between 1760 and 1860, before oyster reefs were degraded by destructive fishing practices between 1870 and 1930. Alternative factors, such as changes in water temperature, salinity, and fishing are less likely to be responsible for this pattern. These results have implications for restoration of oyster reefs in order to mitigate the effects of eutrophication in estuaries, as well as the paleoecological relationship between suspension feeders and paleoproductivity.  相似文献   

9.
The capacity of filter feeders to reduce seston and phytoplankton concentrations in the water column has important implications for restoration and management of coastal ecosystems. We directly measured changes in chlorophyll a concentration on commercially stocked intertidal oyster beds (Crassostrea gigas) in Willapa Bay, Washington, USA by recording water properties near small drifters as they tracked parcels of water across tide flats. Chlorophyll declined 9.6% per half hour in water passing on-bottom adult oysters and 41% for longline adult oysters, whereas chlorophyll concentrations increased as water flowed across tide flats without adult oysters. Field filtration rates, which were fit to exponential declines in chlorophyll and accounted for oyster density and water depth, averaged 0.35 L g− 1 h− 1 (shucked dry weight) for on-bottom aquaculture and 0.73 L g− 1 h− 1 for longline culture, compared to values of 2.5–12 L g− 1 h− 1 reported from laboratory studies of C. gigas. Field filtration rates may be lower than laboratory rates due to unfavorable field conditions (e.g., low initial chlorophyll concentrations) or masked by resuspension of benthic microalgae. In addition to distinctions among on-bottom, longline, and no-oyster habitats, Akaike's Information Criterion analysis showed temperature, initial chlorophyll concentration, and depth related to chlorophyll decline. This research corroborates mathematical models suggesting that benthic suspension feeders are exerting top-down control of pelagic production in this estuary, with strong patterns in chlorophyll emerging across extensive tideflats populated by C. gigas despite low field filtration rates.  相似文献   

10.
夏秋季南黄海浮游植物群落及其调控因子   总被引：1，自引：1，他引：0  
The phytoplankton water samples were collected in two multidisciplinary investigations which were carried out during summer(June) and autumn(November to December) of 2011. Phytoplankton species composition and abundance data were accomplished by Uterm?hl method. The phytoplankton community was dominated by diatoms and dinoflagellates in the southern Yellow Sea(YS) in summer and autumn. In summer, Paralia sulcata and Prorocentrum dentatum were the predominated species, the cell abundance ranged from 0.074 to 107.733×103 cells/L with an average of 9.057×103 cells/L. Two phytoplankton high abundance appeared in northwest part of the survey area and the Changjiang River Estuary, respectively. In autumn, Par. sulcata became the predominant species, and the phytoplankton cell abundance ranged from 1.035×103 to 8.985×103 cells/L, the average was 3.263×103 cells/L. The phytoplankton abundance in surface layer presented the homogeneous distributions. Canonical Correspondence Analysis(CCA) method was applied for discovering the relationship between environmental factors and the common found phytoplankton species. The responses of phytoplankton to nutrients were varied between summer and autumn. The abundance of most predominant species, Par. sulcata was strongly correlated to temperature and salinity in autumn, but not the case in summer.  相似文献   

11.
To verify the hypothesis that the growth of phytoplankton in the Western Subarctic Gyre (WSG), which is located in the northwest subarctic Pacific, is suppressed by low iron (Fe) availability, an in situ Fe fertilization experiment was carried out in the summer of 2001. Changes over time in the abundance and community structure of phytoplankton were examined inside and outside an Fe patch using phytoplankton pigment markers analyzed by high-performance liquid chromatography (HPLC) and flow cytometry (FCM). In addition, the abundance of heterotrophic bacteria was also investigated by FCM. The chlorophyll a concentration was initially ca. 0.9 μg l−1 in the surface mixed layer where diatoms and chlorophyll b-containing green algae (prasinophytes and chlorophytes) were predominant in the chlorophyll biomass. After the iron enrichment, the chlorophyll a concentration increased up to 9.1 μg l−1 in the upper 10 m inside the Fe patch on Day 13. At the same time, the concentration of fucoxanthin (a diatom marker) increased 45-fold in the Fe patch, and diatoms accounted for a maximum 69% of the chlorophyll biomass. This result was consistent with a microscopic observation showing that the diatom Chaetoceros debilis had bloomed inside the Fe patch. However, chlorophyllide a concentrations also increased in the Fe patch with time, and reached a maximum of 2.2 μg l−1 at 5 m depth on Day 13, suggesting that a marked abundance of senescent algal cells existed at the end of the experiment. The concentration of peridinin (a dinoflagellate marker) also reached a maximum 24-fold, and dinoflagellates had contributed significantly (>15%) to the chlorophyll biomass inside the Fe patch by the end of the experiment. Concentrations of 19′-hexanoyloxyfucoxanthin (a prymnesiophyte marker), 19′-butanoyloxyfucoxanthin (a pelagophyte marker), and alloxanthin (a cryptophyte marker) were only incremented a few-fold increment inside the Fe patch. On the contrary, chlorophyll b concentration reduced to almost half of the initial level in the upper 10 m water column inside the Fe patch at the end of the experiment. A decrease with time in the abundance of eukaryotic ultraphytoplankton (<ca. 5 μm in size), in which chlorophyll b-containing green algae were possibly included was also observed by FCM. Overall, our results indicate that Fe supply can dramatically alter the abundance and community structure of phytoplankton in the WSG. On the other hand, cell density of heterotrophic bacteria inside the Fe patch was maximum at only ca. 1.5-fold higher than that outside the Fe patch. This indicates that heterotrophic bacteria abundance was little respondent to the Fe enrichment.  相似文献   

12.
河北沿岸微微型浮游植物的分布特征   总被引：1，自引：0，他引：1  
于2006年7月～ 2007年10月间,分4个季度调查了河北省沿岸微微型浮游植物的丰度和生物量及对浮游植物总生物量的贡献.结果显示:河北近岸海域聚球藻蓝细菌丰度为4.46×103个/mL(0.79×103～ 16.19×103个/mL),生物量(以碳计,下同)为1.31 mg/m3 (0.84～17.47 mg/m3),季节分布特征为秋季＞冬季＞夏季＞春季.微微型光合真核生物丰度为4.43×102个/mL (0.84×102～ 17.47×102个/mL),生物量为1.11mg /m3 (0.21～ 4.37 mg/m3),季节变化变现为秋季＞冬季＞春季＞夏季.微微型浮游植物对浮游植物总生物量的贡献年平均为5.32％(1.84％～ 8.91％),春季最高,秋季最低.温度在较冷季节(冬春季)里是影响聚球藻蓝细菌生长和分布的控制因素.总之,在近岸环境里,微微型浮游植物并不占优势.  相似文献   

13.
Seasonal changes in abundance, growth and mortality of heterotrophic bacteria were investigated monthly from collections and dilution experiments in Kagoshima Bay, the southernmost of Japan. Bacteria occurred abundantly with considerable variation in the surface layers where chlorophyll a concentrations were high, whereas seasonal variations were obscure below 100 m. Especially, bacteria showed a decline of cell density toward summer when heterotrophic nano-flagellates increased their abundance. Seasonal and vertical variations in bacterial cell number during the study period were positively correlated with those of water temperature and pico-sized chlorophyll a concentration. Maximum growth and mortality rates showed positive correlations with water temperature but no positive relationships to size-fractionated chlorophyll a. Net increase rate (i.e. in situ rate if abundance changes) was negatively correlated with cell density of heterotrophic nano-flagellates. It is concluded that bacterial abundance is controlled by the resultant (i.e. net growth rate) of the balance between maximum growth and predatory mortality by heterotrophic nano-flagelllates which are both dependent on ambient temperature.  相似文献   

14.
Chesapeake Bay is a large and productive estuary that has received close scrutiny in recent years because of indications that its water quality and biota have been damaged by man's activities. Data on primary production for the estuary as a whole, however, are surprisingly sparse. We describe here the distribution of photosynthetic carbon assimilation by phytoplankton in Chesapeake Bay, and relate productivity patterns to hydrographic characteristics of the estuary. Between March 1982 and April 1983, a series of four cruises was conducted on Chesapeake Bay, and two cruises on the urbanized Delaware Bay for comparison. The upper Chesapeake and Delaware were highly turbid with high concentrations of suspended particulate matter and dissolved inorganic nutrients. Low chlorophyll concentrations were usually found in these areas of high turbidity, despite the abundance of nutrients, suggesting light limitation. Application of Wofsy's (1983) model of phytoplanton growth confirmed this suggestion. Chlorophyll and productivity maxima usually occurred seaward of the turbidity maxima where light penetration increased and suffient nutrients were present to support active phytoplankton growth. Further seaward of the chlorophyll maxima in the Chesapeake, the photic zone depth increased, concentrations of nutrients decreased, and phytoplankton biomass decreased, suggesting that nutrient availability, rather than light, controlled phytoplankton growth in the lower portion of the estuary. In contrast to the Chesapeake, Delaware Bay was more turbid, had generally higher nutrient concentrations, and was lower in phytoplankton productivity. The chlorophyll maxima and region of rapid phytoplankton growth occurred further toward the lower estuary and shelf regions in Delaware Bay because the high turbidity extended further seaward. Nutrients were never depleted at the shelf end of the estuary sufficiently to retard phytoplankton growth. Photosynthesis-irradiance (P-I) curves from simulated in situ and constant intensity incubations showed a strong correlation of the light-limited slope (aB) with the light-saturated rate ( ) on each cruise. Spatial variations in corresponded to patterns of phytoplankton abundance, as did integral production (PP) and carbon-based growth rates (μC, μm), and photosynthetic parameters varied significantly with temperature.  相似文献   

15.
Concentrations of chlorophyll a and suspended particulate concentrations were measured during three lake-wide surveys of St Lucia, a shallow, turbid estuary on the east coast of South Africa. There was no salinity gradient in the system during any of the surveys, but between the surveys there were considerable salinity differences. Summer turbidities were higher than those of winter and spring, and turbidity along the eastern edge of the system was lower than elsewhere. Chlorophyll a was present over a wide range of salinities and turbidities and was generally highest in summer. However, there was no relationship between salinity and concentrations of chlorophyll a, and the concentrations were not significantly higher along the less turbid eastern shore. Concentrations of total paniculate matter (TPM) and particulate organic matter (POM) in the < 100 μm fraction were significantly correlated with turbidity throughout the year, but chlorophyll a and POM (< 100 μm) were significantly correlated only in summer. Concentrations of TPM in the > 100 μm fraction were two orders of magnitude lower than those in the < 100 μm fraction, but the organic content of the former fraction was very much higher. There was no relationship between turbidity and TPM (> 100 μm), nor between chlorophyll a and POM (> 100 μm) concentrations. Under conditions of high TPM load and in the salinity range 2–25 × 10?3, phytoplankton would probably still occur in St Lucia. Estimates of phytoplankton production ranged between 218 and 252 mg C·m?2·day?1. A comparison of estimates of the standing stocks of carbon from phytoplankton and suspended POM < 100 μm indicated that carbon input from sources other than phytoplankton may be important.  相似文献   

16.
Standing stocks and production rates of phytoplankton and abundance of bacteria were investigated at 39 stations in the Seto Inland Sea, Japan during four crulses in October 1993, January, April and June 1994. Primary productivity was measured by the13C tracer method. Photosynthetic rate varied from 0.41 to 32.1 μgC/1/h with an average value of 4.67 μgC/l/h. Annual primary production was estimated to be 218 gC/m2/year. Annual primary production in this study was 1.8 times as high as the values which were previously reported at same area. The reason for the disagreement between our primary production value and previous values is not thought to be due to the difference of methods used for measuring primary production or the different Chl.a concentrations but to the method of estimating the primary production in the euphotic zone from thein vitro measurements. The distribution of bacterial cells in surface seawater was examined during the same cruises. Bacterial cell density ranged from 0.32 to 3.4×106 cells/ml. The density was relatively high in the eutrophic regions of Hiroshima Bay and Osaka Bay In addition, a high density of bacteria was also observed in an area within Suo Nada where Chl.a was relatively low. The disparity between Chla and bacterial density in Suo Nada suggests that bacterial abundance can be controlled by the availability of substrates other than phytoplankton exudate.  相似文献   

17.
Available data on phytoplankton and bacterial abundance and production off the coasts of southern Africa (to the 500 m depth contour) have been assembled and analysed for a network analysis of carbon flow in the Benguela ecosystem. Phytoplankton carbon biomass (from measurements of chlorophyll a) in the northern Benguela (2 558 300 tons) was considerably higher than in the southern Benguela (671 420 and 516 400 tons for the West and South coasts respectively). However, overall annual production (from C14-uptake measurements) was similar, 77 416 608, 76 399 973 and 78 988 020 tons C·year?1 respectively. Phytoplankton respiration and sedimentation losses were calculated as functions of primary production and therefore followed similar trends. From the most conservative estimates (mean bacterial biomass of 10 mg C·m?3 and average P:B of 0,2·day?1) bacterial biomass is 2–7 per cent of phytoplankton biomass in the northern and southern Benguela, and bacterial production is 3–5 per cent of primary production. Assuming a net growth yield of 30 per cent, bacteria would need to consume 9–15 per cent of the total primary production in order to meet their requirements for carbon consumption. Calculations based on a mean bacterial biomass of 40 mg C·m?3 and a mean growth rate of 0,5·day?1 in the upper 30 m of the water column show bacterial biomass to be 8–27 per cent of phytoplankton biomass and bacterial production to be 26–44 per cent of phytoplankton production. Bacterial carbon consumption requirements at these rates amount to 86–147 per cent of total primary production.  相似文献   

18.
2009年晚春黄海南部浮游植物群落   总被引：3，自引：0，他引：3       下载免费PDF全文
田伟  孙军 《海洋科学》2011,35(6):19-24
在2009年6月对黄海南部及中部海域30个站位进行综合调查,对获得的131个浮游植物样品用Utermohl方法进行初步分析,共鉴定浮游植物4门51属73种（不包括未定名种）,其中硅藻32属47种（不包括未定名种）,甲藻17属24种（不包括未定名种）,定鞭藻1门1种,蓝藻1门1种,硅藻在物种丰富度上占有优势。浮游植物的生...  相似文献   

19.
本文基于2018年5月（春季）、8月（夏季）、11月（秋季）和2019年1月（冬季）季度航次调查，采用冗余分析（RDA）和Bray-Curtis相似性聚类分析方法，讨论了烟台四十里湾及其邻近海域网采浮游植物丰度、优势种组成、多样性指数、均匀度指数的分布特征以及浮游植物与环境因子的关系。本年度调查共发现浮游植物4门69属116种，其中硅藻门50属85种，甲藻门15属27种，着色鞭毛藻门3属3种，未定类1种（三深碎裂藻，Ebria tripartita）。浮游植物丰度在8月份达到年度最高值，为2.89×108cells/m3，秋季次之，春季最低，春、秋、冬季浮游植物丰度均为~105cells/m3。硅藻门在4个季节中均占绝对优势，除春季出现甲藻门（夜光藻）优势种外，其余季节浮游植物优势种均为硅藻门。相邻季节浮游植物优势种更替明显，未出现4个季节共有的优势种。浮游植物多样性和均匀度指数均在夏季达到最低值，分别为1.58和0.31。RDA排序分析显示，不同季节影响浮游植物群落分布的环境因子不同，总体来讲，温度、溶解氧浓度、SiO32-浓度和NO3-浓度对浮游植物的丰度和平面分布有显著影响。Bray-Curtis相似性聚类结果显示，2018年每个季节浮游植物群落分布均可分为两个类群，其分布受营养盐分布的影响较为明显。  相似文献   

20.
We collected surface water along the 142nd E meridian from Tasmania to Antarctica in December 1999. We measured temperature, salinity and total chlorophyll a; additionally, we collected suspended particle size fractions and used fluorometric analysis to determine the quantity of chlorophyll a in each of four cell size classes: picoplankton (<3 μm), two nanoplankton fractions (3–10 μm and 10–20 μm) and microplankton (> 20 μm). Changes in temperature and salinity show that we crossed 6 water masses separated by 5 fronts. We found low abundance (<0.2 mg m−3) of chlorophyll in all size classes, with the exception of higher values near the continent (0.2 to 0.4 mg m−3). Lowest chlorophyll values (<0.1 mg m−3) were found in the Polar Frontal Zone (51° to 54°S). Microplankton made up the largest portion of total chlorophyll throughout most of the region. We conclude that biomass of all phytoplankton fractions, especially pico-and nanoplankton, was constrained by limiting factors, most probably iron, throughout the region and that ecosystem dynamics within a zone are not circumpolar but are regionalized within sectors.  相似文献   

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