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1.
2006年10月在黄海冷水团海域的三个站点开展了微型异养鞭毛虫、异养细菌和蓝细菌的密度和生物量调查，进行了微型异养鞭毛虫的现场摄食实验，通过荧光标记细菌法和消化系数法获得该海区微型异养鞭毛虫对异养细菌和蓝细菌的摄食率，并估算了微型异养鞭毛虫对异养细菌和蓝细菌现存量及生产力的摄食压。结果显示，微型异养鞭毛虫、异养细菌和蓝细菌的密度分别为036×103~113×103，039×106~113×106和004×104~374×104cells/cm3，温跃层以上明显高于底层。微型异养鞭毛虫对异养细菌的摄食率为533~1489个/（HF·h），对蓝细菌的摄食率为026×102~2310×10-2cells/（HF·h），摄食率随深度而下降。微型异养鞭毛虫每天能消耗927%~3308%的异养细菌现存量和812%~1609%的蓝细菌现存量。同时，微型异养鞭毛虫对异养细菌和蓝细菌的日摄食量各占它们生产力的266%~1310%和812%~1609%。研究表明微型异养鞭毛虫的摄食可能不是秋季黄海冷水团海域浮游细菌及其生产力的主归宿。 相似文献
2.
采用DAPI荧光染色技术, 进行了2007年6月和2008年7月黄海底栖异养细菌的丰度和生物量及分布特点研究。结果表明, 2007年底栖细菌的丰度为(1.13±0.39)×109cells/cm3, 生物量为(49.63±17.26)?gC/cm3; 2008年底栖细菌的现存量较2007年低了约43%。南黄海的底栖细菌现存量较北黄海分别低8%(2007年)和13%(2008年), 而中央冷水团则较其外围区域高约10%和37%, 在南黄海呈现中央冷水区域高于近岸的分布特点, 而在北黄海则正相反。统计分析表明, 2007年北黄海底栖细菌丰度与沉积物叶绿素a含量呈极显著正相关, 南黄海细菌丰度与沉积物有机质含量及底层水盐度呈极显著正相关; 而2008年北黄海细菌丰度与环境因子未见明显的相关性, 在南黄海则与底层水的叶绿素含量呈极显著负相关, 显示浒苔暴发可能对底栖细菌产生了明显抑制。 相似文献
3.
采用海域大规模调查和模拟现场流水法测定了桑沟湾海域微食物环主要组分生物(微微型浮游生物、微型鞭毛虫和纤毛虫)在桑沟湾的季节分布和对长牡蛎食物来源的贡献。对桑沟湾海域浮游生物现存量的调查结果显示:微食物环生物丰度和生物量以冬季最低(P0.05)。微食物环组成生物的生物量以微型鞭毛虫最大,占51.69%(无色素体微型鞭毛虫HNF贡献37.31%,有色素体微型鞭毛虫PNF贡献14.38%),其次是异养细菌(39.03%),纤毛虫和微微型真核浮游生物贡献较小,分别为2.31%和0.66%。使用模拟现场流水法,测定了长牡蛎对浮游生物的摄食,其清滤率变化范围为0.26—3.50L/(g·h),随着粒径的增大,长牡蛎对浮游生物的清滤率增加。长牡蛎对不同浮游生物的清滤率由大到小依次为:2μm以上有色素体浮游生物纤毛虫2μm以下有色素体浮游生物无色素体微型鞭毛虫异养细菌,长牡蛎对2μm以上有色素体浮游生物碳截留最大(289.20±62.36μg/(g·h)),其次是无色素体微型鞭毛虫,异养细菌和纤毛虫。传统的对于贝类食物来源的测定忽略了异养细菌、HNF以及纤毛虫,对微食物环框架的研究得出三种生物对长牡蛎的碳贡献为1563.58μg/(g·d)(17.94%),指示原生动物(异养鞭毛虫和纤毛虫)在长牡蛎的食谱组成中的地位不可忽视。异养细菌除了参与微食物环,还能被长牡蛎直接或者间接的摄食,成为长牡蛎的食物来源之一。本文结果为长牡蛎的养殖容量评估和微食物环生物对养殖生态系统的贡献分析提供了重要的数据支撑。 相似文献
4.
于2009年7月20日至8月16日(夏季),2010年1月6日至30日(冬季),2010年10月26日至11月24日(秋季)和2011年4月30日至2011年5月24日(春季)在南海北部调查了微型异养鞭毛虫的生态分布特点。结果表明:春、夏、秋、冬的微型异养鞭毛虫丰度分别为0.05×103~1.93×103,0.03×103~2.65×103,0.09×103~2.05×103和0.04×103~1.84×103 cells/mL,生物量(以碳计)分别为0.56~19.50,0.04~24.11,0.96~14.80和0.29~22.26 μg/L。4个季节的微型异养鞭毛虫丰度均以2~5 μm粒级的为主,其所占比例超过65%,10~20 μm粒级所占比例通常低于10%。在水平分布上,微型异养鞭毛虫的丰度随离岸距离的增加逐渐降低;在垂直分布上,微型异养鞭毛虫的丰度随深度的增加逐渐降低,但夏季微型异养鞭毛虫丰度的高值多出现在次表层叶绿素a极大值层(DCM层)。微型异养鞭毛虫的丰度分布受到多重因素的交互影响,并且其所受调控模式在不同季节存在差异:春季和秋季微型异养鞭毛虫主要受下行调控;夏季微型异养鞭毛虫主要受上行调控;冬季上行和下行调控对微型异养鞭毛虫的影响相近。 相似文献
5.
东海、黄海浮游病毒及异养细菌的分布研究 总被引：3，自引：1，他引：2
采用流式细胞仪对2009年春季东海、黄海浮游病毒和异养细菌的丰度进行了大尺度(119.5°—129°E, 25°—39°N)研究, 并分析了浮游病毒丰度、异养细菌丰度以及其与环境因子之间的相关性。结果表明, 研究海域浮游病毒、异养细菌的丰度范围分别为3.38×105—2.26×107个/mL(平均6.24×106个/mL)、5.83×103—1.23×106个/mL(平均1.22×105个/mL)。在水平分布上, 浮游病毒与异养细菌的变化趋势基本一致, 且均在山东半岛周边养殖海域、浙江东南沿海养殖区及舟山渔场北部形成明显的高值区; 黄海浮游病毒与异养细菌的丰度平均值均高于东海。在垂直分布上, 东海浮游病毒与异养细菌丰度值随水深呈明显下降趋势, 表层丰度值与30m以下各层差异显著(P<0.05); 在黄海, 二者丰度随水深降低趋势不明显。Pearson相关性分析显示: 调查海域浮游病毒丰度与异养细菌丰度显著正相关(r =0.288, P<0.01), 浮游病毒丰度与温度显著负相关(r = -0.243, P<0.05), 异养细菌丰度与盐度显著负相关(r = -0.245, P<0.05)。 相似文献
6.
渤海、黄海沿岸几种经济贝类及其生存环境中的异养细菌 总被引：10，自引：0，他引：10
报道渤海、黄海6个重点沿岸海域(吕四、青岛、北戴河、盘锦、大连、庄河)海水和沉积物及经济贝类样品中的异养细菌总数检测结果.结果表明,整个渤海、黄海沿岸海域经济贝类体内异养细菌总数的变化范围为2.0×103～1.6×106cfu/g湿重,平均值为2.7×105cfu/g湿重,其中异养细菌总数最高的样品是在吕四沿岸3号站采集的四角蛤蜊(1.6×106cfu/g湿重),其次分别在北戴河沿岸2号站采集的杂色蛤(1.2×106cfu/g湿重)和毛蚶(1.1×106cfu/g湿重),而异养细菌总数最低样品是在青岛沿岸采集的镜蛤(2.0×103cfu/g湿重)和在大连沿岸采集的太平洋牡蛎、紫贻贝和皱纹盘鲍(≤5.0×103cfu/g湿重).该海区表层海水中异养细菌总数变化范围为2.5×105～1.0×108cfu/dm3,全海域平均值为1.2×107cfu/dm3.表层沉积物中异养细菌数量变化范围为2.8×103～7.5×105cfu/g干重,全海域平均值为1.3×105cfu/g干重.根据上述结果和欧共体委员会(93/51/EEC)指令要求,对各海区贝类卫生质量进行了初步评价.这在国内尚属首次. 相似文献
7.
秋季东、黄海异养细菌(Heterotrophic Bacteria)的分布特点 总被引：27，自引：1，他引：27
2000年10-11月,乘"北斗号"考察船进行秋季"东、黄海生态系统动力学与生物资源可持续利用"大面调查,研究秋季东、黄海异养细菌的分布.结果表明,异养细菌在黄海和东海的丰度分别在(2.37-13.33)×108 cell/L和(3.05-13.62)×108 cell/L之间.细菌丰度最高值出现在长江口附近,且断面E和断面F各站位的细菌丰度明显高于其他断面.异养细菌丰度大小以长江口为中心向外海依次递减.东、黄海水体异养细菌生物量分别在244.45-1812.90mgC/m2和100.60-940.87mgC/m2之间.东、黄海异养细菌丰度无显著差异,但是东海海域水体异养细菌生物量高于黄海海域.异养细菌空间分布与浮游植物叶绿素在东海有一定的相关性,黄海异养细菌与硝酸盐浓度的相关性极显著. 相似文献
8.
《中国海洋大学学报(自然科学版)》2017,(Z1)
亚洲沙尘是全球沙尘的重要组成部分,黄海是受亚洲沙尘影响较大的海域。沙尘沉降是海洋营养元素的重要来源之一,对海洋异养细菌的生长有重要影响。为研究亚洲沙尘沉降对黄海海域异养细菌丰度和活性的影响,于2014年11月在北黄海S1站位和南黄海S2站位分别进行了船基围隔培养实验,通过添加不同浓度的沙尘和无机磷研究沙尘沉降对海洋异养细菌的作用过程。结果显示,沙尘的添加在南、北黄海海域均显著提高了异养细菌丰度和高核酸菌比例(HNA%),高浓度沙尘对异养细菌丰度和活性的促进作用最显著,培养结束后使北黄海和南黄海异养细菌丰度分别增加了62%和45%;磷的添加在北黄海海域显著提高了异养细菌丰度和高核酸菌比例(HNA%),高浓度磷对异养细菌丰度和活性的促进作用最显著,培养结束后使异养细菌丰度增加了50%。研究表明,沙尘能够缓解北黄海磷对异养细菌生长的限制,促进异养细菌的生长,增强异养细菌的活性,提高异养细菌在海洋生态系统中的生态功能。南黄海海域,沙尘在短期内对异养细菌的生长表现为抑制作用,降低了异养细菌的活性;沙尘在长期内对异养细菌的生长表现为促进作用,增强了异养细菌活性。等量沙尘的沉降方式不同,对生态系统的影响结果存在较大差异。 相似文献
9.
东海异养细菌生产力的时空分布 总被引：11，自引：2，他引：9
1997年 2— 3月和 1 998年 7月 ,在东海海区乘“科学一号”考察船进行两个航次的调查 ,利用异养细菌特异示踪物 [甲基 - 3H]胸腺嘧啶核苷 (3H -Tdr)并入DNA的速率测定东海 (2 7°— 32°N ,1 2 2°— 1 30°E)异养细菌生产力 (BP)。结果表明 ,1 997年 2— 3月 (冬季 )异养细菌生产力较低 [0 46— 2 62 μgC/(L·h) ],1 998年 7月 (夏季 )异养细菌生产力较高 [3 50—1 5 70 μgC/(L·h) ]。冬季和夏季在长江口和 41 0站附近都有一个异养细菌生产力的高值区。通过两个连续站的昼夜观测发现冬季异养细菌生产力变化是底层 >中层 >表层 ,夏季是中层>底层 >表层。异养细菌生产力与初级生产力 (PP)之比 ,即BP PP ,冬季的均值为 0 1 7(0 0 4— 0 30 ) ,夏季的均值为 0 32 (0 2 1— 0 43)。BP PP冬季的高值区在长江口附近 ,夏季的高值区在 1 1 1站附近 ,这与长江冲淡水有密切相关。 相似文献
10.
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
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
11.
A study was carried out to investigate the grazing pressure of heterotrophic nanoflagellates(HNF) on bacteria assemblages in the Yellow Sea Cold Water Mass(YSCWM) area in October, 2006. The results show that the HNF abundance ranges from 303 to 1 388 mL-1, with a mean of 884 mL-1. The HNF biomass is equivalent to 10.6%–115.6% of that of the bacteria. The maximum abundance of the HNF generally occurred in the upper 30 m water layer, with a vertical distribution pattern of surface layer abundance greater than middle layer abundance, then bottom layer abundance. The hydrological data show that the YSCWM is located in the northeastern part of the study area, typically 40 m beneath the surface. A weak correlation is found between the abundances of HNF and bacteria in both the YSCWM and its above water layer. One-way ANOVA analysis reveals that the abundance of HNF and bacteria differs between inside the YSCWM and in the above water mass. The ingestion rates of the HNF on bacteria was 8.02±3.43 h-1 in average. The grazing rate only represented 22.75%±6.91% of bacterial biomass or 6.55%+4.24% of bacterial production, implying that the HNF grazing was not the major factor contributing to the bacterial loss in the YSCWM areas. 相似文献
12.
A. I. Kopylov A. F. Sazhin E. A. Zabotkina A. V. Romanenko N. D. Romanova P. R. Makarevich M. P. Wenger 《Oceanology》2016,56(6):789-798
The paper considers the concentrations and functional characteristics of viruses, bacteria, and heterotrophic nanoflagellates determined for the first time in the Laptev Sea in August-September, 2014. The abundance of bacteria, viruses, and heterotrophic nanoflagellates varied from 110.1 × 103 to 828.4 × 103 cells/mL, from 384.2 × 103 to 2932.8 × 103 particles/mL, and from 108 to 651 cells/mL, respectively. The daily bacterioplankton production varied from 4.2 × 103 to 381.7 × 103 cells/mL, with an average of 117.6 × 103 cells/mL. Electron transmission microscopy has for the first time shown that the frequency of visibly infected bacterial cells varied from 0.2 to 2.0% (0.8% on average) of NB. The average virus-induced mortality of bacteria was 6.3% of bacterioplankton production, with variations ranging from 1.4 to 16.9%. Grazing on bacteria by heterotrophic nanoflagellates contributed more to bacteria mortality than virus-induced bacterial lysis. By grazing on bacteria, heterotrophic nanoflagellates consumed large quantities of viruses located on the surface and inside bacterial cells. 相似文献
13.
Distribution of heterotrophic nanoflagellates and their importance as the bacterial consumer in a eutrophic coastal seawater 总被引：4，自引：0，他引：4
Kimio Fukami Noriyuki Murata Yuuki Morio Toshitaka Nishijima 《Journal of Oceanography》1996,52(4):399-407
Seasonal and vertical changes in abundances of bacteria and heterotrophic nanoflagellates (HNF), and HNF grazing on bacteria were investigated in a small eutrophic inlet of Uranouchi-Wan throughout the years. Bacterial densities in the surface water ranged from 1.2 to 11 (average 4.3)×106 cells ml–1 with a couple of maxima following the algal blooming. Densities of HNF ranged from 0.54 to 73 (average 16.4)×103 cells ml–1 in the surface, and showed almost similar fluctuation pattern to that of bacteria with a time lag of about 1 to 2 weeks. Grazing rates of HNF on bacteria obtained by FLB method were 4.78 to 16.9 (average 10.3±SD 4.8) cells HNF–1h–1 in the surface layer in summer, and consequent total bacterial consumption rates by HNF fluctuated from 4 to 99×104 cells ml–1h–1. In deeper layers, however, as HNF densities and grazing rates on bacteria were low, the grazing pressure of HNF on bacteria was small. Turnover times of bacteria by HNF grazing in the surface layer were calculated as relatively constant values of 40 to 60 h, however, it decreased to as low as 6 to 7 h when the HNF activity was highest. These results indicate that bacteria grew so actively by consuming organic matter in seawater as to compensate high HNF grazing pressure, and that bacteria and HNF in the microbial loop play important roles on the turnover of substrates in coastal ecosystems. 相似文献
14.
台湾海峡小型浮游动物的摄食对夏季藻华演替的影响 总被引：3，自引：2，他引：3
于2004年8月1~6日对台湾海峡南部近岸的藻华过程进行了定点连续跟踪观测,用稀释法研究了浮游植物的生长率和小型浮游动物对浮游植物的摄食死亡率,同时运用高效液相色谱(HPLC)技术,分析了浮游植物不同光合色素类群的生长率和摄食死亡率.结果表明,观测期间处于藻华的消退期.8月1日时,浮游植物生物量(叶绿素a)和丰度分别为2.04μg/dm3和2.99×105个/dm3,主要优势种为尖刺伪菱形藻(Pseudo-nitzschia pungens)、冰河拟星杆藻(Asterionellopsis glacialis)和中肋骨条藻(Skeletonema costatum),8月6日时,浮游植物生物量和丰度分别减为0.37μg/dm3和1.54×104个/dm3;而蓝藻和甲藻的丰度和比例则呈现出逐渐增加的趋势,所占的比重分别从1日的0.04%和0.85%增加到6日的9.59%和41.97%.小型浮游动物主要由无壳纤毛虫、砂壳纤毛虫、红色中缢虫(Mesodinium rubrum)和异养甲藻等类群组成,总丰度于8月2日达到最大值,为3640个/dm3,之后逐渐减少,6日时,仅为436个/dm3.观测期间,小型浮游动物在群落组成上虽一直以无壳纤毛虫和异养甲藻为主,但在具体的类群结构上却表现出了一定的差异,30μm以下的无壳纤毛虫和异养甲藻总体呈下降的趋势,而红色中缢虫、砂壳纤毛虫和大于50μm的无壳纤毛虫总体呈增加的趋势.观测期间,浮游植物的生长率为0.40~0.91d-1,小型浮游动物的摄食率为0.26~1.34d-1,摄食率和生长率总体呈逐渐下降的趋势.结果还表明,小型浮游动物的摄食率与叶绿素a具有很好的相关性(R2=0.89),对各光合色素类群的现存量和初级生产力均具有较高的摄食压力(分别为37.97%~82.24%和70.71%~281.33%),是藻华消亡的重要原因之一;此外,小型浮游动物对甲藻和蓝藻的避食行为,可能是观测期间由“硅藻”水华向“硅藻-甲藻”水华转变的重要原因之一. 相似文献
15.
Evaristo Vázquez-Domínguez Carlos M. Duarte Klaus Jürgens Josep M. Gasol 《Progress in Oceanography》2008,79(1):83-94
The role of microorganisms in the transfer of carbon of marine systems is very important in open oligotrophic oceans. Here, we analyze the picoplankton structure, the heterotrophic bacterioplankton activity, and the predator-prey relationships between heterotrophic bacteria and nanoflagellates during two large scale cruises in the Central Atlantic Ocean (∼29°N to ∼40°S). Latitud cruises were performed in 1995 between March-April and October-November. During both cruises we crossed the regions of different trophic statuses; where we measured different biological variables both at the surface and at the deep chlorophyll maximum (DCM). The concentration of chlorophyll a varied between 0.1 and 0.8 mg m−3, the abundance of heterotrophic bacteria varied between <1.0 × 105 and >1.0 × 106 cells ml−1, and that of heterotrophic nanoflagellates between <100 and >1.0 × 104 cells ml−1. The production of heterotrophic bacteria varied more than three orders of magnitude between <0.01 and 24 μgC L−1 d−1; and the growth rates were in the range <0.01-2.1 d−1. In the Latitud-II cruise, Prochlorococcus ranged between <103 and >3 × 105 cells ml−1, Synechococcus between <100 and >1.0 × 104 cells ml−1, and picoeukaryotes between <100 and >104 cells ml−1.Two empirical models were used to learn more about the relationship between heterotrophic bacteria and nanoflagellates. Most bacterial production was ingested when this production was low, the heterotrophic nanoflagellates could be controlled by preys during Latitud-I cruise at the DCM, and by predators in the surface and in the Latitud-II cruise. Our results were placed in context with others about the structure and function of auto- and heterotrophic picoplankton and heterotrophic nanoplankton in the Central Atlantic Ocean. 相似文献
16.
《Deep Sea Research Part II: Topical Studies in Oceanography》2010,57(16):1537-1550
Studies in epipelagic waters report higher heterotrophic microbial biomass in the productive high latitudes than in the oligotrophic low latitudes; however, biogeographical data are scarce in the deep ocean. To examine the hypothesis that the observed latitudinal differences in heterotrophic microbial biomass in the epipelagic zone also occur at depth, abundance and biomass of heterotrophic prokaryotes, nanoflagellates (HNF), and ciliates were determined at depths of 5–5000 m in the central Pacific between August and September of 2005. Heterotrophic microbial biomass increased from the tropical to the subarctic region over the full water column, with latitudinal differences in prokaryotic biomass increasing from 2.3-fold in the epipelagic zone to 4.4-fold in the bathypelagic zone. However, the latitudinal difference in HNF and ciliate biomass decreased with depth. In the mesopelagic zone, the vertical attenuation rate of prokaryotic abundance, which was calculated as the linear regression slope of log-log plot of abundance versus depth, ranged from –0.55 to –1.26 and was more pronounced (steeper slope) in the lower latitudes. In contrast, the vertical attenuation rate of HNF in the mesopelagic zone (–1.06 to –1.27) did not differ with latitude. In the subarctic, the attenuation rate of HNF was 1.7 times steeper than for prokaryotes. These results suggest the accumulation of prokaryotes in the deep subarctic Pacific, possibly due to low grazing pressure. Although the vertical attenuation rate of ciliates was steepest in the bathypelagic zone, HNF abundance did not further decrease at depths below 1000 m, except for at 2000 m where HNF was lowest across the study area. Ciliate abundance ranged 0.3–0.8 cells l–1 at 4000 m, and were below the detection limit (<0.1 cells l –1) at 5000 m. To our knowledge, this study presents the first data for ciliates below 2000 m. 相似文献
17.
18.
影响北欧海和楚科奇海夏季细菌丰度和生产力的因素 总被引：3，自引：0，他引：3
Abundance and production of bacterioplankton were measured in the Nordic seas and Chukchi Sea during the5 th Chinese Arctic Research Expedition in summer 2012.The results showed that average bacterial abundances ranged from 3.31×10~(11) cells/m~3 to 2.25× 10~(11)cells/m~3,and average bacterial productions(calculated by carbon)were 0.46 mg/(m~3·d) and 0.54 mg/(m~3·d) in the Nordic seas and Chukchi Sea,respectively.T-test result showed that bacterial abundances were significantly different between the Nordic seas and Chukchi Sea,however,no significant difference was observed regarding bacterial productions.Based on the slope of lg bacterial biomass versus lg bacterial production,bacterial communities in the Nordic seas and Chukchi Sea were moderately dominated by bottom-up control.Both Pearson correlation analysis and multivariable linear regression indicated that temperature had significant positive correlation with bacterial abundance in the Chukchi Sea,while no correlations with productions in both areas.Meanwhile,Chl a had positive correlations with both bacterial abundance and production in these two regions.As the temperature and Chl a keep changing in the future,we suggest that both bacterial abundance and production been hanced in the Chukchi Sea but weaken in the Nordic seas,though the enhancement will not be dramatic as a result of higher pressure of predation and viral lysis. 相似文献