Dissolved organic carbon in sediments from the eastern North Atlantic

Profiles of dissolved organic carbon (DOC) were measured in the pore water of sediments from 1000, 2000 and 3500 m water depth in the eastern North Atlantic. A net DOC accumulation in the pore waters was observed, which followed closely the zonation of microbial respiration in these sediments. The concentration of pore water DOC in the zone of oxic respiration was elevated relative to that in the bottom ocean water. The resulting upward gradient across the sediment–water interface indicated a steady state diffusive benthic flux, F_DOC, of 0.25–0.44 mmol m⁻² day⁻¹ from these sediments. Subsequent increase in the concentration of DOC in the pore water occurred only in the sediments from 1000 and 2000 m water depth that supported anoxic respiration, leading to a deep concentration maximum. By contrast, in the sediments from 3500 m water depth, a deep concentration minimum was measured, coincident with minimal postoxic respiration in this near-abyssal setting. The gradient-based F_DOC represented approximately 14% of the total remineralized organic carbon (TCR=sum of F_DOC and depth-integrated organic carbon oxidation rate) in the sediments from 1000 and 2000 m water depth, while it was 36% of the TCR in the sediments from 3500 m water depth. A covariance of particulate organic carbon (POC) and pore water DOC with depth in the sediments was evident, more consistently at the deepest site. While the covariance can be related to biotic processes in these sediments, an alternative interpretation suggests a possible contribution of sorption to the biotic control on sedimentary organic carbon cycling. The steady state diagenetic conditions in which this may occur can be conceivable for some organic-poor deep-sea locations, but direct evidence is clearly required to validate them.     

Meridional carbon dioxide transport in the northern North Atlantic

Combination of estimated water transport and accurate measurements of total carbon dioxide (TCO₂) on a hydrographic section at 58 °N allows the assessment of meridional inorganic carbon transport in the northern North Atlantic Ocean. The transport has been decomposed into contributions from the large-scale baroclinic overturning, the Ekman transport, baroclinic and a barotropic eddy terms, and an estimated contribution of the East Greenland Current. These terms are −0.27 · 10⁶, +0.03 · 10⁶, +0.03 · 10⁶, +0.10 · 10⁶, and +0.05 · 10⁶ mol s⁻¹, respectively, which result in a total southward inorganic carbon transport of only −0.06 · 10⁶ mol s⁻¹. An order of magnitude estimate of the meridional transport of dissolved organic carbon (DOC) has shown that in general this term cannot be ignored in the total carbon flux, this being +0.04 · 10⁶ to +0.16 · 10⁶ mol s⁻¹ at 58 °N. A simple carbon budget has been formulated for the temperate North Atlantic, using our flux estimates as well as those of Brewer et al. (1989). This budget shows that the divergence of the meridional carbon flux, connected with the freshwater balance of the ocean may be of the same order of magnitude as the divergence of the total inorganic carbon flux. For an accurate estimate of the total carbon budget of the ocean it will be necessary to take both the DOC transport and the effects of the freshwater balance into account.     

The oxygen isotope composition of water masses in the northern North Atlantic

The ratio of oxygen-18 to oxygen-16 (expressed as per mille deviations from Vienna Standard Mean Ocean Water, δ¹⁸O) is reported for seawater samples collected from seven full-depth CTD casts in the northern North Atlantic between 20° and 41°W, 52° and 60°N. Water masses in the study region are distinguished by their δ¹⁸O composition, as are the processes involved in their formation. The isotopically heaviest surface waters occur in the eastern region where values of δ¹⁸O and salinity (S) lie on an evaporation–precipitation line with slope of 0.6 in δ¹⁸O–S space. Surface isotopic values become progressively lighter to the west of the region due to the addition of ¹⁸O-depleted precipitation. This appears to be mainly the meteoric water outflow from the Arctic rather than local precipitation. Surface samples near the southwest of the survey area (close to the Charlie Gibbs Fracture Zone) show a deviation in δ¹⁸O–S space from the precipitation mixing line due to the influence of sea ice meltwater. We speculate that this is the effect of the sea ice meltwater efflux from the Labrador Sea. Subpolar Mode Water (SPMW) is modified en route to the Labrador Sea where it forms Labrador Sea Water (LSW). LSW lies to the right (saline) side of the precipitation mixing line, indicating that there is a positive net sea ice formation from its source waters. We estimate that a sea ice deficit of ≈250 km³ is incorporated annually into LSW. This ice forms further north from the Labrador Sea, but its effect is transferred to the Labrador Sea via, e.g. the East Greenland Current. East Greenland Current waters are relatively fresh due to dilution with a large amount of meteoric water, but also contain waters that have had a significant amount of sea ice formed from them. The Northeast Atlantic Deep Water (NEADW, δ¹⁸O=0.22‰) and Northwest Atlantic Bottom Waters (NWABW, δ¹⁸O=0.13‰) are isotopically distinct reflecting different formation and mixing processes. NEADW lies on the North Atlantic precipitation mixing line in δ¹⁸O–salinity space, whereas NWABW lies between NEADW and LSW on δ¹⁸O–salinity plots. The offset of NWABW relative to the North Atlantic precipitation mixing line is partially due to entrainment of LSW by the Denmark Strait overflow water during its overflow of the Denmark Strait sill. In the eastern basin, lower deep water (LDW, modified Antarctic bottom water) is identified as far north as 55°N. This LDW has δ¹⁸O of 0.13‰, making it quite distinct from NEADW. It is also warmer than NWABW, despite having a similar isotopic composition to this latter water mass.     

Dissolved organic carbon export and subsequent remineralization in the mesopelagic and bathypelagic realms of the North Atlantic basin

Dissolved organic carbon (DOC) data are presented from three meridional transects conducted in the North Atlantic as part of the US Climate Variability (CLIVAR) Repeat Hydrography program in 2003. The hydrographic sections covered a latitudinal range of 6°S to 63°N along longitudes 20°W (CLIVAR line A16), 52°W (A20) and 66°W (A22). Over 3700 individual measurements reveal unprecedented detail in the DOC distribution and systematic variations in the mesopelagic and bathypelagic zones of the North Atlantic basin. Latitudinal gradients in DOC concentrations combined with published estimates of ventilation rates for the main thermocline and North Atlantic Deep Water (NADW) indicate a net DOC export rate of 0.081 Pg C yr⁻¹ from the epipelagic zone into the mesopelagic and bathypelagic zones. Model II regression and multiple linear regression models applied to pairwise measures of DOC and chlorofluorocarbon (CFC-12) ventilation age, retrieved from major water masses within the main thermocline and NADW, indicate decay rates for exported DOC ranging from 0.13 to 0.94 μmol kg⁻¹ yr⁻¹, with higher DOC concentrations driving higher rates. The contribution of DOC oxidation to oxygen consumption ranged from 5 to 29% while mineralization of sinking biogenic particles drove the balance of the apparent oxygen utilization.     

Geotechnical characteristics of deep-sea sediments from the North Atlantic and North Pacific oceans

Geotechnical properties from a series of deep-sea sites in the North Atlantic and North Pacific oceans are examined to evaluate overall trends and to compare with similar fine-grained soils found on land. The study areas encompass a range of sedimentary environments dominated by combinations of turbidite and pelagic deposits. Carbonate content in excess of 20% is seen to result in a decrease in liquid limit and compressibility. Vertical profiles of geotechnical properties in the North Pacific show broader changes in down-core geotechnical properties compared to the North Atlantic and reflect the effects of long-term climatic changes and seafloor spreading. Sediments in the North Atlantic indicate significant differences depending on location, which is attributed to variability in turbidite deposition, water depth, distance from sediment sources, and the effects of bottom currents. Compared to equivalent fine-grained soils on land, deep-sea sediments are generally softer, more compressible and have higher friction angles at comparable Atterberg limits. Deeper and older sediments in the North Pacific are characterized by unusually large plastic limits, which are attributed to the presence of volcanic fractions. Empirical relationships for compression index and friction angle are discussed for sediments from both oceans.     

Bacterial abundance and activity in deep-sea sediments from the eastern North Atlantic

Results are presented from four cruises to the Porcupine Abyssal Plain (PAP site) that took place during the BENGAL project from September 1996 to March 1998, and two cruises to the PAP and an oligotrophic site (EUMELI) that took place during the DEEPSEAS project between September 1993 and March 1994. Bacterial abundances in sediment and sediment contact water were measured by epifluorescence microscopy. Bacterial activity was determined by ³H-thymidine incorporation as a measure of DNA synthesis, and by ³H-leucine incorporation as a measure of protein synthesis. Activities were measured under atmospheric and in situ pressures and temperatures. Bacterial activity was usually higher in samples incubated at in situ pressure than those incubated at atmospheric pressure indicating that a barophilic community was dominant. Inter-cruise comparisons of abundance and activity during the BENGAL project showed no firm evidence of there being a seasonal response in the benthic microbial community to any episodic phytodetritus event. This was probably because of inter-annual variations in the quality and quantity of phytodetritus deposition at the PAP site, the rapid remineralization of fresh organic material by the microbial communities and the timing of cruises to the study area. ³H-thymidine and ³H-leucine incorporation in sediments was higher during the BENGAL period than the DEEPSEAS programme. A methodological change in the ³H-thymidine incorporation technique for sediments may explain the differences in DNA synthesis observed between the two projects, whereas the lower levels of protein synthesis observed during the DEEPSEAS programme probably reflected both inter-annual variations in activity at the PAP site and the lower productivity that prevailed at surface at the EUMELI oligotrophic site. Rates of ³H-thymidine incorporation in sediment contact water were similar during both projects.     

The geochemistry of basal sediments from the North Atlantic Ocean

Chemical analyses of North Atlantic D.S.D.P. (Deep Sea Drilling Project) sediments indicate that basal sediments generally contain higher concentrations of Fe, Mn, Mg, Pb, and Ni, and similar or lower concentrations of Ti, Al, Cr, Cu, Zn, and Li than the material overlying them. Partition studies on selected samples indicate that the enriched metals in the basal sediments are usually held in a fashion similar to that in basal sediments from the Pacific, other D.S.D.P. sediments, and modern North Atlantic ridge and non-ridge material.Although, on average, chemical differences between basal sediments of varying ages are apparent, normalization of the data indicates that the processes leading to metal enrichment on the crest of the Mid-Atlantic Ridge appear to have been approximately constant in intensity since Cretaceous times. In addition, the bulk composition of detrital sediments also appears to have been relatively constant over the same time period. Paleocene sediments from site 118 are, however, an exception to this rule, there apparently having been an increased detrital influx during this period.The bulk geochemistry, partitioning patterns, and mineralogy of sediments from D.S.D.P. 9A indicates that post-depositional migration of such elements as Mn, Ni, Cu, Zn, and Pb may have occurred. The basement encountered at the base of site 138 is thought to be a basaltic sill, but the overlying basal sediments are geochemically similar to other metalliferous basal sediments from the North Atlantic. These results, as well as those from site 114 where true oceanic basement was encountered, but where there was an estimated 7 m.y. hiatus between basaltic extrusion and basal sediment deposition, indicate that ridge-crest sediments are not necessarily deposited during active volcanism but can be formed after the volcanism has ceased. The predominant processes for metal enrichment in these deposits and those formed in association with other submarine volcanic features is a combination of shallow hydrothermal activity, submarine weathering of basalt, and the formation of ferromanganese oxides which can scavenge metals from seawater. In addition, it seems as though the formation of submarine metalliferous sediments is not restricted to active-ridge areas.     

Correlation between the low-frequency variability of surface temperature and the heat flux through the surface in the North Atlantic

Using the data of UWM/COADS (University of Wisconsin-Milwaukee/Comprehensive Ocean—Atmosphere Data Set), we have performed cluster and spectral analyses of the average monthly anomalies of temperature and heat balance of the surface of the Atlantic Ocean in three frequency ranges (intraannual, interannual, and decadal). It is shown that these anomalies are closely related on intraannual scales, where the anomalies of the surface temperature of the ocean can be regarded as a result of the direct local generation by heat balance anomalies. The generation mechanism is explained within the known Hasselman model [1, 2]. On interannual scales, this mechanism is not valid, and nonlocal effects related to heat advection become important. On decadal scales, the local generation of anomalies of the surface temperature of the ocean is insignificant, local correlation between fluctuations of heat balance and the surface temperature of the ocean is completely broken, and the spatial structure of anomalies of the surface temperature of the ocean is governed by the global system of currents, which redistributes heat flux from the ocean to the atmosphere. Violations of the local correlation between anomalies of heat balance and the surface temperature of the ocean are observed on intraannual scales in regions with powerful jet currents and in the equatorial region. In some parts of the World's ocean with weak advection, the correlation between heat balance and the surface temperature of the ocean persists up to a decadal period. Translated by Peter V. Malyshey and Dmitry V. Malyshey     

Cross-basin differences in particulate organic carbon export and flux attenuation in the subtropical North Atlantic gyre

We compared in-situ and satellite-derived measures of the biological carbon pump efficiency at the two seemingly similar subtropical North Atlantic gyre time series sites, the Bermuda time series (BATS, Bermuda Atlantic time-series study and OFP, ocean flux program) in the western gyre and the ESTOC time series (European station for time-series in the ocean, Canary Islands) in the eastern gyre. Satellite-derived surface chlorophyll a was slightly lower at Bermuda compared to ESTOC (annual average of 0.10±0.04 vs. 0.14±0.05-mg-m^?3), as was satellite-derived primary production (annual average of 380±77 vs. 440±80-mg C-m^?2 d^?1). However, export production normalized to primary production (export ratio) was higher at Bermuda by a factor of 2–3 when estimated using mesopelagic traps moored at 500-m depth and by a factor of 3–4 when estimated using surface-tethered drifting traps. When averaged seasonally, flux at BATS was highest in spring (March, April, May) at all depths followed by summer (June, July, August) and decreasing towards fall, but this seasonality was less visible at ESTOC. Seasonal comparison showed the fastest flux attenuation at Bermuda in winter and spring, coinciding with the highest POC flux. POC/PIC ratios derived from the moored traps were significantly higher at BATS than at ESTOC in fall and winter, but this difference was not significant in spring (p>0.05). This study shows that while the western and eastern Atlantic subtropical gyres have similar rates of primary production, the biological carbon pump differs between the two provinces. Higher new nutrient input observed at Bermuda compared to ESTOC might explain part of the difference in export ratio but alone is insufficient. Greater winter mixed-layer depths and higher mesoscale eddy activity at Bermuda resulting in pulsed production events of labile organic matter might explain both the higher export flux and export ratios found at Bermuda.     

渤海湾北部和西部海域表层沉积物中无机碳形态研究

采用氯化钠(NaC1)、氨水(NH3·H2O)、氢氧化钠(NaOH)、盐酸羟胺(NH2OH·HC1)溶液对渤海湾北部和西部海域表层沉积物中无机碳进行了连续浸取,并将无机碳分为5种赋存形态:交换态(NaCl相)、弱碱结合态(NH3·H2O相)、强碱结合态(NaOH相)、弱酸结合态(NH2OH·HCl相)和残渣态.同时,结...     

Organic geochemistry of late Cenozoic sediments from the subtropical South Atlantic Ocean

Organic matter has been characterized in samples of Pleistocene, Pliocene, and Miocene sediments from seven Deep Sea Drilling Project sites in the subtropical South Atlantic Ocean. Organic carbon concentrations average 0.3% for most samples, and n-alkanoic acid, n-alkanol, and alkane biomarkers indicate extensive microbial reworking of organic matter in these organic-carbon-lean sediments. Samples from the easternmost parts of the South Atlantic contain an average of 4.1% organic carbon and reflect the high productivity associated with the Benguela Current. Lipid biomarkers show less microbial reworking in these sediments. Eolian transport of land-derived hydrocarbons is evident at most of these oceanic locations.     

北冰洋西部沉积物有机碳、氮同位素特征及其环境指示意义

通过对楚科奇海及邻近的北冰洋深水区表层沉积物中有机碳同位素含量(δ13C)、氮同位素含量(δ15N)及生物成因SiO₂(BSiO₂)含量分析,结果表明海源和陆源有机质的分布受海区环流结构和营养盐结构所制约.楚科奇海中西部和楚科奇海台受太平洋富营养盐海水的影响,海洋生产力高,沉积物中海源有机质和BSiO₂含量高;靠阿拉斯加一侧海域海水的营养盐含量和生产力都偏低,沉积物中陆源有机质比重增加;在研究区北部和东北部的楚科奇高地和加拿大海盆,冰封时间较长,营养盐供应少,海洋生产力低,但来自马更些河和阿拉斯加北部的陆源有机质增多,沉积物中BSiO₂含量小于5%,海源有机质百分含量小于40%.由于亚北极太平洋水通过楚科奇海向北冰洋海盆输送,研究区营养盐池表现为开放系统,营养盐的利用率与它的供应成反比,与海洋生产力成反比.     

Organic carbon and nitrogen isotopes in surface sediments from the western Arctic Ocean and their implications for sedimentary environments

1 IntroductionFor several reasons, the Arctic Ocean and itsmarginal seas are key areas for understanding ocean-ic circulation and global climate system ( Clark,1982; Hansen et al., 1983; Walsh et al., 1996;Overpeck et al., 1997). First, the Arctic Ocean i…     

神狐海域Site4B表层沉积物中脂肪酸组成及其碳同位素分布特征

通过对神狐海域表层5个沉积物样品进行脂肪酸组成及其碳同位素分布特征测试和研究,结果表明总脂肪酸含量分布为5.14~8.99 μg/g,碳数分布范围从C₁₂到C₃₂,类型包括正构饱和脂肪酸、支链脂肪酸、单不饱和脂肪酸、多不饱和脂肪酸和类异戊二烯酸等计48种;样品中饱和的短链脂肪酸主要来自细菌与浮游生物,而长链饱和脂肪酸来自陆源高等植物,其比例表明研究海域中海洋细菌与浮游生物输入量远远大于陆源高等植物的输入。支链脂肪酸10me16:0与单不饱和脂肪酸18:1ω9、16:1ω9主要来自硫酸盐还原菌,而单不饱和脂肪酸16:1ω7很大可能来源于硫氧化菌,比较相对含量得出神狐海域表层沉积物为还原环境。样品中检测出8种类异戊二烯酸,主要是植烷酸和17,21-ββ二升藿烷酸,及少量的姥鲛酸,推测为叶绿素a和细菌微生物的共同贡献。     

Arsenic in sediments of the North Atlantic Ocean and the Eastern Mediterranean Sea

Chemical extraction techniques show that the majority of the arsenic in North Atlantic deep-sea sediments is associated with an iron phase compositionally similar to that found in deep-sea ferromanganese nodules (As/Fe ～ 11 · 10^?4) and is probably of seawater origin. Some sediments also contain As associated with Fe oxides produced by continental weathering. A minority (～8%) of the arsenic is of detrital origin but is not associated with Fe or Mn oxides; it has a content (1.7 ppm) similar to the average crustal abundance. In the Eastern Mediterranean Sea, near-shore sediments contain As associated with land-derived Fe oxides (As/Fe ～ 2 · 10^?4), but As/Fe ratios increase to ～ 13 · 10^?4 in deep-sea sediments as the contribution of seawater derived arsenic becomes dominant. Arsenic is enriched in metalliferous sediments (As/Fe ～ 20?50 · 10^?4) but As/P ratios of metalliferous sediments, deep-sea ferromanganese nodules and deep-ocean water are all similar. Although a hydrothermal contribution cannot be discounted, it is likely that the arsenic is also of seawater origin, suggesting that hydrothermal iron oxyhydroxides remove As more efficiently from seawater than do iron phases (goethite) in deep-sea sediments and nodules. Arsenic accumulates in deep-sea sediments (～ 6 μg cm^?2 10^?3 yr^?1) at sediments (～ 120 μg cm^?2 10^?3 yr^?1) at rate sufficient to balance river input input (～3 · 10¹⁰ g yr^?1). These estimates give an oceanic residence time for arsenic of 1–2 · 10⁵ yr.     

渤海表层沉积物中有机碳的分布和来源

大河影响下的陆架边缘海沉积有机碳的分布和来源是全球碳循环研究的重要内容。本研究于2012年5月采集了渤海海域的29个表层沉积物样品,分析了粒度组成、总有机碳(TOC)、总氮(TN)、木质素含量和稳定碳同位素丰度(δ13C)等参数,结合基于蒙特卡洛模拟的三端元混合模型,定量研究了沉积物中有机碳的分布和来源情况,并讨论了其影响因素。结果表明,研究区域表层沉积物中TOC含量为0.19%~0.81%,渤海中部泥质区站位(大于0.65%)明显高于其周围砂质区域站位(小于0.40%);TOC与黏土含量也有显著的正相关性,说明细颗粒沉积物容易富集有机碳。沉积有机碳的δ13C范围为-23.7‰~-21.8‰,显示沉积有机碳是海源和陆源有机碳的混合输入。木质素参数,如C/V、S/V和LPVI的数值范围显示研究区域表层沉积物中木质素主要来源于被子植物草本组织与木本组织的混合,同时有少量裸子植物的贡献。基于蒙特卡洛模拟的三端元混合模型显示研究区域沉积物中有机碳主要来源于海洋浮游植物,平均为64%,陆源有机碳中来自土壤的贡献最高(平均为27%),C₃维管植物的贡献较少(平均为9%)。海洋浮游植物有机碳主要分布在渤海中部泥质区及离岸较远的区域,而土壤有机碳和C₃维管植物有机碳则主要沉积在河口附近及近岸区,并可以离岸输运到较远的地方。     

Local remineralization patterns in the mesopelagic zone of the Eastern North Atlantic, off the NW Iberian Peninsula

The short-time-scale variability of the remineralization patterns in the domain of Eastern North Atlantic Central Waters (ENACW) off the NW Iberian Peninsula is studied based on biogeochemical data (oxygen, nutrient salts, total alkalinity, pH, dissolved organic matter and fluorescence of dissolved humic substances) collected weekly between May 2001 and April 2002. The temporal variability of inorganic variables points to an intensification of remineralization during the summer and autumn, with an increase of nutrients, total inorganic carbon and fluorescence and a decrease of oxygen. During the subsequent winter mixing, there is a biogeochemical reset of the system, with lower nutrients, total inorganic carbon and fluorescence and higher oxygen. In contrast to inorganic variables, the levels of dissolved organic matter in the ENACW seem to respond to short-term events probably associated with fast sinking particles, where solubilisation of organic matter prevails over remineralization. Applying a previously published stoichiometric model, we observed a vertical fractionation of organic-matter remineralization. Although there is a preferential remineralization of proteins and P compounds in the entire domain of ENACW, the percentage was higher in the upper ENACW (σ<27.10 kg/m³) than in the lower; the percentage of N and P compounds in the oxidised organic matter was >80% for the upper ENACW and 63% for the lower. Likewise, the redissolution of calcareous structures contributes about 6% and 13% to the carbon regenerated in the upper and lower layers of ENACW, respectively.     

Dissolved organic carbon and apparent oxygen utilization in the Atlantic Ocean

Dissolved organic carbon (DOC) distributions along two Atlantic Meridional Transects conducted in 2005 in the region between 47°N and 34°S showed clear latitudinal patterns. The DOC concentrations in the epipelagic zone (0–100 m) were the highest (70–90 µM) in tropical and subtropical waters with stable mixed layers, and lowest (50–55 µM) at the poleward extremities of the transects due to deep convective mixing supplying low DOC waters to the surface. A decrease in DOC occurred with depth, and lowest DOC concentrations (41–45 µM) in the 100–300 m depth range were observed in the equatorial region due to upwelling of low DOC waters. A strong relationship between DOC and AOU was observed in the σ–t 26–26.5 isopycnal layer which underlies the euphotic zone and outcrops at the poleward extremities of the North and South Atlantic Subtropical Gyres (NASG and SASG) in the region ventilating the thermocline waters. Our observations reveal significant north–south variability in the DOC–AOU relationship. The gradient of the relationship suggests that 52% of the AOU in the σ–t 26–26.5 density range was driven by DOC degradation in the NASG and 36% in the SASG, with the remainder due to the remineralisation of sinking particulate material. We assess possible causes for the greater contribution of DOC remineralisation in the NASG compared to the SASG.     

Organic compounds in the aerosols and surface waters of the East Atlantic

The data on the content and composition of lipids and aliphatic hydrocarbons (HC) in aerosols and surface waters obtained during the spring-summer periods of 2001 and 2003 along the vessel route from the North Sea to the Antarctic and backwards are presented. It was shown that the distribution of organic compounds is caused by the influence of the zonal supply of eolian matter from land, anthropogenic, and marine autochtonous sources. The concentrations of organic compounds in the aerosols varied from 0.22 to 13.04 ng/m³ for the lipids and from 0.04 to 7.03 ng/m³ for the aliphatic HC; in the surface waters, it from 9 to 84 and from 1 to 53 μg/l, respectively. There is a correlation between the fluxes of the lithogenic fraction of the aerosols, HC, and lipids. The growth of the aquatic area productivity increases the levels of the HC in the surface waters but to a lower degree than the HC supply with oil contamination.     

北黄海表层沉积物中甲藻孢囊的分布特征

2009年和2010年采集北黄海15个站位的表层沉积物样品进行甲藻孢囊分析,共鉴定出甲藻孢囊28种(隶属13个属)和2种未定种,优势种为膝沟藻(Gonyaulax spp.)、塔马/链状亚历山大藻(Alexandriumcatenella/tamarense)和微小/相似亚历山大藻(Alexandrium minutu...