The distribution and population dynamics of O-group plaice (Pleuronectes platessa L.) on nursery grounds in the Firth of Forth

Midsummer (1 August) population estimates of about 2 million O-group plaice (Pleuronectes platessa L.) were derived for sandy bays around the Firth of Forth in 1979–1980. This is an order of magnitude less than similar estimates made for the Clyde Sea Area in 1973–1974. Autumn population estimates of 0·4–1·0 million fish were comparable to estimates by the Ministry of Agriculture, Fisheries and Food for the area between the Scottish border and Flamborough Head (2·3 million for 1970 and 1973) which represented 4·8% (1973) to 5·3% (1970) of the total number of O-group fish on the English east coast.Largo Bay was the most important nursery area holding 25% of the total population. It is particularly well situated to receive newly metamorphosed plaice carried in water currents along the north side of the Forth from the spawning ground off Fife Ness. Plaice in the Forth are mainly distributed on fine to medium sandy beaches (186–480 μm), the mean number per haul in midsummer (D) being correlated with the median diameter (m.d. in μm) of the low water sediments by the equation: D=−45·7666+0·2327 m.d. (n=11,r=0·68,P<0·02 but>0·01).The shallow inshore water in sandy bays in the outer Firth was well mixed and more marine than estuarine (27·7–35·0‰). The correlation coefficient between fish density and water temperature was low, while that with salinity (S‰) was: D=6·1618+0·2238S (n=23,r=0·62,P<0·005).Regression analysis demonstrated that the relationship between the instantaneous mortality rate (Z) and the initial population density (D_p) was: Z×100=0·7480+0·0546d_p (n=12,r=0·87,P<0·001).The mean mortality rate for the O-group plaice in the Forth nursery areas was 53% month⁻¹.     

Higher plant n-alkane average chain length as an indicator of petrogenic hydrocarbon contamination in marine sediments

The n-alkane average chain length (ACL) is the weight-averaged number of carbon atoms of the higher plant C₂₅–C₃₃ n-alkanes. The abundance of individual n-alkanes from higher plant sources generally increases with increasing carbon number in coastal marine sediments around Taiwan, but this trend is reversed for petrogenic hydrocarbons. The ACL would potentially be lowered if petrogenic hydrocarbons were added to sediments containing biogenic hydrocarbons alone. To test this idea, a marine environment off southwestern Taiwan known to contain both biogenic and petrogenic hydrocarbons and two nearby rivers were selected for investigating possible difference in ACL values between their sediments. The average CPI of C₂₅–C₃₃ n-alkanes was 4.08 ± 2.04 (range 1.90–8.96, n = 15) for the river sediments and 1.70 ± 0.16 (range 1.43–1.97, n = 15) for the marine sediments. The ACL of C₂₅–C₃₃ n-alkanes for river sediments ranged from 29.2 to 30.5 (average 29.9 ± 0.4), and for marine sediments from 28.4 to 29.3 (average 28.9 ± 0.3). The ACL difference between marine and river sediments was significant (Student's t test at 99% confidence) although it appeared small. It is suggested that the ACL can be an additional indicator for detection of petrogenic hydrocarbons in coastal marine sediments.     

白令海北部陆坡全新世以来长链正构烷烃的古环境意义

本文对白令海北部陆坡B2-9站位沉积物岩芯开展了高分辨率的生物标志物分析,获得了研究区近一万年来陆源长链正构烷烃（简写为烷烃）的输入及其源区植被结构的变化等相关记录。结果表明,nC₂₇是烷烃中最高的主碳峰,对烷烃总量的贡献也最大,这可能与源区木本植物的丰度及其分布有关;nC₂₃的含量也较高,可能主要是来源于北半球沿海地区广泛分布的一类沉水植物。全新世期间,烷烃总量分别在7.8 ka B.P.,6.7 ka B.P.和5.4 ka B.P.经历了三次阶梯状的下降过程,呈现出四个相对稳定的阶段,可能主要受控于早全新世海平面上升以及源区气候环境和植被分布的变化。烷烃的分子组合特征各参数（如CPI、ACL以及nC₃₁/nC₂₇等）的变化则表明,烷烃主要来自陆生高等植物,且全新世期间植被结构较为稳定,木本植物占据优势。此外,在几个较短的时期内,烷烃总量及其分子组合特征等参数的变化具有同步性,表明在这些时期特殊的气候条件下,源区木本植物烷烃对烷烃总量的贡献率的增加可能低于草本植物烷烃和化石烷烃。     

Chemical speciation of copper and zinc in surface waters of the western Black Sea

The chemical speciation of Cu and Zn was investigated by voltammetric titration methods in the surface waters (10 m) of the western Black Sea during an Istanbul–Sevastopol cruise conducted in November 1998. Supporting parameters (temperature (T), salinity (S), pH, alkalinity (Alk), suspended particulate matter (SPM) and dissolved and particulate ²³⁴Th) were obtained in order to distinguish hydrographic features against involvement of the metals in biogeochemical processes. In the Turkish continental slope region, the cruise track intersected a narrow vein of colder water originating on the western shelf. The core of this cold water vein was characterised by a relatively low salinity, higher specific alkalinity and higher metal (especially Cu) and metal-binding ligand concentrations.A very large portion of Cu (93–99.8%) and Zn (82–97%) was organically complexed. The degree of complexation was highest in shelf waters and lowest in the central gyre. Titration data for Cu were modelled by two classes of organic binding ligands characterised by (C_L1=3–12 nM, log K₁′=13.1–13.9) and (C_L2=20–70 nM, log K₂′=9.4–11.2). These ligands occurred mainly in the ‘dissolved’ phase, as defined by 0.4-μm filtration. The stronger Cu-binding ligand seemed to be produced in situ in response to Cu concentration, whereas the weaker Cu-binding ligand appeared to be derived from terrestrial sources and/or reducing shelf sediments. Titration results for Zn were generally represented by one class of ligands (C_L1=8–23 nM, log K₁′=9.4–10.2), which were almost uniformly distributed between the ‘dissolved’ (78±8%) and the particulate phase (22±8%). The concentration of these strong Zn-binding ligands showed a very good correlation with SPM (r²=0.64), which improved when the dissolved ligands alone were considered (r²=0.78). It is hypothesised that these ligands were produced in situ by the bacterial breakdown of particulate organic matter.     

合浦珠母贝基质蛋白KRMP-3对二价金属离子选择性的研究

用大肠杆菌表达含有GST标签的基质蛋白KRMP-3。利用圆二色谱(Circular Dichroism, CD)研究不同浓度钙离子和镁离子对基质蛋白 KRMP-3二级结构的影响。结果表明,钙离子对其二级结构的变化远大于镁离子;同时,采用荧光淬灭法研究 KRMP-3对钙,镁,锶,钡等二价金属离子的选择性,结果表明, KRMP-3对钙离子有特异性选择性,钙离子与KRMP-3的结合常数K约为103 L/mol,结合位点数 n 近似为1,表明 KRMP-3与钙离子的结合能力适中,推测基质蛋白 KRMP-3对合浦珠母贝( Pinctada fucata)棱柱层形成起到促进作用。     

南海大鹏湾盐田海域骨条藻数量的多元分析

１９９０年及１９９１年３月３０日－５月３０日，在南海大鹏湾盐田海域设点测定骨条藻数量及各环境要素，以逐步回归，主成分分析及判别分析的方法，分析该海区骨条藻数量与环境因子的关系。１９９０年４、５月与１９９１年４，５月骨条藻数量差异与该期间环境因子值差异显著有关；初步提出用三维主成分分析图及判别分析方程作为盐田海域骨条材料潮预报的方法。     

Distribution and contribution of major phytoplankton groups to carbon cycling across contrasting conditions of the subtropical northeast Atlantic Ocean

The relation between trophic regime and phytoplankton composition and function in oceanic systems is well accepted in oceanography. However, the relative dynamics and carbon cycling contributions of different phytoplankton groups across gradients of ocean richness are not fully understood. In this work we investigated phytoplankton dynamics along two transects from the NW African coastal upwelling to open-ocean waters of the north Atlantic subtropical gyre. We adopted a pigment-based approach to characterize community structure and to quantify group-specific growth and grazing rates and associated carbon fluxes. Changes in pigment cell concentration during the incubation experiments due to photoadaptation were corrected to obtain reliable rates. The oceanic region was dominated by Prochlorococcus (PRO) (45±7% of total chlorophyll a) while diatoms dominated in upwelling waters (40±37%). Phytoplankton grew faster (μ=0.78±0.26 d⁻¹) and free of nutrient limitation (μ/μ_n=0.98±0.42) in the coastal upwelling region, with all groups growing at similar rates. In oceanic waters, the growth rate of bulk phytoplankton was lower (μ=0.52±0.16 d⁻¹) and nutrient limited (μ/μ_n=0.68±0.19 d⁻¹). Diatoms (0.80±0.39 d⁻¹) and Synechococcus (SYN) (0.72±0.25 d⁻¹) grew faster than Prymnesiophyceae (PRYMN) (0.62±0.26 d⁻¹) and PRO (0.46±0.18 d⁻¹). The growth rates of PRO and SYN were moderately nutrient limited (μ/μ_n=0.81 and 0.91, respectively), while the limitation for diatoms (μ/μ_n=0.71) and PRYMN (μ/μ_n=0.37) was more severe. Microzooplankton grazing rate was higher in upwelling (0.68±0.32 d⁻¹) than in oceanic waters (0.37±0.19 d⁻¹), but represented the main loss pathway for phytoplankton in both systems (m/μ=0.90±0.32 and 0.69±0.24, respectively). Carbon flux through phytoplankton, produced and grazed, increased from offshore to coastal (∼2 to ∼200 μg C L⁻¹ d⁻¹), with diatoms dominating the flux in the upwelling region (52%) while PRYMN (40%) and PRO (30%) dominated in the open ocean.     

Some effects of copper on the veliger larvae of the mussel Mytilus edulis and the Scallop Pecten maximus (Mollusca, Bivalvia)

During 1983 and 1985 several batches of laboratory reared veliger larvae of Mytilus edulis and Pecten maximum here subjected to a rank of concentrations of added copper (CuCl₂) over a 15-day period. M. edulis larvae were less sensitive, measured both as mortality (15-day LC₅₀) of 400 μglitre⁻¹) and reduced growth, than P. maximus larvae (15-day LC₅₀ of 85μg litre⁻¹). Both species appeared less sensitive to Cu than other bivallve larvae previously studied. Veliger larvae of M. edulis are from 7 to 10 times more tolerant of Cu than juveniles or adults and this unexpected finding is discussed in relation to the recent literatures on Cu toxicity and accumulation in mussels.     

Solvent extraction of copper acetylacetonate in studies of copper(II) speciation in seawater

A liquid-liquid partition, ligand exchange procedure involving the formation of copper(II) complexes with acetylacetone is presented for the determination of stability constants and concentrations of copper chelators in seawater. Acetylacetone competes with natural ligands for copper, and the equilibrium concentration of the copper acetylacetonate complex is used in speciation calculations. The concentration of the complex is calculated by partitioning a fraction of it into an organic phase and determining the total Cu concentration in that phase by back extracting with acid, and analyzing by flameless atomic absorption spectroscopy. The concentration of Cu acetylacetonate in seawater in equilibrium with the organic phase is calculated from the partition coefficient. The simple, thermodynamically well characterized procedure offers several advantages over previous techniques. Studies using organic free seawater and model ligands show good agreement between experimental and calculated conditional stability constants. Studies from seawater in Biscayne Bay, Florida, indicate two ligand types are present; type 1, K₁ = 1.2 × 10¹², C_L1 = 5.1 × 10⁻⁹ M; type 2, K₂ = 2.8 × 10¹⁰, C_L2 = 1.1 × 10⁻⁷ M. Speciation is dominated by ligand type 1. Depth profiles of [Cu(II)]_free/[Cu(II)]_total measured with the procedure at ambient copper concentrations show an increase from < 5 × 10⁻⁵ at 50–60 m to > 1 × 10⁻³ at the surface at two stations off the Florida coast.     

A comparison of two voltammetric techniques for determining zinc speciation in Northeast Pacific Ocean waters

Two independent voltammetric techniques, differential pulse cathodic stripping voltammetry (DPCSV) and differential pulse anodic stripping voltammetry (DPASV), determined that 95% of the dissolved zinc is organically complexed at two depths (60 and 150 m) within the surface euphotic zone at an open ocean station in the Northeast Pacific. Average values for the concentrations of the natural zinc-complexing organic ligands (C_L) obtained from duplicate determinations at these two depths by DPCSV versus DPASV are in excellent agreement: 1.60 ± 0.01 versus 1.76 ± 0.03 nM at 60 m, and 2.14 (n=1) versus 2.22 ± 0.06 nM at 150 m. Average values for the conditional stability constants (with respect to free Zn²⁺) of the natural zinc-organic complexes (log K^′_ZnL) from duplicate determinations at both depths by DPCSV versus DPASV are 10.3 ± 0.2 versus 11.2 ± 0.2. Additional research is required to assess the significance of the difference in the conditional stability constants determined by these two techniques. These results confirm recent observations that strong zinc complexes formed with an organic ligand class existing at nanomolar concentrations dominates zinc speciation in the North Pacific.     

Formation and stability of mixed Mg/Ca/phytate species in synthetic seawater media: Consequences on ligand speciation

The results of a potentiometric investigation (by ISE-H⁺, glass electrode) on the speciation of phytate ion (Phy¹²⁻) in an ionic medium simulating the major components (Na⁺, K⁺, Ca²⁺, Mg²⁺, Cl⁻ and SO₄²⁻) of natural seawater, at different salinities and t = 25 °C, are reported. The work was particularly aimed at determining the possible formation of mixed Ca²⁺–Mg²⁺–phytate ion pairs, and to establish how including the formation of these mixed species would affect the speciation modeling in seawater media. After testing various speciation models, that considering the formation of the MgCaH₃Phy⁵⁻, MgCaH₄Phy⁴⁻, Mg₂CaH₃Phy³⁻ and Mg₂CaH₄Phy²⁻ species was accepted, and corresponding stability constants were determined at two salinities (S = 5, 10). A discussion is reported both on the choice of the experimental conditions and on the possibility to extend these results to those typical of real seawater. A detailed procedure is also described to demonstrate that the stability of these species is higher than that statistically predicted. As reported in literature, a parameter, namely log X, has been determined in order to quantify this extra stability for the formation of each mixed species at various salinities. For example, at S = 10, log X₁₁₃ = 2.67 and log X₁₁₄ = 1.37 for MgCaH₃Phy⁵⁻ and MgCaH₄Phy⁴⁻ (statistical value is log X_stat = 0.60), and log X₂₁₃ = 6.11 and log X₂₁₄ = 2.15 for Mg₂CaH₃Phy³⁻ and Mg₂CaH₄Phy²⁻ (log X_stat = 1.43), respectively. Results obtained also showed that the formation of these species may occur even in conditions of low salinity (i.e. low concentration of alkaline earth cations) and low pH (i.e., more protonated ligand).     

The combined effect of copper and hydrocarbons on the length growth of Mytilus edulis

The combined effect of copper and North Sea crude oil is tested on juvenile Mytilus edulis. Dissolved CuSO₄ x 5H₂O is added to the seawater in concentrations of 3 and 6 μg Cu litre^-1. Crude oil, microencapsulated in a gelatine/acacia structure, is added in concentrations of 1·5 and 3·0 mg oil litre^-1. The shell length growth is measured every 24 h with laser diffraction. Linear effects were observed for single components within 24 h of exposure and significant antagonistic interaction appeared within 48 h. Reduced growth rate coincided with reduced filtering and defaecation, and reduced byssus production.     

Determination of cadmium(II), copper(II), manganese(II) and nickel(II) species in Antarctic seawater with complexing resins

The strong species of cadmium(II), copper(II), manganese(II) and nickel(II) in an Antarctic seawater sample are investigated by a method based on the sorption of metal ions on complexing resins. The resins compete with the ligands present in the sample to combine with the metal ions. Two resins with different adsorbing strengths were used. Very stable metal complexes were investigated with the strong sorbent Chelex 100 and weaker species with the less strong resin, Amberlite CG-50. Strong species were detected for three of the considered metal ions, but not for Mn(II). Cu(II) is completely linked to species with a side reaction coefficient as high as log α_M(I) = 11.6 at pH = 7.3. The ligand concentration was found to be similar to that of the metal ion, and the conditional stability constant was around 10²⁰ M^− 1. In the considered sample, only a fraction of the metal ions Cd(II) and Ni(II) is bound to the strong ligands, with side reaction coefficients equal to log α_M(I) = 5.5 and 6.5 at pH = 7.3 for Cd(II) and Ni(II), respectively. These findings were confirmed by the test with the weaker sorbent Amberlite CG-50. It can be calculated from the sorption equilibria that neither Mn(II) nor Ni(II) is adsorbed on Amberlite CG-50 under the considered conditions and, in fact, only a negligible fraction of Mn(II) and Ni(II) was adsorbed. A noticeable fraction of Cd(II) was adsorbed on Amberlite CG-50, meaning that cadmium(II) is partially linked to weak ligands, possibly chloride, while no copper(II) was adsorbed on this resin, confirming that copper(II) is only combined in strong species. These results are similar, but not identical, to those obtained for other seawater samples examined in previous investigations.     

Analysis of submarine slumping in the continental slope off the southern coast of Israel

Abstract

The continental slope off the coast of Israel is riddled with numerous large slump scars at depths greater than 400 m. Recent scar slumps are situated in the steepest central portions of the continental slope (400–450 m depth, α=6°), frequently disfiguring older slump scars in its lower portions. The slumping materials were probably largely transported downslope in the form of density currents, and occasionally by sliding of large sediment chunks. Upslope retrogressive slumping phases progressively disfigure the shape of the slump scars until they totally disappear, causing net reduction of the thickness of the sedimentary column. To provide a basis for the quantitative analysis of slumping, laboratory vane tests, triaxial consolidated, undrained compression tests with pore‐pressure measurements, drained direct shear tests, and consolidation tests were performed oh undisturbed samples. Because the sediments consist of normally consolidated silty clays, the geotechnical properties measured on the core samples can be readily extrapolated for greater depths, assuming the sediments are homogeneous. Angles of internal friction measured by direct shearing under drained conditions are ?_d =24°‐25°, designating the maximum possible angle of a stable infinite slope. These angles are appreciably higher than the steepest slopes in the investigated area, and a drained slumping mechanism is therefore considered unlikely. The slopes of the slump scar walls are about 20°; therefore, in the absence of active erosional, sedimentological, or tectonic agents, these walls have long‐term stability (drained shear). Undrained shear failure resulting in slope instability may be attributable to rapid changes in slope geometry (undercutting or oversteepening of the slope), fluctuations in pore pressure, or accelerations associated with earthquakes. Undrained shear‐strength parameters were determined by both laboratory consolidated‐un‐drained triaxial tests and by miniature vane shear tests. The angles of internal friction that were measured are ?_cu =15°‐17°, and the c_u/p_o values range between 0.22 and 0.75. An analysis of the force equilibrium within the sediments leads to the conclusion that horizontal earthquake‐induced accelerations, as little as 5–6% of gravity, are sufficient to cause slope failure in the steepest slope zone (400–450 m depth, α = 6°, c_u /p_o =0.25). Collapse resulting from liquefaction is unlikely, as the sediments are normally consolidated silty clays with intermediate sensitivity, S_t =2–4.

The existence of slump scars in the lower portion of the continental slope, characterized by gentle slopes (α=1°‐3°) and sediments with high shear strength (c _u /p _o=0.30–0.50) is attributed to large horizontal accelerations(k=12–16% of gravity). Owing to the wide range of geotechnical properties of the sediments (c_u /p_o = 0.20–0.75) and the inclination of the continental slope (α=1°‐6°), the same earthquake may generate a wide range of horizontal accelerations in different portions of the continental slope, and slumping may occur wherever the stability equilibrium is disrupted.     

基于几何形态测量学的4种金线鱼矢耳石识别研究

利用2007年9月至2010年9月采自北部湾海域的24尾红棘金线鱼(Nemipterus nemurus)、32尾金线鱼(N.virgatus)、36尾深水金线鱼(N.bathybius)和35尾日本金线鱼(N.japonicus)性成熟后的矢耳石样本,运用几何形态测量学方法研究了4种鱼类矢耳石形态识别问题。耳石经图像处理后提取地标点坐标值,进行相对扭曲主成分分析,通过判别分析区分4种金线鱼的耳石,利用薄板样条分析和网格变形分析耳石形态变异。结果表明:在相对扭曲主成分分析中,第1、2、3主成分分别解释了总变异的30.78%、28.44%和11.75%,可以将四种金线鱼耳石区分开来。其中Ⅰ型地标点6、10、11,Ⅱ型地标点2,Ⅲ型地标点7,贡献作用较大,解释了主要形态变异。相对扭曲主成分的逐步判别分析中,四种鱼的平均判别成功率达91.3%;交互验证结果显示,四种鱼的平均判别成功率达89.8%,表明几何形态测量学分析可以作为鱼种耳石识别的有效方法之一,在耳石形态学与鱼种判别研究中具有重要应用价值。     

Lipids in selected abyssal benthopelagic animals: links to the epipelagic zone?

A detailed study of the lipids of selected zooplankton species and scavenging amphipods in the near-bottom water layer (15–100 m above bottom, mab) was carried out at the BENGAL site in late summer 1998. Copepoda were the main contributors to the zooplankton, comprising 75% of the total abundance, followed by Ostracoda and Chaetognatha. Calanoid copepods of the family Metridinidae were predominant and accounted for more than 50% of all copepods.Two types of storage lipids were distinguished: triacylglycerols and wax esters. Ostracoda and the polychaete Vanadis sp. stored exclusively triacylglycerols whilst the bulk of the Copepoda accumulated wax esters, with the exception of the family Aetideidae. In the amphipods both lipid classes were found: Eurythenes gryllus stored wax esters and Paralicella spp. and Orchomene sp. triacylglycerols.The fatty acid composition was characterized by a high level of monounsaturated 18:1 (n—9), which is described as characteristic for animals living in the deeper layers of the water column, and to a lesser degree by 16:1 (n—7) and 20:5 (n—3), which are typical components of diatom lipids, and 22:6 (n—3), typical of dinoflagellates. The ratio of 18:1 (n—9):18:1 (n—7) fatty acids was between 5 and 10 in the copepods and indicates a carnivorous/omnivorous feeding behaviour in this group, whereas the higher ratios of 8–18 in the amphipods confirm their necrophagy. The fatty alcohols of the animals storing wax esters were dominated by the monounsaturated isomers 18:1 (n—9) and 18:1 (n—7).The predominance of wax esters as storage lipids in the deep-sea copepods indicates a strong seasonality in the availability of food. This is supported by the high levels of 16:1 (n—7), 20:5 (n—3) and 22:6 (n—3) fatty acids, which point to there being a direct link between the surface primary production and deep-sea copepods, probably via the rapid deposition of phytodetritus.     

Increased toxicity of benzo(a)pyrene-7,8-dihydrodiol in the presence of polychlorobiphenylols

Benzo(a)pyrene (BaP) and polychlorinated biphenyls (PCBs) often co-exist in contaminated environments. Polychlorobiphenylols (OH-PCBs), formed by CYP-dependent monooxygenation of PCBs, are potent inhibitors of the glucuronidation of hydroxylated BaP metabolites. We hypothesized that OH-PCBs could drive the biotransformation of (−)BaP-7,8-dihydrodiol (BaP-7, 8-D) away from detoxication and towards formation of the reactive metabolite. A mixture of five OH-PCBs with 4–6 Cl atoms was infused into isolated, perfused, biliary intact livers (n=3 fish) removed from 3-methylcholanthrene-induced channel catfish. Controls (n=3) were infused with vehicle. Subsequently, [³H]-BaP-7, 8-D was infused into each liver and bile was collected for 1 h. The livers were taken for analysis of metabolites and DNA adducts. Induction status was confirmed by EROD assay. Bile was analyzed for metabolites. It was found that preinfusion of the mixture of OH-PCBs reduced the extent of glucuronidation of BaP-7, 8-D and increased the formation of DNA adducts 5-fold over controls. GSH conjugates, tetrols and triols were increased in the OH-PCB-infused fish, providing further support for our hypothesis that if the glucuronidation were inhibited, CYP-dependent activation would increase. These studies suggest a mechanism for synergy of toxicity of PAH and PCBs.     

Sources and preservation of organic matter in Plum Island salt marsh sediments (MA, USA): long-chain n-alkanes and stable carbon isotope compositions

Elemental (TOC, TN, C/N) and stable carbon isotopic (δ¹³C) compositions and n-alkane (nC_16–38) concentrations were measured for Spartina alterniflora, a C₄ marsh grass, Typha latifolia, a C₃ marsh grass, and three sediment cores collected from middle and upper estuarine sites from the Plum Island salt marshes. Our results indicated that the organic matter preserved in the sediments was highly affected by the marsh plants that dominated the sampling sites. δ¹³C values of organic matter preserved in the upper fresh water site sediment were more negative (−23.0±0.3‰) as affected by the C₃ plants than the values of organic matter preserved in the sediments of middle (−18.9±0.8‰) and mud flat sites (−19.4±0.1‰) as influenced mainly by the C₄ marsh plants. The distribution of n-alkanes measured in all sediments showed similar patterns as those determined in the marsh grasses S. alterniflora and T. latifolia, and nC₂₁ to nC₃₃ long-chain n-alkanes were the major compounds determined in all sediment samples. The strong odd-to-even carbon numbered n-alkane predominance was found in all three sediments and nC₂₉ was the most abundant homologue in all samples measured. Both δ¹³C compositions of organic matter and n-alkane distributions in these sediments indicate that the marsh plants could contribute significant amount of organic matter preserved in Plum Island salt marsh sediments. This suggests that salt marshes play an important role in the cycling of nutrients and organic carbon in the estuary and adjacent coastal waters.     

舟山近海日本囊对虾野生群体与越冬养成群体形态性状对体重和肉重影响的比较

于舟山近海日本囊对虾(Marsupenaeus japonicus)海捕野生群体和露天池塘越冬养成群体中各随机选取150尾作为测定样本,依次测量其体重(Y1)、肉重(Y2)、体长(X1)、头胸甲长(X2)、胸宽(X3)、胸高(X4)、第二腹节长(X5)、第二腹节宽(X6)、第二腹节高(X7)、尾节长(X8)、尾节宽(X9)、尾节高(X10)、眼径(X11)、眼窝距(X12)、额剑长(X13)、额剑上缘锯齿数(X14)等16项表型性状,并采用相关分析、通径分析和偏回归分析等方法定量研究了日本囊对虾形态性状对野生海捕群体与露天越冬养成群体体重和肉重的影响效应。结果表明:(1)两实验测定群体的体重和肉重与本研究中除X14外的其它形态性状的相关系数均达到极显著水平(P0.01);(2)经通径分析,海捕野生群体被保留的形态性状与体重和肉重的复相关指数分别为0.944和0.837,露天越冬养成群体被保留的形态性状与体重和肉重的复相关指数分别为0.955和0.907,其中影响露天越冬养成群体体重和肉重的核心变量均为X1,重要变量依次为X2和X6,影响海捕野生群体体重和肉重的核心变量分别为X1和X2,重要变量均为X6;(3)经多元回归分析,得出了用于估算海捕野生群体体重和肉重的回归方程以及估算露天越冬养成群体体重和肉重的回归方程。