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1.
于 2 0 0 2年 1 1月— 2 0 0 3年 4月 ,采用Winkle滴定法和次溴酸盐氧化法对硬壳蛤呼吸排泄进行了研究。结果表明 ,在 5— 35℃温度范围内 ,温度和体重对硬壳蛤 (壳长 0 5— 6cm ,软体部干重 0 0 0 34— 0 5 9g)的耗氧率和排氨率均有显著影响 (P <0 0 5 ) ,其单位体重耗氧率在2 0— 30℃之间达到最大值 ,且随着硬壳蛤个体的增大而下降 ;不同温度下硬壳蛤个体耗氧率OR[mgO2 /(ind·h) ]与软体部干重W(gDFW)之间的关系可用方程OR =aWb 表示 ,其中a值在0 0 4— 0 70之间 ,b值在 0 45— 0 65之间。硬壳蛤的排氨率 温度曲线呈单峰型 ,其单位体重排氨率在 2 5℃附近达到最大值 ,且随着硬壳蛤个体的增大而下降。不同温度下硬壳蛤个体排氨率NR[μgNH4 N/(ind·h) ]与软体部干重W(gDFW)之间的关系可用方程NR =aWb 表示 ,其中a值在 1— 2 7之间 ,b值在 0 40— 0 75之间。硬壳蛤呼吸排泄的氧、氮比在 5℃时最大 ,随后有下降趋势 ,其比值在 1 0— 80之间。  相似文献   

2.
饥饿对二倍体和三倍体长牡蛎呼吸和排泄的影响   总被引:2,自引:2,他引:0  
采用室内实验的方法研究了饥饿对二倍体 (2n)和三倍体(3n)长牡蛎(Crassostreagigas)呼吸和排泄的影响。实验饥饿的时间为2,5,8,11,14,23,32d,实验牡蛎的软体部干质量为M2n=0.347g±0.071g;M3n =0.301g±0.099g。实验结果表明 :(1)二倍体长牡蛎在饥饿2~14d内 ,随着饥饿时间的延长 ,个体的耗氧率增大 ,当饥饿14d以后 ,随着饥饿时间的延长 ,个体的耗氧率下降 ;三倍体长牡蛎则表现出饥饿5d以后 ,随着饥饿时间的延长 ,个体的耗氧率下降。耗氧率与饥饿时间的关系为:Ro ,2n(mg/(个·h))= -0.08 +0.21T-0.01T2-0.01T3,Ro ,3n(mg/(个·h))= -1.97+0.45T-0.12T2+0.01T3;在饥饿2~5d内 ,二倍体和三倍体长牡蛎的耗氧率差异不显著(P>0.05) ,而饥饿5d以后 ,耗氧率的差异达到显著水平(P<0.05) ;(2)二倍体长牡蛎在饥饿2~8d内 ,随着饥饿时间的延长 ,其排氨率增加 ,当饥饿8d以后 ,排氨率则逐渐下降 ;三倍体长牡蛎则表现出饥饿5d以后 ,随着饥饿时间的延长 ,个体的排氨率下降。排氨率与饥饿时间的关系为 :RA ,2n(μg/(个·h))= -16.09 +32.65T-8.11T2 +0.57T3 ,RA ,3n(μg/(个·h))=4.57 +16.07T-5.42T2 +0.44T3 ;在实验的时间范围内 ,二倍体和三倍体长牡蛎排氨率的差异达到显著水平 (P<0.05)。  相似文献   

3.
盐度对二倍体和三倍体长牡蛎呼吸和排泄的影响   总被引:6,自引:1,他引:6  
采用室内实验的方法研究了盐度对二倍体(2n)和三倍体(3n)长牡蛎(Crassostrea gi-gas)呼吸和排泄的影响。实验的盐度(S)梯度为15,20,25,30,35共5个梯度,实验牡蛎的规格为,2n:W(软体部干质量,单位为g)=0.347±0.071 g;3n:W=0.301±0.099g。实验结果表明:盐度对二倍体和三倍体长牡蛎的呼吸和排泄有显著影响。在实验的盐度范围内,随着盐度的升高,二倍体和三倍体长牡蛎的耗氧率逐渐增大,盐度与耗氧率的关系可表示为,2n:Ro[mg/(g·h)]=0.0142S~(1.219),3n:Ro[mg/(g·h)]=0.0085S~(1.391);随盐度的升高,排氨率逐渐增大,当S为35时,二倍体和三倍体长牡蛎的排氨率略有下降,在实验的盐度范围内,盐度与排氨率的关系可表示为,2n:RA[μg/(g·h)]=-12.25+2.902S-0.0573S~2;3n:RA[ug/(g·h )]=-39.39+3.882S-0.06S~2。在实验的盐度范围内,二倍体和三倍体长牡蛎耗氧率的差异未达到显著水平(P>0.05),而排氨率的差异则有所不同,当S为15~20时,二倍体和三倍体牡蛎的排氨率差异达到显著水平(P<0.05),而S为25~35时,其差异不显著(P>0.05)。  相似文献   

4.
泥蚶、缢蛏和僧帽牡蛎呼吸与排泄的周年变化   总被引:1,自引:1,他引:0  
于2005年5月至2006年3月对浙江沿岸重要的3种经济贝类泥蚶、缢蛏和僧帽牡蛎的呼吸率与排泄率进行了周年研究。结果表明:泥蚶、缢蛏和僧帽牡蛎耗氧率的变化范围分别为0.11~5.05 mg/(g·h)、0.77~5.97 mg/(g·h)和0.33~5.47 mg/(g·h),排氨率的变化范围分别为21.51~1 078.63 μg/(g·h),26.97~990.73 μg/(g·h)和32.12~1 378.67 μg/(g·h);耗氧率与排氨率9月份最高,1月份最低。经单因素方差分析发现,3种实验贝类月际间的耗氧率与排氨率均存在极显著差异(p<0.01),经配对T检验发现,缢蛏(SC)和僧帽牡蛎(SCA)之间的耗氧率存在着显著差异TSC-SCA=3.184,p=0.024),泥蚶(TG)与缢蛏、僧帽牡蛎的耗氧率之间都不存在差异(TTG-SC=1.887,p=0.118;TTG-SCA=0.246,p=0.815),泥蚶、缢蛏和僧帽牡蛎之间的排氨率的差异均不显著(TTG-SC=0.977,p=0.373;TTG-SCA=2.369,p=0.064;TSC-SCA=1.002,p=0.362)。3种贝类的耗氧率与排氨率均随温度的升高而升高,经回归分析发现,耗氧率和排氨率与温度的变化均呈较显著的幂指数性相关lnY=lna+blnTY=aebT)。泥蚶呼吸排泄O:N变化范围为4.69~28.55,缢蛏和僧帽牡蛎的O:N变化范围分别为:4.68~37.89和3.04~10.27。  相似文献   

5.
采用静水实验法,研究了在不同温度(15、20、25)和盐度(8、13、18、23、28、33)下对壳长为(25.10±0.84)mm的毛蚶耗氧率和排氨率的影响。结果表明:随着温度的升高,耗氧率和排氨率逐渐增大,在温度25、盐度28时,耗氧率和排氨率均达到最大,分别为1.5111mg/(g·h)、0.2412mg/(g·h);盐度18~28时,耗氧率和排氨率随着盐度的增加而增加,盐度28时达到最大,之后,随着盐度的增加而降低;毛蚶的氧氮比值范围为3.55~5.48,在温度15~25、盐度28时,各实验组均有最大的氧氮比值。经方差分析,温度和盐度以及二者交互作用均对毛蚶的耗氧率和排氨率有显著影响(P<0.05)。  相似文献   

6.
盐度对双齿围沙蚕耗氧率和排氨率的影响   总被引:2,自引:0,他引:2  
为优化双齿围沙蚕养殖条件,促进沙蚕资源的合理开发和利用,作者探讨了不同盐度下(8、16、24、32、40、45)双齿围沙蚕(Perinereis aibuhitensis)耗氧率和排氨率的情况。结果表明:盐度对双齿围沙蚕的耗氧率和排氨率均有显著性影响(P0.05)。在盐度为8~32时,耗氧率随着盐度的升高呈先下降后上升的趋势;在盐度为24时耗氧率最低(0.22 mg/(g·h)±0.01 mg/(g·h));在盐度为32时耗氧率达到最大值(0.37 mg/(g·h)±0.05 mg/(g·h))。在盐度为8~40条件下,沙蚕的排氨率随着盐度的升高呈先降低后上升的趋势;在盐度为24时,双齿围沙蚕的排氨率最低(0.10μmol/(g·h)±0.02μmol/(g·h));当盐度为40时排氨率达到最大值(0.94μmol/(g·h)±0.11μmol/(g·h))。盐度为8~40时,沙蚕的O︰N比值随着盐度的上升呈先升高后降低的趋势,在盐度24和32时,沙蚕的O︰N比值分别为130.84和126.47,且变化较小,当盐度40时,O︰N比值急剧下降到13.3,然后再度上升。综合上述结果,双齿围沙蚕生活的最适盐度为24~32。  相似文献   

7.
盐度对刺参(Apostichopus japonicus)呼吸和排泄的影响   总被引:17,自引:1,他引:17  
采用封闭式呼吸器法研究了(15±0.5)℃水温条件下不同盐度(22、27、31.5、36)对四种规格刺参{S[(39.60±8.77)g]、M[(71.80±14.04)g]、L[(128.30±19.69)g]和XL[(196.65±19.81)g]}呼吸和排泄的影响。结果表明,各规格组刺参单位体重耗氧率[Rwr,μg/(g·h)]和排氨率[(Rwe,μg/(g·h)]在盐度22—31.5范围内均随着盐度的升高而降低,当盐度升高至36时,二者都明显升高;各盐度下实验刺参的单位体重耗氧率分别为17.52、16.32、15.49和17.60μg/(g·h),单位体重排氨率分别为1.05、0.88、0.87和0.95μg/(g·h);在同一盐度下,刺参体重越大,其单位个体耗氧率[Rir,μg/(ind·h)]和排氨率[Rie,μg/(ind·h)]越高,二者呈幂函数关系,可用关系式Rir(或Rie)=aWb表示;关系式Rir=aWb中,a值的变动范围为40.6656—81.1900,b值为0.6432—0.8145;而关系式Rie=aWb中,a值的变动范围为2.0947—4.8489,b值为0.6507—0.8072;盐度对刺参O∶N比的影响不显著,各盐度条件下,不同规格的刺参,其O∶N比均在15左右,表明本实验条件下该参代谢所需要的能量主要由脂肪和碳水化合物提供。从呼吸和排泄的角度来看,刺参在其最适温度(15℃)条件下,具有一定的渗透压调节能力,能够适应较广的盐度变化范围(22—36)。  相似文献   

8.
温度对缢蛏(Sinonovacula constricta)耗氧率和排氨率的影响   总被引:4,自引:0,他引:4  
实验研究温度对不同个体大小缢蛏耗氧率和排氨率的影响。实验结果表明 ,在实验温度(15~ 30℃ )条件下 ,缢蛏的耗氧率 (O) [mg/ h·个 ]和排氨率 (N ) [μg/ h·个 ]与缢蛏软体部干重(W)呈明显的幂函数关系 ;温度的上升使得缢蛏的耗氧率 (OS) [mg/ g· h]、排氨率 (Na) [μg/ g· h]均增大 ;两者之间的比值 (原子数 O∶ N)在 2 0℃时最大 ,随着温度的继续升高其值逐步减小。耗氧率 (O)、排氨率 (N)与温度 (T)、缢蛏软体部干重 (W)二元线形回归方程分别是 :O=- 0 .370 3+0 .32 0 4 W+ 0 .0 2 98T,N =- 15 4 .0 6 77+ 6 9.74 88W+ 7.9332 T。复相关系数 r分别为 0 .9773和0 .92 2 8;F检验表明 ,两个回归方程均极显著。  相似文献   

9.
盐度对近江牡蛎耗氧率、排氨率、O:N 和吸收率的影响   总被引:2,自引:0,他引:2  
以半现场流水槽法研究了不同盐度(5、10、15、20、25、30、35)对近江牡蛎(Crassostrea hongkongensis)耗氧率、排氨率、O:N、吸收率的影响,并测定了盐度为20条件下牡蛎耗氧率和排氨率的周日变化.结果表明,近江牡蛎耗氧率、排氨率、O:N先随着盐度的升高而下降,在20左右降到最低,随着盐度继续上升,又升高;而近江牡蛎的吸收率先随着盐度的升高而升高,在20左右达到最高,然后随盐度升高而下降.根据数据得出耗氧率与盐度的拟合方程: y=0.0033x2-0.1161x+1.5523, R2=0.9018;排氨率与盐度:y=0.0001x2-0.0041x+0.0871, R2=0.9889;O:N与盐度:y=0.0016x3-0.0782x2+0.9051x+10.818, R2=0.955;吸收率与盐度: y=-0.0011x2+0.0399x+0.4393.R2=0.9453.一日内,8时、14时、19时、22时4个时间点,近江牡蛎耗氧率和排氨率变化较大,在14时最大,表明该时点其代谢活动最强.  相似文献   

10.
为了研究温度对方斑东风螺(Babylonia areolata)能量收支的影响,作者采用室内静水法,分析了不同养殖水体温度条件下方斑东风螺幼螺的摄食率、排粪率、耗氧率、排氨率、黏液排泄率的变化规律。结果表明,方斑东风螺摄食率、排粪率、耗氧率和排氨率均随温度升高呈现先上升后下降趋势。其中各温度处理组摄食率差异显著(P<0.05),在23℃时最低为2.548±0.093mg/(g/h),29℃时最高为4.958±0.150 mg/(g/h);排粪率为1.695±0.037~2.892±0.074 mg/(g/h),在29℃时达到最高;耗氧率在29℃时最高为0.437±0.054mg/(g/h), 23℃时最低为0.202±0.027 mg/(g/h);在本实验条件下,方斑东风螺排氨率为0.009±0.001~0.025±0.003mg/(g/h),各温度处理组间均有显著差异(P<0.05),且在29℃时最高为0.025±0.003 mg/(g/h)。黏液排泄率在23℃时最高为0.030±0.001 mg/(g/h),显著高于其他各温度组(P<0.05)。基于不同温度下能量...  相似文献   

11.
In order to assess the impact of deep-sea mining on the in situ benthic life, we measured the microbial standing stock and concentration of organic nutrients in the deep-sea sediments of the Central Indian Ocean Basin in the Indian pioneer area. Sediments were collected using box core and grab samples during September 1996. The total bacterial numbers ranged from 10 10 -10 11 cells per g -1 dry weight sediment. There was a marginal decrease in the number of bacteria from surface to 30 cm depth, though the subsurface section registered a higher number than did the surface. The highest numbers were encountered at depths of 4-8 cm. The retrievable number of bacteria were two orders less in comparison with the direct total counts of bacteria. An almost homogeneous distribution of bacteria, total organic carbon, living biomass, and lipids throughout the depth of cores indicates active microbial and benthic processes in the deep sea sediments. On the other hand, a uniform distribution of total counts of bacteria, carbohydrates, and total organic carbon in all the cores indicates their stable nature and suggests that they can serve as useful parameters for long-term monitoring of the area after the benthic disturbance. Further studies on temporal variability in this region would not only verify the observed norms of distribution of these variables but would also help to understand restabilization processes after the simulated benthic disturbance.  相似文献   

12.
海上大直径钢管桩打桩过程中,桩周土体受到强烈扰动而发生强度弱化,掌握桩周土体强度弱化规律对于准确预测打桩过程、保证工程安全具有重要意义。为研究土体强度弱化规律,开展了环剪试验模拟打桩对桩周土体的扰动,测试土体强度随剪切速率的变化规律,建立了描述土体强度弱化规律的拟合公式,引入到打桩分析软件中。研究结果表明:土体的强度折减程度不仅与土体本身的性质有关还受到土体的埋深和剪切速率的影响,埋深越深土体强度折减程度越低,剪切速率越高土体强度折减越高,在打桩分析中可采用这里推荐的线性折减方法来模拟不同深度处土体强度的折减规律。  相似文献   

13.
An acoustic inversion method using a wide-band signal and two near field receivers is proposed and applied to multiple layered seabed models including a manganese sediment. The inversion problem can be formulated into a probabilistic model comprised of signals, a forward model, and additive noise. The forward model simulates wide-band signals, such as chirp signals, and is chosen to be the source-waveletconvolution plane wave modeling method. The wavelet matching technique, using weighted least-squares fitting, estimates the sediment sound-speed and thickness on which determination of the possible numerical ranges for a priori uniform distribution is based. The genetic algorithm is applied to a global optimization problem to find a maximum a posteriori solution for determined a priori search space. Here the object function is defined by an L 2 norm of the difference between measured and modeled signals. Not only the marginal pdf but also its statistics are calculated by numerical evaluation of integrals using the samples selected during importance sampling process of the genetic algorithm.  相似文献   

14.
This article reviews information recently available from existing marine and coastal mining for responses to environmental issues affecting marine mining at different depths. It is particularly but not exclusively concerned with those issues affecting seabed biodiversity impact and recovery. Much information has been gathered in the past 10 years from shallow mining operations for construction aggregate, diamonds, and gold, from coastal mines discharging tailings to shallow and deep water, and from experimental deep mining tests. The responses to issues identified are summarized in a series of eight tables intended to facilitate site-specific consideration. Since impacts can spread widely in the surface mixing layer SML, and can affect the biologically productive euphotic zone, the main issues considered arise from the depth of mining relative to the SML of the sea. Where mining is below the SML, the issue is whether it is environmentally better to bring the extraction products to the surface vessel for processing (and waste discharge), or to process the extraction products as much as possible on the seabed. Responses to the issues need to be sitespecific, and dependent on adequate preoperational environmental impact and recovery prediction. For deep tailings disposal from a surface vessel, there are four important environmental unknowns: (1) the possible growth of "marine snow" (bacterial flocs) utilizing the enormous quantities of fine tailings particles (hundreds or thousands of metric tons per day) as nuclei for growth, (2) the possibility that local keystone plankton and nekton species may migrate diurnally down to and beyond the depth of deep discharge and hence be subjected to tailings impact at depth, (3) the burrow-up capability of deep benthos and their ability to survive high rates of tailings deposition, and (4) the pattern and rate of dispersion of a tailings density current through the deep water column from discharge point to seabed. Actions to obtain relevant information in general and site-specifically are suggested.  相似文献   

15.
Particle fluxes were measured 7 m above the sea bottom during the predisturbance, disturbance, and postdisturbance periods by using time series sediment traps attached to seven deep-sea moorings deployed in the INDEX experiment site in the Central Indian Basin. The predisturbance particle fluxes varied between 22.3 to 55.1 mg m -2 day -1 . Increased and variable particle fluxes were recorded by the sediment traps during the disturbance period. The increase observed was 0.5 to 4 times more than the background predisturbance fluxes. The increases in particle fluxes (~4 times) recorded by the sediment trap located in the southwestern direction (DMS-1) were the greatest, which could be the result of preferential movement of resuspended particles generated during the deep-sea benthic disturbance along the general current direction prevailing in this area during the experimental period. Also, the traps located closer to the disturbance area recorded greater fluxes than did the traps far away, across the Deep Sea Sediment Resuspension System path. This variability in recorded particle fluxes by the traps around the disturbance area clearly indicates that physical characteristics such as grain size and density of the resuspended particles produced during the disturbance had an important effect on particle movement. The postdisturbance measurements during ~5 days showed a reduction in particle fluxes of ~50%, indicating rapid particle settlement.  相似文献   

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A set of 27 marine planktonic bacteria isolated from the polar regions was characterized by 16S rDNA sequencing and physiological and biochemical testing. More than half of these bacteria were positive for caseinase, gelatinase and 13-glucosidase, and could utilize glucose, maltose or malic acid as carbon source for cell growth. Twelve isolates expressed nitrate reduction activities. Except for one antarctic isolate BSwlO175 belonging to Actinobacteria phylum, these isolates were classified as γ-Proteobacteria, suggesting that γ-Proteobacteria dominated in cultivable marine bacterioplankton at both poles. Genus Pseudoalteromonas was the predominant group in the Chukchi Sea and the Bering Sea, and genus ShewaneUa dominated in cultivable bacterioplankton in the Prydz Bay. With sequence similarities above 97%, genus Psychrobacter was found at both poles. These 27 isolates were psychrotolerant, and significant 16S rDNA sequence similarities were found not only between arctic and antarctic marine bacteria ( 〉 99% ), but also between polar marine bacteria and bacteria from other aquatic environments ( ≥ 98.8% ), including temperate ocean, deep sea, pond and lake, suggesting that in the polar oceans less temperature-sensitive bacteria may be cosmopolitan and have a bipolar, even global, distribution at the species level.  相似文献   

19.
The advanced piston corer (APC) has been used by the Ocean Drilling Program since 1985 for recovering soft sediments from the ocean floor. The pullout force measured on extracting the core barrel from the sediment is shown to correlate with the average shear strength of the sediment core measured in the ship's laboratory. A simple rule of thumb is derived relating the shear strength of the sediment to the pullout force. Multiple APC holes at individual sites allow the consistency of the pullout measurements to be assessed. The effects of different operational procedures during APC coring are also explored. Although generally applicable, the correlation between pullout force and laboratory measurements of shear strength breaks down for some APC holes, possibly because of the disturbance of some sediment types during the APC coring process. A better understanding of the physical process of APC coring, and its effect on the properties of the sediment both inside and immediately outside the core barrel, would indicate what confidence can be put on the measurement of pullout force as a way of evaluating the in situ shear strength of deep sea sediments.  相似文献   

20.
Oedometer tests have been carried out on 70 undisturbed surficial clays (at approximately 250 mm below the mudline), mostly collected by free-fall corers from sites widely scattered throughout the deep-sea North Atlantic. Acoustic measurements were also made, initially on contiguous samples and ultimately on the same sample using a geophysically instrumented oedometer which also collected electrical resistivity data. Apart from those quiescent areas below the carbonate compensation depth, such as north of the West Indies where very fine clays exist, most of the samples are silty clays whose geotechnical-geophysical properties are dependent on the type of clay minerals present (and their ability to take in moisture), the sand-size fraction, and the quantity of carbonate present. Thus the pure clays have high compressibilities which decrease on the addition of coarse particles, while the converse is true for the acoustic parameters, these increasing with the sand fraction. Using the notion of the intrinsic compression line for all samples, and comparison to it of the measured compression curves, it is clear that, contrary to some previously held ideas, most deep-sea clays are normally consolidated; the addition of carbonate has the effect of creating an open, stronger sediment skeleton. Interestingly, where information is available, the variation with depth of a sample's acoustic velocity follows the void ratio pressure relationship of the compression curve. This allows the construction of an in-situ sediment compression curve using the in-situ geophysical observations.  相似文献   

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