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1.
温度对橄榄蛏蚌耗氧率和排氨率的影响 总被引：1，自引：0，他引：1
在室内实验条件下研究了温度对不同规格橄榄蛏蚌耗氧率和排氨率的影响。实验结果表明，15～30℃下，橄榄蛏蚌耗氧率和排氨率为大规格组均小于小规格组。耗氧率和排氨率与橄榄蛏蚌软体部干重(W)呈现明显的幂函数关系。在实验温度(15～30℃)范围内，随温度的上升，橄榄蛏蚌的耗氧率和排氨率均先逐渐增加，后随之下降，两者的高峰值分别出现在25℃和20℃。耗氧率(0)、排氨率(N)与温度(T)和橄榄蛏蚌软体部干重(N)的二元线性回归方程分别为：D=-0．6513 0．0532T 0．1073W，N=32．1626-1．0566T 1．3222W。二方程复相关系数r分别为0．9642和0．8921；F检验分别为极显著和显著。 相似文献
2.
温度对橄榄蛏蚌耗氧率和排氨率的影响 总被引：3，自引：0，他引：3
在室内实验条件下研究了温度对不同规格橄榄蛏蚌耗氧率和排氨率的影响。实验结果表明, 15~30℃下,橄榄蛏蚌耗氧率和排氨率为大规格组均小于小规格组。耗氧率和排氨率与橄榄蛏蚌软体部干重(W)呈现明显的幂函数关系。在实验温度(15~30℃)范围内,随温度的上升,橄榄蛏蚌的耗氧率和排氨率均先逐渐增加,后随之下降,两者的高峰值分别出现在25℃和20℃。耗氧率(O)、排氨率(N)与温度(T)和橄榄蛏蚌软体部干重(W)的二元线性回归方程分别为:O=-0 .651 3+0. 053 2T+0. 107 3W,N=32. 162 6-1. 056 6T+1 .322 2W。二方程复相关系数r分别为0 .964 2和0 .892 1;F检验分别为极显著和显著。 相似文献
3.
采用室内实验生态学方法研究近江牡蛎的耗氧率和排氨率。结果表明,在实验温度13~33℃范围内,近江牡蛎的耗氧率(RO)和排氨率(RN)与体重(W)均呈负相关,可用Y=aW-b表示。耗氧率和温度的关系可表示为RO=-c+b1t-b2 t2,耗氧率为0.626~2.354 mg.g-1.h-1;在温度13~28℃范围内,耗氧率随温度的升高而增加,28℃时,耗氧率达最大值,温度升高至33℃时,耗氧率反而下降。排氨率与温度的关系可表示为RN=c1e d1t,排氨率为0.075~0.318 mg.g-1.h-1,且随温度的升高,排氨率呈持续升高趋势。近江牡蛎呼吸和排泄Q10值范围分别为0.631~3.399和1.046~2.288。在28℃,不同规格近江牡蛎呼吸氧原子数与排出氨氮原子数的比值(nO/nN)均达到最大值。方差分析表明,体重、温度及二者的交互作用对近江牡蛎的耗氧率和排氨率均有极显著的影响(P<0.01)。近江牡蛎的日常代谢明显高于标准代谢,耗氧率和排氨率平均值分别提高46.8%和67.7%。 相似文献
4.
温度对管角螺Hemifusus tuba(Gelin)耗氧率和排氨率的影响 总被引：1，自引：0，他引：1
设置5个温度梯度(14、19、24、29、34℃),海水盐度为32,研究温度和规格对管角螺Hemifusustuba(Gelin)耗氧率和排氨率的影响。结果表明:14～29℃范围内,管角螺耗氧率随温度的升高,29℃时达到最大值;14～34℃范围内,排氨率随温度的升高而增加。在相同温度下,耗氧率和排氨率随单位软体部干重的增加而下降,管角螺软体部干重(W)与单位体重耗氧率(OR)、排氨率(NR)之间的关系分别符合幂函数方程OR=aW-b、NR=cW-d,W与OR、NR呈负相关关系。 相似文献
5.
采用室内实验生态学方法对马氏珠母贝的耗氧率和排氨率进行了研究。结果表明:在温度13～33℃范围内,马氏珠母贝的耗氧率和排氨率均与体重呈负相关,可用Y=aW表示;在13～28℃温度范围内,马氏珠母贝-b的耗氧率随温度的升高而增加,28℃时,耗氧率达最大值,温度升高至33℃时,耗氧率反而下降,而排氨率在此温度范围内则呈持续升高趋势;在13～28℃温度范围内,马氏珠母贝呼吸和排泄Q10值分别为1.51～2.71和1.03～2.73,且在该温度范围内,马氏珠母贝的耗氧率和排氨率的比值范围为7.29～13.14。方差分析表明,体重、温度及二者的交互作用对马氏珠母贝的耗氧率和排氨率均有极显著影响(P<0.01)。马氏珠母贝的日常代谢高于标准代谢,耗氧率和排氨率平均值分别提高40.8%和59.1%。 相似文献
6.
《广东海洋大学学报》2016,(3)
在实验室条件下研究不同pH(5.0、6.0、7.0、8.0、9.0)、亚硝酸盐浓度(0、0.036、0.357、0.714、1.429mmol/L)和氨氮浓度(0、0.036、0.357、0.714、1.429 mmol/L)对双齿围沙蚕(Perinereis aibuhitensis)耗氧率和排氨率的影响。结果表明,在不同p H条件下各组双齿围沙蚕的耗氧率差异无统计学意义(P0.05);pH为7.0时,沙蚕的排氨率较低(2.37±0.51μg·g~(-1)·h~(-1)),pH为9.0时,排氨率最低(0.44±0.13μg·g~(-1)·h~(-1))(P0.05)。随着亚硝酸盐氮浓度的升高,其耗氧率仅在0.714 mmol/L组升高,与其他各组差异无统计学意义(P0.05),而排氨率0.036 mmol/L组升高,之后急速下降,1.429 mmol/L组最低,差异有统计学意义(P0.05)。随氨氮浓度的增加,双齿围沙蚕耗氧率呈下降趋势,当氨氮浓度0.714~1.429 mmol/L时差异有统计学意义(P0.05)。 相似文献
7.
《广东海洋大学学报》2019,(5)
【目的】探讨盐度对不同规格九孔鲍(Haliotis diversicolor supertexta)耗氧量和排氨率的影响。【方法】采用实验室生态学方法,测定7种盐度下(21、24、27、30、33、36和40)3种规格[干质量(1.53±0.14)、(1.11±0.23)和(0.68±0.20)g]九孔鲍的耗氧率和排氨率。【结果】(1)盐度在21～36时,耗氧率随着盐度的上升而增大;盐度为36时,3种规格九孔鲍的耗氧率均达到最大值;当盐度大于36时,耗氧率随盐度上升而下降,九孔鲍的耗氧率(R_O)与软体部干质量(m)的回归关系符合幂函数:R_O=a m~(-b),其中a的波动范围在0.412～1.216之间,平均值为0.818±0.286;b的波动范围在0.311～0.546之间,平均值为0.446±0.074;(2)排氨率在实验盐度范围内呈持续升高趋势,排氨率(R_N)与软体部干质量(m)的回归关系符合幂函数:R_N=c m~(-d),其中c的波动范围在0.174～0.621之间,平均值为0.330±0.154;d的波动范围在0.439～0.668之间,平均值为0.521±0.084;(3)相同盐度下,九孔鲍的耗氧率和排氨率随干质量的增大而显著减小(P <0.05),且耗氧率和排氨率与干质量均符合R=a m~(-b)模型;(4)九孔鲍的规格对O/N比值影响不显著(P> 0.05),当盐度为40时,O/N值显著降低。【结论】盐度、规格及两者间的交互作用均对九孔鲍的耗氧率和排氨率有显著影响。 相似文献
8.
将莫荷罗非鱼(Oreochromis mossambicus×O.urolepis hornorum)幼鱼养殖水体盐度从淡水渐变至12、18、24、30(每天提升6)等4个目标盐度,利用间歇式呼吸仪分析幼鱼在目标盐度下5、10、15、20 d时的呼吸和氨氮排泄的变化。结果表明,在实验前期,莫荷罗非鱼幼鱼耗氧率、排氨率随盐度的升高而增加,各盐度处理组均在5 d时升到最大值,之后开始下降,下降时间、幅度与外界盐度有关。盐度12、18组幼鱼耗氧率10 d时下降至对照组水平,20 d时低于对照组水平,差异有统计学意义(P<0.05);盐度24、30组幼鱼耗氧率则在15 d时下降至对照组水平并维持稳定;幼鱼排氨率随实验时间的延长,各盐度处理组幼鱼排氨率呈先上后下降的变化,盐度24、30组幼鱼排氨率在15 d下降并维持在对照组水平,盐度12、18组幼鱼排氨率在15 d时下降至对照组水平并于20 d时低于其他盐度组,差异有统计学意义(P<0.05)。莫荷罗非鱼幼鱼适应新盐度环境后,盐度18组的耗氧率、排氨率最低,与盐度12组差异无统计学意义(P>0.05),与其他盐度处理组有差异有统计学意义(P<0.05),推测其等渗点在盐度12~18之间。不同盐度条件下,氧氮比值介于18.810~24.216间,氨熵介于0.083~0.108间,表明莫荷罗非鱼幼鱼主要依靠蛋白质和脂肪氧化供能。 相似文献
9.
利用室内实验生态学方法研究不同盐度和体质量对波纹龙虾的呼吸和排泄的影响.结果表明:不同盐度和体质量对波纹龙虾耗氧率和排氨率有显著影响(p <0.05).盐度为18~34时,波纹龙虾的耗氧率和排氨率先下降再升高,盐度26和30时较小,耗氧率分别为0.1305±0.0105 mg/(g·h)和0.1314±0.0052 mg/(g·h),排氨率分别为0.1733±0.0039 mg/(g·h)和0.1724±0.0044 mg/(g·h).波纹龙虾耗氧量(MO)和排氨量(MN)与体质量(m)呈正相关,而耗氧率(RO)和排氨率(RN)与体质量呈负相关,其关系式可表示为:MO =1.4921 m 0.4190和MN=1.1295 m 0.6988;RO=2.9333 m -0.7343和RN=1.1291 m -0.3011. 相似文献
10.
采用流水式的密封装置测定了胭脂鱼鱼种在18~30℃温度范围内的耗氧率,结果表明,在实验温度范围内,胭脂鱼鱼种耗氧率随温度上升逐渐升高,符合函数关系:y=-0.000 8 x2+0.044 0 x-0.438 1,R2=0.990 6。胭脂鱼鱼种耗氧率昼夜变化测定实验表明,其昼均耗氧率(0.204 2±0.011 0)mg?g-1?h-1,略低于夜均耗氧率(0.205 7±0.012 2)mg?g-1?h-1,二者差异不具统计学意义(P>0.05),表明胭脂鱼鱼种耗氧率并不存在明显的昼夜节律。在不同实验温度下,随着胭脂鱼鱼种规格的增大,其耗氧率均呈下降趋势。 相似文献
11.
Metabolism of polychaete Neanthes japonica Izuka： relations to temperature, salinity and body weight
Polychaete Neanthes japonica is a species geographically specific in China and Japan with important scientific implication and commercial value. In this
study, the relations of body weight, salinity and temperature to oxygen consumption and ammonia excretion of N. japonica were determined. Three different groups in body weight (large: 2.34±0.36 g, middle: 1.50±0.21 g and small: 0.62±0.12 g) were
set for all experiments. Results show that the body weight is negatively related to the rates of oxygen consumption and ammonia
excretion; and the relationship is significant. The oxygen consumption and ammonia excretion at 24°C decreased at salinity
from 5 to 30 and increased above 30, indicating that both lower and higher salinity are adverse and certain degree of salinity
stress is necessary for enhancing the energy demand. At salinity 30, rising temperature from 18°C to 30°C, the oxygen consumption
increased before 27°C and then decreased. However, the relation of ammonia excretion and temperature seems more complex. Two-way
ANOVA shows that salinity, temperature and body weight all have a significant effect on the oxygen consumption and ammonia
excretion of the worm. Moreover, interaction between salinity/temperature and body weight is also significant. O:N (oxygen/nitrogen)
ratio varies greatly in this case from 5.97 to 463.22, indicating that N. japonica can regulate the type of metabolic substrate against environment changes.
Supported by the National Natural Science Foundation of China (No. 30490233) and the Three-Gorge Project and the Estuarine
Environment (No. SX2004-018) from the Three Gorges Project Construction Committee 相似文献
12.
在水温18℃±1℃和盐度27.0±0.5条件下,研究了饥饿对褐菖鮋耗氧率和排氨率的影响。结果表明:对照组的平均耗氧率为1.082 mg.g-1.h-1;饥饿组耗氧率随着饥饿时间的延长而下降,饥饿期间,褐菖鲉的平均耗氧率为0.893 mg.g-1.h-1,总体上低于对照组。排氨率随着饥饿时间的延长下降趋势呈阶段性变化:饥饿1 d、3 d后的排氨率略低于对照组但差异不显著(P>0.05);饥饿3～7 d,排氨率下降幅度变大,饥饿7d较饥饿3 d的排氨率下降了185.075%;饥饿14 d、21 d后排氨率分别为0.053 mg.g-1.h-1和0.028 mg.g-1.h-1,呈继续下降趋势,但下降幅度减缓。褐菖鮋的nO∶nN比值始小幅度上升,7 d时开始迅速上升,21 d后升高至27.754,差异显著(P<0.05)。 相似文献
13.
Effects of temperatures and salinities on oxygen consumption and ammonia-N excretion rate of clamMeretrix meretrix were studied in laboratory from Oct. 2003 to Jan. 2004. Two schemes were designed in incremented temperature at 10, 15, 20,
25°C at 31.5 salinity and in incremented salinity at 16.0, 21.0, 26.0, 31.5, 36.0, and 41.0 at 20°C, all for 8–10 days. From
10 to 25°C, both respiration and excretion rate were increased. One-way ANOVA analysis demonstrated significant difference
(P<0.01) in physiological parameters in this temperature range except between 15 and 20°C. The highestQ
10 thermal coefficient value (12.27) was acquired between 10 and 15°C, and about 1 between 15 and 20°C, indicatingM. meretrix could well acclimate to temperature changes in this range. Salinity also had significant effects on respiration and excretion
rate (P<0.05). The highest values of respiration and excretion rate ofM. meretrix were recorded at 16.0 salinity (20°C). These two physiological parameters decreased as salinity increased until reached the
minimumQ
10 value at 31.5 (20°C), then again, these parameters increased with increasing salinity from 31.5 to 41.0.M. meretrix can catabolize body protein to cope with osmotic pressure stress when environmental salinity is away from its optimal range.
No significant difference was observed between 26.0 and 36.0 in salinity (P>0.05), suggesting that a best metabolic salinity range for this species is between 26.0 and 36.0.
This work is supported by National High-Tech R & D Program of China. (863 Program) (2002AA603014). 相似文献
14.
Metabolic rates (oxygen consumption and ammonia excretion) of two dominant copepods, Calanoides acutus and Metridia gerlachei, were measured during the austral summer (December 1998 January 1999), in the marginal ice zone of the Prydz Bay. Their elemental compositions (C and N) were also analysed through these metabolic experiments. The results showed that C. acutus was 48.4% 48.6% of dry weight in carbon content and 6.1% 6.5% of dry weight in nitrogen content. Metridia gerlachei was 47.1% 50.1% and 5.9% 7.4%, relatively. Oxygen consumption rates of C. acutus were variant in the different areas (0.226 to 0.774 μlO2mg-1h-1). And its ammonia excretion rates ranged from 0.014 to 0.105 μgNmg-1h-1. The ratio between the rates (O∶N) exhibited a large difference(5 6 times). For Metridia gerlachei, oxygen consumption rates were 0.488 0.644 μlO2mg-1 and ammonia excretion rates were 0.015 0.034 μgNmg-1h-1. From the results of metabolic rate measurements and elemental analyses, daily losses of body carbon and nitrogen were estimated to be 0.59% 1.99% and 0.44% 3.27%, respectively. The metabolic carbon requirements accounted for 0.6% 29.2% of primary production per day, and their excretion of ammonia occupied 0.2% 38.0% of daily phytoplankton nitrogen demand. 相似文献
15.
We evaluated the effects of salinity andbody mass on the oxygen consumption rate and ammonia excretion rate of mudskipper Boleophthalmus pectinirostris under laboratory conditions.Salinity and body mass had highly significant effects on the oxygen consumption rate(R_O) and ammonia excretion rate(R_N)(P0.01).The interactive effects between salinity and body mass onR_O and R_N were insignificant(P0.05)and highly significant(P0.01),respectively.R_O and R_N of B.pectinirostris decreased significantly as the individual body mass increased.The relationship between R_O and body mass was represented by R_O=aW~b(R~2=0.956,P0.01).The relationship between R_N and the body mass of B.pectinirostris was represented by R_N=cW~d(R~2=0.966,P0.01).The R_O/R_N(O:N) ratios increased significantly as the salinity increased from 12 to 27,but decreased as salinity increased from 27 to 32.The atomic O:N ratios were significantly higher at27 than at other salinity levels.The average O:N ratio was 25.25.Lipid and carbohydrate were the primary energy sources and protein was the secondary energy source within the salinity range 12-32.R_O and R_N were significantly higher at 27 than at other salinity levels.Our results suggest that the optimum salinity level for B.pectinirostris is 27. 相似文献