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1.
Growth and energy budget of the polychaete, Neanthesjaponica, at various temperatures （17, 20, 23, 26 and 29℃） were investigated in this study. The growth, as indicated by final dry weight and specific growth rate （SGR）, increased with increasing temperature, with the maximum level at 26℃, and then decreased significantly at 29℃. A similar trend was observed in feeding rate, food conversion efficiency （FCE） and apparent digestive rate （ADR）. However, no significant differences were detected in ADR among all the temperature treatments. In the pattern of energy allocation, faeces energy was only a small component of energy budget and had little influence on the proportion of food energy allocated to growth. The metabolic energy accounted for a large portion of energy intake for each temperature treatment. The nitrogen excretion was appreciable with changing temperature. The two expenditure terms （respiration energy and excretion energy） in energy budget were the major factors influencing the proportion of food energy allocated to growth. These results revealed that temperature affected the growth of N. japonica mainly by influencing feeding rate and FCE. In addition, regression equations describing the relationship between feeding rate, faecal production, SGR, FCE and temperature were obtained. The optimum temperatures for feeding rate, FCE and SGR were estimated at 25.01 ℃, 24.24℃ and 24.73 ℃, respectively, from the regression equations.  相似文献   

2.
Growth and energy budget of the polychaete, Neanthesjaponica, at various temperatures (17, 20, 23, 26 and 29 ℃) were investigated in this study. The growth, as indicated by final dry weight and specific growth rate (SGR), increased with increasing temperature, with the maximum level at 26℃, and then decreased significantly at 29℃. A similar trend was observed in feeding rate, food conversion efficiency (FCE) and apparent digestive rate (ADR). However, no significant differences were detected in ADR among all the temperature treatments. In the pattern of energy allocation, faeces energy was only a small component of energy budget and had little influence on the proportion of food energy allocated to growth. The metabolic energy accounted for a large portion of energy intake for each temperature treatment. The nitrogen excretion was appreciable with changing temperature. The two expendi-ture terms (respiration energy and excretion energy) in energy budget were the major factors influencing the proportion of food en-ergy allocated to growth. These results revealed that temperature affected the growth of N. japonica mainly by influencing feeding rate and FCE. In addition, regression equations describing the relationship between feeding rate, faecal production, SGR, FCE and temperature were obtained. The optimum temperatures for feeding rate, FCE and SGR were estimated at 25.01 ℃, 24.24℃ and 24.73 ℃, respectively, from the regression equations.  相似文献   

3.
The effects of body weight and temperature on the carbon budget of the juvenile bastard halibut ,Paralichthys olivaceus ,were studied at temperature 13.5,18,21.5 and 24℃,respectively.The carbon intake,faecal and growth carbon were measured ,and the carbon respiration was calculated using the carbon budget equation (Cc=Gc Fc Rc),The combined relationship between different components of the carbon budgent,body weight and temperature could be described by regression equations:Cc=1.0206 W^0.8126E^0.1483T;Gc=0.0042w^1.4096(-5.11 T^3 285.90T^2-5173.72T 30314.03);Fc=0.0485W^0.7711e^0.1624T;Uc=1.4333W^0.6715e^0.1487t,Body weight had no significant effect on the carbon absorption efficiency and the conversion efficiency.  相似文献   

4.
Seasonal and sexual variations as well as the effect of dry feed supplement on total drinking water intake and its utilization were observed in mithun （Bosfrontalis） - a semi-wild animal found in North Eastern Hill Region （NEHR） of India. In a completely randomized design, twelve adult mithuns （B. frontalis） as per their sex and body weight were assigned in two different rearing systems （free grazing and free grazing with dry concentrate feed supplementation）, and ten growing male mithuns as per their body weight assigned in two different levels of dry concentrate feed supplementation （1.o kg and 2.0 kg dry concentrate feeds on green forage based diet） and in two different seasons （summer and winter）. It was observed that the environmental temperature had a significant effect on drinking water intake by mithuns. Drinking water consumption （per unit of body weight） was significantly （P 〈 0.05） higher in summer than in winter. Supplementation of concentrate feed on free grazing animals resulted in increase in water consumption. Total water consumption （drinking as well as performed water） was found to be 15.18 litres per 100 kg body weight by growing mithun. Feed dry matter and digestible nutrient intakes by growing mithun were observed to be increased with the increase of supplementation of dry concentrate feed. Roughage to concentrate ratio did not affect the nutrient digestibility. Mithun calves drank an average of 4.30 litres water for each kg of dry matter intake. Metabolic water was significantly （P〈0.01） increased with the increase of supplementation of concentrate feed whereas water turn over, which depends upon the body weight of the animals, did not differ significantly on offering of lower or higher level of dry feed. Faecal water loss of growing mithun was decreased with the increase in intake of concentrate feed and was estimated to be 33 - 46 % of total water intake. Excretion of water through faeces of mithun was about 3.8 % of body weight. It could, there  相似文献   

5.
Experiment on phosphorus budget of redeye mullet （Liza haematocheila T. ＆ S.） was conducted at water temperature 21℃ and salinity 33. The results showed that the growth phosphorus （phosphorus that allocated into growth, GP） increased from -30.84% to 15.83% by feeding on graded amount of diets （starvation, 1%, 2%, 3%, 4% body weight and satiation）. The GP linearly increased with feeding levels （FL） as GP （mg） = - 0.785 ＋ 0.604 FL, and at satiation the relationship between GP and body weight （BW） was GP （mg） = 1,5991 BW0.7685. In the budget, IP （intake phosphorus） = GP ＋ FP （faecal phosphorus） ＋ EP （excretion phosphorus）. FP showed an irregular tendency with different feeding levels, and EP decreased with increasing feeding levels but rebound at satiation. The P budget at satiation was 100IP = 15.84 GP ＋ 64.62 FP ＋ 19.55 EP.  相似文献   

6.
Maximum rate of food consumption ( Cmax ) was determined for juvenile Sebastodes fuscescens (Houttuyn) at water temperature of 10, 15, 20 and 25℃. The relationships of Cmax to the body weight (W) at each temperature were described by a power equation: lnCmax = a b lnW. Covariance analysis revealed significant interaction of the temperature and body weight. The relationship of adjusted Cmax to water temperature (T) was described by a quadratic equation: Cmax = -0.369 0.456T - 0.0117T^2. The optimal feeding temperature calculated from this equation was 19.5 ℃. The coefficients of the multiple regression estimation relating Cmax to body weight (W) and water temperature (T) were given in the Table 2.  相似文献   

7.
Systematic study on sorption behavior of o-nitrophenol on marine sediments was conducted.Isotherms of sorption of o-nitrophenol on marine sediments could be described by Freundlich model; and the isotherm of sorption of o-nitrophenol on HCl-treated sediment could be described by Langmuir model. The sorption behavior was affected by various factors including organic carbon content, aqueous solution salinity,temperature, and acidity. The sorption amount of o-nitrophenol increased when salinity and acidity of the aqueous solution increase, but decreased with increasing temperature. Organic carbon content in sediments had apparent effect on the behavior except for HCl-treated sediments.  相似文献   

8.
Dietary leucine requirement for juvenile large yellow croaker, Pseudosciaena crocea Richardson 1846 (initial body weight 6.0 g±0.1 g) was determined using dose-response method.Six isonitogenous (crude protein 43%) and isoenergetic (19 kJ g-1) practical diets containing six levels of leucine (Diets 1-6) ranging from 1.23% to 4.80% (dry matter) were made at about 0.7% increment of leucine.Equal amino acid nitrogen was maintained by replacing leucine with glutamic acid.Triplicate groups of 60 individuals were fed to apparent satiation by hand twice daily (05:00 and 17:30).The water temperature was 26-32℃, salinity 26-30 and dissolved oxygen approximately 7 mg L-1 during the experimental period.Final weight (FW) of large yellow croaker initially increased with increasing level of dietary leucine but then decreased at further higher level of leucine.The highest FW was obtained in fish fed diet with 3.30% Leucine (Diet 4).FW of fish fed the diet with 4.80% Leucine (Diet 6) was significantly lower than those fed Diet 4.However, no significant differences were observed between the other dietary treatments.Feed efficiency (FE) and whole body composition were independent of dietary leucine contents (P0.05).The results indicated that leucine was essential for growth of juvenile large yellow croaker.On the basis of FW, the optimum dietary leucine requirement for juvenile large yellow croaker was estimated to be 2.92% of dry matter (6.79% of dietary protein).  相似文献   

9.
Oxygen uptake under starvation and short periods of sudden temperature change was measured forlarval herring (Clupea harengus L.) reared at average temperature of 7.3, 11 and 12.9℃. Larval stagesbetween first feeding and premetamorphosis were used. For comparison, the routine oxygen uptake(ROU) was also investigated and followed the relationship Q=0.974+0. 174 tW~(0.210), where Q is in μg/(mg·h), W is dry body weight in mg and t is temperature in ℃. The oxygen uptake under starvation(SOU, deprived of food for 24 h) was different from the routine when the larval dry weightwas less than 0.6-0.8 mg, it increased with temperature and body weight giving the reationship Q=1.568+0.110 tW~(0.380), if the larval dry weight mp more than 0.6-0.8 mg, it reverted to the norm(Q=1.704+0.078 tW~(-0.349)). The oxygen uptake was tested in short periods (3 h) of sudden temperaturechanges in six groups: 7.3 to 11, 7.3 to 12.9, 11 to 7.3. 11 to 12.9, 12.9 to 7.3 and 1.29 to11℃. The oxygen uptake in the 7.3 to 12.9 and 1  相似文献   

10.
Wang  Nan  Li  Chaolun  Wang  Yantao  Feng  Song 《中国海洋湖沼学报》2018,36(6):2216-2230
Mass occurrences of moon jellyfish have been observed in coastal waters. Strobilation directly determines the initial population size of adult jellyfish, but energy distribution during the strobilation process is not well understood. In this study, strobilation was induced in polyp of Aurelia coerulea by elevating temperature. The different stages in the strobilation process, including polyp budding, strobilation and body growth, were investigated at six temperature levels(8, 10, 13, 15, 17 and 19°C) and five food supply levels(0, 30, 60, 100 and 150 μg C/L). The results showed that the duration of strobilation preparation stage(SP) remarkably decreased with increasing temperature. Food level positively af fected the production of buds and ephyrae and the body growth of parent polyps. Of the six temperatures tested, 13°C was optimal for strobilation. At 13°C, strobilation activity was enhanced, and this treatment resulted in the greatest energy distribution, highest ephyrae production and longest duration of strobilation stage(SS). Polyps tended to allocate 6.58%–20.49% carbon to buds with sufficient food supply regardless of temperature. The body growth of parent polyps was highest at lower temperatures and higher food levels. This study is the first to provide information on carbon-based energy distribution strategy in the polyp strobilation process. We concluded that budding reproduction is a lower-risk strategy for A. coerulea polyps to increase populations. Even during strobilation season, polyps prioritize budding, but at the optimal strobilation temperature, polyps utilize a portion of the energy stored for budding to release ephyrae. The body carbon content of parent polyps may be considered as strategic energy reserves, which could help to support budding activities and strobilation during harsh conditions.  相似文献   

11.
ＩＮＴＲＯＤＵＣＴＩＯＮＴｈｅｍｅｔａｂｏｌｉｓｍｉｎｆｉｓｈｉｎｃｌｕｄｅｓｓｔａｎｄａｒｄｍｅｔａｂｏｌｉｓｍ(ＲＳ)ｒｏｕｔｉｎｅｍｅｔａｂｏｌｉｓｍ(ＲＲ),ｓｐｅｃｉｆｉｃｄｙｎａｍｉｃａｃｔｉｏｎ(ＳＤＡ)ａｎｄａｃｔｉｖｅｍｅｔａｂｏｌｉｓｍ(ＲＡ),ｒｅｌａｔｅｄａｓ:　　ＲＴ=ＲＳ ＲＲ ＳＤＡ ＲＡｗｈｅｒｅＲＳｉｓｔｈｅｍｅｔａｂｏｌｉｓｍｏｆｔｈｅｆｉｓｈａｔｒｅｓｔ;ＲＲｔｈｅｍｅｔａｂｏｌｉｓｍｏｆｔｈｅｒｏｕｔｉｎｅｌｙａｃｔｉｖｅｆｉｓｈ;ＳＤＡｔｈｅｍｅｔａｂｏｌｉｓｍｏｆｔｈ…  相似文献   

12.
1 INTRODUCTION Chironomid larvae are main groups in most aquatic ecosystems, playing a crucial ecological role in decomposition of detritus and material ex- changes between water column and the sediment (Liang et al., 1995a, b; Chen, et al., 1982). They a…  相似文献   

13.
Oxygen uptake under starvation and short periods of sudden temperature change was measured for larval herring (Clupea harengus L.) reared at average temperature of 7.3, 11 and 12.9°C. Larval stages between first feeding and premetamorphosis were used. For comparison, the routine oxygen uptake (ROU) was also investigated and followed the relationshipQ=0.974+0.174tW −0.210, whereQ is in μg/(mg·h),W is dry body weight in mg andt is temperature in °C. The oxygen uptake under starvation (SOU, deprived of food for 24 h) was different from the routine when the larval dry weight was less than 0.6–0.8 mg; it increased with temperature and body weight giving the relationshipQ=1.568+0.110tW 0.380; if the larval dry weight was more than 0.6–0.8 mg, it reverted to the norm (Q=1.704+0.078tW −0.349). The oxygen uptake was tested in short periods (3 h) of sudden temperature changes in six groups: 7.3 to 11, 7.3 to 12.9, 11 to 7.3, 11 to 12.9, 12.9 to 7.3 and 1.29 to 11°C. The oxygen uptake in the 7.3 to 12.9 and 12.9 to 7.3°C groups varied in a way similar to that of the larvae under starvation. The other four groups' oxygen uptake were more or less normal.  相似文献   

14.
Growth and energy budget of the polychaete, Neanthes japonica, at various temperatures (17, 20, 23, 26 and 29°) were investigated in this study. The growth, as indicated by final dry weight and specific growth rate (SGR), increased with increasing temperature, with the maximum level at 26°C, and then decreased significantly at 29°C. A similar trend was observed in feeding rate, food conversion efficiency (FCE) and apparent digestive rate (ADR). However, no significant differences were detected in ADR among all the temperature treatments. In the pattern of energy allocation, faeces energy was only a small component of energy budget and had little influence on the proportion of food energy allocated to growth. The metabolic energy accounted for a large portion of energy intake for each temperature treatment. The nitrogen excretion was appreciable with changing temperature. The two expenditure terms (respiration energy and excretion energy) in energy budget were the major factors influencing the proportion of food energy allocated to growth. These results revealed that temperature affected the growth of N. japonica mainly by influencing feeding rate and FCE. In addition, regression equations describing the relationship between feeding rate, faecal production, SGR, FCE and temperature were obtained. The optimum temperatures for feeding rate, FCE and SGR were estimated at 25.01°C, 24.24°C and 24.73°C, respectively, from the regression equations.  相似文献   

15.
Reproductive rate of a marine planktonic copepodLabidocera euchaeta Giesbrecht in Xiamen Harbor bor was studied during the period from April 1986 to August 1987. Results showed that rate of egg production (F, eggs/(♀, d)) was positively correlated with temperature (T,oC) and body weight of spawning female (Wc, μgC) as:F=0.0637 (T−7)0.7445 Wc. Each month a maximum rate of egg production occurred at one of the five experimental temperatures (10°, 15°, 25°, and 30°C) near the monthly mean field temperature. The available food density (P, μgC/ml) had significant effect on specific rate of egg production (Fc, %C ♀/d) as:Fc=0.1732 (P-0.0179)/P. The gross efficiency of egg production of ca 62% in carbon was independent of food density snd ingestion rate. Observations on in situ egg production and hatching rate demonstrated that this species reproduces continuously all the year round, with summer as its high reproductive season and winter a low one. Ten generations a year is also suggested based on the number of the peaks of average population egg production rate. This agreed well with the result obtained from the generation-time equations. Egg-laying pattern was also observed and discussed.  相似文献   

16.
Scales of the Lake Anchovy in Taihu Lake are used as a basis for its age determination. Annual variation of scale edge growth rate (α) indicates that the annulus forms once a year, mainly in April–June. The relationship formula for body length and scale diameter is L=18.658+118.06R, that for body length and weight isW♀=7.588×10−6 L 2.8301;W♂=5.584×10−6 L 2.8781. The fish before age II have a higher relative growth rate in body length and weight and a higher growth index. Growth is consistent with the growth equation by Von Bertalanffy. The turning point of the body weight growth curve is located between age II and III; the exact position is atW=0.292W ∞. Variation specificity of the growth course can be reflected by the growth rate and its acceleration curves. Time for capture of the fish should preferably be after age II, when they have reached a body length of 170 mm. That is one of the key measures to increase Lake Anchovy production in Taihu Lake.  相似文献   

17.
ＩＮＴＲＯＤＵＣＴＩＯＮＴｈｅＪａｐａｎｅｓｅｓｅａｂａｓｓ (ＬａｔｅｏｌａｂｒａｘｊａｐｏｎｉｃｕｓＣ＆Ｖ)ｄｉｓｔｒｉｂｕｔｅｓｗｉｄｅｌｙｉｎｔｈｅｃｏａｓｔａｌｗａｔｅｒｓａｌｏｎｇｔｈｅＢｏｈａｉＳｅａ ,ＹｅｌｌｏｗＳｅａ ,ＥａｓｔＣｈｉｎａＳｅａ,ａｎｄＳｏｕｔｈＣｈｉｎａＳｅａ .Ａｓａｃａｒｎｉｖｏｒｏｕｓｆｉｓｈ ,ｉｔｏｃｃｕｐｉｅｓｔｈｅｈｉｇｈｔｒｏｐｈｉｃｌｅｖｅｌｉｎｔｈｅｍａｒｉｎｅｅｃｏｓｙｓｔｅｍａｎｄｈａｓａｄａｐｔｅｄｔｏｖａｒｉｏｕｓｅｎｖｉｒｏｎｍｅｎｔａｌｒ…  相似文献   

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