盐度对黄鲷胚胎发育及早期仔鱼生长的影响

The effect of salinity on embryo and early larva development of Dentex tumiforns was discussed. Floating forms of egg in different salinities, optimal salinity for embryonic development and early larva growth was studied. The results showed: 1. In immobile condition, all eggs sank at salinity of 32.0, most of egg ssuspended in the middle of water at 34.0, and all eggs floated on the surface when salinity above 36.0. 2. Eggs did not hatch out at salinity of below 10.0 or above 60.0 and the death time of egg gradually moved up with increase or decline of salinity. Eggs hatched out at salinity range of 15.0 and 50.0, including abnormal larva. There was indistinct difference in speed of embryonic development (about 36-40h) within the salinity of 15.0 and 50.0. However the salinity had a great effect on larval survival after hatching and abnormal rate. The relation between hatching rate and salinity variation showed parabola but abnormal rate showed inverted parabola. The hatching rate was 81%-86% and abnormal rate of yolk sac larva was 27%-30% in suitable salinities of 27.0-39.0. The hatching rate was 89%-91% and abnormal rate was 13%-16% in optimal salinities of 33.0-36.0. The oil ball of abnormal larva was located in the central or front position. With increased extent of salinity, spondyle of larva bended and number of larva with arrhythmia increased. 3. The optimal salinities were 30.0-35.0 based on SAI. The test with SAI showed that SAI of early larvae was 41.25-47.53 at salinities of 30.0-35.0, the yolk and oil ball of 7-8 days larva was completely absorbed with a survival rate of 88%.     

Effects of changing temperature on benthic marine life in Britain and Ireland

• 1. The coastal waters surrounding Britain and Ireland became warmer during the 20th century and, according to the UK Climate Impact Programme 2002 scenarios of change and other sources, average annual seawater temperatures may rise a further 2°C or more by the 2050s. This warming is part of a global rise in sea‐ and air‐surface temperatures that will cause changes in the distribution and abundance of species.
• 2. Initially, there will not be a wholesale movement northwards of southern species or retreat northwards of northern species, because many additional factors will influence the responses of the different organisms. Such factors include the hydrodynamic characteristics of water masses, the presence of hydrographical and geographical barriers to spread and the life history characteristics (reproductive mode, dispersal capability and longevity) of species. Survey data over the past century show how organisms react to changes of the order of 0.5°C, and in the last two decades, when sea temperatures have risen by as much as 1°C, there have been significant local changes in the distribution of intertidal organisms. These past changes provide a clue to more extensive changes expected in the future if global warming develops as predicted.
• 3. Where species affected by climate change are dominant or key structural or functional species in biotopes, there may be a change in the extent and distribution of those biotopes. Some, dominated by predominantly northern species such as the horse mussel Modiolus modiolus, may decline and reduce their value as rich habitats for marine life. Others, characterized by southern species, for example the sea fan Eunicella verrucosa and the alcyonacean Alcyonium glomeratum, may increase in extent.
• 4. Using information on the life history characteristics of species, their present distribution and other factors, a key supported by a decision tree has been constructed to identify ‘types’ of organism according to their likely response to temperature rise. Conspicuous and easily identified rocky substratum species are good candidates to track change. Using the key, many species are shown as likely to increase their range northwards significantly. In contrast, fewer will decline in abundance and extent in the north. If, as anticipated, global warming continues, then species with distributions already accurately mapped, or being mapped at present, will provide baseline data to test forecasts.

Copyright © 2004 John Wiley & Sons, Ltd.     

Seasonal changes in circulating growth hormone (GH), hepatic GH-binding and plasma insulin-like growth factor-I immunoreactivity in a marine fish,gilthead sea bream,Sparus aurata

We have studied the seasonal relationship between growth and circulating growth hormone (GH), hepatic GH-binding and plasma insulin-like growth factor-I immunoreactivity in gilthead sea bream,Sparus aurata. The seasonal increase in plasma GH levels preceded by several weeks the summer increase in growth rates. In contrast, a marked increase in hepatic GH-binding with a high degree of endogenous GH occupancy was found during the period of maximum growth which suggests an enhanced sensitivity of liver to GH action. Thus, circulating levels of immunoreactive IGF-I, probably derived from the liver in response to GH action, were positively correlated with growth throughout the experimental period although a consistent relationship between growth and circulating GH was not found. In spite of this, we consider that, in gilthead sea bream, as in several other teleosts, the availability of endogenous GH can limit growth. Thus, under environmental conditions of suboptimal growth, a single intraperitoneal injection of recombinant rainbow trout GH (rtGH) induced over the dose range tested (0.75, 1.5, 3 μg g BW⁻¹) an increase in plasma IGF-I-like immunoreactivity comparable to that seen during the period of maximum growth.     

Recruitment patterns of six species of cyprinid fishes in the lower River Trent, England

Abstract – Fisheries data were collected for six species of 0-group cyprinid fishes from eight sites in the lower reaches of the River Trent, England, between May and October 1999 inclusive, using a micromesh seine net. Recruitment and growth patterns were observed via monthly length–frequency histograms and estimations of mean length. In the cases of roach and dace, growth was approximately linear through the summer, before declining in September and October. In the cases of chub and gudgeon, and to a lesser extent bream and bleak, however, there were suggestions of multiple recruitment events. It is argued that some of the fish species examined in the present study adopt fractional or protracted spawning strategies in the lower River Trent.     

虾夷扇贝海区采苗技术初步研究

2005—2006年,在大连旅顺沿海进行了虾夷扇贝海区采苗试验。试验结果为:2005年月亮湾海区采苗密度,第1批为231枚/袋,第2批为423枚/袋;2006年月亮湾海区采苗密度为242枚/袋,董砣子海区为456枚/袋。生殖腺指数等调查结果表明,长海县各海区虾夷扇贝开始产卵时间在3月末4月初。虾夷扇贝浮游幼虫附着高峰期出现在5月底。     

Immune response of sea bass <Emphasis Type="Italic">Dicentrarchus labrax</Emphasis> to <Emphasis Type="Italic">Tenacibaculum maritimum</Emphasis> antigens

ABSTRACT:   Seawater fishes are affected by a pathology commonly called 'myxobacteriosis', caused by Tenacibaculum maritimum (formerly Flexibacter maritimus ). The disease is characterized by fin erosion and necrotic ulcers of skin and muscle, and by low but constant mortality in cultured marine fish; in Italy is one of the most important and widely spread diseases affecting sea bass Dicentrarchus labrax , gilthead seabream Sparus aurata , sharp-snouted bream Diplodus puntazzo , white bream Diplodus sargus , and six-tooted bream Dentex dentex . In order to obtain an effective vaccine against the disease, formalin killed cells (FKC), extracellular products (ECPs) and crude lipopolysaccharide (LPS) preparations were obtained from the T. maritimum strain SPVId and injected intraperitoneally twice into the sea bass. The fish immune response to the preparations was studied: agglutinating antibody titer and in vitro phagocytosis were determined after the first and second injection in order to evaluate whether the preparations are immunogenic or not and if the booster effect took place. The results show that FKC and LPS preparations increased the antibody titer after the first injection when compared to the control sea bass. Moreover, all the preparations stimulated a secondary (booster) response. In vitro phagocytosis of the total blood was significantly higher for all the preparations when compared to the controls, but the crude LPS immunized sea bass showed the highest activity.     

A synthesis of the life history and ecology of juvenile Pacific herring in Prince William Sound,Alaska

Physical and biological variables affecting juvenile Pacific herring (Clupea pallasi) in Prince William Sound (PWS) from 1995 to 1998 were investigated as part of a multifaceted study of recruitment, the Sound Ecosystem Assessment (SEA) program. Though more herring larvae were retained in eastern PWS bays, ages‐0 and ‐1 herring used bays throughout PWS as nursery areas. Water transported into PWS from the Gulf of Alaska (GOA) contributed oceanic prey species to neritic habitats. Consequently, variations in local food availability resulted in different diets and growth rates of herring among bays. Summer food availability and possible interspecific competition for food in nursery areas affected the autumn nutritional status and juvenile whole body energy content (WBEC), which differed among bays. The WBEC of age‐0 herring in autumn was related to over‐winter survival. The limited amount of food consumption in winter was not sufficient to meet metabolic needs. The smallest age‐0 fish were most at risk of starvation in winter. Autumn WBEC of herring and winter water temperature were used to model over‐winter mortality of age‐0 herring. Differences in feeding and energetics among nursery areas indicated that habitat quality and age‐0 survival were varied among areas and years. These conditions were measured by temperature, zooplankton abundance, size of juvenile herring, diet energy, energy source (GOA vs. neritic zooplankton), WBEC, and within‐bay competition.     

Fishing gear effects and ecology of the sea whip (Halipteris willemoesi (Cnidaria: Octocorallia: Pennatulacea)) in British Columbia,Canada: preliminary observations

• 1. We conducted a preliminary study of the effects of a shrimp beam trawl and prawn traps on sea whips (Halipteris willemoesi (Cnidaria: Octocorallia: Pennatulacea)) at two bays on Clio Channel, south central coast of British Columbia, Canada. Video and grabs surveys were conducted to estimate abundance and make observations on sea whips and their habitat.
• 2. No adult sea whips were caught in six beam trawls. In 600 prawn (Pandalus platyceros) trap sets at Turnour Bay, 30 sea whips were found entangled in the gear and of these 50% of the colonies were damaged. The length of broken sea whips ranged from 0.09 to 1.03 m. At Turnour Bay, the density of adults observed in video surveys ranged from 7.1 to 14.3 m^?2. Juvenile density in grab samples ranged from 53 to 123 m^?2 and a few adults were also caught. The lengths of intact adult sea whips caught in traps and grabs ranged from 0.20 to 1.98 m and juveniles from 0.3 to 0.7 cm.
• 3. Fewer adult sea whips (<0.1 m^?2) were seen in Bones Bay, where sediments were muddier (grain size <0.25 mm: 84.6 to 97.2%) relative to Turnour Bay (grain size <0.25 mm: 71.4 to 85.9%). Bottom water characteristics at the two bays were similar. Seasonal temperature range was 7.5–8.4°C, salinity 30.63–31.49 psu, and dissolved oxygen 2.76–5.97 mg L^?1. Differences in sediment characteristics and food availability may have been a factor influencing differences in abundance of sea whips between the two bays.
• 4. Further data are needed to investigate the effects of trawling and trapping on sea whips, as sample sizes were small in the present study and only two gear types were evaluated. Studies of effects of otter trawling and heavier traps, such as those used for Dungeness crab (Cancer magister), are warranted.

Copyright © 2005 John Wiley & Sons, Ltd.     

Shell marking by artificial feeding of the tropical abalone Haliotis asinina Linne juveniles for sea ranching and stock enhancement

A method of marking abalone (Haliotis asinina Linne) for sea ranching and stock enhancement purposes was developed. Three‐month‐old abalone juveniles (11.8‐mm shell length, 0.28 g) were fed artificial diets for 1, 2, or 3 weeks. The width of the bluish‐green shell band produced by abalone juveniles was 1.7, 2.6, and 4.2 mm after 1, 2, or 3 weeks of feeding respectively. The growth and survival of juveniles fed artificial diets did not differ from that of juveniles fed the seaweed Gracilariopsis bailinae (control). Feeding the diet‐fed juveniles with the seaweed thereafter produced the natural brownish shell, thus forming a sandwiched bluish‐green band. An experimental release in outdoor tanks with natural growth of seaweeds and diatoms, and in a marine reserve showed that the shell band remained clear and distinct, indicating the usefulness of this shell marking method in sea ranching and stock enhancement of abalone.