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91.
Length frequency data collected from artisanal fisheries in Lake Ayamé I (Côte d'Ivoire) from August 2004 to 2005 were analysed with F isat software using the E lefan package to estimate the population parameters of 11 fish species. Asymptotic values for total length ( L∞ ) ranged from 20.5 cm for Brycinus imberi to 78 cm for Mormyrops anguilloides . Growth rates ( k ) varied from 0.24 year−1 for Chrysichthys nigrodigitatus to 0.57 year−1 for Hemichromis fasciatus . The growth performance estimates were close to the values found by others authors and reported in FishBase 2008. Fishing mortality ( F ) and exploitation rate ( E ) were found to be below optimum levels of exploitation for most fish species. Recruitment was noted as year–round and bimodal for most studied populations. The data sets were limited in most cases, thus this study provides preliminary population parameters only, but for species for which information is scarce. For application in stock assessment, the growth parameters and especially the natural mortality data require further confirmation.  相似文献   
92.
A rudimentary understanding of age, growth, and life-span is lacking for many non-game fishes. Growth characteristics of the central mudminnow ( Umbra limi ) have not yet been accurately described using reliable hard part analysis. The utility of scales and otoliths as ageing structures and quantified growth was examined in one lake and one stream population of central mudminnow. Scales were found to be of no utility in determining age due to inconsistent formation of yearly annuli and a high incidence of regenerated scales, while otoliths were easily extracted and considered to be an accurate ageing structure. Ages determined from scales were low compared to those from otoliths, and the difference in age interpreted from the two structures increased with fish age. A power function was fitted to describe the length-weight relationship for this species ( a  = 0.0069, b  = 3.175). Von Bertalanffy growth parameters were estimated and compared for each population (Lake: L  = 114.20 mm, K  = 0.30, t 0 = −0.93; Stream: L  = 77.59 mm, K  = 0.63, t 0 = −0.76). The lake population showed greater size at age compared to the stream population, especially at older ages, and achieved a larger maximum size. Growth rate was also greater in the lake population (Lake: 1.74; Stream: 1.09 g year−1). Females were larger at age than males in both populations, however all individuals greater than age 3 were males. This work represents the first successful account of central mudminnow growth using hard part analysis.  相似文献   
93.
94.
Reports in the literature show that the dietary fatty acid (FA) composition is reflected in fish muscle, their internal organs and eggs. Fish eggs are used in toxicity tests to determine the subchronic toxicity of various substances. In toxicity tests, physico-chemical test parameters have been standardized. However, parental age and diet may also influence results of toxicity tests and if so would also require standardization. Our investigations hitherto indicate that the FA composition of eggs and testes in zebrafish is caused by the FA composition of fish diet. Diets with different ratios of n-3/n-6 polyunsaturated fatty acids led to different contents of these FA in the reproductive organs and finally to variations in the fertilization rates. This rate is elevated in the eggs of zebrafish ( Danio rerio Hamilton-Buchanan) if the quotient of n-3/n-6 is low.  相似文献   
95.
The food consumption and egg production of 26 adult (13 female and 13 male) Atlantic cod ( Gadus morhua ) were monitored during prespawning, spawning and postspawning periods. Females spawned from late January to mid-April. Feeding activity occurred from December to early January and ceased for females, on average, 36 days (15–54 days) before the onset of spawning. The duration of spawning by females was, on average, 42 days (10–61 days) and feeding was suppressed by both sexes during the first three-quarters of each female's spawning period. Mature females went, on average, 70 days or 19% of the year without eating. An abrupt increase in feeding activity, particularly by females, occurred during the last quarter of spawning or shortly after the release of the last egg batch (on average, feeding started again after 91% of a female's eggs had been released or 82% of egg batches). Females consumed greater quantities of food than males during both winter and postspawning feeding periods. During spawning, females lost, on average, 29% of their body weight and males 14%. Fecundity ranged from 0.75 to 3.97 million eggs per female. The volume of eggs produced by four individual females (range = 1285–5995 ml in four to 11 batches) ranged from 99 to 195% (mean 150%) of a female's postspawning body volume. Six immature cod fed throughout the experimental period and gained, on average, 8% of initial body weight. Laboratory results were supported by stomach fullness index values of Georges Bank cod exhibiting different maturity states.  相似文献   
96.
Summary A board game was developed for use in workshops to demonstrate some theoretical principles underpinning conservation planning at the landscape scale. The game is based on neutral landscape models and demonstrates the effects of habitat removal and arrangement on landscape connectivity for organisms with different mobility characteristics. This paper briefly describes the ecological principles underpinning the game, the equipment required to run a game session, and the rules of the game. The game was piloted in three workshops where it was played by a total of 75 people, primarily extension personnel. It proved to be an effective learning tool that was adopted by a number of the participants for their own communication activities.  相似文献   
97.
Axillary seabream Pagellus acarne (Risso 1826) caught off the Canary Islands from January 1991 to December 1994 were studied. The length range of the catches was between 11 and 31 cm, with a modal distribution between 17 and 21 cm. The overall ratio of males to females was 1:1.74. Males were observed up to a length of 24 cm. Hermaphrodites were recorded at lengths between 15 and 23 cm. The species was characterized by protandric hermaphroditism. The reproductive season extended from October to March, with a peak in spawning activity in December–January. The size at sexual maturity was 15.8 cm total length (2 years old) for males and 19.4 cm total length (3 years old) for females. The total length–total weight relationship for the entire population is described by the parameters a = 0.0068, and b = 3.2401. Otolith age readings showed that the population exploited consisted of 10 age groups (1–10 years), including a very high proportion of individuals between 1 and 4 years old. The von Bertalanffy growth parameters for all individuals were L = 32.98 cm, k = 0.22 years−1, and t0 = −0.87 years. Males grew comparatively slower than females. The instantaneous rates of mortality for all fish were Z = 0.96 years−1, M = 0.30 years−1, and F = 0.66 years−1. The exploitation ratio and the length at first capture were, respectively, E = 0.69 and LC50 = 16.1 cm. The stock is overexploited, therefore measures such as closed seasons or changes in fishing patterns would be desirable to safeguard the spawning stock and recruits.  相似文献   
98.
Heterobranchus longifilis Val. 1840 larvae were reared under two light intensities, 30 lux and 915 lux, and at varying photoperiods. Results show that maximum survival (82.5 ± 6.5% respectively) at 30 lux was obtained at continuous illumination [24 h light (L)], while the minimum (65 ± 21.2%) was at the 6 h L : 18 h dark (D) treatment. Survival at 24 h D averaged 71.3 ± 6.3%, with no significant difference (P < 0.05) in growth of larvae. Maximum larval survival at 915 lux was 87.5 ± 17.7% at the 18 h L treatment. Growth was not significantly different (P < 0.05) in the treatments. Comparison of the two light intensities showed that survival was better at a photoperiod above 12 h irrespective of intensity, while growth was significantly better at the 915 lux intensity.  相似文献   
99.
Summary Concerns about the effects of predation by Feral Cats ( Felis catus ) on native fauna, particularly breeding seabirds, precipitated a decision in 1987 to control and eventually eradicate cats from Gabo Island. The size of the population prior to control was at least 30 animals. A control programme, undertaken between 1987 and 1991, centred on shooting, trapping and an extensive 1080 poison-baiting programme. Trapping and shooting were ineffectual. Poisoning was the most successful and effective technique for the rapid and widespread reduction in the Feral Cat population on Gabo Island. The effectiveness of dead 1-day-old chickens as a poison carrier was demonstrated. Effective poison baiting was attributed to bait selection and strategic timing of baiting to periods when prey was at low levels. Outcomes from the trapping programme and post-control monitoring strongly suggested that the cat population had been reduced to only two or three animals, possibly of the same sex. Monitoring between 1992 and 1998 failed to record any evidence of cats, indicating that the cats remaining after poison baiting had been unable to sustain a viable population. On the basis of the available evidence, Feral Cats appear to have been successfully eradicated from Gabo Island.  相似文献   
100.
Summary For the 70% of New Zealand under private ownership, native biodiversity conservation has to occur within a landscape that must also provide a productive return to land owners. Recent New Zealand legislation, especially the Resource Management Act 1991, promotes sustainable management on private land by allowing for the economic and cultural well-being of local communities while providing for the protection of natural resources including native biodiversity. We suggest that, to effectively conserve native biodiversity in rural landscapes, we need to consider four key issues: (i) what might be realistic goals for native biodiversity conservation; (ii) how might we better arrange different land uses to meet both native biodiversity and production goals; (iii) what is the optimum arrangement of native biodiversity; and (iv) how native biodiversity conservation can improve productive returns to land managers. Options to enhance native biodiversity conservation include a variety of incentives (e.g. management agreements, financial incentives and regulatory systems) and onsite management options (e.g. remnant management, restoration plantings, weed and pest control, use of native species for commercial and amenity purposes, use of exotic species to facilitate native biodiversity). The importance of taking a landscape-based rather than a paddock-based approach to management is emphasized.  相似文献   
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