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61.
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63.
南海北部陆架区蓝圆鲹的生长、死亡及合理利用研究 总被引:10,自引:0,他引:10
本文根据1997年12月至1999年6月在南海北部陆架区进行的大规模底拖网渔业资源调查资料中的蓝圆鲹生物学测定资料,运用FAO开发的最新的体长频率数据分析软件FiSATⅡ对蓝圆鲹的生长、死亡参数进行估算,并进一步应用Beverton-Holt模式对南海北部陆架区的蓝圆鲹最新资源状况进行研究.结果表明:(1)蓝圆鲹的叉长和体重的关系式为:W=1.4084×10~(-2)L~(2.9931),其生长规律可用von Bertalanffy的生长方程描述.(2)其von Bertalanffy生长方程各参数为:渐近叉长L_∞=33.1cm,渐近体重W_∞=498.6g,生长系数K=0.36,t_0=-0.44.(3)总死亡的系数Z=1.87,自然死亡系数M=0.85,捕捞死亡系数F=1.02,开发率E=0.55.在估算结果的基础上,进一步提出南海北部陆架区蓝圆鲹在目前的捕捞强度下的最佳可捕规格叉长为14.7cm,为我国实施拖网目限制提供了科学依据. 相似文献
64.
Myers R. A.; Barrowman N. J.; Hoenig J. M.; Qu Z. 《ICES Journal of Marine Science》1996,53(3):629-640
65.
Abstract. The Philippines is generally accepted to be the center of the international trade of stony corals for ornamental use. Despite existing legal bans on the collection and export of stony corals in the Philippines, the coral trade continues to date, particularly in Cebu. This paper reports on the specific market demand for stony corals in Cebu and the effects of commercial collection based on the results of a quantitative study of two shallow coral reef areas subjected to large differences in collection effort. Comparison of the measured coral community parameters suggests selective population changes and reduced abundance of exploited coral populations as a result of commercial collection. Estimates of the natural mortality, fishing mortality and yield are presented for the two sampled populations of Pocillopora verrucosa , utilizing the method of GRIGG (1976). Based on the study results and a review of reported coral growth rates and coral colony size at reproductive maturity, the potential for resource management of stony corals on a sustainable yield basis is - discussed. 相似文献
66.
南海北部带鱼生长死亡与参数动态综合模式 总被引:9,自引:1,他引:9
根据我国近海带鱼分种研究结果,利用南海北部底拖网调查收集的带鱼属3鱼种的生物学资料,运用长度频率法估算了3鱼种的生长和死亡参数.带鱼、南海带鱼和短带鱼von Bertalanffy生长方程的渐近肛长分别为70.0,54.5和48.0 cm;生长系数分别为0.27,0.27和0.17;理论生长起点年龄分别为-0.60,-0.68和-1.10龄.用长度变换渔获曲线法估算的3鱼种总死亡系数分别为3.02,0.80和2.43;用经验公式估算的自然死亡系数分别为0.39,0.58和0.44;捕捞死亡系数分别为2.63,0.22和1.99.动态综合模式的分析结果表明,3鱼种都能承受较大的捕捞压力,资源利用的不合理之处是大量捕捞1龄以内的幼鱼;在最适利用状态下,带鱼、南海带鱼和短带鱼的开捕年龄分别应为3.0,2.0和2.7龄,对应的肛长分别为44,28和23 cm. 相似文献
67.
Estimating time-based instantaneous total mortality rate based on the age-structured abundance index 总被引:1,自引:0,他引:1
王迎宾 《中国海洋湖沼学报》2015,33(3):559-576
The instantaneous total mortality rate(Z) of a fish population is one of the important parameters in fisheries stock assessment. The estimation of Z is crucial to fish population dynamics analysis,abundance and catch forecast,and fisheries management. A catch curve-based method for estimating time-based Z and its change trend from catch per unit effort(CPUE) data of multiple cohorts is developed. Unlike the traditional catch-curve method,the method developed here does not need the assumption of constant Z throughout the time,but the Z values in n continuous years are assumed constant,and then the Z values in different n continuous years are estimated using the age-based CPUE data within these years. The results of the simulation analyses show that the trends of the estimated time-based Z are consistent with the trends of the true Z,and the estimated rates of change from this approach are close to the true change rates(the relative differences between the change rates of the estimated Z and the true Z are smaller than 10%). Variations of both Z and recruitment can affect the estimates of Z value and the trend of Z. The most appropriate value of n can be different given the effects of different factors. Therefore,the appropriate value of n for different fisheries should be determined through a simulation analysis as we demonstrated in this study. Further analyses suggested that selectivity and age estimation are also two factors that can affect the estimated Z values if there is error in either of them,but the estimated change rates of Z are still close to the true change rates. We also applied this approach to the Atlantic cod(G adus morhua) fishery of eastern Newfoundland and Labrador from 1983 to 1997,and obtained reasonable estimates of time-based Z. 相似文献
68.
Effect of salinity on survival,feeding behavior and growth of juvenile swimming crab P ortunus trituberculatus was investigated under 5 salinity levels of 5,10,20,30 and 40. The results show that the crab juveniles fed 2 or 3 times at the salinity 20 and 30,each lasted for about 25 minutes,for a total feeding time of 73.2±22.65 minutes per day. At these salinities,there were significantly higher in the frequency of feeding and in total feeding time than those at lower salinities of 5 and 10. All crab juveniles moulted when reared at a salinity of 20 during the 5 days duration of the experiment,which is significantly higher than those at other salinities. All juveniles survived at salinity 20,and the survivorship was not significantly different from that at 30,but was signif icantly higher than those at other salinities. The crab juveniles reared at a salinity of 20 had the highest value of food ration of 0.190 8±0.011 3 g/g BW,average body weight gain of 0.796±0.128 g,gain rate of 87%–96%,and food conversion ratio of 1.20±0.09. There was no significant difference in the values found between 20 and 30 but these values were significantly lower than that at the other salinities( P 0.05). Highest activities of digestive enzymes(Amylase,Protease,Lipase) and lowest activities of protective enzymes(SOD,PO,CAT) were also obtained on crab juveniles reared at salinity of 20. 相似文献
69.
Growth hiatuses in massive corals are usually indicative of past ecological or environmental stresses. Among 37 fossil Porites colonies surveyed from the reef flat of Dadonghai fringing reef at Sanya, Hainan Island, northern South China Sea, seven of them were found to show clear evidence of past mortality, representing a population of ~19%. Among these samples, two of them (SYO‐13 and SYO‐28) display clear growth hiatuses reflecting mortality followed by subsequent recruitment, and five others exhibit a well‐preserved mortality surface and no subsequent recruitment. The growth hiatuses were dated using high‐precision thermal ionisation mass spectrometry U‐series techniques. The age results suggest all the dated corals formed and died in the mid Holocene. Multiple dates below the growth hiatuses suggest that SYO‐13 and SYO‐28 died at 6298 ± 11 and 6929 ± 19 a BP (i.e. years before AD 1950), respectively. Multiple dates above the growth hiatuses indicate that growth in SYO‐13 and SYO‐28 resumed at 6257 ± 14 and 6898 ± 20 a BP, respectively. The calculated durations of growth hiatuses are therefore 41 ± 18 a for SYO‐13 and 31 ± 28 a for SYO‐28, respectively, implying growth resumed within decades after the mortality events. U‐series dating of four other samples with dead heads suggests that they died at 6035 ± 53, 6059 ± 23, 6127 ± 22 and 6474 ± 24 a BP, respectively. In addition, using solution inductively coupled plasma mass spectrometry (ICP‐MS), monthly resolution Sr/Ca and Mg/Ca ratios were determined for the annual growth bands below and above the growth hiatuses for three of the dated samples. The Sr/Ca and Mg/Ca profiles indicate that the three corals probably died in different seasons (from spring to autumn), and the mortality appears to be unrelated to anomalous sea surface temperature‐induced bleaching. Copyright © 2010 John Wiley & Sons, Ltd. 相似文献
70.
Gufu Oba Inger Nordal Nils C. Stenseth Jrn Stave Charlotte S. Bjor Josphat K. Muthondeki William K. A. Bii 《Journal of Arid Environments》2001,47(4):499
In the arid zone of central Turkana, north-western Kenya, where soil salinity affects 15–20% of the rangelands, growth performances of trees planted in saline soil rehabilitation trials have not been evaluated. Tree-planting trials have emphasised exotic species over indigenous ones. However, advantages and disadvantages of promoting exotic tree species have not been examined. The current study was aimed at evaluating growth performance of seven exotic and nine indigenous tree species used in saline soil rehabilitation trials. The tree species were established from 6-month-old saplings using microcatchments (FT1) from 1988 through 1990 and pitting treatment (FT2) from 1989 through 1992. The soils in FT1 and FT2 treatments were moderately to highly saline. The exotic tree species produced greater cover and volume during the first year (FT1) but by the second year, production was not sustained due to greater mortality (FT1 & FT2). The indigenous species in general had higher survival rates. Relative growth rates (RGR) of exotic and indigenous species did not differ (FT1 & FT2). Tree mortality was negatively correlated with RGR for exotic species in FT1 but not for indigenous ones. However, changes in plant performance were not in response to salinity alone. Rather, water scarcity superimposed on soil salinity might have influenced plant growth performance. Greater water and salinity stress and subsequently greater mortality in exotic species provided a more convincing reason for promotion of indigenous tree species. In the future, knowledge of salinity distribution and selection of indigenous species to match this will be a better way of rehabilitating sites affected by soil salinity in the arid zone of central Turkana, north-western Kenya. 相似文献