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91.
为明确猕猴桃果园的生产潜力,在普查的基础上对两个管理水平较高的徐香猕猴桃果园的树体结构及土壤养分状况进行分析。结果表明,高产型徐香猕猴桃树体的合理结构为成龄树冬季修剪后单株保留17个左右结果母枝,每枝保留15~21个有效芽,折合每667 m留长枝量为1 496个,留芽量为22 440~23 760个,7月份叶果比为3.33∶1。土壤速效氮为16.5 mg/kg,速效磷64.8 mg/kg,速效钾209.6 mg/kg,速效镁和速效铁分别156.6 mg/kg和3.58 mg/kg,有机质含量1.13%。可见,充足的肥料投入、枝芽数量及合理的叶果比是高产稳产的基本保证。 相似文献
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采用丙酮震荡提取样品,在水解衍生的步骤中创造性地使用试管加入吡啶盐酸盐,于220℃的烘箱里水解1.5 h,经过处理后使用气相色谱ECD进行测定。结果表明:该方法的线性范围为0.005~0.500 ng,相关系数为0.999 9;对香蕉、绿橙、花牛苹果、青苹果、猕猴桃、砀山梨6种空白基质分别进行了0.01、0.10、1.00 mg/kg 3个水平加标,其回收率为81.0%~106.4%,相对标准偏差(RSD,n=5)为0.3%~5.7%;该方法的最低检出限为0.01 mg/kg,并且烘箱水解的新方法操作简便 相似文献
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Epidemiology and control of Menangle virus in pigs 总被引:6,自引:0,他引:6
Kirkland PD Love RJ Philbey AW Ross AD Davis RJ Hart KG 《Australian veterinary journal》2001,79(3):199-206
OBJECTIVE: To describe the epidemiology and eradication of Menangle virus infection in pigs. DESIGN: Field observations and interventions, structured and unstructured serological surveys, prospective and cross-sectional serological studies and laboratory investigations. PROCEDURE: Serum samples were collected from pigs at a 2600-sow intensive piggery in New South Wales that experienced an outbreak of reproductive disease in 1997. Serum samples were also collected from piggeries that received pigs from or supplied pigs to the affected piggery and from other piggeries in Australia. Serum and tissue samples were collected from pigs at piggeries experiencing reproductive disease in New South Wales. Sera and faeces were collected from grey-headed flying foxes (Pteropus poliocephalus) in the region of the affected piggery. Serum samples were tested for neutralising antibodies against Menangle virus. Virus isolation was attempted from faeces. RESULTS: Following the outbreak of reproductive disease, sera from 96% of adult pigs at the affected piggery, including sows that produced affected litters, contained neutralising antibodies against Menangle virus. Neutralising antibodies were also detected in sera from 88% of finisher pigs at two piggeries receiving weaned pigs from the affected piggery. No evidence of Menangle virus infection was found in other piggeries in Australia. In cross-sectional studies at the affected piggery, colostral antibodies were undetectable in most pigs by 14 to 15 weeks of age. By slaughter age or entry to the breeding herd, 95% of pigs developed high antibody titres (> or = 128) against Menangle virus in the virus neutralisation test. Menangle virus was eradicated from the affected piggery following a program of serological testing and segregation. Neutralising antibodies against Menangle virus were also detected in P poliocephalus from two colonies in the vicinity of the affected piggery. Two piggery workers were infected with Menangle virus. There was no evidence of infection in cattle, sheep, birds, rodents, feral cats and a dog at the affected piggery. CONCLUSIONS: Serological evidence of infection with Menangle virus was detected in pigs at a piggery that had experienced reproductive disease, in pigs at two associated piggeries and in fruit bats in the region of the piggery. Two humans were infected. The mode of transmission between pigs is unknown, but spread by faecal or urinary excretion is postulated. This virus can be eradicated by the segregation of pigs into discrete age groups. 相似文献
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97.
Thomas Thomidis 《Phytoparasitica》2001,29(1):47-49
The relative virulence ofPhytophthora cactorum andP. syringae originating from almond trees, and ofP. citrophthora originating from citrus, to apple, pear, peach, cherry and plum rootstocks, was studiedin vivo andin vitro. Results of the different experiments were in good agreement. All testedPhytophthora isolates showed little virulence to pear rootstocks-causing only minor crown rot symptoms - and no virulence at all to apple
rootstocks. In contrast, they were highly virulent to stone fruit rootstocks, causing crown rot disease. The non-pathogenicity
of these isolates to pome rootstocks could be interpreted as strict host specificity. 相似文献
98.
A technique for rearing the progeny of wildCeratitis capitata flies was developed. The method is based on wild captured flies which are allowed to oviposit in artificial fruit containing
larval rearing medium. Flies develop in the fruit from eggs to last larval instar, then exit the fruit and pupate within vermiculite.
This method was shown to be feasible and efficient, and to increase considerably the number of wild flies for testing purposes.
Possible contribution to the Sterile Insect Technique (SIT) and potential applications of the method are discussed. 相似文献
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100.