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1.
Eighty-six Heterobasidion annosum isolates, mainly belonging to the F intersterility group and obtained from 32 different geographical localities in Italy, were subjected to genetic analysis by the Random Amplified Polymorphic DNA (RAPD) markers. The similarity between F and S groups was higher than that between F and P. In UPGMA Cluster Analysis, the F isolates originating from the same locality usually grouped in the same cluster. The isolates also showed a tendency to group at the level of larger geographical areas. Within the F group, isolates from the south of the Italian peninsula showed the highest genetic variation and northern isolates from the Alpine regions showed the lowest. This indicates a gradual cline along the peninsula. The genetic variability in the Italian F group is discussed in relation to the past and present distribution of the host species in Italy and Europe.  相似文献   
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Seven sea otters received a single subcutaneous dose of cefovecin at 8 mg/kg body weight. Plasma samples were collected at predetermined time points and assayed for total cefovecin concentrations using ultra‐performance liquid chromatography and tandem mass spectrometry. The mean (±SD) noncompartmental pharmacokinetic indices were as follows: CMax (obs) 70.6 ± 14.6 μg/mL, TMax (obs) 2.9 ± 1.5 h, elimination rate constant (kel) 0.017 ± 0.002/h, elimination half‐life (t1/2kel) 41.6 ± 4.7 h, area under the plasma concentration‐vs.‐time curve to last sample (AUClast) 3438.7 ± 437.7 h·μg/mL and AUC extrapolated to infinity (AUC0→∞) 3447.8 ± 439.0 h·μg/mL. The minimum inhibitory concentrations (MIC) for select isolates were determined and used to suggest possible dosing intervals of 10 days, 5 days, and 2.5 days for gram‐positive, gram‐negative, and Vibrio parahaemolyticus bacterial species, respectively. This study found a single subcutaneous dose of cefovecin sodium in sea otters to be clinically safe and a viable option for long‐acting antimicrobial therapy.  相似文献   
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An adult, wild-caught, female prairie falcon (Falco mexicanus) was presented with the chief complaint of anorexia. Radiographic findings included increased densities within the air sacs, and coelomic endoscopy revealed numerous slender worms within the air sacs and on the serosal surfaces of the ovary, oviduct, liver, proventriculus, and ventriculus. The bird seemed to improve for a short period of time with antiparasitic therapy (ivermectin and fenbendazole) and supportive care. Twenty-one days after initial presentation, the bird became recumbent with increasing pelvic limb neurologic deficits and was euthanized. On histopathologic examination, mature nematodes and larvated eggs identified as Serratospiculoides amaculata were found within the subdural space of the distal thoracolumbar and synsacral spinal cord and within the coelomic cavity. This case suggests that S. amaculata can cause clinically significant lesions in its falconiform host with potentially fatal results.  相似文献   
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Diagnosis of avian mycobacteriosis, caused by Mycobacterium genavense or species belonging to the Mycobacterium avium complex (MAC), is problematic. Polymerase chain reaction (PCR) offers rapid and sensitive detection of minute quantities of DNA, and conventional protocols have been used for evaluating avian specimens. The recent development of real-time PCR offers several advantages over conventional PCR. In attempts to improve diagnosing avian mycobacteriosis, a real-time TaqMan PCR assay was developed targeting the 65-kD heat shock protein gene of M. genavense and MAC spp. Nineteen reference isolates, 16 clinical isolates, and 32 avian tissue samples were used to evaluate the assay. When sufficient amplicons were produced, the species of mycobacteria was determined by standard sequencing of TaqMan PCR products and compared with results from commercial mycobacteriology laboratories and/or standard sequencing of conventional PCR products. The TaqMan PCR detected DNA from reference isolates of M. genavense, MAC spp., and Mycobacterium tuberculosis complex spp. Of the clinical isolates, the TaqMan PCR detected DNA from 10 of 12 Mycobacterium avium avium isolates and two of three Mycobacterium avium intracellulare isolates. For the tissue samples, the TaqMan PCR amplified DNA in six of nine samples that were identified by sequencing of conventional PCR products and/or by commercial mycobacteriology laboratories as being MAC spp. positive and three of four samples that were positive for M. genavense. There was some disagreement between speciation results from the TaqMan PCR and those from commercial mycobacteriology laboratories or conventional PCR or both. This disagreement was suspected to be because of relatively small numbers of base pairs in the TaqMan PCR products. The TaqMan PCR may provide a useful tool for evaluating clinical samples for DNA from mycobacteria species that most commonly infect birds; however, further refinement is needed in order to improve sensitivity and provide more accurate speciation.  相似文献   
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美国截叶胡枝子的硬实率很高,发芽率只有17.3%.经过种子预处理,如采用不同温度下浸种、98%浓硫酸浸泡、机械破皮和机械破皮结合热水浸种等处理,结果表明,机械破皮后用60℃热水浸种处理的效果最好,发芽势和发芽率分别达到64.0%和74.3%;其次是机械破皮,平均发芽率达到50%;浓硫酸浸种可以显著提高种子发芽势,浓硫酸浸种5min效果最好,发芽率达到44.7%;热水浸种的处理效果不佳,最好的90℃热水浸种处理发芽率也仅有26.7%.  相似文献   
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不同处理方法对美国截叶胡枝子种子发芽的影响   总被引:1,自引:0,他引:1  
截叶胡枝子(Lespedezacunecta)是原产于亚洲东部的一种多年生的豆科植物,在我国南方地区野生分布很广。它具有耐瘠、耐旱、耐酸、耐热、固土能力强、适应性广等特性,在国外也颇受重视。我国于1983年从美国引种,通过对其生物学和生态学特性、经济性状和栽培技术研究证明,引进的美国截叶胡枝子在人工栽培条件下,表现出良好的经济性状,是南方草地改良的希望种子。但是在生产中,由于其硬实的存在,使得种子的发芽率很低,往往造成出苗困难和草地建植缓慢,甚至出现严重缺苗断垄的现象,直接影响田间产量,限制了它的进一步推广应用。试验采用不同处…  相似文献   
9.
不同处理方法对美国截叶胡枝子种子发芽的影响   总被引:2,自引:0,他引:2  
美国截叶胡枝子的硬实率很高,发芽率只有17.3%。经过种子预处理,如采用不同温度下浸种、98%浓硫酸浸泡、机械破皮和机械破皮结合热水浸种等处理,结果表明,机械破皮后用60℃热水浸种处理的效果最好,发芽势和发芽率分别达到64.0%和74.3%;其次是机械破皮,平均发芽率达到50%;浓硫酸浸种可以显著提高种子发芽势,浓硫酸浸种5min效果最好,发芽率达到44.7%;热水浸种的处理效果不佳,最好的90℃热水浸种处理发芽率也仅有26.7%。  相似文献   
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