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51.
Growth, survival, and body composition were evaluated in two feeding trials using juvenile hybrid bluegill Lepomis cyanellus × L. macrochirus . In Experiment 1, hybrid bluegill (20 g) were stocked into 1.25-m3 cages at a rate of 300 fish/cage and fed diets containing 35, 40, 44, or 48% protein for 12 wk. Fish meal comprised 32% of the dietary protein in all diets. Fish were fed all they could consume in 40 min. No significant differences ( P > 0.05) in individual length, individual weight, specific growth rate (SGR), condition factor (K), and feed conversion ratio (FCR) were found among treatments and averaged 13.4 cm, 47.4 g, 1.02%/d, 1.96, and 4.06, respectively. Whole-body composition of hybrid bluegill indicated that fish fed a diet containing 35% protein had a significantly lower ( P < 0.05) percentage protein (56.3%) and a higher ( P < 0.05) percentage lipid (29.3%) compared to fish fed diets containing 40, 44, and 48% protein. In Experiment 2, 15 hybrid bluegill (15 g) were stocked into 110-L aquaria and fed one of four diets containing 28, 32, 36, or 38% protein for 10 wk. Fish were fed twice daily all they would consume in 20 min. Fish fed a diet containing 38% protein had higher ( P < 0.05) percentage weight gain (265%) than fish fed diets containing 28% (203%) and 32% (219%) protein, but were not significantly different ( P > 0.05) compared to fish fed a diet containing 36% protein (251%). Feed conversion ratio (FCR) of hybrid bluegill fed diets containing 36% and 38% protein (average 1.39) were significantly lower ( P < 0.05) than fish fed a diet with 28% protein (1.73). Results from these studies indicate that hybrid bluegill can be fed a practical diet containing 35–36% protein (with fish meal comprising 32% of the protein). Further refinement of the diet formulation may allow producers to reduce diet and production costs.  相似文献   
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In implantation trials carried out with Prosopis chilensis and Prosopis flexuosa, the following variables were considered: implantation time (December and March), implantation technique (direct seeding and seedling transplantation) and age of the seedlings at the time of transplantation (60, 105 and 150 days). Survival was evaluated for more than 9 months after implantation and trials were repeated in 3 consecutive years.

Results from both species were similar and they show that survival after transplantation was higher (60–80%) than from direct seeding (35–45%). Survival from transplantation was independent of the size and age of the seedlings and it was less affected by climatic conditions than direct field sowing. Survival from direct seeding was higher in March than in December. The best time for either implantation alternative would be the end of the summer or beginning of fall, when climatic conditions increase the probability of seedling survival.  相似文献   

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The T2*‐weighted gradient recalled echo sequence is a sensitive means to detect blood degradation products. While not a routine sequence in magnetic resonance imaging of the spine in small animals, it can provide additional valuable information in select cases. The goal of this retrospective, cross‐sectional study was to describe findings when acquiring this sequence during magnetic resonance imaging examination of the spine in small animals. The University of Tennessee's veterinary radiology database was searched for dogs and cats that underwent magnetic resonance imaging for suspect spinal disease in which a T2*‐weighted gradient recalled echo sequence was acquired and susceptibility artifact was identified. The following information was recorded: signalment, clinical signs, location and appearance of susceptibility artifact, and final diagnosis. Thirty‐nine cases were included in the study. Extradural susceptibility artifacts were observed in cases of intervertebral disc herniation with or without associated hemorrhage (n = 28), extradural hemorrhage associated with spinal trauma (n = 2), hemophilia (n = 1), and in a cystic extradural mass (n = 1). Remaining lesions displaying susceptibility artifact were intramedullary and included presumptive acute noncompressive nucleus pulposus extrusion (n = 2), hematoma (n = 1), hemangiosarcoma metastasis (n = 1), intramedullary disc extrusion (n = 1), presumptive meningomyelitis (n = 1), and a mass of undetermined etiology (n = 1). Inclusion of a T2*‐weighted gradient recalled echo sequence may be helpful in spinal magnetic resonance imaging when standard imaging sequences are ambiguous or intramedullary lesions are observed.  相似文献   
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A 13-year-old dog exhibited dramatic, radiographic osteopenia consistent with fibrous osteodystrophy secondary to primary hyperparathyroidism. Following parathyroidectomy, the dog developed severe, prolonged hypocalcemia, but was successfully treated and discharged 32 d after surgery. A variety of factors may have contributed to this dog’s hypocalcemia including hypoparathyroidism and hungry bone syndrome.  相似文献   
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The Standard for the Exchange of Nonclinical Data (SEND), adopted by the US FDA, is part of a set of regulations and guidances requiring the submission of standardized electronic study data for nonclinical and clinical data submissions. SEND is the nonclinical implementation of SDTM (Study Data Tabulation Model), the standard electronic format for clinical regulatory submissions to FDA. SEND, SDTM, and the associated Controlled Terminology have been developed by CDISC (Clinical Data Interchange Standards Consortium). In order to successfully implement SEND, interdisciplinary contributions between sponsors and CROs, need a model for task allocation. This is being undertaken by the Pharmaceutical Users Software Exchange (PhUSE). Because SEND is currently the preferred submission format of the US FDA only and will become required by it starting in December 2016, only American academic societies and companies are actively involved. An exception to this is the INHAND initiative, which leads the way in standardizing terminology for toxicological pathology. On the other hand, international globalization of other clinical and nonclinical practices is not feasible because there are substantial differences between the US and non-US countries in CRO involvement in drug development. Thus, non-US countries must consider and develop approaches to SEND that meet their needs. This paper summarizes the activities of the major organizations involved in SEND development and implementation, discusses the effective use of SEND, and details a compliance scheme (research material of the Showa University School of Medicine) illustrating how pharmaceutical companies can complete a large amount of work up to an FDA application with the effective utilization of CROs and solution providers.  相似文献   
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