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1.
Fasciolosis is an endemic zoonotic parasitic disease with significant impacts on human health and both animal health and production. Early post-infection impacts on the host remain unclear. The objective of this study was to determine the changes, if any, to levels of endotoxin in cattle plasma in response to early-stage infection with Fasciola hepatica. Thirty-six (36) commercial bred cattle were experimentally infected with approximately 400 viable metacercariae. Plasma lipopolysaccharide (endotoxin) levels were examined on 24 occasions from 0 h before infection to 336 h after infection using the Limulus Amoebocyte Lysate chromogenic end point assay and compared with that of six (6) uninfected control animals. Peak lipopolysaccharide levels in infected animals were reached at 52 h after infection and returned to pre-infection levels at time 144 h after infection. Infected animals had significantly elevated lipopolysaccharide levels between 24 and 120 h after infection when compared to uninfected animals. The mean change in endotoxin units (EU)/mL over time after infection was statistically significant in infected animals. Elevations of lipopolysaccharide occurred in all infected animals suggesting a possible repeatable and titratable endotoxemia conducive to therapeutic agent model development. 相似文献
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Purification and characterization of a β–glucan binding protein from the haemolymph of freshwater prawn Macrobrachium rosenbergii 下载免费PDF全文
Jyotirmaya Mohanty Pramoda Kumar Sahoo Bindu R. Pillai Swagatika Mohanty Sushil Kumar Garnayak Shailesh Kumar 《Aquaculture Research》2015,46(1):95-104
β‐glucan binding protein (βGBP), a pattern recognition protein was purified from the haemolymph of freshwater prawn Macrobrachium rosenbergii by heparin affinity chromatography that showed a single band in native gradient PAGE. The β‐glucan binding property of the purified protein was confirmed in a phenoloxidase (PO) assay, where addition of βGBP along with β‐glucan increased the specific PO activity compared with that of β‐glucan alone. The molecular weight of the βGBP was found to be ~316 kDa on gel filtration chromatography. In SDS‐PAGE, βGBP molecule was reduced to one polypeptide chain of molecular weight ~113 kDa. Thus the βGBP in M. rosenbergii is possibly a homotrimeric molecule. The purified sample run on unreduced condition in SDS‐PAGE also revealed a similar size band (~113 kDa) and hence, the polypeptide chains of βGBP are held by non‐covalent interactions. The purified βGBP samples run in native PAGE was stained positively with alcian blue for carbohydrates and Sudan black for lipids indicating the βGBP to be a glycolipoprotein. With rabbit polyclonal anti‐βGBP serum developed, an indirect ELISA was standardized and the normal βGBP concentration in adult M. rosenbergii serum was quantified to be ~2 mg mL?1. Furthermore, the applicability of the developed ELISA is discussed. 相似文献
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Persistence and binding capacity of [14C]p, p′-DDT and [14C]y-HCH were studied for one year in a sandy loam soil of Delhi, India, after surface treatment during monsoon, winter and summer seasons under field conditions. Both DDT and HCH dissipated more rapidly under the Indian subtropical climate than reported for temperate regions. In all three seasons, both insecticides dissipated most rapidly during the initial 60 days. However, in the final six months there was very little change in the residue levels. After one year, the final soil burden of DDT varied from 33 to 36% and of HCH from 14 to 15% of the initial concentrations in the different experiments. HCH bound more with the soil as, out of the total residues present after one year, more than 75% of HCH was in bound form compared with only 24% of DDT. The observed time for 50% initial dissipation of DDT ranged from 60 to 120 days, while in the case of HCH it varied from 30 to 45 days. However, the rate of loss of residues which persisted for more than 6 months was equivalent to a half-life of between 500 and 10000 days for DDT, and between 700 and 2000 days for HCH, thus illustrating the very long persistence of aged residues. Since degradation of both insecticides was apparently minimal, the data indicate that dissipation of DDT and HCH was largely due to volatilisation. 相似文献
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C. HAMBLIN JS SALT SD GRAHAM K. HOPWOOD AM WADE-EVANS 《Australian veterinary journal》1998,76(9):622-629
Objective To study the clinical signs following bluetongue virus serotypes 1 and 3 infection in Poll Dorset sheep.
Design A clinical and pathological study.
Procedure Twenty Poll Dorset sheep were inoculated with bluetongue virus serotypes 1 or 3, each inoculum having a different passage history. The sheep were examined daily and their clinical appearance and rectal temperatures recorded. Heparinised and non-heparinised blood samples were taken at intervals for virological and serological study. Gross pathological findings were recorded for several sheep at necropsy and tissue samples were collected from three sheep for virological studies.
Results All inoculated sheep developed clinical disease. The clinical signs and gross pathological changes varied considerably but were consistent with damage to the vascular endothelial system. There was a decline in the titres of infectious bluetongue virus and of antigen in tissues collected between 7 and 12 days after infection.
Conclusions The severity of disease was related to the speed of onset and duration of pyrexia and not the development or titre of viraemia. Generally, those animals with sensitive mouths, depression, coronitis, recumbency and reluctance to move were the most debilitated. Whole blood was the most reliable source of infectious virus from acutely and chronically infected and convalescent animals. However, tissue samples particularly spleen, collected from dead or killed animals suffering from either peracute or acute forms of disease were most appropriate for the rapid confirmation of a clinical diagnosis. 相似文献
Design A clinical and pathological study.
Procedure Twenty Poll Dorset sheep were inoculated with bluetongue virus serotypes 1 or 3, each inoculum having a different passage history. The sheep were examined daily and their clinical appearance and rectal temperatures recorded. Heparinised and non-heparinised blood samples were taken at intervals for virological and serological study. Gross pathological findings were recorded for several sheep at necropsy and tissue samples were collected from three sheep for virological studies.
Results All inoculated sheep developed clinical disease. The clinical signs and gross pathological changes varied considerably but were consistent with damage to the vascular endothelial system. There was a decline in the titres of infectious bluetongue virus and of antigen in tissues collected between 7 and 12 days after infection.
Conclusions The severity of disease was related to the speed of onset and duration of pyrexia and not the development or titre of viraemia. Generally, those animals with sensitive mouths, depression, coronitis, recumbency and reluctance to move were the most debilitated. Whole blood was the most reliable source of infectious virus from acutely and chronically infected and convalescent animals. However, tissue samples particularly spleen, collected from dead or killed animals suffering from either peracute or acute forms of disease were most appropriate for the rapid confirmation of a clinical diagnosis. 相似文献
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Objective Validation of a stimulation test for determining the steroidogenic capacity of the parrot testis. The major aim was to characterise testosterone secretion after injection of a gonadotropin-releasing hormone agonist (GnRHa), then use the test to investigate seasonal reproduction in the male cockatiel.
Procedure A synthetic GnRHa (buserelin; 8.0 µg of peptide/kg bodyweight) was injected IM into male cockatiels (n = 7) and sulphur-crested cockatoos (n = 3) and serial blood samples collected at 0, 30, 60, 90 and 120 min after administration. Once validated, the technique was subsequently used to examine seasonal changes (23 months) in the testosterone profile of a captive cockatiel population.
Results Injection of buserelin resulted in a significant increase in the testosterone concentration of cockatiel plasma, with maximal concentrations occurring at approximately 60 (1.33 ± 0.08 ng/mL) to 90 min (1.22 ± 0.08 ng/mL) after injection. Although no clear pattern of seasonal variation in testosterone secretion was detected in cockatiel plasma, samples taken 60 and 90 min after administration showed a significant increase in all seasons. Injection of buserelin in the sulphur-crested cockatoo also resulted in increased testosterone secretion, with maximal concentrations obtained after 90 min.
Conclusion Buserelin can be used to obtain a reliable index of the prevailing testosterone capacity of the cockatiel and cockatoo testis. With further studies, this test may be incorporated into clinical assessment of reproductive status. 相似文献
Procedure A synthetic GnRHa (buserelin; 8.0 µg of peptide/kg bodyweight) was injected IM into male cockatiels (n = 7) and sulphur-crested cockatoos (n = 3) and serial blood samples collected at 0, 30, 60, 90 and 120 min after administration. Once validated, the technique was subsequently used to examine seasonal changes (23 months) in the testosterone profile of a captive cockatiel population.
Results Injection of buserelin resulted in a significant increase in the testosterone concentration of cockatiel plasma, with maximal concentrations occurring at approximately 60 (1.33 ± 0.08 ng/mL) to 90 min (1.22 ± 0.08 ng/mL) after injection. Although no clear pattern of seasonal variation in testosterone secretion was detected in cockatiel plasma, samples taken 60 and 90 min after administration showed a significant increase in all seasons. Injection of buserelin in the sulphur-crested cockatoo also resulted in increased testosterone secretion, with maximal concentrations obtained after 90 min.
Conclusion Buserelin can be used to obtain a reliable index of the prevailing testosterone capacity of the cockatiel and cockatoo testis. With further studies, this test may be incorporated into clinical assessment of reproductive status. 相似文献
8.
Agarwal H. C. Mittal P. K. Menon K. B. Pillai M. K. K. 《Water, air, and soil pollution》1986,31(1-2):89-94
Water, Air, &; Soil Pollution - DDT residues in water, bottom sediments and certain non-target organisms from four different sites of the river Jamuna in Delhi were monitored periodically from... 相似文献
9.
The extensive zero-water exchange shrimp farming system in the periphery of Chilka lagoon (Orissa, India) was studied. The study aimed to describe this unique farming system with special reference to dynamics of macrozoobenthos, production characteristics and economics. The study conducted was based on a general survey as well as monitoring of five individual farms over a complete production cycle. The farming practice in this area is characterized by complete absence of water exchange during rearing. Ponds in this area are generally shallow (mean 72 cm). Most of the water and soil quality characteristics of these farms are within acceptable levels. Macrozoobenthos belonging to 12 taxa were collected, amphipods (81%) and polychaetes (13%) being most numerous. Overall macrobenthic density of farms studied varied from 968 to 11,470 individuals/m2 with a gross mean of 5644 individuals/m2. There was no general pattern to the variation in abundance of various taxa in different phases of the rearing cycle, suggesting a low predatory pressure by shrimp in the farms studied. Shrimp production was highly variable (91–250 kg/ha), but generally low with a mean of 145 kg/ha. The net income of these farms was estimated to be Rs. 63,250 per crop per ha. Compared with shrimp farming system with regular water exchange in the same area, Chilka farms generated high benefit-cost ratio indicating high profitability and sustainability. 相似文献
10.
The pH change in 40 ml of buffer caused by 20 g dry soil may be multiplied by 5600 to provide the lime requirement of mud in a fish pond. The buffer contains 10 g p-nitrophenol, 7.5 g boric acid, 37 g potassium chloride, and 5.25 g potassium hydroxide dissolved and diluted to 1000 ml with distilled water; the buffer pH is adjusted to 8.00. 相似文献