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71.
72.
Abstract

AIM: To determine the effects of Cu and levamisole on concentrations of Cu and Fe in plasma and liver, and the effects of levamisole on lipid peroxidation induced by Cu intoxication in broiler chickens.

METHODS: In a 2×4 factorial study, 80 one-day-old Ross PM3 broiler chicks were fed diets for 21 days containing either 8 mg/kg Cu (Low Cu) or 250 mg/kg Cu (High Cu) and were treated with 0 (L0), 4 (L4), 8 (L8) or 16 (L16) mg/kg bodyweight levamisole per day from Day 7 of the study, on three consecutive days in their drinking water. This treatment was repeated three times, at 3-day intervals. On Day 21, blood samples were collected from each bird for analysis of concentrations of Cu, Fe and malondialdehyde, and activities of aspartate aminotransferase (AST), alanine aminotransferase (ALT), superoxide dismutase, catalase and glutathione peroxidase (GSH-Px). The birds were killed and liver samples collected for analysis of Cu and Fe.

RESULTS: Mean concentrations of Cu and Fe in plasma, and Cu in liver, were increased overall in the High Cu groups compared with the Low Cu groups (p<0.001). Compared with the L0 treatment group on the High Cu diet, treatments L4, L8 and L16 decreased concentrations of Cu in plasma, and L8 and L16 increased concentration of Cu in liver (p<0.05). Mean activities of AST and ALT were increased in untreated birds (L0) fed the High compared with Low Cu diets (p<0.01). In birds receiving the High Cu diet, treatments L4 and L8 decreased activities of AST, and L4 and L16 decreased activity of ALT, compared with L0 (p<0.05). The High Cu diet induced an oxidative stress characterised by increased mean concentrations of malondialdehyde and decreased activities of superoxide dismutase, catalase and GSH-Px (p<0.001). Concentration of malondialdehyde, and activities of superoxide dismutase and catalase were not changed following levamisole treatment in birds on the High Cu diet, and activity of GSH-Px was decreased by the L4 and L8 treatments compared with the L0 group.

CONCLUSIONS AND CLINICAL RELEVANCE: The results of the study suggest that treatment with levamisole might alleviate the harmful effects of Cu on the liver, as demonstrated by decreased activities of AST and ALT induced by a diet containing 250 mg/kg Cu.  相似文献   
73.
74.

Purpose

Various soil conditioners, such as biochar (BC) and anionic polyacrylamide (PAM), improve soil fertility and susceptibility to erosion, and may alter microbial accessibility and decomposition of soil organic matter (SOM) and plant residues. To date, no attempts have been made to study the effects of BC in combination with PAM on the decomposition of soil SOM and plant residues. The objective of this study was to evaluate the effects of BC, PAM, and their combination on the decomposition of SOM and alfalfa residues.

Materials and methods

An 80-day incubation experiment was carried out to investigate the effects of oak wood biochar (BC; 10 Mg ha?1), PAM (80 kg ha?1), and their combination (BC?+?PAM) on decomposition of SOM and 14C-labeled alfalfa (Medicago sativa L.) residues by measuring CO2 efflux, microbial biomass, and specific respiration activity.

Results and discussion

No conditioner exerted a significant effect on SOM decomposition over the 80 days of incubation. PAM increased cumulative CO2 efflux at 55–80 days of incubation on average of 6.7 % compared to the soil with plant residue. This was confirmed by the increased MBN and MB14C at 80 days of incubation in PAM-treated soil with plant residue compared to the control. In contrast, BC and BC?+?PAM decreased plant residue decomposition compared to that in PAM-treated soil and the respective control soil during the 80 days. BC and BC?+?PAM decreased MBC in soil at 2 days of incubation indicated that BC suppressed soil microorganisms and, therefore, decreased the decomposition of plant residue.

Conclusions

The addition of oak wood BC alone or in combination with PAM to soil decreased the decomposition of plant residue.
  相似文献   
75.
SUMMARY: Free radical oxidation products, namely conjugated dienes, ultraviolet fluorescence (excitation 325 nm, emission 395 nm) and visible fluorescence (excitation 360 nm, emission 460 nm) were measured in equine synovial fluid exposed to free radicals In vitro and in the plasma and synovial fluids of horses with synovial effusions. The synovial effusions were induced by intra-articularly administered carrageenin (0.3 ml, 1%), which rarely resulted in clinical lameness. The free radicals were generated In vitro by mixtures of iron and ethylene diamine tetra acetate (Fe/EDTA) or mixtures of hypoxanthine and xanthine oxidase (HX/XO). The conjugated diene concentrations and intensity of ultraviolet fluorescence were negligible in plasma and synovial fluid specimens. No increase resulted from incubation of synovial fluids with either a free radical generating system or as a result of the induced inflammation. The intensity of visible fluorescence did not increase in specimens incubated with Fe/EDTA. However, the intensity of visible fluorescence increased in specimens incubated with HX/XO, in synovial effusions induced by carrageenin, in plasma and in synovial fluids aspirated from saline injected controls. The results indicate that the intensity of visible fluorescence of equine synovial fluid increases after exposure to free radicals and during synovitis in the horse, suggesting a possible role for free radicals in the pathogenesis of equine inflammatory joint diseas  相似文献   
76.
A study of phosfolan deposited from sprays indicated that most of it is degraded within a week in the presence of light and air. It disappears more rapidly on cotton leaves than on glass because much of it migrates into the leaf interior within 7 h of application. Degradation within the leaf proceeds more slowly than on the leaf surface or on glass.  相似文献   
77.
The performance of six groups of six calves each from a previous field experiment was followed from the beginning of housing until turning out seven months later. When housed the groups harboured different levels of infection with Ostertagia ostertagi and had corresponding weight and gain reductions. The most heavily infected groups improved rapidly following housing. Elevated serum pepsinogen levels decreased markedly, and approached normal values at eight weeks. Differences in serum pepsinogen levels between groups diminished considerably, but remained significant over the entire stabling period. The serum albumin level was low in the most seriously affected animals at the time of housing, but normal levels were restored within the first twelve weeks. In general, the number of parasite eggs in the faeces of the animals decreased, but there was considerable fluctuation. Apart from a single sampling date, no significant difference in egg per gram (EPG) could be demonstrated between the experimental groups during the stabling period.The calves were fed according to their age. The live weight differences between most and least affected groups diminished from 64 kg at the time of housing to 37 kg at the end of the stabling period. The reduction took place particularly during the first four weeks of housing.Considering both the grazing and stabling periods, it appeared that anthelmintic treatment twice during the period had no effect on the final live weight, whereas remeated treatments at three-week intervals resulted in an increase of 24 kg. Similarly, moving the animals to a clean pasture in mid-July resulted in an increase of 39 kg at the end of the stabling period when compared to calves which were not moved. Treatment of moved animals did not result in further body weight gain after seven months of housing.No significant correlation was found between parasite EPG of faeces and growth rate during the stabling period. However, a positive correlation was found between serum pepsinogen during the first eight weeks of housing and the weight gain over the entire stabling period. This was in contrast to the correlation experienced during the grazing period.  相似文献   
78.
The study was conducted to evaluate the effects of α ‐linolenic acid (ALA) on frozen–thawed quality and fatty acid composition of bull sperm. For that, twenty‐four ejaculates obtained from three bulls were diluted in a Tris extender containing 0 (control), 3, 5, 10 and 15 ng/ml of ALA. Extended semen was incubated at 37°C for 15 min, to allow absorption of ALA by sperm cell membrane. The sample was chilled for 2 h, packed into 0.25‐ml straws and frozen in liquid nitrogen for 24 h. Subsequently, straws were thawed and evaluated for total sperm motility (computer‐assisted semen analysis), membrane functional integrity (hypo‐osmotic swelling test), viability (eosin‐nigrosin), fatty acid composition (gas chromatography) and lipid peroxidation (thiobarbituric acid‐reactive substances (TBARS)). A higher (p < 0.05) percentage of total sperm motility was observed in ALA groups 5 ng/ml (47.74 ± 07) and 10 ng/ml (44.90 ± 0.7) in comparison with control (34.53 ± 3.0), 3 ng/ml (34.40 ± 2.6) and 15 ng/ml (34.60 ± 2.9). Still, the 5 ng/ml ALA group presented a higher (p < 0.05) percentage of viable sperms (74.13 ± 0.8) and sperms with intact membrane (74.46 ± 09) than all other experimental groups. ALA concentration and lipid peroxidation in post‐thawed sperm was higher in all treated groups when compared to the control group. As such, the addition of 5 ng/ml of ALA to Tris extender improved quality of frozen–thawed bull spermatozoa.  相似文献   
79.
80.
The aim of this was to investigate the histology and immunohistochemistry of interstitial glands during non‐breeding season in camel ovaries. A total of 21 mature, non‐pregnant and apparently healthy camels aged between 8 and 12 years were slaughtered. The ovaries were removed within 15 min, cleaned from adipose tissue, weighted and examined grossly. The histological preparation was made, and then, the blocks were cut at 3–5 microns thickness and stained by H&E for histological examinations. Moreover, some sections were stained with Sudan Black for lipid detection. Immunohistochemical analysis of paraffin‐embedded ovarian tissues was performed to detect the localization of S‐100, vimentin, progesterone receptors (PR) and oestrogen receptors (ER). Immunoreactive signals were detected using UltraVision Detection System. The results revealed that the interstitial glands were located in the cortical region and they were arranged in various arrangements either single, in couple or in groups rich in lipid droplet. All interstitial gland arrangements were enclosed by connective tissue capsules containing fibroblasts and collagenous fibres separated them from the surrounding ovarian structures. Both interstitial glands and their surrounding CT were penetrated by several blood vessels. There was a strong immunoreactive signal for S‐100 in the nuclei of interstitial cells, and no signals were detected either in cells of the interstitial glands or their connective tissue with PR. We could conclude that the interstitial gland is distinct in ovary of camel and further studies are needed to elucidate its rule in steroid synthesis.  相似文献   
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