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101.
PD JELINEK T ELLIS RH WROTH SS SUTHERLAND HG MASTERS DS PETTERSON 《Australian veterinary journal》1988,65(7):214-217
SUMMARY: Immunity in 12 weaner Merino sheep fed a low selenium (Se) diet (low Se sheep) was compared with that in 10 matching sheep fed the same diet but each given an intraruminal Se pellet (high Se sheep), while the sheep were housed in individual, sheltered pens. All sheep were challenged with killed Brucella abortus cells (days 0 and 28), rabbit red blood cells (days 0, 7 and 28) and corynebaclerium pseudotuberculosis toxoid (days 0 and 28), and serum antibody titres were measured weekly for 8 weeks from day 0. The sheep were then experimentally infected with Haemonchus conforfus, and slaughtered 8 weeks later. The mean antibody titre to B. abortus, measured by 4 different tests, was significantly higher in the high Se sheep on occasions during the primary immune response phase (Rose Bengal test - day 21 (p < 0.05), day 28 (p < 0.025); complement fixation - day 7 (p < 0.05); enzyme-llnked immunosorbent assay - day 14 (p < 0.01); serum agglutination - no differences), but not during the secondary phase. The mean antibody titre to rabbit red blood cells, measured by haemagglutination test, was marginally higher in the high Se sheep on day 49 (p = 0.049). The mean antibody titre to C. pseudotuberculois, measured by enzyme-linked immunosorbent assay, was not significantly different between the groups at any time during the trial. In addition, the mean invitro responsiveness of peripheral blood lymphocytes to stimulation with phytohaemagglutinin in the high Se sheep was significantly greater than that in 10 sheep from the low Se group on day 22 (p < 0.01), but not day 50. However, there were no significant differences in the mean number of sheep in which the infection with H. contortus established, time to first shedding of eggs in faeces, abomasal worm burdens at necropsy, or inflammatory response in the abomasal mucosa in the sheep in each group. The results showed that the low Se sheep produced strong overall immune responses that were largely comparable to those in the high Se sheep. 相似文献
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104.
Gustavo Henrique Merten Paul D. Capel Jean P. G. Minella 《Journal of Soils and Sediments》2014,14(7):1235-1241
Purpose
Optical turbidity sensors have been successfully used to determine suspended sediment flux in rivers, assuming the relation between the turbidity signal and suspended sediment concentration (SSC) has been appropriately calibrated. Sediment size, shape and colour affect turbidity and are important to incorporate into the calibration process.Materials and methods
This study evaluates the effect of SSC and particle size (i.e. medium sand, fine sand, very fine sand, and fines (silt + clay)) on the sensitivity of the turbidity signal. Three different turbidity sensors were used, with photo detectors positioned at 90 and 180 degrees relative to the axis of incident light. Five different sediment ratios of sand:fines (0:100, 25:75, 50:50, 75:25 and 100:0) were also evaluated for a single SSC (1000 mg l-1).Results and discussion
The photo detectors positioned at 90 degrees were more sensitive than sensor positioned at 180 degrees in reading a wide variety of grain size particles. On average for the three turbidity sensors, the sensitivity for fines were 170, 40, and 4 times greater than sensitivities for medium sand, fine sand, and very fine sand, respectively. For an SSC of 1000 mg l-1 with the treatments composed of different proportions of sand and fines, the presence of sand in the mixture linearly reduced the turbidity signal.Conclusions
The results indicate that calibration of the turbidity signal should be carried out in situ and that the attenuation of the turbidity signal due to sand can be corrected, as long as the proportion of sand in the SSC can be estimated. 相似文献105.
María F Martín PD PhD María S Carrasco MD PhD Jesús Usón-Gargallo DVM PhD Juan R Lima DVM Luis J Ezquerra DVM PhD 《Veterinary anaesthesia and analgesia》2001,28(3):132-139
Objective To compare the magnitude and duration of the peri‐operative haematological, endocrine and metabolic effects of surgery performed under sevoflurane anaesthesia. Study Design Prospective randomized study. Animals Ten, 55‐day‐old lambs of both sexes, mean weight 20.8 ± 0.3 kg (range 18.5–23.6 kg). Methods Animals were randomly allocated to two equal groups. All were anaesthetized with sevoflurane for 3 hours. Surgery (end‐to‐end anastomosis of the right carotid artery and right jugular vein) was performed in animals of Group 1 only. The electrocardiogram, pulse oximetry, cardiac output and noninvasive arterial blood pressure (NIBP) were monitored. Venous blood samples (5 mL) were taken 30 minutes before induction of anaesthesia (T = 0) and 1 (T1), 24 (T2), 48 hours (T3) and 7 days (T4) after anaesthesia in order to measure plasma cortisol, ACTH, insulin, cyclic adenosine monophosphate (cAMP), glucose, protein concentrations and haematological variables. Results Sevoflurane decreased NIBP (minimum mean value: 64 ± 3 mm Hg) in both groups. Plasma cortisol and ACTH concentration increased in Group 1 (maximum mean values: cortisol: 136.2 nmol L?1, ACTH: 54.5 pmol L?1) and Group 2 (maximum mean values: cortisol: 128.7 nmol L?1, ACTH: 44.0 pmol L?1). Cyclic AMP increased only in Group 1 (9.3 nmol) 1 hour after anaesthesia. Neutrophilia, lymphopaenia and a decreased PCV were observed in both groups 1 hour after anaesthesia. Plasma protein and glucose concentrations did not change. Conclusions Increased ACTH and cortisol concentrations recorded 1 hour after anaesthesia suggest that sevoflurane induces a stress response in lambs. Clinical relevance The study did not identify the mechanism by which sevoflurane induces a stress response although hypotension is implicated. 相似文献
106.
Yves PS Moens DVM PD PhD Diplomate ECVAA Peter Gootjes† Ing Jean-Claude Ionita‡ DVM Erkki Heinonen§ Lic Tech PhD & Urs Schatzmann‡ DVM PhD Diplomate ECVAA 《Veterinary anaesthesia and analgesia》2009,36(3):209-219
Objective To remodel and validate commercially available monitors and their Pitot tube-based flow sensors for use in large animals, using in vitro techniques.
Study design Prospective, in vitro experiment.
Methods Both the original and the remodelled sensor were studied with a reference flow generator. Measurements were taken of the static flow-pressure relationship and linearity of the flow signal. Sensor airway resistance was calculated. Following recalibration of the host monitor, volumes ranging from 1 to 7 L were generated by a calibration syringe, and bias and precision of spirometric volume was determined. Where manual recalibration was not available, a conversion factor for volume measurement was determined. The influence of gas composition mixture and peak flow on the conversion factor was studied.
Results Both the original and the remodelled sensor showed similar static flow–pressure relationships and linearity of the flow signal. Mean bias (%) of displayed values compared with the reference volume of 3, 5 and 7 L varied between −0.4% and +2.4%, and this was significantly smaller than that for 1 L (4.8% to +5.0%). Conversion factors for 3, 5 and 7 L were very similar (mean 6.00 ± 0.2, range 5.91–6.06) and were not significantly influenced by the gas mixture used. Increasing peak flow caused a small decrease in the conversion factor. Volume measurement error and conversion factors for inspiration and expiration were close to identity.
Conclusion The combination of the host monitor with the remodelled flow sensor allowed accurate in vitro measurement of flows and volumes in a range expected during large animal anaesthesia.
Clinical relevance This combination has potential as a reliable spirometric monitor for use during large animal anaesthesia. 相似文献
Study design Prospective, in vitro experiment.
Methods Both the original and the remodelled sensor were studied with a reference flow generator. Measurements were taken of the static flow-pressure relationship and linearity of the flow signal. Sensor airway resistance was calculated. Following recalibration of the host monitor, volumes ranging from 1 to 7 L were generated by a calibration syringe, and bias and precision of spirometric volume was determined. Where manual recalibration was not available, a conversion factor for volume measurement was determined. The influence of gas composition mixture and peak flow on the conversion factor was studied.
Results Both the original and the remodelled sensor showed similar static flow–pressure relationships and linearity of the flow signal. Mean bias (%) of displayed values compared with the reference volume of 3, 5 and 7 L varied between −0.4% and +2.4%, and this was significantly smaller than that for 1 L (4.8% to +5.0%). Conversion factors for 3, 5 and 7 L were very similar (mean 6.00 ± 0.2, range 5.91–6.06) and were not significantly influenced by the gas mixture used. Increasing peak flow caused a small decrease in the conversion factor. Volume measurement error and conversion factors for inspiration and expiration were close to identity.
Conclusion The combination of the host monitor with the remodelled flow sensor allowed accurate in vitro measurement of flows and volumes in a range expected during large animal anaesthesia.
Clinical relevance This combination has potential as a reliable spirometric monitor for use during large animal anaesthesia. 相似文献