Husbandry of animals on land and in water: similarities and differences.     

E W Shell 《Journal of animal science》1991,69(10):4176-4182

The husbandry of aquatic animals originated in China in approximately 1,100 B.C., thousands of years after the beginning of animal agriculture. The practice did not reach Europe until the Middle Ages. Aquaculture apparently was not very important in Western Europe. The early immigrants from that region did not include fish with the other food animals that they brought with them to the New World. The practice of aquaculture finally came to the United States in the mid-nineteenth century, where it was used for the production of trout for stocking coldwater ponds and streams for sport fishing. Later, cultural practices were extended to warmwater species such as the largemouth black bass and the channel catfish. Thus, aquaculture in the United States was derived from recreational fishing rather than from food production, and from fisheries management rather than from animal science. There are important differences in the hydrosphere and atmosphere as cultural environments. Differences in composition, density, response to physical force, latent heat of fusion, specific heat, transparency, viscosity, and erosiveness of air and water result in different problems for land animal and aquatic animal culturists. Aquaculturists work primarily with "cold-blooded" ("lower") animals, whereas agriculturists work with "warm-blooded" ("higher") animals. In comparison with warm-blooded land animals, cold-blooded aquatic animals are less independent of changes in their environment.(ABSTRACT TRUNCATED AT 250 WORDS)  相似文献   

Clearance of ovine isolates of Bordetella parapertussis from murine trachea and lungs     

Chen W  Alley MR  Manktelow BW 《New Zealand veterinary journal》1991,39(2):75-76

Thirty-six mice were inoculated intranasally with Bordetella parapertussis organisms (isolated from sheep with chronic non-progressive pneumonia) to study their deposition and clearance in the lower respiratory tract. The deposition of the organism was greater in the trachea than in the lungs. At 48 hours after inoculation, almost 100% of organisms were cleared from the trachea but only 55% of organisms were cleared from the lungs. This result correlates well with the morphological changes seen previously in the pulmonary parenchyma and airways of mice and lambs experimentally infected with this organism.  相似文献   

Epidemiology and preventive medicine: A report of the CAVEPM/ACEMPV 1990 meeting          下载免费PDF全文

McNab WB  Ribble CS 《The Canadian veterinary journal. La revue veterinaire canadienne》1991,32(6):343-346

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Ontario. Abortions and stillbirths associated with generalized cytomegalovirus infection in a swine herd          下载免费PDF全文

Wilson RW  Carman PS  Dulac GC 《The Canadian veterinary journal. La revue veterinaire canadienne》1991,32(6):370

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Proposed criteria for classification of acute myeloid leukemia in dogs and cats     

Jain NC  Blue JT  Grindem CB  Harvey JW  Kociba GJ  Krehbiel JD  Latimer KS  Raskin RE  Thrall MA  Zinkl JG 《Veterinary clinical pathology / American Society for Veterinary Clinical Pathology》1991,20(3):63-82

Blood and bone marrow smears from 49 dogs and cats, believed to have myeloproliferative disorders (MPD), were examined by a panel of 10 clinical pathologists to develop proposals for classification of acute myeloid leukemia (AML) in these species. French-American-British (FAB) group and National Cancer Institute (NCI) workshop definitions and criteria developed for classification of AML in humans were adapted. Major modifications entailed revision of definitions of blast cells as applied to the dog and cat, broadening the scope of leukemia classification, and making provisions for differentiating erythremic myelosis and undifferentiated MPD. A consensus cytomorphologic diagnosis was reached in 39 (79.6%) cases comprising 26 of AML, 10 of myelodysplastic syndrome (MDS), and 3 of acute lymphoblastic leukemia (ALL). Diagnostic concordance for these diseases varied from 60 to 81% (mean 73.3 +/- 7.1%) and interobserver agreement ranged from 51.3 to 84.6% (mean 73.1 +/- 9.3%). Various subtypes of AML identified included Ml, M2, M4, M5a, M5b, and M6. Acute undifferentiated leukemia (AUL) was recognized as a specific entity. M3 was not encountered, but this subclass was retained as a diagnostic possibility. The designations M6Er and MDS-Er were introduced where the suffix "Er" indicated preponderance of erythroid component. Chief hematologic abnormalities included circulating blast cells in 98% of the cases, with 36.7% cases having >30% blast cells, and thrombocytopenia and anemia in approximately 86 to 88% of the cases. Bone marrow examination revealed panmyeloid dysplastic changes, particularly variable numbers of megaloblastoid rubriblasts and rubricytes in all AML subtypes and increased numbers of eosinophils in MDS. Cytochemical patterns of neutrophilic markers were evident in most cases of Ml and M2, while monocytic markers were primarily seen in M5a and M5b cases. It is proposed that well-prepared, Romanowsky-stained blood and bone marrow smears should be examined to determine blast cell types and percentages for cytomorphologic diagnosis of AML. Carefully selected areas of stained films presenting adequate cellular details should be used to count a minimum of 200 cells. In cases with borderline diagnosis, at least 500 cells should be counted. The identity of blast cells should be ascertained using appropriate cytochemical markers of neutrophilic, monocytic, and megakaryocytic differentiation. A blast cell count of > 30% in blood and/or bone marrow indicates AML or AUL, while a count of < 30% blasts in bone marrow suggests MDS, chronic myeloid leukemias, or even a leukemoid reaction. Myeloblasts, monoblasts, and megakaryoblasts comprise the blast cell count. The FAB approach with additional criteria should be used to distinguish AUL and various subtypes of AML (Ml to M7 and M6Er) and to differentiate MDS, MDS-ER, chronic myeloid leukemias, and leukemoid reaction. Bone marrow core biopsy and electron microscopy may be required to confirm the specific diagnosis. Immunophenotyping with lineage specific antibodies is in its infancy in veterinary medicine. Development of this technique is encouraged to establish an undisputed identity of blast cells. Validity of the proposed criteria needs to be substantiated in large prospective and retrospective studies. Similarly, clinical relevance of cytomorphologic, cytochemical, and immunophenotypic characterizations of AML in dogs and cats remains to be determined.  相似文献   

William Moorcroft (1767-1825). Veterinarian, explorer in Asia--and spy?     

W Steinigeweg 《DTW. Deutsche tier?rztliche Wochenschrift》1991,98(5):183-185

From 1790 to 1791 the surgeon William MOORCROFT studied veterinary medicine in Alford. He was the first Englishman with a complete formal veterinary education. In 1808 he gave up his horse practice and went into service of the East India Company as superintendent of the Company's Indian stud. Search for appropriate stud-horses and his efforts for opening up trading-routes from India to inner Asia induced him to exploring expeditions into the regions of the southwest Himalayas, the Hindu kush, Samarkand and Afghanistan. There he made also a lot of geographical and biological observations. He was not only one of the European pioneer Himalaya explorers but became also an early participant of the later so called "Great Game", the struggle between England and Russia for supremacy in Central Asia.  相似文献   

What Is Your Diagnosis?     

Green RA  Kasari TA 《Veterinary clinical pathology / American Society for Veterinary Clinical Pathology》1991,20(4):98-100

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Some nutritional and genetic considerations in the performance testing of beef bulls     

W F Cates 《Veterinary Clinics of North America: Food Animal Practice》1991,7(1):59-76

Performance testing started after it was recognized that growth traits were heritable. In the early years of performance testing there was a tendency to feed higher levels of energy for longer periods of time. More recently, the trend has been to feed lower levels of energy for shorter periods. There are still differences in opinion as to the appropriate level of energy to use. Although it is important that the level of energy fed is adequate to correctly establish a bull's ability to gain, it is essential to know that it will pose no risk of impaired spermatogenesis or cause any degree of laminitis. Clinical observations and research on overfeeding clearly show that both libido and spermatogenesis can be impaired by excess energy intake. The damage in 2-year-old bulls can be very extensive and in some animals it may not be reversible. The scant amount of research in yearling bulls indicates that there is considerable potential danger from overfeeding energy as well. Test stations are under used in regard to performing research that would help identify heritable defects that would interfere with the productive and reproductive efficiency of beef cattle. The first performance testing programs emphasized average daily gain from weaning to 1 year of age, so "performance" has traditionally meant rate of gain to most cattle raisers. The term "performance" is now starting to acquire a broader and more inclusive definition. For many breeders, it now includes weight per day of age, which is in part a maternal trait, and some kind of male evaluation for reproductive potential that can also be extrapolated to the female side. One of the first breakthroughs in this regard was to recognize the heritability of testicular size, and that testicular size could be fairly accurately determined by scrotal circumference measurement. It was also found that there was a favorable relationship between larger testicle size and the ability to produce high quality semen. As a result, it became a common practice to include scrotal circumference measurements in the published bull test results. However, many test station patrons were, and still are, content to consider the scrotal circumference measurement alone as an evaluation of a bull's breeding potential. Unfortunately, less than half of the bulls finishing a performance test at ages ranging from 11 to 14 months will be able to produce semen of completely acceptable quality.(ABSTRACT TRUNCATED AT 400 WORDS)  相似文献   

Open Intestinal Anastomosis with Surgical Stapling Equipment in 24 Dogs and Cats     

SHARON L. ULLMAN DVM  MS    MICHAEL M. PAVLETIC DVM  Dipiomate ACVS  GEOFFREY N. CLARK DVM 《Veterinary surgery : VS》1991,20(6):385-391

Surgical stapling equipment was used to perform open antiperistaltic side-to-side ("functional end-to-end") entero-anastomoses in 20 dogs and 4 cats. Twenty-one anastomoses healed uneventfully. Seven animals with severe bacterial peritonitis required open peritoneal drainage and delayed abdominal closure. There was postoperative leakage at the anastomotic site in two dogs and a localized abscess at the staple line in one cat. No long-term complications occurred in follow-up periods of 3 to 29 months.  相似文献   

Development of a semi-selective medium and an immunofluorescence colony-staining procedure for the detection of Clavibacter michiganensis subsp. sepedonicus in cattle manure slurry     

N. J. M. Roozen  J. W. L. Van Vuurde 《European journal of plant pathology / European Foundation for Plant Pathology》1991,97(5):321-334

Various compounds and basal media were tested for their suitability to create a semi-selective medium for isolation ofClavibacter michiganensis subsp.sepedonicus (Cms) from cattle manure slurry containing c. 10⁸ colony forming units (cfu) per ml.Plating efficiency of Cms in yeast glucose mineral medium (YGM) was 104% compared with yeast peptone glucose medium. Nalidixic acid, polymyxin B sulphate and the experimental disinfectant S-0208 inhibited colony growth of cattle slurry bacteria as compared with Cms in YGM. The optimal concentration of these inhibitors in combination was determined by modified agar diffusion tests and by pour plating in 24-well tissue culture plates. The semi-selective medium YGMI consisted of YGM supplemented with nalidixic acid (2 mg/l), polymyxin B sulphate (30 mg/l) and S-0208 (125 mg/l). Plating efficiency varied for Cms between 50.9 and 69.6%, for cattle slurry bacteria between 1.8 and 2.5% and for saprophytes from potato heel end extracts between 11.5 and 27.4%.Differentiation of Cms colonies from other colonies was based on their small and bluish colony morphology in pour plates and on immunofluorescence colony-staining (IFC). IFC of a pure culture of micro colonies of Cms in YGM was possible after one day incubation (colonies c. 5 cells). Green background fluorescence in the agar gels was prevented by addition of Tween 20 (0.1%) to the washing buffer and the use of 1% agar gels. IFC of macro colonies of Cms in YGMI, visible with 4x objective magnification, was possible after 4 days. The detection level of the target organism in artificially inoculated cattle slurry in YGMI based on colony morphology varied between 1.4×10³ and 2.3×10⁴ cfu per ml of cattle slurry. Miniaturized plating combined with IFC, using wells in tissue culture plates (=16 mm), proved suitable for detection, but was c. 30 times les sensitive. The recovery of Cms was negatively correlated with the number of saprophytic colonies in the agar plates (R ²=0.74).  相似文献