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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
9
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pubmed:dateCreated |
1989-3-22
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pubmed:abstractText |
Fresh fecal specimens from deer were examined for nematode eggs (primarily Haemonchus and Ostertagia), using a flotation technique (sugar, sp gr = 1.27), and then were reexamined for up to 200 days after storage in 2.5, 5, or 10% formalin, absolute methyl alcohol, or 70% ethyl alcohol at room temperature (20 C) or after storage without preservative at 4, 0, or -20 C. For long-term storage, 10% formalin was the best fixative for recovery of eggs (compared with the rate of recovery of eggs from fresh feces). Approximately 50% of the strongyle eggs were detected in feces stored in formalin for 200 days. However, between days 3 and 10 of storage, the recovery rate was low (less than 50%), presumably due to ion binding. Alcohols were unsuitable for preservation, and storage at 0 or -20 C resulted in an egg recovery rate of less than 50%. Storage at 4 C for 50 days resulted in approximately 90% recovery of nematode eggs. Number of Parelaphostrongylus tenuis larvae recovered from fecal specimens stored in 10% formalin for 24 days was greater than that recovered from fresh fecal specimens.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0003-1488
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
189
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1065-7
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pubmed:dateRevised |
2003-11-14
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pubmed:meshHeading | |
pubmed:year |
1986
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pubmed:articleTitle |
Recovery of nematode eggs and larvae in deer: evaluation of fecal preservation methods.
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pubmed:affiliation |
Department of Veterinary Microbiology and Pathology, Washington State University, Pullman 99164.
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pubmed:publicationType |
Journal Article
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