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1.
J Hered ; 89(4): 301-5, 1998.
Article in English | MEDLINE | ID: mdl-9703686

ABSTRACT

The Guadalupe fur seal (Arctocephalus townsendi) population underwent one or two severe bottlenecks due to commercial sealing in the late 19th century. Since then the protected population has been growing steadily around their only rookery, Isla de Guadalupe, Mexico. We probed both nuclear and mitochondrial genomes using multilocus nuclear DNA profiling and mitochondrial DNA sequencing to estimate the level of genetic variability of the present population. Unlike other pinniped populations that have experienced similar historical bottlenecks, such as Hawaiian monk seals and northern elephant seals, high levels of genetic variability were found.


Subject(s)
Fur Seals/genetics , Genetic Variation , Animals , DNA Fingerprinting , Female , Fur Seals/classification , Male , Sequence Analysis, DNA
2.
Mol Ecol ; 6(11): 1091-7, 1997 Nov.
Article in English | MEDLINE | ID: mdl-9394465

ABSTRACT

We describe methods for the preservation, extraction and amplification of DNA from faeces that facilitate field applications of faecal DNA technology. Mitochondrial, protein encoding and microsatellite nuclear DNA extracted and amplified from faeces of Malayan sun bears and North American black bears is shown to be identical to that extracted and amplified from the same individual's tissue or blood. A simple drying agent, silica beads, is shown to be a particularly effective preservative, allowing easy and safe transport of samples from the field. Methods are also developed to eliminate the risk of faecal DNA contamination from hair present in faeces.


Subject(s)
DNA/analysis , Feces/chemistry , Genetic Techniques , Animals , Biochemistry/methods , DNA/blood , DNA/chemistry , DNA, Mitochondrial/analysis , Female , Hair , Male , Polymerase Chain Reaction/methods , Sex Determination Processes , Specimen Handling/methods , Ursidae/genetics
3.
Proc Natl Acad Sci U S A ; 91(3): 1049-53, 1994 Feb 01.
Article in English | MEDLINE | ID: mdl-11607458

ABSTRACT

Populations of the temperate seagrass, Zostera marina L. (eelgrass), often exist as discontinuous beds in estuaries, harbors, and bays where they can reproduce sexually or vegetatively through clonal propagation. We examined the genetic structure of three geographically and morphologically distinct populations from central California (Elkhorn Slough, Tomales Bay, and Del Monte Beach), using multilocus restriction fragment length polymorphisms (DNA fingerprints). Within-population genetic similarity (Sw) values for the three eelgrass populations ranged from 0.44 to 0.68. The Tomales Bay population located in an undisturbed, littoral site possessed a within-population genetic similarity (Sw = 0.44) that was significantly lower than those of the other two populations. Cluster analysis identified genetic substructure in only the undisturbed subtidal population (Del Monte Beach). Between-population similarity values (Sb) for all pairwise comparisons ranged from 0.47 to 0.51. The three eelgrass populations show significantly less between locale genetic similarity than found within populations, indicating that gene flow is restricted between locales even though two of the populations are separated by only 30 km. The study demonstrates that (i) natural populations of Z. marina from both disturbed and undisturbed habitats possess high genetic diversity and are not primarily clonal, (ii) gene flow is restricted even between populations in close proximity, (iii) an intertidal population from a highly disturbed habital shows much lower genetic diversity than an intertidal population from an undisturbed site, and (iv) DNA fingerprinting techniques can be exploited to understand gene flow and population genetic structure in Z. marina, a widespread and ecologically important species, and as such are relevant to the management of this coastal resource.

4.
EXS ; 67: 429-36, 1993.
Article in English | MEDLINE | ID: mdl-8400711

ABSTRACT

The enforcement of wildlife laws and the captive breeding of threatened/endangered species requires the ability to identify individual animals. DNA profiles of a variety of large North American mammals, birds, and fish were generated using ten different oligonucleotide probes. The probes tested were four multilocus probes [33.6, 33.15, JE46, and (TGTC)5] and six 'human unilocus' probes [MS1 (D1S7), CMM101 (D14S13), YNH24 (D2S44), EFD52 (D17S26), TBQ7 (D10S28), and MS43 (D12S11). Each of the probes was chemically synthesized, and labeled by the attachment of alkaline phosphatase; after hybridization, the probes were detected by chemiluminescence catalyzed by the enzyme. Initial screening against zoo blots including samples of bear, wolf, large cat, wild sheep, deer, birds, marine mammals, and fish indicated that three multilocus probes [33.15, 33.6, (TGTC)5] gave informative patterns containing 15-40 bands for most or all of the animals tested, as did two of the 'human unilocus' probes (MS1 and CMM101). The other five probes appeared informative only in some species (for example, YNH24 against canids). Subsequent screenings of populations within species were used to determine genetic diversity by analysis of observed bandsharing (S). Large heterologous populations, such as white-tailed deer, exhibited highly diverse band patterns (S < or = 0.2). Geographically isolated and/or genetically constricted animals, such as endangered Mexican wolves, Tule elk, and Columbian white-tailed deer, exhibited much higher frequencies of bandsharing (0.6 < or = S < or = 0.95).(ABSTRACT TRUNCATED AT 250 WORDS)


Subject(s)
Animals, Wild/genetics , DNA Fingerprinting , Mammals/genetics , Animals , Base Sequence , DNA/genetics , Jurisprudence , Molecular Sequence Data , North America , Oligonucleotide Probes/genetics , Species Specificity
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