By Richard Frankham
Meant for people with a restricted history in genetic reviews, this concise, entry-level textual content in conservation genetics is gifted in a easy structure, with details basically highlighted. Solved difficulties are supplied all through to assist illustrate key equations, even though a simple wisdom of Mendelian genetics and easy statistics is thought. A thesaurus and proposals for extra examining offer extra help for the reader. a number of pen-and-ink pix of endangered species convey the fabric to existence. additionally on hand: advent to Conservation Genetics "...balance[s] pupil want for readability and brevity with the necessities of conservation pros for targeted applications." selection 0-521-63014-2 Hardback $130.00 C 0-521-63985-9 Paperback $50.00 D
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Extra resources for A Primer of Conservation Genetics
An electrical potential gradient applied to the gel causes the proteins to migrate through the gel. Proteins coded for by the same genetic locus but with different charges migrate to different positions (F–fast vs. S–slow), allowing identiﬁcation of the different alleles at the locus. Proteins from speciﬁc loci are usually detected by their unique enzymatic activity, using a histochemical stain. 5 Allozyme genetic diversity in different taxa. 096 Sources: Hamrick & Godt (1989); Ward et al. (1992).
Chapman & Hall, New York. Advanced scientiﬁc reviews on the conservation of major groups of animals and plants, including considerable information on genetic diversity. Smith, T. B. & R. K. Wayne. ) 1996. Molecular Genetic Approaches in Conservation. Oxford University Press, New York. Contains information on genetic diversity in threatened species and the diverse molecular methods for measuring it. Advanced. Chapter 3 Evolutionary genetics of natural populations Populations evolve through the actions of mutation, migration, selection and chance.
AUG CUU GAC GUU. . . . met– leu– asp– val. . . . AUG CUU GGC GUU. . . . met– leu– gly – val. . the protein on the right will migrate more slowly towards the anode in an electrical potential gradient, as a consequence of the substitution of uncharged glycine (gly) amino acid for negatively charged aspartic acid (asp). A gel electrophoresis apparatus (after Hedrick 1983). Soluble protein extracts are placed in spaced positions across the top of the gel. An electrical potential gradient applied to the gel causes the proteins to migrate through the gel.