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Identification biogéographique des principaux stocks exploités en Manche, relations avec ceux des régions voisines ArchiMer
Bennet, D; Casey, J; Dare, P; Dawson, W; Flatman, S; Hulme, T; Macer, C; Millner, R; Pickett, G; Vince, M; Lorance, Pascal; Souplet, A; Giret, M; Morin, Jocelyne; Berthou, A; Latrouite, Daniel; Morizur, Yvon; Bossy, S; Ozanne, S.
At present, the majority of fisheries are monitored and regulated in areas which are delineated by arbitrary ICES boundaries which do not necessarily have logical or consistent relationships with biological processes or fish movements. The biogeographical identification of Channel stocks is, therefore, an important step towards developing a rational strategy for the management of their fisheries. This synthesis is based on the wide available knowledge which has not been yet entirely exploited with the purpose of stock identification, for 25 commercially important species in the Channel. In addition, principal technics for stock identification are reviewed likewise environmental characteristics of the Channel, which represent fundamental components in...
Tipo: Text Palavras-chave: Environnement physico chimique; Méthodes d'identification; Migrations; Zones de ponte; Distribution géographique; Espèces exploitées; Identité de stock; Manche; Physical environment; Identification methods; Migrations; Spawning areas; Geographical distribution; Exploited species; Stock identification; Channel.
Ano: 1993 URL: https://archimer.ifremer.fr/doc/1993/rapport-719.pdf
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Polymerase chain reaction (PCR) identification of terverticillate Penicillium species isolated from agricultural soils in eskişehir province BABT
Demirel,Rasime; Sariozlu,Nalan Yilmaz; İlhan,Semra.
In the present study, nine terverticillate Penicillium isolates (P. griseofulfum, P. puberulum, P. crustosum, P. aurantiogriseum, P. chrysogenum, P. primulinum, P. expansum, P. viridicatum, Eupenicillium egyptiacum) from 56 soil samples were characterized genetically by a PCR method. The DNAs of the strains were isolated using the glass beads and vortexing extraction method and then used for PCR amplification with the internal transcribed spacer 1 (ITS1) and ITS4 universal fungal specific primers. The ITS regions of fungal ribosomal DNA (rDNA) were sequenced through the CEQ 8000 Genetic Analysis System. ITS-5.8S sequences obtained were compared with those deposited in the GenBank Database. The results indicated that the identification of Penicillium...
Tipo: Info:eu-repo/semantics/article Palavras-chave: Penicillium; Identification methods; PCR; ITS.
Ano: 2013 URL: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1516-89132013000600013
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