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The cultivated Gossypium spp. (cotton) represents the single most important, natural fiber crop in the world. In addition to its fiber, the oil and protein portion of the cottonseed also represents significant economic value. To protect the worldwide economic value of cotton fiber and cotton byproducts, coordinated efforts to collect and maintain cotton genetic resources have increased over the last 100 yr. The classified genetic resources of cotton are extensive and include five tetraploid species in the primary gene pool, 20 diploid species in the secondary gene pool, and 25 diploid species in the tertiary gene pool. This report provides information on the status and contents of eight major cotton germplasm collections present across the world. Based on the findings of this report, a number of classified Gossypium species are not maintained in these collections, and several are underrepresented and vulnerable to extinction. This report presents several critical challenges and opportunities facing international efforts to enhance and preserve the world's Gossypium genetic resources. Multinational communication and collaboration are essential to protect, secure, and evaluate the global cotton germplasm resources. Without global, collaborative efforts, the rarest and most unique cotton germplasm resources are vulnerable to extinction.

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-The objective of this work was to characterize the populations of Gossypium barbadense in the states of Amapá and Pará, Brazil. In situ characterization was conducted through interviews with the owners of the plants and environmental observations. Leaf or petal tissue as well as seed samples were collected for genetic characterization by single sequence repeats markers and for storage in germplasm banks, respectively. The plants were maintained in dooryards and used mainly for medical purposes. The genetic analysis showed no heterozygous plants at the loci tested (f = 1), indicating that reproduction occurs mainly through selfi ng. The total genetic diversity was high (H e = 0.39); and a high level of differentiation was observed between cotton plants from the two states (F ST = 0.36). Conventional methods of in situ maintenance of G. barbadense populations are not applicable. The conservation of the genetic variability of populations present in the two states could be achieved through germplasm collection and establishing of ex situ seed banks.Index term: cotton, genetic diversity, germplasm, SSR markers. Caracterização in situ e genética de Gossypium barbadense dos Estados do Pará e do AmapáResumo -O objetivo deste trabalho foi caracterizar populações de Gossypium barbadense dos estados do Amapá e Pará. A caracterização in situ foi conduzida por meio de entrevistas com os proprietários das plantas e por observações sobre o ambiente. Tecidos de folhas ou de pétalas, além de sementes, foram coletados para a caracterização genética com marcadores SSR ("single sequence repeats") e para o armazenamento em bancos de germoplasma, respectivamente. As plantas eram mantidas em fundos de quintal e usadas, principalmente, para fi ns medicinais. As análises genéticas não mostraram plantas heterozigotas nos locos testados (f = 1), o que indica que a reprodução ocorre principalmente por meio de autofecundação. A diversidade genética total foi alta (H e = 0,39), e um alto nível de diferenciação foi observado entre as plantas de algodoeiro dos dois estados (F ST = 0,36). Métodos convencionais para a manutenção in situ das populações de G. barbadense não são aplicáveis. A conservação da variabilidade genética das populações presentes nos dois estados deve ser realizada pela coleta de germoplasma e pela constituição de bancos de sementes ex situ.Termos para indexação: algodoeiro, diversidade genética, germoplasma, marcadores SSR.

A series of 24 general‐purpose yeast plasmid vectors has been constructed. The plasmid series is composed of inter‐replaceable cassettes, allowing for easy interconversion of plasmid types. In addition to the usual replication origins, selectable markers and multiple cloning sites (MCS), cassettes dedicated to counter‐selection have been constructed. A pair of unique 8 bp restriction enzyme recognition sites flank each type of cassette, FseI in the case of yeast replication origins, AscI in the case of selectable markers, PacI in the case of counter‐selectable markers and NotI in the case of the MCS. Thus, any given cassette can be replaced by another cassette of the same type, facilitating interconversion of any given plasmid from one type to another, even after the insertion of DNA into the MCS. Hence, the plasmids have been named pYC for ‘yeast cassettes’. The cassettes consist of either NONE, CEN4/ARS or 2µ as replication origin, either URA3, MET2–CA (Lg–MET2) or the G418 resistance gene (the apt1 gene from bacterial transposon Tn903, encoding aminoglycoside phosphotransferase) as selectable markers, either NONE, PMET25–PKA3 or PCHA1–PKA3 as counter‐selectable marker, and the MCS, containing recognition sites for AflII, AvrII, BspEI, PmeI, SacII, SalI, SunI, BamHI, EcoRI, HindIII, KpnI, MluI, NarI and SacI (of which the seven first are unique in all plasmids). The counter‐selectable markers consist of the PKA3 gene under control of the conditional MET25 or CHA1 promoters. At activating conditions these promoters express the PKA3 gene at toxic levels, facilitating easy selection for loss of plasmid or ‘loop‐out’ of plasmid DNA sequence after genomic integration. Copyright © 2000 John Wiley & Sons, Ltd.