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41.
SIMONE DE PÁDUA TEIXEIRA ELIANA REGINA FORNI-MARTINS NEUSA TARODA RANGA 《Botanical journal of the Linnean Society. Linnean Society of London》2002,138(4):461-471
Microsporogenesis, chromosome number, meiotic behaviour and meiotic index were investigated in Dahlstedtia pinnata and D . pentaphylla , two legume species occurring largely in Brazil, in order to ascertain whether the pollen could limit fertilization events. Archesporial cells originate primary sporogenous and anther wall precursor cells, the tapetum is uniseriate, uninucleate and glandular. Tetrads are tetrahedric or decussate, and cytokinesis is of the simultaneous type. Mature pollen grains are tricolpate and bicellular. No abnormalities in microsporogenesis were found. In both species the chromosome number is n = 11, a number not reported previously. The base number for Dahlstedtia is also 11, because cytological observations include both species of Dahlstedtia . D. pentaphylla has a higher meiotic index and lower individual variation values, and it is considered meiotically stable. Its pollen grains do not limit fertilization. D. pinnata has a lower meiotic index, and the pollen is one of the factors which limit fertilization. Furthermore, D. pinnata has numerous adventitious shoots, which suggest that vegetative propagation is important in its reproductive process. © 2002 The Linnean Society of London, Botanical Journal of the Linnean Society , 2002, 138 , 461–471. 相似文献
42.
Comparison of Coding and Spacer Region Sequences of Chromosomal rRNA-Coding Genes of Two Sequevars of Pneumocystis carinii 总被引:2,自引:0,他引:2
MARIA ORTIZ-RIVERA YONG LIU REGINA FELDER MICHAEL J. LEIBOWITZ 《The Journal of eukaryotic microbiology》1995,42(1):44-49
Two distinct sequevars, denoted Pc1 and Pc2, of the opportunistic pathogen Pneumocystis carinii have been previously identified based on the sequence of their 26S rRNA genes, the location of group I self-splicing introns and pulsed field electrophoretic patterns of chromosomal DNA. This study shows that the sequences of 16S and 5.8S rRNA genes also vary between these sequevars, and that greater variation was seen in the internal transcribed spacer regions. Polymerase chain reaction and restriction analysis can distinguish between these sequevars. 相似文献