FLORAL PIGMENTATION STUDIES IN THE GENUS GOSSYPIUM II CHEMOTAXONOMIC ANALYSIS OF DIPLOID GOSSYPIUM SPECIES

The chromatographic pigment arrays of nine diploid species (G. arboreum, G. anomalum, G. herbaceum, G. stocksii, G. sturtii, G. thurberi, G. gossypioides, G. raimondii and G. klotzschianum) were studied. Among the Old World cottons, G. sturtii of Australia was very different from the species analyzed. The two species of the Herbacea section (G. herbaceum and G. arboreum) were found to have very similar pigment arrays. Both G. anomalum and G. stocksii were more like the Herbacea species than any other species in the genus, but both G. anomalum and G. stocksii had unique pigment characteristics. Although the evidence obtained so far from pigmentation patterns suggests that some pairs of species are closely related, the pigment arrays do not support the classification of the New World diploids into more than one section. From analysis of pigments of interspecific hybrids and their parents, it was found that with a hybrid and one parent species the pigment array of the other parent species could be predicted. Using this approach, the pigment arrays of three New World diploid species were predicted.     

THE ULTRASTRUCTURE OF COTYLEDONARY TISSUE FROM GOSSYPIUM HIRSUTUM L. SEEDS

Quiescent cottonseeds stored in a dry, anaerobic situation for over a year have been shown to contain cells whose contents are ultrastructurally similar to those of normal, fully hydrated plant cells. Plastids, mitochondria, and nuclei of the cells of cotyledon tissue in dry seeds possess normal-looking double membranes even under conditions of extreme desiccation. Previous reports have indicated on the basis of light microscopic work, that the cells of certain dry seeds do not possess nuclear membranes or mitochondria. The cells of the dry cottonseed do contain these structures, however. Dictyosomes have not been observed in the spongy parenchymal cells of the cotyledon tissue; it is suggested that they are concerned with translocation and/or utilization of material. The storage materials in the cells, protein and oil, are contained in vacuolar areas enclosed by a single membrane.     

棉属茎,叶表皮毛的研究

棉属植物茎、叶表皮毛的多少及其形态是识别种或品种的主要特征之一,并且与种或品种的抗虫或抗逆性有密切联系。Ramey(1962)研究指出,多毛性状是受 H_1和H_2两个主效基因和一些修饰基因的控制,H_2具有多效性。较系统地研究棉属茎、叶表皮毛的性状报道较少。本文报道利用扫描电镜对棉属植物的茎、叶表皮毛性状观察的结果。     

INTERSPECIFIC INCOMPATIBILITY IN GOSSYPIUM. IV. TEMPERATURE-CONDITIONAL LETHALITY IN HYBRIDS OF G. KLOTZSCHIANUM

A number of interspecific hybrids involving G. klotzschianum are embryo-lethal or seedling-lethal at temperatures considered optimal for cotton culture (26–32 C). At temperatures between 33–37 C, lethal symptoms (cell-necrosis and vascular plugging) for both stages of lethality are greatly ameliorated and at 40 C lethal symptoms are absent and hybrid ontogeny is normal for embryo- and seedling-lethals. Temperature-repressed lethals revert to type within 12–24 h after being returned to a non-repressive temperature regime.     

COTYLEDON PHOTOSYNTHESIS DURING SEEDLING GROWTH OF COTTON,GOSSYPIUM HIRSUTUM L.

Respiration and net photosynthetic O₂ production by cotton cotyledons were determined from an early age through the senescent stage. Various treatments were applied to cotyledons to assess the importance of current photosynthesis as compared to translocation of reserves to seedling development. Rates of respiration and net photosynthesis per cm² were high on 1-day-old cotyledons, but the rates decreased sharply with rapid expansion to reach a fairly stable rate. Respiration per cotyledon decreased linearly with age until the onset of senescence, then exhibited a distinct climacteric rise followed by a sharp decrease. Net photosynthesis per cotyledon increased until expansion was completed and then decreased linearly and steeply with age. Excision of cotyledons, inhibition of photosynthesis either chemically or by covering, and removal of the terminal bud indicated that current photosynthesis is a potent force behind early epicotyl growth.     

FLORAL PIGMENTATION STUDIES IN THE GENUS GOSSYPIUM. I. SPECIES SPECIFIC PIGMENTATION PATTERNS

Previous work on cotton flower pigments is outlined. The major flavonoids are glycosides of gossypetin, quercetin, and kampferol. Twelve flavonol glycosides have been tentatively isolated and identified, while a number of minor components remain unidentified. The gossypetin glycosides are gossypin, gossypitrin and a C₇-linked glycoside of unknown sugar residue. The quercetin glycosides include isoquercitrin, rutin, a third C₃-linked glycoside with unknown sugar residue, quercimeritrin and a second C₇-linked glycoside with sugar residue unknown. The kampferol glycosides include trifolin, kampferol rutinoside and 2 other C₃-linked glycosides with unknown sugar residues. The major anthocyanin throughout the genus is cyanidin. Mutants which affect visible flower color were studied in 3 species (G. arboreum, G. hirsutum, and G. barbadense). The majority of these mutants act to decrease or prevent the synthesis of gossypetin glycosides. The only exceptions to this are the mutants at the Y_a locus in G. arboreum, which affect all of the C₇-linked glycosides in one case, and in the other reduce over-all flavonol production. In all instances, the species could be positively identified by the residual array of pigments not affected by the mutant alleles concerned; i.e., visual similarity of phenotypes did not obscure the basic pattern of pigmentation characteristic of the different species.     

陆地棉半野生种系的细胞学研究

对原产于墨西哥的8个陆地棉半野生种系进行了核型分析。其根尖细胞的染色体数目均为52。“墨西哥棉”、“阔叶棉”、“帕默尔氏棉”和“尖斑棉”为1B 核型。其中以“墨西哥棉”最为原始,2n=4x=52=44m(6SAT) 8sm。“尤卡坦棉”、“玛利加郎特棉”、“莫利尔氏棉”和“雷奇蒙德氏棉”为2B 核型。其中以后两个种系最进化,2n=4x=52=32m(2或4SAT) 20sm。讨论了各种系之间的可能的演化关系。     

INTERSPECIFIC INCOMPATIBILITY IN GOSSYPIUM. I. STEM HISTOGENESIS OF G. HIRSUTUM X G. GOSSYPIOIDES

The hybrid of Gossypium hirsutum X G. gossypioides develops normally until 10–12 nodes have been produced at which time neoplasms form in the cortex, phloem, and pith of the lower portion of the shoot axis. Neoplasms are characterized by irregular whorls of unusually large cells the central portions of which contain apparently cytolysed cells and a reddish-brown substance that probably represents the products of cytolysis. Neoplastic invasion is followed by inactivation of the vascular cambium, disorganization of the phloem and cortex, and tylosing and plugging of many xylem vessels. Subsequent growth of the shoot, which continues at a very slow rate for up to several years, involves the proliferation of parenchymatous tissue which becomes secondarily vascularized.     

ASSESSMENT OF EVOLUTIONARY AFFINITIES IN GOSSYPIUM BY PROTEIN ELECTROPHORESIS

Protein band patterns from 25 species of Gossypium were obtained by electrophoresis of crude seed extracts on polyacrylamide gel. Band homologies between species were verified by electrophoresis of a mixture of their extracts. The patterns were found to be largely consistent with the conventional classification of the diploids into 6 genomic groups, A–F. However, G. triphyllum and G. bickii showed unique patterns differing respectively from those of the B and C groups, and G. australe showed closer affinity with the Arabian E- than with the Australian C-genome species. Affinities among the D-genome species were different from those implied by their former grouping into taxonomic sections but remarkably similar to those indicated in the most recent taxonomic revision of the genus. They were classifiable into two subgroups, β and ɛ. The clustering pattern of the diploids based on correlation coefficients calculated from densitometer curves of the electrophoretic spectra suggested that the genomic groups were derived from an African progenitor type, and that the American β and ɛ subgroups, most closely related to the African B- and the Arabian E-genome groups respectively, evolved under comparative mutual isolation, possibly separated by the Tertiary Amazonas basin.     

IDENTIFICATION OF MONOSOMES FOR SIX CHROMOSOMES IN GOSSYPIUM HIRSUTUM

Six primary monosomes of the amphidiploid species Gossypium hirsutum have been identified as separate chromosomes of the complement. On the basis of cytogenetic tests involving translocations, a diploid species of the D genome group, and genetic markers, 4 of the 6 monosomes were designated chromosomes 1, 2, 4 and 6 of the A subgenome and 2 were designated chromosomes 17 and 18 of the D subgenome. Fourteen other monosomes were identified as duplicates of 3 of the above 6 primaries.     

FATE MAP OF THE ORGANIZING SHOOT APEX IN GOSSYPIUM

Chimeral seedlings from a “semigametic” strain of cotton were used as the basis for a clonal analysis of events in the progressive organization of the nascent shoot apex. At the time the proembryo becomes a globular stage embryo with a distinct dermatogen, the surface of the embryo contains an eight-celled compartment for each cotyledon, a two-celled compartment for the first leaf, a one-celled compartment for the second leaf, and a three-celled compartment for the apical initials and all subsequent leaves and aerial structures. The developmental history of the first two leaves differs in a fundamental way from that of all the other leaves.     

THE ORIGIN,FERTILITY AND TRANSMISSION OF MONOSOMICS IN GOSSYPIUM

The origin of 51 monosomic plants in Gossypium hirsutum is described, and the great majority are shown to be fertile and transmissible. Both fertility and transmission rate can be increased by outcrossing and selection. Monosomics which have been isolated in a standard hirsutum background can be recognized by distinct morphological characteristics, including modifications of both vegetative and reproductive structures such as smaller or narrower leaves, smaller flowers or flower parts, and smaller, longer, or partially collapsed bolls. Monosomics involving the large chromosomes, i.e., the A genome, are recovered more frequently than are monosomics of the D (small chromosomes) genome. Furthermore, monosomics of certain of the A chromosomes are recovered more frequently than others. Of 20 identified hirsutum monosomics, 7 are chromosome A-2, 7 are A-4, 3 are A-6, and 1 each is A-1, D-17 and D-18.