Thesis (Ph. D.)--University of Alabama at Birmingham, 2007. / Additional advisors: Asim Bej, Gene Hines, Douglas Watson, Douglas Weigent. Description based on contents viewed Oct. 2, 2008; title from PDF t.p. Includes bibliographical references.

Thèse--Université de Strasbourg. / "Index bibliographique": p. 483-497.

Inaug.-diss.--Bonn. / Lebenslauf. "Literaturangabe": p. [28]-29.

Inaug.-diss.--Göttingen. / Lebenslauf. "Verzeichnis der benutzten literatur": p. 26-27.

Chum salmon embryonal discs were smeared and the cells stained with acetocarmine (60° C.) for chromosome content. Thirty-eight chromosomes (granular, sigmoid, and j-shaped) were counted, but the number was not considered absolute. The presence of sex chromosomes could not be established. Chromosomes in cells of differentiating gonads showed such excessive clumping that a count could not be made. Sex differentiation was followed in chum salmon. Sections from alevins (three weeks old) showed the gonads to be indifferent. Isolated nests of germ cells appeared which eventually formed a continuous cord (five weeks). At nine weeks the primordial ovary developed oocytes and in the succeeding week formed an endovarial canal. At this time the testis was first recognized (ten weeks). It was a small compact organ containing spermatogonia. Up to the final examination (fifteen weeks) the ovary showed no new structures excepting a prominent vena commites anteriad, while the testis retained its primitive features. The sex of pink and chum salmon fry migrants were shown by dissection. Ultraviolet light and temperature treatment of developing chum, pink, and sockeye embryos did not show that these factors would influence the sex ratio. Temperature data were decidedly inconclusive. An equal distribution of the sexes in pink and chum fry and sockeye smolts was found in data compiled from migrant runs at Port John, B. C. It is suggested that precocious male sockeye mature in the sea. The sex ratios at stages in the life history of the pink salmon are presented to show that there had occurred a natural sea mortality of 40.2 percent. / Science, Faculty of / Zoology, Department of / Graduate

No description available.

All-male fry are preferred to prevent uncontrolled reproduction before harvest in intensive Nile tilapia (Oreochromis niloticus) aquaculture. Males also grow faster than females. An alternative approach to direct hormonal masculinisation of tilapia fry is to produce fry that are genetically male. However, sex determination system in tilapia is fairly complex. Recent developments have resulted in a linkage map and genetic markers that can be used to analyse the sex determination system. To analyse the genetic sex determination mechanism and to develop marker-assisted selection in the Stirling Nile tilapia population, a fully inbred line of clonal females (XX) was verified using test crosses and DNA markers (mostly microsatellites) to use as a standard reference line in sex determination studies. A series of crosses were performed involving this line of females and a range of males. Three groups of crosses were selected (each group consisted of three families) from progeny sex ratio distributions, and designated as type ‘A’ (normal XY males x clonal XX females), type ‘B’ (putative YY males x clonal XX females) and type ‘C’ (unknown groups of males x clonal XX females), for sex linkage study. For type ‘A’, inheritance of DNA markers and phenotypic sex was investigated using screened markers from tilapia linkage group 1 (LG1) to confirm the LG1-associated pattern of inheritance of phenotypic sex and the structure of LG1. Screened markers from LG1, LG3 and LG23 were used to investigate the association of markers with sex in families of type ‘B’ and ‘C’. In addition, a genome-wide scan of markers from the other 21 LGs was performed to investigate any association between markers and sex, in only families of cross type ‘B’. LG1 associated pattern of inheritance of phenotypic sex was confirmed by genotype and QTL analyses in families of cross type ‘A’. Analyses of genotypes in families of type ‘B’ and ‘C’ showed strong association with LG1 markers but no association with LG3 and LG23 markers. Genome wide scan of markers from all other LGs did not show any significant association between any markers and the sex. The allelic inheritance of two tightly linked LG1 markers (UNH995 and UNH104) in families of type ‘B’ and ‘C’ identified polymorphism in the sex determining locus: one of the alleles was associated mostly with male offspring whereas another allele was associated with both progeny (mostly males in type ‘B’ families, and approximately equal numbers in type ‘C’ families). This knowledge was used to identify and separate supermales (‘YY’ males) that should sire higher proportions of male progeny, reared to become sexually mature for use as broodstock. Two of them were crossed with XX females (one clonal and one outbred) to observe the phenotypic expression of the strongest male-associated allele in progeny sex. The observations of 98% male (99 males out of 101 progeny) and 100% male (N=75) from these two crosses respectively, suggest that a marker-assisted selection (MAS) programme for genetically male Nile tilapia production could be practical. This study also suggests that the departures from the sex ratios predicted using a “simple” XX/XY model (i.e., YY x XX should give all-male progeny) were strongly associated with the XX/XY system, due to multiple alleles, rather than being associated with loci in other LGs (e.g., LG3, LG23). This study also tentatively names the allele(s) giving intermediate sex ratios as “ambivalent” and emphasizes that the presence and actions of such allele(s) at the same sex-determining locus could explain departures from predicted sex ratios observed in some earlier studies in Nile tilapia.

The PhD research studied two aspects in tilapia, firstly the analysis of sex determination in Nile tilapia (evidence of complex sex-determining systems) and secondly the genetic management of the tilapia species, using different genomic analysis approaches. This research started with the development of two techniques: minimally invasive DNA sampling from fish mucus, which was found to be suitable for standard genotyping and double-digest restriction-site associated DNA sequencing – ddRADseq; and pre-extraction pooling of tissue samples for ddRADseq (BSA-ddRADseq), which was found to be suitable for identifying a locus linked to a trait of interest (sex in this case). The first molecular evidence concerning the sex determination in genetically improved farmed tilapia (GIFT) was described using BSA-ddRADseq. Given the multiple stock origin of GIFT, surprisingly only a single locus (in linkage group 23) was found to be associated with the phenotypic sex across the population. The first evidence of LG23 influence on phenotypic sex in the Stirling population of Nile tilapia was also found. Different combinations of estrogen hormones and high temperature were tested for feminising Nile tilapia: a combined treatment of estrogen hormone and high temperature was found to be more efficient in feminising Nile tilapia than the estrogen alone. A set of species-diagnostic SNP markers were tested which were found to be suitable to distinguish pure species (O. niloticus, O. mossambicus and O. aureus), and these were used to analyse species contribution to GIFT and a selected tilapia hybrid strain. The results of the current research added novel information to our understanding of sex determination in Nile tilapia, which will be helpful in the development of marker-assisted selection in GIFT and other Nile tilapia strains towards the production of all male offspring. The methods developed also have broader applicability in genetic and genomics research.

South Florida's loggerhead (Caretta caretta), green (Chelonia mydas) and leatherback (Dermochelys coriacea) sea turtles hatchling have environmentally determined sex. The in situ nest mean hatchling sex ratios (SR) were highly female-biased : loggerhead F=0.89) and green turtle F=0.81; leatherback's SR was nearly balanced (0.55F). Nest temperatures and SRs differed between leatherbacks and loggerhead and green turtles. The latter two did not differ. The loggerhead response parameters were estimated within biological limitations by both 50-65% of incubation and mean middle 1/3 temperature. The maximum middle 1/3 temperature was the best-fit predictor for green turtles. No best-fit sex ratio-temperature response could be identified for leatherbacks. Clutches incubating under natural conditions can vary greatly in SR ; TRT differences may account for differences among species' sex ratios. / by Micah Marie Rogers. / Thesis (M.S.)--Florida Atlantic University, 2013. / Includes bibliography. / Mode of access: World Wide Web. / System requirements: Adobe Reader.

Sex determination in leatherback sea turtles is directed primarily by the temperatures a clutch experiences during the middle third of development. Warmer temperatures tend to produce females will cooler temperatures yield males. Nest temperatures can vary spatially and temporally. During the 2010 and 2011 nesting seasons, this study estimated the hatchling sex ratio of leatherback sea turtles on Sandy Point National Wildlife Refuge (SPNWR), St. Croix, U.S. Virgin Islands. I measured sand temperatures from May- August and across the spatial range of leatherback nesting habitat. I spatially interpolated those temperatures to create maps that predicted temperatures for all nests incubating on SPWNR. Nest temperatures were also directly measured and compared with predicted nest temperatures to validate the prediction model. Sexes of dead-in-nest hatchlings and full term embryos were used to confirm the sex-temperature response. The model showed that microclimatic variation likely impacts the production of both sexes on SPNWR. / Includes bibliography. / Thesis (M.S.)--Florida Atlantic University, 2013.