ha if you think they prove your point your wrong. and as i told you gender may be influenced by genetics but not decided. the decisions is made after germination they only have a genetic predisposition to a gender.
that may have came off a little harsh but its true. as far as genes determining gender it all is a part of the enviro that affects the plants gender choice.
some other good example of where genes do not play into gender as much is in Rodents and Reptiles
You are correct about some reptiles, but wrong about rodents, which are mammals, and their sex is determined early in gestation, having nothing to do with their environment, but with the Y.
In the
gametic life cycle, of which humans are a part, the species is diploid, grown from a diploid cell called the
zygote. The organism's diploid germ-line stem cells undergo meiosis to create haploid gametes (the
spermatozoa for males and
ova for females), which fertilize to form the zygote. The diploid zygote undergoes repeated cellular division by
mitosis to grow into the organism. Mitosis is a related process to meiosis that creates two cells that are genetically identical to the parent cell. The general principle is that mitosis creates somatic cells and meiosis creates germ cells.
The first major breakthrough in understanding sex determination was the discovery of sex chromosomes in the early 1900s. From meticulous analyses of male and female insect chromosomes, scientists discovered that, although most chromosomes were present in equal numbers in both males and females, there were one or two additional chromosomes that were unequally represented in the two sexes. Analyses of additional species over the years has revealed that chromosomal differences are primarily responsible for sex determination in most animals.
Sex Determination in Mammals
Figure 1: The SRY gene is on the Y chromosome and causes the development of male characteristics in humans.
In the absence of SRY gene, the embryo develops as a female.
Used with permission. Copyright 2005 by W. H. Freeman and Company. All rights reserved.
In placental mammals, the presence of a Y chromosome determines sex. Normally, cells from females contain two X chromosomes, and cells from males contain an X and a Y chromosome. Occasionally, individuals are born with sex chromosome aneuploidies, and the sex of these individuals is always determined by the absence or presence of a Y chromosome. Thus, individuals with 47,XXY and 47,XYY karyotypes are males, while individuals with 45,X and 47,XXX karyotypes are females. Humans are able to tolerate supernumerary numbers of sex chromosomes because of
X inactivation and the fact that the human Y chromosome is quite gene-poor.
Although the role of the Y chromosome in mammalian sex determination has been known since the early twentieth century, it was not until 1959 that scientists were able to identify the region of the Y chromosome that controlled this process (McLaren, 1991). Later, researcher David C. Page analyzed the chromosomes of sex-reversed XX men, rare individuals who look like men but have two X chromosomes instead of one X chromosome and one Y chromosome. Using DNA hybridization with probes corresponding to different regions of the Y chromosome, Page discovered that sex-reversed males carried genes from a 140-kilobase region on the short arm of the Y chromosome (Figure 1). Presumably, this region had been transferred to the X chromosome during a translocation (Page et al., 1985). Subsequent experiments narrowed down this region (McLaren, 1991) and found that one gene, the sex-determining region of the Y, or SRY, was the master regulator of sex determination. The presence of just this region from the Y chromosome is thus sufficient to cause male development (Koopman et al., 1991).
Figure 2
In human embryos, the SRY gene encodes a unique transcription factor that activates a testis-forming pathway at about week seven of development. Before this time, the embryonic gonad is "indifferent," meaning that it is capable of developing into either a testis or an ovary (Figure 2). Likewise, the early embryo has two systems of ducts, Wolffian and Müllerian ducts, which are capable of developing into the male and female reproductive tracts, respectively. Once the SRY gene product stimulates the indifferent gonad to develop into a testis, the testis begins producing two hormones, testosterone and anti-Müllerian hormone, or AMH. Testosterone and one of its derivatives, dihydrotestosterone, induce formation of other organs in the male reproductive system, while AMH causes the degeneration of the Müllerian duct. In females, who do not contain the SRY protein, the ovary-forming pathway is activated by a different set of proteins. The fully developed ovary then produces estrogen, which triggers development of the uterus, oviducts, and cervix from the Müllerian duct.