Answer:
double fertilization
Explanation:
Flowering plants or angiosperms are seed-producing plants with the ability to produce reproductive organs-flowers and fruits with seed in it (unlike gimnosperms which contain naked seed). Another distinctive feature of angiosperms is their reduced gametophytes. This feature most likely reduces the time between pollination and fertilization. Fertilization in flowerin plants is double, meaning that two sperm cells fertilize ovule cells(egg cell and central nuclei cell): one forms diploid zygote which will develop in embryo, while other form triploid cell which will develop into endosperm (provides nutrition for the embryo).
Answer:
75%
Explanation:
Hypophosphatemic rickets is a disorder characterized by hypophosphatemia (low level of phosphate in the blood), defective intestinal absorption of calcium, and rickets (impaired mineralization of cartilaginous growth plates) or osteomalacia (impaired mineralization of the osteoid) unresponsive to vitamin D. It can be inherited or acquired.
When it comes to inheritable hypophosphatemic rickets, the disorder is most often inherited in an X-linked dominant manner. This means that the gene is inherited through the X chromosome and that one dominant allele is enough to cause it.
As the mother is heterozygous for the trait, she has one dominant and one recessive allele (XHXh). The father has one X chromosome, which he inherited from his mother, and as he has the condition, the dominant allele will be present on it (XHY).
This means that, if the child is a girl, she will definitely have the disorder. Girls inherit one X chromosome from each of their parents. Even if she inherited the one with the recessive allele from her mother, she would get the one with the dominant allele from her father.
If the child is a boy, he has a 50% chance to inherit the condition. Boys inherit the Y chromosome from their father and the X chromosome from their mother. As the mother is heterozygous, he can either get the chromosome without the dominant allele or the one with it. This means that there is a 50% chance of inheriting the disorder.
If we say that there are equal chances of this couple having female and male children, when we combine these results, we get a 75% chance of them inheriting hypophosphatemic rickets.
What exactly is the question?
The amino acid sequence in protein from the gene fragment for botana curus
is the same with species Z that is valine, histidine, leucine, threonine, proline,
glutamine and glutamine. Meanwhile, species X and species Y has different amino
acid sequence compared to botana curus. Therefore, species Z is most closely
related to botana curus because both species has the same amino acid sequence
and has similar sized DNA fragments.
