The ultimate fate of the universe is a topic in physical cosmology, whose theoretical restrictions allow possible scenarios for the evolution and ultimate fate of the universe to be described and evaluated. Based on available observational evidence, deciding the fate and evolution of the universe have now become valid cosmological questions, being beyond the mostly untestable constraints of mythological or theological beliefs. Many possible futures have been predicted by different scientific hypotheses, including that the universe might have existed for a finite and infinite duration, or towards explaining the manner and circumstances of its beginning.
Answer:
Mitotic phase
Explanation:
The mitotic phase is a multistage process during which the duplicated chromosomes are aligned, separated, and moved to opposite poles of the cell, and then the cell is divided into two new identical daughter cells.
The first portion of the mitotic phase, mitosis, is composed of five stages which includes prophase, prometaphase, metaphase, anaphase, telophase , which accomplish nuclear division before reaching the second stage which is cytokinensis which involves the physical separation of the cytoplasmic componenets into two daughter cells.
Answer:
Depending on the food pyramid, on the side there may be something that says decomposers. These eat from all of the sections of the pyramid.
Energy flows from the bottom to the top, and then to the side with the decomposer.
Answer:
amino acids
Explanation:
proteins are organic matter molecules that perform multitude of function in the body
Answer:
Man's genotype: XᴮY
Woman's genotype: XᴮXᵇ
Daughter's genotype: XᵇXᵇ
The daughter is not the man's child.
Explanation:
Color blindness is a sex-linked trait caused by a recessive allele located in the X chromosome (Xᴮ=normal vision; Xᵇ-color blind).
Women have two X chromosomes, while men have an X and a Y chromosomes. For that reason, women need to have two recessive alleles to be color blind, while men only need one Xᵇ to be colorblind.
Since the man has normal color vision, his genotype would be XᴮY.
If the daughter is her father's, she would have inherited his dominant Xᴮ allele, so she would have normal vision. However, she is colorblind, so her genotype is XᵇXᵇ. She is not the man's daughter.
The mother also has normal color vision, but her daughter inherited a recessive allele from her, so her genotype is heterozygous XᴮXᵇ.
