On primary succession newly exposed or newly formed rock is colonized by living things for the first time. And in secondary succession an area that was previously occupied by living things
To know what happens here, you need to analyze the alleles.
If the father is color blind and the daughter is not, you can suppose that is a recessive allele.
You can tell she is a carrier only, and because we received one sexual allele from each parent. If they ask you about the gender, we can suppose a cross between Xx and XY being lower x the recessive allele (color-blind vision).
When you draw the Punnett square, you'll found the probabilities are XX, XY, Xx, and xY.
So, you have a 50% chance of having a boy and 25% chance of having a color-blind boy.
Answer:
They have uncoiled to form long, thin strands.
Explanation:
Chromosomes are present in cell nucleus and consist of chromatin. Genes are present in linear order on chromosomes. The chromosomes become visible under the microscope as distinct structures during cell division. When cells are not dividing, the chromosomes decondense to loose their individuality and make the mass of chromatin.
Chromatin is complex of DNA and packing proteins. As the cells enter the prophase stage of cell division, condensation of chromatin occurs and individual chromosomes become visible under microscope. Before that (during interphase), chromosomes are not visible as they are present in decondensed form.
Secondary succession occurs after the initial succession has been disrupted and some plants and animals still exist. The disruption occurs afer an event like a forrest fire or hurricane destroys the forest.
