In a study conducted at virginia tech on the development of ectomycorrhizal, a symbiotic relationship between the roots of trees and a fungus, in which minerals are transferred from the fungus to the trees and sugars from the trees to the fungus, 20 northern red oak seedlings exposed to the fungus pisolithus tinctorus were grown in a greenhouse. all seedlings were planted in the same type of soil and received the same amount of sunshine and water. half received no nitrogen at planting time, to serve as a control, and the other half received 368 ppm of nitrogen in the form nano3. the stem weights, in grams, at the end of 140 days were recorded as follows:

answer: blah

explanation:

bc blah

i think that is new experiments yield untrustworthy data and should be carefully considered, because you don't know what will happen with the experiments.

an individual’s sex (i.e., whether they are a male or female) is determined by the sex chromosomes. most people have two sex chromosomes, one that is inherited from their mother and one that is inherited from their father. typically, females have two x chromosomes (xx) and males have one x chromosome and one y chromosome (xy). conditions caused by changes (“mutations”) in genes located on the x chromosome are considered x-linked.

x-linked recessive inheritance

most x-linked conditions are recessive. this means that in a person with two x chromosomes (most females), both copies of a gene (i.e., one on each x chromosome) must have a change or mutation whereas in a person with one x chromosome (most males), only one copy of a gene must have a mutation. a female with a mutation in one copy of a gene on the x chromosome is said to be a “carrier” for an x-linked condition. a male with a mutation in a gene on the x chromosome is typically affected with the condition. because females have two copies of the x chromosome and males have only one x chromosome, x-linked recessive diseases are more common among males than females. however, x-linked recessive diseases can occur in both males and females.

for x-linked recessive disorders, an unaffected carrier mother who has a mutation in a gene on the x chromosome can transmit either the x chromosome with this mutation or a “normal” x chromosome to her children. if the father is unaffected, none of her daughters will be affected and all of her daughters will be unaffected—since they will inherit at least one normal x chromosome from their father. however, each daughter will have a 50% chance of being an unaffected carrier like her mother and a 50% chance of both x chromosomes being normal.

lesson summarykaryotypes a genome is the full set of all the genetic information that an organism carries in its dna. chromosomes arebundles of dna and protein found in the nucleus of a eukaryotic cell.