You are confronted with a box of preserved grasshoppers of various species that are new to science and have not been described. your summer job is to separate them into species. there is no accompanying information as to where or when they were collected. which species concept will you have to use?

The answer is Morphological Species Concept

Explanation:

Species concept includes defining the differences between two or more species, especially similar species.

Morphological Species Concept is also known as Typical Species Concept, it includes defining these differences in species using their morphological attributes such as difference in shapes of their bodies, form, structure, colors, what they look like in the inside.

The Morphological Species Concept takes into account the Anatomical features or structures and not the genetic makeup or DNA of the species.

Morphological Species Concept

The Morphological Species Concept is also known as Typical Species Concept, it includes defining these differences in species using their morphological attributes such as difference in shapes of their bodies, form, structure, colors, what they look like in the inside. It takes into account the Anatomical features or structures and not the genetic makeup or DNA of the species.

i believe it would be the lungs.

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.