Answer:
Following are the ways captive breeding helps conserve biodiversity:
- Captive breeding can increase population numbers
- Captive breeding can help remove species from the Endangered Species List
- Captive breeding can result in the eventual release of offspring into the wild.
Explanation:
Captive Breeding:
Captive breeding is an ex-situ conservation technique (taking the animal out of its natural habitat to increase population numbers in zoos or sanctuaries). Captive breeding involves selective breeding of endangered species to help produce a sizable population that can later be introduced back into the wild when their habitat improves.
Captive breeding programs include zoos, sanctuaries located away from the animal's original habitat. For example, the Toronto Zoo has operated a captive breeding program for the Blanding's turtle since 2012. The turtles are kept their for 2 years after birth and then released back into the wild.
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Answer:
In allosteric inhibition, a regulatory molecule binds to a location other than the active site, resulting in a change in enzyme shape that allows the active site to bind substrate.
Explanation:
Allosteric regulation of an enzyme can be positive or negative, but it always involves effector molecules that bind to non-active site of the enzyme and change its conformation. That site of binding is called allosteric or regulatory site. If the enzyme activity is enhanced effector molecule is called allosteric activator but if the activity is decreased effector molecules are allosteric inhibitors.
A group of tissue that work together is a organ
Answer:
Spindle fibers form a protein structure that divides the genetic material in a cell. The spindle is necessary to equally divide the chromosomes in a parental cell into two daughter cells during both types of nuclear division: mitosis and meiosis. During mitosis, the spindle fibers are called the mitotic spindle.
Explanation:
Answer and Explanation:
The cell division cycle is responsible for increasing and maintaining cell number and size. This cycle is an essential feature of living organisms. There are four phases of cell division mitotic phase (M phase), growth phase 1 (G1), growth phase 2 (G2), and synthesis phase (S). One phase of the cell cycle ends, and the other starts; this is named a phase transition—a unidirectional alteration in the cell cycle phases. During G1, G2, and S phase cell grows and during the M phase cell divides. There are two models of cell reproduction as the clock model and the domino model. The domino model implies that cell division phases must occur in a distinct order and at a definite time. The domino model recommends that the cell cycle events are independent, while the clock model shows that the effectiveness of mitosis entrance was not persuaded by other actions.
