Glycolysis, Link reaction, the Krebs cycle, and the electron transport chain.
The force of gravity causes mass wasting to occur faster.☺
Answer:
The humerus-
A long bone of the upper forelimb. It articulates proximally with the scapula to form the soulder joint and distally with the radius and ulna to form the elbow joint.
Proximally the humerus has a rounded projection known as the head.
Cranially at the lateral aspect of the head is a large prominence- the greater tubercle. The lesser tubercle lies medially. Both tubercles act as a sight for muscle attachment. At the distal end of the humerus is a condyle which articulates with the radius & ulna & forms part of the elbow.
The diaphysis of the humerus is twisted.
In the dog a supra condylar foramen is present- a large hole in the condyle.
The Femur-This is the thigh bone and is the largest bone in the body, it is a long bone and is similar in structure to the humerus in that it has a head, neck, shaft & lateral & medial condyles. The femoral head articulates with the acetabulum proximally to form the hip joint, lateral to the head is the greater trochanter and on the medialTh side is a lesser trochanter (for muscle attachment). At the distal end of the femur are 2 condyles that articulate with the tibia to form the stifle joint. Between the 2 condyles is the trochlear groove along which the patella can move.
Explanation:
To first dive into your question, here are some vocabulary terms that I will be using and will be helpful to you as well.
- Homozygous dominant (BB): <em>Is not affected by cystic fibrosis</em>.
- Homozygous recessive (bb):<em> Is affected by cystic fibrosis</em>.
- Heterozygous (Bb):<em> A carrier for cystic fibrosis</em>.
- Phenotype (Ex: Having cystic fibrosis): <em>The appearance of an allele pair</em>.
- Genotype (Ex: bb): <em>The genetic makeup of an allele pair</em>.
We know that if both of the parents are phenotypically normal, there is no way that they can be homozygous recessive (bb), or have cystic fibrosis. We also know that since they have a child with this disease, they can't be homozygous dominant (BB) either. This means that <u>both parents have to be carriers (Bb)</u> in order for them to have a child with cystic fibrosis.
Below I have attached a Punnett square with both of the heterozygous parents.
<em>Each child they have will have a </em><u><em>1/4</em></u><em> or </em><u><em>25%</em></u><em> chance of having cystic fibrosis.</em>
The alimentary canal includes mouth, esophagus, stomach, small intestine, and large intestine. As food passes through the alimentary canal, it is exposed to the different chemical secretions from the organs of the alimentary canal, as well as from other organs, such as liver and pancreas.
First, in the mouth, salivary glands produce saliva which <span>contains enzymes involved in the food digestions. After the food is passed to the esophagus, it produces mucus to help passage of the food. In the stomach, acid and pepsinogen, as well as mucus are produced. All of these secretions help food digestion. Small intestine also produces some digestive enzymes. Further, bile from liver and enzymes from pancreas are secreted via ducts into small intestine. Finally, large intestine secretes mucus for lubrication.</span>