Answer:
Sea caves
Explanation:
Sea caves is a land form that is formed in a cliff by the action of wave of the ocean or lakes. It is called littoral cave and mainly formed by wave action of a sea which involved the process of mechanical erosion and occur in clogged coast where there is break in the wave or wave action.
A high level of gene flow into a population increases genetic diversity in a population. A high level of gene flow out of a population decreases genetic diversity in a population. Genetic drift is the change in allele frequencies due to "sampling error" factors. Typically, genetic drift has the biggest impact on small populations.
Gene flow (or gene migration) is a mechanism of evolution (change the allele frequencies) which transfers genetic variation among populations due to migration. High level of gene flow decreases the genetic differentiation between the two populations.
Genetic drift is a mechanism of evolution that acts by chance (“sampling error”) often when a population is reduced in size by a natural disaster (bottleneck effect) or when a small group leaves the main population and forms a colony (founder effect).
Our weight on moon is less than it would be on Earth due to a difference of the strength of gravity on the moon. The moon's gravitation force is determined by the mass and the size of the moon. ... This means that if you went to the moon you would weigh less, even though your mass stays the same
Answer:
Asparagine
Explanation:
Glycans are structures made up of chains of simple sugar molecules joined together by chemical bonds. N-linked glycosylation, is the attachment of an oligosaccharide, sometimes referred to as glycan, to the amide nitrogen the amino acid asparagine (Asn) residue of a protein, in a process called N-glycosylation. This linkage is most of the time important for the structure and function of the the protein they are linked to.
Answer: <em>D. Causes an accumulation of lipids in brain cells</em>
Explanation:
Tay-Sachs disease is caused by a genetic mutation in the <em>HEXA</em> gene. It is an autosomal recessive disease that causes the mutation on an enzyme, which metabolizes <em>GM2 Ganglioside</em> in nerve cells, this leads to a build-up of the molecule in brain cells. At the moment there is no cure for the disease, only support treatment is available.