Answer:
Dark yellow ,small volume pea.
Infrequent pea.
Dry mouth and tongue.
Sunken eyes.
Dehydration is a condition in which the rate at which the body looses t fluids is higher than the rate at which it takes fluids in.
It is caused by diarrhoea( watery stools )
2.Excessive sweating.
3 vomiting continusly.
4. No access to water intake
5.Polyuria(excessive urination)
6.Fever leading to hyperthermia.
The kidney is the main organ where the effect of dehydration is managed . As a result of increase in the solute potential of the blood,;the hypothalamus secrets ADH hormones which stimulates the Aquaporins(transmembrane proteins in the collecting duct and the distal convoluted tubules) to open .Therefore water moves in by osmosis to reduce the higher solute potential of the blood. Therfore low volume,high concentrated urine is produced.
This homeostatic function of the kidney ensures balanced in the electrolyte fluids of the body to manage dehydration,before medical intervention.
Explanation:
I believe it would be a because your body is stimulated to drink water when you are dehydrated
Answer:
the conclusive evidence about CFCs (chlorofluorocarbons) and the ozone layer of the earth.
Explanation:
Susan Solomon, Web of Science article reveals the conclusive evidence that CFCs (chlorofluorocarbons) could be destroying the protective layer of ozone in the earth’s upper atmosphere. CFCs are compounds that have the potential to destroy the protective layer of ozone (an oxygen compound) in the earth’s upper atmosphere.
Answer:
B: When severe weather occurs causing large waves to hit the coast.
Explanation:
when coastal flooding occurs, storms push the seasonal high tides towards the shore which causes the flooding
Answer:
Each mutant would be mated to wild type and to every other mutant to create diploid strains. The diploids would be assayed for growth at permissive and restrictive temperature. Diploids formed by mating a mutant to a wild type that can grow at restrictive temperatures identify the mutation as recessive. Only recessive mutations can be studied using complementation analysis. Diploids formed by mating two recessive mutants identify mutations in the same gene if the diploid cannot grow at restrictive temperature (non-complementation), and they identify mutations in different genes if the diploids can grow at restrictive temperature (complementation).
Explanation:
Recessive mutations are those whose phenotypic effects are only visible in homo-zygous individuals. Moreover, a complementation test is a genetic technique used to determine if two different mutations associated with a phenotype colocalize in the same <em>locus</em> (i.e., they are alleles of the same gene) or affect two different <em>loci</em>. In diploid (2n) organisms, this test is performed by crossing two homo-zygous recessive mutants and then observing whether offspring have the wild-type phenotype. When two different recessive mutations localize in different <em>loci</em>, they can be considered as 'complementary' since the heterozygote condition may rescue the function lost in homo-zygous recessive mutants. In consequence, when two recessive mutations are combined in the same genetic background (i.e., in the same individual) and they produce the same phenotype, it is possible to determine that both mutations are alleles of the same gene/<em>locus</em>.