The ribosome, since all organisms need to synthesize proteins.
        
             
        
        
        
Answer: Although both are X-linked recessive conditions, and therefore more likely in males, with the single X-chromosome. The recessive allele in colour blindness occurs at a higher frequency in the population and is a mild condition. Thus colour blindness does occur to a lesser extent in females because it needs the double recessive condition. DMD is a severe, disabling condition with a limited lifespan, and recessive allele frequency much lower, so the double recessive condition in females is very rare.
Explanation: DMD is an X-linked recessive, “nearly always in males” suggest that it also occurs due to a new mutation or some rare condition e.g. double recessive from an affected father and carrier mother, or inactivation of the normal gene in a heterozygote. It is also found that the defective allele is not completely recessive and that female carriers may exhibit mild to moderate effects.
colour blindness is polygenic, although the genes are all X-linked. It is more common in males than females. Females can carry two recessive alleles and so express the phenotype, but this is uncommon because the frequency of the recessive gene is low.
There are similarities in that both are X-linked recessives, therefore commonly expressed in males, who only have one X chromosome. The gene frequency of the colour blindness recessive is much higher than that of DMD, so the double recessive condition, which affects females, is more likely to be seen with colour blindness. In addition, DMD is a severe condition associated with disability and limited lifespan, which reduces the probability of mating between an affected male and carrier female
 
        
             
        
        
        
They changed things up because its mixed or from up further in the family line. like your parents could have green eyes and you could get blue. it shoukd of came from your grandparents or other blood related relatives.
        
             
        
        
        
Answer: Gut microbiome degrade the ingested milk sugars through a biochemical pathway, producing ATP required for the energy needs of infant. 
Explanation:
The human breast milk fed on by infants  contains a high concentration of indigestible oligosaccharides which include lacto-N-tetraose and lacto-N-fucopentaose.
These milk sugars are utilized by microbes in the gut of infants, yielding lactate as the final product of metabolism and releasing several molecules of ATP as useful energy for use by the infant. 
Thus, the presence of these gut microbes at birth, and the feeding of infant with breast milk is vital to fulfilling their energy needs 
 
        
             
        
        
        
Answer:
Krill
Explanation:
All animals in the Antarctic depend on krill, very small crustaceans, for their survival.