Yes, beetles can adapt to almost any environment. they are usually found where they eat, and some species help get rid of garbage, dead plants and even help pollenate flowers. however red beetles feed off of lily’s(i think?), so they feed off of those flowers and if you see them your lilies may be at risk.
Answer:
C. Fi 1:0, F2 3:1
Explanation:
Firstly, Mendel's law of segregation states that the alleles of a gene will randomly separate into gametes during gamete formation. In this case involving a single trait, hence, a single gene. Mendel crossed two purebreeding plants i.e. homozygous plants that produced different phenotypes for the same gene. He obtained his offsprings which he called F1 offsprings. He realized that all the F1 offsprings expressed only one phenotype. For example, when he crossed homozygous tall (TT) and short (tt) plants, he got F1 offsprings that were all tall.
He then self-crossed these F1 offsprings to produce a F2 offsprings that had a phenotypic ratio of 3:1 i.e. 3tall, 1short plant. He concluded that the alleles of the single gene had segregated into the gametes but one allele was capable of masking the expression of another, as seen in the heterozygous F1 offsprings that were all tall (Tt).
Hence, he obtained a 1:O ratio for his F1 offsprings then a 3:1 ratio for his F2 offsprings.
The Mitochondria's main function is to create ATP, otherwise known as <span>adenosine triphosphate. ATP is a type of energy, so mitochondria do create energy. Therefore, the answer to your query is true. Hope this helps and have a great day!</span>
Answer:
Explanation:
Galactosemia is an inherited metabolic disorder caused by changes, or mutations, in both copies of an individual’s GALT gene. In the majority of cases, children with galactosemia do not have parents with galactosemia. Mother and father separately are a silent carrier of the condition, which is expressed in the child (autosomal recessive inheritance).
Each individual has two copies of the GALT gene – one from father and one from mother. In case of any changes of these genes (mutations) that prevents the gene from working correctly. In order to inherit galactosemia, it is necessary for a child to have two GALT gene changes. In case of one GALT gene change there is no galactosemia.
Infants with galactosemia may be identified through newborn screening programs or by symptoms that present during the first few weeks of life. Untreated infants develop liver and kidney disease, cataracts in their eyes, and serious infections.
