The northern red-legged frog, or rana aurora, is found along the western coast from british columbia to northern california. their typical breeding season lasts from january to march. the foothill yellow-legged frog, or rana boylii, is found along the western coast from northern oregon to central california. their typical breeding season lasts from april to july. what mechanism might keep rana aurora and rana boylii from mating?
anatomical isolation
temporal isolation
geographic isolation
behavioral isolation

In a hypothetical breed of dogs, coat color is controlled by two genes. there are six different coat colors in this breed: black, brown, cream, gray, silver, and tan. consider the following crosses.cross 1: black females from a lineage of all black dogs are crossed with brown males from a lineage of all brown dogs. f1 males and females are all black. when f1 are intercrossed, f2 males and females are black or brown.cross 2: black females from a lineage of all black dogs are crossed with tan males from a lineage where all males are tan and all females are cream. f1 males are black, f1 females are gray. when f1 are intercrossed, f2 males and females are black, brown, gray, or tan.cross 3: silver females from a lineage where all females are silver and all males are gray are crossed with brown males from a lineage of all brown dogs. f1 males and females are all gray. when f1 are intercrossed, f2 males are black, brown, gray, or tan, f2 females are cream, gray, silver, or tan.select the correct statements regarding the mode of inheritance of the coat color genes.a) both genes are x-linked.b) both genes are autosomal.c) one of the genes modifies the expression of the other gene.d) each gene has an additive effect on the intensity of coat color.e) each gene independently specifies three colors.f) one of the genes is autosomal, and the other is x-linked.

Approximately 90% of all cases of polycystic kidney disease are inherited in an autosomal dominant fashion. the disease is typically related to mutations to genes (pkd1 and pkd2). pkd genes can be found on chromosome 16. the disease occurs in approximately 1: 800 to 1: 1000 people. here is a hypothetical example. the dominant allele d will cause the development of pkd. the recessive allele is known as d. what genotypes would correspond to suffering from pkd? dd, dd what genotypes would correspond to being normal (not suffering from pkd)? dd consider that 1: 1,000 people have pkd in your population of 325million. consider that pkd is inherited in an autosomal dominant fashion. show you math for all of the following questions: what is the genotypic frequency for dd? what is the genotypic frequency for dd? what is the genotypic frequency for dd? what is p? what is q? how many people in your population would have pkd?

To sciences do not agree on which type of grocery bag is better for the environment what is most likely to come out come out of the disagreement