Answer:
Explanation:
Australopithecina or Hominina is a subtribe in the tribe Hominini. The members of the subtribe are generally Australopithecus (cladistically including the genera Homo, Paranthropus,[2] and Kenyanthropus), and it typically includes the earlier Ardipithecus, Orrorin, Sahelanthropus, and Graecopithecus. All these related species are now sometimes collectively termed australopithecines or homininians.[3][4] They are the extinct, close relatives of humans and, with the extant genus Homo, comprise the human clade. Members of the human clade, i.e. the Hominini after the split from the chimpanzees, are now called Hominina[5] (see Hominidae; terms "hominids" and hominins).
While none of the groups normally directly assigned to this group survived, the australopithecines do not appear to be literally extinct (in the sense of having no living descendants) as the genera Kenyanthropus, Paranthropus and Homo probably emerged as sister of a late Australopithecus species such as A. africanus and/or A. sediba.
The terms australopithecine, et al., come from a former classification as members of a distinct subfamily, the Australopithecinae.[6] Members of Australopithecus are sometimes referred to as the "gracile australopithecines", while Paranthropus are called the "robust australopithecines".[7][8]
The australopithecines occurred in the Plio-Pleistocene era and were bipedal, and they were dentally similar to humans, but with a brain size not much larger than that of modern apes, with lesser encephalization than in the genus Homo.[9] Humans (genus Homo) may have descended from australopithecine ancestors and the genera Ardipithecus, Orrorin, Sahelanthropus, and Graecopithecus are the possible ancestors of the australopithecines.[8]
Answer:
<h2>2. Peter's maternal grandfather has PKU.</h2>
Explanation:
- Such type of the genetic disorder in which two copies of a gene must be mutated at a time is called autosomal recessive disorder such as sickle cell anemia, phenylketonuria, and some other diseases.
- When a sing copy of a gene is mutated in a person then this disorder is not appeared and the person is called a carrier.
- So when a child is born by two carrier parents then there is a chance that a child will be affected if both the parents donate mutated genes.
- In the case of Peter, since peter does not show this defect this means his maternal grandfather was affected by this disorder.
Answer:
Surface area to volume ratio, in simple means the size of surface area to the volume of substance that can pass through it at a particular time.
Amoeba and some bacterias are flat and have large surface area to volume ratio. So the diffusion rate is very high due to large surface area.
Where as humans have small surface area: volume so diffusion is very slow or does not take place at all.
Explanation:
As the ratio gets smaller, it takes longer for items to diffuse.
Explanation:
When the cell increases in size, the volume increases faster than the surface area, because volume is cubed where surface area is squared.
When there is more volume and less surface area, diffusion takes longer and is less effective. This is because there is a greater area that needs to receive the substance being diffused, but less area for that substance to actually enter the cell.
this is actually why cells divide. When they become too large and it takes too long for them to transport materials across the cell, they lose efficiency and divide in half to raise the surface area to volume ratio.
I HOPE TGIS HELPS PKEASE MARK ME AS BRAINLIEST
E.coli because e coli is a bacteria.
Answer:
TCTAAGCTTGGA
Explanation: adenine (A), thymine (T), cytosine (C) and guanine (G). Each base can only bond with one other, A with T and C with G.
