True. If we all work together to conserve our resources, then the earth will be able to sustain its human population. In this century, many people don't really care about conserving resources because they are too careless to think about how much resources we are wasting on a daily basis. If everyone realizes how much resources we are wasting and helps to conserve them, than earth will have sufficient resources to sustain its human population.
hope this helps:)
please mark thanks and brainliest:)
Cuz they combine during fertilization and since 2 halves = 1 whole, u get gametes w a full number of chromosomes
The correct option is A ie the process whereby non-sister chromatids exchange genetic material
- Between prophase I and metaphase I, a process known as crossing over occurs in which two homologous non-sister chromatids join up and exchange various pieces of genetic material to create two recombinant chromosome sister chromatids.
- When genetic material is switched between two chromosomes, this process is known as crossing over.
- It is in charge of causing genetic variation among members of a species.
- Only the reproductive cells known as gametes undergo this process.
- The steps involved in crossing over are as follows:
1) Synapsis.
2) Chromosome duplication
3) Crossing over.
4) Terminalizataion.
Learn more about crossing over here :
brainly.com/question/20662534
#SPJ10
According to the Doppler effect, the sound of a police car siren is louder and high pitched as it approaches the observer.
Answer:
B. The father did not contribute a sex chromosome to his daughter due to nondisjunction of the sex chromosomes. The daughter is XO and her only X chromosome came from her mother, who was a carrier.
A.The mother's X chromosomes failed to separate during meiosis, and the daughter inherited two X chromosomes with the Lesch-Nyhan mutation. The father contributed no sex chromosomes.
Explanation:
As seen in the question above, a little girl was diagnosed with Lesch-Nyhan syndrome, which is an X-linked recessive condition caused by a mutation in the HPRT1 gene responsible for purine metabolism.
The little girl's parents do not have the syndrome, and no one in the little girl's paternal family presented this syndrome, however, we know that the maternal grandfather of the little girl's mother had the syndrome, which means that it was the mother's genetic material that contributed to the development of the syndrome in the little girl. This was because the little girl did not receive any X chromosomes from her father, but she inherited the two X chromosomes from her mother that coded for the Lesch-Nyhan mutation. This happened because the mother's X chromosome disjuction did not occur during meiosis I.
As shown above, the father did not contribute any sex chromosomes to his daughter, which means that the daughter is XO and her only X chromosome came from her mother, who was a carrier.