Answer:
The missing step is oxygen is removed from the water after step 3.
Explanation:
The steps listed by Xavier are:
- <em>Water is drawn in trough pores and enters the central cavity.
</em>
- <em>Food is filtered and digested.
</em>
- <em>Water leaves trough an opening at the top of the body.</em>
Porifera or sponges are aquatic, immobile invertebrates whose structure is saccular with an upper opening, the osculus.
Sponges absorb water through their pores, where the porocytes are found, and through flagellated cells -the coanocytes- the movement that allows the entrance of water to the spongocele or atrium is produced, in addition to the phagocytosis of organic elements.
Once the water is in the interior chamber of the sponges, the organic particles are phagocyted to be digested, and the oxygen is removed from the water, and passes through diffusion into the cell. The waste products, as well as carbon dioxide, are released into the water that will be expelled through the osculus.
<u><em>In Xavier's list, the missing step is the removal of oxygen from the water, before it is expelled from the body of the sponge</em></u><em>.</em>
<em />
Learn more:
Sponge structure brainly.com/question/11256747
Answer:
B
Explanation:
Its 23 in mitosis cell division
During the process of ossification, an existing tissue is replaced by bone.
Answer:
0.095
Explanation:
Phenylkentonuria is a disease caused by a recessive allele.
The frequency of the recessive allele + the frequency of the dominant allele equals 1.
The frequency of the recessive allele is q = 0.05
The frequency of the dominant allele then is p = 1 - q = 0.95
If people mate randomly, the frequency of the homozygous dominant genotype will be p², the frequency of the heterozygous genotype will be 2pq and the frequency of the homozygous recessive genotype will be q² .
2pq=2× 0.05 × 0.95
2pq=0.095
The heterozygote frequency in the population is 0.095
Answer:
e. a and d are correct
Explanation:
Meiosis produces 4 daughter cells that are haploid. Haploid means they have half of the chromosomes of the parent cell.