Answer:
The correct answers are "heterozygous", and "homozygous dominant".
Explanation:
Galactosemia is a condition where people are not able to process the sugar galactose. People with this condition have one gene mutated, which does not allow the proper synthesis of the enzyme that breaks down galactose. Galactosemia is inherited as an autosomal recessive genetic condition, therefore, only children that are homozygous recessive develop the condition. Children that are heterozygous or homozygous dominant, will not develop galactosemia.
Sponges are similar to other animals in that they are multicellular, heterotrophic, lack cell walls and produce sperm cells. Unlike other animals, they lack true tissues and organs, and have no body symmetry.
The shapes of their bodies are adapted for maximal efficiency of water
flow through the central cavity, where it deposits nutrients, and leaves
through a hole called the osculum. Many sponges have internal skeletons of spongin and/or spicules of calcium carbonate or silicon dioxide. All sponges are sessile
aquatic animals. Although there are freshwater species, the great
majority are marine (salt water) species, ranging from tidal zones to
depths exceeding 8,800 m (5.5 mi).
Most irregular galaxies are thought to have formed from <span>collisions between other galaxies.
This is just one wat that irregular galaxies are formed; the collision is due to the interaction of their gravitational forces. These galaxies might have been regular before the collision, but are not deformed.
Another form of irregular galaxies are the ones that are still very young and therefore have not yet reached their symmetrical state.</span>
Increasing the light intensity increases the rate of photosynthesis, until some other factor - a limiting factor - becomes in short supply. At very high light intensities, photosynthesis is slowed and then inhibited, but these light intensities do not occur in nature.
