Bainliesttt - explain how tidal bulges form. -how are high tides and low tides formed? how often do they occur?

Tidal bulges are formed during high tides, when the gravitational pull of the moon causes the surface of the ocean to rise on both the side of the earth facing the moon, and its direct opposite. There are always two lunar tidal bulges on Earth. (http://www.scienceclarified.com/Ti-Vi/Tides.html)

High tides are formed when the moon pulls the surface of the ocean upward. Low tides are formed when that gravitational pull is lessened and the water sinks. Because of the moon's and Earth's orbit, the tides are both a daily occurrence, and a seasonal one. During Spring Tides and "Neap" Tides, there are especially high and low tides around the planet. (https://www.qldscienceteachers.com/junior-science/astronomy/tides-eclipses-day-night-seasons)

this will help (https://www.qldscienceteachers.com/junior-science/astronomy/tides-eclipses-day-night-seasons)

an individual’s sex (i.e., whether they are a male or female) is determined by the sex chromosomes. most people have two sex chromosomes, one that is inherited from their mother and one that is inherited from their father. typically, females have two x chromosomes (xx) and males have one x chromosome and one y chromosome (xy). conditions caused by changes (“mutations”) in genes located on the x chromosome are considered x-linked.

x-linked recessive inheritance

most x-linked conditions are recessive. this means that in a person with two x chromosomes (most females), both copies of a gene (i.e., one on each x chromosome) must have a change or mutation whereas in a person with one x chromosome (most males), only one copy of a gene must have a mutation. a female with a mutation in one copy of a gene on the x chromosome is said to be a “carrier” for an x-linked condition. a male with a mutation in a gene on the x chromosome is typically affected with the condition. because females have two copies of the x chromosome and males have only one x chromosome, x-linked recessive diseases are more common among males than females. however, x-linked recessive diseases can occur in both males and females.

for x-linked recessive disorders, an unaffected carrier mother who has a mutation in a gene on the x chromosome can transmit either the x chromosome with this mutation or a “normal” x chromosome to her children. if the father is unaffected, none of her daughters will be affected and all of her daughters will be unaffected—since they will inherit at least one normal x chromosome from their father. however, each daughter will have a 50% chance of being an unaffected carrier like her mother and a 50% chance of both x chromosomes being normal.

a symbiotic relationship with the mitochondria