Answer:
Volume= 4 cm³
Density= 2 g/cm³
Explanation:
We have the following data:
volume= V= 8 cm³
mass= m= 16 g
The density is the mass per volume of a substance, so the density of the rock is:
density= d= 16 g/8 cm³= 2 g/cm³
When we cut the rock in half, we have a half volume and a half mass:
V= 8 cm³/2= 4 cm³
m= 16 g/2= 8 g
But the density is not altered because it is an intrisic property - it does not change with the amount of subtance. Thus, the density of a half rock is:
d = m/V= 8 g/4 cm³= 2 g/cm³
Answer:
Nutrients support vital functions, including growth, the immune, the central nervous system, and preventing disease.
Explanation:
Water waves are an example of waves that involve a combination of both longitudinal and transverse motions. As a wave travels through the waver, the particles travel in clockwise circles. The radius of the circles decreases as the depth into the water increases. The animation at right shows a water wave travelling from left to right in a region where the depth of the water is greater than the wavelength of the waves. I have identified two particles in orange to show that each particle indeed travels in a clockwise circle as the wave passes.
C) The Cell Would Be Forced To Divide as substances continued to build up inside the cell
Normal colour vision (trichromacy) refers to vision that uses all three types of light cones. People with defected trichromatic vision will be colour blind to some extent and these conditions are called anomalous trichromacy. Three types anomalous trichromacy ( one type of cone perceives light slightly) :
1. Protanomaly – phenotype: reduced sensitivity to red light
2. Deuteranomaly - phenotype: reduced sensitivity to green light
3. Tritanomaly – phenotype: reduced sensitivity to blue
People can also have color blindess as the result of mutation, when loss of function of one cone occurs. This condition is called dichromacy. If there is complete color blindness or monochromacy, the person can’t distinguish any color from grey.
Color blindness is an inherited genetic disorder resulted from mutations on the X chromosome.
