Carbon cycles from the atmosphere into plants and living things. For example, carbon is a pollutant in the atmosphere as carbon dioxide.
...
Photosynthesis. Plants pull in carbon dioxide out of the air through photosynthesis. ...
Decomposition. ...
Respiration. ...
Combustion.
I hope that this one is correct - C
Since transpiration is the process of water movement through a plant and its evaporation from aerial parts, such as leaves, stems and flowers.
All organisms in a certain area make a *community*
We know that Hardy-Weinberg conditions include the following equations:

where 
And where p = dominant, and q = recessive; this means that
is equal to the homozygous dominant,
is the heterozygous, and
is the homozygous recessive .
So we have 100 total cats, with 4 having the recessive white coat color. That means we have a ratio of
or 0.04. Let that equal our
value.
So when we solve for q, we get:


Now that we have our q value, we can use the other equation to find p:



So then we can solve for our heterozygous population:

This is the ratio of the population. So we then multiply this number by 100 to get the number of cats that are heterozygous:

So now we know that there are 32 heterozygous cats in the population.
The formula for finding the kinetic energy of an object is:
KE = 0.5MV^2,
Where:
M= Mass
V = Speed
From the information given above,
M = 21 kg
V = 3 m/s
KE = 0.5 * 21 * 9 = 94.5
Therefore, the canoe's kinetic energy is 94.5 J
Answer:
The C. elegans embryo is a powerful model system for studying the mechanics of metazoan cell division. Its primary advantage is that the architecture of the syncytial gonad makes it possible to use RNAi to generate oocytes whose cytoplasm is reproducibly (typically >95%) depleted of targeted essential gene products via a process that does not depend exclusively on intrinsic protein turnover. The depleted oocytes can then be analyzed as they attempt their first mitotic division following fertilization. Here we outline the characteristics that contribute to the usefulness of the C. elegans embryo for cell division studies. We provide a timeline for the first embryonic mitosis and highlight some of its key features. We also summarize some of the recent discoveries made using this system, particularly in the areas of nuclear envelope assembly/ dissassembly, centrosome dynamics, formation of the mitotic spindle, kinetochore assembly, chromosome segregation, and cytokinesis.
1. The C. elegans embryo as a system to study cell division
The C. elegans embryo is a powerful model system for studying the mechanics of metazoan cell division. Its primary advantage is that the syncytial gonad makes it possible to use RNA interference (RNAi) to generate oocytes whose cytoplasm is reproducibly (>95%) depleted of targeted essential gene products. Introduction of dsRNA rapidly catalyzes the destruction of the corresponding mRNA in many different systems. However, depletion of pre-existing protein is generally a slow process that depends on the half-life of the targeted protein. In contrast, in the C. elegans gonad, the protein present when the dsRNA is introduced is depleted by the continual packaging of maternal cytoplasm into oocytes (Figure 1). Since depletion relies on the rate of embryo production instead of protein half-life, the kinetics tend to be similar for different targets. By 36-48 hours after introduction of the dsRNA, newly formed oocytes are typically >95% depleted of the target protein.
Explanation: