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Amanda [17]
3 years ago
10

Which piece of information would be useful to someone studying evolution, but also to someone trying to identify and classify an

unknown organism that they think is new to science?
Biology
2 answers:
Archy [21]3 years ago
7 0

the linnian taxonomy thingy

ozzi3 years ago
6 0

a phylogenetic tree diagram would be helpful

You might be interested in
In humans, the eye color and hair color genes are located on different chromosomes. Brown eyes (B) are dominant to blue (b), and
Andrej [43]

Answer:

Man's genotype: Bbdd

Woman's genotype: bbDd

First child's genotype: Bbdd

Second child's genotype: bbDd

Explanation:

This is a dihybrid cross involving two genes; one coding for eye color and the other for hair color in humans. The allele for brown eye (B) is dominant over the allele for blue eyes (b) in the first gene while the allele for dark hair (D) is dominant over the allele for red hair (d) in the second gene.

According to the question, A man with brown eyes and red hair will possibly possess genotypes: BBdd or Bbdd while a woman with blue eyes and dark hair will possibly have genotype: bbDD or bbDd. Considering the fact that they produced children with recessive traits for both gene (blue eyes and red hair), it means that they are heterozygous for their dominant trait. This means that the ideal genotype for the man is Bbdd since he will produce gametes containing B and b alleles for the first gene while the ideal genotype for the woman is bbDd since it will produce gametes with D and d allele for the second gene.

Hence, a child with brown eyes and red hair will possess genotype: Bbdd since he/she cannot receive two dominant alleles for the first gene from both parents. A child with blue eyes and dark hair will have genotype: bbDd since he/she cannot receive two dominant alleles of the second gene from both parents.

3 0
2 years ago
How many atoms of nitrogen are in a chemical formula Ni(NO3)2?<br> O 3<br> O 2<br> O 1<br> O 6
Julli [10]
The answer is 2 because its the outside number and not in the parentheses
7 0
3 years ago
Read 2 more answers
when measuring the blood pressure, the cuff is deflated until two consecutive beats are heard through the stethoscope. This meas
dem82 [27]

Answer: Systolic pressure.

Explanation:

Every time the heart beats, it pumps blood into the arteries, which are vessels through which blood circulates from your heart to your tissues with the oxygen and nutrients they need. Blood pressure is the force of the blood pushing against the walls of the arteries, and is highest when the heart beats, pumping blood, which is measured as systolic pressure (i.e., when the heart contracts). On the other hand, diastolic blood pressure refers to the pressure of blood in the artery when the heart relaxes between beats (i.e., when the heart relaxes). Since there are two types of pressures, blood pressure readings are given in two numbers, with the top number being the systolic pressure and the bottom number being the diastolic pressure.  

For example, if the systolic pressure measured in a person is 125 millimeters of mercury (mm Hg) and the diastolic pressure is 85 mm Hg, the blood pressure is recorded as 125/85.  

So, <u>the systolic blood pressure is registered with the stethoscope when the cuff is deflated.</u> When two heartbeats are heard, the pressure gauge reading is recorded. <u>When the heartbeat ceases, the cuff pressure is released and the diastolic pressure is measured at this time.</u>

4 0
3 years ago
Leigh's disease is a mitochondrially inherited disease with symptoms that include seizures, fatigue, impaired reflexes, breathin
Ahat [919]

About the question:

You will find the pedigree in the attached files

Answer:

  • individual 4 → Affected woman → Black circle
  • individual 5 → Affected woman or man → Black circle or square
  • individual 7 → Healthy woman → Empty circle
  • individual 10 → Affected boy → Black Square

Explanation:      

Mitochondrial inheritance is the transmission of a disease or a trait from the maternal line.

<em>Most of the DNI is in the nucleus, but there is also DNI in mitochondria. Sperm cells hardly transfer mitochondrial genes to the progeny</em>, so mitochondrial DNI is mostly inherited from the maternal side. If there exists any mutation in this mitochondrial DNI, the whole progeny of the mutated woman will be affected, as they will get the mother genotype carrying the mutation. On the contrary, if an affected man is carrying a mutation in mitochondrial DNI, non of their descendants will get the disease.

Before answering the question, let us remember the pedigree symbols.

  • Squares represent Males/Men
  • Circles represent Females/Women
  • Empty symbols represent healthy/non-affected individuals
  • Solid black symbols represent sick/affected individuals

In the exposed pedigree, we can see that the mother is affected by the disease (individual number 2), so all her children are also affected (individuals 4, 5, and 6) because the <em>disease is mitochondrially inherited</em>.

Individual 3 is a healthy man, so individual 4 must be an affected woman (Black circle). As she is the one affected, then all her children will also be affected. This couple <em>had one boy and two girls</em>. Individuals 8 and 9 are girls (circle), so individual 10 must be the affected boy (black square).  

On the other hand, individual 6 is an affected man (black square), son of individuals 1 and 2. This man couples with a woman, and they have all healthy children. So this woman (individual 7) must be healthy. Even though the man is affected, all their children are not because their mother (7) is not. Remember that sperm cells do not transmit the mitochondrial genes to the progeny.      

And finally, individual number 5 might be either a man or a woman. In any case, this person is also affected by Leigh's disease.  

5 0
3 years ago
Which of the following organs is NOT a part of the immune system?
morpeh [17]

Answer:

I think is D because I had this question

6 0
2 years ago
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