The environment determines how the genotype is expressed. The environment influences gene activity, which leads to a change in the phenotype of fur color.
Coloration of the fur of Himalayan rabbits is regulated by gene C. The rabbit raised at 20°C (left) has pigmentation on its ears, nose, and paws because the gene is active when environmental temperatures are between 15 and 25°C. These areas are where the rabbit's body loses the most heat. Because gene C is dormant at temperatures above 30°C, the rabbit raised in this environment (on the right) lacks fur pigmentation.
Gene expression for fur color in Himalayan rabbits is influenced by temperature. The follicle cells taken from Himalayan rabbits tend to die when kept at warmer temperatures. Himalayan rabbits use fur color to communicate fitness during the breeding season.
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T/ F
The all-or-none phenomenon as applied to nerve conduction states that the whole nerve cell must be stimulated for conduction to take place.
The all-or-none phenomenon as applied to nerve conduction states that the whole nerve cell must be stimulated for conduction to take place. Reflexes are rapid, automatic responses to stimuli. Efferent nerve fibers may be described as motor nerve fibers.
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is marfan syndrome caused by a substitution, insertion, or deletion mutationin the fbn1 gene
Marfan syndrome has been linked to deletions or errors in the fibrillin-1 (FBN1) gene (pathogenic variations).
What is Marfan syndrome?One defective copy of the Marfan gene inherited from one parent is all that is required to have Marfan syndrome, which is inherited as an autosomal dominant characteristic.
The remaining mutations in the FBN1 gene lead to an aberrant fibrillin-1 protein that is dysfunctional.
Therefore, the fibrillin-1 protein undergoes most of the mutations that result in Marfan syndrome by a single amino acid change.
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One year earlier, J. Herbert Taylor's experiments with Vivia faba came to a similar conclusion as this experiment. John Cairns used radioactively-labelled thymidine to explain why heat denaturation in this experiment occurred only with salmon sperm. A density gradient of cesium chloride was used for the ultracentrifugation step in this experiment. This experiment (*) disproved Max Delbruck's dispersive hypothesis. This experiment used E. coli grown on nitrogen-15, followed by growth on
nitrogen-14, and found that three-quarters of the second generation was light. For 10 points, name this experiment that proved DNA replication is semiconservative.
The Meselson and Stahl Experiment served as a test to demonstrate semiconservative DNA replication. To explore DNA replication, Matthew Meselson and Franklin Stahl performed an experiment in 1958 using the fast-diverging E. coli bacterium.
Who established semiconservative DNA replication?Mathew Meselson and Franklin Stahl established in 1985 that DNA replication is semi-conservative. They carried out their experiment on Escherichia coli bacteria.
How did the Meselson-Stall experiment demonstrate the semi-conservative nature of DNA replication?The semiconservative way of DNA replication is indicated by the lighter strand, which is the new one generated from the culture, and the heavier strand, which stands in for the parents. The replication of DNA in this way proved to be semiconservative.
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a type of bacteria doubles every (t) hours, and we will begin a culture with 10 bacteria. give the function that expresses the amount of bacteria b there will be after t hours
A type of bacteria doubles every (n) hours, and we will begin a culture with 10 bacteria. The amount of bacteria there will be after n hours will be: Y = 10* e²ᵇ
We must simulate the behavior of a function for use in practical applications. In mathematical modeling, we pick a well-known general function with characteristics that imply that it will model the actual phenomenon we want to study. When growth is brisk, we can pick the exponential growth function:
Y= A₀* eᵇⁿ
Y = 10* e²ᵇ
where, A₀ denotes the value at time zero that is initial number of bacteria, (e) denotes the Euler constant, and b is a positive constant that establishes the growth rate (%). Applications involving doubling time, or the time it takes for a number to double (n) , can be solved using the exponential growth function. Wildlife populations, investments, biological samples, and natural resources are examples of phenomena that can grow based on a doubling time.
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shown below are several molecules found in animal cells, along with their mass in daltons. based on the data gathered by loewenstein, et al. which molecule(s) would be excluded from moving through gap-junction channels? molecule approximate mass (daltons) histidine (an amino acid) 100 carnosine (a dipeptide) 226 thyroid-releasing hormone (trh, a peptide hormone) 360 atp 551 insulin (a peptide hormone) 5808 hexokinase (an enzyme) 50,000
Molecules that would be excluded from moving through gap-junction channels are insulin and hexokinase.
Connexins, a family of proteins articulated for most tissues of an organism, form gap junction channels.
Gap junction channels allow ions and other small molecules to pass between contacting cells, synchronizing them both electrically and metabolically. Gap junction channels are highly specialised intercellular connections that connect a wide variety of animal cell types. They connect the cytoplasm of two cells directly, allowing molecules, ions, and electrical impulses to transfer through a governed gate between cells.
Hexokinase is the first glycolytic enzyme, potentiating the phosphorylation of glucose by ATP to glucose-6-P. It is one of the glycolysis rate-limiting enzymes. As regular red cells age, their activity decreases rapidly.
Insulin is a peptide hormone created by pancreatic islet beta cells and encoded by the INS gene in humans. It is thought to be the body's primary anabolic hormone. Hexokinase is a potential insulin regulatory site that is irregular in insulin resistance. The modified regulation of hexokinase may play a significant role in the diminished insulin-mediated glucose flow rates in insulin-resistant skeletal muscle.
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Help help help please help help me 50 points for right answer
Identify the components of protein synthesis in this image. (One of these will not be used .)
In protein synthesis, 1. Ribosomes, 2. tRNA, 3. Amino acids and 4. mRNA.
What do you mean by protein synthesis?Protein synthesis is the creation of proteins by cells that uses DNA, RNA, and various enzymes. It generally includes transcription, translation, and post-translational events, such as protein folding, modifications, and proteolysis.
Moreover, protein synthesis represents the major route of disposal of amino acids. Amino acids are activated by binding to specific molecules of transfer RNA and assembled by ribosomes into a sequence.
Protein synthesis is a vital process because we need our bodies to be able to build the proteins that we need to perform important functions.
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The artery that bifurcates into the right subclavian artery and the right common carotid artery is the:
O brachiocephalic artery
O right common iliac artery
O right brachial artery
O right coronary artery
O superior vena cava
The artery that bifurcates into the right subclavian artery and the right common carotid artery is the brachiocephalic artery
The brachiocephalic artery or brachiocephalic trunk is an artery of the mediastinum that supplies blood to the right arm and the head and neck. It is the first branch of the aortic arch. Soon after it emerges, the brachiocephalic artery divides into the right common carotid artery and the right subclavian artery.
There is no brachiocephalic artery for the left side of the body. The left common carotid, and the left subclavian artery, come directly off the aortic arch. However, there are two brachiocephalic veins. The brachiocephalic artery arises, on a level with the upper border of the second right costal cartilage. The function of Brachiocephalic artery is to bring blood from heart to right arm, head, and neck.
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Things like your eye color and height are not under your control. This is because they are determined by your genes.
So, eye color is a good example of an inherited
A
height
Bestate
C carbohydrate
D
trait
A trait that is inherited is the color of the eyes. Both height and eye color are qualities that are influenced by multiple genes.
Which gene affects eye color?ASIP, IRF4, SLC24A4, SLC24A5, SLC45A2, TPCN2, TYR, and TYRP1 are among the genes with known effects on eye color. There is probably a continuum of eye hues in different persons due to the interactions between these genes, OCA2, and HERC2.
Exactly one gene determines eye color?Brown eyes are more prevalent than blue eyes, and eye color has historically been thought of as a single gene feature. At least eight genes have been found to affect the ultimate color of eyes, according to current research. Melanin levels in the specialized iris cells are regulated by genes.
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What was one weakness of Darwin's theory?
a. It lacked an explanation for adaptations.
b. It lacked an explanation for competition.
c. It lacked an explanation for how evolution occurs.
d. It lacked an explanation for the genetic inheritance of traits.
One weakness of Darwin's theory was that it lacked an explanation for how evolution occurs and is therefore denoted as option C.
What is Evolution?This is referred to as the change in the heritable characteristics of biological populations over successive generations and makes organisms better suited for their ever changing envrironment.
Darwin's theory of evolution on the other hand describes how organisms evolve over generations through the inheritance of physical or behavioral traits but lacked an explanation for how it occurs and it was termed the theory of evolution by natural selection.
It had an explanation about adaptations, competition and genetic inheritance of traits which is the treason why option C was chosen as the correct choice.
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One of the following organs is located on the Inferior surface of the liver in the right hypochondriac regions of the nine region plan:
Gall bladder
Pancreas
Left lobe of the liver
Right Lung
Artificial selection (chosen by person) and natural selection (best changed in the environment) differ in one major way- the forces that select which organisms are able to survive and reproduce. How are these processes different?
a. In natural selection, the organisms best adapted to survive in the environment are more likely to reproduce and pass on their traits, while in artificial selection, humans choose which organisms survive and reproduce.
b. In natural selection, humans choose which organisms survive and reproduce, while in artificial selection, the organisms best adapted to survive in the environment are more likely to reproduce and pass on their traits.
c. In natural selection, both the humans and the environment choose which organisms survive and reproduce, while in artificial selection technology chooses which organisms survive and reproduce.
d. In natural selection, technology chooses which organisms survive and reproduce, while in artificial selection, humans and the environment choose which organisms survive and reproduce.
I think it is A, but I believe two heads are better than one. So, check my answer pelase
The way that the processes of artificial and natural selection are different are: a. In natural selection, the organisms best adapted to survive in the environment are more likely to reproduce and pass on their traits, while in artificial selection, humans choose which organisms survive and reproduce. Option A
What is meant by artificial selection?Individual organisms with certain phenotypic characteristic values are chosen for breeding through a method called artificial selection. If the chosen characteristic exhibits additive genetic variation, it will respond to selection and change over time.
Because humans (rather than nature) choose which creatures get to reproduce, this process is referred to as artificial selection. The image below demonstrates how farmers have artificially selected for certain traits to develop several crops from wild mustard.
Artificial selection is directed by human preferences and differs from natural selection in that it is not random.
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Imagine you are a paleontologist trying to find the “missing link” between different species. In three to five sentences, create a fictional narrative about your discoveries, describing: 1) what two species, mythical or real, you are studying, 2) what evidence you have linking these species, and 3) what evidence you have to define different correlations and causations that support your hypothesis.
Why might a scientist use a physical model of a bacterial cell instead of
studying the cell directly?
In order for something to be considered a 16. Living things are based on a u living thing, it must display. of the eight Characteristics of life
Answer:living?
Explanation:
if two cells have different scaffolding proteins, explain how they might behave differently in response to the same signaling molecule.
If two cells have different Scaffolding proteins, they handle molecular elements of signaling pathways together in a complex. Various Scaffolding proteins would combine afferent protein collections, resulting in distinct cellular responses in the two cells.
Scaffolding proteins, as the name suggests, combine two or even more proteins in a comparatively stabilized configuration. There are numerous Scaffolding proteins found in nature, many of which have multiple protein-protein interaction modules.
The influence of a chromosome on Scaffold comprising non-histone proteins, known as Scaffolding proteins, has been the most significant structural discovery.
the proteins in a signaling pathway that connect with multiple cells. Based on the results of the analysis, 212 proteins were identified as Scaffolding proteins with statistical importance.
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- Most incidental motions:
may be debated after they are amended.
are always debatable.
are not debatable
may be debated if permission is granted.
Answer:
are always debatable.
which of the following crosses will not produce offspring with the recessive phenotype? select all that apply. a.tt x tt b.tt x tt c.tt x tt tt x tt d.tt x tt
The answer is (C). TTxTt, the other crosses will produce at least one offspring of recessive phenotype.
Punnett squares must be drawn in order to determine the probability and what happens to all the children.
The dominant trait is denoted by T, and the recessive by t.
TT x tt = Tt Tt Tt Tt = 100% Tt
The dominant allele will be present in every single offspring.
Tt x Tt = TT Tt tT tt =25% TT 50% Tt 25% tt
In this case, there is a 25% chance that the progeny will carry the recessive allele.
TT x TT = TT TT TT TT= 100% TT
The dominant allele will be present in every single offspring.
Tt x tt = Tt tt tt tt = 25% Tt 75% tt
In this case, there is a 75% likelihood that the progeny will carry the recessive allele. Thus TT x Tt will have the recessive phenotype in the offspring.
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The correct question is:
Which of the following will not produce offspring with the recessive phenotype?
Select one:
a. tt x tt
b. Tt x tt
c. TT x Tt
d. Tt x Tt
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the spinal cord extends from the foramen magnum of the to the first or second lumbar vertebra, where it terminates in the ______
The spinal cord extends from the foramen magnum of the skull to the first or second lumbar vertebra where it terminates in the fibrous extension called the filum terminale.
The spinal cord of a human being originates from the brainstem from which it passes through the cavity in the skull, also known as the foramen magnum and continues through the conus medullaris, which is near the second lumbar vertebra, and finally ends a fibrous extension. This fibrous extension is known as filum terminale. The parts of the brain stem consist of the midbrain, pons, and medulla oblongata, which is responsible for major body functions like body balance, sleep, heart rhythms, breathing, etc. Therefore, any physical damage to this part of the spinal cord can cause heartbeat fluctuations, heavy breathing, or loss of balance.
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Could the biological, psychological, and sociocultural factors behind psychological disorders all be correct, or is there only one factor that dominates
In psychological disorders, the biological, psychological, and sociocultural factors are all correct.
What are psychological disorders?Psychological disorders are disorders that affect the thought process of an individual.
Psychological disorders are all a combination of biological, psychological, and sociocultural factors.
The biological factors that are involved include the structure of the body organs especially the brain and other related organs and tissues. For example, when lesions occur in the brain, it could lead to psychological disorders.
Psychological factors are those factors that are not physical factors but affect the mind and emotions.
Sociocultural factors are the environmental factors that affect an individual.
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11. In 1996 the moose population dropped, what then happened to the wolf population in the following
year? Explain why.
Answer:
Due to the unfortunate loss of the moose population, the wolf population will also drop because primary prey is lost.
Explanation:
When a species becomes extinct or endangered, the life cycle is disarrayed. The butterfly affect is a great example; one factor makes a difference. Without chocolate, there are many recipies one can not make. Without moose, many wolves will starve.
the ability to wiggle your ears is an autosomal recessive trait that does not appear to benefit or harm the people who possess the trait. What is the genotypic ratio
The ability to wiggle the ears is an autosomal recessive trait that does not appear to benefit or harm the people who possess the trait, and the genotype is ee. E is taken for the ear.
What is the recessive trait?A recessive trait is expressed when two recessive alleles are present together, and in the case of an autosomal recessive trait, there are equal chances of inheritance and character expression in both males and females. In a recessive trait for the wiggle ear, the "E" is taken to represent, so the genotype is "ee," and this trait does not harm the person who inherits it.
Hence, this autosomal recessive trait is expressed as ee.
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What is the speed of a wave if it has a wavelength of 12 m and a frequency of 3 hertz?
Answer:
The speed of a wave is 36 m/s
Explanation:
Given;Wavelength (λ) = 12 mFrequency (f) = 3 Hz or s⁻¹To Find;Speed (v)So,
v = λ × f
v = 12 × 3
v = 36 m/s
Thus, The speed of a wave is 36 m/s
DRAW IT : The graph here shows the pH difference across the inner mitochondrial membrane over time in an active respiring cell. At the time indicated by the vertical arrow, a metabolic poison is added that specifically and completely inhibits all function of mitochondrial ATP synthase. Draw what you would expect to see for the rest of the graphed line, and explain graph.
When an ATP synthase is inhibited by a metabolic poison, the H+ concentration in the mitochondrial membrane rises, lowering the pH. As a result, the graphed line decreases gradually, indicating that pH decreases over time.
H+ would be pumped across the membrane into the intermembranous space, increasing the pH difference between the matrix and the intermembranous space. Because H+ cannot flow back through ATP synthase because the enzyme is constricted by the poison, the difference across the membrane will continue to increase rather than remain constant. Eventually, the concentration of H+ in the intermembranous space would become so high that no more H+ could be pumped against the gradient.
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The adrenal medullae are modified autonomic ganglia that secrete hormones that trigger effects similar to those of the ___________.
The adrenal medullae are modified autonomic ganglia that secrete hormones that trigger effects similar to the sympathetic division of the ANS.
The interior of your adrenal gland is called the medulla. hormones that control your autonomic nervous system are released. This system regulates automatic processes like heart rate that you ordinarily wouldn't think about. The hormones that start the flight or fight response are under the control of the adrenal medulla. Both epinephrine (adrenaline) and norepinephrine (noradrenaline), which have comparable roles, are the primary hormones released by the adrenal medulla.
The sympathetic division of autonomic nervous system sympathetic division extends glandular into the adrenal medulla. The medulla releases adrenaline and norepinephrine hormones into the blood stream when the sympathetic division is activated in response to stress or a threat.
Hence, both adrenal medulla and sympathetic division work in similar manner.
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The processes illustrated in the models depicted above all result in which of the following?
A) Transcription
B) An increase in genetic variation
C) horizontal gene transfer
D) an increase in the chromosome number
The process illustrated in the figure shows an increase in genetic variation.
The true choice is B
Genetic variation is a variation that occurs in the genome of an organism either in nucleotide bases, genes, or chromosomes. Genetic variation at the basic level is shown by differences in the base sequences of the nucleotides (adenine, thymine, guanine, and cytosine) that make up DNA in cells.
Genetic variation can be caused by several events, namely crossing over, conjugation, mutation, and fertilization. Genetic variation can be one of the factors that influence evolution.
Genetic variation is very influential in evolution because the greater the genetic variation in a population, the greater the chance for that population to adapt to environmental changes and disease.
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All of the following tools should be used to remove a hair sample from an object except
Osticky tape
tweezers
vacuum
Obrush
Brush are not used , Hair samples are primarily collected using tools tweezers, trace tapes, and vacuuming. Other methods of hair sample collection include combing and clipping methods.
What methods are employed in the forensic examination of hair?Three main types of hair analysis are conducted by forensic scientists: (1) testing the hair shaft for drugs or nutritional deficiencies in an individual's system; (2) analyzing DNA extracted from the root of the hair; and (3) examining hair under a microscope to determine whether it is from an individual or an animal.
How are hair samples collected?A hair drug test, commonly referred to as a hair follicle drug test, looks for both illicit drug use and prescription drug abuse, a little section of hair cut off of your head for this test. After that, the sample is examined for evidence of drug usage in the 90 days prior to the test.
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Gastric glands produce _________ and are part of the _______ system.
A. stomach acid, endocrine
B. oily sebum, endocrine
C. oily sebum, exocrine
D. stomach acid, exocrine
Answer:
Option D
explanation:
Gastric glands produce stomach acid and are part of the exocrine system. The exocrine system is a system of glands that produce and secrete substances directly into ducts that lead to the outside of the body, such as the skin or the digestive tract. Stomach acid is a digestive enzyme that is produced by the gastric glands and secreted into the stomach, where it helps to break down food. Therefore, the correct answer is option D, which states that gastric glands produce stomach acid and are part of the exocrine system.
Assuming no gene linkage, in a dihybrid cross of AABB x aabb with AaBb F1 heterozygotes, what is the ratio of the F1 gametes (AB, aB, Ab, ab) that will give rise to the F2 offspring?a.1:1:1:1b.1:3:3:1c.1:2:2:1d.4:3:2:1
Assuming no gene linkage, in a dihybrid cross of AABB x aabb with AaBb F1 heterozygotes, the ratio of the F1 gametes (AB, aB, Ab, ab) that will give rise to the F2 offspring is 1:1:1:1.
Gene linkage is the proclivity of genes or segments of DNA closely located somewhere along chromosomes to segregate together during meiosis and thus be inherited together.
Gene linkage evaluation is an effective method for determining the chromosomal position of disease genes. It is based on the discovery that genes that are physically close to one another on a chromosome stay connected during meiosis.
Genes that are close enough together on a chromosome will often seem to "stick together," and the variants (alleles) of those genes that are close together on a chromosome will more often than not be inherited as a pair. This is known as genetic linkage or gene linkage.
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Smooth ER makes ___________ and performs other ________________. It also ______________ poisons. It does not have __________ so it does not make _____________.
The generation of lipids and steroids is one of the many cellular processes carried out by the smooth endoplasmic reticulum.
What does the fluid ER produce? The generation of lipids and steroids is one of the many cellular processes carried out by the smooth endoplasmic reticulum.Additionally, it is essential to the detoxification of toxins, drugs, and alcohol.Blood detoxification is largely accomplished by liver cells.The Smooth Endoplasmic Reticulum's functions.The creation of lipids like cholesterol and phospholipids, which make up all of the membranes of the organism, depends on the smooth ER.Additionally, it plays a crucial role in the production and secretion of steroid hormones from lipid precursors like cholesterol.Animal liver cells also have a large number of smooth ER units.The organelle has a unique role in these cells.Enzymes are used in this instance by smooth ER to aid the liver's detoxification process.These enzymes disintegrate harmful substances, notably alcohol's ethanol.To learn more about endoplasmic reticulum refer
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part a which of these dna molecules is the shortest? a gel with the negative electrode at the top and the positive electrode at the bottom. the loading well is located at the top. dna fragments are labeled a, b, c, d, and e. fragment a is located at the top near the loading well. fragment b is located just below fragment a. fragment c is about halfway down the gel, and fragment d is just below it. fragment e is furthest down the gel, closest to the positive electrode. which of these dna molecules is the shortest? a gel with the negative electrode at the top and the positive electrode at the bottom. the loading well is located at the top. dna fragments are labeled a, b, c, d, and e. fragment a is located at the top near the loading well. fragment b is located just below fragment a. fragment c is about halfway down the gel, and fragment d is just below it. fragment e is furthest down the gel, closest to the positive electrode. a b c d e
The shortest DNA molecule is Fragment A. This is because it is located at the top near the loading well.
Fragment B is just below Fragment A, and Fragment C is about halfway down the gel. Fragment D is just below Fragment C, and Fragment E is the furthest down the gel, closest to the positive electrode.
The way gels work is that DNA molecules are loaded into the well at the top of the gel and then an electrical current is applied. The smaller molecules move faster and end up further down the gel. As Fragment A is the closest to the loading well, it is the smallest molecule, and hence the shortest. Therefore, Fragment A is the shortest DNA molecule.
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