which of the letters in the figure indicates the vagus nerve? a) A. b) B. c) C. d) D.

Answers

Answer 1

The parasympathetic cranial outflow includes the vagus nerve (cranial nerve X), which regulates the normal operation of the organs in the thoracic and upper abdominal cavities. Thus, option A is correct.

What is the parasympathetic cranial outflow?

The third, seventh, ninth, and tenth cranial nerves, as well as the second and third sacral nerves, are the exit points for the neurones of the parasympathetic nervous system from the central nervous system. The craniofacial outflow is another name for this branch.

When there is a threat, the sympathetic nervous system gets the body ready for the “fight or flight” reaction.

Therefore, The parasympathetic nervous system, on the other hand, prevents the body from overworking itself and returns it to a calm, collected state.

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Related Questions

Summarize the phases of cellular respiration.

Answers

1. Glycolysis: This is the first phase and takes place in the cytoplasm. During glycolysis, a single molecule of glucose (a sugar) is broken down into two molecules of pyruvate. This process generates some ATP and also prepares the glucose for further breakdown.

2. The citric acid cycle (also known as the Krebs cycle or tricarboxylic acid cycle): This phase takes place in the mitochondria. The pyruvate produced during glycolysis is further metabolized and converted into ATP, carbon dioxide, and water. The citric acid cycle also generates electrons that will be used to generate more ATP in the next phase.

3. Electron Transport Chain (ETC): This is the final phase and also takes place in the mitochondria. The electrons generated during the citric acid cycle are passed through a series of proteins in the inner mitochondrial membrane, generating a proton gradient that drives the production of ATP. This process is known as oxidative phosphorylation and generates the majority of the ATP produced during cellular respiration.

the collection of microorganisms that live on or on a human host in a mutually beneficial way is called the human ______.

Answers

The collection of microorganisms that live on or on a human host in a mutually beneficial way is called the human microbiota

They generally resides in skin and intestines of the host in helping them, play  a crucial role in maintain health of the organism host.

some are infectious too that live on host like, our single celled or multi celled organism ex: candidiasis which causes yeast infection and athelete foot by tinea and also the  helminths parasitic worms that lives on or in host

The role of this microbiota exist in stomach helps in to exists symbiotically within the human digestive system and also helps support energy production, digestion, and immune defense.

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If an increase in global temperatures causes parts of Alaska to remain snow free for two additional weeks each year, what affects might that have on earth? Describe 2-3 effects that may be seen on earth

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There will be a decrease in the planet's albedo or reflectivity if interior Alaska remains snow-free.

What is albedo?

TThe ratio of a surface's radiosity (J) to its irradiance (Ee) (flux per unit area) is known as its albedo. The amount of solar radiation that reaches the Earth's surface and its spectral and angular distribution both influence how much of it is reflected. These variables change depending on the type of atmosphere, the location, and the time (see position of the Sun). Albedo is the directional integration of reflectance over all solar angles in a given period, as opposed to bi-hemispherical reflectance, which is calculated for a single angle of incidence (i.e., for a given position of the Sun). The temporal resolution can be measured in seconds (as determined by flux measurements) or as averages of a day, a month, or an entire year.

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Can someone please help me with this I’ll make you brainliest

Forces of Evolution
The conditions for Hardy-Weinberg equilibrium are unlikely to be met in real populations. The Hardy Weinberg theorem also describes populations in which allele frequencies are not changing. By definition, such populations are not evolving. How does the theorem help us understand evolution in the real world?
From the theorem, we can infer factors that cause allele frequencies to change. These factors are the forces of evolution. There are four such forces: mutation, gene flow, genetic drift, and natural selection.
Mutation
Mutation creates new genetic variation in a gene pool. It is how all new alleles first arise. In sexually reproducing species, the mutations that matter for evolution are those that occur in gametes. Only these mutations can be passed to offspring. For any given gene, the chance of a mutation occurring in a given gamete is very low. Thus, mutations alone do not have much effect on allele frequencies. However, mutations provide the genetic variation needed for other forces of evolution to act.
Gene Flow
Gene flow occurs when people move into or out of a population. If the rate of migration is high, this can have a significant effect on allele frequencies. Both the population they leave and the population they enter may change.
During the Vietnam War in the 1960s and 1970s, many American servicemen had children with Vietnamese women. Most of the servicemen returned to the United States after the war. However, they left copies of their genes behind in their offspring. In this way, they changed the allele frequencies in the Vietnamese gene pool. Was the gene pool of the American population also affected? Why or why not?
Genetic Drift
Genetic drift is a random change in allele frequencies that occurs in a small population. When a small number of parents produce just a few offspring, allele frequencies in the offspring may differ, by chance, from allele frequencies in the parents. This is like tossing a coin. If you toss a coin just a few times, you may by chance get more or less than the expected 50 percent heads or tails. In a small population, you may also by chance get different allele frequencies than expected in the next generation. In this way, allele frequencies may drift over time. Genetic drift occurs under two special conditions. They are called bottleneck effect and founder effect.
1. Bottleneck effect occurs when a population suddenly gets much smaller. This might happen because of a natural disaster, such as a forest fire. By chance, allele frequencies of the survivors may be different from those of the original population.
2. Founder effect occurs when a few individuals start, or found, a new population. By chance, allele frequencies of the founders may be different from allele frequencies of the population they left.

Answers

Answer:

Explanation:

1. The forces of evolution are the mechanisms that drive the process of evolution and lead to changes in populations over time. There are four main forces of evolution:

Natural Selection: This is the process by which certain traits become more or less common in a population over time due to differences in survival and reproductive success. Individuals with advantageous traits are more likely to survive and reproduce, passing on those traits to their offspring.

Genetic Drift: This is a random change in the frequency of an allele (a variant form of a gene) in a population due to chance events, such as a genetic mutation or the death of individuals carrying certain alleles.

Mutation: This is the process by which new genetic information is introduced into a population. Mutations can lead to new traits and can be the source of variation that drives evolution.

2. Mutations are changes in the DNA sequence of an organism, and they can play a significant role in the process of evolution. There are several types of mutations that can affect evolution, including:

Point mutations: These are mutations that change a single nucleotide in the DNA sequence, which can lead to changes in the amino acid sequence of a protein and potentially affect its function.

Insertion and deletion mutations: These mutations result in the addition or removal of nucleotides in the DNA sequence, respectively. They can disrupt the reading frame of a gene and change its function or lead to the formation of a premature stop codon, causing a truncated protein to be produced.

Frameshift mutations: These are mutations that shift the reading frame of a gene, causing a significant change in the amino acid sequence of the protein produced.

Chromosomal mutations: These are mutations that affect the structure or number of chromosomes, leading to changes in the quantity or organization of genetic information.

These types of mutations can lead to evolution by producing new variations of traits within a population. If these mutations provide a beneficial advantage, they can increase in frequency within a population through natural selection. Over time, the accumulation of beneficial mutations can lead to the evolution of new species.

Therefore, mutations are important in evolution because they provide the raw material for natural selection to work on, leading to the development of new traits and ultimately to speciation.

3. Yes, the gene pool of the American population was affected by the gene flow described above. Gene flow refers to the transfer of genes from one population to another, and it can have a significant impact on the gene pool of a population. In the case of America, the gene pool was affected by the influx of immigrants from various countries, each bringing their own unique genetic background and diversity.

For example, the American population has a significant contribution from European, African, and Asian ancestry. This mixture of different ancestral gene pools has resulted in a diverse and complex genetic landscape in the American population.

Additionally, the intermarriage between individuals from different ancestral backgrounds has also contributed to the gene flow and the diversity of the American gene pool.

4. Genetic drift is one of the four forces of evolution and refers to a random change in the frequency of an allele (a variant form of a gene) in a population over time. This change can occur due to chance events, such as a genetic mutation or the death of individuals carrying certain alleles.

Genetic drift is particularly important in small populations, where chance events can have a larger impact on the frequency of alleles. For example, in a small population, if a single individual carrying a certain allele dies, the frequency of that allele in the population could decrease significantly. Over time, this random process can lead to the loss of genetic variation in a population and can contribute to the divergence of populations and the formation of new species.

Overall, genetic drift is an important force of evolution that can shape the genetic structure of populations and contribute to the diversity of life on Earth.

5. One special condition under which genetic drift occurs is an isolated population. Genetic drift is a mechanism of evolution that refers to the random fluctuations in the frequency of alleles in a population. In an isolated population, the genetic drift process can be more pronounced because the population size is small, and there is limited gene flow from other populations.

As a result, random events such as mutations, deaths, and migrations can have a greater impact on the frequency of alleles in an isolated population. Over time, these random events can lead to the loss or fixation of alleles, shaping the genetic makeup of the population.

What other types of evidence or features might be used to ascertain whether the tree of life is best represented according to the three-domain or the eocyte hypothesis?
-DNA sequence data
-the fossil record
-cell biology

Answers

In addition to DNA sequence data, the fossil record and cell biology are other types of evidence or features that can be used to ascertain whether the tree of life is best represented

according to the three-domain or the eocyte hypothesis.

The fossil record provides physical evidence of past life and can be used to infer the evolutionary history of organisms. By examining the fossil record, scientists can determine the morphological characteristics of ancient organisms and how they are related to modern organisms. This information can be used to support or refute different hypotheses about the evolutionary history of life.

Cell biology can also provide evidence for different hypotheses about the tree of life. For example, the presence or absence of certain cellular features, such as the presence of peptidoglycan in bacterial cell walls or the occurrence of unique metabolic pathways, can help to distinguish between different groups of organisms and support different hypotheses about their relationships.

In summary, while DNA sequence data is a powerful tool for understanding the evolutionary history of life and for determining the relationships between different groups of organisms, the fossil record and cell biology can also provide important evidence for testing different hypotheses about the tree of life. Combining evidence from multiple sources is often necessary to obtain a more complete picture of the evolutionary history of life.

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when two or more monomers join together to form a polymer, water is produced. this is called what?

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When two or more monomers combine to create a polymer, a reaction called a dehydration or condensation occurs, which results in the production of water.

DefinitionCovalent bonds are used to join the monomers together to create polymers, which are bigger molecules. Monomers produce water molecules as byproducts as a result of this process. Dehydration synthesis, which literally translates to "to bring together while losing water," is the term used to describe this kind of process.Covalent bonds are created when one monomer combines with another and releases a water molecule. The terms "dehydration reactions" or "condensation reactions" refer to these processes.Through hydrolysis processes, in which the addition of a water molecule lyses (or breaks) a link), polymers are converted into monomers.

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what is an environmental agent that significantly increases the rate of mutation above the spontaneous rate called? tautomer mutagen transposon missense agent ames agent

Answers

An environmental agent that significantly increases the rate of mutation above the spontaneous rate is called mutagen.

A mutagen is a substance that can cause DNA mutations by chemical or physical means. Tobacco products, radioactive compounds, x-rays, ultraviolet radiation, and a wide range of chemicals are a few examples of mutagens. DNA mutations that cause or support the development of some diseases can result from exposure to a mutagen.

The following are the impacts of mutagens: DNA is altered by mutagens, which can result in issues with transcription, replication, and, in severe situations, cell death. Chromosome breakages and rearrangements including translocation, deletion, and inversion can be brought on by strong mutagens that produce chromosomal instability. Certain mutagens can result in aneuploidy, which is a change in the number of chromosomes in a cell.

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why would you expect to find amino acids with nonpolar side chains tucked into the inside of a folded protein?

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Amino acids with nonpolar side chains are hydrophobic, meaning they do not interact well with water. Because the interior of a folded protein is generally shielded from the aqueous environment,

It is energetically favorable for hydrophobic amino acids to be tucked into the interior of the protein, where they can avoid contact with water.

Proteins are made up of long chains of amino acids that fold into complex three-dimensional structures. The specific sequence and arrangement of amino acids in a protein determines its shape and function. A protein's shape is critical to its function, and the interior of the protein is often tailored to meet specific functional needs.
Amino acids with nonpolar side chains, such as alanine, leucine, and phenylalanine, are hydrophobic, meaning they do not interact well with water. In contrast, amino acids with polar or charged side chains are hydrophilic and interact well with water. Because water is abundant in cells and is the medium through which many biochemical reactions occur, it is energetically unfavorable for hydrophobic amino acids to be exposed to the aqueous environment.

Therefore, it is common to find hydrophobic amino acids buried in the interior of a folded protein, away from water, and in close proximity to other hydrophobic amino acids. This arrangement reduces the protein's surface area, increases its stability, and enables it to carry out its biological function more effectively.

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what happens to the products of digestion after absorption?​

Answers

The products of digestion after absorption is passed by the circulatory system to other parts of your body to store or for different types of uses.

What is Digestion?

This is referred to as the breakdown of large insoluble food molecules into small water-soluble food molecules so that they can be absorbed into the watery blood plasma.

The circulatory system which comprises of the blood etc passes them on to other parts of your body to store or use through the help of special cells help absorbed nutrients cross the intestinal lining into your bloodstream.

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petunia is very skilled at sniffing out the fungus, which this farmer can then sell for as much as $3,600 per pound. what fungus is the farmer trying to grow and what group of fungi does it belong to?

Answers

White truffles,  is the farmer trying to grow and Ascomycota group of fungi does it belong to

It is primarily found in the Piedmont region of northern Italy's Langhe and Montferrat areas, as well as the countryside around the cities of Alba and Asti. Acqualagna, in the northern Marche near Urbino, is another hub for the cultivation and commercialization of white truffles, with one of the most prominent yearly festivals in Italy.

Ascomycota is a monophyletic group of organisms (it contains all descendants of one common ancestor). Asexual (or anamorphic) ascomycetes, which were previously classified as Deuteromycota along with asexual species from other fungal taxa, are now identified and categorised based on morphological or physiological similarities to ascus-bearing taxa, as well as phylogenetic analyses of DNA sequences.

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Full Question: A farmer in France has tried very unsuccessfully to cultivate a valuable type of fungus as a means to augment her income. Due to her unsuccessful attempts (so far at least) to cultivate this fungus, she continues to rely on her pet pig Petunia to find and harvest the wild fungus, which grows naturally on the wooded part of her property. Petunia is very skilled at sniffing out the fungus, which this farmer can then sell for as much as $3,600 per pound. What fungus is the farmer trying to grow and what group of fungi does it belong to?

Which of the following mRNA modifications are common in human cells?A) 5' cap additionB) intron removal and exon joiningC) 3' poly-A tail additionD) alternative splicingE) All of the above are common mRNA modifications in human cells.

Answers

The correct answer is E) All of the above are common mRNA modifications in human cells.

All of the listed mRNA modifications - 5' cap addition, intron removal and exon joining, 3' poly-A tail addition, and alternative splicing - are common in human cells and play important roles in gene expression and protein synthesis.

The 5' cap addition involves the addition of a modified guanine nucleotide to the 5' end of mRNA, which helps to protect the mRNA from degradation and assists in translation initiation. Intron removal and exon joining is a process in which non-coding regions (introns) of pre-mRNA are removed and the remaining coding regions (exons) are joined together to form mature mRNA. The 3' poly-A tail addition involves the addition of a long chain of adenine nucleotides to the 3' end of mRNA, which plays a role in mRNA stability and nuclear export.

Alternative splicing is a process in which different combinations of exons within a pre-mRNA molecule are spliced together to generate multiple mRNA isoforms, leading to the production of multiple protein isoforms from a single gene. Alternative splicing is a common mechanism used to generate protein diversity in eukaryotes, and it is estimated that over 90% of human genes undergo alternative splicing.

In summary, all of the listed mRNA modifications are common in human cells, and they play important roles in the regulation of gene expression and protein synthesis.

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Dump the sand along one side of the pan and form a shoreline, as shown in the
image. Fill the pan with room temperature water so there's at least one inch of water
in the pan and the top of the shoreline is above the water. If you are using food
coloring, add a few drops to your oil and mix thoroughly. Pour the oil in the middle of
the ocean you created, and write down what you observe.

Answers

The oil will be found to float on the surface of the water

What happens when oil is poured into an ocean?

When oil is spilled into an ocean, it can have severe environmental impacts. Oil is a toxic substance that can harm marine life, such as fish and birds, and their habitats.

The oil floats on the surface of the water, forming a slick that can cover large areas. This can limit the amount of light and oxygen that penetrate the water, killing plants and animals that live near the surface. The oil can also coat birds and sea mammals, making it difficult for them to fly or swim, and potentially causing them to suffocate.

Oil can also contaminate the food chain, as small organisms that are covered in oil can be eaten by larger organisms, leading to the accumulation of toxic chemicals in their bodies.

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roth ira contribution limits 2023 married filing jointly

Answers

In 2022 and 2023, Roth IRA annual contribution caps are the same as traditional IRA annual contribution caps.

The maximum contribution for tax year 2022 is $6,000 for those under 50 and $7,000 for those over 50. For 2023, you may not contribute more than the following amounts to all of your regular and Roth IRAs: $6,500 ($7,500 if you are 50 or older); or. if less, your taxable income for the entire year.

If you are married and filing jointly, your combined MAGI must be less than $214,000 in 2022 or $228,000 in 2023. A $1,000 catch-up contribution for a total of $7,500 is allowed to be made to a Roth IRA in 2023 if you are 50 years old or older.

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the primary consequence of hypercarotenemia is multiple choice question. yellowing of the skin. softening of the bones. poor muscular coordination. night blindness.

Answers

The primary consequence of hypercarotenemia is yellowing of the skin.

What is hypercarotenemia?

Hypercarotenemia is a condition where there is an excess of carotenoids, which are plant pigments that give fruits and vegetables their yellow, orange, and red color, in the body. This excess can lead to yellowing of the skin, especially in the palms of the hands and soles of the feet.

Carotenoids build up in the stratum corneum of the epidermis and plasma carotenoid levels rise in hypercarotenemia, which causes the skin to appear yellowish.

However, hypercarotenemia is usually not harmful and is generally a cosmetic issue. In severe cases, it can lead to other symptoms, but those are not the primary consequence.

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which eukaryotic structures are not present in prokaryotic cells?

Answers

Answer:

Endoplasmic reticulum, microtubules, and the Golgi apparatus

What is the structure of the vesicle membrane?

Answers

The structure of the vesicle membrane is composed of a lipid bilayer, which is composed of two layers of phospholipid molecules. The head of each phospholipid molecule is hydrophilic (water-loving) and the tail is hydrophobic (water-fearing). The hydrophobic tails face each other in the center of the bilayer, forming a barrier that separates the interior of the vesicle from the outside environment. The hydrophilic heads face outward, making contact with the water-based environment inside and outside the vesicle. This lipid bilayer structure allows the vesicle to maintain its shape and separate its contents from the surrounding environment. Additionally, certain proteins can be embedded within the lipid bilayer, serving various functions such as the transport of molecules in and out of the vesicle.

Answer:

The vesicle membrane is composed of a phospholipid bilayer, which is a double layer of phospholipid molecules. The phospholipids are arranged in a "head-to-tail" fashion, with the hydrophilic (water-loving) heads facing outward and the hydrophobic (water-fearing) tails facing inward. The membrane also contains proteins, cholesterol, and other molecules that help to regulate the movement of substances in and out of the vesicle.

Explanation:

what ingredients are broken down by enzymes during the modification of barley?

Answers

Through the activity of enzymes released from the aleurone layer and perhaps the scutellum during germination, modification refers to the disintegration of cell walls and the conversion of starch to sugars in the endosperm of grains.

The modification of barley is also known as Malting. Malting is a test of practical biochemistry, particularly enzymology. Both the carbohydrate, protein, and nucleic acid molecules stored in barley grains and the fermentation processes carried out by brewing yeasts are not supported by these molecules. Before the yeast can utilize these big and physically complicated molecules, they must first partially or, in some cases, completely breakdown into their constituent sugars, amino acids, and nucleotides. When barley seeds sprout, hydrolytic enzymes are created or transformed into active forms that can quickly break down these heavy substances.

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an ecologist estimated 800 star-nosed moles, condylura cristata, per square mile in one woodlot and 1,600 per square mile in another woodlot. what was the ecologist comparing?

Answers

An ecologist calculated that there were 1,600 star-nosed moles (Condylura cristata) per square mile in one woodlot and 800 in another. The   comparisons that  ecologist made are density of star-nosed moles

The ecologist was comparing the density of star-nosed moles (Condylura cristata) between two different woodlots, specifically the number of moles per square mile.

The ecologist estimated that there were 800 star-nosed moles per square mile in one woodlot and 1,600 per square mile in another woodlot.

The term "density" refers to the number of individuals of a particular species per unit area or volume of habitat, and it is an important metric for understanding population dynamics and ecology.

By comparing the densities of star-nosed moles between the two woodlots, the ecologist may be able to identify factors that contribute to differences in population size, such as variations in food availability, predator abundance, or habitat quality.

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the layer of the skin called the lacks blood vessels.

Answers

The epidermis layer of the skin called the lacks blood vessels.

The skin has three layers: The epidermis, the outermost layer of skin, provides a waterproof barrier and creates our skin tone.

The dermis, beneath the epidermis, contains tough connective tissue, hair follicles, and sweat glands.

The deeper subcutaneous tissue (hypodermis) is made of fat and connective tissue.

The epidermis is visible to the eye and works to provide protection to the body. It does not contain any blood vessels and is, therefore, dependent on the dermis, the layer of the skin underneath it, to provide access to nutrients and dispose of waste. Hence, the epidermis is the layer of skin that does not contain blood vessels.

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Are enzymes reused or consumed?

Answers

Enzymes may be reused again and again since they are not reactants and do not deplete throughout a reaction. An enzyme can be employed for other reactions after it has catalyzed a reaction and been freed from its binding to a substrate.

A biological catalyst is an enzyme. In a chemical process, catalysts are not consumed; rather, they just increase the pace of the reaction without being consumed. Technically speaking, they provide another route for a reaction to take place and are eventually used up, but a subsequent chemical reaction using the alternate route produces the catalyst molecule once again, thus we say that the catalyst is not used up again.

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Describe the TWO ways in which CRISPR works in gene editing

Answers

Crispr / cas 9 edits genes by precisely cutting dna and then letting natural dna repair processes to take over. The system consists of two parts: the cas 9 enzyme and a guide rna. Rapidly translating a revolutionary technology into transformative therapies.

Answer:

CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) works in gene editing through two main mechanisms:

CRISPR-Cas9: This mechanism involves the use of the Cas9 endonuclease enzyme and a guide RNA molecule (gRNA) to find and cut the specific DNA target. The broken DNA is then repaired by the cell's natural processes, resulting in specific mutations or changes in the genetic code.

CRISPR-Cpf1: Similar to CRISPR-Cas9, this mechanism also involves the use of a nuclease enzyme (Cpf1) and a gRNA to target and cut DNA. However, it has some distinct differences from CRISPR-Cas9, such as its ability to target different sites within the genome and create a more stable cut in DNA.

Explanation:

Both of these CRISPR-based mechanisms have the potential to be used for a variety of applications, including the treatment of genetic diseases and the development of new treatments for various medical conditions.


ALLEN

What level of protein structure has α helixes or β pleated sheets?

Answers

The level of protein structure that has α helixes or β pleated sheets is the Secondary Protein Structure.

The Secondary Protein Structure refers to the three-dimensional structure of individual polypeptide chains. The arrangement of these polypeptide chains includes helixes, pleated sheets, and a few unique forms.

The right-handed spiral structure of the polypeptide backbone results in the formation of alpha helices. The amide group of one amino acid forms hydrogen bonds with the carbonyl group of the amino acid four places downstream, stabilising this secondary structure.

On the other hand, when two or more polypeptide backbones are arranged side by side, pleated sheets are created. The sheets are held together by hydrogen bonds formed by the side chains of the amino acids on the backbones.

This secondary structure is critical for protein stability and has a role in functional activity. Proteins' tertiary structure, or the overall three-dimensional form of the protein, is dependent on the secondary structure of the protein.

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the thoracic and sacral curvatures of the vertebral column, which develop to accommodate the thoracic and abdominopelvic viscera, are classified as

Answers

The thoracic and sacral curvatures of the vertebral column, which develop to accommodate the thoracic and abdominopelvic viscera, are classified as  primary curves.

In general , the thoracic and sacral curvatures are also known as the primary curves because they are found  in the fetus and often remains the same in the adult. During the developmental period in child they lift their head, and begins to assume an upright position, this when the secondary curves known as cervical and lumbar  develop.

Their are other curves present known as kyphotic curve which is convex towards the back of the spine. A lordotic curve is concave towards the back of the spine found in the cervical and lumbar levels of the spine.

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Fill in the blank.In the CNS, _____ are cells that line the fluid-filled cavities and which produce, transport, and circulate the fluid surrounding the brain and spinal cord.

Answers

Ependymal cells are the cells that line the fluid-filled cavities and create, transport, and circulate the fluid that surrounds the brain and spinal cord in the central nervous system (CNS).

The fluid that covers the brain and spinal cord is created, moved, and circulated by ependymal cells, which line the fluid-filled cavities in the central nervous system (CNS).

The spinal cord and brain are both parts of the central nervous system (CNS). In addition to respiration, heart rate, hormones, and body temperature, it also regulates everything else, including thought, movement, and emotion.

Because it integrates information from every part of the body and organizes movement throughout the entire organism, the CNS is referred to be "central."

A brief description of the CNS is given on this page. The various cell types that are involved, various brain regions, spinal circuitry, and potential impacts of illness and damage on the CNS are all examined.

skin cellular structure Ependymal cells line the cavities of the CNS. Ependymal cells create the cerebrospinal fluid (CSF), and they also act as crucial barriers between the CSF and the extracellular space of the brain.

The choroid plexus epithelial cells create the majority of the CSF that hydrates the ventricles, spinal cord, and subarachnoid spaces.

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How many molecules of carbon dioxide are in the balanced equation?

H2O + CO2 ---------> C6H12O6 + O2

Answers

Answer:

Six I think

Explanation:

Answer:

In the balanced equation:

H2O + CO2 -> C6H12O6 + O2

there are 6 molecules of carbon dioxide (CO2).

why do some species employ both mitosis and meiosis, whereas other species use only mitosis? see concept 13.2 (page) view available hint(s)for part a why do some species employ both mitosis and meiosis, whereas other species use only mitosis? see concept 13.2 (page) they need both if they are producing plant gametes. a single-celled organism only needs mitosis. they need meiosis if the cells are producing organs such as ovaries. they need only meiosis if they produce egg cells. they need only mitosis to make large numbers of cells such as sperm.

Answers

Some species use both mitosis and meiosis, others only use mitosis since they must use both to produce animal gametes.

Animals divide their sex and non-sex cells through meiosis, while plants divide their sex and non-sex cells through both mitosis and meiosis. The non-sex cells, such as skin, muscle, and blood cells, are divided through mitosis in humans and all other animal species. This is the case because these cells need to be retrieved quickly because they decrease quickly. Sex cells, including male and female gametes, are haploid and divide via meiosis. Cell division during mitosis and meiosis are both necessary for gamete production in plants. If they are to produce plant (or animal) gametes, they must have both sides.

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which is one reason scientists produce transgenic organisms? A. to treat certain types of diseases. B. to create new species of organisms. C. to create new habitats for endangered species.

Answers

Option A is correct. One reason why scientists create transgenic organisms is to treat certain types of diseases.

What are transgenic mean?

Transgenic refers to an organism or cell whose genome has been artificially altered by the introduction of one or more exogenous DNA sequences from another species. There are many examples of transgenic organisms such as: Insect resistant corn. BT cotton. glow fish. 

What are transgenic organisms used for?

Transgenic organisms are created in the laboratory for research purposes. Transgenic organisms are important research tools and are often used to study gene function. Transgenesis is also related to the medical practice of gene therapy, which introduces DNA into a patient's cells to treat disease. Transgenic organisms are widespread in agriculture.

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What makes membrane potential more positive?

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The membrane potential normally becomes more positive in response to neurotransmitters that open Na+ channels.

Whereas the membrane potential typically becomes more negatively responsive to neurotransmitters that open K+ channels.

The voltage known as the membrane potential is caused by variations in the concentrations of ions on the opposing sides of a cellular membrane. The typical membrane potential ranges from -70 mV to -40 mV. Potassium (K+), which has a high concentration inside the membrane and a low concentration outside, is one of the ions that have a concentration gradient across it. In the extracellular and intracellular regions, respectively, sodium (Na+) and chloride (Cl) ions are present in high and low amounts.

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discuss two examples of how cell death affects the development and functioning of a multicellular organism.

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Multicellular organisms use physiological mechanisms of cell death for development and morphogenesis, to regulate cell quantity, and as a defensive tactic to eliminate infected, mutant, or damaged cells.

Almost all multicellular creatures require cell death for optimal development, which frequently entails the synthesis of extra cells and the removal of those that are unnecessary. The cytoplasm or structural parts of the dead cell frequently play crucial roles in plants and sporadically in other species. Apoptosis, a form of cell death used by metazoans for development, is highly conserved and is distinguishable morphologically. In a multicellular organism, the unintentional death of cells causes swelling and membrane rupture as well as the inevitable leakage of cell contents into the surrounding tissue, which is harmful to the organism. The cells of metazoans have evolved sophisticated self-destruction mechanisms, collectively referred to as programmed cell death, that ensure the orderly elimination of surplus cells, in order to avoid this type of necrotic death.

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Is blood pressure higher in the pulmonary circuit?

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Because the coronary veins are not as muscularly developed as their systemic counterparts, the pulmonary circulation is a comparatively low pressure system in comparison to the systemic circulation.

Is the pulmonary circuit blood pressure higher?

The pulmonary circulation has a lower blood pressure than the systemic circulation. Comparable arteries in the blood circulation have thicker walls than do pulmonary capillaries.

Why does the pulmonary artery have greater blood pressure?

Blood arteries in the lungs that are thickened, constrained, blocked, or damaged make it harder for blood to pass through them. As a result, pulmonary hypertension develops, a condition brought on by an increase in the blood pressure inside the lungs.

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