How does the wasp Ichnuemon eumerus manipulate ant colonies to gain a host butterflies? Releases pheromone that makes ants attack each other Releases pheromone that mimics the queen Releases pheromone that makes ants leave nest Releases pheromone that kills ants

Answers

Answer 1

The wasp Ichnuemon eumerus has developed an unusual way to manipulate ant colonies to gain a host butterflies. The wasp's larvae require a live caterpillar to feed upon, but caterpillars are often heavily defended by ants.

The wasp is therefore required to penetrate ant nests undetected and lay its eggs on the caterpillar while it is within the protection of the ant colony.

How does the wasp Ichnuemon eumerus manipulate ant colonies to gain a host butterfly?

Ichnuemon eumerus uses a chemical that smells similar to the ant queen's scent, called a cuticular hydrocarbon, to evade detection by ants. The chemical compounds are located on the outer layer of the wasp's body and can be sensed by ants that make contact with them.

When the wasp enters the ant colony, it carries out a complex set of behaviours that result in the release of a chemical signal that causes the ants to behave as if they are protecting their queen.

The ants stop moving and huddle together, and the wasp is able to lay its eggs on the caterpillar without being attacked by the ants.

The eggs hatch, and the larvae are raised by the ants alongside the caterpillar. As the larvae grow and consume more caterpillar tissue, they release more of the chemical signals that cause the ants to protect them, creating a self-reinforcing cycle that leads to the death of the caterpillar and the eventual release of adult wasps.

The chemicals used by Ichnuemon eumerus are a fascinating example of chemical mimicry in the animal kingdom. By creating a scent that smells like the ant queen, the wasp is able to evade detection by ants and lay its eggs on the caterpillar without being attacked.

Once the larvae are in place, they release more of the same chemical, causing the ants to protect them as if they were their own. This unique strategy allows the wasp to gain access to an otherwise inaccessible host, providing an important resource for its survival.

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Related Questions

Spatial summation refers to the process of adding up postsynaptic potentials coming from the same presynaptic neuron True False al aladin Moving to another question waves Haunter Our 2 points In a reflex are the nerve impulse travels along the following pathway (sort Afferent nerve fiber ✓ Skeletal muscles Somatic receptors Efferent nerves fibers Intereurons

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Spatial summation is defined as the process of adding up postsynaptic potentials coming from the same presynaptic neuron. The process occurs when the activity of one neuron affects the activity of another neuron through synapses.

This mechanism is crucial for the propagation of signals in the brain and the spinal cord.



Spatial summation refers to the process of adding up postsynaptic potentials coming from the same presynaptic neuron. This statement is True.In a reflex arc, the nerve impulse travels along the following pathway: afferent nerve fiber, somatic receptors, interneurons, efferent nerve fibers, and skeletal muscles.

When a stimulus activates a sensory receptor, it generates a nerve impulse that is transmitted along the sensory (afferent) nerve fiber to the central nervous system (CNS).

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a chicken farmer choose chickens with the most amount of breast meat to breed. after many generations, she had breed chickens with breasts so large the chickens had trouble walking. this is an example of:

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This is an example of artificial selection or selective breeding, which is the intentional breeding of animals or plants for specific traits by humans.

In this case, the chicken farmer selectively bred chickens with the most amount of breast meat to create a new generation with even more breast meat. However, over time, this process led to unintended consequences, such as difficulty walking due to the excessive weight of the breasts.

Artificial selection has been used for thousands of years by humans to breed plants and animals with desirable traits, such as increased yield, resistance to disease, or better taste. Through careful selection of the individuals with the desired traits, humans can guide the evolution of domesticated species in ways that would not occur naturally.

However, as in the example of the chicken farmer, artificial selection can also have unintended consequences if it is taken too far or focused too narrowly on a specific trait. In some cases, artificially selected traits may reduce the overall fitness of the organism or lead to health problems that can negatively impact their well-being.

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Capsaicin, the active ingredient in hot peppers, creates a burning sensation because it causes the local temperature of the exposed tissue to increase dramatically leading to depolarization of thermoreceptors O it causes an inflammatory response that attracts immune cells that release soluble cytokines that bind and depolarize nociceptors O it destroys cells in the tongue releasing acid (H+) onto taste buds O it binds and opens an ion channel on nociceptors that also happens to open in response to heat

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Capsaicin, the active ingredient in hot peppers, creates a burning sensation because it binds and opens an ion channel on nociceptors that also happens to open in response to heat.

Nociceptors are sensory neurons that are specialized in detecting and transmitting signals related to pain and temperature. The ion channel involved in this process is known as the transient receptor potential vanilloid 1 (TRPV1) channel. When capsaicin comes into contact with nociceptors, it binds to and activates the TRPV1 channels. These channels are normally activated by high temperatures, but capsaicin can also bind to them, leading to their opening and depolarization of the nociceptor membrane. This depolarization sends a signal to the brain, resulting in the perception of a burning or painful sensation. It is important to note that capsaicin does not cause an actual increase in temperature or destroy cells. Instead, it interacts with the sensory system, specifically targeting the TRPV1 channels on nociceptors, leading to the perception of heat and pain. This mechanism explains why capsaicin creates a burning sensation when it comes into contact with tissues or receptors in the body, and it is also responsible for the sensation of heat when consuming spicy foods containing capsaicin.

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Which variable rises after capillary beds?
a. Blood pressure
b. Blood vessel area
c. blood velocity
d. blood volume

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A blood velocity After capillary beds, the blood velocity of the blood rises because of the following reasons. After capillary beds, blood velocity increases. Explanation:Capillaries are the smallest and the thinnest vessels in the human body. These vessels play a vital role in the body as they help in the exchange of various substances such as nutrients, waste, and oxygen. It connects the arterial and venous systems.

The narrowing of the capillaries from tiny vessels increases the resistance of the flow of blood. This then leads to a drop in blood pressure and an increase in blood velocity.The sum of the cross-sectional area of the capillaries is bigger than the cross-sectional area of the arteries and veins; this means that the blood that flows in the capillaries moves at a much slower pace than the blood that flows in the arteries and veins.

This causes a drop in the speed of blood flow, thus leading to a rise in blood velocity.Along with blood velocity, the blood pressure and blood volume may also change after capillary beds. Blood pressure decreases after capillary beds while the blood vessel area and blood volume vary depending on the situation or condition.

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Tachycardia with marked rise of blood pressure occur after administration of : Select one O a. Isoprenaline b. Noradrenaline O c. Dobutamine d. Adrenaline d e. Atropine

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Tachycardia with a marked rise in blood pressure is observed when adrenaline is administered. Adrenaline is a naturally occurring hormone, also known as epinephrine.

That plays a vital role in the fight or flight response in the body.Tachycardia, an abnormally high heart rate, and hypertension, or high blood pressure, are among the possible side effects of the drug administration. Adrenaline is a medication that is often used in emergency situations.

The medication is administered by injection, and the dosage is determined by the patient's weight, the severity of their condition, and other factors. The medication stimulates beta receptors in the body, resulting in increased heart rate and constriction of blood vessels.

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An example of an evolutionary homology would be
Group of answer choices
a. your arms and the flippers of a seal
b. the fur on your dog and the feathers on your parrot
c. nest-building of a bird and hive-building of a honeybee
d. fins of a fish and flipper of a seal

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Evolutionary homology is when organisms share a common ancestry and have similar structures. The structures can have different functions in different organisms, but they are similar in their underlying structure. Therefore, an example of an evolutionary homology would be fins of a fish and flipper of a seal. correct option is d ) .

These structures are different in their function, but they have similar structures and the same embryonic origin.

The flipper of a seal and fins of a fish have the same basic structure. For example, they both have a humerus, radius, and ulna bones.

The structure is a result of their shared ancestry, and it is an example of an evolutionary homology.

Other examples of evolutionary homologies are wings of bats and wings of birds.

Even though they have different functions, they have similar structures. The bones, muscles, and other structures that make up their wings are similar because they are derived from a common ancestor.

Another example is the limbs of mammals.

Whether they are used for walking, swimming, or flying, they share a basic structure that is an example of evolutionary homology.

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What are the infective stage and diagnostic stages for the following diseases?
1. Giardia Lamblia.
2. Leishmania.
3. Ascaris lumbricoides.
4. Toxoplasma Gondi.
5. african trypanosomiasis.
6. Chagas disease.
7. Trichomoniasis Vagainalis.
8. Malaria.
9. Hookworms.
10. Enterobiasis.
11. Entermba Histolatika

Answers

1. Giardia Lamblia: Infective stage - Cyst; Diagnostic stage - Trophozoite.

2. Leishmania: Infective stage - Promastigote; Diagnostic stage - Amastigote.

Certainly! Here are the infective stages and diagnostic stages for the mentioned diseases:

1. Giardia Lamblia:

  - Infective Stage: Cyst

  - Diagnostic Stage: Trophozoite

2. Leishmania:

  - Infective Stage: Promastigote

  - Diagnostic Stage: Amastigote

3. Ascaris lumbricoides:

  - Infective Stage: Eggs

  - Diagnostic Stage: Adult worm

4. Toxoplasma gondii:

  - Infective Stage: Oocyst

  - Diagnostic Stage: Tissue cyst

5. African trypanosomiasis (Sleeping sickness):

  - Infective Stage: Metacyclic trypomastigote

  - Diagnostic Stage: Bloodstream trypomastigotes, intracellular amastigotes

6. Chagas disease:

  - Infective Stage: Trypomastigote

  - Diagnostic Stage: Amastigote

7. Trichomoniasis vaginalis:

  - Infective Stage: Trophozoite

  - Diagnostic Stage: Trophozoite (observed in vaginal secretions or urine)

8. Malaria:

  - Infective Stage: Sporozoite

  - Diagnostic Stage: Merozoite

9. Hookworms:

  - Infective Stage: Infective larvae (L3)

  - Diagnostic Stage: Adult worm, eggs in stool

10. Enterobiasis:

   - Infective Stage: Infective eggs

   - Diagnostic Stage: Adult pinworm or eggs on perianal swab or tape test

11. Entamoeba histolytica:

   - Infective Stage: Cyst

   - Diagnostic Stage: Trophozoite or cyst in stool sample.

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no explanation needed pls answer
quick.
Answer all short answer questions and the essay DQuestion 23 Crossing over occurs between..... Sister chromatids during prophase 1 of mitosis O Sater chromatics during prophase I of meiosis O Non-sist

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Crossing over occurs between sister chromatids during prophase 1 of mitosis (option a).

Crossing over occurs during prophase 1 of meiosis. It is the exchange of genetic material between non-sister chromatids of homologous chromosomes. During meiosis, two rounds of cell division occur which produces haploid cells. During prophase 1 of meiosis, crossing over occurs between non-sister chromatids of homologous chromosomes. During this stage, the two homologous chromosomes exchange genetic material. This process leads to the creation of new combinations of genetic material and increases genetic diversity. The correct option is: Sister chromatids during prophase I of meiosis

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Positioning of the first Met tRNA on the mRNA is a critical step in translation inititiation. Selection of the first correct AUG is achieved by a complex of Met tRNA with a. initiation factors
b. initiation factors plus poly A binding protein
c. small subunit ribosome d.small subunit ribosome plus initiation factors

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The positioning of the first Met tRNA on the mRNA during translation initiation is a crucial step. The correct selection of the first AUG codon is achieved by a complex of Met tRNA with the small subunit ribosome plus initiation factors. This complex ensures the accurate initiation of protein synthesis.

Translation initiation is the process by which protein synthesis begins in cells. It involves the assembly of the ribosome, mRNA, and initiator tRNA at the start codon of the mRNA molecule. The first Met tRNA, carrying the amino acid methionine, plays a crucial role in this process.

To ensure accurate initiation, a complex is formed between the small subunit ribosome, the initiator tRNA, and several initiation factors. These initiation factors help in the proper positioning of the components and facilitate the recognition of the start codon. Among the initiation factors, one important factor is the initiation factor 2 (IF2) that interacts with the initiator tRNA and the small subunit ribosome.

The initiation complex scans the mRNA molecule until it reaches the correct start codon, which is typically AUG. The start codon is recognized by the anticodon of the initiator tRNA, which is base-paired with the AUG codon. The interaction between the Met tRNA and the start codon is facilitated by the small subunit ribosome and the initiation factors. Once the correct start codon is recognized, the large subunit of the ribosome joins the complex, and protein synthesis begins. The initiator tRNA occupies the P-site of the ribosome, ready to receive the next amino acid and initiate the elongation phase of translation.

In conclusion, the positioning of the first Met tRNA on the mRNA during translation initiation is achieved by a complex consisting of the small subunit ribosome plus initiation factors. This complex ensures the accurate selection of the first AUG codon and facilitates the proper initiation of protein synthesis.

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Which of the following is an incorrect statement about "calories"?
a. All one needs to know to accurately calculate one's daily calorie needs is knowledge of their sex and their weight. b. Two hundred calories from an avocado (which offers healthy fats and other nutrients) can be a better choice than eating 100 calories of deli meat. c. Fiber helps to slow the absorption of sugar. d. Healthy eating and drinking choices is about more than calories.
e. A zero-calorie pop/soda, for example, might also provide zero nutrients, and come packed with artificial sweetners. f. Consuming 100 calories in the form of an apple will provide a more "full" feeling than drinking 100 calories of pop/soda/Red Bull, etc.

Answers

An incorrect statement about "calories" is: a. All one needs to know to accurately calculate one's daily calorie needs is knowledge of their sex and their weight.

Option (a) is the incorrect statement. While sex and weight are important factors in estimating daily calorie needs, they are not the sole factors. Other variables, such as age, height, activity level, and metabolic rate, also play a significant role in determining individual calorie requirements. Therefore, relying solely on sex and weight to calculate daily calorie needs would not provide an accurate estimation.

Options (b), (c), (d), (e), and (f) are all correct statements about calories. Option (b) highlights that the nutrient content and overall health benefits of food should be considered along with calorie content. Option (c) emphasizes the role of fiber in slowing down sugar absorption, which is important for managing blood sugar levels. Option (d) acknowledges that healthy eating is not solely about calorie intake but also about nutrient quality and overall dietary choices. Option (e) points out that zero-calorie beverages may lack nutrients and contain artificial sweeteners. Option (f) highlights the difference in satiety and fullness between consuming calories from different sources, such as whole foods versus sugary beverages.

Therefore, option (a) is the incorrect statement among the given options.

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Yersinia pestis the causative agent of the bubonic plague, killed 50% of Europe's population in the middle ages. It is considered the most successful pathogen infecting humans. When engulfed by a macrophage the bacterium prevents acidification of the phagosome and is transported to the lymph nodes unharmed. Here it multiplies and creates the buboes (extremely swollen lymph nodes) that characterize this disease.
Though Y. pestis can grow in a macrophage, it is destroyed inside dendritic cells that process the antigen and initiate an adaptive immune response. If a person is to survive this infection without antibiotics, what type of cells would need to be activated by the dendritic cell to combat this pathogen as it replicates inside a macrophage.
plasma cells
Cytotoxic T cells
T-helper 1 cells
neutrophils
mast cells

Answers

As a result, activating Th1 cells by dendritic cells to combat this pathogen as it replicates inside a macrophage is crucial for the survival of an infected person without antibiotics.

When engulfed by a macrophage, the bacterium prevents the acidification of the phagosome and is transported to the lymph nodes unharmed, where it multiplies and creates the buboes (extremely swollen lymph nodes) that characterize this disease.

Though Y. pestis can grow in a macrophage, it is destroyed inside dendritic cells that process the antigen and initiate an adaptive immune response.

If a person is to survive this infection without antibiotics, T-helper 1 cells would need to be activated by the dendritic cell to combat this pathogen as it replicates inside a macrophage.

The T-helper 1 (Th1) cells are a subpopulation of T-helper cells, which are involved in the immune system's response to infectious agents, including viruses, intracellular bacteria, and parasites.

They stimulate macrophages to kill phagocytosed microbes, and the cytokines they produce, such as IFN-γ and IL-2, play a critical role in the response to intracellular pathogens.

The Th1 response is crucial for the host defense against Y. pestis, which is known to survive and replicate inside macrophages.

T-helper 1 cells activate macrophages through a series of signaling events, resulting in increased phagocytosis, enhanced intracellular killing, and the release of microbicidal molecules such as reactive oxygen species (ROS) and nitric oxide (NO).

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Gene flow will
will cause increase genetic drift in populations
reduce the frequency of rare alleles in a population
reduce genetic differentiation among populations
promote in

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Gene flow has several effects on populations, including increased genetic drift, reduced frequency of rare alleles, reduced genetic differentiation among populations, and promotion of genetic diversity.

Gene flow refers to the movement of genes from one population to another through the migration and subsequent breeding of individuals. This process has significant implications for population genetics.

One effect of gene flow is an increase in genetic drift within populations. Genetic drift is the random fluctuation of allele frequencies in a population, and increased gene flow can introduce new alleles or change the frequencies of existing alleles, leading to increased genetic drift. By facilitating the exchange of genetic material, gene flow can blur the genetic distinctions between populations, leading to increased genetic similarity.

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Which of these statements about hetersporous plants is false? a.All seed plants are heterosporous. b.Their spores develop into either male gametophytes or female gametophytes. c.All seedless plants are are heterosporous. d.They produce two types of spores.

Answers

The false statement about heterosporous plants is that all seedless plants are heterosporous.

Heterospory is a reproductive strategy found in some plants where they produce two different types of spores: microspores and megaspores. These spores develop into separate male and female gametophytes, respectively. Now let's analyze each statement to determine which one is false:

a. All seed plants are heterosporous: This statement is true. All seed plants, which include gymnosperms (such as conifers) and angiosperms (flowering plants), exhibit heterospory. They produce microspores that develop into male gametophytes and megaspores that develop into female gametophytes.

b. Their spores develop into either male gametophytes or female gametophytes: This statement is true. In heterosporous plants, the microspores give rise to male gametophytes, which produce male gametes (sperm), while the megaspores develop into female gametophytes, which produce female gametes (eggs).

c. All seedless plants are heterosporous: This statement is false. Seedless plants, such as mosses, liverworts, and ferns, are generally homosporous, meaning they produce only one type of spore. This single type of spore develops into a bisexual gametophyte, which can produce both male and female gametes.

d. They produce two types of spores: This statement is true. Heterosporous plants indeed produce two distinct types of spores: microspores and megaspores. These spores differ in size and eventually give rise to separate male and female gametophytes.

In conclusion, the false statement about heterosporous plants is that all seedless plants are heterosporous. Seedless plants, including mosses and ferns, are typically homosporous, producing a single type of spore that develops into a bisexual gametophyte.

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no
explanation needed:) just answer!
Which of the following are accurate related to the ethical considerations with the Tuskegee Syphilis study? O A. Once realized there was an effective treatment, it was provided immediately O B. Study

Answers

Among the following options, the accurate option related to the ethical considerations with the Tuskegee Syphilis study is that: The study did not provide the participants with the appropriate treatment when it was available. Option (C) is correct.

The Tuskegee Syphilis study is regarded as an unethical study conducted in the United States. In 1932, the U.S. Public Health Service initiated this study to examine the effects of untreated syphilis. This study continued for four decades and ended in 1972 when it was uncovered by the media that the participants were not receiving appropriate treatment when it was available and effective.The study caused widespread outrage among the medical and non-medical community.

The study violated the basic ethical principles of human research. Participants were deliberately not given appropriate treatments to allow the progression of the disease, and the medical team had no interest in their welfare. Ultimately, the study ended after media coverage and multiple lawsuits were brought against it.

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OPTION A
A large tract of South-Australian Mallee has been donated to long-term conservation. It has been
heavily cleared and grazed for >100-years, and is negatively affected by alien invasive pests and
weeds, 15-years of drought, and poor management of fire and irrigation practices.
You have been tasked with developing a new monitoring program to evaluate the impacts of a
broad-scale restoration project. This project will include a variety of components, including: (i) alien
species removal and exclusion; (ii) planting and restoration; and (iii) experimental landscape
watering.
Whilst you have been funded to develop the program, you do not have an infinite budget. Choose
one of the three components above (i – iii) and discuss the following aspects of your program.
Provide a rationale for your decisions based on the broad goals of the program.
Page 3 of 5
Page 4 of 5
(A) Identify how you might use rapid assessment methods, or similar, to collect the necessary
data for your chosen restoration component.
(B) How will these methods be implemented over the long term to allow the consequences of
your restoration program to be detected?
Specify what part of the ecological community you will target for monitoring the response outcome
of your chosen restoration component, and identify the spatial and temporal scales of sampling.

Answers

Rapid evaluation techniques can be utilised to gather the essential information for the selected restoration component of alien species removal and exclusion.

Rapid surveys could be one strategy for determining the presence or absence of the target alien species. This can require making observations in the field, making a visual identification, or even spotting invasive species via remote sensing methods. By providing a snapshot of the current status of alien species within the restoration region, rapid assessment methods enable effective data collection. (B) The rapid evaluation techniques can be applied frequently to enable the long-term detection of effects emerging from the restoration programme. To keep track of any changes in the presence of a substance, routine monitoring can be carried out at predetermined intervals, such as annually or biennially.or a large number of foreign species. Repeating the assessments over time makes it possible to spot patterns and evaluate the long-term success of the removal and exclusion activities. significant variations in the structure and composition of vegetation. The native plant community may be the ecological community targeted for monitoring in terms of the response outcome of the selected restoration component. This community is essential for supporting the environment as a whole and for providing habitat. Choosing representative plots or transects within the restoration area that include a variety of habitats and vegetation types can be done as part of the spatial scale of sampling. With monitoring carried out over a number of years to evaluate the progress, the temporal scale of sampling would rely on the restoration schedule and the predicted rate of return of the native plant community.

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Help
2. What is the advantage of using Sabouraud agar?

Answers

The advantage of using Sabouraud agar is it relatively easy to prepare, has higher yield rate than other fungal growth media, will change colour as the pH changes, and can differentiate between fungal species.

Sabouraud agar is a selective and differential medium used for fungal growth, it has a distinct composition with lowered pH that inhibits bacterial growth and improves fungal growth. One of the advantages of using Sabouraud agar is that it's relatively easy to prepare and relatively inexpensive. Secondly, it has a higher yield rate than other fungal growth media, which is why it is commonly used for clinical specimen cultures. Sabouraud agar can also be used for the isolation and identification of fungi from food, water, soil and other materials, this is due to the fact that it has a high degree of sensitivity and specificity.

Another advantage is that the pH indicator of Sabouraud agar will change colour as the pH changes, which makes it easier for the detection of fungal colonies. Lastly, it can differentiate between fungal species by the color and texture of their growth, which helps identify the type of fungal infection a patient has. So therefore the advantage of using Sabouraud agar is it relatively easy to prepare has higher yield rate than other fungal growth media, will change colour as the pH changes, and can differentiate between fungal species.

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9. Which of the following sunlight classes of UV radiation has the shortest wavelength? a) UVA b) UVB c) UVC d) UVD 10. Human Papillomavirus is the main cause of _____.
a) testicular cancer b) cervical cancer c) breast cancer d) hepatocarcinoma 11. The phenomena in which the integration of viral DNA into host chromosome that cause activation or disruption of a normal gene is known as ______.
a) insertional mutagenesis b) proliferating mutagenesis c) transforming mutagenesis d) constitutive mutagenesis

Answers

UVC has the shortest wavelength among the sunlight classes of UV radiation. Cervical cancer is mainly caused by Human Papillomavirus (HPV). The underlying mechanism is thought to be insertional mutagenesis, a process by which there is an integration of viral DNA into the host chromosome that causes activation or disruption of the normal host gene.

Among the sunlight classes of UV radiation, UVC has the shortest wavelength. UVA has the longest wavelength, followed by UVB and then UVC.

Human Papillomavirus (HPV) is the man causative agent of cervical cancer. HPV is a sexually transmitted infection that can lead to the development of abnormal cervical cells, which, if left untreated, can progress to cervical cancer. It is important for individuals, particularly females, to undergo regular screening tests, such as Pap smears and HPV testing, to detect and prevent cervical cancer.

The phenomenon in which viral DNA integrates into the host chromosome and causes activation or disruption of a normal gene is known as insertional mutagenesis. Viral DNA can insert itself into the host genome and affect the expression and function of genes.

This integration can lead to genetic changes that contribute to the development of various diseases, including certain types of cancer. Insertional mutagenesis is a mechanism through which viruses can alter the normal functioning of host cells and potentially drive cellular transformation.

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If
anyone can help explain this?
EXERCISE 9.2 Question Worksheet 1 Explain why the lymphatic system is considered an open system. How is this different from the circulatory system?

Answers

The lymphatic system is considered an open system because it lacks a centralized pump and has multiple points of entry and exit for fluid. This is different from the circulatory system, which is a closed system with a centralized pump (the heart) and a continuous loop of blood vessels.

The lymphatic system is an open system because it operates without a centralized pump, like the heart in the circulatory system. Instead, lymphatic fluid, called lymph, flows through a network of lymphatic vessels, lymph nodes, and other lymphoid organs. The movement of lymph is facilitated by muscle contractions, body movements, and pressure changes within the body.

The lymphatic system also has multiple points of entry and exit for fluid. Lymphatic capillaries collect excess interstitial fluid, which includes proteins and cellular waste products, from the tissues. This fluid enters the lymphatic vessels and eventually drains back into the bloodstream through the thoracic duct or right lymphatic duct.

In contrast, the circulatory system is a closed system with a centralized pump, the heart, which actively propels blood through a network of blood vessels. Blood flows in a continuous loop, delivering oxygen, nutrients, and hormones to the tissues and removing metabolic waste products.

Therefore, the main difference between the lymphatic system and the circulatory system is that the lymphatic system is an open system without a centralized pump, while the circulatory system is a closed system with a centralized pump and a continuous loop of blood vessels.

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All the following about telomerase and telomeres are true except: there is no telomerase activity in somatic cells. the telomerase enzyme carries an RNA template. telomerase adds RNA nucleotides to the lagging strand. O telomere length and age-at-death appear to be correlated. human telomeres are repeats of 6 nucleotides. Question 10 1 pts Which of the following statements about DNA replication is correct? Does not require a primer to replicate the leading strand. The lagging strand is synthesised discontinuously in the 5' to 3' direction. Proceeds in one direction from the origin of replication. Topoisomerase unwinds and separates the parental DNA strands. O Uses DNA ligase to form the H-bonds holding the two complementary strands together.

Answers

All the following about telomerase and telomeres are true except there is no telomerase activity in somatic cells.The statement, “there is no telomerase activity in somatic cells” is false as somatic cells, due to the constant cell division they undergo, need telomerase to prevent shortening of telomeres. The rest of the given statements are true regarding telomerase and telomeres:Telomerase carries an RNA template.Telomerase adds RNA nucleotides to the lagging strand.Telomere length and age-at-death appear to be correlated.Human telomeres are repeats of 6 nucleotides.The correct statement about DNA replication is - Proceeds in one direction from the origin of replication.DNA replication is a process by which a cell duplicates its DNA and replicates it. This is an important process during the cell division as each daughter cell needs to have an exact copy of the genetic material of the parent cell. During DNA replication, DNA polymerase moves along the parental DNA and creates a new strand of DNA that is complementary to the parental DNA molecule. It proceeds in one direction from the origin of replication.Topoisomerase unwinds and separates the parental DNA strands, and Uses DNA ligase to form the H-bonds holding the two complementary strands together. DNA polymerase can only add nucleotides in the 5' to 3' direction, so it replicates the leading strand continuously but has to replicate the lagging strand discontinuously in the 5' to 3' direction and then uses DNA ligase to seal the gaps to form a continuous strand. It requires a primer to replicate the leading strand.

Q18. Describe the negative feedback loop that controls the rate
of erythropoiesis. Under what circumstances would you expect the
rate of erythropoiesis to increase? How would it be possible to
tell if

Answers

The negative feedback loop controlling the rate of erythropoiesis involves EPO and responds to low oxygen levels or decreased red blood cell count. The rate of erythropoiesis increases under circumstances such as hypoxia or anemia.

Erythropoiesis is the process of red blood cell production in the bone marrow. The rate of erythropoiesis is regulated by a negative feedback loop involving the hormone erythropoietin (EPO) and the oxygen-carrying capacity of the blood.

When oxygen levels in the body decrease or when there is a decrease in red blood cell count, the kidneys sense the low oxygen levels and release EPO into the bloodstream. EPO stimulates the bone marrow to produce more red blood cells, increasing the rate of erythropoiesis.

Once the oxygen levels in the body are restored or the red blood cell count returns to normal, the kidneys sense the adequate oxygenation and reduce the release of EPO. This negative feedback loop helps maintain a balance in the production of red blood cells.

To determine if the rate of erythropoiesis has increased, one can measure the levels of EPO in the blood. Elevated EPO levels indicate an increased rate of erythropoiesis. Additionally, a complete blood count can be performed to assess the red blood cell count and hemoglobin levels, which would be higher if erythropoiesis has increased.

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In humans, normal arches are due to a dominant gene (A), flat feet are due to its recessive allele (a). a) If a heterozygous normal arched individual mates with a flat-footed individual, what type of offspring could be produced? Show your work. b) A normal-arched male mates with a flat-footed female. The mother of the normal arched male had flat feet. What are the possible phenotypes and genotypes of this couple's offspring?

Answers

A heterozygous normal arched individual has one allele for normal arches (A) and one allele for flat feet (a). The gametes produced by the heterozygous normal arched individual are A and a. A flat-footed individual has two alleles for flat feet (aa), so the gametes produced are also aa.

a) If a heterozygous normal arched individual mates with a flat-footed individual, then the type of offspring could be produced are as follows:   Gametes produced by heterozygous normal arched individual: A, a Gametes produced by flat-footed individual: a, a Possible genotypes of offspring:      AA    (Normal arched individuals)      Aa    (Normal arched individuals)      aa     (Flat-footed individuals)Possible phenotypes of offspring:      Normal arched individuals.      Flat-footed individuals.

b) A normal-arched male mates with a flat-footed female, and the mother of the normal arched male had flat feet. The possible phenotypes and genotypes of this couple's offspring are:    Gametes produced by normal-arched male: A, a Gametes produced by flat-footed female: a, a Possible genotypes of offspring:    AA    (Normal arched individuals)     Aa    (Normal arched individuals)     aa     (Flat-footed individuals)Possible phenotypes of offspring:     50% Normal arched individuals (AA or Aa).     50% Flat-footed individuals (aa).

The possible gametes produced by the normal-arched male are A and a. The flat-footed female has two alleles for flat feet (aa), so the possible gametes produced are aa. When the two individuals mate, the possible genotypes and phenotypes of their offspring can be determined using a Punnett square.

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3. For the plant DNA amplification, what size DNA fragment do
you expect?
A) 455 base pairs
B) None of the above
C) 200 base pairs
D) Both 455 and 200 base pairs

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It consists of four bases (A, G, C, and T) that pair with each other to form base pairs. Plant DNA amplification involves duplicating a specific fragment, and in this case, the expected size of the amplified DNA fragment is 200 base pairs. This amplification allows for further analysis and study of the targeted DNA region.

For plant DNA amplification, the size of the DNA fragment that you expect is 200 base pairs.What is amplification?Amplification is a process of increasing the number of copies of a particular piece of DNA. The most common method of amplifying a DNA fragment is through the polymerase chain reaction (PCR).What is DNA?DNA stands for Deoxyribonucleic acid. It is the molecule that carries the genetic information in all living organisms. DNA is made up of four chemical bases, namely, adenine (A), guanine (G), cytosine (C), and thymine (T). These bases pair with each other to form base pairs (bp).In summary, for the plant DNA amplification, the size of the DNA fragment that you expect is 200 base pairs (Option C).Amplification is the process of increasing the number of copies of a specific DNA fragment. It is commonly achieved through PCR, which selectively targets and replicates the desired DNA sequence. DNA, or Deoxyribonucleic acid, is a molecule that carries genetic information in all living organisms.

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MATCHING Place the most appropriate number in the blank provided. Zymogenic cells 1. Hydrochloric acid Pancreatic islets 2. Pancreatic juice Heparin 3. Regulates blood Crypts of Lieberkuhn sugar level Parietal cells Brunner's glands 4. Phagocytosis Lacteals 5. Pepsinogen Kupffer cells 6. Absorb fats Acini 7. Chyme Insulin 8. Neutralizes acid in chyme 9. Intestinal glands 10. Anticoagulant 11. Secrete hormones 12. Amylase

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Here is the matching for the provided terms:

Zymogenic cells - 5. PepsinogenPancreatic islets - 11. Secrete hormonesHeparin - 10. AnticoagulantCrypts of Lieberkuhn - 9. Intestinal glandsParietal cells - 1. Hydrochloric acidBrunner's glands - 8. Neutralizes acid in chymePhagocytosis - 4. Kupffer cellsLacteals - 6. Absorb fatsAcini - 2. Pancreatic juiceChyme - 7. ChymeInsulin - 3. Regulates blood sugar levelAmylase - 12. Amylase

Zymogenic cells, also known as chief cells, are found in the stomach lining within structures called gastric glands. These cells are responsible for producing and secreting an inactive enzyme called pepsinogen. Pepsinogen is later activated by the acidic environment in the stomach, converting it into its active form called pepsin. Pepsin plays a vital role in the digestion of proteins by breaking them down into smaller peptides.

Pancreatic islets, also known as islets of Langerhans, are small clusters of cells located in the pancreas. They are responsible for producing and releasing hormones that help regulate blood sugar levels. The main cell types within the pancreatic islets are alpha cells, which secrete glucagon, and beta cells, which secrete insulin. Glucagon acts to increase blood sugar levels, while insulin acts to decrease blood sugar levels by facilitating the uptake and storage of glucose in various cells of the body. The balance between these hormones is essential for maintaining proper blood sugar control and preventing conditions like diabetes.

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What bonds do proteases cleave? Name one protease and draw an example of the bond cleaved by such protease .

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Proteases cleave peptide bonds in proteins. One example of a protease is trypsin, which cleaves peptide bonds following the amino acid lysine or arginine.

Proteases are enzymes that catalyze the hydrolysis of peptide bonds in proteins. Peptide bonds are the covalent bonds that link amino acids together in a protein chain. Proteases act by breaking these bonds, leading to the fragmentation of the protein into smaller peptides or individual amino acids.

One well-known example of a protease is trypsin. Trypsin is a serine protease that cleaves peptide bonds following the amino acid lysine (K) or arginine (R). It recognizes specific sequences of amino acids and cleaves the peptide bond on the carboxyl side of either lysine or arginine residues. For example, if we have the peptide sequence "Gly-Lys-Ala-Arg-Ser," trypsin would cleave the peptide bond between the arginine (R) and serine (S) residues.

The cleavage of peptide bonds by proteases is essential for various biological processes, including protein digestion, post-translational modifications, and protein turnover. By selectively cleaving specific peptide bonds, proteases play a crucial role in regulating protein structure, function, and degradation within cells.

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Quantity which refers to the number of reaction process that each active site of the enzyme catalyzes per unit time.
a. Turnover number
b. Catalytic efficiency
c. Enzyme activity
d. Specific enzyme activity

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Quantity which refers to the number of reaction process that each active site of the enzyme catalyzes per unit time Turnover number. The correct option is a.

The turnover number refers to the number of reaction processes that each active site of an enzyme catalyzes per unit time. It is also known as kcat and is a measure of the catalytic activity of an enzyme. The turnover number provides information about how efficiently an enzyme can convert substrate molecules into product molecules. It is expressed as the number of substrate molecules converted per active site per second.

Option a, turnover number, accurately describes the quantity mentioned in the question. Options b, c, and d (catalytic efficiency, enzyme activity, and specific enzyme activity) are related concepts but do not specifically refer to the number of reaction processes per active site per unit time.

Therefore, the correct answer is a.

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A mutation causing an addition or a deletion of one base pair resulted in the production of a nonfunctional mutant protein. The sequences of the normal and mutant proteins are given below. Normal: Met - Gly - Glu - Val - Asp Mutant: Met - Gly - Lys - Ser - lle - Lys - Trp - Arg - . Was this mutation cause by an insertion or a deletion? Below, fill in the codons in the coding sequence of the mRNA that is translated into the mutant protein. If more than one codon is possible, just enter a single codon. NH₂ Met Gly Lys Ser lle codons 5' AUG

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The mutation that caused the nonfunctional mutant protein was due to an insertion.

 The coding sequence of the mRNA that is translated into the mutant protein has one additional codon, thus the frameshift mutation that caused the protein to be nonfunctional can be inferred to have been an insertion mutation. A deletion mutation would have caused one of the amino acids to be missing, and the mRNA sequence to be shorter than the normal sequence.

Hence, the mutation causing the nonfunctional mutant protein was due to an insertion.Let us fill in the codons in the coding sequence of the mRNA that is translated into the mutant protein.NH₂ Met Gly Lys Ser lle codons 5' AUG GGUAAGUCAUCAGGAC The codons in the coding sequence of the mRNA that is translated into the mutant protein are 5' AUG GGUAAGUCAUCAGGAC.

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Which of the following is NOT a role of the kidneys? * 1 point regulates ion balance rids the body of metabolic waste egestion of nitrogenous wastes regulates water balance secretion of hormones involved in the production of RBCs Urea is produced * * 1 point by the liver in every cell of the body when amino acids are dephosphorylated by the kidneys by birds and reptiles

Answers

The kidneys are the pair of organs that perform a variety of important functions that are important for a healthy body. The primary roles of kidneys are the regulation of water balance, maintenance of acid-base balance, regulation of blood pressure, filtration of waste products from the body, and production of urine.

The kidney's main job is to filter the blood to remove excess waste products and fluids from the body.

The following functions are performed by the kidneys except for the secretion of hormones involved in the production of red blood cells.

Erythropoietin is a hormone that regulates the production of red blood cells in the body, and it is produced by the kidneys.

Kidneys regulate the body's ion balance by filtering the blood.

Kidneys remove metabolic waste products such as urea, uric acid, and creatinine from the body. Kidneys are involved in the egestion of nitrogenous wastes, which include excess urea, uric acid, and creatinine.

Kidneys are involved in regulating the water balance of the body by regulating the concentration of urine and maintaining blood pressure.

Urea is produced by the liver in every cell of the body when amino acids are dephosphorylated. Urea is a waste product that is filtered by the kidneys.

Birds and reptiles excrete nitrogenous waste products in the form of uric acid rather than urea, which is the case in mammals. Hence, this is not a role of the kidneys.

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Chain Reactions Linking Acorns to Gypsy Moth Outbreaks and Lyme Disease Risk Oak trees (Quercus spp.) produce large autumnal acorn crops every two to five years, and produce few or no acorns during intervening years. Acorns are a critical food for white-footed mice (Peromyscus leucopus). Mice are important predators of the pupal stage of the gypsy moth (Lymantria dispar). This introduced insect periodically undergoes outbreaks that defoliate millions of hectares of oak forests, decreasing tree growth, survival, and acorn crop production. An abundance of acoms provides food for white-tailed deer (Odocoileus virginianus). Mice and deer are the primary hosts of the black-legged tick (Ixodes scapularis), which carries Lyme disease.

Answers

The chain of events linking acorns to gypsy moth outbreaks and Lyme disease risk can be summarized as follows:

1. Acorn Production: Oak trees produce large acorn crops every two to five years, with intervening years having few or no acorns.

2. White-Footed Mice: Acorns are a critical food source for white-footed mice. During years with abundant acorn production, the mouse population increases due to the availability of food.

3. Gypsy Moth Predation: White-footed mice play a crucial role in controlling gypsy moth populations. They are important predators of the pupal stage of the gypsy moth.

4. Gypsy Moth Outbreaks: The gypsy moth, an introduced insect, periodically undergoes outbreaks. During these outbreaks, the gypsy moth larvae defoliate millions of hectares of oak forests. This defoliation can have detrimental effects on tree growth, survival, and acorn crop production.

5. Deer and Acorns: An abundance of acorns provides a food source for white-tailed deer. Deer play a role in dispersing acorns and can consume large quantities when they are available.

6. Tick Hosts: Both white-footed mice and white-tailed deer are primary hosts for the black-legged tick, also known as the deer tick (Ixodes scapularis). These ticks are responsible for transmitting Lyme disease.

7. Lyme Disease Risk: The black-legged tick carries the bacterium that causes Lyme disease. When ticks feed on infected hosts, such as white-footed mice and white-tailed deer, they can acquire the bacterium. Subsequently, these ticks can transmit the bacterium to humans when they bite.

The chain reaction begins with the production of acorns by oak trees, which supports an increase in the population of white-footed mice. These mice, in turn, prey on gypsy moth pupae, helping to control gypsy moth populations. However, when gypsy moth outbreaks occur, they can defoliate oak forests and impact tree health and acorn production. Abundant acorns also attract white-tailed deer, which are hosts for black-legged ticks carrying Lyme disease. Thus, the interconnectedness of these factors contributes to the risk of Lyme disease transmission to humans.

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The nucleotides in a single strand of DNA are connected by... [Select the best answer.] a. hydrogen bonds between phosphates b. covalent bonds between sugars c. hydrogen bonds between complementary bases d. covalent bonds between the sugar of one nucleotide and the phosphate of the next nucleotide.

Answers

The nucleotides in a single strand of DNA are connected by covalent bonds between the sugar of one nucleotide and the phosphate of the next nucleotide.

The structure of DNA consists of two strands that are held together by hydrogen bonds between complementary bases (adenine with thymine and guanine with cytosine). However, within each individual strand, the nucleotides are connected by covalent bonds.

A nucleotide is composed of three main components: a phosphate group, a sugar molecule (deoxyribose in DNA), and a nitrogenous base. The sugar-phosphate backbone forms the structural framework of the DNA molecule. The covalent bonds between the sugar of one nucleotide and the phosphate of the next nucleotide create a strong and stable linkage, known as a phosphodiester bond.

These covalent bonds form a continuous chain of nucleotides in a single strand of DNA. The phosphate group of one nucleotide is covalently bonded to the sugar molecule of the adjacent nucleotide, forming a repeating pattern along the DNA strand.

It is important to note that the hydrogen bonds between complementary bases occur between the two strands of DNA, holding them together in a double helix structure, while the covalent bonds within each strand provide stability and maintain the integrity of the DNA molecule.

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humans may have one or four blood types: A, B, AB, or O. explain why a person with tupe O blood is referred to as universal donor yet can recieve only from othe rindividuals with type O blood 5 sentences

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A person with type O blood is referred to as the universal donor because their red blood cells do not express the A or B antigens on their surface.

This means that their blood can be transfused into individuals with any blood type (A, B, AB, or O) without triggering an immune response. However, individuals with type O blood can only receive blood from other individuals with type O blood. This is because if they receive blood that contains the A or B antigens, their immune system will recognize them as foreign and mount an immune response, leading to potentially severe complications. Therefore, while type O blood can be donated to anyone, individuals with type O blood can only receive blood from others with type O blood.

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