.What is one piece of evidence for the endosymbiotic hypothesis?
A-Mitochondria have 70S ribosomes.
B-Mitochondria have linear DNA.
C-Vibrio cholerae bacteria produce cholera toxin when infected by a phage.
D-Mitochondria have cell walls made of peptidoglycan, like those of Bacteria.

Answers

Answer 1

The correct answer is A- Mitochondria have 70S ribosomes. The endosymbiotic hypothesis proposes that eukaryotic cells originated from the incorporation of free-living bacteria into primitive host cells.

Mitochondria are believed to have originated from the endosymbiosis of aerobic bacteria, which were engulfed by the host cell. One of the pieces of evidence for this hypothesis is that mitochondria have their own circular DNA, which is similar to bacterial DNA, and they also have their own 70S ribosomes, which are smaller and structurally different from the eukaryotic 80S ribosomes. The presence of 70S ribosomes in mitochondria supports the idea that they originated from bacterial ancestors and were subsequently incorporated into eukaryotic cells through endosymbiosis.

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Related Questions

pathway of sperm cells from testis to external urethral orifice is called_____.

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The pathway of sperm cells from the testis to the external urethral orifice is called the male reproductive tract, or the spermatic tract.

This pathway comprises of a series of organs and structures, each playing an important role in the production and transport of sperm cells. Starting at the testes, sperm cells are produced in the seminiferous tubules. They are then transported to the epididymis, where they undergo maturation and storage. From the epididymis, sperm cells move through the vas deferens, which is a long, muscular tube.

At the end of the vas deferens lies the seminal vesicles, which secrete a nutritious fluid that helps to nourish the sperm cells. The sperm cells then pass through the prostate gland, which adds additional fluid to the semen. The fluid then passes through the ejaculatory ducts, which lead to the urethra.

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what is the medial attachment of the rhomboid major muscle

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The medial attachment of the rhomboid major muscle is the spinous processes of the upper thoracic vertebrae (T2-T5).

The medial attachment of the rhomboid major muscle is the vertebral border of the scapula. Specifically, it attaches to the spinous processes of the upper thoracic vertebrae (T2 to T5).

The rhomboid major is a deep back muscle located between the scapula and the spine. It works in conjunction with the rhomboid minor muscle to retract and stabilize the scapula.

The medial attachment of the rhomboid major muscle plays a crucial role in its function. When the muscle contracts, it pulls the scapula medially toward the spine, helping to retract the scapula and maintain proper posture. This action is important for various upper limb movements, such as pulling the shoulder blades together during activities like rowing or squeezing the shoulder blades together during exercises like scapular retractions.

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a mother chimpanzee is sitting behind her offspring, grooming the offspring. what sensory stimulus is the young chimpanzee taking in from this interaction?

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The young chimpanzee in this interaction is likely taking in tactile sensory stimuli from the grooming session with its mother. Grooming involves physical contact, such as the mother's hands or fingers touching the offspring's body and skin.

Through tactile sensations, the young chimpanzee can perceive the gentle touch, pressure, and movements of its mother's grooming actions. Tactile sensory information is important for social bonding, communication, and comfort among primates, including chimpanzees. Grooming not only helps to maintain hygiene and remove parasites but also serves as a social behavior that strengthens the bond between the mother and offspring. The tactile stimulation received during grooming can provide a sense of security, reassurance, and physical closeness for the young chimpanzee, fostering a positive emotional connection with its mother.

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laci codes for a(n) ________, and a null mutation in laci would cause the lac operon to be _________ in low-glucose conditions

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Laci codes for a repressor protein, which is responsible for inhibiting the expression of the lac operon in the absence of lactose.

A null mutation in laci would cause the lac operon to be constitutively expressed, even in low-glucose conditions. This means that the lac genes would be transcribed and translated into their respective proteins regardless of the presence or absence of lactose. This is because the repressor protein is no longer functional and cannot bind to the operator region of the lac operon to block transcription. As a result, the lac operon would be "switched on" all the time, leading to the constant production of lactose-metabolizing enzymes, even when glucose is available. This could be problematic for the cell, as it would require energy to produce these enzymes, even when they are not needed. However, in the presence of lactose, the inducer molecule binds to the repressor protein and changes its shape, making it unable to bind to the operator region. This allows RNA polymerase to transcribe the lac genes and produce the necessary enzymes to metabolize lactose.

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Which of the following are proteins that interact directly with antigens during the adaptive immune response?
A) immunoglobins
B) major histocompatibility complex
C) T cell receptors
D) all of these

Answers

All the given options - immunoglobulins, major histocompatibility complex, and T cell receptors - interact directly with antigens during the adaptive immune response.

All three options (A) immunoglobulins, (B) major histocompatibility complex, and (C) T cell receptors are proteins that interact directly with antigens during the adaptive immune response.

Immunoglobulins (antibodies) bind to antigens, major histocompatibility complex (MHC) molecules present antigens to T cells, and T cell receptors recognize and bind to the antigen-MHC complex.


Summary: All the given options - immunoglobulins, major histocompatibility complex, and T cell receptors - interact directly with antigens during the adaptive immune response.

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Which of the following vessels gives rise to the peritubular capillaries?
a. Glomerulus
b. Vasa recta
c. Efferent arteriole
d. Afferent arteriole

Answers

Efferent arteriole vessels gives rise to the peritubular capillaries. Option(c).

The efferent arteriole gives rise to the peritubular capillaries in the kidney. The peritubular capillaries are a network of tiny blood vessels that surround the renal tubules in the kidney. They play a crucial role in the reabsorption of water and solutes from the filtrate back into the bloodstream.

The efferent arteriole carries blood away from the glomerulus, which is a specialized capillary network involved in the initial filtration of blood in the renal corpuscle. As the efferent arteriole leaves the glomerulus, it gives rise to the peritubular capillaries, which then surround the renal tubules throughout the kidney.

The glomerulus (option a) is not directly involved in giving rise to the peritubular capillaries but rather functions as the initial filtration site in the nephron.

The vasa recta (option b) is a specialized network of blood vessels that descends into the medulla of the kidney and plays a role in maintaining the concentration gradient in the renal medulla. It is not directly associated with the peritubular capillaries.

The afferent arteriole (option d) carries blood into the glomerulus and is not directly responsible for giving rise to the peritubular capillaries.

Therefore, the correct answer is c. Efferent arteriole.

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which of the following statements is true about the biceps femoris muscle?
It is an antagonist of the biceps femoris. This is the tensor fasciae latae. It flexes the knee It flexes the thigh It is a synergist of the iliopsoas.

Answers

The statement that is true about the biceps femoris muscle is that it flexes the knee.

The biceps femoris muscle is one of the muscles located in the back of the thigh and is part of the hamstring muscle group. Its main function is to flex the knee joint and also assist in extending the hip joint. It works in opposition to the quadriceps muscles, which are responsible for extending the knee joint. The tensor fasciae latae muscle is not an antagonist of the biceps femoris but rather a muscle that works to abduct and flex the hip joint. Additionally, the biceps femoris muscle is not a synergist of the iliopsoas, which is a muscle group located in the front of the hip joint that works to flex the hip joint. The iliopsoas muscle is responsible for flexing the hip joint, whereas the biceps femoris muscle is responsible for flexing the knee joint.

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In anatomical position, the lateral forearm bone is the radius. T/F.

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The given statement "In anatomical position, the lateral forearm bone is the radius" is True because the anatomical position is a standardized reference position used in anatomy and medicine.

It is a standing position with the arms at the sides, the palms facing forward, and the feet parallel and flat on the ground. In this position, the lateral forearm bone is the radius. The radius is one of the two bones in the forearm and is located on the lateral side of the forearm, which is the side away from the body's midline.

The other bone in the forearm is the ulna, which is located on the medial side of the forearm, towards the body's midline. The radius and the ulna work together to enable the movement of the forearm and the rotation of the wrist.

Knowing the anatomical position and the location of the bones is important for healthcare professionals as it helps them to understand the orientation and relationships of structures in the body, which is crucial for accurate diagnosis and treatment.

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what compound couples glycolysis to acetyl coa formation?

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The compound that couples glycolysis to acetyl-CoA formation is pyruvate.

In glycolysis, glucose is broken down into two molecules of pyruvate in the cytoplasm of the cell. Pyruvate then enters the mitochondria, where it is converted into acetyl-CoA by the enzyme pyruvate dehydrogenase.

The conversion of pyruvate to acetyl-CoA is a key step in linking glycolysis to the citric acid cycle, also known as the Krebs cycle. Acetyl-CoA enters the Krebs cycle, where it is further metabolized to produce energy in the form of ATP.

Therefore, pyruvate plays an important role in coupling glycolysis to acetyl-CoA formation and ultimately to the production of ATP.

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The pieces of DNA produced by restriction endonucleases are termed restriction fragments. true or false?

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The statement, "The pieces of DNA produced by restriction endonucleases are termed restriction fragments." is true.

Restriction endonucleases, also known as restriction enzymes, are proteins that cut DNA at specific sequences known as recognition sites.

The DNA pieces of different lengths produced by these enzymes are called restriction fragments.

Restriction endonucleases are enzymes that cleave DNA at specific recognition sites, which are usually palindromic sequences.

These fragments can be analyzed and manipulated in various ways, such as in DNA fingerprinting, genetic engineering, cloning, gene editing, and gene sequencing.

The discovery and use of restriction enzymes have revolutionized the field of molecular biology and have greatly advanced our understanding of genetics and gene regulation.

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Which ranking has subcellular structures ordered from the largest to the smallest? A. ribosome, nucleus, pyruvate dehydrogenase complex. B. pyruvate ...

Answers

To rank subcellular structures from largest to smallest. The correct ranking is B. Pyruvate dehydrogenase complex, nucleus, ribosome.


1. Pyruvate dehydrogenase complex is a large enzyme complex that plays a key role in the conversion of pyruvate to acetyl-CoA. Its size ranges from 4 to 10 MDa (millions of Daltons), making it the largest among the given options.

2. The nucleus is an organelle found in eukaryotic cells, which contains most of the cell's genetic material. Its size varies, but typically, the diameter of the nucleus ranges from 5 to 10 micrometers.

3. Ribosomes are small cellular structures responsible for protein synthesis. They have a size of about 20-30 nanometers in diameter or around 2.5 MDa in molecular weight, making them the smallest among the given options.

So, the correct order from largest to smallest is the pyruvate dehydrogenase complex, nucleus, and ribosome.

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Secondary Antibody Staining of Drosophila embryos
Q9.7 Are drosophila embryos too large for effective visualization with a standard fluorescent scope?

Answers

No, drosophila embryos are not too large for effective visualization with a standard fluorescent microscope.

Drosophila embryos are typically between 0.1 to 0.3 millimeters in size, which is well within the resolution range of most standard fluorescent microscopes.

In fact, fluorescent microscopy is commonly used to visualize and study drosophila embryos.

Additionally, there are specialized microscopes and imaging techniques, such as confocal microscopy, that can provide even higher resolution images of these embryos.

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the organisms belonging to these different lineages are thought to be different species. which of these observations would most support this hypothesis?

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The most supporting observation for the hypothesis that organisms belonging to different lineages are different species would be the presence of reproductive isolation between the lineages.

If organisms cannot interbreed or produce viable offspring, they are considered to be separate species. Other observations that may support this hypothesis include differences in morphology, behavior, genetics, and ecology.

To support the hypothesis that organisms belonging to different lineages are different species, the most crucial observation would be reproductive isolation. This means that when individuals from these lineages attempt to interbreed, they either fail to produce offspring or produce offspring that are infertile or have reduced fitness. This demonstrates that these lineages have distinct genetic backgrounds and are separate species.

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across the lifespan, a nurse knows that the female heart

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Answer:

Is normally smaller than the male heart.

The total size of the heart is approximately that of a clenched adult fist. The female heart is normally smaller and weighs less than the male heart across all age groups.

The female heart does not consistently beat more slowly than a male heart.

Across the lifespan, a nurse knows that the female heart undergoes changes and experiences different risks compared to the male heart.

For instance, women have a higher risk of developing heart disease after menopause due to the decrease in estrogen levels. Additionally, pregnancy can put stress on the heart and increase the risk of complications such as preeclampsia and gestational diabetes. It is important for nurses to educate women on lifestyle modifications such as maintaining a healthy weight, exercising regularly, and managing stress to promote heart health throughout their lifespan.

The nurse would say that the age group of infants is most at risk for these imbalances.

A balance of electrolytes to change fluid levels, the brain can actively move electrolytes into or out of cells. As a result, maintaining electrolyte balance—also known as maintaining correct ion concentrations—is necessary to maintain fluid equilibrium between the compartments. The kidneys maintain proper electrolyte concentrations. Maintaining the right balance of electrolytes benefits your body's other activities, including muscular contraction and blood biochemistry. Sodium, calcium, potassium, chloride, phosphate, and magnesium are examples of electrolytes. You get them from the foods and drinks you eat.

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you record from a squid giant axon in which the reversal potential for potassium ions is at -90 mv. you hyperpolarize the membrane to -110 mv. what will happen?

Answers

When you record from a squid giant axon and hyperpolarize the membrane potential to -110 mV, the potassium ions will move out of the cell due to the increased driving force. This happens because the membrane potential is now more negative than the potassium reversal potential, which is at -90 mV.

As the potassium ions move out of the cell, the membrane potential will become even more negative, reaching a value closer to the potassium reversal potential. At this point, the outward movement of potassium ions will be balanced by their inward movement due to their electrochemical gradient, and the membrane potential will stabilize at the potassium reversal potential of -90 mV.

Therefore, hyperpolarizing the membrane potential to -110 mV will result in an outward movement of potassium ions and a stabilization of the membrane potential at the potassium reversal potential of -90 mV.

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besides genetics, [blank1] can change a trait

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Besides genetics, environment can change a trait.

There are other factors that can influence and change a trait besides genetics. The environment is a major influence on development. Environmental factors include food availability, temperature, humidity, and exposure to certain chemicals and pollutants.

For instance, a plant's growth and development can be affected by the amount of sunlight and water it receives. The same is true for animals, as their environment can shape their behavior and physiology. Depending on the species, different environmental conditions can influence their size, color, behavior, and even life expectancy.

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GFR regulation mechanisms primarily affect which of the following?
a. blood osmotic pressure (OPg)
b. glomerular hydrostatic pressure (HPg)
c. capsular hydrostatic pressure (HPc)
d. capsular osmotic pressure (OPc)

Answers

GFR regulation mechanisms primarily affect blood osmotic pressure (OPg) and glomerular hydrostatic pressure (HPg).

Correct option is A and B.

OPg is the pressure of the solutes in the blood that is generated by the kidneys, and HPg is the pressure of the fluid in the glomerulus that is generated by the heart. Both OPg and HPg play a major role in the reabsorption of fluid and solutes from the glomerular filtrate back into the blood.

The pressure of the fluid in the capsular space (HPc) and the pressure of the solutes in the capsular space (OPc) are both affected by the regulation of GFR, but to a lesser extent. The regulation of GFR is essential for maintaining homeostasis and optimal functioning of the body.

Correct option is A and B.

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When your body temperature is too high, which of the following does not occur? Heat radiates from the skin. Blood vessels in the skin constrict. The thermostatic control center of the brain is activated. Blood vessels at the body surface fill with warm blood. Evaporative cooling occurs.

Answers

When your body temperature is too high, the blood vessels in the skin do not constrict. Rather, they dilate, allowing more blood to flow to the surface of the skin and dissipate heat through radiation. This process is known as vasodilation and it helps to cool the body down.

The thermostatic control center of the brain is activated and sends signals to the body to initiate cooling mechanisms such as sweating, which leads to evaporative cooling. This process helps to lower the body temperature. If the body is unable to effectively cool itself down, it can lead to heat exhaustion or heat stroke, which can be dangerous and even life-threatening. It is important to stay hydrated and avoid overexertion in hot weather to prevent overheating. Additionally, wearing loose-fitting clothing and seeking shade or air conditioning can also help to keep the body cool. Vasodilation is the widening of blood vessels as a result of the relaxation of the blood vessel's muscular walls. Vasodilation is a mechanism to enhance blood flow to areas of the body that are lacking oxygen and/or nutrients.

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side effect of hormonal therapy used for behavior modification is increased

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It seems you may be referring to hormonal therapies used for behavior modification in certain contexts, such as in the treatment of sexual disorders or gender dysphoria.

In such cases, the side effect you may be referring to is an increased risk of certain health conditions.

For example, in the context of hormone therapy for gender dysphoria, individuals undergoing masculinizing hormone therapy (testosterone) or feminizing hormone therapy (estrogen and anti-androgens) may experience increased health risks associated with hormonal changes. These risks can include:

Cardiovascular effects: Hormone therapy can potentially increase the risk of cardiovascular conditions such as high blood pressure, heart disease, and blood clotting disorders.

Metabolic effects: Hormone therapy may affect metabolic parameters, including changes in lipid profiles, insulin sensitivity, and body composition. This can lead to an increased risk of metabolic disorders such as diabetes or dyslipidemia.

Liver function: Hormonal therapy may impact liver function, particularly in individuals using certain hormone formulations or at higher doses. Regular monitoring of liver function is essential in such cases.

Bone health: Hormonal therapy can affect bone density and increase the risk of osteoporosis or bone fractures. Adequate calcium and vitamin D intake, along with regular bone health monitoring, are important.

Mental health effects: While hormone therapy can alleviate gender dysphoria and improve mental well-being in individuals with gender incongruence, some individuals may experience mood changes, including increased risk of depression or anxiety.

It is important to note that the side effects and risks associated with hormonal therapy can vary depending on the specific context, individual factors, and the specific hormonal agents used. Close monitoring by healthcare professionals and regular follow-up appointments are crucial to manage potential side effects and ensure overall health and well-being during hormonal therapy.

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on what layer of the skin are the friction ridges located

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The friction ridges are located on the outermost layer of the skin, known as the epidermis.

Friction ridges, which are responsible for forming fingerprints, are located on the outermost layer of the skin called the epidermis.

The epidermis is composed of multiple layers, with the outermost layer being the stratum corneum.

This layer consists of dead skin cells that have flattened and fused together to form a protective barrier.

Beneath the stratum corneum is the stratum lucidum, followed by the stratum granulosum, stratum spinosum, and finally the basal layer, which is in direct contact with the dermis.

Friction ridges form during fetal development and are determined by genetic factors.

They are unique to each individual and do not change throughout their lifetime, making them a valuable tool for identification purposes.

The ridges are formed by the interaction between the dermis and the epidermis during development, with the dermal papillae protruding into the epidermis and forming the ridges.

In conclusion, friction ridges are located on the outermost layer of the skin, the epidermis, specifically on the stratum corneum layer.

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True or false: Meiosis occurs in specialized animal organs known as gonads.

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The following statement “Meiosis does occur in specialized animal organs known as gonads.” is True.  

In animals, including humans, meiosis takes place in the testes of males and the ovaries of females. The gonads are responsible for producing gametes (sperm cells in males and egg cells in females) through the process of meiosis.

During meiosis, the number of chromosomes in the cells is halved, resulting in the formation of haploid gametes. This is necessary for sexual reproduction, as when the gametes combine during fertilization, the resulting zygote will have the correct number of chromosomes for the species.

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select the main ways that mitosis and meiosis are different.

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Here are the main ways in which mitosis and meiosis differ:

1. Purpose: Mitosis is the process of cell division for growth, tissue repair, and asexual reproduction, resulting in two genetically identical daughter cells. Meiosis, on the other hand, is a specialized form of cell division that occurs in the reproductive cells (gametes) and is involved in sexual reproduction, resulting in four genetically diverse daughter cells.

2. Number of divisions: Mitosis involves a single division of the cell, resulting in two daughter cells. Meiosis involves two consecutive divisions, resulting in four daughter cells.

3. Chromosome number: Mitosis preserves the diploid chromosome number, where the daughter cells have the same number of chromosomes as the parent cell. Meiosis, however, reduces the chromosome number by half, resulting in daughter cells with a haploid chromosome number.

4. Genetic variation: Mitosis produces genetically identical daughter cells, as the chromosomes are replicated and divided equally. Meiosis, through the processes of crossing over and independent assortment, generates genetic diversity among the daughter cells, leading to genetic variation.

5. Role in reproduction: Mitosis is involved in the growth and maintenance of the body, while meiosis is specifically dedicated to the production of gametes (sperm and egg cells) for sexual reproduction.

These are the key differences between mitosis and meiosis, highlighting their distinct roles and outcomes in cellular division and reproduction.

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Which one out of the following enzymes acts in the pentose phosphate pathway? select one: a. pyruvate kinase b. glycogen phosphorylase c. 6-phosphogluconate dehydrogenase d. aldolase

Answers

The enzyme that acts in the pentose phosphate pathway is c. 6-phosphogluconate dehydrogenase.

The pentose phosphate pathway, also known as the hexose monophosphate shunt, is a metabolic pathway that operates alongside glycolysis. It plays a crucial role in the generation of pentoses (5-carbon sugars) and reducing power in the form of NADPH. These products are important for various cellular processes, including the synthesis of nucleotides and fatty acids and the detoxification of reactive oxygen species.

6-phosphogluconate dehydrogenase is an enzyme involved in the oxidative phase of the pentose phosphate pathway. It catalyzes the conversion of 6-phosphogluconate to ribulose-5-phosphate while generating a molecule of NADPH. This step is important for the production of reducing power needed for biosynthetic reactions and cellular antioxidant defense.

On the other hand, pyruvate kinase is an enzyme involved in glycolysis, specifically the conversion of phosphoenolpyruvate (PEP) to pyruvate. Glycogen phosphorylase is an enzyme involved in glycogenolysis, the breakdown of glycogen to release glucose. Aldolase is an enzyme involved in the cleavage of fructose-1,6-bisphosphate during glycolysis.

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identify if each cranial nerve is mainly sensory motor or both

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There are 12 pairs of cranial nerves in the human body, and each of these nerves has different functions that are classified as sensory, motor, or both.

The sensory nerves are responsible for transmitting information from the body's sensory organs, such as the eyes, ears, nose, and tongue, to the brain, while the motor nerves transmit signals from the brain to the body's muscles, allowing for movement and coordination. The first two cranial nerves, the olfactory and optic nerves, are primarily sensory nerves, responsible for transmitting the sense of smell and vision to the brain, respectively. The third, fourth, and sixth cranial nerves, the oculomotor, trochlear, and abducens nerves, are primarily motor nerves that control the movements of the eyes. The fifth cranial nerve, the trigeminal nerve, is both sensory and motor, responsible for transmitting sensation from the face and head and controlling the muscles used in chewing. The seventh and ninth cranial nerves, the facial and glossopharyngeal nerves, are also both sensory and motor, responsible for transmitting taste and controlling facial expressions and swallowing, respectively. The eighth cranial nerve, the vestibulocochlear nerve, is primarily sensory, responsible for transmitting hearing and balance information to the brain. The tenth cranial nerve, the vagus nerve, is both sensory and motor, responsible for transmitting information from the organs in the chest and abdomen and controlling various organs, including the heart, lungs, and digestive system. Finally, the eleventh and twelfth cranial nerves, the accessory and hypoglossal nerves, are primarily motor nerves, responsible for controlling the muscles in the neck and tongue, respectively.

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Veins functions as ________ reservoirs due to their ________ compliance.
A) pressure : high
B) volume : high
C) pressure : low
D) volume : low
E) pressure : lack of

Answers

Veins function as volume reservoirs due to their high compliance. Compliance refers to the ability of a vessel to expand and accommodate an increased volume of blood without a significant increase in pressure.

Veins have a thinner muscular wall than arteries, which allows them to stretch and hold a larger volume of blood at a lower pressure. This function is particularly important during times of decreased blood flow, such as when standing for long periods or during dehydration. In these situations, the veins can dilate and hold onto more blood, helping to maintain adequate blood pressure and perfusion to vital organs. Additionally, the compliance of veins can help to prevent damage to smaller blood vessels by acting as a cushion against rapid changes in pressure.
In summary, veins function as volume reservoirs due to their high compliance. This allows them to accommodate changes in blood volume without significantly altering blood pressure and helps to prevent damage to smaller blood vessels.

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in the family below, the affected people have an autosomal dominant mutation. please describe the pattern of activity in this gene. be as specific as possible.

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In an autosomal dominant inheritance pattern, the presence of a single copy of the mutant gene is sufficient to cause the phenotype or disease.

It means that individuals who inherit the mutated gene from one affected parent have a 50% chance of inheriting the condition. The trait or disorder associated with the gene will be expressed in each generation, and both males and females can be affected. The mutant gene is not limited to one sex and does not skip generations. Additionally, unaffected individuals do not transmit the condition to their offspring.

It is important to note that without specific information about the family and the specific gene involved, it is not possible to provide more detailed information about the pattern of activity in this gene.

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list the full steps of the simplified viral reproductive cycle

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The list of full steps of the simplified viral reproductive cycle includes,

1. Attachment

2. Entry

3. Uncoating

4. Replication and Transcription

5. Translation

6. Assembly

7. Maturation

8. Release

9. Transmission

1. Attachment: The virus attaches to specific receptors on the surface of a host cell. This attachment is usually mediated by viral proteins interacting with host cell receptors.

2. Entry: The virus enters the host cell, either through direct fusion with the host cell membrane or by being engulfed into the cell through endocytosis.

3. Uncoating: Once inside the host cell, the viral genetic material is released from its protein coat (capsid) or envelope. This step allows the viral genome to be accessible for replication and gene expression.

4. Replication and Transcription: The viral genome is replicated and transcribed by utilizing the host cell's machinery. The viral genes are used to produce new copies of the viral genetic material and viral proteins.

5. Translation: The newly synthesized viral proteins are translated using the host cell's ribosomes. These proteins are necessary for the assembly of new virus particles.

6. Assembly: The viral components, including the newly synthesized viral genetic material and proteins, come together to form new virus particles, often inside the host cell.

7. Maturation: The newly assembled virus particles undergo maturation, during which they acquire their final structural and functional characteristics. This step may involve modifications to the viral proteins or packaging of the genetic material into the capsid.

8. Release: The mature virus particles are released from the host cell, either through cell lysis (rupture) or budding. In budding, the virus acquires a portion of the host cell membrane as it exits, resulting in the formation of an enveloped virus.

9. Transmission: The released virus particles can then infect new host cells, either within the same organism (horizontal transmission) or to different organisms (vertical transmission).

It's important to note that viral reproductive cycles can vary depending on the specific type of virus, host, and other factors. This simplified outline captures the general steps involved in a viral reproductive cycle.

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How would you isolate Benzyl alcohol, if you had the benzyl alcohol in diethyl ether? I would extract with M HCl, separate distill the aqueous layer. • I would gently distill the diethyl ether the benzyl alcohol should be in the receiver • I would gently distill the diethyl ether, the benzyl alcohol should be in the distillation flask

Answers

To isolate Benzyl alcohol from diethyl ether, I would first extract it with M HCl to obtain an aqueous layer.


To isolate benzyl alcohol from a diethyl ether solution, you can follow these steps:

1) Perform an extraction using M HCl to form an aqueous layer containing benzyl alcohol;

2) Separate the aqueous layer from the diethyl ether layer;

3) Gently distill the diethyl ether, leaving the benzyl alcohol in the distillation flask. This process allows for the separation and purification of benzyl alcohol from the diethyl ether solution.

Overall, the key steps to isolating Benzyl alcohol from diethyl ether involve extraction with M HCl and distillation of the aqueous layer and ether.

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most hominin fossils older than 3 million years are called

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Most hominin fossils older than 3 million years are called Australopithecus. This term refers to a group of extinct hominins that lived in Africa between approximately 4.2 and 1.2 million years ago.

The Australopithecus genus is divided into several species, such as Australopithecus afarensis, Australopithecus africanus, and Australopithecus sediba.

Australopithecus fossils are significant because they provide valuable insights into the evolutionary history of early humans. For example, the famous fossilized skeleton of Lucy, an Australopithecus afarensis, revealed that these hominins were bipedal, meaning they walked on two legs. This was a crucial step in human evolution, as bipedalism allowed early humans to travel long distances and use their hands for other tasks, such as tool-making.

In addition to bipedalism, Australopithecus fossils also show that these hominins had relatively small brains and robust, muscular bodies adapted to living in trees and on the ground. Over time, as hominins evolved and their environments changed, these characteristics would shift, leading to the emergence of new species, such as Homo erectus and eventually Homo sapiens.

Overall, most hominin fossils older than 3 million years are called the Australopithecus fossils representing an important chapter in the story of human evolution, and their study continues to shed light on the origins of our species.

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Most commonly, which cerebral hemisphere is responsible for controlling speech? A. Left B. Right

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A. Left hemisphere is most commonly responsible for controlling speech.

In the majority of individuals, the left hemisphere of the brain is primarily responsible for controlling speech. This phenomenon is known as left hemisphere dominance for language. The left hemisphere contains specialized regions, such as Broca's area and Wernicke's area, which play crucial roles in language processing and production.

Broca's area, located in the frontal lobe of the left hemisphere, is involved in the production of speech and the coordination of speech-related muscles. Damage to this area can result in expressive language difficulties, such as difficulty forming words or sentences (a condition known as Broca's aphasia).

Wernicke's area, located in the temporal lobe of the left hemisphere, is involved in language comprehension. Damage to this area can lead to receptive language difficulties, where individuals may have trouble understanding spoken or written language (known as Wernicke's aphasia).

While the left hemisphere is typically dominant for speech, it's important to note that there can be variations among individuals, and in some cases, speech control can involve contributions from both hemispheres.

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