explain why cord-mediated reflexes are generally much faster than those involving input from the higher brain centers.

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Answer 1

Cord-mediated reflexes are generally much faster than those involving input from the higher brain centers because cord-mediated reflexes involve only spinal cord neurons, while brain centers (such as the cerebral cortex and brainstem) are involved in reflexes that require sensory input from other areas of the body.

Cord-mediated reflexes involve a direct connection between sensory neurons and motor neurons in the spinal cord. When a sensory neuron is stimulated, it sends an electrical impulse to the spinal cord, which then activates a motor neuron, causing a muscle to contract. This process takes only a few milliseconds, and the reflex response is almost instantaneous.

Brain centers, on the other hand, are involved in reflexes that require sensory input from other areas of the body. For example, when you touch a hot stove, your sensory neurons send a signal to the spinal cord, which then sends a signal to the brainstem. The brainstem then sends a signal to the cerebral cortex, where the signal is processed and a decision is made about how to respond. This process takes much longer than a cord-mediated reflex and can take up to half a second or more.

Therefore, cord-mediated reflexes are generally much faster than those involving input from the higher brain centers.

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Related Questions

the thick filament is composed of what molecule? myosin pivoting the head of this molecule provides what is known as the

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The thick filament is composed of the myosin molecule. Pivoting the head of this molecule provides what is known as the power stroke. The thick filament is a component of the sarcomere, which is the basic unit of contraction in skeletal muscle.

The thick filament, which is made up of myosin molecules, is responsible for generating the force of muscle contraction.  

Myosin is a protein that makes up the thick filaments of muscle fibers. The molecule consists of two main regions: the head region and the tail region.

The tail region of each myosin molecule is responsible for binding to other myosin molecules in order to create the thick filament.

The head region of the myosin molecule is responsible for binding to and interacting with the thin filament during the process of muscle contraction.

When the myosin head binds to the thin filament, it undergoes a conformational change that results in the power stroke. This power stroke is what causes the thick filament to slide past the thin filament, generating the force of muscle contraction.

Overall, the thick filament and the myosin molecules that make it up are essential for muscle function and movement.

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which structural layer of blood vessels is most responsible for maintaining blood pressure? group of answer choices tunica intima subendothelial tunica media tunica externa

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The tunica media is the structural layer of blood vessels most responsible for maintaining blood pressure. Option C.

It is made up of a layer of smooth muscle cells and elastic connective tissue, which act together to regulate blood flow and pressure. The elastic connective tissue is able to stretch and expand, helping to maintain a constant pressure within the vessel walls.

When the pressure increases within the vessel, the muscle cells contract to restrict the flow, while when the pressure decreases the muscle cells relax to allow more blood flow.

The tunica intima, or innermost layer of the vessel wall, is composed of endothelial cells and helps to protect the vessel from damage. The subendothelial layer lies beneath the endothelial cells and provides a framework for the endothelial cells to attach to. Lastly, the tunica externa is the outermost layer of the vessel wall and helps to provide strength and support.
Together, these three layers of the blood vessel help to maintain consistent blood pressure and ensure the flow of blood throughout the body.

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mutations can occur with a single nucleotide change. the misfolding of the hemoglobin protein results from

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Mutations can occur with a single nucleotide change. The misfolding of the hemoglobin protein results from amino acid substitution.

A mutation is an alteration in the DNA sequence that results in a modified gene product or a modified regulatory element. A mutation is a permanent alteration to the DNA sequence that makes up a gene.

A mutation can occur in any part of the DNA sequence. A mutation can occur with a single nucleotide change. The misfolding of the hemoglobin protein results from amino acid substitution. Misfolding is a term used to describe the folding of a protein molecule into an incorrect three-dimensional structure.

Misfolding occurs when a protein does not fold correctly into its normal, biologically functional state. Misfolding of proteins is linked to a variety of diseases. Hemoglobin is a protein that is crucial for the transport of oxygen in the body. Hemoglobin is the oxygen-carrying protein in the red blood cells of mammals.

Hemoglobinopathy is a term used to describe diseases caused by mutations in the hemoglobin gene. These illnesses can have a variety of consequences, ranging from minor symptoms to serious, life-threatening illnesses.

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true or falsein type 2 diabetes, the body's cells do not respond adequately to the hormone insulin

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The statement "In type 2 diabetes, the body's cells do not respond adequately to the hormone insulin" is true because when the cells don't respond, the body cannot adequately use the glucose from the bloodstream for energy, resulting in high blood sugar levels.

When the cells don't respond, the body cannot adequately use the glucose from the bloodstream for energy, resulting in high blood sugar levels. Insulin helps regulate blood sugar levels by allowing glucose from the bloodstream to enter the body's cells for energy.Type 2 diabetes is caused by a combination of factors, including genetics and lifestyle.

Being overweight or obese, having a sedentary lifestyle, and consuming a diet high in processed foods and sugar are all risk factors. Treatment for type 2 diabetes typically involves making lifestyle changes such as exercising more and eating a healthy diet, as well as taking medications or insulin if needed.

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if two brain cells become more active at the same time, the connections between them grow stronger. this process is called

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This process is called synaptic plasticity. Synaptic plasticity is the ability of two neurons to form a stronger connection when they become active at the same time. This process is important for learning, memory formation, and other cognitive processes.

If two brain cells become more active at the same time, the connections between them grow stronger. This process is called Hebbian Learning.The learning process that occurs when the firing of one neuron strengthens the synapse that leads to a neighboring neuron is known as Hebbian learning. It is named after Canadian psychologist Donald Hebb, who first proposed the concept in 1949.

This theory is based on the idea that the two neurons that fire together become connected, and the synaptic link between them grows stronger when they do. Hebbian learning has been related to a variety of learning processes in the brain, including the development of perceptual maps in the visual cortex, the refinement of motor control, and the learning of higher-order cognitive abilities. It is thought to underlie most types of memory and plays a critical role in neural development, memory formation, and learning.

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how would you describe the physical structure of the feeding part of the colony? what are the individuals threadlike until called?

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Throughout its life cycle, it has two different forms: polyp and medusa. Its DNA molecule is bundled into thread-like chromosomal structures in the nucleus of the each cell, giving rise to the first form, called diploblastic.

What is a nucleic acid strand that resembles a thread?

A chromosome is indeed a gene-carrying, protein-coated linear thread of DNA that is found in the cell's nucleus and is responsible for transmitting genetic information.

Before it replicates, threadlike DNA is known as what?

Response and justification Chromosomes are the thread-like DNA bundles that are visible during cell division. These DNA structures arise from the coiling of DNA strands around histone proteins, which resemble thread on a spool, during in the prophase phase of mitosis.

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What do you think lead to the evolutionary differences between Owls and Falcons? Answer in at least four sentences.

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Answer:

Owls and Falcons belong to distinct families, each evolving uniquely to suit their distinctive hunting requirements. Specializing in hunting, Falcons rely on speed and agility to catch their prey featuring a streamlined body with long, pointed wings and sharp talons. In contrast, Owls are nocturnal hunters that heavily rely on stealth and silence to capture their prey with the use of forward-facing large eyes and sensitive hearing under low-light conditions. Owls possess flight feathers that are fringed with soft edges enabling them to fly silently. Falcons employ stiff, smooth feathers that promote fast flight. These diverse hunting methodologies have resulted in the animals' unique adaptations and evolutionary diversity.

Explanation:

based on the data, what is the relationship between temperature and water uptake by the radish seeds?

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According to the data interpretation, the water uptake by radish plant seeds increases with increasing temperature. This implies that water intake is directly proportional to temperature.

How temperature affects water uptake by plants ?

Because of the increased concentration of sunlight and warm air, transpiration will increase as the temperature rises. However, if temperatures remain high for an extended period of time, resulting in drought, transpiration may decrease to conserve water in the plant.

What is transpiration ?

Transpiration is the movement of water through a plant and the evaporation of water from aerial parts such as leaves, stems, and flowers. Water is essential for plants, but only a small portion of the water absorbed by the roots is used for growth and metabolism. Transpiration and guttation account for the remaining 97-99.5%. Leaf surfaces are dotted with pores known as stomata (plural "stoma"), which are more numerous on the undersides of the foliage in most plants. Guard cells and their stomatal accessory cells (collectively known as the stomatal complex) surround the stomata, which open and close the pore. Transpiration occurs through the stomatal apertures and can be thought of as a necessary "cost" associated with opening the stomata to allow air to pass through.

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what would most likely happen to a periplasmic protein in the general secretion pathway if the gene sequence is modified and the n-terminal sequence is significantly shortened

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If the gene sequence is altered and the N-terminal sequence is significantly shortened, the most likely thing that will happen to a periplasmic protein in the general secretion pathway is that it will be prevented from being targeted and processed to the periplasm. It could also be degraded or exported to the cytoplasm, depending on the degree of modification made.

A signal sequence is present at the N-terminal of a protein to direct it to the secretion pathway. This N-terminal signal sequence is necessary for the export and secretion of proteins to the periplasm.

If this signal sequence is absent, the protein might fail to be processed in the pathway or it might be directed to the cytoplasm.

Hence, a significant shortening of the N-terminal sequence in a gene sequence would fail the protein to be targeted to the periplasm, and it would not be able to get exported correctly in the general secretion pathway.

This would ultimately result in the non-secretion of periplasmic proteins. Therefore, modification of the gene sequence and the N-terminal sequence of the protein could have significant implications on the processing and secretion of periplasmic proteins.

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which of the following contain oxygenated blood? group of answer choices pulmonary veins lobar arteries pulmonary trunk pulmonary arteries

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Answer:  Pulmonary veins

Explanation:

Pulmonary veins contain oxygenated blood, while pulmonary arteries contain deoxygenated blood.

The pulmonary veins are the vessels that transport oxygenated blood from the lungs to the left atrium of the heart. The pulmonary arteries are the vessels that transport deoxygenated blood from the heart to the lungs. The pulmonary trunk is a large artery that carries blood from the right ventricle to the lungs, and the lobar arteries are branch arteries that connect the pulmonary trunk to the smaller bronchial arteries.

Oxygenated blood is blood that has passed through the lungs, where it has been oxygenated, and is rich in oxygen. This oxygenated blood is pumped out of the heart through the pulmonary veins, and is directed to the left atrium. From here, it is sent to the left ventricle, then distributed to the rest of the body.
Deoxygenated blood is blood that has already been used by the body, so it contains less oxygen and more carbon dioxide. This deoxygenated blood is sent to the lungs via the pulmonary arteries, where it is oxygenated and sent back to the heart.
The pulmonary trunk is a large artery that carries blood from the right ventricle of the heart to the lungs. The lobar arteries are branch arteries that connect the pulmonary trunk to the smaller bronchial arteries. These small bronchial arteries are the vessels that deliver oxygenated blood to the bronchi, which are the passageways that supply oxygen to the lungs.

In summary, the pulmonary veins contain oxygenated blood, the pulmonary arteries contain deoxygenated blood, the pulmonary trunk carries blood from the right ventricle to the lungs, and the lobar arteries are branch arteries that connect the pulmonary trunk to the smaller bronchial arteries.

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what is the main function of the cytoplasm in an animal cell?

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The main function of the cytoplasm in an animal cell is to provide a supportive environment for the cell's organelles and to facilitate various cellular processes.

In detail, the cytoplasm serves the following purposes:

1. Structural support: The cytoplasm consists of a jelly-like substance called cytosol, which provides a medium for the cell's organelles to remain suspended and maintain their structure.

2. Metabolic reactions: The cytoplasm houses numerous metabolic reactions, such as protein synthesis, glycolysis, and the citric acid cycle, all of which are vital for the cell's survival and proper functioning.

3. Transportation of molecules: The cytoplasm acts as a medium for the movement of molecules and ions within the cell. This includes the transportation of nutrients, waste products, and other essential molecules between different organelles and the cell membrane.

4. Enzyme activity: Many enzymes required for various biochemical reactions are present in the cytoplasm, ensuring proper functioning of the cell.

5. Storage of molecules: The cytoplasm serves as a storage space for molecules such as glycogen and lipids, which can be utilized when needed by the cell for energy production.

6. Cell signaling: The cytoplasm plays a crucial role in cell signaling processes, as it contains numerous signaling molecules and proteins that facilitate communication between cells and organelles.

In summary, the main function of the cytoplasm in an animal cell is to provide structural support, facilitate metabolic reactions, ensure transportation and storage of molecules, maintain enzyme activity, and play a crucial role in cell signaling.

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umbilical cord blood is promoted as a rich source of multipotent stem cells for autologous (self) transplants. can you see a problem with the use of baby's cord blood to treat a disease in that child at a later date?

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There are also ethical concerns surrounding the use of cord blood as a medical treatment, as some people believe that it is wrong to use stem cells from a baby in this way.

The use of a baby's cord blood to treat a disease at a later date can create a problem as it has several limitations. Some of these limitations include limited availability, high cost, and the need for a perfect match to the HLA of the recipient. Additionally, cord blood stem cells also have a lower stem cell count than bone marrow, which can make it difficult to transplant them into an adult patient. Moreover, there are other ethical concerns related to the use of cord blood as a medical treatment. One problem with using cord blood is that it contains a limited number of stem cells, which makes it less effective than other treatments. Furthermore, the costs associated with collecting, storing, and processing cord blood stem cells are often quite high, which can make it difficult for families to access this treatment option. Additionally, since cord blood stem cells must match the HLA of the recipient, it may be difficult to find a donor who is a perfect match.

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if you observe a live cell moving under the microscope, what structure might be producing the motion? select all that apply.

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The interior structure of a cell is observed to move when viewed under a microscope. The cytoskeleton, which causes cytoplasmic streaming, is what causes this movement in the interior skeletal-like component.

Which microscope is used to view live cells?

The two most common methods for seeing living cells are phase-contrast microscopy and differential interference-contrast microscopy. The cell, which Robert Hooke first discovered in 1665, has a long and fascinating history that has ultimately led to many of today's scientific breakthroughs.

What is the cell's microscopic structure?

The cell membrane, the nucleus, and the cytoplasm make up a cell's three components. The cytoplasm contains hundreds or perhaps thousands of tiny, distinct structures known as organelles, as well as intricate arrangements of microscopic fibers.

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which statement is not true about mutations? a mutation is a change in the dna that can generate offspring less fit for survival than their parents

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No, a mutation is not necessarily a change that results in an offspring less fit for survival than its parents.

Mutations can result in more fit offspring, no change, or less fit offspring depending on the particular mutation.

Mutations are changes in the genetic material (DNA) of a cell and can occur naturally through errors in the replication of DNA, or can be caused by environmental factors such as radiation or chemical mutagens. These mutations can be beneficial, neutral, or deleterious and may or may not result in a change of phenotype in the organism.

If a mutation is beneficial, it may result in offspring that are more fit for survival than their parents. If the mutation is deleterious, it may result in offspring that are less fit for survival than their parents. Neutral mutations have no effect on fitness and may or may not result in a change in phenotype. Regardless of the mutation, it is important to note that the offspring will always have some variation from its parents.

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immediately after absorption, what circulatory system carries the fat-soluble vitamins and large fats?

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Immediately after absorption, the circulatory system carries the fat-soluble vitamins and large fats is: lymphatic system

Immediately after absorption, the lymphatic system carries the fat-soluble vitamins and large fats. The lymphatic system is made up of a network of vessels and organs, including lymph nodes, that work together to transport lymph, a clear fluid containing white blood cells and other substances, throughout the body.

After fats and vitamins are absorbed from the digestive system, they are moved through the lymphatic system via lymphatic vessels and lymph nodes. The lymphatic vessels pick up the fat-soluble vitamins and large fats and carry them to the lymph nodes where they are filtered before entering the bloodstream. From there, they are distributed to the organs and tissues of the body.

In summary, the lymphatic system is responsible for carrying fat-soluble vitamins and large fats immediately after absorption. It is made up of vessels and organs that transport lymph, which is then filtered by lymph nodes and then distributed to the organs and tissues of the body.

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write two alternative hypotheses about how these lizards might have speciated/evolved on and between these islands.

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The first hypothesis suggests that the genetic divergence between the populations of the lizard species may have been facilitated by physical isolation. According to this hypothesis, the lizards may have become genetically and phenotypically different as a result of geographic isolation. The lizards may have been physically separated on these islands, either by natural barriers such as water bodies or by human activities such as farming or logging, for long periods of time.

The second hypothesis suggests that the genetic divergence between the populations of the lizard species may have been facilitated by different selection pressures. According to this hypothesis, the lizards may have become genetically and phenotypically different as a result of different environmental pressures on different islands. This hypothesis suggests that the lizards may have adapted differently to the different environments of different islands.

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true/false. one strategy for purifying an expressed protein from a mixture of bacterial proteins is to modify the protein's gene to encode a series of amino acid residues at the n- or c-terminus of the protein.

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The given statement is true because one strategy for purifying an expressed protein from a mixture of bacterial proteins is to modify the protein's gene to encode a series of amino acid residues at the N- or C-terminus of the protein.

This strategy, known as fusion protein expression, involves adding a sequence of amino acids to either the N- or C-terminal of the target protein. This additional sequence, called a fusion tag, typically consists of several amino acids and is used to purify the target protein from the mixture of other proteins. The fusion tag acts as a recognition site for affinity purification resins, allowing for the target protein to be selectively bound and subsequently eluted from the mixture.

Another advantage of using fusion protein expression is that it allows for increased expression levels of the target protein due to the presence of the fusion tag. Additionally, it is also possible to control the level of expression of the target protein by controlling the level of the fusion tag.

In conclusion, fusion protein expression is an effective strategy for purifying expressed proteins from a mixture of bacterial proteins. By adding a sequence of amino acids to the N- or C-terminal of the target protein, the target protein can be selectively bound and eluted from the mixture using affinity purification resins. Additionally, this strategy can also be used to increase expression levels and control the level of expression of the target protein.

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where do speaking primates come from? what is the difference brain wise and larynx-wise among the following: australopithecus afarensis, homo erectus and homo neanderthalensis? how long ago did humans begin to speak? by what time-frame were anatomically humans speaking as we would understand it today?

Answers

Answer:

A new study has thought about various primate species' brains. It uncovered that primates with more extensive vocal repertoires had more of their cerebrum committed to controlling their vocal apparatus. That recommends that our own talking has further adapted to fit modern standards vs chimpanzees who have the apparatus to talk but can't because they can't evolve as we did.

Explanation:

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we saw that signaling based on channel-linked receptors is the fastest signaling mechanism. why is this faster than other mechanisms?

Answers

Signaling based on channel-linked receptors is the fastest signaling mechanism because it involves direct communication between the receptor and the target cell.

The receptor binds with the ligand, which opens the ion channel, allowing ions to pass through. This rapid transmission of ions causes an electrical signal to be transmitted along the cell membrane to the target cell, allowing the signal to be processed quickly.

Other mechanisms, such as second messenger systems, involve more steps and thus take longer to complete.

In a second messenger system, the ligand binds to the receptor, causing a conformational change in the receptor and activating an enzyme, which in turn activates a second messenger molecule.

This second messenger molecule then binds to and activates a different enzyme, leading to a response in the target cell. This process takes significantly more time than the channel-linked receptor mechanism and therefore is not as fast.

In summary, signaling based on channel-linked receptors is faster than other mechanisms because it involves direct communication between the receptor and the target cell, eliminating the need for the multiple steps of a second messenger system. This direct transmission of ions results in a faster response in the target cell.

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describe the different mechanisms (e.g., reuptake, enzymatic breakdown, diffusion) by which neurotransmitter activity at a synapse can be terminated.

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Neurotransmitter activity at a synapse can be terminated by three main mechanisms: reuptake, enzymatic breakdown, and diffusion.

Reuptake is when neurotransmitters are taken back into the presynaptic neuron, while enzymatic breakdown is when enzymes break down neurotransmitters into smaller molecules. Diffusion is when neurotransmitters move away from the synapse, which causes the neurotransmitter concentration to decrease.

Reuptake is a process by which the neurotransmitter is taken back into the presynaptic neuron and broken down, either for reuse or for storage. This process is known as active reuptake and is very efficient in preventing the build-up of neurotransmitters in the synapse.

Enzymatic breakdown is when enzymes break down neurotransmitters into smaller molecules, and this process can occur both within and outside of the synapse.

Finally, diffusion is the process by which neurotransmitters move away from the synapse and the concentration of neurotransmitter decreases over time. This process is known as passive diffusion and is the most common way neurotransmitter activity is terminated at the synapse.

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which lymph nodes are located under the tip of the chin and are easier to explore with one hand?

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The lymph nodes located under the tip of the chin are called: submandibular lymph nodes.

They are easier to explore with one hand because they are found just below the mandible, or jawbone. These lymph nodes help filter lymphatic fluid, which is a key component in the immune system. This fluid contains white blood cells that help fight infections and other foreign substances that enter the body.

To explore these nodes with one hand, you should start by placing your hand underneath the chin, just below the jawbone, and then carefully feel the area with your fingers. You may be able to feel some small, roundish lumps or nodes underneath your fingertips. Be gentle and take your time when exploring, as pressing too hard may cause pain or discomfort.

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describe where cartilage is found on the surface of a long bone. what function dose cartilage serve in this location?

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Cartilage is found on the surface of long bones and it serves to cushion the joint, reduce friction, and provide tensile strength. It also contains proteoglycans which keep it hydrated and flexible.



Cartilage is composed of cells, fibers, and ground substance. The cells in cartilage produce the fibers and ground substance, which act as a cushion between the bones. The fibers also provide tensile strength, which helps maintain joint integrity. The ground substance is a gel-like material which helps cushion the joint and provides flexibility to the cartilage.


Cartilage also contains proteoglycans, which are molecules that help keep the cartilage hydrated. This helps to keep the cartilage flexible and helps prevent it from becoming too stiff and brittle. The proteoglycans also help keep the cartilage from drying out and wearing away.

In conclusion, Cartilage is found on the surface of long bones at the ends of the bone, where it forms a joint. Cartilage serves to cushion the joint and absorb shock. It also acts as a cushion between the bones and prevents them from grinding against each other. Cartilage also helps to reduce friction at the joint, allowing for smoother, more efficient movement.

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determine the correct answer
* sphinchter muscle block urine as it"
1- voulantry muscle
2-sync with urinary bladder muscle
3_it will relax to exert urine
4-all the aaboe

Answers

Option 2. The sphincters' muscle block urine as it sync with urinary bladder muscle

What does the  sphinchter muscle do?

The sphincter muscle is a ring-shaped muscle that surrounds the urethra, the tube that carries urine from the bladder out of the body. There are two sphincter muscles that control the flow of urine: the internal sphincter, which is made up of smooth muscle and is under involuntary control, and the external sphincter, which is made up of skeletal muscle and is under voluntary control.

The sphincter muscle works in coordination with the bladder muscle to control the flow of urine. When the bladder is full, the bladder muscle contracts to expel urine, while the internal sphincter muscle relaxes to allow urine to pass through the urethra. The external sphincter muscle remains contracted to maintain continence.

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early weight gain is mainly: a. bone growth. b. muscle growth. c. internal organ growth. d. increase in fat.

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Early weight gain is mainly due to bone growth, muscle growth, and internal organ growth. An increase in fat cells also contributes to weight gain, but it happens later in the development process.

The early weight gain of an infant is mainly due to the growth of bones, muscles, and internal organs. Bone growth accounts for about half of the weight gained by infants in the first few months of life. Muscle growth also contributes significantly to early weight gain. Internal organ growth, particularly the growth of the brain, accounts for the remainder of the weight gain. An increase in fat is also a contributing factor, but it generally happens later in the development process.


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the gel electrophoresis apparataus creates an electrical field with positive and negative poles at each end. were the dyes tested postively or negatively charged? how do you know?

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The dyes used in gel electrophoresis are usually negatively charged because they move towards the positive electrode. The positively charged particles are attracted to the negative electrode. Hence, it can be inferred that the dyes tested were negatively charged in gel electrophoresis.

In the gel electrophoresis apparatus, the dyes are tested positively or negatively charged. It is known that the apparatus creates an electrical field with positive and negative poles at each end. The charged particles are separated based on the strength of the charge they possess.

The gel electrophoresis is a technique that helps in the separation of DNA or RNA molecules based on their size and charge. The samples are loaded into a well that is created in a gel and exposed to an electric field.

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which statement describes the primary difference between centrally acting muscle relaxants and direct-acting antispasmodics?

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The primary difference between centrally acting muscle relaxants and direct-acting antispasmodics is that centrally acting muscle relaxants function by blocking impulses within the central nervous system, whereas direct-acting antispasmodics function by relaxing smooth muscle contractions directly in the affected area.

Centrally acting muscle relaxants function by blocking impulses within the central nervous system, which helps to relax skeletal muscles. It does so by acting on the spinal cord or brain. These drugs are used in conjunction with rest and physical therapy to treat conditions such as back pain, muscle spasms, and muscle strains.

Direct-acting antispasmodics function by relaxing smooth muscle contractions directly in the affected area. These drugs are used to treat gastrointestinal and urinary disorders, menstrual cramps, and muscle spasticity related to conditions like cerebral palsy, multiple sclerosis, and stroke.

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which group is considered a population? responses the birds of guam the birds of guam all birds and snakes of hoi polloi all birds and snakes of hoi polloi the arc-crested fruit doves of hoi polloi the arc-crested fruit doves of hoi polloi, all brown snakes on earth

Answers

A population refers to a group of individuals of the same species living in the same geographic area and potentially interbreeding. Based on this definition "The birds of Guam," is considered a population. Here option A is the correct answer.

The birds of Guam share the same species identity, and they all live in the same geographic area, providing the potential for interbreeding.

In contrast, option B, "All birds and snakes of Hoi Polloi," includes multiple species, and option D, "The arc-crested fruit doves of Hoi Polloi, all brown snakes on Earth," includes only one species of bird and one species of snake, but from different geographic locations.

Option C, "The arc-crested fruit doves of Hoi Polloi," refers to a single species, but it is unclear if all members of that species in the area are included or if they are limited to a specific geographic area.

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Complete question:

Which group is considered a population?

A) The birds of Guam.

B) All birds and snakes of Hoi Polloi.

C) The arc-crested fruit doves of Hoi Polloi.

D) The arc-crested fruit doves of Hoi Polloi, all brown snakes on Earth.

the tree stages of cellular respiration are glycolysis

Answers

glycolysis, the citric acid cycle, and oxidative phosphorylation. Glycolysis takes place in the cytosol, the citric acid cycle occurs in the mitochondrial matrix, and oxidative phosphorylation occurs on the inner mitochondrial membrane.

approximately what percentage of the human genome consists of noncoding dna? approximately what percentage of the human genome consists of noncoding dna? 98.5% 77.5% 67.0% 87.0%

Answers

Only about 1 percent of DNA is made up of protein-coding genes; the other 99 percent is noncoding. The correct answer is 98.5%.

The total number of noncoding genes in the human genome is controversial. Some scientists think that there are only about 5,000 noncoding genes while others believe that there may be more than 100,000 (see the article on Non-coding RNA). The difference is largely due to debate over the number of lncRNA genes.

The proportion of coding versus noncoding DNA varies significantly between species. In the human genome for example, almost all (98%) of the DNA is noncoding, while in bacteria, only 2% of the genetic material does not code for anything.

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which statement describes a gene? the pair of dna sequences an organism has for a trait a section of dna in which the code for a protein is located the physical trait produced by an organism's genetic makeup one variation of the code for a protein

Answers

The statement "A gene is a section of DNA in which the code for a protein is located" best describes a gene.

What is a gene?

A gene is a basic unit of heredity in living organisms. It is a specific sequence of DNA nucleotides that contains the instructions for making a functional product, such as a protein or RNA molecule.  

In other words, a gene is a specific sequence of nucleotides within DNA that contains the instructions for making a functional product, such as a protein or RNA molecule.

Genes are responsible for determining the physical and behavioral traits of an organism, such as eye color, height, susceptibility to certain diseases, and many other characteristics.

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