select all of the following that provide evidence that modern species have evolved from prior species. a. molecular biology b. biogeography c. biogeography d. comparative anatomy e. the fossil record

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Answer 1

Molecular biology, biogeography, comparative anatomy, and the fossil record all provide evidence for common descent, and that modern species have evolved from prior species. By studying these sources, one can gain a better understanding of the evolutionary process, and how species have changed over time.

Molecular biology provides evidence for common descent by comparing the genetic sequences of different species. Genetic sequences are like fingerprints that are unique to each species, and by comparing the genetic sequences of two species, one can determine how closely related the two species are. For example, if two species have similar genetic sequences, then it is likely that the two species are closely related, and are descended from a common ancestor.

Biogeography is the study of the geographic distribution of species. By looking at the geographic distribution of species, one can infer how the species might have evolved from their ancestors. For example, if two species are found in the same geographic area, then it is likely that the two species are related, and descended from a common ancestor.

Comparative anatomy is the study of the anatomy of different species. By comparing the anatomy of different species, one can determine how closely related they are. For example, if two species have similar anatomical features, then it is likely that the two species are closely related, and are descended from a common ancestor.

The fossil record provides evidence for common descent by looking at the transition of species over time. Fossilized remains provide a snapshot of the evolution of species over time, and by looking at the transition of species over time, one can infer how one species evolved into another.

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Related Questions

the hypothesis that processes similar to those at work in microevolution can, over eons of time, transform an organism into a completely different kind of organism.

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The hypothesis that processes similar to those at work in microevolution can, over eons of time, transform an organism into a completely different kind of organism is one of the most important theories in evolutionary biology.

This hypothesis proposes that small, incremental changes in an organism's genes, traits, and behavior can accumulate over long periods of time to yield substantial changes in the species. In other words, small differences in characteristics can accumulate and become much larger ones, eventually leading to the emergence of an entirely new species.

The primary process at work in this hypothesis is natural selection. Over time, certain traits become more advantageous than others, and those that are beneficial are more likely to be passed on to future generations. This leads to the gradual accumulation of beneficial traits, which can eventually lead to a major change in the organism. For example, a species of birds living in an environment with a great deal of wind may gradually evolve larger wings to help them better navigate the air currents.

Another process important to the hypothesis is genetic drift. This occurs when random changes in the gene pool occur due to chance, rather than due to natural selection. These changes can sometimes be beneficial, and they can accumulate over time, leading to significant changes in the species.

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a complete halt to trading with a particular nation or in a particular product is called an embargo.

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An embargo is a full halt to trade with a specific country or in a specific good. . true.

When a product is exported in huge quantities, is the price lower than what it would be if it were sold domestically or less than what it would cost to make the product?

Dumping happens when a nation or business exports a good at a cost that is less expensive in the foreign market than it is in the exporter's home market.The ability of flood the market with goods at prices that are frequently thought to be unfair is the main benefit of dumping.

Is indeed the exportation of a commodity in big numbers at a cheaper cost than the domestic market price?

Dumping is the export of a product in big quantities at a cheaper rate than the domestic market price for the same product.

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Which of the following musculoskeletal injuries has the GREATEST risk for shock due to blood loss? A. pelvic fracture B. posterior hip dislocation C. unilateral femur fracture D. proximal humerus fracture

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Pelvic Fracture is a musculoskeletal injury which has a greater risk for shock due to blood loss, among the rest of the options.

A break in one or more of your pelvic bones is known as a pelvic fracture. The severity of pelvic fractures, which are a rare kind of fracture, can range from minor to severe. While minor pelvic fractures typically heal without surgery, major fractures necessitate treatment.

With a shattered pelvis, it is painful to stand, sit, or move around. The bladder, intestines, and other significant blood arteries are shielded either by the pelvis. Numerous significant abdominal and leg muscles also link to the pelvis, enabling proper body motion and function.

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Please concisely explain the difference between ecosystem function and ecosystem services. Your answer
should be a single complete and grammatical sentence.

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Answer: Ecosystem function refers to the processes and interactions that take place within an ecosystem, such as the cycling of nutrients and energy through the food web. Ecosystem services, on the other hand, are the benefits that humans derive from ecosystems, such as the provision of food, clean water, and air, as well as the regulation of climate and other environmental factors.

sickle-cell anemia is a genetic disorder that occurs when an individual has two recessive alleles. scientists have discovered that some people who are carriers of one allele for sickle-cell anemia are protected against malaria. deduce which genotype would be the most advantageous to protect people against malaria without causing sickle-cell anemia.

Answers

Sickle-cell anemia is a genetic disorder that occurs when an individual has two recessive alleles.

Scientists have discovered that some people who are carriers of one allele for sickle-cell anemia are protected against malaria. Aa Heterozygous genotype would be the most advantageous to protect people against malaria without causing sickle-cell anemia.

A genetic disorder called sickle cell anemia manifests from birth. The changed or mutated genes from your mother, father, or both parents are the root cause of many genetic disorders.

Red blood cells in sickle cell anemia sufferers have a crescent or sickle shape. A hemoglobin gene mutation is the cause of this odd form. Red blood cells' haemoglobin component enables them to carry oxygen to tissues all over your body.

Red blood cells' sickle shape can cause a number of difficulties. They can get caught inside blood arteries because of their atypical structure, resulting in uncomfortable symptoms. Furthermore, sickle cells age more rapidly than regular red blood cells, which can cause anemia. Some genetic disorders, but not all of them, can be passed down from one or both parents. One such disorder is sickle cell anemia. It has an autosomal recessive pattern of inheritance.

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A group of stone age farmers settles on a remote island. The allele frequency of this first generation is P=0.8 and Q=0.2, with P being the dominant allele frequency and Q being the recessive allele frequency. One thousand years later, no member of this population has the recessive allele. This is an example of: A) Natural Selection B) Genetic Drift C) Mutation D) Gene Flow

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A group of stone-age farmers settles on a remote island, and the allele frequency of this first generation is P = 0.8 and Q = 0.2. One thousand years later, no member of this population has the recessive allele, and this is an example of the genetic drift present in Option B.

What is genetic drift?

Genetic drift occurs when genes from one population migrate to another through migration, mating, or other means, causing changes in the gene pool of that population. In this way, after a thousand years, the recessive allele is lost.

Hence, this population has no recessive allele, and this is an example of the genetic drift present in Option B.

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Peter went swimming at a lake with his friends. They arrived early in the morning. Peter walked on the sand around the lake with his bare feet. The sand is cool. At noon, when Peter walked around the lake with his bare feet, the sand is very hot.

What has made the sand hot at noon?
A heat from the motion of the waterheat from the motion of the water
B hot rock under Earth’s surfacehot rock under Earth’s surface
C radiant energy from the Sunradiant energy from the Sun
D warmth from human bodies

Answers

Answer:

A

Explanation:

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The radiation from the sun warms the sand. Therefore, option "C" is correct.

What is low specific heat?

Sand has low unambiguous intensity, meaning it needs almost no energy from the sun to warm up quickly. Sand can store a significant amount of the gained thermal energy due to its high density.

The amount of intensity expected to raise the temperature of one gram of a substance by one Celsius degree is referred to as the specific heat. Typically, calories or joules per gram and Celsius degrees are the units of specific heat. Water, for instance, has a specific heat of 1 calorie (or 4.186 joules) per gram for every degree Celsius.

Therefore, matters having low specific heat get warm easily which they get in contact with the heating material.

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The data in the graph are the result of a paramecium being placed in a hypertonic salt solution.

A graph entitled Paramecium Contractile Vacuole Contractions has salt concentration on the horizontal axis and contractions per minute on the vertical axis. A very low salt concentration has 30 contractions per minute, low: 22, medium: 15, high: 8, very-high: 2.

Based on the data in the graph, which would most likely happen if the paramecium were placed in distilled water?

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Based on the data in the graph, the most likely thing that will happen if the paramecium were placed in distilled water is that the contractions would increase.

What is paramecium?

Paramecium is described as a genus of eukaryotic, unicellular ciliates, commonly studied as a representative of the ciliate group.

The most likely thing that will happen if the paramecium were placed in distilled water is that the contractions would increase as the result of a hypertonic solution.

The total movement of water in an aqueous solution is from the higher water concentration to a lower water concentration and so because a hypertonic solution has higher solute in the cell than the outside. The movement is from the cell to the outside and so the cell will shrink.

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Answer:

The contractions would increase.

Explanation:

The pelvic splanchnic nerves are formed by preganglionic parasympathetic fibers from the ______ region of the spinal cord.

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Preganglionic parasympathetic fibers from the sacral region of the spinal cord form the pelvic splanchnic nerves.

The pelvic splanchnic nerves are preganglionic nerves that emerge from the spinal cord's lateral horn grey matter at the sacral segments of the S2, S3, and S4. The S3 nerve usually contributes the most of these fibers.

Sympathetic nerve fibers emerge from the gray matter of the spinal cord's intermediolateral horns between segments T-1 and L-3. There are no sympathetic nerve fibers that originate in the cervical or lumbar or sacral segments of the cord below L-3.

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Which of the following best describes how a cell uses alcohol fermentation as a mechanism of breaking down food to generate ATP?a. Oxygen is absent; electron transport chain is not used.b. Oxygen is absent; electron transport chain is used.c. Oxygen is present; electron transport chain is not used.d. Oxygen is present; electron transport chain is used.

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The following best describes how a cell uses alcohol fermentation as a mechanism of breaking down food to generate ATP Oxygen is absent; the electron transport chain is not used.

Many fermentation processes require enzymes to speed up the process. Since the amylase enzyme is responsible for breaking down starch into simple sugars, alcohol cannot be produced without the amylase enzyme. Furthermore, fermentation without enzymes is never possible.

Alcoholic fermentation is a complex biochemical process in which yeast converts sugars into ethanol carbon dioxide and other metabolic by-products that contribute to the chemical composition and sensory properties of fermented foods. The main purpose of fermentation is to produce ATP an energy source for use and storage at the cellular level.

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in the r- vs. k-selection classification, which of the following best describes a k-selected species? individuals grow larger, live longer, reproduce later, and invest more resources into each offspring. individuals reproduce early and often, maximizing fecundity with little investment in each offspring. individuals live longer and reoroduce later but invest verv little in offspring. individuals reproduce earlv and often and invest more resources into each offspring.

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K-selected species have relatively steady populations that fluctuate near the environment's carrying limit.

These animals are distinguished by having a small number of offspring while providing extensive parental care. Humans, elephants, and bison are all k-selected species.

Reproduction is the biological process through which new individual organisms - "offspring" - are formed from their "parent" or parents. Each individual organism exists as a result of reproduction, which is a fundamental aspect of all known life.

Semelparity. A member of a species reproduces just once during its lifespan and then dies in semelparity. Species with this pattern deplete the majority of their resource budget in a single reproductive event, risking their health to the point of extinction.

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manipulations that decrease blood glucose level cause ; manipulations that increase blood glucose level cause . group of answer choices an increase in hunger; a decrease in hunger an increase in general arousal; a decrease in general arousal a decrease in general arousal; an increase in general arousal a decrease in hunger; an increase in hunger

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An increase in hunger is a side effect of blood glucose level manipulations. A decrease in hunger is a side effect of blood glucose level manipulations.

The quantity of glucose dissolved in a person's blood is known as blood glucose. For their energy needs, the body's many cells obtain this glucose. Diabetes, on the other hand, is a condition where the cells do not absorb the dissolved glucose.

Hunger is an organism's desire to consume food. The hormone ghrelin causes the body to produce the sensation of hunger. When the stomach is empty, it is let go. It causes the hypothalamus to send a signal that makes someone feel hungry.

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Which of the following pieces of evidence most strongly supports the common origin of all life on Earth ? A. All organisms require energy . B. All organisms reproduce . C. All organisms show heritable variation . D. All organisms use essentially the same genetic code .

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Cell function is often strongly supports the common origin of all life on Earth as all organisms reproduce. Thus, option B is correct.

What are centrioles?

Centrioles has been considered as the small, cylindrical cell organelles, which is present just near the nuclei of the animal cells. It has been involved in the formation of the spindle fibers at the time of the cell division that help in the proper separation of the chromosomes during cell division.

Nucleus as well as ribosomes has been present in both animal and plant cells, while cell wall is found only in plant cell. The organelle in the diagram that should be listed under animal only will be 'centriole.'

Therefore, Cell function is often strongly supports the common origin of all life on Earth as all organisms reproduce. Thus, option B is correct.

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look over the pedigree you constructed in part a. based on the inheritance pattern, which mode of inheritance must be the cause of galactosemia? view available hint(s)for part b look over the pedigree you constructed in part a.based on the inheritance pattern, which mode of inheritance must be the cause of galactosemia? sex-linked dominant autosomal dominant sex-linked recessive autosomal recessive

Answers

Autosomal recessive, Galactosemia must be an autosomal recessive trait as their daughter has the same ailment and there is no indication of a sex-linkage.

Galactosemia is a form of mutation, right?

CRM+ missense mutations, the most prevalent type, CRM- missense mutations, and splicing mutations are the three kinds of disease-causing mutations that have been identified. Due to the well-documented clinical diversity associated with galactosemia, it is interesting that the illness is heterogeneous at the molecular level as well.

Is the deletion mutation galactosemia present?

Galactosemia is a metabolic condition brought on by a GALT (galactose-1-phosphate uridyltransferase) enzyme deficiency. We have previously demonstrated that the Duarte (D2) allele is related with a deletion in the GALT gene's 5' upstream (promoter) region.

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Defective proteins are often degraded quickly, making their effects temporary. Single amino acid substitutions caused by errors in mRNA transcription would not affect protein function. Unlike DNA mutations, mRNA transcripts have short half-lives and are not inherited across many generations. Degradation of defective proteins activates mRNA repair pathways RNA polymerases synthesize many transcripts per gene, so only a small fraction of RNA transcripts would have errors. ch mRNA molecule is only translated once and then degraded. Incorrect At least one of the reasons you have selected does not explain why RNA polymerases do not require rigorous error correction. Transcription can produce many mRNA transcripts that then can be translated into many proteins. If only one of these mRNAs contains an error, not all the copies of that particular protein will contain an error. Additionally, mRNAs and proteins have a finite lifetime and can be degraded while DNA persists from generation to generation. Identify answers that are consistent with these features of transcription and translation.

Answers

It is true to say that defective proteins are often degraded quickly, making their effects temporary.

Protein degradation assumes a focal part in numerous cell capabilities. Misfolded and harmed proteins are taken out from the cell to keep away from harmfulness. The convergences of administrative proteins are changed by degradation at the fitting time. Both unfamiliar and local proteins are processed into little peptides as a feature of the versatile safe reaction. In eukaryotic cells, an ATP-subordinate protease called the proteasome is liable for quite a bit of this proteolysis.

Proteins are focused on for proteasomal degradation by a two-section degron, which comprises of a proteasome restricting sign and a debasement inception site. Here we depict how the two parts add to the particularity of corruption. Single amino acid substitutions  can do degradation of defective proteins which activates mRNA repair pathways.

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(Complete question) is:

Defective proteins are often degraded quickly, making their effects temporary. Single amino acid substitutions caused by errors in mRNA transcription would not affect protein function. Unlike DNA mutations, mRNA transcripts have short half-lives and are not inherited across many generations. Degradation of defective proteins activates mRNA repair pathways RNA polymerases synthesize many transcripts per gene, so only a small fraction of RNA transcripts would have errors. ch mRNA molecule is only translated once and then degraded. Incorrect At least one of the reasons you have selected does not explain why RNA polymerases do not require rigorous error correction. Transcription can produce many mRNA transcripts that then can be translated into many proteins. If only one of these mRNAs contains an error, not all the copies of that particular protein will contain an error. Additionally, mRNAs and proteins have a finite lifetime and can be degraded while DNA persists from generation to generation. Identify answers that are consistent with these features of transcription and translation.Select statement is true or false.

which of the following correctly describes the order of how information is sent through the papez circuit?

Answers

C. Thalamus → cingulate cortex → hippocampus → mammillary bodies → thalamus is the correct order of how information is sent through the Papez circuit.

The Papez circuit is a circuit of neurons that starts in the thalamus, which then connects to the cingulate cortex. The cingulate cortex then connects to the hippocampus, and then to the mammillary bodies, which then connect back to the thalamus. This circuit is thought to be involved in processing emotions and memory.

The circuit includes the hippocampus, the entorhinal cortex, the mammillary bodies, the anterior thalamic nuclei, the cingulate gyrus, and the prefrontal cortex. This circuit helps the brain to store and retrieve memories, as well as process emotions.

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which of the following correctly describes the order of how information is sent through the Papez circuit?

A.

Cingulate cortex → thalamus → hippocampus → mammillary bodies → cingulate cortex

B.

Cingulate cortex → hippocampus → thalamus → mammillary bodies → cingulate cortex

C.

Thalamus → cingulate cortex → hippocampus → mammillary bodies → thalamus

D.

Thalamus → cingulate cortex → mammillary bodies → hippocampus → thalamus

ADH (Anti-diuretic hormone) is important in maintaining homeostasis in mammals. ADH is released from hypothalamus in response to high tissue osmolarity (=less water in blood). In response to ADH, the collecting duct and distal tubule In the kidney become more permeable to water; which Increases water reabsorption Into caplllaries: The amount of hormone released is controlled by a negative feedback loop. Based on the model presented, what is the relationship between ADH release, osmolarity and production of urine? poni As tissue osmolarity rises, more ADH is released, causing less water to be excreted 05 urine As tissue osmolarity rises, less ADH is released, causing less water to be excreted as unne As tissue osmolarity rises more ADH is released, causing more water t0 be excreted as urine As tissue osmolarity rises, less ADH is released, causing more water to be excreted 0: unne Tivo of the above

Answers

Option a. As tissue osmolarity RISES, MORE ADH is released, causing LESS water to be excreted as urine.  The relationship between ADH release, osmolarity and production of urine.

Antidiuretic hormone (ADH) is a chemical produced within the brain that causes the kidneys to release less water, reducing the quantity of urine produced. A high ADH stage reasons the frame to provide less urine. A low degree results in greater urine production.

ADH is a substance produced naturally in a place of the brain known as the hypothalamus. it is then launched by using the pituitary gland at the bottom of the mind.

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explain the following terms: dna,chromosomes,sister chromosomes homologous chromosomes and replication chromosomes

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DNA stores the genetic code, chromosomes are thread-like structures, and sister chromatids are two halves of chromosomes.

Your genetic code is stored in every cell of your body in the form of deoxyribonucleic acid (DNA). It makes your body's instruction manual. The DNA molecule is packaged into thread-like structures called chromosomes in each cell's nucleus. The term "homologous chromosome" refers to chromosomes that share the same genetic foundation but may also have variants caused by replication. The two halves of a given chromosome that are held together at the centromere are called sister chromatids. After the cell has gone through the process of DNA replication in order to get ready for cell division, chromosomes are known as "replication chromosomes" emerge.

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in checkpoint inhibition therapy, which of the following is a protein targeted by therapeutic monoclonal antibodies?

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Monoclonal antibodies or targeted therapies are how checkpoint inhibitors are characterized.

How do blood antibodies work?

Antibody-containing proteins are found in plasma. They are a part of the natural defenses that your body has. They recognize foreign substances, such as germs, and alert your immune system, which subsequently gets rid of them. Red blood cells' surface shell contains glycoprotein known as antigens.

What do dangerous antibodies do?

Autoimmune diseases can be brought on by the "bad" antibodies, which also are known to fight against body's own tissues. It was formerly believed that they were rendered inactive over time or that the immune eliminated them because of this.

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french biologist, living in the late 1700s and early 1800s, who was the first to propose a mechanism by which evolution might occur. although this mechanism was later found to be incorrect, he was the first to emphasis how the environment plays a key role in evolution and that the environment can help explain changes in organismal forms seen in the fossil record.

Answers

Answer:

Jean Baptiste Lamarck

select the correct statement(s) about the origin of fungi. select all that apply. select the correct statement(s) about the origin of fungi.select all that apply. fungi evolved after the first plants colonized land. fungi are more closely related to plants than to animals. multicellularity probably arose independently in fungi and animals.

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The correct statement about the origin of fungi is:

B. Multicellularity probably arose independently in fungi and animals.

Although there is little information regarding fungi's fossil history, research suggests that they likely initially appeared roughly a billion years ago.

Fungi are a very old group of organisms, as shown by the presence of fungal hyphae in the tissues of the oldest plant fossils. Prototaxites, which date back to the Devonian Period (419.2 million to 358.9 million years ago) and are among the earliest terrestrial plantlike fossils known, are actually believed to be enormous saprotrophic fungi (possibly even Basidiomycota).

It is believed that the remains of the filamentous fungus Tortotubus protuberans, which belong to the early Silurian Period (440 million years ago), are the oldest fossils of a terrestrial life.

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Primary motor neurons of the __________ motor pathway originate in the primary motor cortex, whereas primary motor neurons of the __________ motor pathway originate in the brainstem
direct, indirect

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Primary motor neurons of the direct motor pathway originate in the primary motor cortex, whereas primary motor neurons of the indirect motor pathway originate in the brainstem.

The term "motor neuron" refers to a specific type of neuron whose cell body is found in the motor cortex, brainstem, or spinal cord and whose axon (fiber) travels to the spinal cord or to sites outside the body to directly or indirectly control effector organs, primarily muscles and glands. The two different types of motor neurons are upper motor neurons and lower motor neurons. Interneurons in the spinal cord allow upper and lower motor neuron axons to occasionally connect directly. The axons from the lower motor neurons are the efferent nerve fibers that transmit signals from the spinal cord to the effectors. Lower order motor neuron types include alpha and beta motor neurons.

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Help me with this questions​

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Answer:

(1) In this experiment, the variable that should be changed is the temperature at which the seeds are germinated.

(2) The variable that should be measured is the rate of germination, or the percentage of seeds that germinate within a certain time period.

(3) Some important variables that should be kept constant in this experiment include the type of seeds used, the amount of moisture the seeds are exposed to, and the amount of light the seeds receive. These variables can all affect the rate of germination, so it is important to keep them constant in order to accurately measure the effect of temperature on germination.

Propose a hypothesis in an attempt to find explanations for this curiosioty ​

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Answer:

True As you find an hypotheses to learn something new. I hope this is what you meant.

The typical skeletal muscle fiber contains several components that facilitate the production of ATP. Check All That Apply a. Mitochondria b. Myoglobin c. Myosin d. Glycogen

Answers

The normal skeletal muscle fiber has a number of parts that help ATP generation.

The mitochondria of muscle fibers produce ATP during routine tasks and modest exercise, a process known as aerobic respiration. In order to break down food energy (often glucose and fat) and produce ATP for muscular contractions, aerobic respiration needs oxygen. The three following processes—glycolysis, tricarboxylic acid cycle, and lastly oxidative phosphorylation—catabolize glucose, the primary energy source for cellular metabolism, to create ATP. Slow-twitch muscle fibers, also known as type I fibers, are red in color and have a lot of mitochondria. Myoglobin, a protein that both stores oxygen in muscle and transports oxygen in the blood to the mitochondria, is correlated with fiber color.

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be able to describe the environmental conditions that might give rise to semelparity vs. iteroparity.

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Salmon in the Pacific are semelparous, putting enormous energy into a single, massive reproductive attempt. Iteroparous individuals have recurrent reproductive cycles (most vertebrates, shrubs, and trees).

Why is semelparity more common than iteroparity?

The average individual in the iteroparous population will generate 340 seeds in its lifetime, more than in the semelparous population, if adult mortality in the population is 30% annually. Semelparity will be preferred over iteroparity in populations with a high enough mortality rate.

Why is semelparity advantageous?

Semelparity has the benefit of enabling an organism to invest as much as possible in reproduction, leading to larger clutch sizes, greater parental investment, or quicker generation times.

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Which one of these series of events is in the correct
chronological order of first appearance?
A. Photosynthesis, multicellularity, eukaryotic
cells, prokaryotic cells
B. Prokaryotic cells, photosynthesis,
multicellularity, eukaryotic cells
C. Photosynthesis, prokaryotic cells,
multicellularity, eukaryotic cells
D. Prokaryotic cells, photosynthesis, eukaryotic
cells, multicellularity
E. None of the above

Answers

Among these series of events D) Prokaryotic cells, photosynthesis, eukaryotic cells, multicellularity is correct.

The process includes of three distinct but brief phases: the growth phase, during which the mass of the cell increases; the chromosomal replication phase; and the final phase, during which the chromosomes are divided and the cells are physically split into two independent new cells. To begin with, whether a cell has a nucleus determines which of two primary classes it belongs to. Eukaryotic cells, which include bacteria, have a nucleus where the genetic material is segregated from the cytoplasm. Prokaryotic cells, which include bacteria, lack a nuclear envelope. Comparing prokaryotic and eukaryotic cells, the former are often smaller and more basic. Despite these distinctions, prokaryotes and eukaryotes both rely on the same fundamental molecular pathways for survival, proving that all modern cells are descendants of a single primordial progenitor. The process by which plants convert carbon dioxide, water, and sunshine into oxygen and sugar-based energy is known as photosynthesis. The four stages of photosynthesis include light absorption, electron transfer, ATP production, and carbon fixation.

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Can anyone do this for me like 10-20 minutes?

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The six geneticists can be Gregor Mendel, Francis Collins, Wilhelm Johannsen, William Bateson, Hugo DeVries, and Tschermak.

What is genetics?

The scientific study of genes and heredity i.e., how particular traits or qualities are passed from parents to children as a result of changes in DNA sequence is known as genetics.

Gregor Mendel We have a better understanding of the fundamentals of inheritance because to Gregor Mendel's work on the pea plant. The originator of genetics

Francis Collins, an American geneticist and former head of the National Institutes of Health, uncovered the genes that cause hereditary disorders (NIH).

Wilhelm Johannsen, a botanist, first used the term "gene" to refer to the Mendelian units of heredity. From the word gene, William Bateson created the term genetics in 1905.

A generation after Mendel published his papers, Hugo DeVries, Carl Correns, and Tschermak each independently rediscovered Mendel's work in the same year.

Thus, these are some geneticists who are well known for their works.

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In the general population, 1 in 300 individuals is a carrier for Tay-Sachs disease, while 1 in 30 individuals of Ashkenazi Jew descent are carriers. Tay-Sachs also affects 1 in 30 individuals with French-Canadian ancestry, although two completely unique mutations are responsible for the Ashkenazi and French-Canadian mutations.Part A What are the chances of two individuals having a child with Tay-Sachs if both individuals are not of Ashkenazi or French-Canadian descent? Enter your answer using scientific notation. For the multiplication symbol, use an asterisk ). 2.77×10-8 Submit My Answers Give Up CorrectPart B What are the chances of two individuals having a child with Tay-Sachs if one individual is of Ashkenazi descent and one is not? 2.77*10-5 Submit My Answers Give Up CorrectPart B What are the chances of two individuals having a child with Tay-Sachs if one individual is of Ashkenazi descent and one is not? 2.77*10-5 Submit My Answers Give Up CorrectPart D What are the chances of two individuals having a child with Tay-Sachs if the father is an Ashkenazi carrier and the mother is a French-Canadian carrier?

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(1/30) × (1/300) × 1/4 = 2.77 × 10⁻⁵,Chance of mom being a carrier × Chance of dad being a carrier × Chance of having an affected child if both parents are carriers), In the general population, 1 in 300 individuals is a carrier for Tay-Sachs disease, while 1 in 30 individuals of Ashkenazi Jew descent are carriers

Tay-Sachs disease is a rare genetic ailment that is inherited from both parents. It is brought on by the lack of an enzyme that aids in the breakdown of fatty materials. These fatty compounds, known as gangliosides, accumulate to toxic amounts in the brain and spinal cord and impair the nerve cells' ability to function. By the age of 3 to 5 years, the illness is typically deadly, frequently as a result of complications from a lung infection (pneumonia). Juvenile Tay-Sachs disease and other uncommon forms of the disease first manifest in early adulthood or later in childhood (late-onset Tay-Sachs disease).

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learned guidelines for sexual expression that provide individuals with a sense of culturally appropriate sexual behaviors and sexual desires are known as .

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Sexual scripts are learned norms for sexual expression that provide people an understanding of acceptable sexual behaviors and desires, depending on their culture.

A person's capacity for sexual feelings and their emotional and sexual attraction to a particular gender is referred to as their sexuality (male or female).The ability to evaluate gender and sexuality as social rather than biological characteristics depends on the distinction between sex and gender. Heterosexuality, which is attraction to people of the opposite sex; homosexuality, which is attraction to people of one's own sex; Bisexuality, which is attraction to people of either sex; and asexuality, which is the lack of attraction to either gender, are the four main categories of sexuality or sexual orientation. Currently accepted scientific theory holds that people typically become conscious of their adolescence.

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