HELP PLEASE. Compare and contrast how people taste sweetness, with how people taste spiciness.

The ampulla of the ductus deferens joins with an excretory duct of the seminal gland, marking the beginning of the ejaculatory duct.

The ejaculatory duct is a portion of the male anatomy's urethral system that is located within the prostate gland. It connects the vas deferens to the urethra and transports semen during ejaculation. The vas deferens and seminal vesicles join to create the ejaculatory duct in the male reproductive system.

Each ampulla of the ductus deferens joins the excretory duct of the seminal gland, which is the start of the ejaculatory duct. The ejaculatory duct then transports the semen into the prostatic urethra, from which it exits the body during ejaculation.

Therefore, the joining of the ampulla of ductus deferens with the excretory duct is the beginning of the ejaculatory duct.

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a. The evaluationof the passage above to determine the specific characteristics of embryos that biologists assume to provide a barrier to behavioral thermoregulation are immobility.

According to the passage, biologists have assumed that the (immobile) embryonic stage cannot thermoregulate behaviorally. This means that embryos are unable to use behavioral tactics like sun-seeking and shade-seeking to maintain their body temperatures within selected bounds. Behavioral thermoregulation requires an ability to detect spatial thermal heterogeneity and to move to favorable sites. Thus, because embryos are immobile, they cannot move to favorable sites, and this lack of mobility creates a barrier to behavioral thermoregulation. The concept of behavioral thermoregulation refers to the ability of animals to control their body temperature by changing their behavior.

Many ectotherms, for example, use behavioral tactics like sun-seeking and shade-seeking to maintain their body temperatures within selected bounds. These animals are able to detect spatial thermal heterogeneity and move to favorable sites, which helps them to avoid extremes of temperature. However, embryos cannot do this because they are immobile, and this immobility creates a barrier to behavioral thermoregulation. Thus, biologists assume that embryonic stages cannot thermoregulate behaviorally because they lack the necessary mobility to move to favorable sites.

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The ability to maintain a constant body temperature was the key factor for the success of vertebrates in relatively dry environments.

The ability to maintain a constant body temperature was the most important factor for vertebrate success in relatively dry environments. This ability allowed vertebrates to withstand harsher temperatures and survive longer in the dry environment. It allowed them to conserve more energy by regulating their body temperature. The shelled, amniotic egg was a key adaptation for surviving in relatively dry environments. The amniotic egg allowed the embryo to develop in a fluid-filled environment and was able to retain moisture longer. This protected the embryo from drying out, which allowed the vertebrates to live longer.

Two pairs of appendages also helped vertebrates survive in the dry environment. The limbs allowed the vertebrates to move around in the dry environment and access food and water. They also allowed them to search for shelter and escape predators.  Bony scales were also essential for the survival of vertebrates in a dry environment. The scales were a protective layer that kept the vertebrates warm and insulated. It also provided a barrier against harmful elements and diseases.
A four-chambered heart was also important for the success of vertebrates in relatively dry environments. The four-chambered heart allowed the vertebrates to regulate their blood flow, which improved their overall health and allowed them to live longer in the dry environment.
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Curators create living collections for a variety of reasons, such as scientific study and education. Living collections for plants contain plant genetic resources that are preserved for study and conservation in germplasm repositories, such as the largest in the world, the National Plant Germplasm System (NPGS) of the USDA.

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Advantages of having children in one's twenties are as follows: The parents have more physical energy. The mother is likely to have fewer health problems. The parents are less likely to build up expectations for their children.

Being pregnant and giving birth is a tiring and physically demanding job. In addition, taking care of a child, especially a young one, can be equally exhausting. It is said that having children in your twenties will provide you with more physical energy. When a mother gives birth at an early age, her body is much more capable of bouncing back than it would be at a later age. The mother is also likely to have fewer health problems than an older mother, making the child's early years much easier.

There is also an advantage for parents in that they are less likely to build up expectations for their children. The younger parents don't have to worry about things like paying for their children's education, so they can simply focus on the enjoyment of raising their child.

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The probability that two people with moderate flushing will have three children with extreme flushing is 1/8. The correct option is a.

The answer to this question is that the probability of two people with moderate flushing having three children with extreme flushing is 1/8. Two working copies of ALDH2 result in little to no flushing reaction to alcohol, one working copy results in moderate flushing, and no working copies result in extreme flushing.The genotype of each individual is determined by two copies of each gene. An individual can inherit two identical copies of a gene or one copy from each parent. If two heterozygous individuals (i.e. individuals with one working copy and one non-working copy of a gene) mate, each of their children will have a 1/4 chance of inheriting two non-working copies, a 1/2 chance of inheriting one working and one non-working copy, and a 1/4 chance of inheriting two working copies.The probability of a child inheriting two non-working copies of the ALDH2 gene from two heterozygous parents is therefore 1/4 * 1/4 = 1/16.

However, this only applies to each individual child. The probability of having three children with this genotype is calculated by multiplying this probability by itself three times: 1/16 * 1/16 * 1/16 = 1/4096. This means that the probability of having three children with the extreme flushing reaction is very low. However, the probability of having one or two children with this reaction is higher than zero.

Therefore, the correct answer is 1/8.

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If conditions are not restore to optimal conditions, the enzymes of the body do not function correctly because they are denatured, potentially leading to organ failure and possible death.

The term "denatured" is used to describe the condition of an enzyme that is unable to function properly. When an enzyme becomes denatured, it loses its structure and shape, which causes it to be unable to perform its intended function. This can happen due to a number of different factors, such as changes in temperature or pH levels. When an enzyme becomes denatured, it is unable to interact with the substrate that it is supposed to act on. As a result, the chemical reaction that the enzyme is supposed to catalyze cannot occur. This can lead to a number of different problems within the body, such as organ failure or even death, in extreme cases.

Therefore, it is very important to maintain optimal conditions for enzymes to function properly in the body. Denatured enzymes are unable to carry out their designated chemical reactions, and this can have drastic consequences on the body's metabolic processes.

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The important difference between the effect of selection against a recessive allele and selection against a dominant allele is that selection against a recessive allele reduces the frequency of the allele in the population.

Whereas selection against a dominant allele reduces both the frequency of the allele and the frequency of the homozygous recessive genotype in the population. To break it down further, a recessive allele will only produce an observable phenotype in an individual who is homozygous for that allele, meaning that two copies of the allele must be present for it to be expressed. Selection against a recessive allele will only act upon individuals that are homozygous for that allele. Therefore, the frequency of the allele will be reduced in the population, but the frequency of the homozygous recessive genotype will remain unaffected.

In contrast, a dominant allele will produce an observable phenotype in an individual who is either homozygous or heterozygous for the allele. Therefore, selection against a dominant allele will act upon both individuals that are homozygous and heterozygous for that allele. This means that the frequency of the allele, as well as the frequency of the homozygous recessive genotype in the population, will be reduced.

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Radiometric dating and stratigraphy were two important technologies that helped to support Hutton and Lyell's hypothesis that the Earth is much older than previously believed.

Radiometric dating techniques allowed scientists to accurately determine the age of rocks and fossils by measuring the decay of radioactive isotopes. This helped to confirm the geological time scale developed by Hutton and Lyell, which showed that the Earth had undergone many changes over a long period of time. Stratigraphy, the study of rock layers and their relationships to each other, helped to construct a timeline of geological events and determine the relative ages of different rock formations.

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The given description is related to the following processes:

Meiosis II and Mitosis both involve the separation of sister chromatids. In mitosis, this occurs during the anaphase stage, where spindle fibers pull apart the sister chromatids towards opposite poles of the cell. In meiosis II, sister chromatids are separated during the second round of division after the cells have already undergone meiosis I.

Mitosis results in diploid cells, this is because, during mitosis, the parent cell replicates its DNA, separates the sister chromatids, and divides the cytoplasm to produce two genetically identical daughter cells with the same number of chromosomes as the parent cell.

Meiosis I is the process that separates homologous chromosomes. During this process, the two homologous chromosomes (one from each parent) pair up and exchange genetic material in a process called crossing over. Then, they separate from each other and move towards opposite poles of the cell during anaphase I. The resulting daughter cells are haploid, containing only one chromosome from each homologous pair.

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The risk for a woman who had retinoblastoma in early childhood due to a partial deletion on one number 13 chromosome to have a child who also develops the disorder is 50%.

Retinoblastoma is a type of cancer that grows in the retina. It is caused by mutations or genetic changes in the DNA of cells in the retina, which cause them to divide and multiply uncontrollably.

Retinoblastoma is classified into two categories: hereditary and sporadic. Sporadic retinoblastoma occurs randomly without any clear cause, whereas hereditary retinoblastoma is caused by a genetic mutation that is passed down from one or both parents.

The risk for a woman who had retinoblastoma in early childhood due to a partial deletion on one number 13 chromosome to have a child who also develops the disorder is 50%. If the mother has a mutation in one copy of the RB1 gene on one chromosome 13, there is a 50% chance that she will pass the mutation on to her offspring.

If the child receives the mutation, they will inherit a single copy of the mutated RB1 gene and will be at an increased risk of developing retinoblastoma. If the mother passes on the normal RB1 gene, her child will not have an increased risk of developing retinoblastoma.

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The skeletal and muscular systems both provide body movement, but they do so in different ways. The skeletal system provides movement through its bones, while the muscular system provides movement through its muscles. These two systems are connected in that the muscles attach to the bones and use them as leverage to move the body.

The skeletal system is the body system responsible for providing structural support and protection to the body's internal organs. It consists of bones, cartilage, and ligaments.

The muscular system is the body system responsible for producing movement. It consists of skeletal muscles, smooth muscles, and cardiac muscles. The skeletal system provides movement through its bones.

The muscles are attached to the bones by tendons, which are strong connective tissues that are capable of withstanding the forces generated by muscle contractions. When a muscle contracts, it pulls on the tendon, which in turn pulls on the bone, causing movement.

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Answer:

x=4

Explanation:

Therefore, theoretically speaking, I shall be the one who must thou answer such answer. In addition, I hail to speak tho truth must come out of one's mouth, in other words, spitting facts (aka. spittin fax )

You shall thank me later.

Kind Regards,

Penguin Man.

The order of the eukaryotic gene elements in which their appearance in the direction travelled by RNA polymerase along the gene is

- Promoter

- Transcription start site

- 5' UTR

- Start codon

- Intron start

- Stop codon

- Polyadenylation signal

- Polyadenylation site

А promoter is а region of DNА thаt is locаted upstreаm of а gene аnd contаins the elements necessаry for trаnscription initiаtion аnd regulаtion. The trаnscription stаrt site is the nucleotide sequence of а gene's DNА where RNА polymerаse binds аnd initiаtes trаnscription of thаt gene. 5' UTR is а nucleotide sequence locаted аt the 5' end of аn mRNА molecule thаt is upstreаm of the stаrt codon. It is аlso referred to аs leаder sequence.

The stаrt codon is the first codon of аn mRNА trаnscript thаt is trаnslаted by the ribosome аnd is responsible for stаrting the synthesis of а protein. The intron stаrt is the beginning of аn intron, which is а non-coding sequence of nucleotides thаt interrupts а coding sequence of а gene. The stop codon is а nucleotide triplet within аn mRNА molecule thаt signаls the end of trаnslаtion аnd protein synthesis.

Polyаdenylаtion signаl is the RNА sequence thаt is locаted аt the 3' end of most eukаryotic messenger RNА (mRNА) molecules аnd is responsible for the terminаtion of trаnscription. Polyаdenylаtion site is the point аt which the polyаdenylаtion signаl is cleаved by аn enzyme to releаse the mRNА from the trаnscription mаchinery.

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For patient A the treatment of broken bone is with splints or surgery. For patient B the treatment of diabetic peripheral neuropathy is with insulin medications. For patient C, the treatment of muscle sprain is using pain relief medications.

Nervous and musculoskeletal injuries occurs when there is damage to the nerve or the musculoskeletal system due to a direct impact or an underlying illness.

Patient A sustained a direct injury to the bone after an incidence of a bike accident.

Treatment plan: The treatment plan for a bone fractures is either through surgery or through the use of splints to immobilize the broken bones and hasten recovery.

Patient B who is a diabetic patient reported to the hospital complaining of numbness and tingling in his right foot. This is a nervous injury or damage that occurred due to the underlying illness.

Treatment plan: This involves managing blood sugar with insulin and using medication to control nervous symptoms.

Patient C who sustained muscle sprain during a track event complained of tightness and pain in the back of her calf.

Treatment plan: This should include pain relievers, ice or splinting but depends on the extent of injury.

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Full Question ;

FIRST TO ANSWER THIS WITH THE CORRECT INFORMATION GETS BRAINLIEST AND PLS DO FAST

Nervous and Musculoskeletal Worksheet

Instructions: Fill in the sections below based on the Helping Dr. Homeostasis interactive. You may use articles, videos, books, or journals to get treatment suggestions. Make sure you use reliable sources, like those from medical, educational, or government agencies.

Patient A

Diagnosis:

Treatment plan—list at least two possible treatments:

Cite the sources you used to create the treatment plan:

Patient B

Diagnosis:

Treatment plan—list at least two possible treatments:

Cite the sources you used to create the treatment plan:

Patient C

Diagnosis:

Treatment plan—list at least two possible treatments:

Cite the sources you used to create the treatment plan:

Patient A came to the clinic after having a bike accident. She has severe pain in her left forearm. The pain increases when she moves the arm, and her arm is quite swollen. The X-ray shows an abnormality with the radius bone in the forearm.

Use the internet to search for treatments for broken bones.

Record possible treatments on your activity report.

Make sure you list the websites you use to create a treatment plan.

Patient B came to the clinic complaining of numbness and tingling in his right foot. He described the pain as feeling like pins and needles. There is no swelling, bruising, or redness. The X-ray shows no breaks or fractures, but the patient states that he has type 2 diabetes. A blood glucose test shows high blood glucose levels.

Use the internet to search for diabetic peripheral neuropathy treatments.

Record possible treatments on your activity report.

Make sure you list the websites you use to create a treatment plan.

Patient C came to the clinic complaining of pain in her left calf. Her calf is swollen and hurts even when at rest. Before coming in to the clinic, Patient C had been running track. All of a sudden, she felt tightness and pain in the back of her calf. The X-ray shows no breaks or fractures, and an MRI shows no nerve damage.

Use the internet to search for muscle sprain treatments.

Record possible treatments on your activity report.

Make sure you list the websites you use to create a treatment plan.

The feature of Huntington's disease that supports the claim is that the symptoms of this disease generally begin appearing in middle age.

The neurological condition known as Huntington's disease (HD), commonly referred to as Huntington's chorea, is primarily hereditary. The first signs are frequently modest issues with mood or cognitive function. The result is frequently a general lack of coordination and a shaky walk.

A uncommon hereditary disorder called Huntington's disease causes the progressive death of brain nerve cells. Huntington's illness, which frequently results in mobility, cognitive, and psychological problems, has a substantial impact on a person's functional capacities.

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Alleles of a gene are typically located at the same position on homologous chromosomes, which are a pair of chromosomes that have the same genes in the same location.

Homologous chromosomes are derived from each parent, and they pair up during meiosis, the process of cell division that produces gametes (sperm and egg cells).

Each gene on a homologous chromosome pair has two versions, one from each parent. These versions of a gene are called alleles. Homologous chromosomes ensure that each gamete receives one allele for each gene, which is important for genetic diversity in offspring.

The location of a gene on a chromosome is called its locus, and the specific alleles present at that locus determine an individual's genetic makeup. Dominant alleles are expressed when present in a heterozygous state with a recessive allele, while recessive alleles are only expressed when present in a homozygous state.

The study of the inheritance of genes and alleles is called genetics, and it has significant implications for understanding biological diversity, evolution, and human health.

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Phenotypic ratio of F1 is 4:0 (green: white seeds). Phenotypic ratio of F2 is 9:7 (green: white seeds). Phenotypic ratio of F2 of dihybrid cross = 9:3:3:1.

The F1 phenotypic ratio will be all green seeds, as only one dominant allele is sufficient to produce green seeds. This will result in a phenotypic ratio of 4:0 green: white seeds.

F2 Phenotypic ratio for the F2 generation, we will get a phenotypic ratio of 9:7 green: white seeds.

Parents- WWWW x A genotype produces all WAWA gametes, while wwww produces all wawa gametes. On crossing these parents, hybrid produced will be:

WWAW x wawA

Offspring genotypes: WWAW – green, WWAw – green, WwAW – green, WwAw – green, WWaA – green, WwaA – green, Wwaa – white, wwAW – white, wwAw – white, wwaA – white, wwaa – white.

F2 Phenotypic ratio of a dihybrid cross, the ratios are as follows

Parents - WWWWAAAA x wwwwaaaa

The possible gametes from the WWAW genotype are WAWA, WAWa, WaWA, and WaWa. The wawa genotype produces only wawa gametes. The multiplication of these two results in the following:

WWAW x wawa = WAWAaWAWa x wawa = WAWaaWaWA x wawa = WaWAWawa x wawa = WaWaWaAW x wawa = WawaAaWaAw x wawa = Wawaa waWA x wawa = waWAwawa x wawa = wawa

The phenotypic ratio will be the same as the F2 generation’s phenotypic ratio, which is 9:7 green: white seeds.

The F2 ratio would be 9 dominant W and dominant A individuals: 3 dominant W and recessive a individuals: 3 recessive w and dominant A individuals: 1 recessive w and recessive a individuals.

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The plasma membrane forms a barrier which is amphipathic on the outer and inner surface and hydrophobic on the interior.

The lipid bilayer of the plasma membrane is made up of a double layer of phospholipids that is amphipathic on the outer and inner surface and hydrophobic on the interior. This feature aids in the separation of the cell from its environment.

The lipids are amphipathic, meaning they have both hydrophobic and hydrophilic regions. This provides the membrane with its fundamental barrier characteristics. In addition to phospholipids, there are other membrane lipids and membrane proteins that contribute to the membrane's function.

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The endomembrane system has all of the following properties except encasing cellular components and products in the membrane to protect them

The endomembrane system is a network of membranes and organelles found within eukaryotic cells, which work together to facilitate the transport of materials both within the cell and to the outside of the cell. This system includes the endoplasmic reticulum (ER), Golgi apparatus, lysosomes, and vesicles.

The endoplasmic reticulum is a complex network of flattened sacs and tubules that are involved in protein synthesis and lipid metabolism. The Golgi apparatus is responsible for modifying, sorting, and packaging proteins and lipids into vesicles for transport to their final destination. Lysosomes are involved in intracellular digestion, breaking down waste materials and macromolecules. Vesicles are small membrane-bound sacs that transport materials within the cell or to the outside of the cell.

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Complete Question:

The endomembrane system has all of the following properties except _____.

(a) encasing cellular components and products in the membrane to protect them

(b) provides a passageway for messenger RNA after it exits the nucleus

(c) includes lysosomes and mitochondria in the system

(d) includes rough and smooth endoplasmic reticulum in the system

(e) All of these are properties of the endomembrane system.

The core RNA polymerase of a bacterium is composed of four subunits: two α subunits, one β subunit, and one β' subunit. The α subunits have regulatory roles, while the β and β' subunits are responsible for catalyzing RNA synthesis.

The β subunit is responsible for binding the DNA template and the incoming ribonucleotides, while the β' subunit is responsible for catalyzing the formation of the phosphodiester bonds between the ribonucleotides.

The core RNA polymerase is able to carry out elongation of the RNA transcript, but additional subunits called sigma factors are required for the initiation of transcription at specific promoter sequences. Different sigma factors confer specificity to the RNA polymerase by recognizing different promoter sequences and binding to the core enzyme to form a holoenzyme.

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Complementation has taken place of two recessive mutations occur at the same locus, producing a mutant phenotype.

What is complementation? Complementation is the production of a normal phenotype from two organisms that carry homozygous recessive mutations at different loci. When two homozygous recessive mutations occur at the same locus, the mutant phenotype is produced (i.e., there is no complementation).

Option D is correct because two recessive mutations occurring at the same locus will produce a mutant phenotype. The complementation of two mutant alleles is a common genetic technique utilized to test whether the mutant phenotypes arise from distinct or identical genetic events.

If the mutations are caused by distinct genetic events, the heterozygous offspring will express the wild-type phenotype because the two complementing genes will provide the necessary enzymatic activity or structural proteins.

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There are only about 40 tRNA molecules that represent 40 anticodons but there are 61 codons that each specify the addition of a specific amino acid.

It is possible that different tRNA molecules with different anticodons can recognize and bind to the same codon. As a result, a single tRNA molecule can be used to read multiple codons that all specify the same amino acid. The wobbling or degeneracy of the genetic code makes it possible for multiple codons to encode the same amino acid, allowing for fewer tRNAs to be utilized.

To provide an example, there are 4 codons that specify the amino acid alanine (GCN, GCU, GCC, and GCA), but only two tRNA molecules with the anticodon 5′-CGA-3′ are needed to bind all four codons because the third position of the codon can wobble to bind the G or the A base. This saves the cell's energy and resources while also simplifying the transcription and translation processes.

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Answer:

The mineral found in beef, fish, turkey, grape juice, and broccoli is iron.

Answer:

The pairing of homologous chromosomes occurs during the first stage of meiosis, known as prophase I. Specifically, during the early stages of prophase I, the homologous chromosomes find each other and come together to form a tetrad, which consists of two pairs of sister chromatids (four chromatids in total). This pairing is also known as synapsis and it allows for the exchange of genetic material between the homologous chromosomes through a process called crossing over.

The article describes how biologist Kenneth Lohmann discovered that baby loggerhead turtles use the Earth's magnetic fields and waves to orient themselves and direct their swims, through experiments tying newborns to a device and observing their movements in a large glass tank filled with water.

The question being investigated is: How do baby loggerhead turtles orient themselves and navigate long distances across the ocean to return to their birthplace.

The hypothesis is that baby loggerhead turtles use the Earth's magnetic fields and waves to orient themselves and navigate long distances.

The independent variable is the Earth's magnetic fields and waves.

The dependent variable is the direction in which the turtles swim.

The constants are the size and age of the loggerhead turtle hatchlings, the water temperature and composition, the darkness in the tank, and the location of the experiment.

The data shows that the loggerhead turtle hatchlings swam in the same direction within minutes of being placed in total darkness and that the direction was between magnetic north and east, leading away from Florida's east coast and toward the Gulf Stream currents. When the magnetic field was reversed, the turtles swam in the opposite direction - towards the southwest. The analysis shows that the turtles are using the Earth's magnetic fields to orient themselves.

The conclusion is that baby loggerhead turtles use the Earth's magnetic fields and waves to orient themselves and navigate long distances, allowing them to return to the same beach where they were born years later. This is an example of the scientific method, in which a question is asked, a hypothesis is developed, an experiment is conducted, data is collected and analyzed, and a conclusion is drawn.

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The question is -

Turtles Ahoy! (A real implementation of the scientific method) Did you ever wonder how baby sea turtles can run down into the ocean after hatching, paddle thousands of miles across the North Atlantic, and find their way back years later to the same beach they were born in?

Curious about these creatures, a biologist at the University of North Carolina at Chapel Hill have discovered at least part of the answer. Baby loggerhead turtles, no bigger than a child's hand, use the Earth's magnetic fields and waves to orient themselves and direct their marathon swims. In a recent issue of Scientific American magazine, biologist Kenneth Lohmann describes experiments showing their biological compass. Working with Florida Atlantic University science researchers, Lohmann tied loggerhead turtle hatchlings (newborns) to a device and placed them in a large glass tank filled with water.

Within minutes of placing the hatchlings in total darkness, researchers observed that the turtles all swam in the same direction. In fact, most of them swam towards points located between magnetic north and east, directions that would lead them away from Florida's east coast and toward the Gulf Stream currents. The biologists also found that when they reversed the magnetic field, the turtles swam in the opposite direction- toward the southwest.

1. Circle and label the question that is going to be investigated.

2. What is the hypothesis?

3. What is the independent variable?

4. What is the dependent variable?

5. What are the constants?

6. Describe the data and analysis.

7. What is the conclusion?

In an aphotic zone of a body of water, there is no photosynthesis. The correct answer is option B.

The aphotic zone, which is also known as the abyssal zone, is a section of the ocean or other bodies of water that is entirely devoid of light. It is the area below the photic zone, where sunlight is abundant enough for photosynthesis to occur.However, in an aphotic zone, the sun's light does not reach the ocean floor. This implies that no photosynthesis occurs in this area since plants and other photosynthetic organisms require light to survive. So,there is no photosynthesis in an aphotic zone of a body of water.

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Answer:Its D

Explanation:

The lunar-linked rhythm of fiddler crab courtship is similar to the seasonal timing of plant flowering in terms of mechanism and function.

The lunar-linked rhythm of fiddler crab courtship is similar in mechanism and function to the seasonal timing of plant flowering in the following ways:

Therefore, the lunar-linked rhythm of fiddler crab courtship and the seasonal timing of plant flowering are examples of biological timing mechanisms that are influenced by environmental factors.

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