Which of these statements is true about the gametophyte tissue that surrounds the pine embryo?
a) It functions as a diploid food reserve.
b) It functions as a triploid food reserve.
c) It develops from the fusion of a microspore and a megaspore.
d) It functions as a haploid food reserve.
e) It is the remnant of the pollen tube.
d) it functions as a haploid food reserve
(This gametophyte tissue is a source of nourishment for the embryo.)

Answers

Answer 1

The following is accurate regarding the gametophyte tissue that envelops the pine embryo: (d) It serves as a haploid food reserve (The embryo receives nutrients from this gametophyte tissue.

What is gametophytic tissue?

A gametophyte is one of the two alternate multicellular stages that occur during the life cycles of plants and algae. It grows from a single-chromosome haploid spore to become a haploid multicellular creature. The sexual stage of plants and algae's life cycles is known as the gametophyte. All tissues and organs produced by the haploid generation are referred to as gametophytes. The protonema and the gametophore are two separate phases in the formation of the gametophyte. The protonema is the first element of the moss to emerge from the spore.

Where is gametophyte found?

Within anther sacs, the male gametophyte begins to develop inside the flower. Microsporocytes are the name for the big cells that make up their precursors and can be found in a stacked column at the middle of the anther sacs (or microspore mother cells). Microsporocytes go through meiosis to produce four microspore-like cells.

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Related Questions

Select the products of the preparatory reaction and the Krebs cycle after two turns. Select all that apply.

Multiple select question.

A) 2 FADH2
B) 3 CO2
C) 8 NADH
D) 1 ATP
E) 1 FADH2
F) 2 ATP
G) 4 NADH
H) 6 CO2

Answers

The products of the preparatory reaction are 2 NADH and 2 acetyl CoA. The products of the Krebs cycle after two turns are 6 NADH, 2 FADH2, 4 CO2, and 2 ATP. So, the total products after two turns are 12 NADH, 4 FADH2, 6 CO2, and 4 ATP.

What is Krebs cycle?

The Krebs cycle, also known as the citric acid cycle, is a series of chemical reactions that take place in the mitochondria of cells. It is the second of three main stages in cellular respiration and generates molecules that carry energy to the electron transport chain. The cycle produces ATP, NADH, FADH2, and CO2 as byproducts.

The products of the preparatory reaction are 2 NADH and 2 acetyl CoA. The products of the Krebs cycle after two turns are 6 NADH, 2 FADH2, 4 CO2, and 2 ATP. So, the total products after two turns are 12 NADH, 4 FADH2, 6 CO2, and 4 ATP.

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which of the following statements is false? which of the following statements is false? eukaryotes have a much simpler genetic makeup than prokaryotic cells. eukaryotic cells evolved from prokaryotic cells. prokaryotes are unicellular and lack a membrane-bound nucleus. eukarya is a eukaryotic domain. archaea and bacteria are prokaryotic domains.

Answers

The following statement is false : eukaryotes have a much simpler genetic makeup than prokaryotic cells.

Prokaryotes are always unicellular, while eukaryotes are often multicellular. Furthermore, eukaryotic cells are over 100-10,000 times larger than prokaryotic cells and are much more complex. Prokaryotic DNA is kept in the cytoplasm, whereas eukaryotic DNA is retained in the nucleus.

A distinct feature that distinguishes prokaryotic and eukaryotic cells is the cell nucleus. A true nucleus does not exist in prokaryotic cells and membrane-bound organelles exist only in eukaryotic cells.

Eukaryotic cells rarely have cell walls. If present, they are of a simple chemical nature. A true core exists. Cytoplasm is present in prokaryotic cells but absent in most organelles. In eukaryotic cells, they are composed of both cytoplasm and organelles, both of which are present.  

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Which of the following are features of lymphatic vessels? Select all that apply.
A tunica interna is present
Smooth muscle is present in the vessel wall
They resist moderate to high pressure
They have thick walls
Valves are present

Answers

The features of lymphatic vessels include a tunica interna is present, smooth muscle is present in the vessel, and valves are present. Lymphatic vessels are a part of the lymphatic system, which is a network of vessels and organs that is responsible for the circulation of lymph.

Lymphatic vessels are thin-walled vessels that collect excess fluid and waste products from the tissues and return them to the bloodstream. The structure of lymphatic vessels is similar to that of veins, with a tunica interna (inner layer), tunica media (middle layer), and tunica adventitia (outer layer). However, lymphatic vessels have thinner walls than veins and do not have as much smooth muscle in the vessel wall. Lymphatic vessels also have valves, which prevent the backflow of lymph and help to direct its flow towards the lymph nodes. Lymphatic vessels are low-pressure vessels, with pressures ranging from 1-5 mmHg. They are not able to resist moderate to high pressure and do not have as thick walls as arteries. This is because the lymphatic system relies on the contraction of surrounding muscles and the movement of body tissues to help move lymph along the vessels.

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a twisted, double strand of nucleotide bases and sugar phosphates is the structure of: group of answer choices mrna dna a protein rna

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A twisted, double-stranded strand of nucleotide bases, and sugar phosphates is the structure of option B: DNA.

Nucleic acids, which are the information-carrying molecules of the cell, include DNA (deoxyribonucleic acid) molecules. As nucleotides are made up of numerous smaller molecules, DNA molecules are polymers. A phosphate group, a sugar molecule, and a nitrogenous base are all components of each nucleotide.

The genetic code, or all the information necessary for an organism to function, is stored in DNA molecules, which are housed in the nucleus. Two DNA strands make up DNA molecules, which are then wound around one another to form the double helix, a spiral pattern. James Watson, Francis Crick, and Rosalind Franklin made the initial discovery of the double helix structure of DNA in 1953.

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Does protein expression begin with transcription or translation? a. translation b. transcription.

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The process of protein expression begins with the transcription of genetic information from DNA to RNA, followed by the translation of RNA into a protein.So option b is correct.

Transcription is the first step in protein expression, during which the genetic information encoded in a DNA sequence is transcribed into RNA. This process is carried out by RNA polymerase enzymes, which bind to the DNA template strand and synthesize a complementary RNA molecule that carries the genetic information for the protein being expressed. The RNA molecule produced during transcription is known as messenger RNA (mRNA), and it serves as a template for the next step in protein expression, which is translation.

Translation is the process by which the genetic information contained in mRNA is translated into a sequence of amino acids, the building blocks of proteins. This process occurs on ribosomes, which read the codons on the mRNA and use this information to select the appropriate amino acids and link them together to form a protein chain.

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gram positive cellshave a second, outer membrane that helps retain the crystal violet stain.have multiple layers of peptidoglycan that help retain the crystal violet stain.have a thick capsule that traps the crystal violet stain.none of these options.

Answers

Gram positive cells have a option B. multiple layer of peptidoglycan that helps to retain the crystal violet stain.

Gram staining is a technique for determining whether bacteria are gram-positive or gram-negative. These bacteria will be distinguished based on whether the stain reveals the bacteria to be purple or pink.

Gram-positive cells have several layers of peptidoglycan that allow them to maintain the crystal Violet stain. As a result, gramme positive bacteria appear violet during the gramme staining method.

As a result, the right answer is B. a multiple layer of peptidoglycan that aids in the retention of the crystal violet stain

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Complete Question is:

Gram positive cells have a

A. second outer membrane that helps to retain the crystal violet stain

B. multiple layer of peptidoglycan that helps to retain the crystal violet stain

C. thick capsule that traps the crystal violet stain

D. periplasmic space that traps the crystal violet

the thin space between the parietal and visceral layers of the serous pericardium is the ______ cavity.

Answers

The thin space between the parietal and visceral layers of the serous pericardium is the pericardial cavity.

The pericardium is a double-layered sac that surrounds and protects the heart. The two layers of the pericardium are the parietal pericardium, which is the outer layer, and the visceral pericardium, which is the inner layer. The space between these two layers is called the pericardial cavity. The pericardial cavity is a thin, fluid-filled space that contains a small amount of serous fluid. This fluid acts as a lubricant and reduces friction between the parietal and visceral layers of the pericardium, allowing the heart to move smoothly within the pericardial sac during its contractions and relaxation. The pericardial cavity is an important part of the cardiovascular system and plays a crucial role in protecting and facilitating the movement of the heart. Any accumulation of excess fluid in the pericardial cavity, such as in pericardial effusion, can interfere with the normal functioning of the heart and require medical intervention.

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Do homozygous dominant and heterozygous organisms for a specific trait have different genotypes?

Answers

homozygous dominant and heterozygous organisms will look identical that is, they will have different genotypes but the same phenotype.

Genotype is a way to describe the combination of alleles that an individual has for a certain gene . For each gene, an organism has two alleles, one on each chromosome of a homologous pair of chromosomes (think of it as one allele from Mom, one allele from Dad). The genotype is represented by letter combinations, such as TT, Tt, and tt. When an organism has two of the same alleles for a specific gene, it is homozygous (homo means "same") for that gene. An organism can be either homozygous dominant (TT) or homozygous recessive (tt). If an organism has two different alleles (Tt) for a certain gene, it is known as heterozygous (hetero means different). To identify whether an organism exhibiting a dominant trait is homozygous or heterozygous for a specific allele, a scientist can perform a test cross. The organism in question is crossed with an organism that is homozygous for the recessive trait, and the offspring of the test cross are examined

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in an isolated population of elephants, 16 percent of the individuals have large ears, a homozygous recessive condition, and 84 percent have the dominant small ears phenotype. what percentage of the population are heterozygotes?

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A homozygous recessive condition, and 84 percent have the dominant small ears phenotype, percentage of population of heterozygotes is 0.36.

In an isolated population of elephants, 16 percent of the individuals have large ears, a homozygous recessive condition, and 84 percent have the dominant small ears phenotype, In a population that is in Hardy-Weinberg equilibrium, the frequency of homozygous dominant individuals is 0.36.

p = the frequency of the dominant allele in a population. q = the frequency of the recessive allele in a population. 2 p q 2pq 2pq = the frequency of the heterozygous dominant genotype. p 2 p^2 p2 = the frequency of homozygous dominant genotype.

The frequency of genotypes in a population can be represented by p2+2pq+q2= 1, with p2 equal to the frequency of the homozygous dominant genotype, 2pq equal to the frequency of the heterozygous genotype, and q2 equal to the frequency of the recessive genotype.

Homozygous and heterozygous are terms that are used to describe allele pairs. Individuals carrying two identical alleles (RR or rr) are known as homozygous. While individual organisms bearing different alleles (Rr) are known as heterozygous.

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How does the structure of eukaryotic chromosome during mitosis differ from its structure during the rest of the cell cycle

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Chromosome: replicating itself, looks like 2 lines, come back together at both ends; during the rest of the cell cycle, just one singular line.

The term "eukaryotic chromosome structure" describes the many stages of packaging of DNA, from unprocessed DNA molecules to the chromosomal structures seen during metaphase in mitosis or meiosis. Long DNA strands that carry genetic data are found in chromosomes. Eukaryotic chromosomes are linear, much larger than prokaryotic chromosomes, and have more nucleotides per base.While prokaryotic cells' chromosomes are not stored in a nucleus, eukaryotic cells' chromosomes are. Because there is more DNA present on eukaryotic chromosomes, more packaging is needed to fit the DNA molecules inside the cell nucleus. Condensed nucleosomes are created by wrapping DNA around histone proteins at this stage of packing.

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Eukaryotes have more ways to obtain energy than prokaryotes.
a. True
b. False

Answers

This statement is true. Eukaryotes, which are organisms that have a nucleus and other membrane-bound organelles, have more ways to obtain energy than prokaryotes, which are organisms without a nucleus or membrane-bound organelles.

One of the ways eukaryotes obtain energy is through aerobic respiration, which occurs in the mitochondria. This process requires oxygen and involves breaking down glucose to produce ATP, the molecule that provides energy for cellular processes.

Eukaryotes can also obtain energy through anaerobic respiration, which occurs in the absence of oxygen. This process occurs in the cytoplasm and is less efficient than aerobic respiration.

In addition, eukaryotes have the ability to perform photosynthesis, a process that converts light energy into chemical energy in the form of glucose. This process occurs in organelles called chloroplasts and is carried out by pigments such as chlorophyll.

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which of the following statements is correct? prokaryotic cells and eukaryotic cells evolved at about the same time. prokaryotic cells evolved a lot earlier (over a billion years) than eukaryotic cells. eukaryotic cells evolved a lot earlier (over a billion years) than prokaryotic cells.

Answers

Prokaryotic cells evolved a lot earlier (over a billion years) than eukaryotic cells.

Prokaryotic cells, such as bacteria, are the simplest and most primitive type of cells. They first appeared on Earth around 3.5 billion years ago and have been highly successful, thriving in a wide range of environments. On the other hand, eukaryotic cells, which are more complex Prokaryotic cells and include all animal and plant cells, evolved around 2 billion years ago. The evolution of eukaryotic cells was a major event in the history of life, as it made possible the development of complex multicellular organisms. The presence of a nucleus and other membrane-bound organelles in eukaryotic cells allowed for the specialization of cellular functions, which was crucial for the evolution of higher life forms.

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Rank the following items in order from largest to smallest: cell, chromosome, gene, DNA,

organism, nucleus

Answers

DNA, genes, and chromosomes are listed in size order, smallest to largest. The four various types of the double DNA molecules that compose a chromosome are determined by the bases they are connected to.

Adenine (A), thymine (T), guanine (G), & cytosine (C) are the four different kinds of DNA (C). Cells, tissues, organs, and organ systems are listed in order from smallest to the largest among these structures. A type of nucleic acid called deoxyribonucleic acid (DNA) was smaller than a gene. Two lengthy chemical chains termed nucleotides that form a double helix around one another make up this molecule. Your chromosomes, genes, and DNA all contribute to who you are. In cells, chromosomes transport DNA. Your human anatomy is created and maintained by your DNA. Rank the following items in order from largest to smallest: cell, chromosome, gene, DNA, organism, nucleus.

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how is atp used in the digestion, respiration, and excretion processes in all cells?

Answers

Adenosine triphosphate (ATP), an energy-rich compound that absorbs the chemical energy obtained from the breakdown of food molecules and releases it to fuel other cellular processes, is one goal of the degradation of foodstuffs.

ATP is created when the energy contained in chemical bonds is converted from one form to another. The chemical energy contained in food molecules is captured and then released to power the work being done by the cell. Consider ATP as the universal currency of your body's cells. Your body breaks down the food you eat into tiny macronutrient components. Your body converts all the carbs in your food to glucose, a simple sugar. A series of chemical processes known as cellular respiration convert glucose into ATP, which can then be used as energy to fuel many reactions throughout the body.

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what cell organelle is the fluid of dissolved molecules that fills the cell and suspends the organelles?
A. Cytosol
B. Chromoplast
C. Chromoplast
D. None of the above

Answers

The cell organelle that is the fluid of dissolved molecules that fills the cell and suspends the organelles is called the cytosol.

Cytosol, also known as intracellular fluid or cytoplasmic matrix, is the liquid part of the cytoplasm that is found within cells. It is composed of water, ions, small molecules, and various biomolecules, such as enzymes and structural proteins. Cytosol provides a medium for metabolic reactions and cellular processes to occur, and it also serves as a buffer to maintain the proper pH and osmotic balance within the cell.

The other options presented in the question, chromoplast and chloroplast, are organelles found in plant cells that are involved in photosynthesis and pigment synthesis. Chromoplasts are responsible for synthesizing and storing pigments other than chlorophyll, while chloroplasts contain chlorophyll and are involved in photosynthesis. However, neither of these organelles serves as the fluid that fills the cell and suspends the organelles, which is the function of the cytosol.

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When you use a field guide to identify a species by its appearance, you are applying the _____ conceptA. morphospeciesB. biological speciesC. ecological speciesD. evolutionary species

Answers

Applying the morphospecies theory or morphological species concept, you can identify a species by looking at it in a field guide.

The morphological species concept applies to both asexual and sexual organisms and describes a species according to its body shape and other structural characteristics. It differs from the modern definition of a species, where a collection of organisms that can breed with one another and produce fertile offspring are considered to belong to the same species. The Morphospecies concept seeks to explain speciation by examining structural similarities between different species. The forelimbs of mammals are an illustration of this. The forelimbs of a human, a cat, a whale, and a bat are similar.

It defines species as groups of individuals that share morphological characteristics and differ from other groups of similar individuals. When two organisms meet certain morphological (anatomical) requirements, they are categorised as belonging to the same species. When a species cannot reproduce sexually—some of which are only known from fossils—this is used.

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which types of kernels have the parental phenotypes? which types of kernels have recombinant or non-parental phenotypes? how many of them are there?

Answers

Homozygous kernels have parental phenotypes, whereas heterozygous kernels have recombinant phenotypes. Each is available in pairs.

The seed of a plant is referred to as the "kernel" in genetics. According to the genes they acquire from each parent, kernels during genetic crossings may exhibit various phenotypes.

Kernels that exhibit the same traits as one or both of their parents are said to have parental phenotypes. Recombinant or non-parental phenotypes are features that arise from the mixing and recombination of genetic material from both parents and are displayed by kernels.

Genetic crosses can produce two parental kinds and two recombinant types of kernels, giving rise to a total of four different types of kernels. The dominant homozygote and the recessive homozygote are the parental kinds, whilst the two heterozygotes make up the recombinant types.

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what ion enters a neuron causing depolarization of the cell membrane?

Answers

Depolarization is caused when positively charged sodium ions rush into a neuron with the opening of voltage-gated sodium channels.

When positively charged sodium ions (Na+) abruptly flood into an open voltage-gated sodium channel in a neuron, it results in the depolarization, also known as the rising phase. The membrane potential actually changes polarity when extra sodium pours in. The membrane develops a temporary positive value (+40 millivolts) during this polarity transition.

Slow sodium channel closure and voltage-gated potassium channel opening result in the repolarization, or falling phase. The membrane's sodium permeability consequently decreases to resting levels. Slow voltage-gated potassium channels open when sodium ion input decreases, allowing potassium ions to quickly exit the cell. The cell's specific negative membrane potential is restored by this expulsion.

Sodium channels reset during the hyperpolarization phase, during which certain potassium channels remain open. Before the potassium channels close, there is a period of enhanced potassium permeability, which leads to an excessive potassium efflux. A small dip that follows the surge indicates that this causes hyperpolarization.

Action potential spread is influenced by refractory periods rather than stimulus intensity. The absolute refractory period is the time from when sodium channels open until they start to reset. No matter how powerful the stimulation, the cell is unable to respond during this time.

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what is the largest type of lymphatic vessel, which deposits lymph into the subclavian veins?

Answers

The collecting lymphatics throughout the body eventually merge into bigger lymph trunks, the biggest of which, the thoracic duct and right lymph duct, discharge directly into the subclavian veins.

The right lymphatic duct drains lymph into the right subclavian vein, whereas the thoracic duct links to the left subclavian vein. The biggest lymphatic veins are lymphatic ducts. These two ducts pour lymph into neck veins (the right and left subclavian veins at their junctures with the internal jugular veins).

The efferent vessels that carry lymph from lymphatic organs to nodes and then to the right lymphatic duct or thoracic duct, the body's biggest lymph channel.

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what earth layer has a temperature that runs as high as 6,600 Celsius

Answers

Answer: The inner core.

The inner core has the highest temperature

Why would one use basic dyes instead of acidic dyes for simple stains?

Answers

Since they contain differing charges, basic dyes are more effective at staining bacteria than acidic dyes.

A basic dye has a positive charge and stains a cell's interior, whereas an acidic dye has a negative charge and stains a cell's outside.

We are aware that basic dyes are positively charged and acidic dyes have a negative charge. Moreover, the majority of organisms including bacteria have negatively charged cell walls. As both are similarly charged, they do not attract when the bacterial cell wall is dyed with acidic dyes.Therefore, generally, people use the basic dye instead of acidic dyes for simple stains.Which simply means that the basic dyes are being more preferred as compared to acidic dyes for simple stains.

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a genetic mutation preventing the production of the enzyme tyrosinase would result in the condition known as

Answers

A genetic mutation preventing the production of the enzyme tyrosinase would result in the condition known as Oculocutaneous albinism

Oculocutaneous albinism (OCA) is an uncommon genetic illness characterized by a decrease or complete absence of melanin pigment in the skin, hair, and eyes. Mutations in certain genes required for the generation of melanin pigment in specialized cells called melanocytes cause these diseases.

Oculocutaneous albinism is a type of albinism that affects the eyes (oculo-), skin (-cutaneous), and hair. Oculocutaneous albinism affects around one in every 20,000 people worldwide.

OCA is caused by abnormalities in many genes that govern melanin synthesis within melanocytes.

There are seven kinds of oculocutaneous albinism, all of which are caused by a breakdown in melanin synthesis and are all autosomal recessive illnesses.

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Normal cells have a contact inhibition feedback mechanism that prevents the cells from replicating when other cells are touched. A diagram of cells with contact inhibition and cells without contact inhibition is shown.

Cells with contact inhibition. cells without contact inhibition.
Top view.
Side view.

Which statement best describes what will happen to cells in an organism that lack contact inhibition?

Answers

Answer:

Cells in an organism that lack contact inhibition are likely to continue replicating uncontrollably and form a mass of tissue known as a tumor. This uncontrolled cell growth can lead to the development of cancer if the cells become abnormal and continue dividing even when they should stop. Normal cells, on the other hand, have a contact inhibition mechanism that prevents them from replicating when other cells are in close proximity, helping to regulate the growth and division of cells in the body.

An ecologist recorded 12 white-tailed deer per one square mile in one woodlot and 20 per one square mile in another woodlot. What was the ecologist comparing?

Answers

A comparison of (A) density was made by an ecologist who found 12 white-tailed deer per square mile in one woodlot and 20 per square mile in another woodlot.

What is the job of ecologist?

Ecologists study how organisms as well as their surroundings interact. They examine the wildlife and plant life that exist in a specific area and provide information on the potential effects of any proposed development projects. Most ecologists are scientists by training and hold degrees on chemistry, environmental science, geologist, biology, climatology, statistics, and occasionally economics.

Why do we need ecologists?

Ecologists investigate not only how ecosystems work, but also what happens when they don't work as they should. Numerous variables, such as illnesses spread by local species, temperature rises, and increasing human activity, can cause changes in ecosystems. It offers fresh understanding of the connection of humans and nature, which is essential for food production, preserving clean air and water, and preserving biodiversity in the face of climate change.

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The complete question:

An ecologist recorded 12 white-tailed deer, Odocoileus virginianus, per square mile in one woodlot and 20 per square mile on another woodlot. What was the ecologist comparing?

A) density

B) dispersion

C) carrying capacity

D) quadrats

E) range

explain how temperature and rainfall affect the distribution of biomes

Answers

The increase in temperature and an increase of rain increases forests. Less water and cooler temperature can result in grasslands biome.

forest is an important biome as it evolves maximum oxygen and resources for the organisms.

The maximum growth rate of the forest depends on the temperatures rise above 10 °C and is in the warmest months and the annual rain is more than 200 mm, heavy rainfall is needed to grow the forest.

In biome growth takes place in region of high latitudes (60° to 90°) which is farthest from the equator which receive the least amount of sunlight and have lower temperatures.

taiga and tundra is the example of biome.

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How would administering a non-hydrolyzable form of GTP to cell affect its G protein-coupled signal transduction pathways? a. The pathways would lose their specificity of response b. The pathways would become hypersensitive to stimuli. c. The pathways would respond in unpredictable ways.
d. The pathways would not turn off.
e. The pathways would become nonresponsive to stimuli.

Answers

d) The pathways would not turn off, if administering a non-hydrolyzable form of GTP to cell is in its G protein-coupled signal transduction pathways

In the pathway of G protein coupled signal transduction pathways, there are two principal signal transduction pathways involving the G protein-coupled receptors: the cAMP signal pathway and the phosphatidylinositol signal pathway.

there are 2 subunit which is alpha and beta subunits and when alpha subunit the interaction increases the alpha subunit affinity for the GDP. when these 2 subunits are separated they help in either inhibiting or  help in activation of secondary messengers

so, we can say ligand binding to G receptor, changes its conformation, which leads to lower affinity of binding GDP and less affinity of GTP.

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injection of calcium chelators, such as edta, into a postsynaptic neuron would most likely have what effect on synaptic plasticity?

Answers

Injection of calcium chelators, such as edta, into a postsynaptic neuron would most likely have LTP would not be observed

What is synaptic plasticity ?

Synapses, the connections that allow neurons to communicate with one another, undergo change known as synaptic plasticity. Donald Hebb, a Canadian psychologist, was the first to postulate that synapses could alter and that this change depended on how active or passive they were.

Examples of short-term plasticity in response to outside stimulus include paired-pulse depression and paired-pulse facilitation.

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Background Information: In incomplete dominance, the heterozygous genotype will express a phenotype somewhere in-between the dominant and the recessive. With codominance, the heterozygous genotype will express both phenotypes. Answer in

________________________________________________________________

In a chestnut horse, their coat (hair) color can be reddish brown (AA), light red/pink (Aa), and creamy white (aa). Fill in the Punnett square and determine the expected genotypes and phenotypes from crossing heterozygous and heterozygous parents.


My question is Is this an example of incomplete or codominance? And how can I tell the two incomplete and codominance apart in a problem

Answers

From this Punnett square, we can determine that there is a 25% chance of producing homozygous dominant offspring (AA), a 50% chance of producing heterozygous offspring (Aa), and a 25% chance of producing homozygous recessive offspring (aa).

In the case of chestnut horses, this is an example of incomplete dominance. This is because the heterozygous genotype (Aa) expresses a phenotype that is intermediate between the homozygous dominant (AA) and homozygous recessive (aa) phenotypes. In this case, the heterozygous genotype (Aa) will result in a coat color that is a light red/pink color, rather than the darker reddish-brown of the homozygous dominant (AA) or the creamy white of the homozygous recessive (aa).

In contrast, codominance occurs when the heterozygous genotype expresses both phenotypes simultaneously. This means that the offspring will exhibit characteristics of both the dominant and recessive traits, rather than an intermediate phenotype. For example, in the case of blood type, a person with AB blood type has both A and B antigens present on their red blood cells, rather than an intermediate phenotype.

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imagine a population that is polymorphic at the a locus. if the frequency of the a allele is 80% and the frequency of the a allele is 20%, what proportion of the population would you expect be heterozygotes?

Answers

You would estimate that 0.0016 of something like the population would be heterozygotes. if the frequency of one allele is 20% and indeed the frequency of another is 80%.

What is an example of an allele?

An allele is a component of a group of genes that govern the same feature, such as red cells or color blindness, and are located at a specific place on a specific chromosome. The alleles you received from your parent define your blood group.

Why is there two alleles in humans?

Diploid humans exist. As a result, everyone of our genes has just two alleles. This is mostly due to the fact that we only receive one copy of each parent's chromosomes. We all have pairs of chromosomes because we each have two parents.

AA × AA = 0.4096

AA × Aa = 0.4096

AA × aa = 0.0512

Aa × Aa = 0.1024

Aa × aa = 0.0256

aa × aa = 0.0016

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the fibula group of answer choices articulates with the femur. crosses the tibia when the leg is rotated. forms the lateral border of the knee joint. stabilizes the ankle joint.

Answers

The fibula or calf bone is a leg bone on the lateral side of the tibia, to which it is connected above and below.

The fibula or calf bone is a leg bone on the lateral side of the tibia, to which it is connected above and below. It is the smaller of the two bones and, in proportion to its length, the most slender of all the long bones.

The structure of the fibula can be broken down into the head, neck, shaft, and distal end of the fibula. As the head becomes narrow distally, the fibular neck is formed. The fibular shaft lies distal to the neck and has three surfaces, lateral, medial, and posterior. The lower leg is comprised of two bones, the tibia and the smaller fibula. The thigh bone, or femur, is the large upper leg bone that connects the lower leg bones (knee joint) to the pelvic bone (hip joint).

The fibular collateral ligament is a strong ligament that originates from the lateral epicondyle of the femur, just posterior to the proximal attachment of the popliteus, and extends distally to attach on the lateral surface of the fibular head.

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