. There are many abiotic factors that affect the rate of photosynthesis in terrestrial plants. Wheat is an important cereal crop in many parts of the world. Wheat seedlings were grown at three different concentrations of carbon dioxide (in parts per million) and the rate of photosynthesis was measured at various light intensities. 50- 40- 30- Rate of photosynthesis /ul CO, min! key: A 1300 ppm CO2 500 ppm CO2 280 ppm CO2 20- O 10- 0 0 T 15 5 10 20 Light intensity / x 10 lumen m3-2 (Source: Adapted from JP Kimmins, 1997 Forest Ecology, (2nd edition) page 161) (a) Describe the relationship between the rate of photosynthesis and light intensity for wheat seedlings grown at a CO2 concentration of 500 ppm

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Answer 1

The graph shows the relationship between the rate of photosynthesis and the light intensity for wheat seedlings grown at CO2 concentrations of 500 ppm. The rate of photosynthesis increased as the light intensity increased.

At a light intensity of 0 lumen m-2, the rate of photosynthesis was around 0 ul CO2 min-1. At a light intensity of 10 lumen m-2, the rate of photosynthesis was around 20 ul CO2 min-1. At a light intensity of 20 lumen m-2, the rate of photosynthesis was around 40 ul CO2 min-1.

As the light intensity continued to increase, the rate of photosynthesis did not increase at a proportional rate but rather started to level off. This is because there was a limit to the rate of photosynthesis that could be achieved by the wheat seedlings.

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Related Questions

Strenous exercise should cause an increase in systemic capillary blood flow due to the sympathetic nervous system. True False QUESTION 7 In myocardial contractile cells, the action potential will occu

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The given statement is false.

Strenuous exercise causes an increase in systemic capillary blood flow primarily due to vasodilation of arterioles, not the sympathetic nervous system. The sympathetic nervous system plays a role in regulating heart rate and cardiac output during exercise, but its effect on capillary blood flow is limited. Vasodilation of arterioles is mediated by factors such as metabolic demands, local factors (e.g., nitric oxide release), and hormonal responses (e.g., epinephrine), which increase blood flow to active tissues during exercise.

Solution of Question 7:

In myocardial contractile cells, the action potential occurs as a result of a series of electrical changes. The action potential begins with the depolarization phase, initiated by the influx of sodium ions through fast voltage-gated sodium channels. This rapid depolarization leads to the opening of calcium channels, resulting in a plateau phase, where calcium influx balances potassium efflux, thus prolonging the action potential and allowing for sustained contraction. Finally, repolarization occurs as potassium channels open, leading to potassium efflux and restoring the resting membrane potential. This sequential pattern of electrical changes allows for coordinated contraction and relaxation of the myocardium, enabling the heart to pump blood effectively.

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Oxidative decarboxylation of pyruvate and the TCA cycle in muscles are stimulated by increased acrobic exercise. These processes operate only when O, is present, although oxygen does not participate directly in these processes. Explain why oxidative decarboxylation of pyruvate is activated under aerobic conditions. For the answer: a) describe the overall reaction catalyzed by the pyruvate dehydrog complex (PDH) and its regulation; b) outline the intermediates and enzymes of the TCA cycle; e) explain the relationship between the reactions of PDH and the TCA cycle and the respiratory chain.

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Oxidative decarboxylation of pyruvate is activated under aerobic conditions because the oxidative decarboxylation of pyruvate requires the participation of oxygen indirectly. Aerobic respiration yields ATP as well as carbon dioxide and water by the breakdown of glucose in the presence of oxygen. The aerobic oxidation of pyruvate, which occurs in mitochondria in a series of coordinated enzyme-catalyzed reactions, is a key metabolic pathway for aerobic organisms to extract energy from nutrients.

In the mitochondria, the pyruvate dehydrogenase complex (PDH) catalyzes oxidative decarboxylation of pyruvate to form acetyl-CoA and CO2 by converting the 3-carbon pyruvate molecule to the 2-carbon acetyl group attached to CoA. The reaction catalyzed by the PDH complex is regulated by phosphorylation/dephosphorylation, which is under the control of pyruvate dehydrogenase kinase and pyruvate dehydrogenase phosphatase. In the TCA cycle, acetyl-CoA enters the cycle by condensing with the 4-carbon oxaloacetate to form citrate. The cycle then proceeds through several enzymatic reactions to regenerate oxaloacetate, which can accept another acetyl-CoA molecule.

The intermediates and enzymes of the TCA cycle include citrate synthase, aconitase, isocitrate dehydrogenase, alpha-ketoglutarate dehydrogenase, succinyl-CoA synthetase, succinate dehydrogenase, fumarase, and malate dehydrogenase. The NADH and FADH2 produced by the TCA cycle are utilized in the electron transport chain to produce ATP through oxidative phosphorylation. In conclusion, the reactions of the PDH complex and the TCA cycle are closely related to the respiratory chain as they generate the substrates for the electron transport chain to produce ATP.

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3. DISCUSS THE ZONES OF BASE OF 5TH METATARSAL BONE?

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The fifth metatarsal bone, located in the foot, has specific zones that are important to understand, particularly in relation to injuries such as fractures. The zones of the base of the fifth metatarsal bone are commonly referred to as the Lawrence and Botte classification system.

Zone 1: Tuberosity Avulsion Fracture:

This zone is characterized by an avulsion fracture at the base of the fifth metatarsal, specifically at the insertion point of the peroneus brevis tendon. It typically occurs due to a sudden forceful contraction of the peroneus brevis tendon, resulting in the pulling away of the bone fragment.

Zone 2: Jones Fracture:

This zone is located distal to the tuberosity avulsion fracture. A Jones fracture involves a fracture through the metaphyseal-diaphyseal junction of the fifth metatarsal bone. It is a common type of fracture that occurs due to repetitive stress or acute trauma.

Zone 3: Diaphyseal Fracture:

Zone 3 is the diaphyseal or shaft region of the fifth metatarsal bone. Fractures in this zone are less common than in zones 1 and 2. They usually result from direct trauma or excessive bending or twisting forces.

Understanding these zones is important because the treatment and prognosis of fractures in each zone may differ. Zone 1 fractures usually have a good prognosis, while zone 2 fractures (Jones fractures) can be more challenging to heal due to a limited blood supply in that area.

Zone 3 fractures may have varying treatment approaches depending on the fracture pattern and severity.

It's worth noting that this classification system provides a general framework for understanding and discussing fractures in the base of the fifth metatarsal bone. However, individual cases may present variations and require thorough evaluation by a healthcare professional.

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.What are the major concerns or factors you would like to consider, when implementing protein purification?
This question is related to performing protein purification as a lab technique to identify an expressed protein.

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Some well-known variables (molecular weight, theoretical IEC, amino acid composition, extinction coefficient) help to improve the rate of protein purification. Some variables (pH and salt concentration) are expected from the homologously composed protein structure.

Proteins need to be stored in a well-oxygenated environment to avoid rapid changes in pH levels that could cause irreversible changes in their structure, solubility, and function.

Purification is a set of steps designed to separate one or more proteins from a complicated mix, typically composed of cells, tissues, or entire organisms. Purification plays an important role in understanding the functions, structure, and interactions of a protein of interest.

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pleas help homework questions I dont know any of these
QUESTION 19
Which muscle is involved with shoulder abduction?
subscapularis
supraspinatus
teres minor
teres major

Answers

The supraspinatus muscle is involved in shoulder abduction. Shoulder abduction refers to the movement of raising the arm away from the body in a lateral direction.

The supraspinatus muscle, located in the upper back, plays a vital role in this movement. It is one of the four rotator cuff muscles and is specifically responsible for initiating and assisting with shoulder abduction. When the supraspinatus contracts, it helps to stabilize the shoulder joint and facilitates the lifting of the arm away from the body. The other muscles listed (subscapularis, teres minor, and teres major) are involved in different movements of the shoulder but not directly related to abduction.

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true or false Here is a phylogeny of eukaryotes determined by DNA evidence. All of the supergroups contain some photosynthetic members.

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The statement "All of the supergroups contain some photosynthetic members" in reference to a phylogeny of eukaryotes determined by DNA evidence is a true statement.

Supergroups are a collection of phylogenetically related eukaryotes. These lineages, which were once referred to as "Kingdom Protista," are now grouped into the six supergroups that make up the eukaryotic tree of life. In each supergroup, some members engage in photosynthesis.

The six supergroups are as follows:

ExcavataChromalveolataRhizariaArchaeplastidaAmoebozoaOpisthokonta

As a result, it is correct to say that all supergroups contain some photosynthetic members.

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Drawing on the theory of the vulnerability (to extinction) of small populations, in the discipline of Conservation Biology, explain why increasing propagule pressure (number of individuals introduced) increases the likelihood of a species establishing a novel alien population, outside its’ native range.

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Increasing propagule pressure, which refers to the number of individuals introduced into a new environment, increases the likelihood of a species establishing a novel alien population outside its native range.

When small populations are introduced to a new habitat, they often face challenges and uncertainties that can lead to high extinction risks. These risks arise due to various factors such as limited genetic diversity, reduced adaptive potential, and increased vulnerability to environmental fluctuations and stochastic events. However, increasing the number of individuals introduced, or the propagule pressure, can help mitigate these risks and enhance the chances of successful establishment.

Higher propagule pressure provides several advantages. Firstly, it increases the genetic diversity within the introduced population, which is crucial for adaptation and resilience to new environmental conditions. A larger number of individuals bring a wider range of genetic variation, increasing the likelihood that some individuals possess traits advantageous for survival and reproduction in the new environment.

Secondly, larger populations have a greater chance of overcoming demographic and environmental stochasticity. They are more resilient to random events such as disease outbreaks, predation, or unfavorable weather conditions. With more individuals, the probability of some individuals surviving and reproducing increases, thereby enhancing the establishment success of the alien population.

Lastly, higher propagule pressure can facilitate the formation of self-sustaining populations. A critical threshold of individuals is often required to establish viable breeding populations and prevent inbreeding depression. By introducing a larger number of individuals, the chances of meeting this threshold are improved, increasing the long-term survival and persistence of the species in the new habitat.

In summary, increasing propagule pressure enhances the likelihood of a species establishing a novel alien population outside its native range by promoting genetic diversity, improving resilience to environmental challenges, and facilitating the formation of self-sustaining populations.

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4. Create a box-and-arrow model that shows how information stored in the SRY gene is stored in a somatic cell of a typical male. Your model must be contextualized to this case and should include the following structures, although you may add or repeat structures as needed: nucleotides, chromosomes, DNA, gene

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The SRY gene, located on the Y chromosome in a typical male somatic cell, stores information that directs the development of male characteristics. This information is transcribed into mRNA, translated into the SRY protein, which then triggers male reproductive structure development and hormone production.

In a typical male somatic cell, the SRY gene plays a crucial role in determining the development of male characteristics. Here is a box-and-arrow model illustrating how information stored in the SRY gene is stored:

1. Nucleotides: The fundamental units of DNA, composed of adenine (A), thymine (T), cytosine (C), and guanine (G).

2. Chromosomes: The SRY gene is located on the Y chromosome, one of the two sex chromosomes in males.

3. DNA: The SRY gene is a specific sequence of nucleotides within the DNA molecule on the Y chromosome.

4. Gene: The SRY gene contains the genetic instructions for the development of male characteristics. It codes for the SRY protein.

5. Transcription: The information stored in the SRY gene is transcribed into a messenger RNA (mRNA) molecule through a process called transcription.

6. mRNA: The mRNA molecule carries the genetic information from the nucleus to the cytoplasm.

7. Translation: In the cytoplasm, the mRNA is translated into a protein molecule through a process called translation.

8. SRY Protein: The protein synthesized from the SRY gene binds to specific target genes involved in male sexual development.

9. Male Development: The binding of the SRY protein to its target genes triggers a cascade of molecular events that direct the development of male reproductive structures, such as the testes, and the production of male hormones, such as testosterone.

Overall, this box-and-arrow model illustrates how the information stored in the SRY gene on the Y chromosome is transcribed and translated into a protein that orchestrates male development in somatic cells.

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if its right ill give it a
thumbs up
Question 6 Hormone signaling results in transcription. O True O False

Answers

False.

Hormone signaling does not directly result in transcription.

Hormone signaling is a complex process that involves the transmission of chemical signals from endocrine glands to target cells throughout the body. These hormones bind to specific receptors on the surface of target cells, triggering a series of intracellular events. While hormone signaling can ultimately lead to changes in gene expression, it does not directly result in transcription.

Once a hormone binds to its receptor on the cell surface, it initiates a cascade of intracellular signaling events, typically involving second messenger molecules. These signaling pathways can activate or inhibit various enzymes and proteins within the cell, leading to the activation of specific transcription factors. Transcription factors are proteins that bind to DNA and regulate gene expression by promoting or inhibiting the transcription process.

Therefore, it is the activation of transcription factors, rather than the hormone itself, that ultimately leads to changes in gene expression and subsequent transcription. Hormone signaling serves as a crucial regulatory mechanism in coordinating various physiological processes, but its effects on transcription are mediated through intracellular signaling pathways and transcription factor activation.

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I am a member of the phytoplankton community that is covered with calulose plates called a theca dominate the phytoplankton in late summer in mid-lattudes, and am almost always dominant in the tropics I am also bioluminescent To which group do I belong? a. diatoms b. coccolithophores c. cyanobacteria d. dinoflagellates

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I belong to the Dinoflagellates group.

Dinoflagellates are a group of single-celled organisms that belong to the Protista kingdom. Dinoflagellates have two flagella that help them move in the water column. These organisms are the largest group of marine phytoplankton. Dinoflagellates are important members of the food chain in the ocean. They are also known for producing bioluminescence, which means they emit light. A member of the phytoplankton community that is covered with calcite plates called a theca is a coccolithophore. They are a group of single-celled algae that have calcified external coverings. Coccolithophores are also dominant in the tropics and have bioluminescence. But, they are not the dominant phytoplankton in late summer in mid-latitudes. Diatoms are another type of phytoplankton. They are single-celled organisms that have cell walls made of silica. However, diatoms are not bioluminescent and do not have theca. Cyanobacteria are also known as blue-green algae. They are a group of photosynthetic bacteria that are typically found in freshwater. They do not have a theca and are not bioluminescent. Therefore, the correct option is (d) dinoflagellates.

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Which of the following events would elicit a response by a natural killer cell? A. A cell is infected with a virus B. A parasitic worm invades the body. C. Pollin is encountered in the respiratory tract. D. A skin cell becomes cancerous E. A bacterium invades the blood stream.

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Natural killer (NK) cells belong to the innate immune system and respond to numerous types of cellular tension that can arise due to viral infections, cancerous transformation, and other events.

The correct answer is A. A cell is infected with a virus. Viruses can enter and disrupt healthy cells and hijack their protein synthesis machinery to produce viral particles that spread the disease throughout the body.

A virus-infected cell displays markers of abnormality on its surface that NK cells can recognize, allowing them to differentiate between healthy and infected cells. The NK cell will subsequently launch an attack against the infected cell by releasing granules containing cytotoxic molecules, such as perforin and granzymes.

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_________ is a term used to describe abnormal gut function

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Irritable bowel syndrome (IBS) is a term used to describe abnormal gut function. It is a common disorder that affects the large intestine and causes symptoms such as abdominal pain, bloating, diarrhea, and constipation.

The exact cause of IBS is unknown, but it is believed to involve a combination of factors including abnormal muscle contractions in the intestine, increased sensitivity to pain, and changes in the gut microbiome. Treatment for IBS usually focuses on managing symptoms through dietary changes, stress reduction, and medication.

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This Activity explored the big idea that gene expression can change. Specifically, • changes in the sequence of DNA can have beneficial, neutral or deleterious effects; • transcription can be enhanced or inhibited by changes in a cell's environment; • changes in chromosome structure can also change gene expression. In your own words, speak briefly to demonstrate each of the three ways in which gene expression can be affected or changed.

Answers

Gene expression can be affected or changed through alterations in DNA sequence, modulation by the cell's environment, and changes in chromosome structure.

a brief explanation of the three ways in which gene expression can be affected or changed:

Changes in the sequence of DNA: The DNA sequence contains the instructions for building proteins and regulating gene expression. Alterations in the DNA sequence, such as mutations, can have different effects on gene expression.

Beneficial mutations may enhance protein function or provide new traits, while deleterious mutations can disrupt protein production or function. Neutral mutations have no significant effect on gene expression.

Transcription modulation by the cell's environment: Gene expression can be influenced by changes in the cellular environment. Various external factors, such as temperature, nutrient availability, chemical signals, or stress conditions, can enhance or inhibit transcription—the process of synthesizing RNA from DNA.

Environmental cues can activate or suppress certain genes, allowing cells to adapt their gene expression to different conditions.

Changes in chromosome structure: Chromosomes play a vital role in gene expression, as they contain genes organized into DNA sequences. Structural changes in chromosomes, such as inversions, deletions, or translocations, can impact gene expression.

These alterations can disrupt the normal regulation of genes, affecting their accessibility to transcription machinery or altering the interaction of regulatory elements with specific genes.

In summary, gene expression can be affected by changes in DNA sequence, transcription modulation by the cellular environment, and alterations in chromosome structure.

These various mechanisms highlight the dynamic nature of gene expression and its responsiveness to internal and external factors.

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Hypothesis: The presence of solute impacts osmosis, causing cells to gain or lose mass. You are given the following materials: 10% sucrose solution, dialysis bags, orange clips, distilled water, beakers, electronic balance, graduated cylinders, weigh boat, timer, a funnel. REMEMBER: SUCROSE IS TOO LARGE TO PASS THROUGH THE PORES OF THE DIALYSIS BAGS. Identify the independent variable (0.5pt): Identify the dependent variable (0.5 pt): State at least 2 confounding variables (1 pts): Identify any controls (1 pt): Now, devise a protocol to test the above hypothesis to demonstrate the gain of mass by a dialysis bag, using the materials listed above. DETAILS MUST BE PROVIDED TO RECEIVE FULL CREDIT. (4 pts) Finally, you construct a graph using data collected from your experiment. What specifically will you put on the X axis? How will label it? (1 pt) What specifically will you put on the Y axis? How will you label it? (1 pt) What type of graph will you construct? (1 pt)

Answers

The independent variable in the experiment is the presence of solute in the dialysis bag. The dependent variable is the change in mass of the dialysis bag.

Two potential confounding variables could be the initial mass of the dialysis bag and the temperature of the surrounding environment. The control group would involve using a dialysis bag filled with only distilled water.

To test the hypothesis, the protocol involves filling dialysis bags with different concentrations of sucrose solution, placing them in separate beakers with distilled water, and measuring the change in mass over a specific time period.

The X-axis of the graph will represent the concentration of solute in the dialysis bag, labeled as "Concentration (sucrose %)." The Y-axis will represent the change in mass of the dialysis bag, labeled as "Change in Mass (grams)." A line graph would be suitable for displaying the data.

The independent variable in this experiment is the presence of solute, specifically the concentration of sucrose solution in the dialysis bag. The experiment aims to investigate how the presence of solute impacts osmosis and the resulting change in mass of the dialysis bag.

By varying the concentration of sucrose solution, the effect on osmosis can be observed.

The dependent variable is the change in mass of the dialysis bag. The mass of the dialysis bag before and after the experiment will be measured, and the difference will indicate whether the dialysis bag gained or lost mass.

Two potential confounding variables that should be considered are the initial mass of the dialysis bag and the temperature of the surrounding environment.

The initial mass of the dialysis bag may vary between different bags, which could affect the overall change in mass. The temperature can also impact the rate of osmosis, as higher temperatures may increase the rate of molecular movement.

To conduct the experiment, the protocol involves filling multiple dialysis bags with different concentrations of sucrose solution, ranging from 0% (distilled water) to 10%. Each bag will be securely sealed with an orange clip.

The bags will then be placed in separate beakers filled with distilled water. The beakers will be labeled with the corresponding sucrose concentration.

The bags will be left in the beakers for a specific time period, allowing osmosis to occur.

After the designated time, the dialysis bags will be removed from the beakers, gently blotted dry, and weighed using an electronic balance.

The change in mass for each bag will be calculated by subtracting the initial mass from the final mass.

For constructing the graph, the X-axis will represent the concentration of solute in the dialysis bag and will be labeled as "Concentration (sucrose %)." The Y-axis will represent the change in mass of the dialysis bag and will be labeled as "Change in Mass (grams)."

Since the concentration of solute is a continuous variable, a line graph would be suitable for displaying the data and showing any trends or patterns.

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Create a concept map that will link the following words. Use connecting words to complete concepts. 1. Allele 2. Genetics 3. Gene 4. Dominance 5. Recessiveness 6. Heterozygous 7. Homozygous 8. Blending theory 9. Elementen 10. Genotypic ratio 11. Aristotle 12. Mendel 13. Peas 14. Thomas Hunt Morgan 15. Fruit fly

Answers

Allele, Genetics, Gene, Dominance, Recessiveness, Heterozygous, Homozygous, Blending theory, Elementen, Genotypic ratio, Aristotle, Mendel, Peas, Thomas Hunt Morgan, Fruit fly can be linked in a concept map as follows:

Genetics: Genetics is the branch of biology that focuses on the study of genes, heredity, and variation in organisms.

Gene: A gene is a segment of DNA that contains the instructions for the synthesis of a specific protein or functional RNA molecule.

Allele: An allele is a variant form of a gene that arises through mutation and is located at a specific position on a chromosome.

Dominance: Dominance refers to the relationship between alleles of a gene, where one allele (dominant) masks the expression of another allele (recessive) in the phenotype.

Recessiveness: Recessiveness refers to the phenomenon where an allele is expressed only in the absence of a dominant allele.

Heterozygous: Heterozygous refers to an individual having different alleles at a particular gene locus.

Homozygous: Homozygous refers to an individual having identical alleles at a particular gene locus.

Blending theory: The blending theory of inheritance was an early hypothesis that suggested that traits from parents blend together in the offspring.

Elementen: Elementen refers to the term used by Gregor Mendel to describe the hereditary units that determine specific traits.

Genotypic ratio: The genotypic ratio refers to the ratio of different genotypes observed in the offspring resulting from a genetic cross.

Aristotle: Aristotle was a Greek philosopher who made observations on the inheritance of traits in organisms.

Mendel: Gregor Mendel was an Austrian monk and botanist who conducted experiments with pea plants and established the fundamental principles of inheritance.

Peas: Peas were the plants used by Gregor Mendel in his experiments on inheritance.

Thomas Hunt Morgan: Thomas Hunt Morgan was an American geneticist known for his work on fruit flies and the discovery of sex-linked inheritance.

Fruit fly: The fruit fly (Drosophila melanogaster) is a common model organism used in genetics research due to its short generation time and easily observable traits.

Conclusion: The concept map connects various terms related to genetics, including key figures, concepts, and model organisms. It demonstrates the interconnectedness of these terms and their significance in understanding the principles of inheritance and genetic variation.

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Case Study: Part One Saria is at the doctor to get the lab results of the samples she brought in to be tested. From the results, it appears that she is getting the rashes due to Pseudomonas aeruginosa infection that she contracted from the sponge she was sharing with her roommates. Now, we have to run further tests to check for the appropriate antibiotic needed to get rid of the infection. We also need to make sure to protect the normal flora in Saica so only the bad germs die. To do this we will use a gene transfer method to protect her healthy germs from the effects of possible antibiotics we can use. Introduction/Background Material: Basics of Bacterial Resistance: Once it was thought that antibiotics would help us wipe out forever the diseases caused by bacteria. But the bacteria have fought back by developing resistance to many antibiotics, Bacterial resistance to antibiotics can be acquired in four ways: 1. Mutations: Spontaneous changes in the DNA are called mutations. Mutations happen in all living things, and they can result in all kinds of changes in the bacterium. Antibiotic resistance is just one of many changes that can result from a random mutation. 2. Transformation: This happens when one bacterium takes up some DNA from the chromosomes of another bacterium 3. Conjugation: Antibiotic resistance can be coded for in the DNA found in a small circle known as a plasmid in a bacterium. The plasmids can randomly pass between bacteria (usually touching as seen in conjugation) 4. Recombination: Sharing of mutations, some of which control resistance to antibiotics. Some examples are: A. Gene cassettes are a small group of genes that can be added to a bacterium's chromosomes. The bacteria can then accept a variety of gene cassettes that give the bacterium resistance to a variety of antibiotics. The cassettes also can confirm resistance against disinfectants and pollutants. B. Bacteria can also acquire some genetic material through transduction (e.g., transfer through virus) or transformation. This material can then lead to change in phenotype after recombination into the bacterial genome. The acquired genetically based resistance is permanent and inheritable through the reproductive process of bacteria, called binary fission. Some bacteria produce their own antibiotics to protect themselves against other microorganisms. Of course, a bacterium will be resistant to its own antibiotic! If this bacterium then transfers its resistance genes to another bacterium, then that other bacterium would also gain resistance. Scientists think, but haven't proved, that the genes for resistance in Saica's case have been transferred between bacteria of different species through plasmid or cassette transfer. Laboratory analysis of commercial antibiotic preparations has shown that they contain DNA from antibiotic-producing organisms.

Answers

The resistance of bacteria to antibiotics is a major concern for public health. Bacterial resistance to antibiotics can be acquired in four ways; mutations, transformation, conjugation, and recombination.

In this case, Saria contracted Pseudomonas aeruginosa infection through a sponge she shared with her roommates.

To get rid of the infection, the appropriate antibiotic needs to be used while ensuring the healthy germs are protected from the effects of the antibiotic. This bacterium is antibiotic-resistant. Bacterial resistance to antibiotics can be acquired in four ways: Mutations, Transformation, Conjugation, and Recombination. Antibiotic resistance can be caused by random mutations in bacterial DNA. Antibiotic resistance can be coded for in the DNA found in a small circle known as a plasmid in a bacterium. The plasmids can randomly pass between bacteria.

This can be achieved through a gene transfer method.


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What structure is necessary for the reversible binding of O2
molecules to hemoglobin and myoglobin? At what particular part of
that structure does the protein-O2 bond form?

Answers

The structure that is required for the reversible binding of O2 molecules to hemoglobin and myoglobin is known as heme. Heme is a complex organic molecule consisting of a porphyrin ring that binds iron in its center, which is the binding site for O2.

The iron atom is held in a fixed position by four nitrogen atoms that form a planar structure. The fifth position is occupied by a histidine residue, which is supplied by the protein. The sixth position is where O2 binds in the presence of heme. The binding of O2 to heme is an electrostatic interaction between the positively charged iron atom and the negatively charged O2 molecule.

This interaction causes the O2 molecule to be slightly bent, which enables it to fit more tightly into the binding site. The strength of this bond is affected by various factors such as pH, temperature, and pressure, which can cause the bond to weaken or break. The protein-O2 bond forms at the sixth position of the heme structure.

The sixth position is where the O2 molecule binds to the iron atom, forming a complex that is stabilized by the surrounding amino acids. The histidine residue in the protein provides one of the nitrogen atoms that hold the iron in place. The other three nitrogen atoms are provided by the porphyrin ring.

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a b . Which letter represents the area where ATP binds? Choice B Choice A O Choice C O Choice D O Choice E A B 2. 2 4. D с 3 Which letter represents the binding of ATP? B OA

Answers

The correct answer is letter E. The letter E represents the area where ATP binds.

ATP stands for Adenosine Triphosphate, which is a high-energy molecule that cells use to power metabolic reactions. ATP is generated in the mitochondria and chloroplasts of eukaryotic cells. Adenosine Triphosphate (ATP) binds with myosin to help muscles contract, and it can also bind with enzymes and proteins to power cellular processes.ATP can provide energy for cellular processes because it has high energy phosphate bonds. It is referred to as the "energy currency" of cells because it transports chemical energy within cells.ATP binds to enzymes or proteins in the cell to donate energy for chemical reactions. When it binds, the molecule splits, releasing a phosphate group and generating energy that can be used by the cell. ATP binds to an enzyme or protein at the binding site. The area of an enzyme or protein where ATP binds is called the binding site. When ATP binds to an enzyme or protein at the binding site, it is referred to as a substrate of the enzyme or protein, and the enzyme or protein is referred to as an ATPase. The area where ATP binds is denoted by the letter E.

In conclusion, ATP binding is crucial for cells to power cellular processes. The binding site is where ATP binds, and it is denoted by the letter E. When ATP binds to an enzyme or protein at the binding site, it generates energy that can be used by the cell. The correct answer is the letter E.

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In studies that are conducted over lengthy periods, researchers
may sometimes end up studying milder cases, or people who are
farther along in the disease process. This may contribute to
Group of answ

Answers

In studies that are conducted over lengthy periods, researchers end up studying milder cases, The option that best fits the statement is D) Exposure to a milder disease form may produce immunity.

When researchers conduct studies over lengthy periods, they may end up studying milder cases or individuals who are farther along in the disease process. This can contribute to the understanding that exposure to a milder form of a disease may produce immunity.

Exposure to a mild form of a disease can stimulate the immune system to recognize and respond to the pathogen responsible for the disease. The immune response includes the production of specific antibodies and the activation of immune cells that can effectively eliminate smallpox the pathogen. As a result, the individual develops immunity to the pathogen, meaning they are protected against future infections or may experience a milder form of the disease.

Studying milder cases or individuals who have progressed further in the disease process allows researchers to observe the effects of previous exposure and the development of immunity. This knowledge is valuable in understanding the dynamics of infectious diseases and can contribute to the development of preventive measures such as vaccines.

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The Complete question is

In studies that are conducted over lengthy periods, researchers may sometimes end up studying milder cases, or people who are farther along in the disease process. This may contribute to

Group of answers

A) A weakened microorganism will not cause disease.

B) Disease is caused by viruses.

C) Someone who recovers from a disease will not acquire that disease again.

D) Exposure to a milder disease form may produce immunity.

E) Pathogenic microorganisms infect all humans and animals in the same manner.

Why is it important for bacteria to maintain a constant fluidity at different growth temperatures? Suggest what might happen to bacteria with membranes that are (a) too fluid, (b) too rigid. (c) How could you test these hypotheses?

Answers

Bacteria are the most successful living organisms on the earth. They have the ability to adapt to a wide range of temperatures, from as low as -20oC to as high as 110oC. This is attributed to the fact that they have the ability to alter their lipid composition of their membranes to maintain fluidity at different growth temperatures.

Maintaining membrane fluidity is important for the survival of bacteria. This is because the structure and function of bacterial membranes are crucial to their survival, and if the membrane is damaged, the bacteria will die. Hence, it is important to maintain membrane fluidity in order to ensure that the bacteria are able to grow and reproduce. If the membrane is too fluid, the bacteria will not be able to maintain their shape and may burst. This can happen when bacteria are exposed to higher temperatures or when the fatty acid composition of the membrane is altered.

On the other hand, if the membrane is too rigid, the bacteria will not be able to grow and reproduce. This can happen when bacteria are exposed to lower temperatures or when the fatty acid composition of the membrane is altered. To test the hypothesis that bacteria with membranes that are too fluid or too rigid are less likely to survive, the following experiments can be performed. A bacterial culture can be grown in a nutrient medium containing different concentrations of fatty acids.

The growth rate of the bacteria can then be measured. If the concentration of fatty acids is too low, the bacteria will not be able to grow and reproduce, indicating that the membrane is too rigid. If the concentration of fatty acids is too high, the bacteria will not be able to maintain their shape and may burst, indicating that the membrane is too fluid.

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Different types of cancer have different combinations of characteristics. There are some characteristics that characterize cancer cells in general and make them different from normal cancer cells.
Explain what properties this is.

Answers

Different types of cancer have different combinations of characteristics.

However, there are some properties that characterize cancer cells in general and make them different from normal cells.

Cancer cells usually divide uncontrollably.

Here is a detailed explanation of the properties of cancer cells:

Properties of cancer cells

Cancer cells usually divide uncontrollably, and they are different from normal cells in several ways.

Here are the main properties of cancer cells:

Uncontrolled growth:

Cancer cells don't respond to the signals that regulate cell growth.

This means that they divide uncontrollably and form tumors.

Avoidance of apoptosis:

Apoptosis is the programmed cell death that occurs in normal cells.

Cancer cells have a mechanism that allows them to avoid apoptosis and survive.

Angiogenesis:

Cancer cells need a blood supply to grow and divide.

They secrete signals that promote the growth of new blood vessels around the tumor site.

Metastasis:

Cancer cells can spread to other parts of the body through the bloodstream or lymphatic system.

This is known as metastasis.

Genetic instability:

Cancer cells have unstable genomes.

They accumulate genetic mutations that can lead to changes in the properties of the cell.

Cancer cells have properties that make them different from normal cells, and these properties contribute to the development and progression of cancer.

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Match the following terms with their description: Column A 1. Oats rich in soluble fiber Bran rich in insoluble fiber Sugar replacer Wheat flour White jasmine rice Satiety Artificial sweeteners Fiber

Answers

Fiber is a vital nutrient for the human body, which helps maintain normal digestion and is also essential for reducing the risk of chronic diseases such as heart disease, stroke, cancer, and diabetes.

Soluble fiber is known to bind with water and slows down digestion, which in turn makes us feel full longer. Insoluble fiber is not easily digestible and helps prevent constipation by adding bulk to the stool. Here is how the terms are matched with their description.1. Oats rich in soluble fiber - Soluble fiber2. Bran rich in insoluble fiber - Insoluble fiber3. Sugar replacer - Artificial sweeteners4. Wheat flour - Fiber5. White jasmine rice - Satiety6. Artificial sweeteners - Sugar replacer7.

Fiber - Wheat flour8. Satiety - White jasmine riceA healthy diet is the key to good health. Whole foods, fruits, vegetables, nuts, and legumes are all good sources of dietary fiber. To increase fiber intake, you should aim to eat at least 25 grams of fiber per day.

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Match the description to the appropriate process. Occurs in cytoplasm outside of mitochondria Creates a majority of ATP
Hydrogen ions flow through ATP synthase proteins within the inner mitochondrial membrane.
Occurs in the matrix of mitochondria. Strips electrons from Acetyl-CoA molecules Produces the 3 carbon molecule pyruvate Utilizes the proton gradient established from the electron transport chain.
1. Glycolysis
2. Citric Acid Cycle
3. Oxidative

Answers

1. Glycolysis occurs in the cytoplasm outside of mitochondria and produces a majority of ATP.

2. Citric Acid Cycle occurs in the matrix of mitochondria and strips electrons from Acetyl-CoA molecules, producing the 3 carbon molecule pyruvate. It utilizes the proton gradient established from the electron transport chain.

Glycolysis is the process that occurs in the cytoplasm outside of mitochondria. It breaks down glucose into two molecules of pyruvate, producing a small amount of ATP and NADH. Although glycolysis is the initial step of cellular respiration, it does not require oxygen and can occur in both aerobic and anaerobic conditions. The net gain of ATP in glycolysis is two molecules.

The Citric Acid Cycle, also known as the Krebs cycle or TCA (Tricarboxylic Acid) cycle, takes place in the matrix of mitochondria. It is the second stage of cellular respiration and completes the breakdown of glucose. The cycle begins with the formation of Acetyl-CoA, which is derived from pyruvate produced during glycolysis. The Citric Acid Cycle oxidizes Acetyl-CoA, generating NADH and FADH2, which carry high-energy electrons to the electron transport chain. Additionally, the cycle produces ATP, CO2, and more electron carriers (NADH and FADH2) that will enter the electron transport chain.

Therefore, the process described as occurring in the cytoplasm outside of mitochondria and producing a majority of ATP is glycolysis (Option 1), while the process occurring in the matrix of mitochondria, stripping electrons from Acetyl-CoA to produce pyruvate, and utilizing the proton gradient from the electron transport chain is the Citric Acid Cycle (Option 2).

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What is the cell concentration here? How many μL of cell suspension do you need to seed 10000 cells per well in a 96-well plate?

Answers

The required cell concentration to seed 10,000 cells per well in a 96-well plate is 104.16 cells/μL. To prepare the required cell suspension, 96.15 μL of cell suspension is needed per well.

The cell concentration can be defined as the number of cells present in a unit volume of the cell suspension. It is usually expressed in cells/μL or cells/mL. The cell concentration can be calculated by dividing the number of cells by the volume of the cell suspension. In this case, the cell concentration required to seed 10,000 cells per well in a 96-well plate can be calculated as follows:10,000 cells ÷ 96 wells = 104.16 cells/wellTo calculate the volume of cell suspension needed to seed 10,000 cells per well, we can use the following formula: Volume of cell suspension = Number of cells ÷ Cell concentration. Therefore, the volume of cell suspension needed to seed 10,000 cells per well in a 96-well plate can be calculated as follows: Volume of cell suspension = 10,000 cells ÷ 104.16 cells/μL = 96.15 μL/ wellThus, 96.15 μL of cell suspension is needed per well to seed 10,000 cells per well in a 96-well plate.

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-Know the three ways that the atmosphere is get cleans?
-What are hydroxyl ions? How are they formed?
• What are the two types of smog and how do they differ?

Answers

The three ways in which the atmosphere is cleansed are the following: i. Through natural occurrences such as the greenhouse effect, precipitation, and the hydroxyl radical.

The three ways in which the atmosphere is cleansed are the following: i. Through natural occurrences such as the greenhouse effect, precipitation, and the hydroxyl radical. ii. Through the man-made process which includes reduction in the emission of pollutants. iii. Through the exchange of air between the ground level and higher altitudes. Hydroxyl ions are the result of the oxidation of dissolved organic matter present in water. The OH radical can be formed through either of the two primary ways: i. through photochemical reaction ii. through catalytic reaction involving molecular hydrogen and ozone. The two types of smog are classical and photochemical smog. The primary differences between the two are their locations and composition. While classical smog is typically formed in areas with low wind speeds and high humidity, photochemical smog is usually formed in regions with lots of sunlight and high temperatures.

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Question 7 0.5 pts The ammonia smell of stale urine results from bacteria metabolizing which of the following urine chemicals? O Urochrome Urea Glucose Sodium

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The correct option for the given question is "Urea." The ammonia smell of stale urine is the result of bacteria metabolizing "urea" in the urine.

Urea is a waste product formed in the liver by the breakdown of proteins and is usually excreted in urine by the kidneys. Urine is composed of around 95% water and 5% waste substances. These waste substances comprise urea, uric acid, creatinine, ammonia, and other chemicals.

Bacteria break down urea in the urine, generating ammonia, which is responsible for the strong, pungent odor of stale urine. The bacteria that cause urine to smell stale, such as Escherichia coli and Proteus mirabilis, can also produce hydrogen sulfide, which adds to the unpleasant odor.

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(a) With the aid of a detailed labelled diagram, give an account of the structure of the cell surface membrane, explaining the function of the various components. (b) Explain the role of the major organelles found in an animal cell and explain the importance of their membranes.

Answers

(a) The cell surface membrane, also known as the plasma membrane, is a vital component of the cell that separates the intracellular environment from the extracellular space. It is composed of a phospholipid bilayer embedded with various proteins and other components. The phospholipid bilayer consists of two layers of phospholipids, with their hydrophilic heads facing outward and hydrophobic tails facing inward, creating a selective barrier.

The various components of the cell surface membrane include integral proteins, peripheral proteins, cholesterol, and glycoproteins. Integral proteins span the entire phospholipid bilayer, while peripheral proteins are found on the inner or outer surface. These proteins play key roles in transport of molecules, cell signaling, and maintaining the structural integrity of the membrane. Cholesterol molecules are interspersed within the phospholipid bilayer, contributing to membrane fluidity and stability. Glycoproteins, which have carbohydrate chains attached, participate in cell recognition and immune response.

The cell surface membrane functions as a selective barrier, controlling the movement of substances into and out of the cell. It regulates the exchange of ions, nutrients, and waste products, maintaining homeostasis. The proteins embedded in the membrane facilitate cell signaling and communication with the external environment. Additionally, the membrane provides mechanical support, allowing the cell to maintain its shape.

(b) Animal cells contain several major organelles, each with its own specific functions. These organelles are enclosed by membranes that play crucial roles in compartmentalization and maintaining specialized conditions within the organelles.

The nucleus is the most prominent organelle and is surrounded by the nuclear membrane or envelope. It houses the genetic material and controls the cell's activities by regulating gene expression.

Mitochondria are responsible for generating energy in the form of adenosine triphosphate (ATP) through cellular respiration. Their double membrane structure allows for efficient ATP production.

Endoplasmic reticulum (ER) is a network of membranes involved in protein synthesis and lipid metabolism. The rough ER is studded with ribosomes and participates in protein synthesis, while the smooth ER is involved in lipid synthesis and detoxification.

Golgi apparatus consists of a series of flattened membranous sacs. It modifies, sorts, and packages proteins and lipids for transport to specific destinations inside or outside the cell.

Lysosomes contain digestive enzymes that break down cellular waste and foreign substances. Their membrane prevents the enzymes from damaging other cellular components.

The plasma membrane, as mentioned earlier, is also a vital organelle that regulates the exchange of materials between the cell and its environment.

The membranes surrounding these organelles compartmentalize cellular processes, allowing for efficient and specialized functions. They regulate the movement of molecules, facilitate selective transport, and maintain distinct chemical environments necessary for specific cellular processes. Membrane-bound organelles ensure that various metabolic reactions occur in separate compartments, enhancing cellular efficiency and organization.

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1. Describe a method of clustering gene expression data obtained from microarray experiments.
2. Describe the bioinformatics methods you would use to infer the evolutionary history of genomes in an infectious disease outbreak.

Answers

1. Clustering gene expression data obtained from microarray experiments Clustering is an essential process in the analysis of gene expression data obtained from microarray experiments.

It aims to group genes that have similar expression patterns across samples and identify significant genes that may be associated with particular biological processes or diseases. In general, clustering methods can be divided into two types, namely hierarchical clustering and partition clustering. Hierarchical clustering is a top-down approach that builds a tree-like structure to represent the relationships among genes. Partition clustering, on the other hand, is a bottom-up approach that assigns genes to a fixed number of clusters.In both types of clustering methods, the choice of distance measure and linkage method can affect the clustering results significantly. Commonly used distance measures include Euclidean distance, Pearson correlation coefficient, and Spearman correlation coefficient. Linkage methods can be single linkage, complete linkage, average linkage, or Ward's method, each of which has its own advantages and disadvantages.

2. Bioinformatics methods to infer the evolutionary history of genomes in an infectious disease outbreakBioinformatics methods can be used to analyze the genomic data of infectious disease outbreaks and infer the evolutionary history of the pathogen. One popular method is the maximum likelihood phylogenetic analysis, which uses a mathematical model to estimate the most likely evolutionary tree that explains the observed genomic variation. Another method is the Bayesian phylogenetic analysis, which uses a Bayesian approach to estimate the posterior probabilities of different evolutionary trees and can incorporate prior knowledge into the analysis.Both methods require a high-quality alignment of the genomic sequences and a suitable model of sequence evolution. Other bioinformatics methods such as network analysis, comparative genomics, and molecular epidemiology can also be used to complement the phylogenetic analysis and provide additional insights into the origin, transmission, and evolution of the pathogen. However, it is important to note that the interpretation of the genomic data in the context of the epidemiological data is critical for a comprehensive understanding of the infectious disease outbreak.

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1. A mutation in the I gene of the lac operon changes the structure of the allolactose binding site such that allolactose cannot bind. No other properties of the protein are changed. Which of the following describes the expression of the structural genes of the lac operon?
They will show constitutive expression
They will show normal expression
They will never be expressed
They will only be expressed in the absence of lactose
They will only be expressed in the absence of glucose
2. In humans, a protein encoded by gene A on chromosome 13 binds to a region upstream from gene B on chromosome 17 and causes the transcription of gene B. Which of the following describes how gene A acts on gene B?
cis
trans
positive control
both a and c
both b and c

Answers

Gene A acts on Gene B through cis-trans positive control. Cis-trans positive control, also known as cis-acting regulatory elements, involves regulation that occurs within the same chromosome.

Specifically, gene A encodes a protein that binds to a region upstream from gene B on chromosome 17 and causes the activation of gene B’s transcription. This type of regulation is important in maintaining gene expression, as it allows the regulation of gene expression based on the interactions of regulatory molecules.

Cis-trans positive control is essential in systems where multiple genes are regulated by the same transcription factor. In the case of humans, gene A binding to upstream gene B on chromosome 17 results in gene B transcription. In this way, gene A acts on gene B through cistranspositive control.

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The heat associated with inflammation is due to the water in the plasma. True False

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The heat associated with inflammation is due to the water in the plasma is a statement which is false.

Inflammation is a process by which the body's white blood cells and substances they generate defend us from infection with foreign organisms, such as bacteria and viruses. It is a natural response that occurs when tissues are harmed. Without inflammation, infections and wounds would never heal since it is the first step in the healing process.The primary response of inflammation includes heat, pain, redness, and swelling.

The increase in blood flow to the region is due to the relaxation of blood vessels, which causes heat and redness. Due to the immune system releasing chemicals that trigger pain receptors, the area becomes painful. Lastly, the increased flow of fluid and white blood cells causes swelling in the region.The heat associated with inflammation is caused by vasodilation of blood vessels, which increases blood flow to the region, and the subsequent increase in metabolic rate and heat production.

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