To determine how old Neandertal fossils are, researchers must use radiometric dating. They use an isotope with a half-life of 12,000 years, and find that fossils from one Neandertal have 1/256th (=1/28) of the isotope found in currently living organisms. How old would you predict these Neandertal fossils to be?

Answers

Answer 1

Final answer:

Using an isotope with a half-life of 12,000 years and calculating that the fossils have only 1/256th of the original isotopic amount, we can determine that the Neandertal fossils have undergone 8 half-lives, which equates to an age of 96,000 years.

Explanation:

To determine the age of the Neandertal fossils, researchers use radiometric dating techniques involving isotopes with known half-lives. In this case, the researchers are using an isotope with a half-life of 12,000 years. Since the fossils have 1/256th (which is 1/28) of the original isotopic concentration, this indicates that the fossils have undergone 8 half-lives. The age of the fossils can be calculated as follows:

Half-life of the isotope = 12,000 yearsNumber of half-lives (n) = 8Total age = Half-life × Number of half-lives (n)Total age = 12,000 years × 8 = 96,000 years

Therefore, we can predict that these Neandertal fossils are 96,000 years old.


Related Questions

Blood flow
The necessity of the normal pattern of blood flow through the heart is graphically illustrated in a pathology known as Transposition of the Great Vessels (TGV). About 4/10,000 infants are born with the congenital heart defect TGV. In this disorder, the origin of the aorta and the pulmonary trunk are switched, however the destinations of these vessels are normal. You may have to do some online research to find a diagram and a description in order to understand this pathology.
1. Select each answer choice that describes the NORMAL sequence of structures through which blood flows, starting with vena cavae. Note that not all structures are listed and that more than one answer may be correct.

a. Bicuspid → right ventricle → aortic valve → pulmonary circulation
b. Right atrium → semilunar valve right ventricle → AV valve → systemic circulation
c. Left atrium → bicuspid → left ventricle → AV valve → systemic circulation
d. Tricuspid → right ventricle → pulmonary valve → pulmonary circulation

Answers

Answer:

D. Tricuspid → right ventricle → pulmonary valve → pulmonary circulation

Explanation:

The circulatory system is the system of organs and blood vessels which is associated with the circulation of the blood in the body.

The circulatory system is divided into two portions: the systemic circulatory system (body) and the pulmonary circulatory system (lungs).

The vena cava brings the oxygen-poor blood from the body to the right atrium from where the blood is transferred to the same side of the ventricle controlled by the tricuspid valve (atrioventricular valve).

From the right ventricle, the blood is pumped to the pulmonary artery which transports the blood to the lungs where the oxygen will be exchanged.

Thus, Option-D is correct.

Explain why global climate models typically work by treating the planet as a set of connected boxes

Answers

Answer:

Global climate models usually work by managing the planet as a set of connected boxes because this facilitates the management of the calculations applied in a climate system that is dynamic, variable and complex, which is due to the fact that there is not an equal pattern of climate in each area of the planet.

Explanation:

Climate models have been designed to show the dynamics of the planet's climate and what can be expected from the changes that occur in the future.

The scientific basis of a climate model is physical phenomena and chemical reactions to which a series of differential calculations are applied to determine the behaviour of:

Winds.Temperature.Relative humidity.Rainfall.Pressure changes.Heat transfer.Hydrological dynamics.

Global climate models usually divide the planet into sections -such as boxes- making the calculations in each sector, as well as the interaction of each section with the adjacent sections, which greatly facilitates making the differential calculations, showing the climate at a given time and making predictions of future climate behavior.

It is important to mention that a climate model also explains the changes that occur in the climate due to human activity, which is different in each region of the world.

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Third-base wobble allows some tRNAs to recognize more than one mRNA codon. Based on this chapter's discussion of wobble, what is the minimal number of tRNA molecules necessary to recognize the following amino acids?
a. leucine
b. arginine
c. isoleucine
d. lysine

Answers

Answer:

a. leucine

Explanation:

In the case of the amino acid leucine alone, there are six different codons (TTA, TTG, CTT, CTC, CTA, and CTG) that can recognize and translate tRNA. Since there is only one codon to be translated, only one tRNA is required. The anti-codon in the tRNA identifies complementary positions on the codon, and due to the characteristic of the third-base motif, there is no 1: 1 ratio between the number of codons present and the required anti-codon.

For years, biologists called most prokaryotes “bacteria.” Which statement best explains why a biologists now divide prokaryotes into two distinct categories?

Answers

Answer:

Genetically, archaea are in some ways more similar to eukaryotes than to bacteria.

Explanation:

Biologists now classify prokaryotes into two distinct categories because genetically, archaea are more similar to eukaryotes than to bacteria. This classification is due to differences in evolutionary history, genetics, metabolic pathways, and cell wall composition. Hence, the correct answer is option A.

While both archaea and bacteria are prokaryotes and lack a nucleus, they differ significantly in several aspects:

Evolutionary History: Archaea have a distinct evolutionary lineage that makes them more closely related to eukaryotes.Genetics: When comparing genetic material, archaea and eukaryotes share more similarities than archaea and bacteria.Metabolic Pathways: Differences in metabolism and biochemical pathways are observed between these groups.Cell Wall and Membrane Composition: The cell walls and membranes of archaea contain unique lipids and proteins not found in bacteria.

This genetic and functional diversity has led biologists to classify archaea and bacteria into separate domains within the prokaryotic umbrella.

Complete question as follows:

For years, biologists called most prokaryotes “bacteria.” Which statement best explains why a biologists now divide prokaryotes into two distinct categories?

A. Genetically, archaea are in some ways more similar to eukaryotes than to bacteria.

B. Archaea are small, cellular, and lack nuclei.

C. Biologists compared the appearance of archaea and bacteria under the microscope.

D. Archaea can live in high-temperature environments.

1. Pathogens have ________ on their surface that bind to B cells with complementary _______.
2. B cells that bind to the pathogen divide, forming ________ of identical cells with the same antigen______________.
3. Some cells of the clone develop into short-lived ________ that secrete ________ specific for the antigen.
4. Some cells develop into long-lived ________, which produce larger __________ of memory and effector cells upon later exposure to the same antigen.

Answers

Final answer:

Pathogens carry antigens that B cells recognize through their BCRs, leading to the formation of plasma cells that produce antibodies and memory B cells that enhance future immune responses. The activation of B cells is a critical aspect of the immune system's ability to combat pathogens by creating a directed antibody response.

Explanation:

Understanding B Cells and Antibodies

1. Pathogens have antigens on their surface that bind to B cells with complementary antibody receptors (BCRs).

2. B cells that bind to the pathogen divide, forming clones of identical cells with the same antigen specificity.

3. Some cells of the clone develop into short-lived plasma cells that secrete antibodies specific for the antigen.

4. Some cells develop into long-lived memory B cells, which produce larger numbers of memory and effector cells upon later exposure to the same antigen.

Each B-lymphocyte, during its development, becomes genetically programmed to produce an antibody molecule with a unique 3-dimensional shape capable of binding to a specific epitope of an antigen and displays this as a B-cell receptor on its surface. When an antigen is encountered, these receptor-binding episodes can lead to clonal selection and activation of B-cells, followed by differentiation into plasma cells that secrete antibodies and memory B cells that retain the information for more rapid response upon re-exposure to the antigen.

A living thing that eats other living things?

Answers

Would probably be consumer

Answer:

It is a consumer

Explanation:

It cannot make its own food like plants, so it eats, or consumes other animals. Hope this helps.

Fill in the blanks with appropriate option.
The process of Transcription occurs in the ___ and involves the copying of _____. This copied information will then be _____ in the cytoplasm to create a _____, which is composed of smaller building blocks called _____. During translation, individual ____are attached to one another via _____. As the protein strand gets larger and leaves the ribosome, it begins to fold into the first phase of its 3 dimensional structure (secondary structure). _____ give rise to the protein's secondary structure. In the tertiary/quaternary structure of a protein, _____ amino acids are typically found towards the center of the structure, while ____are found towards the outside of the protein, facing the watery environment of the cell.Options:protein, covalent bond, hydrophobic, translated, amino acids, a portion of genome, hydrogen bonds, cytoplasm, the entire genome, transcribed again, hydrophillic, half the genome, mRNA strand, nucleus, replicated, nucleotides

Answers

Answer:

The process of Transcription occurs in the __nucleus_ and involves the copying of ___genome__. This copied information will then be ___translated__ in the cytoplasm to create a _protein____, which is composed of smaller building blocks called __aminoacids___. During translation, individual _amino acids___are attached to one another via __covalent bond___. As the protein strand gets larger and leaves the ribosome, it begins to fold into the first phase of its 3 dimensional structure (secondary structure). __Hydrogen bond___ give rise to the protein's secondary structure. In the tertiary/quaternary structure of a protein, ___hydrophobic__ amino acids are typically found towards the center of the structure, while _hydrophilic___are found towards the outside of the protein, facing the watery environment of the cell.

Explanation:

Final answer:

The process of transcription occurs in the nucleus and involves copying the entire genome. The copied information is transcribed again in the cytoplasm to create an mRNA strand composed of nucleotides. Translation then occurs, where amino acids are attached to one another via covalent bonds and the protein structure begins to fold.

Explanation:

The process of transcription occurs in the nucleus and involves the copying of the entire genome. This copied information will then be transcribed again in the cytoplasm to create a mRNA strand, which is composed of smaller building blocks called nucleotides. During translation, individual amino acids are attached to one another via covalent bonds. As the protein strand gets larger and leaves the ribosome, it begins to fold into the first phase of its 3 dimensional structure (secondary structure). Hydrogen bonds give rise to the protein's secondary structure. In the tertiary/quaternary structure of a protein, hydrophobic amino acids are typically found towards the center of the structure, while hydrophilic amino acids are found towards the outside of the protein, facing the watery environment of the cell.

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n horses, the hair color gene has a dominant allele B (Black) and a recessive allele b (Chestnut). The gait gene has a dominant allele T (Trotter), and a recessive allele t (Pacer). If a Black Trotter is heterozygous for both traits, how many types of allele combinations for these 2 traits can be found in the gametes it produces

Answers

Answer:

The answer is 9.

Explanation:

There are dominant and recessive genes for both the hair color gene and the gait gene in horses, B, b, T and t respectively.

If a black trotter is heterozygous that means it's genotype is going to be Bb and Tt, therefore it will possess both dominant and recessive genes for the two traits.

The allele combinations in the gametes it produces can be BBTT, BBTt, BBtt, BbTT, BbTt, Bbtt, bbTT, bbTt and bbtt .

I hope this answer helps.

Answer:

Four (4). BT, Bt, bT and bt

Explanation:

The hair color has two alleles, dominant B for black and recessive b for chestnut.

The gait also has two alleles, dominant T for trotter and recessive t for pacer.

Heterozygous black trotter will have the genotype BbTt.

Gametes usually have half the amount of allele of the parents

BbTt can have the the following allelic combination in its gamete: BT, Bt, bT and bt.

Hence, there are four (4) possible types of allele combinations for the two traits and they are BT, Bt, bT and bt.

You can see the attached image for the Punnet square analysis of the gametic alleles.

Which animal is a great hunter? Why?

Answers

Answer:

the lion

Explanation:

the lion is a great hunter becuse it likes to hunt more then to kill

Answer:

Orcas.

Explanation:

Orcas are on of the deadliest predators in the world. They have no predators and hunted animals such as seal, dolphin, shark, and many more marine creatures.

Which system is matched with the correct physiological change that occurs in pregnancy?
Hormonal (Endocrine) = breakdown of the corpus luteum
Cardiovascular = Decrease in output
Metabolic = decreased food intake
Integumentary = stretch marks

Answers

Physiological change that occurs in pregnancy is given below.

Explanation:

The enlarging uterus, growing fetus, placenta, amniotic fluid, normal increase in body fat, and increase in water retention all contribute weight gain during pregnancy.As the fetus grows and develops, several anatomical changes must occur to the female body to accommodate the growing fetus, including placental development, weight gain, abdominal extension, breast enlargement, glandular development, and posture changes. ... The abdomen drops and fetal movement can become quite strong.Your uterus begins to support the growth of the placenta and the fetus, your body adds to its blood supply to carry oxygen and nutrients to the developing baby, and your heart rate increases. These changes accompany many early pregnancy symptoms, such as: fatigue. morning sickness.Physiological changes occur with aging in all organ systems. The cardiac output decreases, blood pressure increases and arteriosclerosis develops. The lungs show impaired gas exchange, a decrease in vital capacity and slower expiratory flow rates.

Billy is an 11-year-old boy who was admitted to hospital with dehydration. His parents said that over the last few months, he had seemed tired and lacking in energy, and that despite eating well and drinking large quantities of fluids he had lost about 7 kg (15 lbs) in weight. He also seemed to be going to the toilet frequently, not only during the day but also during the night. On examination, there was evidence of dehydration (sunken eyes, loss of tissue turgor); his pulse rate was 115 BPM, blood pressure was 95/55 mmHg, respiratory rate was 20 breaths per minute, and his breath smelled of acetone.

1. Comment on the history and findings following the physical examination of Billy.

2. Comment on and interpret the test strip results. Are they consistent with your provisional diagnosis based on the history and physical examination findings?

Answers

Answer:

Billy  showed signs of type 1 diabetes.This is because,

1.His dehydration was from polyuria- excessive urination.

2. because of failure of his  pancreas to secrete insulin, for cellular utilization of glucose by beta cells-  he retains glucose in his  blood, and  lost  a lot of  glucose in his urine, thus water follow by osmosis, leading to polyuria causing dehydration.

His urge to replace lost glucose and fluids leads to great thirst polydipsia, another symptoms of type1. However, his  drop  in weight is  because, the solute concentration  of blood glucose is high due to lack  of  insulin.Therefore large amount is lost in the urine, with large volume of fluids leading to drop in  weight, and energy because cells lack glucose for biochemical reaction of energy production.

The dehydration leads to sunken eyes, loss of tissue turgor, and low fluid levels results in drop in blood pressure,-Hyportension.

Due to lack of glucose in the blood gluconeogensis sets in. Fats is converted to glucose by the liver  to supplement the lost glucose. The major by product of this reaction is a ketone-acetone. This explains the reason for the smell of acetone in his  breath.

2, The Test strip indicated large quantity of ketones. above ,3.0mmol/L .This is a confirmation of the Type 1 diabetes mellitus in Billy.As more fats molecules are broken down to glucose.

Explanation:

Final answer:

Billy's history and physical examination findings suggest he may have type 1 diabetes and be in a state of ketoacidosis. The test strip results are consistent with this diagnosis.

Explanation:

The history and physical examination findings of Billy suggest that he may have type 1 diabetes. The symptoms of tiredness, weight loss, increased urination, and dehydration are common signs of diabetes. His elevated pulse rate and blood pressure along with the smell of acetone on his breath indicate that his body may be in a state of ketoacidosis, which can occur in uncontrolled diabetes.

The test strip results are consistent with the diagnosis of diabetes. The presence of glucose in the urine indicates that Billy has high blood sugar levels, which is a characteristic of diabetes. The presence of ketones in the urine confirms that he is indeed experiencing ketoacidosis.

Based on the history, physical examination findings, and test strip results, it is likely that Billy has type 1 diabetes and is currently in a state of ketoacidosis. He should be treated immediately to restore his fluid balance, stabilize his blood sugar levels, and prevent further complications.

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The incidence of Tay Sachs, an autosomal recessive disorder, is approximately 1 in 3,500 in a certain population. Assuming Hardy-Weinberg equilibrium, what is the probability that Sarah, who is phenotypically normal with no family history, and Tom, who despite having an affected sister is phenotypically normal like his parents, will have a child with Tay Sachs

Answers

Answer:

If Tom is either normal in genotype or an heterozygote, and mates with Sarah: with no history, there is zero percent chance of producing a child with Tay Sachs.

Explanation:

The incidence of Tay Sachs, an autosomal recessive disorder. For the trait to  be expressed, two copies has to be inherited from both parent meaning both parents has to be carriers of the trait.

Thus, Tom, who has a sis that is affected can either be a genotypically normal individual or an heterozygote like his parent.

If Tom is either normal in genotype or an heterozygote, and mates with Sarah: with no history, there is zero percent chance of producing a child with Tay Sachs.

Tom        T    T      or        T      t

Sarah

  T        TT   TT               TT    Tt

  T        TT   TT               TT    Tt

Which of the following statements about enzyme function is true? A. Enzyme function is independent of physical and chemical environmental factors such as pH and temperature. B. Enzymes increase the rate of chemical reactions by providing activation energy to the substrate. C. Enzymes increase the rate of chemical reactions by lowering activation energy barriers. D. Enzyme function is generally increased if the three-dimensional structure or conformation of an enzyme is altered.

Answers

Answer:

C. Enzymes increase the rate of chemical reactions by lowering activation energy barriers.

Explanation:

Enzymes are biological catalysts which increases the rate of a chemical reaction. They do so by lowering the activation energy barrier between reactants and products.

Enzyme function are dependent of physical and chemical environmental factors such as pH and temperature. High temperature will denature the enzyme and reduce or stop its activity while pH outside the range of that of the enzyme will slow down its activity.

They don’t provide activation energy to the substrate.

The option that give description of function of enzymes among the given options is Enzymes increase the rate of chemical reactions by lowering activation energy barriers.

An enzyme can be regarded as substance which acts as a catalyst in living organisms, they helps in regulation of  the rate at which chemical reactions proceed and at the end of the reaction, the catalyst themselves remains unaltered.

When Enzymes are introduced to a reaction, then the rate of reaction will increase since the Enzymes will lower the activation energy barriers

Functions of Enzyme are considered dependent on  physical as well as chemical environmental factors.

These factors includes  pH and temperature.

Enzymes does not involve in  provision of activation energy to the substrateAt a  High temperature enzymes can be denatured.

Example is Amylase, this particular enzyme can be found in saliva.

Therefore, enzymes acts as catalyst.

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What description refers to stratus clouds

Answers

The given question is incomplete, the complete question is:

Which description refers to stratus clouds?

are thin and wispy

are round and fluffy

cover all or most of the sky

form at high altitudes

Answer:

The correct answer is that it covers the majority or all the of the sky.

Explanation:

The low layered clouds, which entirely envelopes the sky in the form of a blanket are known as stratus clouds. These clouds are typically grey in appearance. These clouds are known as fog when they are witnessed on the ground or close to the ground. These clouds generally generate a small amount of snow or drizzle.  

The formation of stratus clouds generally takes place above 2000 meters of the surface of the Earth.  

What is the Function of cambium

Answers

Answer:

 the function of the cambium: layer of actively dividing cells between xylem (wood) and phloem (bast) tissues that is responsible for the secondary growth of stems and roots (secondary growth occurs after the first season and results in increase in thickness).

Explanation:

Answer:

Your answer would be "B"

Explanation:

You have a 15kb plasmid. EcoRI cuts the plasmid into 7kb and 8kb pieces, and BamHI cuts the plasmid into 1kb and 14kb pieces. If you do a double digest with both EcoRI and BamHI on your plasmid, which of the following band patterns are possible on your gel?a. Bands at 1kb, 6kb and 8kb.b. Bands at 1kb, 7kb and 8kb.c. Bands at 1kb, 6kb and 14kbd. Bands at 7kb, 8kb and 14kb.

Answers

Answer:

a. Bands at 1kb, 6kb and 8kb

Explanation:

The EcoRI and BamHI are the restriction enzymes which cut the DNA sequence especially a plasmid at specific sites called the restriction sites.

The restriction enzymes produces bands of specific length therefore these restriction enzymes are used to estimate the approximate length of the DNA.

In the given question, the

1. EcoRI- produces two strands of 7 kb and 8 kb

2. BamHI- produces two strands of 1kb and 14kb

This shows that the length of DNA sequence is 15kb

But when the DNA strand are digested with both the enzymes simultaneously then it will produce three bands as:

i) 14 kb can be broken down in 2 bands of 6 kb and 8 kb

ii) 1 kb band is already produced by the Bam HI.

This shows that 1+6+8= 15 kb

Thus, Option-A is correct.

Please help. This is bio question.

Answers

Answer:

D: 1:2:1

Explanation:

The answer is D- 1:2:1

How many cells are produced in Mitosis

Answers

Answer:

Mitosis produces two diploid somatic cells that are genetically identical to each other and the original parent cell.

Explanation:

When a cell divides by way of mitosis, it produces two clones of itself, each with the same number of chromosomes.

Two cells are produced in Mitosis. However, in Meiosis, four cells are produced.

A, B, C and D are genes that are linked on the same chromosome. Given the following recombination frequencies, what is the gene order? A-B 15%, B-C 26%, C-D 30%, A-C 11%, A-D 19%, and B-D 4%. (Hint: what are recombination frequencies equivalent to?)

Answers

Answer and Explanation:

We need to know that 1% of recombination frequency = 1 map unit = 1cm. And that the maximum recombination frequency is always 50%.

The map unit is the distance between the pair of genes for which one of the 100 meiotic products results in a recombinant one.

The recombination frequencies between two genes determine their distance in the chromosome, measured in map units. So, if we know the recombination frequencies, we can calculate distances between the four genes in the problem and we can figure the genes order out. This is:

Recombination frequencies:

1% of recombination frequency = 1 map unit (MU)A-B 15% = 15 MUB-C 26% = 26 MUC-D 30% = 30MUA-C 11% = 11 MUA-D 19% = 19 MUB-D 4% = 4MU

We know that 15 plus 4 equals 19. So we can infer that we have the gen sequence A--B--D, because the distance between A-B= 15, and the distance between B-D=4, and finally the distance between A-D=19.

A----B----D

  15↔4

      19

We also know that 11 + 19 = 30. So we can assume that C is next to A at a distance of 11 MU.

C----A-----B---D

   11   15 ↔ 4

     11 ↔19    

         30                

The gene order is C, A, B, D

Final answer:

The gene order on the chromosome, based on given recombination frequencies, is most likely B, D, A, C. The recombination frequency corresponds to the relative distances between the genes on the chromosome, and is measured in centimorgans (cM).

Explanation:

In order to determine the gene order based on given recombination frequencies, we'll use the principle that the recombination frequency between two genes corresponds to their relative distances on the chromosome. Recombination frequencies are measured in centimorgans (cM), where 1 cM equals a 1% chance of recombination occurring between two genes.

First, sum the given frequencies: A-B (15%) + B-C (26%) + C-D (30%) = 71%. However, B-D is only 4%, implying that B and D are very close. The discrepancy can be explained by double crossovers, which are not counted. Thus, the order is most likely B, D, A, C, based on their respective distances from each other.

Next, to find the distance between genes, subtract the lesser frequency from the greater: B-A (15%) - B-D (4%) = 11 cM, and C-D (30%) - C-A (11%) = 19 cM. We can now confirm that the gene order (from least to greatest) appears to be B, D, A, C.

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Please help me :(((
What type of inheritance is shown by the genes that control sickle cell anemia?

Answers

Answer: The genes have a codominant pattern of inheritance because the heterozygous forms both traits equally.

Explanation:

Final answer:

The genes that control sickle cell anemia are inherited through autosomal recessive inheritance. Those with two mutated genes have sickle cell anemia (HbSS), while carriers (AS) are resistant to malaria.

Explanation:

Inheritance of Sickle Cell Anemia

The type of inheritance exhibited by the genes that control sickle cell anemia is autosomal recessive inheritance. This condition affects the hemoglobin in the blood, leading to red blood cells that take on a crescent or "sickle" shape. Individuals with two copies of the mutated hemoglobin gene (HbS), one inherited from each parent, will develop sickle cell anemia, with a genotype of HbSS. Conversely, an individual without sickle cell alleles has a genotype of HbAA, with two normal adult hemoglobin variants.

Carriers of the disease, known as heterozygotes with genotype AS, do not typically suffer from the full spectrum of symptoms but have increased resistance to malaria, which explains the prevalence of the sickle cell trait in malaria-endemic regions.

distinguish common name and scientific name​

Answers

A scientific name is a taxonomic name of an organism that consists of the genus and species. Scientific names usually come from Latin or Greek. A common name is a name by which a species is known to the general public, rather than its taxonomic or scientific name. For example “Tyto alba”, is the scientific name. While “Barn Owl” is the common name.
Final answer:

Common names are everyday names used to refer to organisms, whereas scientific names use the binomial naming system and consist of the genus and species name to provide a standardized identification system for organisms.

Explanation:

In biology, a common name refers to the name by which an organism is commonly known in everyday language, while the scientific name, also known as the binomial name, is a two-part name consisting of the genus and species name, used to uniquely identify a species. Common names are often based on physical characteristics or cultural associations and can vary across regions, whereas scientific names provide a standardized and universal identification system for organisms. For example, the North American blue jay has the scientific name Cyanocitta cristata.

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Which of the following statements is not true regarding mutations? A. Mutations are always harmful B. Mutations may be helpful C. Mutations generate the raw material for natural selection D. Mutations create variety in the gene pool

Answers

Final answer:

Mutations are changes to an organism's DNA and can be harmful, advantageous, or neutral. They are not always harmful.

Explanation:

Mutations are changes to an organism's DNA and are an important driver of diversity in populations. Some mutations are harmful, some are advantageous, and some are neutral. Advantageous mutations lead to changes that improve an individual's survival and/or chances of reproduction. For example, the mutation for resistance to insecticide in mosquitos improved their survival. Neutral mutations have no effect on survival or reproduction. The statement that mutations are always harmful (A) is not true, as mutations can be beneficial or neutral as well.

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Final answer:

The statement that mutations are always harmful is not true. Mutations can be beneficial, neutral, or harmful and are essential for evolution as they create genetic diversity upon which natural selection can act.

Explanation:

The statement that is not true regarding mutations is: Mutations are always harmful. This is incorrect because mutations can have various impacts, including beneficial, neutral, or harmful effects on the organism. Mutations are the primary source of genetic variation, which is essential for evolution. They provide the raw material upon which natural selection acts. Most mutations are indeed neutral, having no significant effect on an organism's fitness. However, some mutations may confer an advantage in certain environments and will be selected for, thereby becoming more common in the population. Conversely, harmful mutations that negatively impact survival or reproduction are typically eliminated from the population by natural selection. In this way, mutations contribute to the diversity in a population's gene pool and play a critical role in the process of evolution.

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In guinea pigs, black fur is dominant and white fur is recessive. A homozygous dominant black guinea pig is bred with a homozygous recessive white guinea pig. The dominant allele is represented by F, and the recessive allele is represented by f. Create a Punnett Square and answer the following question: What is the probability of having white fur guinea pigs with this combination

Answers

Answer:

The following cross represents the parent genotype for the offspring whose phenotype is to be determined.

Homozygous dominant black guinea pig FF

                                  X

Homozygous recessive white guinea pig ff

The probability of having white fur guinea pig offspring is zero in the first generation because all of the offspring will be Ff, which is the genotype for black fur.

Punnett Square:

            F             F

f           Ff            Ff

f           Ff            Ff

Hope that answers the question, have a great day!

Identify each statement as TRUE or FALSE. a. Plants are defined as multicellular, eukaryotic, photosynthetic autotrophs. b. Plants are defined by their chloroplasts, which contain chlorophyll a and b. c. Charophytes and land plants share four derived traits that suggest they share a relatively recent common ancestor. d. Charophytes are embryophytes.

Answers

Answer:

A. True

B. True

C. True

D. False

Explanation:

A. Plants in general are multicellular organisms, they are often referred to as eukaryotic autotrophs because they are make their own foods. They carry out photosynthesis, meaning the obtain their energy from sunlight.

B. Plants can be characterized by the presence of chloroplast, an organelle that helps in absorption of sunlight, because of the presence of green pigment called chlorophyll. There two major forms of chlorophyll in plants which are chlorophyll a and b.

C. Charophytes are a type of green algae, but several studies shows they have similar traits to land plants compared to other algae, making them have a common ancestor as plants. Some of the traits similarities to land plants compared to other algae are: they have similar enzymes, they have similar type of cell division, also their sperm is also similar to that of land plants.

D. Charophytes are not embryophytes. Embryophytes are also referred to as land plants, they are multicellular in nature, they include ferns and mosses. Charophytes are a type of green algae similar in traits embryophytes. Although embryophytes are a sister group to charophytes, they are not the same.

Final answer:

The statements identify key characteristics defining plants as multicellular, eukaryotic, photosynthetic autotrophs with chlorophyll in chloroplasts, shared traits between charophytes and land plants, but incorrectly classify charophytes as embryophytes.

Explanation:

Identify each statement as TRUE or FALSE regarding plants:

a. Plants are defined as multicellular, eukaryotic, photosynthetic autotrophs. TRUEb. Plants are defined by their chloroplasts, which contain chlorophyll a and b. TRUEc. Charophytes and land plants share four derived traits that suggest they share a relatively recent common ancestor. TRUEd. Charophytes are embryophytes. FALSE

Plants, being multicellular eukaryotes, have distinctive features including chloroplasts containing chlorophyll for photosynthesis. Though charophytes share common traits with land plants pointing to a shared ancestry, they are not classified as embryophytes, highlighting the distinction and evolutionary pathway between aquatic and terrestrial plants.

Select the true statements about the electron transport chain.

a) In the electron transport chain, a series of reactions moves electrons through carriers.
b) The products of the electron transport chain are H2O and either NAD or FAD.
c) The electron transport chain operates independently of other metabolic processes.
d) Coenzyme A is a component of the electron transport chain.
e) The electron transport chain is a series of oxidation-reduction reactions that occurs in the inner mitochondrial membrane.

Answers

Answer: A. In the electron transport chain, a series of reactions move electrons through carriers.

B. The products of the electron transport chain are H2O and either NAD or FAD.

E. The electron transport chain is a series of oxidation-reduction reactions that occur in the inner mitochondrial membrane.

Explanation:

the best suitable statement is it transfers energy stepwise from one compound to another, The electron transport chain is a series of proteins and organic molecules found in the inner membrane of the mitochondria. Electrons are transferred from one member of the transport chain to another in a series of redox reactions.

Answer:

The correct statements are: a), b) and e)

Explanation:

The high energy electrons are released from NAD and FAD and move along the electron transport chains, these are in the inner membrane of the mitochondria. As the high energy electrons are transported along the chains, part of their energy is captured. This energy is used to pump hydrogen ions (from NAD and FAD) through the inner membrane, out of the matrix into the intermembrane space. The electron transport chain serves the sole purpose of transporting protons from one side of these membranes to the other. The protons, thus, are concentrated on one side of the membrane. ATP synthase acts as a channel protein, helping hydrogen ions cross the membrane. It also acts as an enzyme, forming ATP from ADP and inorganic phosphate. After passing through the electron transport chain, the "spent" electrons combine with oxygen to form water. This is why oxygen is needed; in the absence of oxygen, this process cannot occur.

The very rare Bombay blood phenotype in humans results in blood type O because of the lack of both the A and B antigens in individuals who are of hh genotype. This genotype results in blood type O regardless of the genotype at the unlinked I locus. If a man with the genotype IAIO Hh has a child with a woman with the IAIB hh genotype, what is the probability that their first child will also have type blood B? Show your work for full credit.

Answers

Answer:

50% chances of AB blood group

25% chances of O,A and B is 25%

Explanation:

See attached picture.

Which of the following describes empirical evidence?
A
dogs are good pets

B
dogs can speak English

C
dogs have two eyes and two ears

D
pet dogs should be allowed at school prom

Answers

C because it’s evidence based on means of the senses. So seeing for yourself and seeing the dog has 2 eyes and 2 ears
Final answer:

Empirical evidence is information that is verifiable through observation or experimentation. Out of all the presented options, the fact that 'dogs have two eyes and two ears' qualifies as empirical evidence.

Explanation:

Empirical evidence refers to information that can be verified by observation or experimentation. In the listed options, C 'dogs have two eyes and two ears' best describes empirical evidence. This statement is factual and can be supported through observation and experiment, unlike claims that 'dogs are good pets', which is subjective, or that 'dogs can speak English', which is inaccurate, or that 'pet dogs should be allowed at school prom', which is an opinion.

Learn more about Empirical evidence here:

https://brainly.com/question/24121333

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How does the use of fertilizer affect the nitrogen cycle?

Answers

The nitrogen cycle is a natural process that adds nitrogen to the soil. However, the use of fertilizers has increased the amount of usable nitrogen in the soil. The extra nitrogen seems appealing from the agricultural viewpoint that more nutrients in the soil means higher yield crops...

Answer:

When farmers harvest crops, a lot of the plant material is also removed. Little is left to decay and return nitrogen to the soil. If the soil stays this way, it will start producing fewer crops. Fertilizer contains the nitrogen compounds that are essential for plant growth. It can be used to replace the nitrogen in the soil to ensure the growth of healthy crops.

Explanation:

eukaryotic cells. Classify each statement according to whether it occurs in eukaryotic cells, prokaryotic cells, or both.

Eukaryotic Cell Only Both Prokaryotic Cell Only
1. The start codon is often AUG.

2.There are multiple ribosome binding sites.

3. The ribosome is 70S.

4. The large subunit of the ribosome is 60S.

5. Translation occurs in the cytoplasm.

6. The ribosome initially binds the 5' of mRNA.

Answers

Answer:

Both:

The start codon is often AUG

Eukaryotic cell only:

The larger subunit of the ribosome is 60s.The ribosomes initially binds the 5' end of mRNA.

Prokaryotic cell only:

The ribosome is 70sTranslation occurs in the cytoplasmThere are multiple ribosome binding site

Explanation:

AUG is the common start codon for both eukaryotic as well prokaryotic cells. In eukaryotic cell, it codes for methionine . While in prokaryotic cell, it codes for formyl methionine.In prokaryotic cell, ribosomes are found in cytoplasm, hence the translation occurs in cytoplasm.Eukaryotic ribosome consists of two subunits; 40s and 60s(larger subunit)Prokaryotic ribosomes have 70s ribososme, which consists of 50s and 20s subuints in eukaryotic cell, 40s ribosome initially binds to the cap at the 5' end of mRNA.Bacterial mRNA contain multiple ribosome binding sites.

Like DNA, RNA has
bases.

Answers

RNA also contains four different bases. Three of these are the same as in DNA: adenine, guanine, and cytosine. RNA contains uracil (U) instead of thymine (T).

Final answer:

RNA, like DNA, consists of four nitrogenous bases, where thymine (T) in DNA is replaced by uracil (U) in RNA; adenine (A), cytosine (C), and guanine (G) are found in both.

Explanation:

Like DNA, RNA has nitrogenous bases that are essential for storing and transferring genetic information. DNA contains four bases: adenine (A), thymine (T), cytosine (C), and guanine (G). RNA also consists of four bases, but with a crucial difference: instead of thymine, it has uracil (U). The bases adenine, cytosine, and guanine are common to both DNA and RNA. In the structures of DNA and RNA, adenine pairs with thymine/uracil, and guanine always pairs with cytosine. This base pairing is essential for the replication of DNA and the synthesis of proteins, as RNA uses the information from DNA to assemble amino acids into proteins.

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