The likely evolutionary steps that led to a complex eye like we see in humans likely involved . The earliest form of eye may have been a simple light-sensitive cells in a cup, which allowed organisms to detect changes in light intensity.
Over time, these light-sensitive spots evolved into a cup-like structure, which provided a greater ability to detect the direction of incoming light. This was followed by the development of a pinhole lens, which allowed for more precise detection of light direction. Finally, the evolution of a complex lens, cornea, and retina with photoreceptor cells provided the ability to form an image and process visual information with high resolution.These gradual improvements in eye structure and function likely arose through natural selection, as organisms with better vision had a survival advantage over those with less developed eyes. The evolution of a complex eye like we see in humans likely took millions of years and involved many small changes, each of which provided a small advantage to the organisms that possessed them. This gradual process of improvement likely allowed organisms to better navigate their environments, detect and avoid predators, locate food, and perform other important tasks that required good vision.
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The full question was here:
which of the following best describes the likely evolutionary steps that led to a complex eye like we see in humans?
a flat sheet of light-sensitive cells;
light sensitive cells in a cup;
a pinhole camera without a lens;
a pinhole camera with a lens
some scientists speculate that the ability of modern humans to survive in the tibetan highlands was a result of the interbreeding of homo sapiens and which of the following?
Some scientists speculate that the ability of modern humans to survive in the Tibetan highlands was a result of the interbreeding of homo sapiens and Denisovans.
Researchers have discovered proof that the Denisovans, an extinct type of humans, lived in Tibet's high mountains. Until recently, Homo sapiens had been thought to be the only species capable of surviving in such harsh conditions. A gene that enables current people survive at high altitudes appears to have been passed down from the ancient ancestor.
Before contemporary humans like us spread throughout the globe tens of thousands of years ago, there was a mysterious human species called the Denisovans that lived in Asia. The only fossils discovered up until recently were a few shards of bone and teeth from Denisova Cave, a single location in Siberia. But DNA analysis had revealed that they belonged to a separate branch of the human family.
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true/false. The pedigree below shows the inheritance of fur color in Bruins. Fur color in Bruins is determined by a single autosomal gene with three alleles (blue, gold, and white) that exhibit an unknown hierarchy of dominance. Genetic testing shows that individuals I-1 and III-4 are each homozygous for one allele. Use this information and the pedigree to answer the following questions.
T/F:
II-5 and II-6 are more likely to have a white Bruin than a gold Bruin
It is FALSE that II-5 and II-6 are more likely to have a white Bruin than a gold Bruin.
I-1 has a homozygous genotype. I-1 should have the WW genotype.
Blue and white phenotypes are present in the offspring of I-1 and I-2. This shows that at least one white allele exists in I-2. I-2 has a WG genotype. When compared to the white allele, B is dominant.
Given that it is white, genotype II-4 is WG.III-4 is the homozygous person. Its genotype is GG as a result.
Only the progeny with the golden phenotype and GG genotype have the genotype II-5, which has at least one G allele. II-5 has the BG genotype (See Checker board). Here, B has the dominant position against G.
As a result, II-4 and II-5 have more blue than white. However, it was shown that both white and gold bruin have equal probability.
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The complete question is:
The pedigree(See Pic 1) below shows the inheritance of fur color in Bruins. Fur color in Bruins is determined by a single autosomal gene with three alleles (blue, gold, and white) that exhibit an unknown hierarchy of dominance. Genetic testing shows that individuals I-1 and III-4 are each homozygous for one allele. Use this information and the pedigree to answer the following questions.
T/F:
II-5 and II-6 are more likely to have a white Bruin than a gold Bruin.
some aspect of the environment, biotic or abiotic, selects what traits will pass to the next generation during the process of
Answer: Natural selection i think
Explanation:
Some aspect of the environment, biotic or abiotic, selects what traits will pass to the next generation during the process of natural selection.
Natural selection describes how organisms are more likely to survive and reproduce when they possess characteristics that are best adapted to their environment.
In 1859, Charles Darwin published "On the Origin of Species," a book that detailed the process of natural selection.
An evolutionary mechanism is natural selection. Environment-adapted organisms have a higher chance of surviving and dispersing the genes that contributed to their success.
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Will mark brainly!
Define osmosis and osmotic pressure.
Osmosis a process where solvent molecules move from a less concentrated solution to a more concentrated one by tending to pass across a semipermeable membrane while the osmotic pressure is the least amount of pressure that must be applied to a solution in order to block the passage of the solution's pure solvent through a semipermeable membrane.
History of osmosis studyThe crucial biological process was initially in-depth investigated in 1877 by German plant physiologist Wilhelm Pfeffer. Previous researchers had conducted less precise examinations of leaky membranes (such as animal bladders) and the transport of water and escape chemicals through them in opposite directions. Thomas Graham, a British chemist, coined the term "osmose," which is still used to refer to the process, in 1854.
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problem 10. (10 pts) determine if each of the following sets is a subspace of pn for an appropriate value of n. you should use the subspace test from the lectures to show that a given set is a subspace, or, if it is not a subspace, exhibit one of the axioms of a vector space that fails to be satisfied. (a) w1 is the set of all polynomials of the form p(t)
The set of all polynomials of the form p(t) is a subspace of pn for an appropriate value of n.
To show that a set is a subspace of pn, it must satisfy the three axioms of a vector space: closure under addition, closure under scalar multiplication, and the existence of an additive identity. The set of all polynomials of the form p(t) satisfies all three of these axioms, and therefore it is a subspace of pn for an appropriate value of n. This means that any linear combination of polynomials in this set will also be a polynomial in the same set, and any scalar multiple of a polynomial in the set will also be a polynomial in the same set. Furthermore, there exists a zero polynomial in the set which acts as the additive identity.
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(pls help) Which two statements best describe why chromosomes are important to the function of a cell?
Answer: I believe that ans is options c and d
Explanation:
Chromosomes allow DNA to be accurately copied during these cell divisionChromosomes are also responsible for gene regulation⇒hope this helpsWhich statement regarding Next-Generation Sequencing is not true?
a. DNA fragments are mounted in separate locations on the platform.
b. Flashes of light are emitted whenever a base is added during 454 sequencing.
c. Fluorescent dyes are used in Illumina sequencing.
d. No dideoxynucleotides are used in next-generation sequencing.
e. Replication in vitro is not necessary for next-generation sequencing.
The correct option is E ; Replication in vitro is not necessary for next-generation sequencing.
The fundamental method of next-generation sequencing is fragmenting DNA/RNA into numerous pieces, adding adapters, sequencing the libraries, and reassembling them to generate a genomic sequence. In theory, it is analogous to capillary electrophoresis.
The primary distinction between Sanger sequencing and NGS is the amount of data sequenced. While the Sanger method only sequences a single DNA fragment at a time, NGS is massively parallel and can sequence millions of fragments at the same time per run. This method allows for the simultaneous sequencing of hundreds to thousands of genes.
The requirement for PCR amplification prior to sequencing is the major limitation of all 2G NGS approaches. This is due to PCR bias during library creation (sequence GC-content, fragment length, and false diversity) and analysis (base errors/favoring specific sequences over others).
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the pedigree shows the segregation of an autosomal recessive trait. assuming that the mutant allele is a and the normal allele is a, what is the genotype of ii-4? (assume that all individuals from outside the family are homozygous for the normal allele.)
The genotype of II-4 is aa.
The pedigree shows the segregation of an autosomal recessive trait, meaning that the phenotype of an individual with the mutant allele (a) is only expressed when the individual is homozygous for the allele (aa). If the normal allele is represented by the letter A, then the individual with the genotype AA is homozygous for the normal allele and will not express the mutant phenotype.In the case of individual II-4, their genotype can be determined based on the information available in the pedigree.
If their parents (I-2 and I-3) are both heterozygous for the allele (Aa), then there is a 50% chance that they will pass on either the normal allele A or the mutant allele a to their offspring. If II-4 is showing the mutant phenotype, then they must be homozygous for the mutant allele (aa). Therefore, the genotype of II-4 is aa.
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which of the following taxonomic approaches could be used to most accurately classify e. coli k12 and e. coli o157:h7 as separate strains but the same species?
Polyphasic approach is used to most accurately classify E. coli k12 and E. coli o157:h7 as separate strains but the same species.
The three interconnected domains of categorization, nomenclature, and identification that make up bacterial taxonomy are meant to reflect phylogeny and evolution. A consensus style of taxonomy known as polyphasic taxonomy seeks to make use of all the information at hand in defining consensus groupings that will be important for the judgments made in the end.
The bare minimum requirements for obtaining useful polyphasic data are:
(i) a preliminary screening for groups of related strains;
(ii) determining the phylogenetic placement of these groups;
(iii) measuring the relationships between the groups and their closest neighbors; and
(iv) gathering various descriptive data, focusing primarily on various facets of the cell.
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The complete question is:
which of the following taxonomic approaches could be used to most accurately classify e. coli k12 and e. coli o157:h7 as separate strains but the same species?
1) Psychopathic approach
2) Phylogenetics approach
3) Polyphasic approach
4) Polygenic approach
TRUE/FALSE. enzymes secreted by the trophoblast digesting the surface of the endometrium to facilitate implantation.
True, enzymes secreted by the trophoblast digesting the surface of the endometrium to facilitate implantation.
The outermost layer of cells in a blastocyst is called a trophoblast. Four days following fertilization, trophoblasts are seen in human embryos. The two develop into a sizable portion of the placenta and supply the embryo with nutrition. They develop during the first trimester of pregnancy and are the first cells to separate from the fertilized egg to become extraembryonic structures, which are structures that do not directly contribute to the embryo. The term trophectoderm is used to describe the region of the trophoblast that is continuous with the embryo's ectoderm after gastrulation. Since they are unable to develop into trophoblasts, the cells in the human embryo lose their totipotency after the first differentiation and are no longer totipotent stem cells. At this point, they are pluripotent stem cells.
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DNA is one of the features common to all known forms of life; it is the blueprint that guides the growth, development, behavior, and reproduction of all organisms. Contained within the genetic material are the instructions for regulating and manufacturing the proteins that control cellular function, but, it was not until the twentieth century that scientists began to perform a series of experiments that ultimately determined the genetic material and the basic structure of the molecule. The first two experiments, Griffith's transformation experiments and Hershey-Chase's experiments using radioactive DNA and proteins, supported that DNA, not proteins, was the genetic material. By the 1950s, the competition to describe the genetic materials structure began. DNA was first examined by x-ray diffraction analysis, a technique for determining the three-dimensional atomic structure of a molecule. The early x-ray diffraction results of Rosalind Franklin indicated that DNA was composed of two strands of the polymer wound into a helical structure. The observation that DNA was double-stranded was of crucial significance and provided one of the major clues that led to Watson-Crick's proposed structure of DNA. Only when this model was proposed did DNA's potential for replication and information encoding become apparent.
The discovery that DNA was double-stranded was significant in revealing its potential for replication and information encoding.
The discovery that DNA was composed of two strands was of crucial significance in understanding the structure of the molecule. The double-stranded nature of DNA provided one of the major clues that led to Watson and Crick's proposed structure of DNA, which was based on the idea that the two strands could separate and serve as templates for the synthesis of new complementary strands. This realization of DNA's potential for replication was a key factor in establishing its role as the genetic material. Additionally, the discovery that DNA was double-stranded allowed for the potential encoding of information in the specific sequence of nucleotides along the length of each strand. This information encoding capability is what allows DNA to direct the growth, development, behavior, and reproduction of all organisms.
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The Complete Question is:
What was the significance of the discovery that DNA was composed of two strands in determining its potential for replication and information encoding?
Which of the following hazards is specific only to sub-surface mining?
Responses
poor air quality
dust
equipment malfunction
Poor air quality hazard is specific to sub-surface mining.
What is sub-surface mining?Subsurface mining is the process of taking a metal or fossil fuel out of the ground. The best and most well-known mining technique is this one. In the process of mining for gold, silver, lead, and even jewels, the subsurface mining method is useful. In addition, mining for coal, salt, and oil sands all benefit significantly from it.
What is mining?Mining is the process of removing valuable geological components from the earth and other astronomical objects. Most materials that cannot be produced artificially in a lab or factory or grown via agricultural methods must be obtained through mining.
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please select all of the microbes that require live media for growth. check all that apply viruses - rickettsias. certain forms of bacteria - fungi. viruses - rickettsias.
Viruses require live media for growth.
According to their shapes, viruses may be divided into four categories: filamentous, isometric (or icosahedral), enveloped, and head and tail. For easier cell membrane permeability and subsequent reproduction inside the cell, many viruses adhere to their host cells.
Viruses must be grown within appropriate host cells rather than in conventional microbiological broths or on agar plates.
Viral culture is a laboratory procedure in which samples of a virus are added to several cell lines to examine the virus' capacity to infect them. The culture is successful if the cells exhibit modifications, also referred to as cytopathic effects. However, most viruses are developed in lab animals, embryonated hen eggs, or cultured cells.
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write two things about the motherboard
Motherboard provides a single socket for CPU and also provide ports to attach the drive.
What is the role of mother board?The motherboard is considered as the backbone that attach the computer's components with another at one place and allows them to talk with each other. Without it, no part of the computer, like the CPU, GPU, or hard drive, could interact with each other. Total motherboard functionality is important for a computer to work effectively.
It provides a single socket for CPU, while on the other hand for memory, normally one or more parts are available. Motherboards provide ports to attach the hard drive, and optical drives through ribbon cables. Motherboard carries fans and place designed for power supply.
So we can conclude that a single socket for CPU and ports to attach the drive by the Motherboard.
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Modern humans (Homo sapiens) and archaic humans called Neanderthals (Homo neanderthalensis) shared a common ancestor in Africa but diverged in different geographic areas. When modern humans migrated out of Africa and dispersed around the world starting about 100,000 years ago, they overlapped with Neanderthals in Europe. What evidence would support the idea that the two species are relatively closely related?
1%–4% of modern individuals with European ancestry human have Neanderthal DNA in our genomes.
Around 500,000 years ago, Homo sapiens, modern humans, and Neanderthals, had a common ancestor. Following their separation, humans in Africa and Neanderthals in Europe underwent parallel evolution. Finally reaching Eurasia, humans had intercourse with Neanderthals and exchanged DNA throughout this time. Their split, according to certain genetic calibrations, occurred roughly 650,000 years ago. Scientists are now unsure as to whether Homo heidelbergensis, Homo antecessor, or another species was the last common heritage of Neanderthals and modern humans due to both date problems and fossil anatomy. A broad head, strong supraorbital ridges (brow ridges), and the absence of a prominent chin are characteristics of archaics that set them apart from anatomically modern humans.
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12. The daily condition of the Earth's temperature is:
a) Weather
b) Climate
c) Biotic factors
d) Biome
Answer: weather
Explanation:
Weather refers to day-to-day temperature, precipitation, and other atmospheric conditions, whereas climate is the term for the averaging of atmospheric conditions over longer periods of time.
Albinism, a genetic abnormality which is inherited as a recessive trait, is characterized by a lack of melanin (skin pigment) production. A normal person marries a known carrier for albinism. What is the probability of their having an albino child?
Answer:
It all depends on whether you AND your wife carry an albinism gene. If the two of you do, then each child has a 1 in 4 chance of having albinism. If only one or neither of you is a carrier, then each child has pretty close to a zero chance for albinism. To end up with albinism you need to inherit it from both parents.
Explanation:
which of the following depicts the correct order of levels in biological organization from broadest to most specific? Biosphere- ecosystems- communities - populations - organisms organ and organ system- tissues- cells- organelles- molecule and atoms.
The correct order of levels of biological organization from broadest to most specific is:
Biosphere > Ecosystems > Communities > Populations > Organisms > Organ Systems > Tissues > Cells > Organelles > Molecules and Atoms.
Different levels of biological organization are:
Biosphere: It is the sum total of all living organisms on Earth and the physical environment that supports them, including air, water, and soil.Ecosystems: It is a community of living and non-living things interacting with each other in a specific geographic area.Communities: It is a group of different populations of species that live together in an ecosystem and interact with each other.Populations: It is a group of individuals of the same species that live together in a specific geographic area.Organisms: It is an individual living being.Organ Systems: It is a group of organs that work together to perform a specific function.Tissues: It is a group of similar cells that perform a specific function in an organism.Cells: It is the basic unit of life, and all living things are made up of one or more cells.Organelles: It is a specialized structure within a cell that performs a specific function.Molecules and Atoms: It is the smallest unit of matter that retains the chemical properties of an element.Learn more about Biosphere here:
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explain why methicillin resistant staphlococcus aureus (mrsa) is more prevalent now than it was only 30 years ago. see section 1.7 (page) .
Frequent and inappropriate use of methicillin-type antibiotics has provided selective pressure that has resulted in an increase in the proportion of methicillin-resistant strains of Staphlococcus aureus.
The methicillin-resistant Staphlococcus aureus is an illustration of Darwin's Theory of Evolution. He believed that three principles drive evolution: Variation - the diversity of organisms permits them to adapt better to their surroundings. Heridity is the transmission of traits required for survival to the following generation. Natural Selection - the organism that is most fitted to its surroundings lives and passes on its features;
There are strains of Staphlococcus aureus that are resistant to antibiotics. The frequent use of the medication, and sometimes misuse of it, might select resistant strains. Because these traits are critical to their survival, they are handed down to the following generation.
This is why the rate of methicillin-resistant Staphlococcus aureus has increased along the years.
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Full Question :Explain why methicillin resistant Staphlococcus aureus (MRSA) is more prevalent now than it was only 30 years ago. See Section 1.7 (Page) . Explain why methicillin resistant Staphlococcus aureus (MRSA) is more prevalent now than it was only 30 years ago. See Section 1.7 (Page) . Methicillin resistance causes an infection to spread more rapidly. Antibiotics cause mutations in Staphlococcus aureus that lead to an increase in the number of methicillin-resistant strains. Frequent and inappropriate use of methicillin-type antibiotics has provided selective pressure that has resulted in an increase in the proportion of methicillin-resistant strains of Staphlococcus aureus. Diseases like AIDS have made people more vulnerable to infections from Staphlococcus aureus.
an overheated and sick dog in a hot environment will have an impaired thermoregulatory response when its
An overheated and sick dog in a hot environment will have an impaired thermoregulatory response when its body temperature increases to match the environmental temperature.
The hypothalamus, which controls the autonomic nervous system and maintains the balance of temperature, is also in charge of this function. In order to keep the body's temperature within one or two degrees of 98.6 degrees, it responds to both internal and external stimuli.
It also regulates the release of chemicals and hormones linked to temperature. It aids in maintaining salt concentrations and balancing bodily fluids.
The epidermis, sweat glands, and blood vessels, as well as the vents, condensers, and heat ducts of your body's heating and cooling system, are all involved in the hypothalamus' role in controlling body temperature.
Water from the body is kept in the dermis, the middle layer of skin. Perspiration glands are stimulated by heat, and when they do, they release water and salt from the body to the skin's surface as sweat. Water evaporates after reaching the surface. The cooling effect of the body's water evaporation from the skin helps to maintain a healthy body temperature.
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Please Hurry!!!!I if I cross AaDd x AaDd, what is the probability that I get aadd?
The probability of getting "aadd" if you cross "AaDd" with "AaDd" is low. This is because the chances of getting two dominant alleles (AA) and two recessive alleles (dd) in a single offspring is relatively low.
In a cross between two individuals that are heterozygous for a given trait (Aa), the offspring will have a 50% chance of inheriting each allele (A or a) from each parent. This means that the offspring will have a 25% chance of inheriting the dominant homozygous genotype (AA) and a 25% chance of inheriting the recessive homozygous genotype (dd).
So, the probability of getting "aadd" from a cross between "AaDd" and "AaDd" is (1/4) * (1/4) = 1/16, or approximately 6.25%.
Which of the following diseases can be passed to another person through food, soil, or water?
I. Lyme disease
I. Malaria
III. Cholera
II only
III only
I and II
II and III
Answer: III.Cholera only that one
Explanation:
Foodborne diseases are caused by contamination of food and occur at any stage of the food production, delivery and consumption chain. They can result from several forms of environmental contamination including pollution in water, soil or air, as well as unsafe food storage and processing.
Cholera, among the diseases listed, is the disease that can be passed to another person through food, soil, or water. Lyme disease is transmitted via ticks bites and Malaria through mosquito bites.
Explanation:Of the options given: I. Lyme disease, I. Malaria, and III. Cholera, the disease that can be passed to another person through food, soil, or water is cholera, or option III. Lyme disease is typically transmitted through the bites of infected ticks and Malaria is mainly spread by mosquitoes. However, cholera is a bacterial infection that can spread through contaminated food or water.
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which of the following is not described in the lecture presentation as a definitive characteristics of organisms, separating them from non-living things?
"They have mass and take up room" is not described in the lecture presentation as a definitive characteristics of organisms, separating them from non-living things.
Numerous essential traits or capabilities are shared by all living things:
1) Order: Cells make up organisms, which are highly coordinated, ordered structures. Even very basic, single-celled creatures are astonishingly complicated because within each cell, atoms form molecules, which in turn form cell organelles and other cellular inclusions.
2) Reproduction: DNA replication is the first step in the reproduction of single-celled organisms. Then, as the cell is about to split into two new cells, they equally divide it. Specialized reproductive germline cells that develop into new individuals are frequently produced by multicellular organisms. DNA-containing genes are transferred to the progeny of an organism during reproduction. The presence of these genes guarantees that the progeny will be of the same species and will share traits like size and shape.
3) Expansion and development: Each organism's growth and development are governed by particular instructions encoded in its genes. A species' offspring will develop into adults who share many traits with their parents thanks to the instructions provided by these genes, which control cellular growth and development.
4) Energy conversion: For their metabolic processes, all living things need an energy source. Others use the chemical energy found in the molecules they consume as food. Some species use the chemical energy found in food molecules.
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The complete question is:
Which of the following is NOT described in the lecture presentation as definitive characteristics of organisms, separating them from non-living things?
1) They have mass and take up room.
2) They either partially or fully replicate.
3) They alter both matter and energy.
4) They are built upon one or more cells.
the lentiform nucleus, or lenticular nucleus, comprises the putamen and the globus pallidus within the basal ganglia. with the caudate nucleus, it forms the dorsal striatum. it is a large, lens-shaped mass of gray matter just lateral to the internal capsule. true or false
True. The lentiform nucleus, also known as the lenticular nucleus, is a part of the basal ganglia and is comprised of two structures: the putamen and the globus pallidus
The caudate nucleus is also part of the basal ganglia and, together with the lentiform nucleus, they form the dorsal striatum. The lentiform nucleus is a large, lens-shaped mass of gray matter that is located just lateral to the internal capsule. It plays an important role in motor control and regulation of voluntary movements. It also has a role in processing sensory information, regulating mood, and cognitive function. Dysfunction in the basal ganglia and specifically the lentiform nucleus is implicated in various neurological and psychiatric disorders including Parkinson's disease, Huntington's disease, and schizophrenia.
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In DROSOPHILA MELANOGASTER the genes for normal bristles and normal eye color are known to be about 20 map units apart on the same chromosome. Individuals homozygous dominant for these genes were mated with homozygous recessive individuals. The F1 progeny were then test-crossed. If there were 1,000 offspring from the test cross, how many of the offspring would you predict would show cross-over phenotypes?
The genes for normal bristles and normal eye color in DROSOPHILA MELANOGASTER are located on the same chromosome, roughly 20 map units apart. You predicted that 200 of the offspring would exhibit cross-over traits.
The ratio is 1:2 for a diploid drosophila that possesses XY (1 X to 2 sets of autosomes, since it is diploid). The components that the Drosophila sex chromosome ratio encodes are what improve the production of the sxl protein, which in turn activates the female-specific pathway.
The fruit fly is another name for the drosophila. It serves as a model organism in the fields of developmental biology and genetics. On the X chromosome is the gene responsible for eye color.
= 200 (Since 1000 x 0.20 = 200).
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Correct Question:
In DROSOPHILA MELANOGASTER the genes for normal bristles and normal eye color are known to be about 20 map units apart on the same chromosome. Individuals homozygous dominant for these genes were mated with homozygous recessive individuals. The F1 progeny were then test-crossed. If there were 1,000 offspring from the test cross, how many of the offspring would you predict would show cross-over phenotypes?
which of the following are reasons why eukaryotes have a more complex gene regulation than prokaryotes?
-RNA polymerase must have access to the DNA double helix
-RNA polymerase must be capable of binding the promoter
Option B, RNA polymerase must be capable of binding the promoter Eukaryotic cells are more complex than prokaryotic cells and therefore have a more complex system of gene regulation.
This is because eukaryotic cells contain a nucleus and other cellular compartments, such as the endoplasmic reticulum and Golgi apparatus. RNA polymerase ,These compartments create a more diverse cellular environment that requires a more sophisticated system of gene regulation to coordinate the expression of genes. Eukaryotic cells also have a greater number of regulatory elements, such as enhancers and silencers, that can control gene expression in a tissue-specific manner. All of these factors contribute to the more complex gene regulation seen in eukaryotic cells compared to prokaryotic cells.
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The complete Question is:
What are the reasons why eukaryotes have a more complex gene regulation than prokaryotes?
A) RNA polymerase must have access to the DNA double helix
B) RNA polymerase must be capable of binding the promoter
describe why you think the United States has declined to switch from the imperial system to the metric system. What potential problems does this create in an undeniably global society?
Which two molecules that form during cellular respiration have more energy than the two molecules they were produced from?
A. ATP
B.FAD
C.FADH2
D.ADP
Answer:
During this stage, high-energy electrons are released from NADH and FADH2, and they move along electron-transport chains found in the inner membrane of the mitochondrion. An electron-transport chain is a series of molecules that transfer electrons from molecule to molecule by chemical reactions.
Which of the following statements describes when or how recombinant chromosomes add to genetic variability?
a. they are formed as a result of random fertilization when two sets of chromosomes combine in a zygote
b. they are the result of mutations that change alleles
c. they randomly orient during metaphase II, and the nonequivalent sister chromatids separate in anaphase II
d. genetic material from two parents is combined on the same chromosome
e. both c and d
Recombinant chromosomes add to genetic variability through combination of genetic material from two parents on the same chromosome.
Recombinant chromosomes are chromosomes that contain a mixture of genetic material from two different parent chromosomes. They add to genetic variability because they bring together different combinations of alleles, leading to new and unique genetic traits. Recombinant chromosomes are formed during meiosis, when homologous chromosomes exchange genetic material through a process called crossing over. Recombinant chromosomes can also be formed as a result of random fertilization, when two sets of chromosomes combine in a zygote, but this is not the main process by which they add to genetic variability.
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complete the following statements to demonstrate an understanding of the difference between science and technology.
It is usual to miss the distinctions between science and technology, which are commonly employed interchangeably, due to their similar resemblance.
Science's fundamental goal is to learn about natural events and the factors that contribute to them. As an illustration, why is the sky blue? Why do leaves turn green? How come it rains? What colors are there in the rainbow? How can a plant produce food? I could continue. When this information is used to answer requests or problems that concern people, technology is what emerges. As a result, while technology is all about things like products, methods, and designs, science concentrates on ideas, laws, and principles.
The complete question is:
Complete the following statements to demonstrate an understanding of the difference between science and technology.
We use the term __ to refer to the systematic way in which we go about learning about the world around us.
When this knowledge is applied to the interests of humans, we call it ____.
Examples of ___ include cellular telephones and pharmaceutical drugs, both of which could be created based on (science) and its investigations into observable phenomena.
Answer 1: (science)
Answer 2: (technology).
Answers 3: (technology),
Answers 4: (science)
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