Answer:
the second bird below the first one
Explanation:
birds need a big beak to crack shells while some need small ones to eat small seeds.
An enzyme catalyzes a chemical reaction, where A and B are joined to yield C.
What statement is correct about this reaction?
- A and B are products.
- B and C are substrates.
- A and C are products.
- A and B are reactants.
The answer is B and C are substrates
what is the correct equation for cellular respiration showing the reactants on the left of the equal sign and products on the right of the equal sign?
The correct equation for cellular respiration showing the reactants on the left of the equal sign and products on the right of the equal sign is: C6H12O6 + 6O2 → 6CO2 + 6H2O + ATP.
Cellular respiration is a process that occurs in the cells of living organisms in order to release energy from food molecules (such as glucose). There are three main stages of cellular respiration: glycolysis, the Krebs cycle, and oxidative phosphorylation.
During these stages, glucose is broken down into carbon dioxide and water, and ATP (adenosine triphosphate) is produced as an energy source for the cell. The balanced equation for cellular respiration shows that glucose and oxygen react to produce carbon dioxide, water, and energy (in the form of ATP).
Learn more about Cellular respiration at https://brainly.com/question/14158795
#SPJ11
which is a true statement about polygenes? polygenes are located on the same chromosome. polygenes are used to predict the genotype of progeny. polygenes interact and allow for continuous variation. polygenes allow geneticists to maintain any genotype.
Polygenes are a group of genes that are involved in the expression of a single trait and are located at different positions on different chromosomes. The first statement, which claims that polygenes are located on the same chromosome, is false.
Polygenes cannot be used to predict the genotype of progeny. Instead, they contribute to the phenotype of the individual. The second statement is false.The third statement is true. Polygenes are responsible for a range of continuous variation in quantitative traits such as height, weight, and skin color, among others. The variation in these traits is caused by the interaction of several genes at different locations, with each gene contributing a small effect.Polygenes are not capable of maintaining any genotype. While they play an important role in the expression of traits, they do not determine the genotype of an individual. Therefore, the fourth statement is false.To sum up, polygenes are a group of genes located at different positions on different chromosomes that interact to produce continuous variation in quantitative traits. However, they do not predict the genotype of progeny or maintain any genotype.
To learn more about Polygenes :
https://brainly.com/question/521134
#SPJ11
10. Without spliceosomes, _______. a) exons would be missing in the mature mRNA b) introns would remain in the mature mRNA c) RNA processing would remain intact d) transcription would cease
Without spliceosomes, introns would remain in the mature mRNA. This is because spliceosomes are responsible for removing introns from the pre-mRNA during the process of RNA splicing to produce the mature mRNA.
The correct option is b.
In order to provide a long answer, let us go over some more information regarding RNA splicing and the role of spliceosomes in it. RNA splicing is a post-transcriptional process that involves the removal of introns from the pre-mRNA molecule and the ligation of exons to produce the mature mRNA molecule that can be translated into a protein. The process of splicing occurs in the nucleus of eukaryotic cells and involves the interaction of various RNA molecules and protein factors.The major RNA molecules involved in splicing are the pre-mRNA, small nuclear RNA (snRNA), and small nucleolar RNA (snoRNA). The pre-mRNA molecule contains both exons and introns that are initially transcribed from the DNA template by RNA polymerase II. The snRNA molecules combine with protein factors to form small nuclear ribonucleoprotein particles (snRNPs), which recognize specific sequences at the boundaries of the introns and exons in the pre-mRNA molecule.
The snRNPs assemble at the splice sites to form the spliceosome complex that carries out the splicing reaction.The spliceosome complex undergoes a series of steps to excise the intron and ligate the exons together. The intron is cleaved at the 5' end and the cleaved end is attached to the branch site of the intron through a unique 2'-5' phosphodiester bond. The 3' end of the intron is then cleaved, and the resulting free end of the exon is ligated to the 5' end of the downstream exon to form the mature mRNA molecule.Spliceosomes are essential for RNA splicing to occur, and without them, the introns would remain in the mature mRNA molecule, leading to an incorrect protein sequence. Therefore, option b is correct.
To know more about spliceosomes visit:-
https://brainly.com/question/31864341
#SPJ11
i need help please...........
Answer:
Yes
Explanation:
In physics, energy is the quantitative property that must be transferred to an object in order to perform work on, or to heat, the object. Energy is a conserved quantity; the law of conservation of energy states that energy can be converted in form, but not created or destroyed. Wikipedia
1. Using the line of nucleic bases provided complete the complimentary DNA base pair strand?
TATCGAGCCGTATGACGATGAACGAATTCCTAA
2. How many base pairings did you make?
3. Using the line of DNA nucleic bases provided complete the copy as messenger RNA (mRNA) to leave the nucleus and go to a ___________ site for the ordering of specific amino acids and production of _______________.
To complete the complementary DNA base pair strand, we need to match each nucleic base with its complementary base. The complementary bases are:
A -> T
T -> A
C -> G
G -> C
Using this information, we can complete the complementary DNA base pair strand:
ATAGCTCGGCATACTGCTACTTGCTTAAGGATT
We made a total of 34 base pairings.
To convert the DNA sequence into mRNA, we need to replace each DNA base with its corresponding mRNA base. The conversion rules are as follows:
A -> U
T -> A
C -> G
G -> C
Using these rules, the mRNA sequence would be:
UAUCGAGCCGUAUGACGAUGAACGAAUUCUAA
The mRNA leaves the nucleus and goes to a ribosome site for the ordering of specific amino acids and the production of proteins.
3. A few years ago the population of male blue moon butterflies on the island of
Samoa declined. One hypothesis for the decline of the male butterflies is that a
parasite infected the cells of female butterflies. The parasite was passed to
offspring through the females' eggs and killed the male butterfly embryos. At
one point during the decline, nearly all the butterflies in the population were
females, but after five years the number of males in the population increased
significantly.
Blue Moon Butterfly.
Which explantion most likely accounts for the increase in the number of male butterflies in the five years after the initial parasite problem. Please anwser this
Answer:
It wont let me magnify the image srry.
Explanation:
What percentage of your body should be water?
Approx. 60% of the body should be water.
Water is essential for the proper functioning of the human body as it helps regulate body temperature, transports nutrients, removes waste, and acts as a lubricant for joints. The recommended daily intake of water varies but, on average, 60% of the body should consist of water. This percentage may vary based on age, sex, body weight, and physical activity levels. It's important to stay hydrated by drinking enough water and consuming water-rich foods to maintain optimal health.
Learn more about Water here:
https://brainly.com/question/28465561
#SPJ4
Considered the "Command Center for the Endocrine System", the ______________ is a major link between the nervous and endocrine system as it is a major regulatory center in the nervous system, as well as a crucial endocrine gland that can synthesize at least nine different hormones.
Answer:
"Command Center for the Endocrine System", the hypothalamus is a major link between the nervous and endocrine system as it is a major regulatory center in the nervous system, as well as a crucial endocrine gland that can synthesize at least nine different hormones.
True or False: DNA polymerase can only work to elongate DNA in the 5` --- 3` direction?
True. DNA can only be extended by DNA polymerase in the 5' to 3' direction. This is so that the 5' phosphate group and the phosphodiester bond can be formed, which is catalysed by DNA polymerase.
Why does DNA grow 5 to 3 times longer?Using a deoxyribonucleotide, DNA polymerase separates the two terminal phosphates from the nucleotide's 5' end and then uses the free energy to create a phosphodiester bond.
Why only one way of DNA polymerase action?DNA polymerase can only synthesise in one direction by extending the 3' end of the previous nucleotide chain because it needs a free 3' OH group to begin synthesis. As a result, DNA polymerase travels in a 3'–5' direction along the template strand.
To know more about polymerase visit:-
https://brainly.com/question/29377728
#SPJ1
Mutation may occur in gametes or in body cells. In which cell type is a mutation likely to be source of genetic variation for ?
Answer:
Una mutación es el cambio al azar en la secuencia de nucleótidos o en la organización del ADN (genotipo) de un ser vivo,1 que produce una variación en las características de este y que no necesariamente se transmite a la descendencia. Se presenta de manera espontánea y súbita o por la acción de mutágenos. Este cambio estará presente en una pequeña proporción de la población (variante) o del organismo (mutación). La unidad genética capaz de mutar es el gen, la unidad de información hereditaria que forma parte del ADN.2
En los seres pluricelulares, las mutaciones solo pueden ser heredadas cuando afectan a las células reproductivas.3 Una consecuencia de las mutaciones puede ser, por ejemplo, una enfermedad genética. Sin embargo, aunque a corto plazo pueden parecer perjudiciales, las mutaciones son esenciales para nuestra existencia a largo plazo. Sin mutación no habría cambio, y sin cambio la vida no podría evolucionar.
Explanation:
HELP ASAP
Which of the following choices represents the approximate percentage of geologic time that humans have existed on Earth since its origin?
less than 1%
1.8%
11.8%
more than 25%
Answer:
less than 1%
Explanation:
The approximate percentage of the geologic time that humans have existed on the Earth since its origin is less than 1%.
The earth is about 4.6 billion years and much of its history has been without the present of human activities.
Hominis were the first human to appear on the surface of the earth. This was in the Miocene epoch which was about 6 million years ago. Compared to the age of the earth, this time lapse is very small and not up to 1%. Life first appeared on earth about 3.5billion years. Since then evolution has taken its due course to give what we have today.when hydrogen peroxide is mixed with catalase, water and oxygen gas are produced. In this reaction, hydrogen peroxide is the
A. Substrate
B. Enzyme
C. Product
D. Inhibitior
Answer:
enzyme I'm pretty sure Goodluck
what are some sources of nitrogen
The main source of nitrogen include: atmospheric precipitation, geological sources, agricultural land, livestock and poultry operations and urban waste. Agricultural emissions show a strong increase due to the application of fertilizer to agricultural soils, grazing of animals and spreading of animal manure.
Step 1: drag the lac promoter to the stretch of dna. do not drag the lacz gene to the dna. now drawwing the lacz gene to the dna. inject some lactose. specifically,what is lactose being converted into?
This leads to the production of beta-galactosidase, which can then break down lactose into glucose and galactose.
What is DNA?
DNA (Deoxyribonucleic Acid) is a complex molecule that carries genetic information in all living organisms. It is made up of nucleotides, which consist of a sugar molecule (deoxyribose), a phosphate group, and a nitrogenous base. The order of these bases determines the genetic code, or the instructions for the development, function, and reproduction of all living things.
Lactose is being converted into glucose and galactose by the enzyme beta-galactosidase, which is encoded by the lacZ gene that is downstream of the lac promoter in the lac operon. When lactose is present, it binds to the repressor protein that usually binds to the operator region of the lac operon, preventing the repressor from binding to the operator and allowing RNA polymerase to transcribe the lacZ gene and other genes in the operon.
Learn more about DNA from given link
https://brainly.com/question/2131506
#SPJ1
can someone help pls
Answeram está en ingles
Explanation:
Why is it necessary to separate oxgynated blood and deoxgynated blood in living organisums?
Answer:
For efficient transportation of blood.
Explanation:
*Platelets (also called thrombocytes)-
Answer:
yes
Explanation:
To determine a genetic profile of an individual, his/her hair ,blood,saliva or semen/ vaginal secretion can be analyzed and one would obtain exactly the same result regardless of which sample was tested
To determine a genetic profile of an individual, his/her hair ,blood, saliva or semen/ vaginal secretion can be analyzed and one would obtain exactly the same result regardless of which sample was tested, the genetic profile obtained will be the same as it is derived from an individual's unique DNA sequence.
To determine a genetic profile of an individual, various samples can be analyzed such as hair, blood, saliva, semen, or vaginal secretion. These samples contain DNA, which can be extracted and analyzed to determine an individual's unique genetic profile. It is important to note that regardless of which sample is tested, the genetic profile obtained will be the same as it is derived from an individual's unique DNA sequence. Therefore, whether a blood, saliva, or semen/vaginal secretion sample is analyzed, the resulting genetic profile will be identical.
Learn more about genetic profile at https://brainly.com/question/28342490
#SPJ11
PLEASE IN QUICK!!! Why do patients seem to get sicker when they are using chemotherapy and radiation therapy?
Which two conditions do most seeds need in order to germinate?
A. Adequate sunlight
B. Enriched soil
C. Adequate water
D. Warm temperatures
Answer:
I believe it is a and c because plants need sunlight and water
Explanation:
The correct answer of the question about seed germination is that Adequate water and Enriched Soil are the two most important condition in order to germinate seed.
What do you mean seed germination?The fundamental process by which many plant species develop from a single seed into a plant is known as seed germination. This method has an impact on crop output and quality.The growth of a seedling from an angiosperm or gymnosperm seed is a frequent example of seed germination.Rapid water uptake by the seeds during the early stages of germination causes swelling and optimal temperature induced softening of the seed coat. Imbibition is the name given to this phase. Enzymes are activated to begin the growth process. The seed starts to create proteins, respire, and metabolise the food that has been stored after activating its internal physiology. This is the lag phase of seed germination.The seed coat bursts, allowing the radicle to emerge and develop into a main root. The seed begins to take up water from underground. After the radicle and plumule have emerged, the shoot begins to ascend.The seed cell lengthens, divides, and becomes metabolically active in the last stage of seed germination to produce the seedling.
Thus, we can conclude that after analysing and understanding the above given theory the best two realistic conditions in order to germinate good quality of seeds can be that Soil should be enriched and Adequate water supply should be there.
Learn more about Seed Germination here:
https://brainly.com/question/20413259
#SPJ2
Which one is the prokaryotic? And which one is the eukaryotic?
The cell that has the nucleus is eukaryotic and the cell that doesn't have a nucleus is eukaryotic
hope it helps
\(GraceRosalia\)
Answer: the right one is prokaryotic and the other is eukaryotic
Explanation: i am in this seg
which human activities are responsible for the addition of carbon dioxide ( co2 co 2 ) to the environment? select all that apply. increased use of agricultural fertilizers overfishing marine populations burning fossil fuels clearing land for agriculture
Human activities that contribute to the increase of carbon dioxide (CO2) in the environment include burning of fossil fuels such as oil, coal, and natural gas. Therefore the correct option C.
For energy, clearing of forests and land for agriculture and urban development, and overuse of agricultural fertilizers.
Additionally, the loss of species that aid in absorbing CO2 from the seas due to overfishing of marine populations can raise atmospheric CO2 levels further.
All of these activities have helped to raise the amount of CO2 in the atmosphere, which has caused climate change and the resulting effects on ecosystems and human societies. Therefore the correct option C.
For such more question on fossil fuels:
https://brainly.com/question/15603154
#SPJ11
The per capita ecological footprint is the total ecological footprint for a given country or area
O True
O False
The per capita ecological footprint is the total ecological footprint for a given country or area is false and is therefore denoted as option B.
What is Ecological footprint?This is referred to as the amount of land which is required to ensure that there is adequate use and sustainability of the resources which are present in area at a given period of time.
The per capita ecological footprint is the average ecological footprint for a given country or area and not the total ecological footprint which is therefore the reason why false was chosen as the most appropriate choice.
Read more about Ecological footprint here https://brainly.com/question/14441911
#SPJ1
Some viruses are associated with cancer. There are a variety of ways in which viruses may affect a cell in a way that may lead to cancer. Based on your knowledge of the life cycles of viruses and of molecular genetics, what is one way that this might happen
One way that viruses might lead to cancer is by integrating their genetic material into the host cell's DNA. Viruses are small infectious agents that replicate inside the living cells of other organisms.
They have two life cycles: the lytic cycle and the lysogenic cycle.The lytic cycle occurs when the virus infects a host cell, produces copies of itself, and then bursts out of the cell, killing the host cell in the process. In the lysogenic cycle, the virus integrates its DNA into the host cell's DNA, allowing the virus to be replicated each time the cell divides.This may cause problems if the viral DNA gets integrated into a gene that controls cell division or cell growth. If the virus disrupts the normal regulation of cell division, it may lead to the uncontrolled cell growth that is characteristic of cancer.In some cases, the virus may also produce proteins that interfere with the normal function of tumor suppressor genes or oncogenes, which can also lead to cancer.
Viruses are one of many factors that can contribute to the development of cancer, but they are a particularly interesting one because they are infectious agents that can be transmitted from person to person.
To know more about DNA visit-
https://brainly.com/question/30993611
#SPJ11
If mendel had crossed a true breeding dominant plant with a true breeding recessive plant, in which of the three generations is the recessive trait visible? f1 generation only p generation only f1 generation and f2 generation p generation and f2 generation
After the crossing, the recessive trait is visible in the p generation and f2 generation.
What is genetics?The term genetics has to do with the science of inheritance. It is the study of patterns of inheritance. True breeding organisms are hom-ozygous.
Hence, when a true breeding dominant plant is crossed with a true breeding recessive plant, the recessive trait is visible in the p generation and f2 generation.
Learn more about genetics: https://brainly.com/question/12985618
Answer:
it’s D
Explanation:
the P generation (parent generation) and the f2 generation are the ones that have it visible, the f1 generation doesn’t
ur welcome:)
Explain why some mutations cause differences in phenotype and others do not?
The ABO blood type in humans is based on a single gene for which three different allelic forms exist. Indicate the genotypes of two parents that are expected to be able to produce offspring with blood types A, B and O but not offspring with blood type AB.
The ABO blood type system in humans is controlled by a single gene with three different alleles: A, B, and O. Individuals with blood type A have two A alleles, those with type B have two B alleles, while those with type O have two O alleles.
To produce offspring with blood types A, B, and O, but not AB, both parents must have at least one A and one B allele each, with both parents having an O allele. Therefore, the genotypes of these parents can be AOBO and ABOO. When gametes are formed, each parent can pass on either an A or a B allele, resulting in a child with blood type A or B, while both parents can pass on an O allele, resulting in a child with blood type O. However, since both parents lack the AB allele, they cannot produce a child with blood type AB.
The ABO blood type in humans is determined by a single gene with three allelic forms: IA, IB, and i. These alleles result in four blood types: A, B, AB, and O. To produce offspring with blood types A, B, and O, but not AB, the genotypes of the parents should be IAi and IBi.
Parent 1 with genotype IAi can produce gametes with IA or i alleles, and Parent 2 with genotype IBi can produce gametes with IB or i alleles. Their offspring can inherit the following combinations: IAIB (blood type AB), IAi (blood type A), IBi (blood type B), and ii (blood type O). However, since we want to avoid blood type AB, we consider only IAi x IBi crosses, resulting in blood types A, B, and O among the offspring.
Learn more about Blood visit:
https://brainly.com/question/17052766
#SPJ11
what is the basis for the difference in how the leading and lagging strands of dna molecules are synthesized? group of answer choices
Because only the 3' end of the template strand receives additional nucleotides from DNA polymerase.
The DNA molecule has two strands. Leading is the name given to one of the strands, which is continually reproduced in the direction of the fork (3'–5'). The other strand is known as the lagging strand and it replicates in a discontinuous manner (5'-3' direction toward the fork). These two strands are free when DNA helicase opens the replication fork, waiting for complementary nucleotides. However, only the 3' end of the template strand receives additional nucleotides from DNA polymerase. DNA polymerase may easily add nucleotides at the 3' end toward the 5' end (direction 3' to 5') because the leading strand's free end is at the 3' end.
DNA polymerase cannot begin from the lagging strand's 5' free end because it is not free. As a result, replication begins in various locations along the lagging strand so that DNA polymerase can add nucleotides from the 3' end to the 5' end.
To know more about DNA, visit:
https://brainly.com/question/264225
#SPJ4
Which of the following best describes the producers in a terrestrial food web?
A) They are at the top of the energy pyramid.
B) They obtain their energy from consumers.
C) They are unaffected by decomposers.
D) They convert energy from the sun to chemical energy.
Answer:
The correct answer is - D. They convert energy from the sun to chemical energy.
Explanation:
In any food web, producers are the organism that can make their own food and energy by converting light energy coming from the sun into chemical energy, this process called photosynthesis.
Normally producers are green plants. These are present at the bottom of the energy pyramid as these are the highest in the number. Consumers et energy from producers by feed on them.