Answer:
The correct answer is - economic, social, environmental, and geopolitical
Explanation:
Natural Resources are the resources that are formed in nature on their own and can be renewable or non-renewable. There are various risks and benefits are associated with the production of all forms of energy other resource extraction.
These costs or risk includes economic, environmental, social, and geopolitical risks. These risks have various factors that decide if these risk or benefit and can be altered by the new technologies using for the extraction and production of various forms of energy.
Joe and Sam were adopted as infants into different families. They have just met and noticed how much they look alike. They are also the same age and suspect that they are twins who were separated at birth. They wish to know the truth, so have their DNA analyzed. Study this DNA fingerprint (RFLP method) and write a short essay that answers the following questions:
a. In the last column of the DNA fingerprint, what does "frequency of occurrence" mean?
b. What is the probability that Joe and Sam are not twins (i.e., that the DNA in the fingerprints could have come from unrelated men)?
Answer:
Explanation:
The missing diagram in the question is attached in the image below.
(A)
From the image below, the frequency of occurrence is shown in the last column.
The frequency of occurrence means the particular band for the entire whole population.
As an example:
1 in 15 frequency of occurrence means; ⇒ One (1) out of every fifteen (15) people has the band.
1 in 450 frequency of occurrence means; ⇒ One (1) out of every 450 people has the band.
(B)
However, Let the probability that Joe and Sam are twins be = A
and the probability that they are not twins be denoted with B;
Then;
P(B) = 1 - P(A)
where;
P(A) = Probability of specific bands appearing on the gel in every one of them
[tex]P(A) =\Big( \dfrac{1}{15}\times \dfrac{1}{15}\Big)\times \Big( \dfrac{1}{450}\times \dfrac{1}{450}\Big)\times \Big( \dfrac{1}{32}\times \dfrac{1}{32}\Big)\times \Big( \dfrac{1}{70}\times \dfrac{1}{70}\Big)[/tex]
[tex]P(A) =\Big( \dfrac{1}{225}\Big)\times \Big( \dfrac{1}{202500}\Big)\times \Big( \dfrac{1}{1024}\Big)\times \Big( \dfrac{1}{4900}\Big)[/tex]
P(A) = 4.37 × 10⁻¹⁵
∴
P(B) = 1 - P(A)
P(B) = 1 - 4.37 × 10⁻¹⁵
P(B) ≅ 1
Using and spectrophotometer, you measure 2 dilutions of NADH, and get absorbance values of 0.4 for sample A, and 0.2 for sample B. You know that the path length is 1 cm, and the extinction coefficient for NADH is 6220 (L Morcm). Using the Lambert-Beer Law equation (below), calculate the concentrations of sample A Select] and Sample B (Select ] A = log10 () = Ecl Where: A- Absorbance C- Concentration (mol 1 - Path length (cm) E = molar decadic extinction coefficient L mol. cm 1o - Intensity of the incident light 1 - Intensity of the transmitted Night
Answer:
The answer is "The concentration sample A= 0.00006[tex]\frac{mol}{L}[/tex] and concentration of sample B is 0.00003[tex]\frac{mol}{L}[/tex]".
Explanation:
Length of path [tex](l)=1 \ cm\\\\[/tex]
Coefficient extinction[tex](\varepsilon )=6220\ \frac{L}{Mol \ cm}\\\\[/tex]
Absorbace of sample [tex](A)=0.4\\\\[/tex]
Absorbace of sample [tex](B)=0.2\\\\[/tex]
For sample A:
[tex]A=\varepsilon cl\\\\0.4=6220 \times c \times 1\\\\c=\frac{0.4}{6220}\\\\[/tex]
[tex]=0.00064\ \frac{mol}{L}[/tex]
For sample B:
[tex]A=\varepsilon cl\\\\0.2=6220 \times c \times 1\\\\c=\frac{0.2}{6220}\\\\[/tex]
[tex]=0.00003\ \frac{mol}{L}[/tex]
7. I'm full of holes flexible and thin. I control what gets out
As well as what Comes in .
Answer:
cell membrane
Explanation:
Answer:
CELL MEMBRANE AND NUCLEAS
Orange tree adaptation
Answer:
Blue tree adaptation...
approximately how far away is the epicenter for an earthquake if the p-waves arrive three minutes 20 seconds before the S Wave
Answer:
Only P-waves were recorded at seismic station C because P-waves travel At different avival times
Explanation:
....
What term is used to describe the number of chromosomes in a gamete, such as
an egg cell or a sperm cell?
Answer:
The biology term, haploid can also refer to the number of chromosomes in egg or sperm cells, which are also called gametes
The term used to describe the number of chromosomes in a gamete would be haploid.
Gametes are usually formed by meiosis and meiosis is referred to as reductional division. When a normal diploid (2n) cell divides by meiosis, the daughter cells would have half the number of chromosomes of the parent cell. In other words, the daughter cells will have n number of chromosomes as opposed to 2n.
Cells with n chromosome numbers are generally referred to as haploid while those with normal 2n chromosome numbers are said to be diploid. Egg and sperm cells are haploid cells.
More on haploid cells can be found here: https://brainly.com/question/15475325
Is this right ????????????????????
I do believe they made a mistake ???
Answer: yes it is correct
Explanation:
Hope this helps you with your science work :)
what is the thing that represents mitosis?
(and it has to be a living thing)
In plant cells, the first part of mitosis is the same as in animal cells. (Interphase, Prophase, Metaphase, Anaphase, Telophase). Then, where an animal cell would go through cytokineses, a plant cell simply creates a new cell plate in the middle, creating two new cells.
plant cells
the interest on Rs 4050 in five years is Rs 2050 what will be interest on Rs 5000 in 8 years at the same rate of interest
Answer:
Explanation:
for first principle = Rs. 4050 Time =5yrs, interest =Rs. 2050 R%= ?
By the formula, R=?\\
[tex]For the first,\\P =RS 4050, I=RS2050, R=?\\\\R= \frac{I*100} {P*T}\\ = \frac{2050*100}{4050*5} \\=\frac{205000}{20250} \\=10%\\Again, for 2nd \\ P= Rs 5000, T= 8yrs, R= 10% Same as First ,I=?\\\\I=\frac{P*T*R}{100} \\=\frac{5000*8*10}{100} \\=RS=4000.[/tex]
Explain why insertions and deletions are called frameshift mutations, usingthe terms reading frame, codons, and amino acids in your answer.
Answer: A reading frame shift mutation involves the insertion or deletion of a certain number of nucleotides that is not divisible by three, because the cell reads a gene in groups of three bases (a codon). This type of mutation can change the reading frame causing a different translation from the original, because it will code for different amino acids.
Explanation:
DNA is the double-stranded molecule composed of nucleotides which are the functional unit of nucleic acids and are composed of a base (which can be Adenine, Thymine, Guanine, Cytosine, and Uracil replacing Thymine in RNA), a phosphate group and a sugar which can be ribose in RNA and deoxyribose in DNA. The reading frame is one of the possible ways in which a sequence of DNA or RNA nucleotides can be divided to form a group of codons that are consecutive and non-overlapping. A codon consists of a set of three nucleotides and each codon codes for an amino acid during translation or protein synthesis. When DNA is transcribed into messenger RNA (mRNA), this mRNA is read on ribosomes during translation and the three bases of each codon will code for an amino acid.
A single-stranded nucleic acid (RNA) molecule has a phosphate end, called the 5' end (read five prime end) and a hydroxyl end, called the 3' end. These ends define the 5'-3' direction. There are three possible reading frames in which a nucleotide sequence can be read in the 5'-3' direction. Each of these reading frames could start at a different nucleotide of the same codon. In a double-stranded nucleic acid (DNA), there are also three additional reading frames corresponding to the complementary strand, but in an antiparallel direction. Since the two strands of a double-stranded nucleic acid are antiparallel, the 5'-3' direction of the second strand corresponds to the 3'-5' direction of the first strand.
Generally, there is at most, a single biologically relevant reading frame for a given section of a nucleic acid, and that reading begins when a start codon indicating the initiation of protein synthesis is found in the messenger RNA. And the process stops when a stop codon is reached.
An insertion is a type of mutation that involves the addition of genetic material. It can be small and involve a single DNA base pair, or large and involve a fragment of a chromosome. A deletion is a type of genetic mutation in which genetic material is lost, from a single DNA nucleotide pair to an entire chromosome fragment. A reading frame shift mutation involves the insertion or deletion of a certain number of nucleotides that is not divisible by three, because the cell reads a gene in groups of three bases, as it was explained before. This type of mutation can change the reading frame causing a different translation from the original.
pls help!! ill give brainlest !!
Answer:
meiosis
Explanation:
meiosis occurs first in the sex gametes while mitosis occurs later in growing cell
BEST ANSWER GETS BRAINLIEST!!!!!!1
A polygraph test is conducted, and the findings indicate that there is an 80 percent chance of deception. What does this mean for the investigation?
The suspect is guilty and should be arrested for the crime.
The suspect is probably just nervous since 80 percent is a pretty high number and usually indicates a false positive.
The suspect might be guilty, but more information is needed from other parts of the investigation.
There has been a mistake in the polygraph test, and the test should be conducted again to get better results.
Answer:
The suspect might be guilty, but more information is needed from other parts of the investigation.
Explanation:
Due process states innocent until proven guilty. Having an 80 percent chance of deception is not solid proof of anything. It does, however, bring more speculation to the table that this person is indeed guilty, but because there is no actual proof, the investigators must find more information on the matter.
g Explain the meaning of ploidy (haploid, diploid, aneuploid etc.) and how it relates to the number of homologues of each chromosome
Answer:
The correct answer is - Ploidy is the number of sets of chromosomes in a biological cell.
Explanation:
Ploidy is the number of sets of the chromosome in a living cell. Ploidy is known for different condition such as haploid, diploid, and aneuploid, and many more depends how many homologues chromosome numbers are present in the cell.
Diploid cells are common in many organisms where one chromosome come from the mother gamete and the other from the father gamete and makes the homologues chromosomes. In diploid homologues, chromosome are 2n where n is the number of homologues of each chromosome.
In haploid there is only one set of each chromosome and mainly takes place by meiosis. In aneuploidy is the condition where the number of homologues chromosomes are not as the normal genome of the organism for example in humans instead of 46 chromosomes there 45 or 47 chromosome found.
Dominant traits are...
A.Traits that everyone wants
B. Traits that are shown over traits
C.Traits that are hidden by other traits
D. Trants that no one wants
Answer:
its b
Explanation:
Answer:
It would be C , for Pluto
Explanation:
Using complete sentences:
Describe the difference(s) between local and global winds.
Explanation:
The term global winds refers to the six major wind belts that encircle the globe.
Local winds, however, are the winds, or breezes, that are stirred up by the temperatures and topographical features of a small region or area. This is especially true of coastal areas.
what is neuroplasticity and why was its discovery significant
Answer:
Explanation:
I can tell you that Neuroplasticity is how easily someone picks up idea's. Generally kids have more Neuroplasticity than adults. However, I don't really know the answer to the second part of the question. Hopefully it's multiple choice :)
"According to the theory of neuroplasticity, thinking, learning, and acting actually change both the brain's functional anatomy from top to bottom, and its physical anatomy. Canadian psychiatrist Norman Doidge has called neuroplasticity one of the most extraordinary discoveries of the twentieth century." -?
"The brain's anatomy ensures that certain areas of the brain have certain functions. ... Part of the body's ability to recover following damage to the brain can be explained by the damaged area of the brain getting better, but most is the result of neuroplasticity – forming new neural connections." -?
Hope this helps!
WILL MARK BRAINLIEST!
--------------------------------------------------
Which best describes salts?
a. organic substances
b. inorganic substances
c. made of carbohydrates
d. made of lipids
(15 pts)
(its really environmental science but thats not a subject on here so sorry ;-;)
Answer:
inorganic substances
Explanation:
There are both organic and inorganic salts. However, salts like table salt (sodium chloride), baking soda (sodium chloride), calcium carbonate, and muriatic acid (industrial-grade hydrochloric acid) are some of the commonly known inorganic compounds. So, to highlight it, table salt or food salt that humans consume are inorganic compounds.
(I really need this to boost my grade)
Label the permeable and impermeable rock layers
Answer: HI your question is incomplete but i will provide a general answer that can help you
answer : Permeable Rock layers allow the flow of fluid like substances through them, While Impermeable rock layers do not allow the flow of fluid like substance through them.
Explanation:
Permeable rocks are rocks containing pores through Fluid like substances can penetrate through in the rocks. examples of Permeable rocks are ; Sandstones and Chalk
While an Impermeable rock is a rock that does not allow the flow of fluid like substance through it due to the absence of pores in its rock layers . examples of such rock are ; Clay and marble
Although some permeable rocks might exhibit low level of permeability as well but generally Rock sample with pores are classified as permeable rock layers.
PLS HELP FAST NO LINKS!
If you live in a region that has hot, dry summers, and cool, wet winters, what climate might you live in?
A. arid
B.temperate
C.tropical
D.Mediterranean
Answer:
Mediterranean climate
Explain why fish would not be able to navigate their surroundings nearly as well if the light-absorbing molecules in their eyes were an order of magnitude larger or smaller than retinal.
Answer:
Fishes use a different vision mechanism than mammals and other land animals. They have rods and cone photoreceptors to see the colorful visions and adjust their focal point by moving the lens closer to or away from their retina.
In the water bodies, a difference in the amount of light moves with the depth because water absorbs the light and this change occurs due to the optical nature of water.
The light bounces once it back in the retina, leads to the gain of the small packets of energy of light a second chance to be trapped by photoreceptors. However, vision remains blurry. The changes and distortion of the light-absorbing molecules present in the eyes of fishes make it tough to perceive a clear vision.
Which type of reproduction provides organisms with the following advantages? Desirable traits can be selectively bred for in a population of organisms. More genetic diversity that might benefit individuals when environment changes.
A. Asexual reproduction
B. Sexual reproduction
Answer:
Sexual Reproduction
Explanation:
Since sexual reproduction automatically causes genetic diversity(crossing over, DNA from both parents, etc.) it produces desirable traits for organisms. Asexual reproduction does not bring in new and desirable traits and is more of a copy of the parent.
Chromosomes consist of ________ and ________.
Answer:
[tex]\huge\boxed{Answer\hookleftarrow}[/tex]
➟ Chromosomes consist of DNA and protein.ʰᵒᵖᵉ ⁱᵗ ʰᵉˡᵖˢ
# ꧁❣ RainbowSalt2²2² ࿐
The theory of endosymbiosis is based on Multiple Choice similarities between chloroplasts and other organelles in animals. evidence from the fossil record. the knowledge that ribosomes are structures found in bacteria, plants, and animals. the experiments in which bacteria were made to grow in plant cells forming chloroplasts. the observations that chloroplasts and mitochondria resemble bacteria.
Answer:
the observations that chloroplasts and mitochondria resemble bacteria
Explanation:
The Endosymbiotic Theory is a theory that enables us to understand the origin of eukaryotic cells. The Endosymbiotic Theory posits that the mitochondria and chloroplast, which are organelles found in the eukaryotic cells, were once prokaryotic microbes that were first ingested by amoeba-like organisms and subsequently evolved by developing a symbiotic relationship with them. Some of the most important lines of evidence that supports this theory are: 1-chloroplasts and mitochondria resemble prokaryotic cells, i.e., they have a similar size, replicate by binary fission and there are unicellular eukaryotic protists that have filamentous temperature-sensitive proteins at their division plane (similarly to bacteria), and 2- chloroplasts and mitochondria are organelles with their own DNA and their own ribosomes (which are similar to those of bacteria).
Answer:
the observations that chloroplasts and mitochondria resemble bacteria
Explanation:
Replication. Mitochondria and chloroplasts make more of themselves in much the same way as bacteria reproduce. ... Like bacteria, mitochondria and chloroplasts grow in size, duplicate their DNA and other structures, and then divide into two identical organelles.
WILL MARK BRAINLIEST!!!
Which of these is a benefit for a parent who sees a genetic counselor?
A. Deciding whether or not to take medications before pregnancy.
B. Being able to plan in advance for a genetic disorder in a child.
C. Knowing that society must make decisions about genetic disorders.
D. Having a source of long-term psychological help to live with a genetic disorder.
Answer:
B. Being able to plan in advance for a genetic disorder in a child.
Being able to plan in advance for a genetic disorder in a child is an advantage for a parent who sees a genetic counselor. So, the correct option is (B).
What is Genetic Disorder?A genetic disorder is a type of disease caused in whole or in part by a change in a DNA sequence away from the normal sequence.
It can be caused by several reasons like
1. Monogenic Disorder
It is caused by a mutation in one gene
2. Multifactorial Inheritance Disorder
It is caused by mutations in multiple genes
3. Combination of gene mutations and environmental factors.
4. Damage to chromosomes by the changes in the number or structure of entire chromosomes, the structures that carry genes.
Genetic counseling helps parents for better understand test results and treatment options, helps deal with emotional concerns, and provides referrals to other healthcare providers and advocacy and support groups.
Thus, being able to plan in advance for a genetic disorder in a child is an advantage for a parent who sees a genetic counselor. So, the correct option is (B).
Learn more about Genetic Disorders, here:
https://brainly.com/question/17404085
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Homeostasis is maintained through feedback mechanisms.
a. True
b. False
Answer:
a. True
Explanation:
An endocrine system refers to a series of ductless glands and organs responsible for the production and secretion of hormones that are used by the body for the performance of various functions such as metabolism, controlling growth, reproduction, mood, sleep, etc. These hormones are secreted directly into the circulatory system (blood) and then transported to the organs and tissues in the body.
Basically, the endocrine system contributes significantly to the state of homeostasis in the body.
Homeostasis can be defined as a process through which a living organism maintains a steady or stable physical, internal and chemical environment that is ideal to enhance life and proper functionality.
Homeostasis is maintained through feedback mechanisms, which are either positive or negative feedback.
During a negative feedback, a sensor and a control center in the body of a living organism maintains blood glucose to regulate blood pressure by releasing glucagon to increase blood sugar or releasing insulin to decrease blood sugar.
For a positive feedback, a sensor and a control center aids child birth by causing the uterine to contract.
Plz someone help. This is due tonight!!!! I will give brainiest if you fill it out and NO LINK!!
Answer: I am not sure i will try to figure out
Explanation:
Put the following items in order from largest to smallest
cell
nucleotide
organism
chromosome
gene
Answer:
The correct answers is - Organism > Cell > Chromosome > gene > nucleotide.
Explanation:
Organisms are the largest among all these as they are made up of organs that made up of tissues and tissues are made up of cells. Cells are the second largest item among these items which contains various components in them and known as a unit of the structure of organisms.
In cells chromosome presents that are made up of protein and DNA, a particular sequence of DNA is known as gene, therefore, it is smaller than the chromosomes and in the last monomer of the DNA which is nucleotide made up of phosphate group, sugar and nitrogenous bases.
Diminished bone mineral density can result from inactivity. In contrast _______________ can stop if not reverse the loss of bone mineral density.
Answer: Resistance exercise
Explanation:
A decrease in the quantity of mineral in the bone can occur due to inactivity or less body movements which may be as a result of old age or a disease condition.
RESISTANCE EXERCISE is a type of training in which the muscles are subjected to work against a weight to help increase the strength of the muscles. Below are the different forms of resistance exercise:
--> Resistance bands: these bands provides resistance when they are stretched.
--> Suspension equipment: this training tool uses the body weight and gravity to form resistance.
--> Your own body weight: one can conveniently use the body weight for push ups and squats.
Generally, the resistance exercise helps to reverse the loss of bone mineral density through increasing muscle strength and tone and reducing inactivity in the muscles that led to diminished bone mineral density.
How do genetic scientists use dna to investigate homocide and determine ancestor connections?
Answer:
Actually there are plenty methods
such as proceeding,
genetic screening
PCR
fluorescence screen
electrophoresis
and after to compare the amino acid sequences and the DNA base triplets(codons) of the relevant samples.
if it matches well it concludes that they are closely related
if atleast a small % of similarity is visible they may/can conclude that there was a connection between them in the past(ancestor).
Answer:
They put it in sciednce machine thing
Explanation:
Receptor binding motifs such as RGD have highly selective recognition for cell adhesion. Outline a strategy for incorporating a cell adhesive recognition domain to a biomaterial. Address the problems surrounding domain quantity, type, and affinity in your discussion.
Answer:
Explanation:
RGD stands for Arginine Glycine Aspartate and is a three-amino-acid peptide. It is the most extensively utilized adhesive peptide for adhering diverse cell types to a variety of biomaterials. Integrins, fibrinogen, osteopontin, fibronectin, and bone sialoprotein, as well as collagens and laminins, all include an RGD primary binding domain. As a result, the synthetic (artificial) peptide RGD may bind to a wide range of integrin types. The artificial RGD retains its functioning through the sterilizing and processing processes of biomaterial creation because of its recognition advantage. This feature denotes the immune reactivity and pathogen transmission during xenograft.
Affinity can be modulated by the conformation of artificial RGD. The efficacy of RGD is also determined by the in vitro deposition of cells on the surface of the material sample.
The molecular processes unravel its effectiveness throughout its use as a scaffold foundation in in-vivo models. The fact that artificial RGD cannot work well in isolation is now a major aspect that defines its activity.
It has been discovered that cells release a variety of integrin-binding proteins that are more effective in activating integrin signalling than pure RGD. As a result, most biomaterials will bind and adsorb these proteins rather than RGD. As a result, a serum-free medium is employed in the majority of in vitro research.
As a result, biomaterials are supplied with RGD as well as quasi polymers such as polyethylene glycol to reduce the variance produced by native proteins. The addition of additional amino acids to RGD based on natural sequences can increase its biological activity, which can aid in the development of new tissues and the stimulation of cellular responses and signalling.
The amino terminal endpoint of the peptide, as well as the carboxyl group of the material surface, establish a covalent connection, which binds the peptide to just the surface of its biomaterial. Cell adhesion biomaterials are made from a variety of cell adhesion materials, including poly-L-lysine, mussels adhesive protein (MAP), and outer membrane (extracellular matrix) proteins.
Because MAPS are high in Dihydroxyphenylalanine and lysine, RGD is coupled with either of these to boost its cell adhesion capability. As a result, they can also aid in the attachment to damp or moist surfaces. It may also firmly adhere to glass, metals, and plastics. The addition of thiol groups to a peptide can also aid in its orientation and boost its stability.
The gap and density of this peptide sequence and structure on the biomaterial surface may be adjusted using a micro and nanotechnology (nanoscale patterning) method, which also improves ligand binding accuracy. Cellular reactions and cell activity are also under its control. Integrin receptors have been shown to be between 9 - 12 nm in size, therefore nanoscale surface patterning is crucial.
As a result, the above methods serve as a strategy for incorporating a cell adhesion recognition domain into a biomaterial while taking into account all of the technical intervention affecting its quantity, type, and affinity to the top layer for cell adhesion as a functioning tissue rather than a monolayer.