Answer:
D
Explanation:
Because there is only one carbon it says they are equal
A. CC and C. C.C.C
Carbon has four valence electrons, so it can achieve a full outer energy level by forming four covalent bonds.When it bonds only with hydrogen, it forms compounds called hydrocarbons. Carbon can form single, double, or triple covalent bonds with other carbon atoms.A carbon atom can form the following bonds:
Four single bonds. One double and two single bonds. Two double bonds. One triple bond with one single bond.In options, B and D there are single and double formation between carbon atoms. Thus these are correct bonding patterns.
Therefore, bonding pattern cannot be formed by carbon is option A and C.
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Name how soil and water are negatively affected by food production
Answer:
- Water: salinization due to irrigation, water pollution, etc.
- Soil: erosion (mechanization), porosity, accumulation of harmful pesticides/herbicides, loss of microbe biodiversity, etc.
Explanation:
Improper agricultural practices are associated with the pollution of soil and water. It is well known that the overuse of fertilizers or pesticides/herbicides contaminates both the soil and water and disturbs the composition of nutrients in the soil. Moreover, improper agricultural practices also reduce soil porosity, produce soil erosion and increase soil salinity/alkalinity. Moreover, improper practices may also increase pollution by increasing the concentrations of nutrients and toxic pollutants in both water and crops. Finally, irrigation techniques increase salinity levels in water and soil.
Smallholders have historically been for-profit commercial horticulturalists rather than subsistence farmers.
True
False
A segment of a DNA strand is shown. AGGTCAGG
a. What is the complementary DNA strand?
b. What is the mRNA strand?
c. What amino acids are produced as a result (use the codon chart to help you)
Answer:
b. messenger ribonucleic acid
a. The complementary DNA strand is the sequence that pairs with the given DNA strand. In DNA, adenine (A) pairs with thymine (T), and cytosine (C) pairs with guanine (G). Therefore, the complementary DNA strand of "AGGTCAGG" would be "TCCAGTCC".
b. The mRNA strand is synthesized based on the complementary DNA strand. In mRNA, thymine (T) is replaced by uracil (U). Therefore, the mRNA strand corresponding to the given DNA sequence "AGGTCAGG" would be "UCCAGUCC".
c. To determine the amino acids produced, we need to identify the codons (groups of three nucleotides) in the mRNA strand and refer to a codon chart (also known as a genetic code chart). Here's an example of how the codons in the mRNA strand "UCCAGUCC" can be translated:
UCC (Serine)
AGU (Serine)
CCU (Proline)
Therefore, the resulting amino acid sequence would be Serine-Serine-Proline.
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define the term chylomicron
Where are ribosomes produced?
Answer:
In bacterial cells, ribosomes are synthesized in the cytoplasm through the transcription of multiple ribosome gene operons. In eukaryotes, the process takes place both in the cell cytoplasm and in the nucleolus, which is a region within the cell nucleus.
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In which chromosome are sex-linked genes usually found? Explain why these genes are called "sex-linked"
Explanation:
Sex linked is a trait in which a gene is located on a sex chromosome. In humans, the term generally refers to traits that are influenced by genes on the X chromosome. This is because the X chromosome is large and contains many more genes than the smaller Y chromosome. In a sex-linked disease, it is usually males who are affected because they have a single copy of X chromosome that carries the mutation. In females, the effect of the mutation may be masked by the second healthy copy of the X chromosome.
Normal mitotic cell division results in each daughter cell having 1/2 the chromosomes
A True
B False
Answer:
B
Explanation:
it should be a whole number and not 1/2
In humans most of an of offsprings genes comes from the father true or false
Answer:
False. You actually have more from your mother.
biological classification is important because it allows scientists to study organisms in a ___ way
Answer:
Systematic.
Explanation:
Biological classification is important because it allows scientists to study organisms in a systematic way.
In Science, this biological classification of living organisms based on similarities or characteristics such as eyes, number of legs, etc., is generally referred to as taxonomy.
Taxonomy can be defined as the process of naming, classification and description of living organisms such as plants and animals. The eight (8) biological classification (taxonomy) used for grouping and organizing organisms are; kingdom, domain, phylum, family, order, class, species and genus.
Hence, taxonomy helps scientist to have a good understanding and knowledge when studying various organisms.
define organic agriculture production for at least three to five sentences
Answer
Organic farming can be defined as an agricultural process that uses biological fertilisers and pest control acquired from animal or plant waste. Organic farming was initiated as an answer to the environmental sufferings caused by the use of chemical pesticides and synthetic fertilisers.
Please help. I have been stuck on this diagram. Can someone help me fill it in.
Answer:
The definitions are the following.
Explanation:
Transpiration is the process in which water is evaporated from the body of plants.
Sublimation is the changing of state of a substance directly from the solid to the gas state, without passing through the liquid state.
Precipitation is the falling of water from the cloud in the form of rain and snowfall due to condensation of water vapors.
Runoff is the excess liquid that flows across the surface of the land.
Infiltration is the process in which water that are present on the ground surface enters the soil.
Cohesion is the sticking together of particles of the same substance with one another.
Adhesion is the clinging of dissimilar particles or surfaces to one another.
polarity is a state of an atom or a molecule which gain positive and negative charges.
26. the first documented patient in a disease epidemic within a population?
A. The suspect
B. The definitive host
C. The carrier
D. The index case
27. During the lab, the time was needed for E. Coli to show some growth after UV light exposure which indicates some DNA repair?
A. 0 second
B. 30 seconds
C. 1 minute
D. 2 minutes
28. Mannitol salt agar is classified as:
A. Enriched medium
B. Selective medium
C. Differential medium
D. A. and b.
E. B. and c.
29. Mannitol salt agar is used to identify & differentiate
A. Fungi
B. Enteric bacteria
C. Staphylococcus
D. Streptococcus
E. Gram (-) cocci
30. The Ingredient in Mannitol salt plate which makes the agar selective is?
A. Salt
B. Glucose
C. Mannitol
D. Bile acids
Answer:
a a c
Explanation:
Do Birds Really Abandon Their Chicks If Humans Touch Them? 25 points!!
Answer:
Yes they do.
Explanation:
birds will abandon their young after being touched by human hands because they can smell the scent of the human on their babies. This then causes the mother bird to become afraid of possible predators and to leave its children to the elements
answer: no
explanation: parent birds do not recognize their young by smell. They will not abandon a baby if it has been touched by humans.
How does the shape of the red blood allow diffusion to occur efficiently
Answer:
The partial pressure of oxygen determines the affinity of hemoglobin for oxygen. Red blood cells have the shape of a flattened disk, generating a broad surface area for the diffusion of oxygen. Since their only purpose is carrying oxygen throughout the body, they lack many typical cell structures, including a nucleus.
Explanation:
Hope this helps
Answer:
* Because of their viscoelastic characteristic, red blood cells are able to squeeze through very thin capillaries in order to deliver oxygen and remove carbon dioxide. * The biconcave shape of red blood cells helps maximize the overall surface area required for oxygen absorption.
Explanation:
Lymph capillaries Lymph capillaries filter lymph. originate as closed-ended tubes associated with blood capillary networks. cannot be discerned structurally from cardiovascular system capillaries. include layers of smooth muscle for peristalsis. concentrate lymph prior to passing it to larger lymphatic vessels.
Answer:
The correct answer is ''originate as closed-ended tubes associated with blood capillary networks.''
Explanation:
The lymphatic vessel system begins within the tissues in the form of tubes closed at one end called lymphatic capillaries (chyliferous in the intestine). These have an internal endothelial lining, similar to that of blood capillaries. These vessels are found in greater numbers in the skin, the digestive tract, and the respiratory system. The tissue fluid penetrates the lymphatic capillaries by diffusion, with the help of a small indirect pressure gradient, which gives it the arterial pressure. The walls of the lymphatic capillaries offer little resistance to the entry of substances; they are more permeable than capillaries in the blood system. The tiny capillaries form larger vessels, similar to the venules and veins of the blood vessel system. The walls are thinner than those of the veins of the blood system and its valves much more numerous.
Which property (quality) of fossils allows scientists to determine the relative ages of rock layers?
A.Fossils show change over time as species evolve.
B.Fossils form from the remains of living organisms.
C.Fossils are usually found only in sedimentary rock.
D.Fossils can be analyzed to determine their exact age
The property (quality) of fossils allows scientists to determine the relative ages of rock layers are fossils show change over time as species evolve.
What is the minimum age of a fossil?A living being that lived more than 11 thousand years ago is considered a fossil, that is, before the Holocene, which is the current geological epoch. Ancient remains or evidence, but less than 11,000 years old, such as sambaquis, are classified as subfossils.
Chemistry is present in this process, more precisely the element Carbon. The dating of a fossil can be done based on the already known percentage of Carbon-14 (C14) in relation to Carbon-12 (C12) of living matter (without decomposition).
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id- 5121786233 p/w- tepQ3w
Answer:
I need 1 Brainliest before I can become Virtuoso
Explanation:
Answer:................. I just needed the points so I can get help on my math work........
Explanation:
what do you think would be a LIMITING FACTOR for elk populations in Yellowstone and why
HELP EASY QUESTION Definition: This is an organism's response to a stimulus developed by being taught or watching another organism. Example: how to open a soda when you're thirsty
RNA is used in the process of translation to build proteins. Which of these correctly describes the role of the different types of RNA in
protein synthesis? Choose ALL that apply.
A)
rRNA makes up the ribosome.
B)
ERNA carries amino acids to ribosome.
C)
tRNA carries nucleotides to the ribosome.
D
mRNA copies the genetic code from DNA and carries it to the ribosome.
mRNA code is read to determine the sequence of amino acids in the
protein
Answer:
I think its A and D
Explanation:
Sorry if I'm wrong good luck.
How much oxygen does the
atmosphere contain?
O 12%
0 76%
O 35%
0 26%
Answer:
20.95%
Explanation:
By volume, dry air contains 78.09% nitrogen, 20.95% oxygen, 0.93% argon, 0.04% carbon dioxide, and small amounts of other gases. Air also contains a variable amount of water vapor, on average around 1% at sea level, and 0.4% over the entire atmosphere.
Describe in your own words, human ovulation and the menstrual cycle
Answer:
Ovulation occurs around 14 days before your period. If your average menstrual cycle is 28 days, you ovulation is on most likely on day 14. If the usual menstrual cycle is 35 days ovulation most likely happens day 21.
Explanation:
hope this helped!
Genetic movement is also known as genetic what?
Explanation:
Genetic disorders of the central nervous system have a propensity to cause movement disorders or ataxia, as a part of the phenotype, or sometimes as the main phenotypic manifestation. The Online Mendelian Inheritance in Man (OMIM) database lists over 500 entries for disorders of which ataxia or a movement disorder form part. Neurologists should be alert to the possibility that patients with complex disorders involving involuntary movements or unsteadiness may have a genetic disorder.
Only those gene loci with relevance to the practising neurologist will be discussed; a more complete listing of other loci, many of which apply only to individual kindreds, is available in referenced review articles.
HUNTINGTON’S DISEASE
Huntington’s disease (HD) is the prototypic neurogenetic disorder, one of the first to be mapped (1983) and subsequently cloned (1993), and the model on which presymptomatic genetic testing is based.
The clinical triad of movement disorder, psychiatric features, and eventual dementia will be well known to neurologists. Chorea is the first manifestation in about two thirds of patients, initially a mild fidgetiness apparent only to the careful observer, which gradually progresses and may be the only clinical manifestation of HD for several years. Severe chorea may respond well to neuroleptics such as sulpiride. Personality change and eye movement disorders including slow saccades, and head thrusting or blinking to generate saccadic eye movements, are also common early features. A wide range of movement disorders including parkinsonism, loss of postural stability, and dystonia eventually supervene, leading to increasingly functional impairment. Progressive weight loss, often resulting in cachexia, is common. Presentation is usually in the forth or fifth decades, but may be at almost any age. The juvenile onset form of HD may present with parkinsonism, the so-called Westphal variant, while late onset forms may cause chorea alone.
Expansion of a polyglutamine (CAG) trinucleotide repeat beyond the critical threshold of 36 repeats results in disease, and forms the basis of the polymerase chain reaction based genetic test. Expansion size is inversely related to age at onset, but the range in age at onset for a given repeat size is so large that repeat size is not a useful predictor for individuals. Inheritance is dominant with full penetrance, meaning that almost all mutation carriers will eventually develop the disease, except those with 36–39 repeats where penetrance is reduced. Meiotic instability with a tendency to increasing expansion size, particularly during spermatogenesis, provides the molecular basis for the phenomenon of anticipation. Thus, juvenile onset cases with very large expansions usually have an affected father. A small minority (< 1%) of individuals have expansions in an intermediate range (29–35 repeats), believed to be an asymptomatic but unstable pre-mutation range, which may expand to cause disease in offspring. Dentatorubropallidoluysian atrophy (DRPLA), also caused by a trinucleotide repeat expansion, may be difficult to distinguish clinically from early onset HD, and so is usually tested for with HD.
Predictive genetic testing of asymptomatic at-risk relatives of affected patients is governed by international guidelines (see Hanna and Wood on page ii2). Prenatal testing in known mutation carriers is routinely available, while linkage based exclusion testing is available to those at-risk women who do not wish to know their own gene status. The latter depends on termination of a pregnancy where linkage shows the fetus to have the same 50% genetic risk as the mother. Preimplantation diagnosis based on selection of unaffected IVF embryos is available in some centres.
THE DYSTONIAS
Dystonia is a feature of many hereditary neurodegenerative and metabolic disorders. In most of these disorders, dystonia usually occurs in the setting of a broader clinical phenotype, and careful clinical assessment reveals other features such as cognitive involvement, pyramidal signs, or ocular abnormalities.
Primary dystonias
In this group of disorders, dystonia or dystonic tremor is (with the exception of parkinsonism in dopa responsive dystonia (DRD)) the only clinical manifestation, and imaging and pathology are usually unrevealing. These disorders have a genetic basis, with dominant inheritance in most cases. The most important of these disorders to the neurologist are DYT1 dystonia and DRD.
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Why do you think Community Health Workers serve as connectors to the community?
Answer:
CHWs may perform the following roles: Create connections between vulnerable populations and healthcare providers. ... Ensure cultural competence among healthcare providers serving vulnerable populations. Educate healthcare providers and stakeholders about community health needs
Explanation:
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HELP PLS!!
Match the following terms and definitions.
1. Glycolysis
2. electron transport chain
3. Krebs cycle
breaks down glucose into pyruvic acid and ATP
picks up hydrogens and produces ATP
produces carbon dioxide, water, and ATP
Answer:
1. Glycolysis - breaks down glucose into pyruvate and ATP.
2. Electron Transport Chain - picks up Hydrogen and produces ATP.
3. Krebs Cycle - produces carbon dioxide, water, and ATP.
Explanation:
1. Glycolysis takes a molecule of glucose and breaks it down into two molecules of glyceraldehyde-3-phosphate(G3P) which ends up as pyruvate producing 4 molecules of ATP ( two from each G3P molecule). However, there is technically a net gain of 2 ATP molecules.
2. Electron Transport Chain - takes Hydrogen from energy-rich molecules, NADHH and FADH2, and produces ATP through a series of steps in the mitochondria.
3. Krebs Cycle - produces carbon dioxide, water, and ATP from pyruvate oxidation which occurs in the mitochondrial matrix (in eukaryotes).
We have two kinds of rats, dark brown and white rats in a population. In a rain forest scenario, with dark top soil, which kind of rats can survive better, taking into consideration, natural selection?
a.
White rat
b.
Both of them will survive
c.
Brown rat
d.
Neither
Answer:
C
Explanation:
they blend in with the soil color
Which of the following endocrine conditions is this patient at risk of developing?
A. Hyperthyroidism
B. Pheochromocytoma
C. Addison's disease
D. Cushing's syndrome
The dwarf phenotype is recessive to the tall phenotype in pea plants. When one tall plant and one dwarf plant are crossed together, 50% of their offspring are tall, and the other 50% displays dwarfism. What is the genotype of each parent in this cross?
Answer:
Tt (heterozygous tall) and homzygous short (tt)
Explanation:
This question involves one gene coding for height in pea plants. The allele for tallness (T) is dominant over the allele for shortness (tt). This means that dwarf phenotype is recessive to the tall phenotype in pea plants.
According to this question, a tall plant and a dwarf plant (tt) are crossed together. 50% of their offspring are tall, and the other 50% displays dwarfism. This is an equal ratio. Since the dwarf plant can only be "tt", the tall plant must be heterozygous "Tt" to be produced.
Hence, a cross between Tt vs tt will produce ½tall plants and ½short plant.
Please help?.?.?.?.?
Answer:
1.fungi
2.Temperature and Light
3.If the living organism does not get the air, water, food, nutrients, or light it needs to survive then it will die.
4.The relation ship is they need each other to live
Explanation:
np give brainliest and thank!
Why dos a single X chromosome that carriers the allele for red-green color blindness cause males to be color blind but doesn’t cause females to be color blind?
Answer:
Because females have two X chromosomes and the red-green color blindness allele has to be in both chromosomes to cause the woman to be color blinded. In the case of males, they only have one X chromosome, so if the allele for red-green color blindness is in the chromosome, the male will be color blinded since there is no other X chromosome with the normal allele as in females.
Explanation:
What determines if a person's sex is the genes X and Y. A sperm carries one of these two genes. When it meets the egg, this one will give the other chromosome, which is always X. So, if the sperm carries the X chromosome, the result, when the egg's fertilized, will be XX, which will give the information to develop a female human. If the sperm carries the Y chromosome, the result will be XY, which is a male.
As females are XX, if the red-green color blindness gene is in one of them, the other chromosome, which does not have this allele, will prevent the woman from being color blinded. We can say that women have a backup copy that prevents color blindness.
In the case of males, as they are XY, there is no extra copy that can prevent them from being red-green color blinded, so when a male has an X chromosome with this allele, they will be color blinded. In the case of women, they will only be carriers of the gene and will be color blinded if the two X chromosomes have the red-green color blindness allele.