Hydras are simple freshwater animals that have a tube-like body with a mouth surrounded by tentacles at one end and a basal disk for attachment at the other. The feeding and digestion process in hydras involves both extracellular and intracellular digestion.
Hydras use their tentacles to capture small organisms such as tiny crustaceans, insect larvae, and worms, which are then transported to the mouth. The mouth leads to a central cavity called the gastrovascular cavity, which functions as both the digestive and circulatory system.
In extracellular digestion, enzymes are secreted into the gastrovascular cavity by the cells lining its walls. The enzymes break down the captured prey into smaller molecules such as amino acids, glucose, and fatty acids, which can be absorbed by the cells. The nutrients are then transported throughout the body via diffusion.
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Which of the following is NOT an adaptation of the
parasitic tapeworm?
A. No digestive system because food is already digested.
B. Hooks to hang onto host intestine.
C. Fangs to pierce intestine wall and absorb nutrients.
D. Mucus for protection from being digested.
PLEASE HELP!
What claim or claims can you make about the impact of climate change on sea level rise?
What is your evidence for this claim?
Answer:
POLUTION
Explanation:
Answer:
I can make the claim that climate change and the sea level rise have a positive correlation. The graph shows that as the impact of climate change increases so does the sea level conveying that they are positively correlated.
What is the meaning of a Bioscope
Answer:
This is a cinema where people go to watch movies or a film someone watches.
Explanation:
a puppy has long floppy ears like his mother and dark brown for like his father how did the puppy get these traits
Answer:
genes
Explanation:
the puppy got half their mother's chromosomes and half their dad's chromosomes therefore inheriting parts of their genes
I NEED HELP PLEASE!
Answer:
The phenotypic ratio of this crossing is 9:3:3:1 whereas the genotypic ratio is 1:2:1:2:4:2:1:2:1.
Explanation:
If we cross red color organism with the yellow color organism, the phenotypic ratio of this crossing is 9:3:3:1 whereas the genotypic ratio is 1:2:1:2:4:2:1:2:1. In the F1 generation, all offspring are identical to each other means that all offspring resembles to male parent due to the presence of dominant allele while on the other hand, in the F2 generation, the ratio is 9:3:3:1 in which 9 ratio represents male parent, 1 represents female parent and the middle 3 represents hybrid which is different from their parents.
WARM-UP
Look at the two skulls on the right. Use the drop-
down menus below to decide whether certain
components of the human and chimpanzee skull
are similar or different.
Overall skull shape:
Teeth:
Nose shape:
Parts of jaw:
Skull size:
Answer:
overall skull shape- similar
nose shape- different
teeth- different
parts of jaw- similar
skull size- similar
Explanation:
correct on edge:)
The correct match of the components of the human and chimpanzee skull is:
overall skull shape- similarnose shape- differentteeth- differentparts of jaw- similarskull size- similarWhat is the difference between the skull of humans and chimpanzees?Chimp skulls have prominent brow ridges that extend considerably in front of the cranium. In contrast, the human skull's forehead rises immediately from the brows. A prominent nasal bone in the human skull between the eyes contrasts sharply with the flat curvature that leads to the chimp nasal hole.
In comparison to human cranial anatomy, apes have a more projecting face, a larger brow ridge, a longer face, and larger teeth in the front than in the back.
Therefore, the correct match is
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Could two humans (or two cows) have some differences in their DNA sequences for insulin, yet still make the exact same insulin proteins? Explain.
Answer: Yes
Explanation:
2 humans (or 2 cows) could have some differences in their DNA, yet still make the exact same insulin proteins because some codons code for the same amino acids
Which factor could have resulted in differing amounts of DNA collected from the strawberries?
Select one:
a. The location the strawberries were grown.
b. Number of cells in volume of strawberries used.
c. The brand of rubbing alcohol used.
d. The number of copies of DNA each cell contains.
Answer:
b. Number of cells in volume of strawberries used.
Additionally, because strawberries are octoploid and contain eight copies of each chromosome, there is a significant amount of DNA that has to be isolated, hence option B is correct.
What is the amount of DNA collected from the strawberries?Watch where the strawberry combination and the alcohol meet, at this point, a white cloud that resembles a thread will start to emerge. Strawberry DNA is seen here, as it rises to the top of the alcohol layer, the DNA will collect and congeal.
Due to their simple pulverization and the presence of the cell wall-degrading enzymes pectinases and cellulases, ripe strawberries are an ideal source for DNA extraction.
Therefore, the number of cells in the volume of strawberries used, the presence of the cell wall-degrading enzymes pectinases and cellulases, and ripe strawberries are ideal sources for DNA extraction, hence option B is correct.
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The dominant type of extracellular protein fiber in dense connective tissue is.
collagen fibers, I hope this was helpful to you :)
Drag each label to the current location on the table.
Sort the descriptions or examples into inherited or somatic mutations
Exists in all the cells of the body
Skin cancer caused by UV exposure
Not passed onto offspring
Transferred via egg and sperm cells
Found only in a specific cell type.
Help!! This is worth a lot of points!
Sort the descriptions or examples into inherited or somatic mutations. inherited: Exists in all the cells of the body. inherited: Transferred via egg and sperm cells somatic mutations, Found only in a specific cell type. somatic mutations: Skin cancer caused by UV exposure,somatic mutations: Not passed onto offspring.
Somatic mutations are alterations to a person's DNA that take place in any cell that isn't a germ cell after conception (egg or sperm cell). Somatic mutations are not inherited, occur intermittently or randomly, and are not related to a person's family history. Additionally, they cannot be passed on to subsequent generations.
Genetic alterations from the germline can be inherited. The DNA is altered in reproductive cells during this sort of mutation (egg or sperm). The mutation is inherited because sperm and eggs are passed from parents to their offspring.
Somatic mutations cannot be passed on since they happen at random in cells other than sperm or eggs.
Germline mutations happen in a parent's reproductive cells. The genetic material a kid inherits from their parents is altered by these mutations.
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You want to study the relationship between daily alcohol consumption and prostate-specific antigen levels. It was suggested that these two parameters have a linear relationship and as you increase your alcohol consumption your prostate-specific antigen level increases. What kind of a linear model would represent this relationship?
The kind of linear model that would represent this relationship is a positive linear model.
In a positive linear model, as the independent variable (alcohol consumption) increases, the dependent variable (prostate-specific antigen levels) also increases in a linear fashion. This implies that there is a positive correlation between the two variables, suggesting that higher alcohol consumption is associated with higher levels of prostate-specific antigen.
A linear model represents a straight-line relationship between the variables, and in this case, it would show a positive slope. The slope of the line indicates the rate at which the prostate-specific antigen levels increase with each unit increase in alcohol consumption.
By studying this relationship, researchers can gain insights into the impact of alcohol consumption on prostate-specific antigen levels and potentially understand the association between alcohol and prostate health.
However, it is important to note that further research and analysis are necessary to establish a causal relationship and consider other factors that may influence prostate-specific antigen levels.
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What is the relationship between Hox genes and embryological development?
Answer:
Hox genes control the timing of development and growth of embryos. Organisms A and B have very similar Hox genes, and their embryos, in the earliest stages of development, are also very similar.
Explanation:
Hox genes are a family of transcription factors that play a critical role in the development of the body plan during embryogenesis by controlling the spatial patterning of the developing embryo.
What are hox genes?Hox genes play a critical role in embryological development by controlling the formation and patterning of the body segments in animals. These genes are responsible for specifying the identity of different regions of the body, such as the head, thorax, and tail, during the early stages of development. They do this by regulating the expression of other genes that control the differentiation and growth of cells in specific regions of the embryo.
Hox genes are arranged in clusters on chromosomes and are activated in a specific order along the anterior-posterior (front-to-back) axis of the developing embryo. This sequential activation pattern helps to establish the body plan and shape of the organism. For example, the Hox genes that are activated in the head region will determine the formation of the head and brain, while those activated in the thorax region will control the formation of the heart and lungs.
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What is the main strategy to remove the high levels of organic and inorganic nutrients (high bod) from wastewater?
Aerate the wastewater so microorganisms either oxidize the organic matter into CO2 or bind the nutrients into their biomass. Then, the cells are removed from the water.
What's microorganisms?A microorganism, or microbe,( a) is an organism of bitsy size, which may live in its single- celled form or as a colony of cells.The possible actuality of unseen microbial life was suspected from ancient times, similar as in Jain Holy Writ from sixth century BC India. The scientific study of microorganisms began with their observation under the microscope in the 1670s by Anton van Leeuwenhoek. In the 1850s, Louis Pasteur set up that microorganisms caused food corruption, debunking the proposition of robotic generation. In the 1880s, Robert Koch discovered that microorganisms caused the conditions tuberculosis, cholera, diphtheria, and anthrax.What's microorganisms and its function?Microorganisms are set up far and wide in the terrain and play a commanding part in innumerous natural processes. Among other effects, they operate the introductory medicine cycles that are necessary for the shops' force of nutrients via the response of organic matter in soil.Learn more about microorganisms here:
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population of bacteria is growing according to the equation P(t)=1000e0.12t, where P(t) is the population and t is the time in hours. Estimate when the population will reach 5000 . Round to the tenths. Provide your answer below:
The estimated time it will take for the population to reach 5000 bacteria is approximately 13.4 hours.
To estimate when the population will reach 5000 bacteria, we can set up the equation P(t) = 5000 and solve for t.
The given equation for population growth is P(t) = 1000e^(0.12t). To solve for t, we can substitute 5000 for P(t):
5000 = 1000e^(0.12t)
To isolate the exponential term, we can divide both sides of the equation by 1000:
5 = e^(0.12t)
Next, we can take the natural logarithm (ln) of both sides to remove the exponential:
ln(5) = ln(e^(0.12t))
Using the property of logarithms, ln(e^(0.12t)) simplifies to 0.12t:
ln(5) = 0.12t
Now, we can solve for t by dividing both sides by 0.12:
t = ln(5) / 0.12
Using a calculator, we find that ln(5) is approximately 1.6094. Dividing this by 0.12 gives us an approximate value for t:
t ≈ 1.6094 / 0.12 ≈ 13.4117
Rounding to the tenths place, the estimated time it will take for the population to reach 5000 bacteria is approximately 13.4 hours.
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g why are the number of atp molecules produced per nadh or fadh2 not an integer? in other words, why is the p/o ratio not an integer?
The exact number of ATP molecules produced per NADH or FADH2 depends on various factors such as the specific electron transport chain complex involved, the availability of oxygen, and other metabolic conditions.
The number of ATP molecules produced per NADH or FADH2 is not an integer because the electron transport chain is a complex system that involves multiple enzymes and cofactors, each with their own efficiency and energy requirements. Additionally, some of the energy released during the electron transport chain is used to pump protons across the inner mitochondrial membrane, creating an electrochemical gradient that is used to generate ATP. The exact number of protons pumped and the efficiency of ATP synthesis can vary, leading to non-integer values for the P/O ratio.
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what is the function of rna polymerase? a all of the above. b it unwinds the double helix and adds nucleotides to a growing strand of rna. c it adds nucleotides to the 5' end of the growing mrna molecule. d it proceeds slowly along the dna strand, requiring about a minute to add two nucleotides to the growing mrna molecule.
In order to add nucleotides to an expanding strand of RNA, RNA polymerase unwinds the double helix.
What are the three roles that RNA polymerase plays?RNA Pol I: It synthesizes the pre-rRNA subunits that make up ribosomes, which is one of many forms of RNA Pol enzymes found in eukaryotes. RNA Pol II: It creates mRNA, snRNA, and microRNA precursors. RNA Pol III: It produces short RNAs, other rRNA precursors, and tRNA.
The double helix is it unwound by RNA polymerase?According to the DNA wrapping model of transcription, DNA bending and wrapping around RNA polymerase results in the DNA helix being unwound at the enzyme's catalytic site, which induces strand separation both before and during transcript elongation.
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a cell in prophase i has a diploid number (2n) of 36. at the end of meiosis ii, how many sets of chromosomes will each gamete have?
In a typical diploid cell, meiosis reduces the number of chromosomes to half. Consequently, if a cell contains 36 chromosomes before meiosis The four cells that are created during meiosis will each have 18 chromosomes.
With 30 chromosomes, each daughter cell will have 30. At the conclusion of meiosis I, each gamete in an organism with 36 chromosomes comprises 18 chromosomes, or 36 chromatids. The chromosomes duplicate prior to meiosis to produce 36 chromosomes, or 72 chromatids.
Each gamete cell has 23 chromosomes after meiosis II, when each parent cell is divided into two gametes. Each gamete is still haploid at this stage. The cell will possess only half of the real chromosomal 23 chromosomes at the conclusion of meiosis II.
sets of chromosomes = 36/2
= 18 chromosomes
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A student performs a diffusion lab using a starch/glucose solution, iodine solution, and dialysis tubing (cell membrane). The student waits 10 minutes before making observations. The student reports that iodine moved across the cell membrane. What observation helped the student draw their conclusion?
Answer:
Diffusion takes place in this process where iodine and glucose molecule diffuses through the dialysis tubing whereas the starch did not. Diffusion takes place on the basis of the size of the molecules.
Starch molecules are large in size whereas iodine and glucose are much smaller therefore they are able to diffuse. If both iodine and starch would have diffuses through the tubing the color would change into dark purple by mixing thee both molecules.
Which process turns glucose into energy?
Breathing
Cell division
Cellular respiration
Photosynthesis
Answer:
cellular respiration
Explanation:
Are gender traits completely a result of societal expectations?
No, Gender traits are not as a result of societal expectations. They are as a
result of biophysical processes in the body.
Both genders have their unique chromosomes composition in which
Males have XY.Females have XX.During reproduction, the male sex cell passes either the X or Y chromosome
to the offspring while the female pass only the X chromosomes.
This depicts that the male sex cells which is the sperm is the main
determinant in the gender of a child.
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assume that a man with hemophilia marries a normal woman whose father had hemophilia. what is the probability that their first son will have hemophilia?
When a man with hemophilia marries a normal woman whose father had hemophilia. Then the probability that their first son will have hemophilia will be 1/4
Hemophilia is a x hereditary disease.
Since the mother is a carrier mother and the father is a hemophilia father.
So there will be a total of four cases will arise. One hemophilia daughter, one carrier daughter, one normal son, and one hemophilia son.
Therefore the probability that when a man with hemophilia marries a normal woman whose father had hemophilia then their first son will have hemophillia is 1/4
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a Punnett square between a cross of a female who is a carrier for hemophilia and a male who does not have hemophilia.
1.) Correctly identify the alleles
2.) Identify parental genotypes
3.) Correctly assign them on them and complete a Punnett square
4.) Show BOTH your genotypes and phenotypes
The X chromosome contains the hemophilia gene, hence the two alleles are XH (normal clotting) and Xh (hemophilia). The female carrier of hemophilia must have the gene XHXh and be heterozygous.
For beginners, what is a Punnett square?A Punnett Square is a helpful tool for predicting the potential alterations and outcomes of cross-breeding. This includes foreseeing the mating of different species, including humans and animals.
A Punnett square example is what?For instance, Punnett square may predict that all the progeny will be tall and that they will all be heterozygous for both the allele for shortness and when pollen from a true-breeding tall pea plant crosses with pollen from a true-breeding short pea plant, the tallness gene is produced.
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this is the condition in which one living organism serves as a food source for another
Answer:
Producer
Explanation:
A producer provides food for other organisms and a consumer is an organism that eats the producer.
What organism from the example are most closely related to humans? How do we know this?
What organism do they share a common ancestor with?
Answer:
The organism that is most closely related to humans is the chimpanzee. We know this through various forms of evidence, including genetic, anatomical, and behavioral similarities between humans and chimpanzees. For example, the DNA sequence of chimpanzees and humans is approximately 99% identical, and many anatomical features of chimpanzees are very similar to those of humans.
Humans and chimpanzees share a common ancestor that lived between 6 and 8 million years ago, which is thought to have given rise to both the human and chimpanzee lineages. This ancestor was likely a hominid species, similar to modern-day gorillas, chimpanzees, and bonobos, but not identical to any living species. Over time, the evolutionary paths of humans and chimpanzees diverged, leading to the distinct species we see today.
Explanation:
2023
Answer:
Humans, chimpanzees, gorillas, orangutans and their extinct ancestors form a family of organisms known as the Hominidae. Researchers generally agree that among the living animals in this group, humans are most closely related to chimpanzees, judging from comparisons of anatomy and genetics.
Explanation:
Many monosaccharides bonded together would make a
-nucleic acid
-protein.
-lipid.
-polysaccharide.
Answer:
D
Explanation:
polysaccharide
pollen tubes multiple choice transport pollen to the stigma. allow sperm to fertilize the egg. are present during spermatogenesis. package sperm into pollen granules. facilitate the growth of pollen.
Pollen tubes allow sperm to fertilize the egg.
A pollen tube is generated from the pollen that extends down its style into the ovule during pollination process of higher plants. Pollen nuclei move down the pollen tube and fertilize the ovule after the pollen germinates upon that stigmatic surface.
Sperm- An ovum (egg cell), which would be produced by the a biologically female body, is the target of a sperm cell, which is intended to be discharged during sexual activity. Once they are joined, the sperm will enter the egg and fertilize it to produce new genetic material. A pollen grain is a microscopic male gametophyte or male plant (gamete-forming plant).
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true or false: the light microscope drawn is also known as a compound microscope as it has more than one set of lenses
Answer:
its True
Explanation:
do apes have a postorbital closure
Apes do indeed have a postorbital closure. This anatomical feature refers to the complete bony ring surrounding the eye socket, providing protection for the eye and separating it from the muscles used for chewing.
Yes, apes have a postorbital closure. This means that they have a bony plate or bar that completely closes off the eye socket behind the eye, separating it from the temporal fossa. This is a characteristic feature of primates and is important for providing support and protection to the eye and its associated structures.
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why the circulatory system is considered to be a closed system?
Explanation:
human have closed circulatory system. this means blood is always enclosed in the vessels and the heart while circulating throughout the body IN this type of system blood is pumped by heart through arteries and veins and does not fill the body cavities thats why the circulatory system is considered to be a closed system
who were the neurosurgeons who performed the first major series of commissurotomies for the treatment of intractable epilepsy?
A neurosurgeon is a medical professional who focuses on the surgical diagnosis and treatment of conditions affecting the central and peripheral nervous systems, such as congenital anomalies, trauma, tumors, vascular issues, infections of the brain or spine, strokes, or degenerative diseases of the spine.
There is a misconception that neurosurgeons only practice surgery. They actually have a ton of other duties. It can be challenging to anticipate all that will be covered during a consultation with a neurosurgeon.
As some of the most skilled and knowledgeable medical specialists, neurosurgeons spend a lot of time discussing unique cases with other physicians. They also have a list of their own cases, all of which present different difficulties. Although many of these patients will probably require surgery, not all of them will.
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