Experiments with faulty design or inconsistent data:
-decreases the experiment's reliability and validity
- wastes time and resources
- destroys the scientist's credibility in their field
- may lead to issues of safety to the experimenter/s due to faulty design
- is discouraged especially in hard sciences where data obtained should be accurate and precise
Explanation:
There are many<span> reasons that experiments with faulty </span>styles<span> or with incorrect </span>knowledge are<span> problematic for scientists. One reason for them to be problematic </span>is that if<span> he or she were to poorly </span>live<span> what </span>they're learning<span>. </span>as an example<span>, </span>somebody<span> measured the mass of a book </span>properly<span> to be </span>two<span> pounds, and </span>somebody else<span> measured it </span>erroneously<span> to be </span>one<span> pound. </span>differently<span>, that faulty designed experiments and inconsistent </span>knowledge will be<span> problematic is lack of accuracy and </span><span>exactness.</span>
The nurse is auscultating for abdominal bruits, on carotid artery the nurse auscultate last.
The bruits are a swishing sounds due to turbulence in the blood vessel in the abdomen and it heard due to atherosclerotic changes in the abdomen, whereas the carotid artery may be auscultating for bruits.
The auscultate abdominal bruits are present initially, at the right lower quadrant, it move in the sequence up to right upper quadrant, then to left upper quadrant and then finally to the lower quadrant. The auscultating for bruits are present over the aorta, renal arteries, femoral arteries and iliac arteries.
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It can be either diffusion, osmosis or active transport. depending on what is transported and how in which net direction they're moving.
The kinetic energy that occurs when your hands are rubing together
The creation of DNA fragments with ends that can join with other DNA is achieved by the use of restrictive enzyme analysis.
<h3>What are restriction enzymes?</h3>
They are enzymes utilized in genetic engineering or gene recombination technology to cut DNA at some specific points in other to have sticky ends.
The sticky ends DNAs are able to join with other DNAs using these ends. Another enzyme (Ligase) is utilized to join the DNA back once the desired DNA has been inculcated.
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