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Difference Between Hypothesis and Research Question
It is important to distinguish between biological null and alternative hypotheses and statistical null and alternative hypotheses. "Sexual selection by females has caused male chickens to evolve bigger feet than females" is a biological alternative hypothesis; it says something about biological processes, in this case sexual selection. "Male chickens have a different average foot size than females" is a statistical alternative hypothesis; it says something about the numbers, but nothing about what caused those numbers to be different. The biological null and alternative hypotheses are the first that you should think of, as they describe something interesting about biology; they are two possible answers to the biological question you are interested in ("What affects foot size in chickens?"). The statistical null and alternative hypotheses are statements about the data that should follow from the biological hypotheses: if sexual selection favors bigger feet in male chickens (a biological hypothesis), then the average foot size in male chickens should be larger than the average in females (a statistical hypothesis). If you reject the statistical null hypothesis, you then have to decide whether that's enough evidence that you can reject your biological null hypothesis. For example, if you don't find a significant difference in foot size between male and female chickens, you could conclude "There is no significant evidence that sexual selection has caused male chickens to have bigger feet." If you do find a statistically significant difference in foot size, that might not be enough for you to conclude that sexual selection caused the bigger feet; it might be that males eat more, or that the bigger feet are a developmental byproduct of the roosters' combs, or that males run around more and the exercise makes their feet bigger. When there are multiple biological interpretations of a statistical result, you need to think of additional experiments to test the different possibilities.
You should decide whether to use the onetailed or twotailed probability before you collect your data, of course. A onetailed probability is more powerful, in the sense of having a lower chance of false negatives, but you should only use a onetailed probability if you really, truly have a firm prediction about which direction of deviation you would consider interesting. In the chicken example, you might be tempted to use a onetailed probability, because you're only looking for treatments that decrease the proportion of worthless male chickens. But if you accidentally found a treatment that produced 87% male chickens, would you really publish the result as "The treatment did not cause a significant decrease in the proportion of male chickens"? I hope not. You'd realize that this unexpected result, even though it wasn't what you and your farmer friends wanted, would be very interesting to other people; by leading to discoveries about the fundamental biology of sexdetermination in chickens, in might even help you produce more female chickens someday. Any time a deviation in either direction would be interesting, you should use the twotailed probability. In addition, people are skeptical of onetailed probabilities, especially if a onetailed probability is significant and a twotailed probability would not be significant (as in our chocolateeating chicken example). Unless you provide a very convincing explanation, people may think you decided to use the onetailed probability after you saw that the twotailed probability wasn't quite significant, which would be cheating. It may be easier to always use twotailed probabilities. For this handbook, I will always use twotailed probabilities, unless I make it very clear that only one direction of deviation from the null hypothesis would be interesting.
the null hypothesis is rejected when it is true b.
How do we determine whether to reject the null hypothesis? It depends on the level of significance , which is the probability of the Type I error.
Alpha levels are controlled by the researcher and are related to . You get an alpha level by subtracting your confidence level from 100%. For example, if you want to be 98 percent confident in your research, the alpha level would be 2% (100% – 98%). When you run the hypothesis test, the test will give you a value for p. Compare that value to your chosen alpha level. For example, let’s say you chose an alpha level of 5% (0.05). If the results from the test give you:
the null hypothesis is not rejected when it is false c.
In the second experiment, you are going to put human volunteers with high blood pressure on a strict lowsalt diet and see how much their blood pressure goes down. Everyone will be confined to a hospital for a month and fed either a normal diet, or the same foods with half as much salt. For this experiment, you wouldn't be very interested in the P value, as based on prior research in animals and humans, you are already quite certain that reducing salt intake will lower blood pressure; you're pretty sure that the null hypothesis that "Salt intake has no effect on blood pressure" is false. Instead, you are very interested to know how much the blood pressure goes down. Reducing salt intake in half is a big deal, and if it only reduces blood pressure by 1 mm Hg, the tiny gain in life expectancy wouldn't be worth a lifetime of bland food and obsessive labelreading. If it reduces blood pressure by 20 mm with a confidence interval of ±5 mm, it might be worth it. So you should estimate the effect size (the difference in blood pressure between the diets) and the confidence interval on the difference.
Here are three experiments to illustrate when the different approaches to statistics are appropriate. In the first experiment, you are testing a plant extract on rabbits to see if it will lower their blood pressure. You already know that the plant extract is a diuretic (makes the rabbits pee more) and you already know that diuretics tend to lower blood pressure, so you think there's a good chance it will work. If it does work, you'll do more lowcost animal tests on it before you do expensive, potentially risky human trials. Your prior expectation is that the null hypothesis (that the plant extract has no effect) has a good chance of being false, and the cost of a false positive is fairly low. So you should do frequentist hypothesis testing, with a significance level of 0.05.
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the null hypothesis is probably wrong b.
The null hypothesis (H_{0}) is a statement of no effect, relationship, or difference between two or more groups or factors. In research studies, a researcher is usually interested in disproving the null hypothesis.
the result would be unexpected if the null hypothesis were true c.
The alternative hypothesis (H_{1}) is This is usually the hypothesis the researcher is interested in proving. The alternative hypothesis can be (only provides one direction, e.g., lower) We often use twosided tests even when our true hypothesis is onesided because it requires more evidence against the null hypothesis to accept the alternative hypothesis.
the null hypothesis is probably true d.
Watch the video or read the article below:
A p value is used in to help you . The p value is the evidence against a . The smaller the pvalue, the strong the evidence that you should reject the null hypothesis.
One can never prove the truth of a statistical (null) hypothesis.
The significance level (denoted by the Greek letter alpha— ) is generally set at 0.05. The smaller the significance level, the greater the burden of proof needed to reject the null hypothesis, or in other words, to support the alternative hypothesis.
failing to reject the null hypothesis when it is false.
One of the main goals of statistical hypothesis testing is to estimate the P value, which is the probability of obtaining the observed results, or something more extreme, if the null hypothesis were true. If the observed results are unlikely under the null hypothesis, your reject the null hypothesis. Alternatives to this "frequentist" approach to statistics include Bayesian statistics and estimation of effect sizes and confidence intervals.
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