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Statistics Explained, An Introductory Guide for Life Scientists
Statistics Explained, An Introductory Guide for Life Scientists available in Paperback
 ISBN10:
 0521543169
 ISBN13:
 9780521543163
 Pub. Date:
 12/15/2005
 Publisher:
 Cambridge University Press
Overview
Statistics Explained is a readerfriendly introduction to experimental design and statistics for undergraduate students in the life sciences, particularly those who do not have a strong mathematical background. Hypothesis testing and experimental design are discussed first. Statistical tests are then explained using pictorial examples and a minimum of formulae. This classtested approach, along with a wellstructured set of diagnostic tables, will give students the confidence to choose an appropriate test with which to analyze their own data sets. Presented in a lively and straightforward manner, Statistics Explained will give readers the depth and background necessary to proceed to more advanced texts and applications. It will therefore be essential reading for all bioscience undergraduates, and will serve as a useful refresher course for more advanced students.
Product Details
ISBN13:  9780521543163 

Publisher:  Cambridge University Press 
Publication date:  12/15/2005 
Pages:  280 
Product dimensions:  5.98(w) x 8.98(h) x 0.55(d) 
Read an Excerpt
Cambridge University Press
052183550X  Statistics Explained  An Introductory Guide for Life Scientists  by Steve McKillup
Excerpt
1 Introduction
1.1 Why do life scientists need to know about experimental design and statistics?
If you work on living things it is usually impossible to get data from every individual of the group or species in question. Imagine trying to measure the length of every anchovy in the Pacific Ocean, the haemoglobin count of every adult in the USA, the diameter of every pine tree in a plantation of 200 000, or the individual protein content of 10 000 prawns in a large aquaculture pond.
The total number of individuals of a particular species present in a defined area is often called the population. Since a researcher usually cannot measure every individual in the population (unless they are studying the few remaining members of an endangered species), they have to work with a carefully selected subset containing several individuals, often called experimental units, that they hope is a representative sample from which the characteristics of the population can be inferred. You can also think of a population as the total number of artificial experimental units possible (e.g. the 125 567 plots of 1 m^{2} that would cover a coral reef) and your sample being the subset (e.g. 20 plots) you have chosen to work with.
The best way to get a representative sample is usually to choose a proportion of the population at random  without bias, with every possible experimental unit having an equal chance of being selected.
The trouble with this approach is that there are often great differences among experimental units from the same population. Think of the people you have seen today  unless you met some identical twins (or triplets etc.), no two would have been the same. Even species that seem to be made up of similar looking individuals (like flies or cockroaches or snails) show great variability. This leads to several problems.
Image not available in HTML version Figure 1.1 Even a random sample may not necessarily be a good representative of the population. Two samples have been taken at random from the same population. By chance, sample 1 contains a group of relatively large fish, while those in sample 2 are relatively small.
First, even a random sample may not be a good representative of the population from which it has been taken (Figure 1.1). For example, you may choose students for an exercise experiment who are, by chance, far less (or far more) physically fit than the population of the college they represent; a batch of seed chosen at random may not represent the variability present in all seed of that species; and a sample of mosquitoes from a particular place may have very different insecticide resistance than the same species from elsewhere.
Image not available in HTML version Figure 1.2 Samples selected at random from very different populations may not necessarily be different. Simply by chance sample 1 and sample 2 are similar.
Therefore, if you take a random sample from each of two similar populations, the samples may be different to each other simply by chance. On the basis of this you might mistakenly conclude that the two populations are very different. You need some way of knowing if the difference between samples is one you would expect by chance, or whether the populations really do seem to be different.
Second, even if two populations are very different, samples from each may be similar, and give the misleading impression the populations are also similar (Figure 1.2).
Image not available in HTML version Figure 1.3 Two samples of fish were taken from the same population and deliberately matched so that six equalsized individuals were initially present in each group. Fish in the treatment group were fed a vitamin supplement for 300 days, while those in the untreated control group were not. The supplement caused each fish in the treatment group to grow about 10% longer, but this difference is small compared with the variation in growth among individuals, which may obscure any effect of treatment.
Finally, natural variation among individuals within a sample may obscure any effect of an experimental treatment (Figure 1.3). There is often so much variation within a sample (and a population) that an effect of treatment may be difficult or impossible to detect. For example, what would you conclude if you found that 50 people given a newly synthesised drug showed an average decrease in blood pressure, but when you looked more closely at the group you found that blood pressure remained unchanged for 25, decreased markedly for 15, and increased slightly for the remaining 10? Has the drug really had an effect? What if tomato plants treated with a new fertiliser yielded from 1.5 to 9 kg of fruit per plant, compared with 1.5 to 7.5 kg per plant in an untreated group? Would you conclude there was a meaningful difference between these two groups?
These sorts of problems are usually unavoidable when you work with samples and mean that a researcher has to take every possible precaution to try and ensure their samples are likely to be representative and thus give a good estimate of conditions in the population. Researchers need to know how to sample. They also need a good understanding of experimental design, because a good design will take natural variation into account and also minimise additional unwanted variation introduced by the experimental procedure itself. They also need to take accurate and precise measurements to minimise other sources of error.
Finally, considering the variability among samples described above, the results of an experiment may not be clearcut. So it is often difficult to make a decision about a difference between samples from different populations or different experimental treatments. Is it the sort of difference you would expect by chance, or are the populations really different? Is the experimental treatment having an effect?
You need something to help you decide, and that is what statistical tests do, by calculating the probability of obtaining a particular difference among samples. Once you have the probability, the decision is up to you. So you need to understand how statistical tests work!
1.2 What is this book designed to do?
An understanding of experimental design and statistics is important, whether you are a biomedical scientist, ecologist, entomologist, genetic engineer, microbiologist, nursing professional, taxonomist, or human movement scientist, so most life science students are made to take a general introductory statistics course. Many of these courses take a detailed mathematical approach that a lot of life scientists find uninspiring. This book is an introduction that does not assume a strong mathematical background. Instead, it develops a conceptual understanding of how statistical tests actually work, using pictorial explanations where possible and a minimum of formulae.
If you have read other texts, or have already done an introductory course, you may find that the way this material is presented is unusual, but I have found that nonstatisticians find this approach very easy to understand and sometimes even entertaining. If you have a background in statistics you may find some sections a little too explanatory, but at the same time they are likely to make sense. This book most certainly will not teach you everything about the subject areas, but it will help you decide what sort of statistical test to use and what the results mean. It will also help you understand and criticise the experimental designs of others. Most importantly, it will help you design and analyse your own experiments, understand more complex experimental designs, and move on to more advanced statistical courses.
2 'Doing science'  hypotheses, experiments, and disproof
2.1 Introduction
Before starting on experimental design and statistics, it is important to be familiar with how science is done. This is a summary of a very conventional view of scientific method.
2.2 Basic scientific method
The essential features of the 'hypotheticodeductive' view of scientific method (see Popper, 1968) are that a person observes or samples the natural world and uses all the information available to make an intuitive, logical guess, called an hypothesis, about how the system functions. The person has no way of knowing if their hypothesis is correct  it may or may not apply. Predictions made from the hypothesis are tested, either by further sampling or by doing experiments. If the results are consistent with the predictions then the hypothesis is retained. If they are not, it is rejected, and a new hypothesis formulated (Figure 2.1).
The initial hypothesis may come about as a result of observations, sampling, and/or reading the scientific literature. Here is an example from ecological entomology.
The Portuguese millipede Ommatioulus moreleti was accidentally introduced into southern Australia from Portugal in the 1950s. This millipede lives in leaf litter and grows to about four centimetres long. In the absence of natural enemies from its country of origin (especially European hedgehogs, which eat a lot of millipedes), its numbers rapidly increased to plague proportions in South Australia. Although it causes very little damage to agricultural crops, O. moreleti is a serious 'nuisance' pest because it invades houses. In heavily infested areas of South Australia during the late 1980s it
Image not available in HTML version Figure 2.1 The process of hypothesis formulation and testing.
used to be common to find over 1000 millipedes invading a moderate sized house in just one night. When you disturb one of these millipedes it ejects a smelly yellow defensive secretion. Once inside a house the millipedes would crawl across the floor, up the walls, and over the ceiling, where they fell into food and on to the faces and even into the open mouths of sleeping people. When accidentally crushed underfoot they stained carpets and floors, and smelt. The problem was so great that almost half a million dollars was spent on research to control this pest.
While working on ways to reduce the nuisance caused by the Portuguese millipede I noticed that householders who reported severe problems had welllit houses with large, uncurtained windows. In contrast, nearby neighbours whose houses were not so well lit, and who closed their curtains at night, reported far fewer millipedes inside. The numbers of O. moreleti per square metre were similar in the leaf litter around both types of houses. From these observations and very limited sampling of less than ten houses, I formulated the hypothesis, 'Portuguese millipedes are attracted to visible light at night.' I had no way of knowing whether this simple hypothesis was the reason for home invasions by millipedes, but it seemed logical from my observations.
Image not available in HTML version Figure 2.2 Arrangement of a 2 × 5 grid of lit and unlit tiles across a field where millipedes were abundant. Filled squares indicate unlit tiles and open squares indicate lit tiles.
From this hypothesis it was straightforward to predict, 'At night, in a field where Portuguese millipedes are abundant, more will be present on white tiles illuminated by visible light than on unlit white tiles.'
This prediction was tested by doing a simple and inexpensive manipulative field experiment with two treatments  lit tiles and a control treatment of unlit tiles.
Since any difference in millipede numbers between one lit and one unlit tile might occur just by chance or some other unknown factor(s), the two treatments were replicated five times. I set up ten identical white ceramic floor tiles in a two row × five column rectangular grid in a field where millipedes were abundant (Figure 2.2). For each column of two tiles, I tossed a coin to decide which of the pair was going to be lit. The other tile was left unlit. Having one lit tile in each column ensured that replicates of both the treatment and control were dispersed across the field rather than having all the treatment tiles clustered together and was a precaution in case the number of millipedes per square metre varied across the field. The coin tossing eliminated any likelihood that I might subconsciously place the lit tile of each pair in an area where millipedes were more common.
I hammered a thin two metre long wooden stake vertically into the ground next to each tile. For every one of the lit tiles I attached a pocket torch to its stake and made sure the light shone on the tile.
I started the experiment at dusk by turning on the torches. Three hours later I went back and counted the numbers of millipedes on all tiles. The tiles within each treatment were the experimental units (Chapter 1).
From this experiment there were at least four possible outcomes:
No millipedes were present on the unlit tiles but lots were present on each of the lit tiles. This result is consistent with the hypothesis, which has survived this initial test and can be retained.

High and similar numbers of millipedes were present on both the lit and unlit tiles. This is not consistent with the hypothesis, which can probably be rejected since it seems light has no effect.

No (or very few) millipedes were present on any tiles. It is difficult to know if this has any bearing on the hypothesis  there may be a fault with the experiment (e.g. the tiles were themselves repellent or perhaps too slippery, or millipedes may not have been active that night). The hypothesis is neither rejected nor retained.

Lots of millipedes were present on the unlit tiles, but none were present on the lit ones. This is a most unexpected outcome that is not consistent with the hypothesis, which is extremely likely to be rejected.
These are the four simplest outcomes. A more complicated and much more likely one is that you find some millipedes on the tiles in both treatments, and that is what happened  see McKillup (1988). This sort of outcome is a problem, because you need to decide if light is having an effect on the millipedes, or whether the difference in numbers between lit and unlit treatments is simply happening by chance. Here statistical testing is extremely useful and necessary because it helps you decide whether a difference between treatments is meaningful.
2.3 Making a decision about an hypothesis
Once you have the result of the experimental test of an hypothesis, two things can happen:
either the results of the experiment are consistent with the hypothesis, which is retained;
or the results are inconsistent with the hypothesis, which may be rejected.
If the hypothesis is rejected it is likely to be wrong and another will need to be proposed.
If the hypothesis is retained, withstands further testing, and has some very widespread generality, it may progress to become a theory. But a
© Cambridge University Press
First Chapter
Cambridge University Press
052183550X  Statistics Explained  An Introductory Guide for Life Scientists  by Steve McKillup
Excerpt
1 Introduction
1.1 Why do life scientists need to know about experimental design and statistics?
If you work on living things it is usually impossible to get data from every individual of the group or species in question. Imagine trying to measure the length of every anchovy in the Pacific Ocean, the haemoglobin count of every adult in the USA, the diameter of every pine tree in a plantation of 200 000, or the individual protein content of 10 000 prawns in a large aquaculture pond.
The total number of individuals of a particular species present in a defined area is often called the population. Since a researcher usually cannot measure every individual in the population (unless they are studying the few remaining members of an endangered species), they have to work with a carefully selected subset containing several individuals, often called experimental units, that they hope is a representative sample from which the characteristics of the population can be inferred. You can also think of a population as the total number of artificial experimental units possible (e.g. the 125 567 plots of 1 m^{2} that would cover a coral reef) and your sample being the subset (e.g. 20 plots) you have chosen to work with.
The best way to get a representative sample is usually to choose a proportion of the population at random  without bias, with every possible experimental unit having an equal chance of being selected.
The trouble with this approach is that there are often great differences among experimental units from the same population. Think of the people you have seen today  unless you met some identical twins (or triplets etc.), no two would have been the same. Even species that seem to be made up of similar looking individuals (like flies or cockroaches or snails) show great variability. This leads to several problems.
Image not available in HTML version Figure 1.1 Even a random sample may not necessarily be a good representative of the population. Two samples have been taken at random from the same population. By chance, sample 1 contains a group of relatively large fish, while those in sample 2 are relatively small.
First, even a random sample may not be a good representative of the population from which it has been taken (Figure 1.1). For example, you may choose students for an exercise experiment who are, by chance, far less (or far more) physically fit than the population of the college they represent; a batch of seed chosen at random may not represent the variability present in all seed of that species; and a sample of mosquitoes from a particular place may have very different insecticide resistance than the same species from elsewhere.
Image not available in HTML version Figure 1.2 Samples selected at random from very different populations may not necessarily be different. Simply by chance sample 1 and sample 2 are similar.
Therefore, if you take a random sample from each of two similar populations, the samples may be different to each other simply by chance. On the basis of this you might mistakenly conclude that the two populations are very different. You need some way of knowing if the difference between samples is one you would expect by chance, or whether the populations really do seem to be different.
Second, even if two populations are very different, samples from each may be similar, and give the misleading impression the populations are also similar (Figure 1.2).
Image not available in HTML version Figure 1.3 Two samples of fish were taken from the same population and deliberately matched so that six equalsized individuals were initially present in each group. Fish in the treatment group were fed a vitamin supplement for 300 days, while those in the untreated control group were not. The supplement caused each fish in the treatment group to grow about 10% longer, but this difference is small compared with the variation in growth among individuals, which may obscure any effect of treatment.
Finally, natural variation among individuals within a sample may obscure any effect of an experimental treatment (Figure 1.3). There is often so much variation within a sample (and a population) that an effect of treatment may be difficult or impossible to detect. For example, what would you conclude if you found that 50 people given a newly synthesised drug showed an average decrease in blood pressure, but when you looked more closely at the group you found that blood pressure remained unchanged for 25, decreased markedly for 15, and increased slightly for the remaining 10? Has the drug really had an effect? What if tomato plants treated with a new fertiliser yielded from 1.5 to 9 kg of fruit per plant, compared with 1.5 to 7.5 kg per plant in an untreated group? Would you conclude there was a meaningful difference between these two groups?
These sorts of problems are usually unavoidable when you work with samples and mean that a researcher has to take every possible precaution to try and ensure their samples are likely to be representative and thus give a good estimate of conditions in the population. Researchers need to know how to sample. They also need a good understanding of experimental design, because a good design will take natural variation into account and also minimise additional unwanted variation introduced by the experimental procedure itself. They also need to take accurate and precise measurements to minimise other sources of error.
Finally, considering the variability among samples described above, the results of an experiment may not be clearcut. So it is often difficult to make a decision about a difference between samples from different populations or different experimental treatments. Is it the sort of difference you would expect by chance, or are the populations really different? Is the experimental treatment having an effect?
You need something to help you decide, and that is what statistical tests do, by calculating the probability of obtaining a particular difference among samples. Once you have the probability, the decision is up to you. So you need to understand how statistical tests work!
1.2 What is this book designed to do?
An understanding of experimental design and statistics is important, whether you are a biomedical scientist, ecologist, entomologist, genetic engineer, microbiologist, nursing professional, taxonomist, or human movement scientist, so most life science students are made to take a general introductory statistics course. Many of these courses take a detailed mathematical approach that a lot of life scientists find uninspiring. This book is an introduction that does not assume a strong mathematical background. Instead, it develops a conceptual understanding of how statistical tests actually work, using pictorial explanations where possible and a minimum of formulae.
If you have read other texts, or have already done an introductory course, you may find that the way this material is presented is unusual, but I have found that nonstatisticians find this approach very easy to understand and sometimes even entertaining. If you have a background in statistics you may find some sections a little too explanatory, but at the same time they are likely to make sense. This book most certainly will not teach you everything about the subject areas, but it will help you decide what sort of statistical test to use and what the results mean. It will also help you understand and criticise the experimental designs of others. Most importantly, it will help you design and analyse your own experiments, understand more complex experimental designs, and move on to more advanced statistical courses.
2 'Doing science'  hypotheses, experiments, and disproof
2.1 Introduction
Before starting on experimental design and statistics, it is important to be familiar with how science is done. This is a summary of a very conventional view of scientific method.
2.2 Basic scientific method
The essential features of the 'hypotheticodeductive' view of scientific method (see Popper, 1968) are that a person observes or samples the natural world and uses all the information available to make an intuitive, logical guess, called an hypothesis, about how the system functions. The person has no way of knowing if their hypothesis is correct  it may or may not apply. Predictions made from the hypothesis are tested, either by further sampling or by doing experiments. If the results are consistent with the predictions then the hypothesis is retained. If they are not, it is rejected, and a new hypothesis formulated (Figure 2.1).
The initial hypothesis may come about as a result of observations, sampling, and/or reading the scientific literature. Here is an example from ecological entomology.
The Portuguese millipede Ommatioulus moreleti was accidentally introduced into southern Australia from Portugal in the 1950s. This millipede lives in leaf litter and grows to about four centimetres long. In the absence of natural enemies from its country of origin (especially European hedgehogs, which eat a lot of millipedes), its numbers rapidly increased to plague proportions in South Australia. Although it causes very little damage to agricultural crops, O. moreleti is a serious 'nuisance' pest because it invades houses. In heavily infested areas of South Australia during the late 1980s it
Image not available in HTML version Figure 2.1 The process of hypothesis formulation and testing.
used to be common to find over 1000 millipedes invading a moderate sized house in just one night. When you disturb one of these millipedes it ejects a smelly yellow defensive secretion. Once inside a house the millipedes would crawl across the floor, up the walls, and over the ceiling, where they fell into food and on to the faces and even into the open mouths of sleeping people. When accidentally crushed underfoot they stained carpets and floors, and smelt. The problem was so great that almost half a million dollars was spent on research to control this pest.
While working on ways to reduce the nuisance caused by the Portuguese millipede I noticed that householders who reported severe problems had welllit houses with large, uncurtained windows. In contrast, nearby neighbours whose houses were not so well lit, and who closed their curtains at night, reported far fewer millipedes inside. The numbers of O. moreleti per square metre were similar in the leaf litter around both types of houses. From these observations and very limited sampling of less than ten houses, I formulated the hypothesis, 'Portuguese millipedes are attracted to visible light at night.' I had no way of knowing whether this simple hypothesis was the reason for home invasions by millipedes, but it seemed logical from my observations.
Image not available in HTML version Figure 2.2 Arrangement of a 2 × 5 grid of lit and unlit tiles across a field where millipedes were abundant. Filled squares indicate unlit tiles and open squares indicate lit tiles.
From this hypothesis it was straightforward to predict, 'At night, in a field where Portuguese millipedes are abundant, more will be present on white tiles illuminated by visible light than on unlit white tiles.'
This prediction was tested by doing a simple and inexpensive manipulative field experiment with two treatments  lit tiles and a control treatment of unlit tiles.
Since any difference in millipede numbers between one lit and one unlit tile might occur just by chance or some other unknown factor(s), the two treatments were replicated five times. I set up ten identical white ceramic floor tiles in a two row × five column rectangular grid in a field where millipedes were abundant (Figure 2.2). For each column of two tiles, I tossed a coin to decide which of the pair was going to be lit. The other tile was left unlit. Having one lit tile in each column ensured that replicates of both the treatment and control were dispersed across the field rather than having all the treatment tiles clustered together and was a precaution in case the number of millipedes per square metre varied across the field. The coin tossing eliminated any likelihood that I might subconsciously place the lit tile of each pair in an area where millipedes were more common.
I hammered a thin two metre long wooden stake vertically into the ground next to each tile. For every one of the lit tiles I attached a pocket torch to its stake and made sure the light shone on the tile.
I started the experiment at dusk by turning on the torches. Three hours later I went back and counted the numbers of millipedes on all tiles. The tiles within each treatment were the experimental units (Chapter 1).
From this experiment there were at least four possible outcomes:
No millipedes were present on the unlit tiles but lots were present on each of the lit tiles. This result is consistent with the hypothesis, which has survived this initial test and can be retained.

High and similar numbers of millipedes were present on both the lit and unlit tiles. This is not consistent with the hypothesis, which can probably be rejected since it seems light has no effect.

No (or very few) millipedes were present on any tiles. It is difficult to know if this has any bearing on the hypothesis  there may be a fault with the experiment (e.g. the tiles were themselves repellent or perhaps too slippery, or millipedes may not have been active that night). The hypothesis is neither rejected nor retained.

Lots of millipedes were present on the unlit tiles, but none were present on the lit ones. This is a most unexpected outcome that is not consistent with the hypothesis, which is extremely likely to be rejected.
These are the four simplest outcomes. A more complicated and much more likely one is that you find some millipedes on the tiles in both treatments, and that is what happened  see McKillup (1988). This sort of outcome is a problem, because you need to decide if light is having an effect on the millipedes, or whether the difference in numbers between lit and unlit treatments is simply happening by chance. Here statistical testing is extremely useful and necessary because it helps you decide whether a difference between treatments is meaningful.
2.3 Making a decision about an hypothesis
Once you have the result of the experimental test of an hypothesis, two things can happen:
either the results of the experiment are consistent with the hypothesis, which is retained;
or the results are inconsistent with the hypothesis, which may be rejected.
If the hypothesis is rejected it is likely to be wrong and another will need to be proposed.
If the hypothesis is retained, withstands further testing, and has some very widespread generality, it may progress to become a theory. But a
© Cambridge University Press
Table of Contents
Reading Group Guide
Preface; 1. Introduction; 2. 'Doing Science'  hypotheses, experiments and disproof; 3. Collecting and displaying data; 4. Introductory concepts of experimental design; 5. Probability helps you make a decision about your results; 6. Working from samples  data, populations and statistics; 7. Normal distributions  test for comparing the means of one or two samples; 8. Type 1 and Type 2 error, power and sample size; 9. Single factor analysis of variance; 10. Multiple comparisons after ANOVA; 11. Two factor analysis of variance; 12. Important assumptions of analysis of variance: transformations and a test for equality of variances; 13. Two factor analysis of variance without replication, and nested analysis of variance; 14. Relationships between variables: linear correlation and linear regression; 15. Simple linear regression; 16. Nonparametric statistics; 17. Nonparametric tests for nominal scale data; 18. Nonparametric tests for ratio, interval or ordinal scale data; 19. Choosing a test; 20. Doing science responsibly and ethically.
Interviews
Preface; 1. Introduction; 2. 'Doing Science'  hypotheses, experiments and disproof; 3. Collecting and displaying data; 4. Introductory concepts of experimental design; 5. Probability helps you make a decision about your results; 6. Working from samples  data, populations and statistics; 7. Normal distributions  test for comparing the means of one or two samples; 8. Type 1 and Type 2 error, power and sample size; 9. Single factor analysis of variance; 10. Multiple comparisons after ANOVA; 11. Two factor analysis of variance; 12. Important assumptions of analysis of variance: transformations and a test for equality of variances; 13. Two factor analysis of variance without replication, and nested analysis of variance; 14. Relationships between variables: linear correlation and linear regression; 15. Simple linear regression; 16. Nonparametric statistics; 17. Nonparametric tests for nominal scale data; 18. Nonparametric tests for ratio, interval or ordinal scale data; 19. Choosing a test; 20. Doing science responsibly and ethically.