What is the difference between a sample and a population?

How do we look at the distribution of data in a sample

How do we measure aspects of a distribution

What is a normal distribution?

First let’s generate some synthetic data and talk about how to visualize it.

#generate a normal distributionExNorm <-rnorm(1000, mean =5) |>as_tibble()#look at distributions#histogramExNorm |>ggplot(aes(value)) +geom_histogram()

`stat_bin()` using `bins = 30`. Pick better value with `binwidth`.

#pdfExNorm |>ggplot(aes(value)) +stat_density()

#Let's generate a plot that makes comparing these two easier

4.2.1 Stack plots to compare histogram and pdf

We will save each plot as ggplot object and then output them using the patchwork package (loaded in the setup chunk).

What is the difference between a histogram and a pdf?
What features of the histogram are preserved? Which are lost?

#histogramexhist <- ExNorm |>ggplot(aes(value)) +geom_histogram()#pdfexpdf <- ExNorm |>ggplot(aes(value)) +stat_density()#put the plots side by side with + or on top of each other with /exhist/expdf

`stat_bin()` using `bins = 30`. Pick better value with `binwidth`.

4.3 What is the difference between a sample and a population.

Simply put: a population is the thing you are trying to measure. A sample is the data you measure in an effort to measure the population. A sample is a subset of a population.

Let’s write some code for an example:

We will create a POPULATION that is a large set of numbers. Think of this is as the concentration of Calcium in every bit of water in a lake. Then we will create a SAMPLE by randomly grabbing values from the POPULATION. This simulates us going around in a boat and taking grab samples in an effort to figure out the concentration of calcium in the lake.

We can then run this code a bunch of times, you’ll get a different sample each time. You can also take a smaller or larger number of samples by changing “size” in the sample() function.

How does your sample distribution look similar or different from the population?
Why does the sample change every time you run it?
What happens as you increase or decrease the number of samples?
What happens if you set the number of samples to the size of the population?

all_the_water <-rnorm(10000, mean =6) |>as_tibble()sample_of_water <-sample(all_the_water$value, size =100, replace =FALSE) |>as_tibble()population_hist <- all_the_water |>ggplot(aes(value))+geom_histogram()+ggtitle("Population: All the water in the lake")sample_hist <- sample_of_water |>ggplot(aes(value))+geom_histogram()+ggtitle("Your sample of the lake")population_hist + sample_hist

`stat_bin()` using `bins = 30`. Pick better value with `binwidth`.
`stat_bin()` using `bins = 30`. Pick better value with `binwidth`.

4.4 Measuring our sample distribution: central tendency.

When we take a sample of a population, there are a few things we will want to measure about the distribution of values: where is the middle, how variable is it, and is it skewed to one side or another?

The first of these, “where is the middle?” is addressed with measures of central tendency. We will discuss three possible ways to measure this. The mean, median, and weighted mean.

To explain the importance of choosing between the mean and median, we will first import some discharge data. Read in the PINE discharge data.

pineQ <-read_csv("PINE_Jan-Mar_2010.csv")

Rows: 2160 Columns: 8
── Column specification ────────────────────────────────────────────────────────
Delimiter: ","
chr (2): StationID, surrogate
dbl (5): cfs, year, quarter, month, day
dttm (1): datetime
ℹ Use `spec()` to retrieve the full column specification for this data.
ℹ Specify the column types or set `show_col_types = FALSE` to quiet this message.

To find the mean (average), you just sum up all the values in your sample and divide by the number of values.

To find the median, you put the values IN ORDER, and choose the middle value. The middle value is the one where there are the same number of values higher than that value as there are values lower than it.

Because it uses the order of the values rather than just the values themselves, the median is resistant to skewed distributions. This means it is less effected by very large or very small values compared to most values in the sample data.

Let’s look at our normal distribution from earlier (ExNorm) compared to the Pine watershed discharge (pineQ)

Note that distributions like pineQ, that are positively skewed, are very common in environmental data.

#Calculate mean and median for cfs in pineQ and values in ExNormpineMean <-mean(pineQ$cfs)pineMedian <-median(pineQ$cfs)xmean <-mean(ExNorm$value)xmedian <-median(ExNorm$value)#plot mean and median on the ExNorm distributionEx <- ExNorm |>ggplot(aes(value)) +geom_histogram()+geom_vline(xintercept = xmean, color ="red")+geom_vline(xintercept = xmedian, color ="blue")#plot mean and median on the pineQ discharge histogramPineP <- pineQ |>ggplot(aes(cfs)) +geom_histogram()+geom_vline(xintercept = pineMean, color ="red")+geom_vline(xintercept = pineMedian, color ="blue")Ex / PineP

`stat_bin()` using `bins = 30`. Pick better value with `binwidth`.
`stat_bin()` using `bins = 30`. Pick better value with `binwidth`.

4.4.1 So what’s a weighted average?

When you compute a standard mean or median, you are giving equal weight to each measurement. Adding up all the values in a sample and dividing by the number of samples is the same as multiplying each value by 1/# of samples. For instance if you had ten samples, to calculate the mean you would add them up and divide by 10. This is the same as multiplying each value by 1/10 and then adding them up. Each value is equally weighted at 1/10.

There are certain situations in which this is not the ideal way to calculate an average. A common one in hydrology is that you have samples that are supposed to represent different portions of an area. One sample may be taken to measure a forest type that takes up 100 ha of a watershed while another sample represents a forest type that only takes up 4 ha. You may not want to simply average those values!

Another example is precipitation gages. In the image below, you see there are 5 rain gages. To get a precipitation number for the watershed, we could just average them, or we could assume they represent an area of the watershed and then weight their values by the area they represent. One method of designating the areas is by using Theissen polygons (the middle watershed). Another method of weighting is isohyetal contours, but we won’t worry about that for now!

In the weighted situation, we find the average by multiplying each precipitation values by the proportion of the watershed it represents, shown by the Thiessen polygons, and then add them all together. Let’s do an example.

Measures of variability allow us to measure the width of our sample data histogram or pdf. If all the values in our sample are close together, we would have small measures of variability, and a pointy pdf/histogram. If they vary more, we would have larger measures of variability and a broad pdf/histogram.

We will explore four measures of variability:

4.5.0.1 Variance:

Sum of the squared difference of each value from the mean divided by the number of samples minus 1. var()

**Both variance and standard deviation are sensitive to outliers.

4.5.0.3 CV: Coefficient of Variation

CV is simply the standard deviation divided by the mean of the data. Because you divide by the mean, CV is dimensionless. This allows you to use it to compare the variation in samples with very different magnitudes.

4.5.0.4 IQR: Interquartile Range

IQR is resistant to outliers because it works like a median. It measures the range of the middle 50% of the data in your distribution. So the IQR is the difference between the value between the 75th and 25th percentiles of your data, where the 75th percentile means 75% of the data is BELOW that value and the 25th percentile means 25% is below that value. Using the same vocabulary, the median is the same as the 50th percentile of the data.

If you ask R for the QUANTILES of your sample data, it will give you the values at which 0%, 25%, 50%, 75%, and 100% of the data are below. These are the 1,2,3,4, and 5th quantiles. Therefore, the IQR is the difference between the 4th and 2nd quantile.

Okay, code time.

First, let’s explore how changing the variability of a distribution changes the shape of it’s distribution. Create a plot a random normal distribution using rnorm() and set sd to different numbers. Make the mean of the distribution 0, the sample size 300, and the standard deviation 1 to start. Then increase the standard deviation incrementally to 10 and see what happens. Make the limits of the x axis on the plot -30 to 30.

rnorm(300, mean =0, sd =1) |>as_tibble() |>ggplot(aes(value))+stat_density()+xlim(c(-30,30))

Now let’s calculate the standard deviation, variance, coefficient of variation, and IQR of the Pine discharge data.

#standard deviationsd(pineQ$cfs)

[1] 84.47625

#variancevar(pineQ$cfs)

[1] 7136.237

#coefficient of variationsd(pineQ$cfs)/mean(pineQ$cfs)

[1] 2.800221

#IQR using the IQR funcitonIQR(pineQ$cfs)

[1] 8.1325

#IQR using the quantile functionquants <-quantile(pineQ$cfs)quants[4] - quants[2]

75%
8.1325

4.5.0.5 What about how lopsided the distribution is?

There are several ways to measure this as well, but we are just going to look at one: The Quartile skew. The quartile skew is the difference between the upper quartiles (50th-75th) and the lower quartiles (25th-50th) divided by the IQR (75th-25th).

Let’s look at the quartile skew of the two distributions we’ve been measuring. Calculate it for the pineQ discharge data and the random normal distribution we generated.

4.6 What is a normal distribution and how can we determine if we have one?

The distribution we generated with rnorm() is a normal distribution. The distribution of pineQ discharge is not normal. Now that we’ve looked at different ways to characterize distributions, we have the vocabulary to describe why.

Normal distributions:

mean = median, half values to the right, half to the left

symmetric (not skewed)

single peak

Many statistical tests require that the distribution of the data you put into them is normally distributed. BE CAREFUL! There are also tests that use ranked data. Similar to how the median is resistant to outliers, these rank-based tests are resistant to non-normal data. Two popular ones are Kruskal-Wallis and Wilcoxon rank-sum.

But how far off can you be before you don’t consider a distribution normal? Seems like a judgement call!

R to the rescue! There is a built in test for normality called shapiro.test(), which performs the Shapiro-Wilk test of normality. The hypothesis this test tests is “The distribution is normal.” So if this function returns a p-value less than 0.05, you reject that hypothesis and your function is NOT normal.

You can also make a quantile-quantile plot. A straight line on this plot indicates a normal distribution, a non-straight line indicates it is not normal.

shapiro.test(pineQ$cfs)

Shapiro-Wilk normality test
data: pineQ$cfs
W = 0.27155, p-value < 2.2e-16