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Caswell Memorial State Park Field Study & Lab: by Luke Basaca
Caswell Memorial State Park Field Study & Lab: by Luke Basaca
by Luke Basaca
Background
Caswell Memorial State Park, located on the banks of the Stanislaus River near Ripon,
California, was where the field study was conducted. The state park itself is unique in the sense
that it has certain characteristics that set it apart from other state parks. Caswell was founded in
1958 by local landowners who wanted to save this piece of land from development; it eventually
opened in 1958, its size initially 134 acres, but with additional donations increased to its current
size of 258 acres. Within the state park resides many qualities unique to not only the area but the
world. Caswell includes the largest collection of Valley Oak Trees within the Central Valley. It
also is the home of the elusive Riparian Brush Rabbit, a species of rabbit not found anywhere
Caswell State Park's main reason for being such a unique place within the Central Valley
is mainly due to the fact that it represents a very important and somewhat uncommon ecosystem,
called a riparian woodland or zone. Riparian woodlands are usually considerably smaller in size
compared to surrounding ecosystems. However, they are typically more ecologically diverse
with a larger amount of different species of both plants and animals residing within its'
boundaries. Riparian ecosystems are an important source of food, shelter, and resources for the
many animals not only residing in it, but also for animals surrounding it. The ecosystem itself
also serves as a type of filtration system for the rivers and streams crossing through it and as a
type of flood control system, controlling and slowing down the flow of water in a river.
Due to riparian ecosystems being typically small in size and relatively close in proximity
to major rivers and streams, they are usually most affected by ongoing human development and
alteration. Farming and construction has been a great issue in the Central Valley's riparian
ecosystems, contributing to the shrink of the number of remaining woodlands. As the field study
was conducted, great care was taken to make sure not to disturb the habitat of the native plants
and animal species. When any disturbances did occur, however, great care and effort was taken
The healthiness of a riparian woodland ecosystem, like any ecosystem, relies on two
factors: abiotic and biotic. Abiotic factors are the non-living elements that affect an ecosystem.
Examples of abiotic factors measured in the field study and lab were light levels, temperature,
moisture levels, and soil content (pH; potassium, nitrate, and phosphorus levels). Biotic factors,
on the other hand, is quite the opposite; they are the living components of an ecosystem. Biotic
factors measured in the lab included the abundance, diversity, and density of biomass.
Purpose:
To observe and explain the biotic and abiotic characteristics of a Reparian Woodland in
Hypotheses:
1. If the abiotic factors are helpful to organisms in an ecosystem, then these organisms will
2. If the organisms in an ecosystem are numerous and equal, then the ecosystem itself is
healthy.
Materials:
-Group Field Equipment -Group Lab Equipment
Procedures:
1) equipment setup:
1. The ziploc bags were weighed and labeled.
2. Four popsicle sticks were obtained and were formed into a square measuring 0.1 m2.
3. All Group Field Equipment, including the sampling quadrat square, was placed into large
bag.
2) data sheet:
3. A data sheet was created that recorded all the information from the field needed for the
lab. Include:
light levels (in foot candles)
temperature (in 0C)
1.0 meters above ground level
0.1 meters below ground level
at ground level
• soil contents:
• pH levels
• phosphate levels
• nitrate levels
• potassium levels
• abundance (number of species)
2. Also included were measurements while in the lab:
• total biomass (wet and dry)
• moisture level (soil and organic material)
• diversity levels (using the Simpson diversity Index)
3) Site Selection:
1. A 100 meter transect line that ran north/south was created using a tape measure and
compass.
2. Tape was used to mark the transect line (see figure 1)
Figure 1:
3. Within three points along the transect, three stage quadrats were then established,
measuring 10 m2.
4. The boundaries of the stage quadrats were marked by dividing tape.
5. Within each stage quadrat, smaller group quadrats, measuring 1 m2, were chosen at
random (ex: throw square over shoulder without looking, throw square with eyes closed,
etc.).
6. Four meter sticks created into a square marked a chosen group quadrat.
7. A sampling qaudrat was chosen at random by throwing the 10 cm2 popsicle square into
the group quadrat. (see figure 2)
4) Field Measurements:
• Sunlight
1. A light meter was obtained and should have been set to the “sun and high
intensity” setting.
2. You were to wait until the time is at 11:50 am, or solar noon at a randomly
chosen spot within your group quadrat, at ground level. (see figure 3)
3. You were then to read the measurements at 11:50 am at ground level and record
them in foot candles.
• Temperature:
• 1.0 meters above and at ground level:
1. A regular thermometer and meter stick was obtained.
2. Sampling site was then chosen at random and the meter stick was then
placed in the spot.(see figure 4):
3. The temperature was taken at solar noon, or 11:50 am, in degrees Celsius.
4. Temperatures were recorded onto data sheet.
• 0.1 meters below ground level :
1. A soil thermometer was used to take the temperature.
2. The soil thermometer spike was marked at 10 centimeters, or .01 meters,
with a sharpie.
3. Like the regular thermometer reading, the site was chosen at random
within the group quadrat.
4. The soil thermometer was then driven into the ground until the sharpie
mark wasn't visible.(see figure 5)
5. The temperature was taken at solar noon, or 11:50 am, in degrees Celsius.
6. Temperature was recorded onto data sheet.
• Soil Contents (pH, nitrate, phosphate, and potassium levels) :
1. A soil auger was obtained and used to take a soil sample within a random spot in
the group quadrat.
2. Four soil samples from the soil auger were obtained.
3. A chemical test set was then obtained.(see figure 6)
4. Tests were done for pH, phosphates, nitrates, and potassium levels in accordance
to the instructions provided inside the chemical test set.
5. The measurements were recorded.
6. The remaining soil sample was put into a pre-weighed ziploc bag
• Abundance of individuals:
1. Within the group quadrat, five sampling quadrats were created at random.
2. A count of every individual plant species was then done in each sampling quadrat.
3. The number of each individual plant species was also done.
4. Species classified into “A, B, C” categories (ex. Species A)
5. Recorded data onto data sheet.
6. Biomass from each sampling quadrat was collected. (see figure 7)
7. Two pre-weighed ziploc bags were used to collect the biomass.
5) Lab measurements (see figure 8) :
• Moisture level (soil and biomass)
1. The pre-weighed ziploc bags containing the soil sample and biomass was weighed
and the weights were recorded.
2. An aluminum pan was obtained and weighed; pan's weight was then marked.
3. The aluminum pan was then filled with the biomass and soil samples that were
inside the ziploc bags.
4. The aluminum pan were weighed again and marked.
5. An oven was pre-heated to 450 degrees Fahrenheit (232.22 degrees Celsius).
6. Aluminum pan was placed into oven for 24 hours.
7. After 24 hours, the aluminum pan with soil was reweighed and recorded.
8. The moisture level of the soil was obtained by subtracting the weight of the baked
soil(X) from the original weight(Y), then dividing it by the original weight(X):
X-Y
X x 100 = moisture level (in percent)
9. Repeated steps 1-8 for biomass.
• Total dry biomass:
1. An electronic balance was used to weigh the two biomass-filled ziploc bags.
2. The difference between the total weight of each bag and the weight of each
individual bag provided the weight of the total wet biomass in each bag.
3. An aluminum pan was obtained and weighed; pan's weight was then marked.
4. The aluminum pan was then filled with the biomass that was inside the ziploc
bags.
5. Aluminum pans were weighed again and marked.
6. An oven was pre-heated to 450 degrees Fahrenheit (232.22 degrees Celsius)
7. Aluminum pan placed into oven for 24 hours.
8. Aluminum pan was reweighed and recorded after 24 hours.
• Calculating Diversity Level
1. Diversity level was measured using the Simpson Reciprocal Index:
ni
A
ni = amount of an individual species
A = area the individual of species inhabits
• Relative Density (RDi)
1. Relative density found using the data gathered for finding the number of all
species present, group quadrat and overall using the equation:
Di
ΣDi
Di = density of a species
ΣDi = total density in a given area for all species
Data:
1) Observations
• Quadrat Coordinates
-Group Quadrat (4.5 Meters/2 Meters)
Figure 10: Stage and Group Quadrat coordinates
• Site Description
• 3 living trees in stage quadrat
• detrius material (plant leaves, twigs, grasses) all over ground
• partial sunlight due to tree canopy
• soil rich in detrius material
2) Data Tables and Graphs
• Table #1: Abiotic Factors:
Light Levels:
(taken at 11:50 1500 N/A N/A N/A
am) foot candles
Temperature: 1.0 meters above 0.1 meters below @ ground level:
(taken at 11:50 ground level: ground level: N/A
am) 25oC 17oC 25oC
Soil Composition pH: Phosphates: Nitrates: Potassium:
6.0 low low medium to low
A (Johnson
Grass)
B (Crab Grass)
C (Blackberry)
D (Valley Oak
Tree)
A (Johnson
Grass)
B (Crab Grass)
C (Blackberry)
D (Valley Oak
Tree)
3) Simpson Diversity Index:
• Table #5 & Math: Diversity Index (group quadrat)
97(96) 9,312
D = 7,218 = 7,218 = 1.29
185(184) 34,040
D = 19,070 = 19,070 = 1.78
4)Density and Relative Density (Di & RDi)
• Density (Di):
• Table #7 & Math: Density Data
Example:
• Species A (group quadrat & overall)
• Group Quadrat
850 Di
970 Di = .878 RDi
• Overall (Class Data)
22.66 Di
30.82 Di = .7352 RDi
• Table #9: Relative Density (group quadrat & overall class data)
The original purpose of this lab was to “To observe and explain the biotic and abiotic
hypotheses were that: 1. “If the abiotic factors are helpful to organisms in an ecosystem, then
these organisms will be healthy and numerous”; 2. “If the organisms in an ecosystem are
numerous and equal, then the ecosystem itself is healthy.”. This hypotheses were actually proven
while doing both the field study and the lab in a more negative way.
Solid pattens were found while calculating all the measurements. Both the class data and
the individual group quadrat data for diversity and relative density seemed to be quite similar.
Both showed that species A (Johnson Grass) took up a majority of the entire plant population
within both the group quadrat and the other 6 group quadrats of other groups. Diversity levels in
both the group data and the overall class data were very similar, both saying diversity levels in
the area are low. This may be connected to the fact that Johnson grass may be better suited to
grow in an environment with partial sunlight, due to the tree coverage, than the other species
present like blackberries, which were absent in our data and only 9 recorded as a whole. Johnson
grass was numerous in numbers, but compared to the other plant species in the area, it
dominated. Johnson grass took 87.8 % of the total count of species in the group data and 73.53
% in the overall data, showing a overwhelming dominance of that particular plant species in the
area. This led to a lower diversity index showing this site was actually very unhealthy. Soil
content also showed low nitrate, phosphate, and potassium levels, indicating soil with a low
amount of nutrients for a diverse amount of plants, possibly inhibiting different kinds of plant
species growing in the area . With both abiotic and biotic factors combined, the data showed that
have might been some room of errors and mistakes. For instance, while taking the measurements
for solar noon, the switch was mistakenly turned to “florescent” instead of the required “sun and
high intensity” setting. Conversion of the data was then required when we returned back to
school and did the lab measurements. Another possible mistake was when the biomass and soil
samples were collected. The soil sample, for example, was poor due to an object obstructing the
soil auger while it was in the ground. The collection of biomass may have also not have been all
that random, mainly due to us looking as we threw the sampling quadrat square onto the ground.
This factor could have affected the density, relative density, and diversity indexes of all the plant
species. It was also strange that the class data for collected plant species was just only 185, out of
6 separate groups. Our group collected 97, or roughly 52 % of all the recorded species population
count.
An obvious improvement that could be done, if we ever did a similar lab again, would be
to simply double-check the data and compare it to other groups in the same area. This way we
could see any inconsistencies with any of our data and act accordingly to fix it. Another
improvement that could be done is to repeat certain steps that may have been failures at first. For
example, if the soil sample was poor in quality, another one could have been done by simply
picking a different sampling quadrat at random. Lastly, one major improvement that needs to be
done in not just this lab but in any lab is to make sure each lab group does each step. The
inconsistency of the number of species counted could be avoided next time by assigning each
If further investigation was done in this same lab, I would suggest a few things to
challenge our current hypotheses. To diversify our data, we could go to Caswell at different
times of the year, comparing the data and concluding whether if abiotic and biotic factors are
consistent throughout the year. Another suggestion is to go to another test site, possibly ones
totally unrelated to riparian woodlands entirely to compare whether if all ecosystems share