Seneca Lake Lab Report
Introduction: Seneca Lake is approximately 3.7 miles at the widest
point and 630 feet at the deepest point. According to the packet the lake
can get as warm as 72 degrees F and as cold as 38 degrees F. The lake
contains several types of macro invertebrate that live all over the lake such
as stonefly
larva, crayfish, amphipod, and mayfly larva. On a website it is shown that
areas with lower depths result in higher amounts of macro invertebrate
variations and levels. Seneca Lake is one of the eleven Finger Lakes and
is the largest lake when it comes to total area and it is also the
deepest of the eleven Finger Lakes.
Research
Question: How does water depth and water
temperature affect the amount and diversity of zooplankton (or macro invertebrate) in the water?
Hypothesis: I believe that the deeper the portion of the lake is the more
diverse and the higher of a quantity there will be in that section,
and as the temperature increases so does the amount and variety of macro
invertebrate will increase as well. This is supported by the website I
mentioned earlier, it states that as the site gets deeper the variety of
macro invertebrate and the quantity of the macro-invertebrate increase as well.
Variable
Identification:
Independent Variables
|
Dependent Variable
|
Spots of sampling
|
Macro invertebrate levels
|
Relative depth of water
|
Temperature of water
|
Experimental
Setup: In order to keep these sample locations constant I will use the
same boat and use the same procedure for each location in order to keep my
findings constant. To limit variability I will use the same net to collect the
macro invertebrate and the same thermometer to collect data from each of the
three locations.
Procedure:
1. Go to a very shallow depth location on Seneca Lake.
2. Measure for temperature at this location.
3. In order to collect macro invertebrate information you will first need to make sure you have a firm grip on the nets rope.
4. You MUST make sure the clasp at the bottom of the net is closed.
5. Next lower the net over the side of the boat and walk from stern to bow, back and forth, slowly.
6. Bring the net back up and wash the remaining plankton into a cup at the end of the net.
7. Take plankton back to lab for analysis.
8. Next go to a medium depth in the lake and repeat steps 2-7.
9. Next go to deeper portion of the lake and repeat steps 2-7.
2. Measure for temperature at this location.
3. In order to collect macro invertebrate information you will first need to make sure you have a firm grip on the nets rope.
4. You MUST make sure the clasp at the bottom of the net is closed.
5. Next lower the net over the side of the boat and walk from stern to bow, back and forth, slowly.
6. Bring the net back up and wash the remaining plankton into a cup at the end of the net.
7. Take plankton back to lab for analysis.
8. Next go to a medium depth in the lake and repeat steps 2-7.
9. Next go to deeper portion of the lake and repeat steps 2-7.
Data: Fortunately
for us the weather the day of the sampling was fair, the temperature for all
locations that day were pretty average for that time of year with a slight breeze in the air. All locations
were within a degree of each other and there were no significant changes (other
than the depth) between each location. As for the depths we recorded the
deepest we got our dredge samples was 62.6m and the shallowest depth we got was
7.5m. Our dredge sample contained a lot of mussels but the majority of the
sample was sediments including sand, silt and clay.
Sample
1 A
|
Sample
1 P
|
Sample 2 A
|
Sample
2 P
|
Sample
3 A
|
Sample
3 P
|
|
Latitude
|
N
42D 49.9’
|
N
42D 49.92’
|
N
42D 51’
|
N
42D 52’
|
N
42D 52’
|
N
42D 52’
|
Longitude
|
W
76D 58’
|
W
76D 57.49’
|
W
76D 58’
|
W
76D 58’
|
W
76D 58’
|
W
76D 58’
|
Sample
temp.
|
13D
Celsius
|
7D
Celsius
|
13D
Celsius
|
14D
Celsius
|
13D
Celsius
|
13D
Celsius
|
Sample
depth
|
38.9m
|
54m
|
10m
|
10m
|
0m
|
0m
|
P.H.
|
7.3
|
7.4
|
7.4
|
7.4
|
7.5
|
7.3
|
Chloride
|
200
ppm
|
180
ppm
|
300
ppm
|
143
ppm
|
200
ppm
|
140
ppm
|
Dissolved
Oxygen
|
30
ppm
|
10.4
ppm
|
6
ppm
|
10
ppm
|
10
ppm
|
10
ppm
|
Bold
sample location on bottom chart means zebra mussels are present
Sample
|
Species
total
|
1
|
2
|
3
|
4
|
5
|
6
|
7
|
8
|
1A
|
9
|
2
|
2
|
2
|
3
|
0
|
0
|
0
|
0
|
1P
|
21
|
1
|
1
|
1
|
16
|
2
|
0
|
0
|
0
|
2A
|
15
|
2
|
2
|
1
|
7
|
2
|
1
|
0
|
0
|
2P
|
17
|
1
|
1
|
1
|
2
|
5
|
2
|
4
|
1
|
3A
|
9
|
1
|
1
|
3
|
1
|
1
|
1
|
1
|
0
|
3P
|
19
|
6
|
1
|
7
|
3
|
1
|
1
|
0
|
0
|
Discussion:
Compared to the logger data graphic my
data is fairly similar in multiple of the categories. One of these similar
categories includes the temperature, according to both my data and the data
logger graphic as you get farther down in the lake the temperature drops, the
is especially at approximately 32m down. Another category we have in common is
dissolved oxygen, according to the graphic and my data the deeper you get in
the lake the less dissolved oxygen there is, the drop happens at around 45m
according to the data logger graphic.
Evaluation: To
complete my report I would need the names and exact numbers of the macro invertebrate
in the water. I would also need to have more trials because the numbers of
macro invertebrate were insufficient for reliable analysis. Based on my data my hypothesis was not correct because the deeper the lake got the less macro invertebrate were present. In this experiment
human error was a prevalent force throughout the course. This experiment could
have been improved if we got more time to get more precise numbers. Our experiment
also needed to be better explained and have more precise directions. These are
the weaknesses our class faced during this experiment.
Conclusion:
During this experiment I learned that
as depth of almost any body of water is decreased the temperature and dissolved
oxygen are decreased as well, I got this from my data as well as the data
logger graphic. Along with these things I learned I believe with more time I could
have gotten a lot experience and learned a lot more. Also if we received more
precise directions I feel we would not need more time, but if not more time
would be necessary to get the best experience. Overall this experiment was a
lot of fun and even though it was fun it didn’t mean we didn’t learn anything making
one of the best labs I’ve ever done.
References: "Lake County Water Atlas." Seneca, Lake: Ecology.
N.p., n.d. Web. 29 Oct. 2015.
"Does Water Level Affect Benthic Macro-invertebrates of a Marginal Lake in a Tropical River-reservoir Transition Zone?" Does Water Level Affect Benthic Macro-invertebrates of a Marginal Lake in a Tropical River-reservoir Transition Zone? N.p., n.d. Web. 29 Oct. 2015.
"Seneca Lake." - A Guide to Hotels, Bed and Breakfasts in the Finger Lakes. N.p., n.d. Web. 29 Oct. 2015.
"Does Water Level Affect Benthic Macro-invertebrates of a Marginal Lake in a Tropical River-reservoir Transition Zone?" Does Water Level Affect Benthic Macro-invertebrates of a Marginal Lake in a Tropical River-reservoir Transition Zone? N.p., n.d. Web. 29 Oct. 2015.
"Seneca Lake." - A Guide to Hotels, Bed and Breakfasts in the Finger Lakes. N.p., n.d. Web. 29 Oct. 2015.


i claim this post
ReplyDeleteComplete. All requirements of the assignment are met. Something that could have made your lab stronger would be to include the Simpson's diversity index value for each sample of plankton.
ReplyDeleteQuestion: What are the diversity values for each sample of plankton?
Overall, nice work. You were definitely creative with your graphs, but the units were a little confusing, and I don't think it makes sense to use the average sample depth (for comparison between AM and PM collection) instead of the 3 individual depths for each trip.
ReplyDelete