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'''1/28/15 ''Lab 3: Microbiology and Identifying Bacteria with DNA Sequences''
'''
''I. Purpose:'' 
''II. Materials and Methods:''
''III. Data and Observations:''
''IV. Conclusions:''
'''1/21/15 ''Lab 2: Identifying Algae and Protists''
'''1/21/15 ''Lab 2: Identifying Algae and Protists''
'''
'''


''I. Purpose:''
''I. Purpose:'' The purpose of this lab is to examine and understand the characteristics of algae and protists from my transect.  I hypothesize the transect have copious amounts of bacteria living in the niche.  If water is added to the gathered materials and is allowed to incubate, then the bacteria from the niche (in the soil) will grow in the new ecosystem created.
 
 
 
''II. Materials and Methods:''
 
· Make a wet mount from the niche at the top of the jar and make a wet mount from the niche at the bottom of the jar
 
· View at 4x, 10x, and 40x.
 
· Make observations of at least 3 different organisms from each niche
 
· Use a dichotomous key to identify the organisms
 
 
''III. Data and Observations:''  My Hay Infusion Culture has a foul smell, almost like rotten garbage.  The top of the jar has a layer of film, maybe mold, with a gray/green color.  The water is yellow/brown tinged.  The bottom of the jar has a thin layer of dirt on it.
 
Figure 1. [[Image:Topviewgroup3.JPG]]      Figure 2. [[Image:Sideviewgroup3.JPG]]
 
Figure 1. is the top view of my Hay Infusion Culture for Group 3
 
Figure 2. is the side view of my Hay Infusion Culture for Group 3
 
 
The organisms below were found at the top of the jar niche.
 
Figure 1. [[Image:Organism_1_AB.jpg]]
 
Figure 1. is of Organism 1.  In lab I established this organism to be a Didinium Cyst, however after further research, that is not what Organism 1 is.  At the moment, Organism 1 is still unknown.  It is ~30μm , almost circular with two indentations at the top and bottom of the cell, little oval specks inside moving, and colorless.
 
Figure 2. [[Image:Organism2.jpg]]
 
Figure 2. is of Organism 2.  In lab, I established this organism to be Colpidium.  The organism varied in size, one I measured was ~50μm, packman-like face, spins, type of motility undetected, and colorless.
 
Figure 3. [[Image:Organism3.jpg]]
 
Figure 3. is of Organism 3.  In lab, I established this organism to be Euglena, however after extensive google image searches, I believe it to be Fusarium graminearum.  It is ~50μm, peapod/canoe shaped, long, thin, some are segmented inside, and colorless.
 
Figure 4. [[Image:Organism4.jpg]]
 
Figure 4. is of Organism 4.  In lab, I could not determine the genus and species.  It is ~75μm, disc-like, pods in the middle and colorless.
 
The organisms below were found at the bottom of the jar niche.
 
Figure 5. [[Image:Organism5.PNG‎]]
 
Figure 5. is of Organism 5.  In lab, my lab partners could not determine the organism.  It is colorless at ~60μm.


''II. Materials and Methods''
Figure 6. [[Image:Organism6.JPG‎]]


''III. Data and Observations''
Figure 6. is of Organism 6.  In lab, my lab partners could not determine the organism.  It is colorless, and kidney bean shaped.


''IV. Conclusions''
Figure 7. [[Image:Organism7.JPG]]
 
Figure 7. is of Organism 7.  In lab, my lab partners determined this to be algae.
 
 
''IV. Conclusions:'' After observing and identifying 6 or more organisms residing in the two niches of my Hay Infusion Culture, I have determined my hypothesis to be true.  There were multiple organisms growing in my group's Hay Infusion Culture that we observed and we were able to identify a few of them. 
 
 
--[[User:Alison D. Bunnen|Alison D. Bunnen]] 18:33, 29 January 2015 (EST)




'''1/14/15 ''Lab 1:'' ''Biological Life at AU'''''
'''1/14/15 ''Lab 1:'' ''Biological Life at AU'''''


''I. Purpose:'' The purpose of today's lab was to observe and record characteristics of an assigned transect. My assigned transect was group 3: Tall Bushes. I recorded macroscopic observations of abiotic and biotic components in my transectThen my group made a Hay Infusion Culture from materials gathered from our niche.
''I. Purpose:'' The purpose of today's lab was to observe and record characteristics of an assigned transect. We took samples from our niche to create a Hay Infusion Culture. I hypothesize the transect have copious amounts of bacteria living in the nicheIf water is added to the gathered materials and is allowed to incubate, then the bacteria from the niche (in the soil) will grow in the new ecosystem created.
 


''II. Materials and Methods:''  
''II. Materials and Methods:''  
Line 31: Line 99:
· Place the jar in designated lab section area with the jar labeled and lid off
· Place the jar in designated lab section area with the jar labeled and lid off


''III. Data and Observations:''  
 
''III. Data and Observations:'' My assigned transect was group 3: Tall Bushes.  I recorded macroscopic observations of abiotic and biotic components in my transect.  Then my group made a Hay Infusion Culture from materials gathered from our niche.  The Hay Infusion Culture was a mix of ~10 grams of soil and vegetation from my transect, 500 mL of deerpark water, and 0.1 gm of dried milk.


The abiotic components inside the transect included:
The abiotic components inside the transect included:
Line 46: Line 115:


· Rocks
· Rocks


The biotic components inside the transect included:  
The biotic components inside the transect included:  
Line 56: Line 124:
· Bushes
· Bushes


''IV. Conclusions''
Figure 1. [[Image:Aerial-view_diagram111.png]]


Figure 2. [[Image:Niche_Group_3_pic_111.png]]


Figure 3. [[Image:Niche_Group_3_pic_2.png‎]]


[[Image:Niche Group 3 pic 2.png]]
Figure 1. is an aerial-view diagram of my transect labeled with it's abiotic and biotic components.
[[Image:Niche Group 3 pic 1.png]]


This transect is located north of the Battelle-Tompkins at American University. This is an aerial-view diagram of my transect labeled with it's abiotic and biotic components:
Figure 2. is a satellite view of Group 3's transect.


[[Image:Aerial-view_diagram.png‎]]
Figure 3. is a map view of Group 3's transect.


''IV. Conclusions:''  There are abiotic and biotic components in Group 3's transect.  I will not know if my hypothesis is correct until further examination of the incubated Hay Infusion Culture is done.




--[[User:Alison D. Bunnen|Alison D. Bunnen]] 22:24, 26 January 2015 (EST)
--[[User:Alison D. Bunnen|Alison D. Bunnen]] 22:24, 26 January 2015 (EST)
'''References'''
Bentley, M., Walters-Conte, K., Zeller, N. 2015. A Laboratory Manual to Accompany General Biology II. American University Department of Biology: Washington, DC. 19-23.

Revision as of 19:36, 29 January 2015

1/28/15 Lab 3: Microbiology and Identifying Bacteria with DNA Sequences

I. Purpose:

II. Materials and Methods:

III. Data and Observations:

IV. Conclusions:


1/21/15 Lab 2: Identifying Algae and Protists

I. Purpose: The purpose of this lab is to examine and understand the characteristics of algae and protists from my transect. I hypothesize the transect have copious amounts of bacteria living in the niche. If water is added to the gathered materials and is allowed to incubate, then the bacteria from the niche (in the soil) will grow in the new ecosystem created.


II. Materials and Methods:

· Make a wet mount from the niche at the top of the jar and make a wet mount from the niche at the bottom of the jar

· View at 4x, 10x, and 40x.

· Make observations of at least 3 different organisms from each niche

· Use a dichotomous key to identify the organisms


III. Data and Observations: My Hay Infusion Culture has a foul smell, almost like rotten garbage. The top of the jar has a layer of film, maybe mold, with a gray/green color. The water is yellow/brown tinged. The bottom of the jar has a thin layer of dirt on it.

Figure 1. Figure 2.

Figure 1. is the top view of my Hay Infusion Culture for Group 3

Figure 2. is the side view of my Hay Infusion Culture for Group 3


The organisms below were found at the top of the jar niche.

Figure 1.

Figure 1. is of Organism 1. In lab I established this organism to be a Didinium Cyst, however after further research, that is not what Organism 1 is. At the moment, Organism 1 is still unknown. It is ~30μm , almost circular with two indentations at the top and bottom of the cell, little oval specks inside moving, and colorless.

Figure 2.

Figure 2. is of Organism 2. In lab, I established this organism to be Colpidium. The organism varied in size, one I measured was ~50μm, packman-like face, spins, type of motility undetected, and colorless.

Figure 3.

Figure 3. is of Organism 3. In lab, I established this organism to be Euglena, however after extensive google image searches, I believe it to be Fusarium graminearum. It is ~50μm, peapod/canoe shaped, long, thin, some are segmented inside, and colorless.

Figure 4.

Figure 4. is of Organism 4. In lab, I could not determine the genus and species. It is ~75μm, disc-like, pods in the middle and colorless.

The organisms below were found at the bottom of the jar niche.

Figure 5.

Figure 5. is of Organism 5. In lab, my lab partners could not determine the organism. It is colorless at ~60μm.

Figure 6.

Figure 6. is of Organism 6. In lab, my lab partners could not determine the organism. It is colorless, and kidney bean shaped.

Figure 7.

Figure 7. is of Organism 7. In lab, my lab partners determined this to be algae.


IV. Conclusions: After observing and identifying 6 or more organisms residing in the two niches of my Hay Infusion Culture, I have determined my hypothesis to be true. There were multiple organisms growing in my group's Hay Infusion Culture that we observed and we were able to identify a few of them.


--Alison D. Bunnen 18:33, 29 January 2015 (EST)


1/14/15 Lab 1: Biological Life at AU

I. Purpose: The purpose of today's lab was to observe and record characteristics of an assigned transect. We took samples from our niche to create a Hay Infusion Culture. I hypothesize the transect have copious amounts of bacteria living in the niche. If water is added to the gathered materials and is allowed to incubate, then the bacteria from the niche (in the soil) will grow in the new ecosystem created.


II. Materials and Methods:

· 20 x 20 meter transect to study

· Use a sterile 50 mL conical tube to gather materials such as soil and vegetation from transect

· Place 10-12 grams of gathered materials into a large jar

· Add 500 mLs of deerpark water to the jar

· Add 0.1 gm of dried milk into the jar and screw on lid

· Mix contents gently for 10 seconds

· Place the jar in designated lab section area with the jar labeled and lid off


III. Data and Observations: My assigned transect was group 3: Tall Bushes. I recorded macroscopic observations of abiotic and biotic components in my transect. Then my group made a Hay Infusion Culture from materials gathered from our niche. The Hay Infusion Culture was a mix of ~10 grams of soil and vegetation from my transect, 500 mL of deerpark water, and 0.1 gm of dried milk.

The abiotic components inside the transect included:

· Light

· Water/snow

· Concrete

· A metal lamp post

· Dirt

· Rocks

The biotic components inside the transect included:

· Grass

· Shrub

· Bushes

Figure 1.

Figure 2.

Figure 3.

Figure 1. is an aerial-view diagram of my transect labeled with it's abiotic and biotic components.

Figure 2. is a satellite view of Group 3's transect.

Figure 3. is a map view of Group 3's transect.


IV. Conclusions: There are abiotic and biotic components in Group 3's transect. I will not know if my hypothesis is correct until further examination of the incubated Hay Infusion Culture is done.


--Alison D. Bunnen 22:24, 26 January 2015 (EST)


References

Bentley, M., Walters-Conte, K., Zeller, N. 2015. A Laboratory Manual to Accompany General Biology II. American University Department of Biology: Washington, DC. 19-23.