User:Lauren Lit/Notebook/Biology 210 at AU
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== ''' 2/16/14 - Lab 3:Microbiology and Identifying Bacteria with DNA ''' ==
Revision as of 15:40, 16 February 2014
2/16/14 - Lab 3:Microbiology and Identifying Bacteria with DNA
Materials and Methods:
1.Using the swirled up Hay infusion from Lab 1 and 2, 100 ml of the hay infusion culture was added to 10mls of nutrient broth into a tube. This made a 1:100 dilution or 10^-2. Next 100microliters from that tube was placed into 10mls of nutrient broth to make a dilution of 1:10,000 or 10^-4. Next 100microliters from tube 4 was placed into 10mls of nutrient broth to make a dilution of 1:1,000,000 or 10^-6. Next 100microliters from tube 6 was placed into 10mls of nutrient broth to make a dilution of 1:10,000,000 or 10^-8.
2. Four nutrient agar plates were labeled. 10^-3, 10^-5,10^-7,10^-9. Another set of Agar plates with tetracycline were labeled with the same labels.
2/9/14 - Lab 2: Identifying Algae and Protists
Introduction: Understanding and Identifying Unicellular Organisms, specifically Algae and Protists. Algae and Protists have very specialized characteristics. While they are different organisms they both come from a common ancestor and are both unicellular eukaryote.
Materials and Methods: - A wet mount was created using 8 different known organisms --> A drop of the specimen solution containing various organisms were placed on the slide and covered with a coverslip -The wet mount and specimens were viewed under tthe microscope -Once an organism was located it was characterized using a Dichotomous Key
Observations and Data:
1. Euglena - 20-25 micrometers - multicellular 2. Chlamydomonas - 10 micrometers - multicellular 3. Paramecium Caudatum - 180 micrometers
-Smalls musty -mold is growing on the sides -Leaves and plants are on the top layer -Algae is growing on the very bottom of the jar -algae coating on the top.
-Top of Jar: Brown Algae
-Immobile -10 micrometers in length
-Bottom of Jar:
-Spirostimum -brown algae -Colpidium - 62 micrometers
Conclusions: The hay infusion is expected to grow more mold agae and other organisms. The smell is expected to get progressively worse. The niches are expected to become more specialized and more organisms with more distinct roles will develop. LL
1/31/14 - Lab 1: Biological Life at AU
The objective of Lab 1 Proceedure 1 is to understand Natural Selection. To get an understanding of natural selection 3 members of the volvacine line were observed under the microscope. They included Chlamydomonas, gonium, and volvox.
Chlamydomonas Number of cells: 1 Colony Size: 23 Functional specialization Cells: Flagellum for movement and chloroplast
Gonium Number of cells: 75-100 Colony Size: 3 Functional specialization Cells: Flagellum
Vovox Number of cells: about 500 Colony Size: 1
Picture to be added here.
The objective of part 2 is to understand the biotic and abiotic aspects of a niche at American University outside the Katzen Arts Center.
Abiotic Factors Pebbles, large rocks, little rocks dead leaves wood chips bricks soil
Biotic Factors Cotton Tails Red Bushs Grass Weeds
Picture to be added here.
In the future I will be going back to the niche to observe any changes that may have occured to the factors, individually and how they interact together. LL.
Good start. Could be improved with more substance. Address red text from protocol include detailed descriptions, analysis and conclusions. For more instructions see TA notebook. SK
1/26/14 - Lauren Lit's Lab Notebook - Bio210. LL