User:Whitney Morales/Notebook/Biology 210 at AU

January 30, 2014 (Lab 3)

Water level in hay infusion culture slightly decreased, possibly due to evaporation. Smell wasn't as repugnant as it the week prior probably due to the lack of nutrients in the jar compared to their initial habitat. Water albeit its brownish tint appeared a little more translucent. The three niches as described in Lab 2, soil based bottom, liquid water middle and film like layer on surface, remained in tact with the exception that the film layer top disintegrated and therefore wasn't visible to the eye.

Microbiology and identifying Bacteria with DNA Continuing where we left off in lab 2 with spreading samples of our serial dilutions from the hay infusion cultures on petri dishes with nutrient agar and tetracycline, bacteria and possibly some fungi might have grown on the surfaces. Multiple bacteria that form together to make one bacterium form what is called a colony, which is very visible to the eye. Colony morphology is a characteristic for each species. We counted the total number of colonies on each plate where depending on the dilution. there would be a range of bacteria colonies on each plate.

Table 1 100-fold Serial Dilutions Results

Dilution (Plate Table) Agar Colonies Counted Conversion Factor Colonies/ml 〖10〗^(-3) Nutrient 200 X〖10〗^3 200.000 ml 〖10〗^(-5) Nutrient 6 X〖10〗^5 600,000 ml 〖10〗^(-7) Nutrient 0 X〖10〗^7 0 ml 〖10〗^(-9) Nutrient 0 X〖10〗^9 0 ml 〖10〗^(-3) Nutrient +Tet 107 X〖10〗^3 107,000 ml 〖10〗^(-5) Nutrient +Tet 2 X〖10〗^5 200,000 ml 〖10〗^(-7) Nutrient +Tet 0 X〖10〗^7 0 ml

- In the case of hay culture infusion bacteria, they seem to have been antibiotic resistant bacteria as they still formed colonies in the presence of tetracycline. Comparing the colonies size of that in nutrient agar with that in nutrient + tet agar, the colony size are close with few exceptions due to the dilution of those samples. In the most dilute samples 10^-9 (nut) and 10^-7 (nut + tet) there was no bacteria present even with the addition of tetracycline as it should. Tetracycline is supposed to work by preventing the growth and spread of bacteria; however in our case there was growth on those agar plates with tet indicating that our bacteria species in the prairie transect is resistant to it.

Bacteria Cell Morphology Observations - We observed both a native wet mount preparation and a gram stain of two well defined colonies taken from the nutrient agar plate and one taken from the tetracycline plate. We used the 10^-3 and 10^-5 nutrient agar and 10^-3 tetracycline plate to observe.

Wet mount preparation: 1)scoop a tiny amount of growth from the surface of the agar, and mix it into a drop of water on a slide. 2)place a cover slip over the drop before observed with microscope

Gram stain preparation: 1)

January 23, 2014 (Lab 2) As a preparation in identifying unknown organisms in our prairie transect, wet mounts were made with known organisms provided in lab where they were observed under the microscope. Using the Dichotomous Key, we were able to identify the known organisms according to observations made based on their size, shape, movement, and color.

After having a sample of our prairie transect in a jarred container with deer park water and powdered milk, the following: - semi- thick film on surface of water - some underlying mold-like substance underneath globs of soil that float on top of water's surface - greenery remained intact in the plant stem - 3-apparent niches

    1) a soil based bottom
    2)liquid water middle (water pretty transparent)
    3) a thin film layered surface

- water in the container again is transparent with a brownish tint - mildew surrounding the perimeter of the jar at the surface layer

Using the Dichotomous Key just as we did in preparation, we were able to identify unknown organisms in our hay infusion of prier transect. I specifically focused on the possible unknown organisms found at the bottom of the jar of our hay infusion. That area being a soil based niche in regards to the other niches mentioned earlier (Liquid water middle and thin film layered surface).

Organisms found in soil based bottom niche

1) Paramecium Vorticella (40x) - 6oc(ocular spaces)=15 um -small cell with elongated body -swims rapidly in a corkscrew fashion -body covered entirely with cilia

2)Colpidium (40x) - 10oc= 25 um -white/colorless -small body, oval shaped with small mouth -fast swimmer

3)Amoeba (40x) - 1oc= 2.5 um -small -creeps using false feet -single disk-shaped nucleus

4)Gonium (40x) -14oc=35 um -colony flat, disc-shaped, usually containing 16 cells -organ of locomotion is long whip-like flagella -white/colorless

- Amoeba, one of the four organisms found in the soil based niche of our hay infusion demonstrates the qualities of being "alive" as: it acquires energy from its by means of using its pseudopods, it's single-celled, processes information (genes), is cable of replicatingasexually (binary fission), and are a product of evolution

- Some selective pressures that may have affected the composition of our samples may be the lack of or increase in sunlight exposure, which in turn has an affect on how much/little energy is acquired by the organisms. As well as the lack/ increase of oxygen(air), where the organisms that are aerobic would have definitely been affected.

Preparing Serial Dilutions Procedure: 1) Four tubes were obtained each containing 10 mls of sterile broth and labeled 2,4,6,8 respectively. 2)Obtained four nutrient plates with agar labeled (10^-3, 10^-5, 10^-17, 10^-9)and three nutrient plates with agar and the addition of tetracycline labeled (10^-3 T, 10^-5 T, 10^-17T), *the T representing tetracycline 3)Swirled the hay infusion order to mix up all the organisms and then took 100 microliters using a micropipette from the mix and aseptically added it to the to mls of sterile vroth in test tube 2 (10^-2 dilution). The inoculated tube was then swirled 4)100 microliters of broth fro test tube 2 was then taken and inserted in test tube 4 (10^-4 dilution). 5)The process was then repeated to make 10^-6 and 10^-8 dilutions. 6) 100 microliters from test tube 2 were taken ans easptically placed on the surface of the nutrient agar plate (10^-3). the sample was then carefully spread on the surface. 7) The procedure (step 6) was repeated exactly with the nutrient agar plate containing tetracycline (10^-3 T). 8) The procedures taken place in steps 6 and 7 were then repeated using test tube 4 for the 10^5 plates, and test tube 6 for the 10^-7 plates. 9) Finally the agar plates were incubated at room temperature over the next week.

After snowfall that occurred on 1/21/14, our prairie transect was naturally covered with snow

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January 16, 2014 (Lab 1)

- Prior to defining our niche on campus, samples of green algae were looked at in determining the Volvecine Line - Compared the following green algae using microscopes: 1)Chlamydomonas 2)Gonium 3)Volvox - When comparing the evolutionary specialization of members of the volvocine line we looked at: number of cells, colony size, any functional specialization of cells, and reproductive specialization - classifying these cells according to their special functions (ie reproduction) provided insight on the evolution of green algae in the volvocine line by observing an differences or similarities between unicelluar algae such as Chlanydomonas and muticellular green algae such as Volvox.

Group 5: Prairie

Goal/objective: Analysis of 20 by 20 transect of prairie land

- Determining what what set of specific requirements collectively make the niche prairie land. - What interactions, if any, are there between the organisms within the community inhabiting prairie land? - what organisms are there to even begin with? Is there much biodiversity? - How does weather/ change in season affect the prairie transects topography and the organisms that reside there?

Materials Used: - 50 ml conical tube - 10 grams of sample of prairie transect - open jar for hay infusion culture - 0.1gram dried milk - 500 ml deer park water

Procedure: Exactly as followed from Lab 1:Biological Life at AU Step 1: describe the general characteristics of the prairie Step 2: take a sample of soil and vegetation from transect and put it in the 50 ml conical tube. Step 3: make a hay infusion culture

       - weigh 10 grams of soil sample, place in jar with 500 mls of deerpark water
       - add 0,1 gram dried milk into the jar containing at this point water, and soil sample
       - place jar cover on and mix up all the components for 10 seconds
       - remove the jar lid and let it sit

- The fact that the jar lid was not left on, poses the question of how oxygen will affect the hay infusion culture over a period of time. Will our initial prairie niche stay in tact? is there the possibility hat other niches may form? will there be any new organisms?

Characteristics of Prairie land

Abitotic Elements:concrete benches, walkway stones, metal lining surrounding soil, rocks pebbles

Biotic Elements:soil/fertilizer, bushes/shrubs, leaves, flowers, grass, birds (chicks)

- Area mostly consists of biotic elements with the implementation of man made factors such as the concrete benches and walkway stones (abiotic elements) - Due to the current winter season, the plot of land is essentially barren. Dead flowers on the bushes/shrubs, little to no grass directly on the soil. - On this particular day, there was a good amount of sunlight (source of energy for any potential growth of the biotic factors)