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draft evo HW

Submitted by jkswanson on Sun, 12/09/2018 - 15:18

Part A: If the apple maggot flies preference for the apples so much that it is equal between the two trees, then the incipient species will begin to interbreed because there is now no reason for them to not mate, because the previous prezygotic barrier is now abolished.  They will no longer remain separated, they will over time either grow into one species as they continue to interbreed, or another barrier will be formed and reinforced by the apple maggots not having a preference and the hawthorne prefereing hawthorne. This allows for the separtion back into the two trees they prefer.

 

Part B: The two species will definitely diverge as they have a reproductive post-zygotic barrier that is causing hybrid offspring to be sterile.  This will not allow the two species to merge in the long run. This is because the hybrid offspring cannot reproduce leading to a very short lived new hybrid species that is merged from the two.  The two species with the mutations listed will diverge as they are unable to produce a viable merged hybrid off spring. If new mutations occur it could either reinforce this seperation or it could lead to a merging over a long period of time.

 
 

reflection bio 551

Submitted by kruzzoli on Sat, 12/08/2018 - 14:46

This course involved a lot of group work and outside class involvement. Most of my classes before did not involve forming groups and all the work was individual and I have had very few research projects. I have improved as a student because I had to significantly improve my study habits in order to do well in this class. I had to work on bettering my study habits and focus on doing a lot of outside class work. I saw improvement in myself as a student throughout this semester in the fact that I improved greatly on the second exam and  I started to understand the material a lot more. Towards the end I was allowing myself time to actually go through class notes and do the readings which is not how I started the semester. I greatly improved my time management skills and I was better able to figure out what work I needed to do during a certain week and I was able to make a plan to effectively get all the work done in. Having to rely on myself to learn a lot of the material improved my skills as a student because I started to be better at finishing assignments ahead of time and I did the readings throughout the weeks instead of ignoring them. I also improved as a team member because I had to not only do well to account for myself, but to account for my partners as well. This meant I did not have the option of slacking. I also used a lot more software this semester that I have never used before such as Raven and JWatcher. Learning how to use these softwares gave me a wider range of professional skills and will also help me in learning how use new software in the future because I know I will have to read manuals and practice in order to properly utilize a new software given to me.

 

reflection bio 551

Submitted by kruzzoli on Sat, 12/08/2018 - 09:20

This was the first specified biology class that I have taken that was more in depth than just “evolution” or “ecology”. I had a lot of prior knowledge about evolution and some animal behavior in terms of environment from other biology classes, but I learned a lot more in depth examples of how to apply evolutionary concepts to the roles of animals. I never looked deeply into animal communication before this class but now I notice a lot more animal interactions and I find myself trying to reason certain behaviors that I observe. When I went home throughout this semester I noticed how my cat interacts with us more and that there are certain things he does that will always be indicators of something he wants. When he wants to be fed he will nudge me and meow, so I know he’s hungry. When he wants to be let outside, instead of nudging me he’ll walk around my feet until I follow him to the door. I’ve noticed that there are different signals for different reasons, which is something I did not think about prior to this course. We also recently got a new cat and I’ve noticed that my cat has started to act differently when in the presence of the new cat. Now,  I try to observe behaviors and think of reasons that could explain a certain meow or tail movement and then observe to see if I can reason it. This is a new behavior of mine that I developed from this class because I did not think about my cat having different signals and different ways to communicate before this class. From this class I have become more curious about how animals interact with one another and I observe my pets a lot more than I would have without taking this course.

 

Sphyraenidae

Submitted by mtracy on Sat, 12/08/2018 - 00:03

The family Sphyraenidae contains the barracudas. This family contains only 1 genus and 29 species. Originally barracudas were considering to be in the genus of esox, though it is now in sphyarena. Small barracuda tend to congregate in schools, however when they become large enough the become solitary fishes. Generally these fish get up to 1.5m in length. Barracudas are specialized to be fast start, rather than distance swimmers. Thus, their fins are located more caudally than rostralling. Ciguatera posioning tends to build up in their tissues, and when eaten it may cause the indavudal to become sick. This is passed from microorgansims which small fish eat, and then the barracuda will eat the small fish. Over time bioaccumulation occurs and the posion builds in the barracudas tissue. One hypothesis about why the poison does not effect the fish, but effects a human that eats the fish is that, the posion itself is in a tissue not being broken down (ie: its muscles, unless under starvation conditions). However when eaten, this tissue is broken down, thus releasing the posion.

part of intro draft

Submitted by msalvucci on Fri, 12/07/2018 - 13:10

For the control and cool conditions, the spiders were placed in a plastic cup which was enclosed in a Styrofoam box; the cool condition had a layer of ice underneath the plastic cup with a cardboard barrier to achieve the cool temperature. The spiders in the heated condition were kept in plastic cups that were placed under a heat lamp. Each condition was monitored over a four-day period to ensure the temperatures were constant. Following the four days, the spider contraptions were weighed to get final measurements of the spider web densities.

 

abstract draft

Submitted by msalvucci on Fri, 12/07/2018 - 13:07

The aim of this experiment was to test the effects of temperature on spider web production for the species Pholcus phalangioides. We had hypothesized that the warmer the temperature a spider occupied, the denser the web it would create. During this experiment, spiders were placed in 3 environments set at different temperatures. The control enclosure was kept at 19℃, the warm enclosure was kept at 26℃, and a cool enclosure was kept at 11℃. Two spiders for each condition were observed for four days; the spider web enclosures were weighed on the final day in order to measure spider web production. Following the data collection and analysis, the results indicated denser web production in the warm enclosure compared to cool and control conditions.

 

my thoughts on paper draft

Submitted by msalvucci on Fri, 12/07/2018 - 13:02

Overall, I found this research project highly conclusive regarding the function of the V1 nerve in reed warblers. I admire the team’s strong efforts in keeping this experiment controlled. For example, the scientists did not know which bird population they were analyzing in order to keep the results unbiased. The team also used a sham-surgery in order to prevent the possibility of there being any skewed data due to surgical setbacks in one group of birds. I find this tactic reasonable and necessary to control the variables in this project, but also a bit unethical as the excess surgeries may have been prevented. This article creates a strong foundation for research regarding how exactly birds utilize map information transmitted through the V1 nerve.

Draft

Submitted by cgualtieri on Fri, 12/07/2018 - 12:48

In conclusion, this experiment was able to obtain CFU/ml values for one dilution of E.

coli. There were approximately 8.9x104 CFU/ml of E. coli in one ml of the 10-2 dilution. This

number was obtained using The 10-1 dilution produced to many colonies to count, making

obtaining a CFU/ml value impossible. The other dilutions did not produce more than 30 colonies,

possibly due to a mistake in the dilution process. Another explanation for this could be that when

the dilutions were prepared, the aliquots may have had a lower CFU/ml than other aliquots by

random chance. This experiment showed that using viable counts is a reliable and effective way

to count the number of bacteria in an inoculated sample.

Draft

Submitted by cgualtieri on Fri, 12/07/2018 - 12:47

In the viable counts portion of this lab we used viable counts to observe the number of cells

present on Petri dishes inoculated with decreasing dilutions of E. coli. The E. coli were diluted in

sterile saline and spread at dilutions of 10-1, 10-2, 10-3, 10-4, 10-5, 10-6, 10-7, and 10-8. Dilution and

viable counts is a useful technique because it allows live cells to be counted, eliminating the

variable of dead cells contributing to a cell count. Colony forming units per ml (CFU/ml) were

calculated to determine the number of cells growing at each dilution. I expected the highest

CFU/ml would be from dilutions containing a higher concentration of cells, and the lowest from

the more dilute samples. . I expected that as the solutions increased in dilution, , the CFU/ml

would decrease due to less E. coli being transferred and inoculated onto the Petri dish.

Draft

Submitted by cgualtieri on Fri, 12/07/2018 - 12:46

The results of this experiment showed that E. coli grown at 37°C had the highest growth

rate (k), at 1.92 generations/hour and lowest generation time (g) at 31.4 minutes. The E. coli

grown at 27°C had a growth rate of 1.02 generations/hour and a generation time of 59.3 minutes.

At 45°C, the growth rate of E. coli was 0.9 generations/hour and the generation time was 66.6

minutes. The E. coli grown at 55°C did not grow sufficiently enough to calculate k and g values,

due to the high temperatures causing the cells to lyse.

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