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| | #1 (permalink) |
| New Member Join Date: Jun 2005
Posts: 9
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28 Dec 2005, 12:24 PM ![]() | Biology Exam You can hide this advertisement by registering. An absolute killer of an exam. |
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| | #2 (permalink) |
| Senior Member | I found it easy. Haha, I just won $20 when I predicted the Homo Florensiesis question was bound to come out. What did you guys put down for the UV mutation and DNA repair graph question? I decided that the greatest UV damage would be at the intersection between those two values, which was if I remember correctly 270nm Last edited by anarchron; 31 Oct 2005 at 11:24 AM. |
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| | #3 (permalink) |
| Junior Member | It was easier than Exam 1 - there were less difficult conclusions to write. The question relating to the patient with tuberculosis - I wrote out the evolution of the organism into an antibiotic strain, then read that the tuberculosis returned *after* the antibiotic course had finished. Overall I was surpised on how little there was on (In-depth descriptions of) *PCR *Linkage *Protein Synthesis and *Meiosis and Mitosis No real 'NFI' questions for me though, just some questions took a fair amount of time to complete - probably spent too much time on this year's fairly easy Multiple Choice questions. Last edited by rlaws06; 31 Oct 2005 at 11:27 AM. |
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| Senior Member | Quote:
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| | #9 (permalink) | |
| Junior Member | Quote:
Maybe the antibiotic-resistant strain of bacteria were selected for in the prescense of antibiotics, but their resistance may have caused them to be less virulent. When the antibiotics stopped, the resistant bacteria may have had a selective disadvantage, and the possibly more virulent anti-biotic sensitive form of the bacteria returned (assuming some organisms managed to survive the antibiotics somehow) to cause the symptoms which were not caused by antibiotic-resistant bacteria. With that said, there were 3 marks available, so I just went through the standard natural selection evolution template RE: Antibiotic resistance. | |
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| | #10 (permalink) |
| Senior Member | Yep well, the question was regarding how the bacteria managed to come back after the course of the antibiotics. The antibiotics was meant to finish off all the bacteria, but variation existed. Then there was a differentiation of survival with all the non-resistant bacteria being wiped off. The surviving ones then manage to multiply etc etc. I don't think it really mattered that they bacteria reappeared when the antibiotics was stopped, it was how they survived it. |
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| | #11 (permalink) |
| Junior Member | Cool - what did everyone put down for the experiment RE: Stem colours (Wild Type and V---- something) and Cross 3 and 4's genotypes? I was running low on time when I got around to finishing that question, so I wrote that Cross 3 and Cross 4 offspring should both be tested at 20 and 37 degrees, and if they produce the same offspring ratios in each, then they (the parents of Cross 3 and 4) are the same genotype I'm not sure if that was correct, or if you should put both cross parents through a test cross to determine their genetype |
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| | #12 (permalink) |
| Senior Member HSC: 2006 Gender: Male Location: Victoria
Join Date: Oct 2004
Posts: 211
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20 Feb 2007, 4:53 PM ![]() | I had test cross at both 20C and 37C from memory, although not entirely sure. What did you have as a control for this?
__________________ Class of 2006 VCE 2004-2006 |
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| | #13 (permalink) |
| Senior Member | I had: Isolate those two groups of parents in a controlled environment at 37 degrees. Redo the cross. If the cross produced 3:1 ratio then they have the same genotype. If they produced all whatever the phenotype was, then they are both homozygous for that trait. |
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| | #15 (permalink) | |
| New Member HSC: N/A Gender: Male
Join Date: Oct 2005
Posts: 8
Last Activity:
15 Jun 2007, 11:36 PM ![]() | Quote:
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