Hello lovelyherring
RNA Polymerase; it has a built-in Helicase-like component. Whereas DNA Helicase is typically present in DNA replication.
Hope this helps
Hello lovelyherring
RNA Polymerase; it has a built-in Helicase-like component. Whereas DNA Helicase is typically present in DNA replication.
Hope this helps
Hi bioho4!
Most of diagram was irrelevant, and it included everything you needed to answer the question - given that you knew your standard bio content. The two, and only, pieces of information that was needed was that:
Allow me to elaborate;
Given that the biochemical pathway represented was the light-dependent stage of photosynthesis this narrows down all possible inputs to be Water, ADP, and NADP+; and all outputs to be Oxygen, ATP, and NADPH.
Looking at the boxes and arrows, we know that the question asks for the identity of one input (W), and two outputs (V and Z).
To summarise those two points, the answer we are looking for must be a combination of one input and two outputs; that must belong to the light-dependent stage of photosynthesis.
...
Ok, now, with that knowledge lets take a look at all four options;
Option A - 'Water, ATP and NADP+' - We have two inputs and one output here, so that doesn't work.
Option B - 'Oxygen, ATP and NADPH' - We have no inputs and three outputs, this does not work either.
Option C - 'Oxygen, ADP and NADPH' - Ah, one input and two outputs, all of the light-dependent stage of photosynthesis .
Option D - 'Carbon Dioxide, ADP and NADP+' - Carbon Dioxide is not apart of the light-dependent stage of photosynthesis, so we need not bother with this option at all.
...
So, in conclusion, Option C was the correct answer, and you didn't need detailed knowledge of the light-dependent stage either.
As the maths shill in me would say, Q.E.D.
...
This was a fairly lengthy post for a MCQ, but I think it was an important post to make.
When you do VCE Biology, you can have faith in that no non-SD content will be assessed - you would (and should) expect that much. And honestly, from personal experience, learning non-SD content is basically useless for many areas of the VCE Biology Study Design; I think doing so would be a regrettable decision, especially in Year 12.
Chances that you get tested on it are extremely slim, and if it is truly non-SD I think consequentials would be awarded anyways. And yes, the extra background knowledge helps, but the tradeoff for time on other subjects is not favourable (this one comes from personal experience ).
...
My Bio journey is finished for now, but hopefully those still in it (or are yet to begin) will have better luck. Happy studying .
No, this is for the next SD
Hmmmm... I haven't done the 2022 sample yet, so I cannot assist you with that.
However on the latter point, I have heard that the chief VCAA assessor for VCE Biology is also a Psychology teacher. Which would explain your observation (VCE Psychology is a borderline English subject, where you have 10 mark questions with explicit mark allocations for paragraph and sentence structuring). It is just a rumour though, do not take it as fact.
If it is really true, I think it would be a shame.
VCE Biology's content is very enjoyable, possibly the best science in the VCE in terms of theory. However I think this "subjective application", style as you call it, is the incorrect approach taken by the assessors, the proper assessment approach for Biology, would be to test "technical application" where the same theory is mapped onto unfamiliar contexts (e.g. Enzyme theory for ribozymes... etc)...
Privet NG900!
Attenuation inhibits expression of the structural genes of the TrpOperon in conditions of mild-to-high concentration of loaded tryptophan tRNA.
There is a sequence of DNA located downstream of the promoter, and upstream of the structural genes, of the TrpOperon called the TrpLeader sequence. It contains two triplets, that when transcribed, become two codons (so mRNA) for tryptophan.
(Recall that transcription and translation occurs concurrently in prokaryotes)
When the ribosome reaches these two codons, it will stall in conditions of low loaded tryptophan tRNA -- and attenuation will not occur --, it will continue normally otherwise -- and attenuation will occur --.
Why you ask? This you don't really need to know in detail, but basically the time taken for the ribosome to translate those two codons will determine how the mRNA section ahead is folded. Different folding patterns will result in attenuation or not, depending [again, on the time the ribosome takes to reach it].
Apologies if I confused you haha
Hey chemistry1111!
Every protein has tertiary structure, no exceptions.
Hello MinahilMehr!
In short, no, allergic responses are "overreactions" and do not have any real meaning or purpose.
Hello Smartiestarz!
Hi guys- could someone please help explain Q13 (Multiple Choice) of the VCAA 2003 Exam 1 (sorry I don't really know how to add pictures on this like it dosent seem to be working for me)
The examiners report dosent have a marked answer.. Why wouldn't N be correct if the cell was undergoing anaerobic respiration? Wouldn't the alcohol levels increase with c02 as both are products of the reaction?
The examiners report says its not N
I think its P because even though the rate of co2 production is decrease, the amount is probs still increasing as the graph is in the positive axis right- so at point P when oxygen is introduced it undergoes aerobic cellular respiration and with this as the rate of production of co2 increases the alcohol levels would decrease.. thats why its not Q
Does my logic make sense? Basically im confused between point N and point P
so if someone could explain the concept behind how to think about this question thatd be great!
thanks so much!!
You are right, the answer is P because the question asks for concentration (amount) of alcohol, which is cumulative. If it asked for rate of alcohol production then the answer would be N instead, but that would be a different question altogether.
Hello Smartiestarz!
Can someone please explain part b of this question from the 2019 VCAA exam? Like i get that the mitochondrial DNA of the girlβs finger bone will be very similar to the mtDNA of her female ancestors, but I dont get why. MtDNA has a high mutation rate but it remains relatively unchanged from one generation to another- can someone pls explain what the concept is behind mtDNA and how that links to this question? Cos the way the edrolo textbook has explained it is kinda contradictory..
mtDNA does not change from generation to generation as much as nuclear DNA because it does not undergo recombination. It is solely inherited maternally (well... in most cases anyways).
Think about it like this; suppose you have a deck of cards. Which would result in a more drastic change?
Scenario 1 would be comparable to spontaneous mutations in mtDNA, and Scenario 2 would be comparable to genetic recombination. Sure, mtDNA may accumulate mutations faster than nuclear DNA, but it is still relatively insignificant when compared to nuclear DNA recombination.
Also can someone explain Q4 from the 2020 VCAA examβs multiple choice section? How do we know that substrate B is gonna be a competitive reversible inhibitor? I actually thought substrate B wouldnβt even bind to the active site cos its not forming a product
- Iβve been a bit confused with these two questions since yesterday so if someone could help clarify this in detail thatβd be great. Thanks so much!
This was a bad question. Usually we would not call an inhibitor a "substrate" at all, we would call them inhibitors.
Basically you had to choose the most plausible option, option C. The other options didn't really have any coherence.
Again, the question is pretty bad. Is the experiment under timed conditions? If not, reversible competitive inhibitor shouldn't make a difference in the end... etc.
Hey chimichurri!
VCAA probably wouldn't ask you about this specifically.
I would only include it in the context of a Translation question.
οΈ
Hello hello tubes!
Ah, human evolution question! My [least] favourite!
I will try to give some tips, advice, and some suggested answers. However please note that I am not a teacher, so other advice (i.e. from your VCE Biology teacher) is highly recommended.
a) Which currently known hominin species is most likely the ancestor of Aboriginal Australians? Explain
your response by referring to the different species and other information presented in the article. (3 marks)
a) Homo heidelbergensis that evolved into Homo sapiens 300,000ya in Africa and then migrated to Australia 50,000 ya. Already present before the arrival of the ancestors of Indigenous Australians was Homo erectus - an earlier hominin- that had previously migrated out of Africa and had diverged into Homo floresiensis in Indonesia also coexisted with Homo sapiens.
You should make it clearer which hominin species you are selecting for your answer (e.g. "Homo heidelbergensis, evolved into Homo sapiens...").
The question stem specifically asks for an explanation using hominin species referenced in the provided article, you made a tangent which references hominins referenced in the article; these are very different things.
In this question/example, Homo denisova would have been the best hominin species to reference in your answer, because we are told (presented information) that Aboriginal Australians share some common DNA with H. denisova. Even more compelling evidence presented in the article is that it specifically states no other currently known ancestral species shares similar nuclear DNA with Aboriginal Australians.
b) Comparisons of genomes of Aboriginal Australian populations on the west coast and east coast suggest
that there were two distinct pathways of migration across Australia.
Using supporting evidence from the article, explain likely reasons for the differences seen in the
genomes of the populations. (2 marks)
tubes b) Migration to Australia occurred in 2 distinct pathways, were one group reached and travelled along the East coast 40,000 ya and the 2nd group travelled across the western coast and settled 41000, because the 2 main groups were geographically isolated by Australia's mainland, gene flow was limited and hence different mutations occurred and accumulated in each population's genome
This is good, you have the main guts of it down; as you mentioned gene flow is limited and accumulation of different mutations lead to differences. I would only suggest polishing it up a little bit.
E.g.
Overall pretty good answer for this part, goodjob
οΈ
c) Analysis of mtDNA from Aboriginal Australians and phylogeographic patterns support the contention
that there was a continuous presence of distinct populations in discrete geographic areas for up to
50000 years.
i) Identify two types of artefacts that may be found in a particular geographic area if Aboriginal
Australians had lived in that area for long periods of time (thousands of years)? (2 marks)
i) Evidence of art (cultural evolution) such as cave paintings. The presence of stone tools.
VCAA has specifically stated in their 2022 VCE Biology FAQs that "...ability to distinguish between biological evolution and cultural evolution is not required."
So I think this is a typical case of VCAA blunder, and am not so sure you will encounter such questions on the end of year exam.
However, in the case that it does show up, answers such as cave paintings, burial sites... etc. are perfectly fine, I think (stress "I think" ).
ii) Explain how mtDNA phylogeny provides evidence for the continuous presence of Aboriginal
Australian populations in discrete geographic areas. (3 marks)
ii) The large genetic variation in mtDNA indicates that a long time had elapsed since migration hence the time for mutations to accumulate, supporting a continuous presence in Australia as well as in discrete areas as many different mutations occurred in specific isolated population and hence accumulated because of the lack of gene flow leading to 111 mtDNA genomes to diverge
This is a hard question. I had to think about it for a while. What do they mean by continuous presence?
The question asks for an explanation, you need to give a structured and logical line of thought in order to explain this.
Perhaps you could say "When Aboriginal Australian populations formed in discrete geographic locations, they became isolated from other populations; which then limited gene flow between these populations. Consequently, over long (and continuous) periods of time, differences in their gene pools from mutations, natural selection and genetic drift accumulated. MtDNA phylogeny can serve as evidence of these differences, and hence the continuous presence of these populations."
Or perhaps we can take a different angle of attack and say "Large differences between genetics of Aboriginal Populations of discrete geographical areas illustrated in mtDNA phylogeny, evidence that these populations have been established a very long time ago and have been continuously present. As those are the conditions required for these differences to arise, conditions required for factors such as lack of gene flow, different mutations, different natural selection pressures acting, and genetic drift to act on these populations; and create such differences."
Feel free to add anything to these "suggested" answers (or dispute their validity), I feel like VCAA expects a fairly meaty answer for this type of question; perhaps some more information from the article can be utilised?
Be careful, as it is very easy to fall into the trap of making an answer which uses false logic/circular reasoning for this sort of question, yuck .
Hope this helps!
(Apologies if I may have used harsh wording.)
Hello again tubes
But in that VCAA question by determining absolute age of the igneous rock you could determine the absolute age of the ancient mollusk (as specified in the stem) by using relative dating techniques, since its found in the same stratum (after first using absolute dating techniques on the igneous rock),
You misinterpreted the VCAA question (/suggested answer).
Scientists take samples of igneous rock from igneous rock strata above and below the mollusc fossils. Then they use the ratio of Potassium-40 to Argon-40, and the half-life value of Potassium-40 to calculate the age of these igneous rock strata. Since the mollusc is in between these two strata of igneous rock scientists can kind of average the two values and get an approximate age* of the mollusc fossil. This is absolute dating.
*I know the name of the dating method would suggest that it yields an absolute value, but unfortunately it is not always possible to directly date a fossil.
Hey tubes!
- Firstly radiometric dating is utilized to date igneous rock associated with (near) sedimentary layer that the index fossil is found within, percentage of parent isotope is compared to broken down products, hence using stratigraphy it can be inferred that the age of the index fossil = ____.
Here you must mention that calculations are made based on the half life of the particular radioisotope measured in the radiometric dating; otherwise, how does the ratio of parent to daughter nuclei help?
It might also be good to mention the type of radiometric dating technique you are referring to (i.e. K-Ar dating), as they all have ranges.
- Using stratigraphy, the fossil found in the same strata is the same age as the index fossil, ____.
Yes, you are correct here as well, but because the unknown fossil is more often than not in another strata from the index fossil used, the index fossils are often used in conjunction with the principle of superposition (which states that rock strata are arranged in a order of progressing age, with the newest at top, in normal conditions). That is to say, if there is a fossil of unknown age and it is found below an index fossil, it can be inferred that the unknown fossil is older than a certain age (i.e. that of the index fossil); and vice versa.
So if the question asked whether using index fossils is absolute or relative (point 2) what would be say?
Relative - because the age of the fossil is being determined by using the index fossil nearby?
or Absolute - because the NUMERICAL value of the fossil is known because of the INDEX fossils whose NUMERICAL age is also known?
Relative. If an index fossil is used it is always relative. Because it is in relation -- or in other words, relative to -- the index fossil (also links back to my previous point that the unknown fossil is more often than not, in a different rock strata to the index fossil, so the approximate numerical age is not known anyway).
Hope this helps .
Ah ok I see,
The VCAA question explicitly states a tissue has entered the body; presumably transplanted but that doesn't really matter.
And, yes, MHC class 1 on the cells of the tissue is what allows Cytotoxic T Cells to recognise them.
Also, the cells themselves aren't considered pathogens, just foreign.
RBCs don't have MHC/HLA markers but some will have "red cell antigens". Most times these atigens will fall under either type-A or type-B (there are a few minor ones but they are very very uncommon so don't worry about it).
You may have heard of the term "blood type", which can be either O, A, B or AB (for all intents and purposes).
Ok, due to Immunological Tolerance, and the relatively conservative nature of these A and B antigens, people with a certain blood type will be able to accept any blood with the same or less antigens. Since they are recognised as self. That is to say, a person with type-A blood will be able to accept Type-O (no antigens, less) and Type-A (same) blood; but not Type-B or Type-AB blood.
Blood transplants are rejected is because the antigens in the transfusion are not recognised as self (i.e. foreign).
EDIT: just to be extra clear, this is quite a simplified view of blood types, as there are more red cell antigens types than just A and B; rhesus factors also need to be taken into consideration (which is technically just another type of antigen).