2013 HSC COURSE
HSC biology, physics, economics, english & four unit mathematics
HSC biology, physics, economics, english & four unit mathematics
Kartei Details
Karten | 417 |
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Sprache | English |
Kategorie | Allgemeinbildung |
Stufe | Mittelschule |
Erstellt / Aktualisiert | 10.04.2013 / 10.09.2024 |
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experiment on structures in plants that assist the in conservation of water
aim: to investigate structures in plants that assist in the conservation of water
risk: cacti has sharp spines that may cause injury. As such wear gloves when handling
materials 1x cacti sample 1x banksia sample 1x spinifex grass sample 1x magnifying glass 1x pencil
method: 1. use the magnifying glass to observe samples 2. identify and sketch features that assist with water conservation
independant variable
variable that the experimenter changes
dependant variable
variable that the experimenter measures
xylem tissue
tissue in plants responsible for the unidirectional passive movement of water from roots to shoots.
structure: 1. arranged end to end to form a continuous column 2. pits to allow sideways movement of water 3. narrow lumen to increase height that water can reach 4. walls thick with lignin to increase strength 5. composed of dead cells (doesnt absorb water)
Osmoregulators
able to regulate salt water concentration and keep it constant regardless of changes in the external environment
osmoconformers
body fluids isotonic (same concentration as the environment)
unable to adjust internal salt water concentration
carries out enantiostasis
Phloem tissue
living tissue responsible to the bilateral movement of organic substances in plants from source to sink
composed of: 1. sieve tube elements and compagnion cells linked end to end 2. sieve tube plates perforated with pores linked by plasmodesmata
James watson contribution to determining the structure of DNA
suggested with crick that DNA molecule was made up of 2 chains of nucleotides each in a helix by one going up and the other going down
realised that A - T pair held togethor by 2 hydrogen bonds was identical to G - C pair - therefore these pairs of bases could serves as rungs on the twisting ladder of DNA
Francis crick contribution to determining the structure of DNA
deduced that the matching base pairs of which there were similar amounts interlocked in the middle of the double helix to keep the distance between the chains constant
Relative importance of Watson and Crick in determining the structure of DNA
Concluded that the DNA molecules was made up of 2 chains of nucelotides, bonded in a double helix shape with one going up and the other going down
Rosalind franklin contribution to the determination of the structure of DNA
Produced the "world's best" X ray diffraction images of DNA
Extracted fine DNA fibers than ever before and arranged them in paralled bundles before studying reaction to humid conditions
Found her images showed that the 'wet' form of DNA had the characteristics of a helix
Rosalind Franklin relative importance in the determining of DNA structure
X ray diffraction images became the basis of watsons and cricks conclusion
Showed that the chains of nucleotides in DNA were in the shape of helixes - crucial to watsons and cricks conclusions
Maurice wilkins contribution to the determining of DNA structure
Found DNA could exist in 2 forms depending on humidity of surrounding air
deduced that the phosphate part of DNA was on the outside
Showed watson one of franklins X ray diffraction images giving vital information
Relative importance of Maurice wilkins to the determining of DNA structure
Enabled the combination of Franklins images and Watsons and Cricks research leading to watsons and cricks conclusion on the structure
Impact of collaboration and communication on the determination of DNA structure
Franklin's reluctance to share her works ultimately meant she was not directly credited for her work and the discovery of the structure was retarded
Good collaboration between watson and crick helped find a quicker solution
Principle of segregation
for any particular trait the pair of alleles / factors each each parent seperate and only one allele / factor passes from each parent to an offspring
principle of independant assortment
different pairs of alleles are passed to offspring interpendant of one another
e.g. if a pea plant inherits purple flower its is no more likely to inherit yellow seeds
roles of Sutton and Boveri in identifying the importance of chromosomes
- Two scientists are credited with the discovery of the role of chromosomes in 1902. They were the German scientist Theodor Boveri and the American microbiologist Walter Sutton.
- Boveri worked on sea urchins and showed that their chromosomes were not all the same and that a full complement was required for the normal development of an organism.
- Sutton worked on grasshoppers and showed that their chromosomes were distinct entities. He said even though they duplicate and divide they remain as a distinct structure. He associated the behaviour of chromosomes with Mendel's work on the inheritance of factors and concluded that chromosomes were the carriers of hereditary units.
- Together their work became known as the Sutton-Boveri chromosome hypothesis.
Chemical nature of chromosomes and genes
– Each chromosome is made up of about 60% protein and 40% DNA – The DNA is coiled tightly around a protein core (histone proteins) – A gene is a section on a chromosome, made up of DNA – DNA is further made up made up of a particular sequence of bases – Different genes are different lengths (diameter of locus), hence differing lengths of DNA.
Structure of DNA
DNA (deoxyribonucleic acid): - A double stranded helix - Made up of sub-units called nucleotides, each nucleotide is made up of a phosphate, a deoxyribose sugar and a nitrogenous base. - The four different nitrogenous bases are adenine, thymine, guanine, and cytosine - Adenine pairs with thymine (A-T) and guanine with cytosine (G-C) - A single DNA strand is made up of a chain of nucleotides (a polynucleotide) where the phosphate and sugar alternate as the backbone of the strand
Meiosis
Meiosis is the process of division in which sex cells are produced(ie gamates)
In the process half the number of chromosomes are in each sex cell (compared to a normal cell)
occurs in the sex organs
Jelly snakes model
models the process of meiosis using jelly snakes to represent chromosomes
cell with diploid number of 2 (2 pairs of 2 chromosomes) 1 pair short homologous 1 pair long homologous with each chromsome in the homologous pair a different colour
Chromosomes were doubled keeping colours consistant (copy attached to original at centromere)
crossing over was modelled between homologous chromosomes by breaking off pieces from the homolougous chromatid and rejoining to the other homologous chromatid
random segregation was modelled as each homologous pair lined up at the equator in random order
The homologous chromosomes then moved away from each other to the poles of the cell by the spindle
cytokinesis occurs
Chromosomes are once again drawn to the equator and then the chromatid are seperated drawn by the spindle to the poles
cytokinesis
4 cells each with 2 seperate chromosomes
Advantages of jelly snakes model
Colours of the snakes helped understand the idea of homologous chromosomes and made crossing over clear as well as the random segregation of chromosomes (different possibilities)
The snakes being soft and sticky demonstrated crossing over clearly
Moving the snakes around to simulate movement in meiosis helped to understand the dynamic nature of the process
The snakes could be resized to make chromosome pairs different sizes
relationship between the structure and behaviour of chromosomes during meiosis and the inheritance of genes
- Chromosomes are made of DNA. Genes are coded within the DNA on the chromosomes. Meiosis in four genetically different sex cells (due to crossing over and random segregation) that are haploid, (ie contain half the chromosome number of the original cell) thereby creating 4 possibilities for the inheritance of genes
Gamete formation and sexual reproduction in genetic variation
Gamete formation results in the halving of the chromosome number (n) (diploid to haploid) and sexual reproduction results in combining gametes (haploid to diploid) to produce a new diploid organism (2n).
The processes involved in forming this new organism result in variability of the offspring as not only does 2 different genetic makeups combine through sexual reproductioon, but in gamete formation each sex cell is also genetically different each other due to random segregation and crossing over during meiosis
experiment: demonstrating the effect of environment on phenotype
aim: to demonstrate the effect of the environment on the phenotype of bean sprouts
hypothesis: The different environmental condition will result in different phenotypes
risk: spilt water is a slipping hazard and may cause injury. As such clean up any split water immeadiatly
materials 100 x bean sprouts 10 x plastic contrainer 1x cotton wool 1 x 1L water 1x light impermiable sheet
method: 1x place a layer of cotton wool into each of the plastic containers 2. soak cotton so that it is damp 3. place 10 bean sprouts into each container equally spaced 4. store 5 containers under the light impermiable sheet and 5 in a light abundant area 5. leave for 2 days and return 6. record results
process of DNA replication
1. DNA double helix unwound by helicase enzyme
2. DNA unzips to form two seperate strands
3. Complementary nucleotides are brought over by DNA enzyme polymerase and form hydrogen bonds with the single strands resulting in two identical strands of DNA
4. DNA double helix rewinds
DNA replication
takes place during interphase in preparation for nuclear division that occurs during meiosis or mitosis
Ensures daughter cells receive a copy of DNA from parent cells in asexual reproduction and mitosis and half the genetic information in meiosis
Semi conservative (each new double helix has one original and one new strand)
DNA and the production of polypeptides
DNA carries the instruction for making a polypeptide and therefore a protein
RNA is used to transcribe the message from DNA (as it is small enought to fit through the nuclear pore to the ribosome) it does so through helicase enzyme unwinding the enzyme, and RNA polymerase building a complementary strand of mRNA
The ribosomes translates the DNA sequence 3 bases at a time and tRNA (transfer RNA) molecule brings over the corrosponding amino acid (the amino is based on the mRNA condon)
Peptide bonds form between neighbouring amino acids
tRNA molecule is released back into the cytoplasm
Chain of amino acids form a polypeptide chain
sequence stops when ribsosome reaches a stop sequence and starts again when it reaches a start condon
Simple model: DNA production of polypeptides
DNA ---> transcription ---> RNA ---> translation ---> polypeptide
Relationship between a polypeptide and a protein
Polypeptides are the basic units of proteins
Sometimes more than one polypeptide chain is needed to create a protein (and therefore more than one gene may be needed to create a protein)
polypeptide
A chain of amino acids
How changes in DNA sequences can result in changes in cell activity
Beedle and tatum
hypothesized that if there really was a one-to-one relationship between genes and specific enzymes, it should be possible to create genetic mutants that are unable to carry out specific enzymatic reactions. To test this theory, they exposed spores of Neurospora crassa (a bread mold) to X-rays or UV radiation and studied the resulting mutations. The mutant molds had a variety of special nutritional needs. Unlike their normal counterparts, they could not live without the addition of particular vitamins or amino acids to their food. Genetic analysis showed that each mutant differed from the original, normal type by only one gene and biochemical analysis showed a build up of the substrate the enzyme normally used These results led them to the one gene/one enzyme hypothesis, which states that each gene is responsible for directing the building of a single, specific enzyme. Subsequent work has led to further refinement of this hypothesis. We now know that a gene infact codes for a particular polypeptide rather than a protein and a protein can be composed of multiple polypeptides (e.g. Hb). Its also been shown that proteins dont just code for enzymes, but are also coded for structural uses
how mutations can lead to new alleles
- Any change in the base sequence in DNA by mutations may result in different polypeptides being produced and therefore a new allele
- if the mutation occurs in the sex cells of the organism the mutated code may be passed off to offspring
- The offspring may therefore have a new allele/s from the changed protein/s depending on the effect of the mutation
effect of mutations
depending on types of mutations mutations may have:
no effect - as mutation produces the same amino acid
neutral effect - eye colour
harmful effect - e.g. sickle cell anaemia
beneficial effect - e.g. sickle cell anaemia immunity to HIV
Chromosomal mutations
Changes in the number and/or structure of entire chromosomes
may occur during meiosis when homologous chromosomes dont seperate properly
e.g. down's syndrome (trisome 21)
Causes of mutations
inheritance from parents (if mutation occurs in sex cells)
environmental damage (radiation)
mistakes when DNA is compied
modern day natural selection example DDT
insecticide DDT was used to eradicate maleria carrying mosquito
however widespread use cause resistance to occur arising from a mutation in a single genen DDT-R (occured in the sex cellsand was passed on)
evidence for the mutagenic nature of radiation
A mutagen is a natural or human-made agent (physical or chemical) which can alter the structure or sequence of DNA.
Mutagens can be carcinogens (cancer causing) or teratogens (birth defects causing).
Beadle and Tatum used X-rays to produce mutations in bread mould in the formulation of their “one – gene one – polypeptide” hypothesis. The atomic bombs dropped on Hiroshima and Nagasaki also increased the evidence for mutations caused by radiation. There was a tenfold increase in cancer deaths directly after the bombs were dropped. Rosalind franklin died very young after using x ray cyrstalography to examine DNA structure Mutagens may cause death in the individual but unless they affect the sex cells the effect is not passed on to the next generation.