SD206 Examination Essay questions (Set G)

Outlines of the answers for these questions are given below.

They give you some indication of what is asked for in these exam essays, but note that the marking scheme is somewhat different from that currently adopted. As you should be aware from the guidance notes for TMA essays, as a general rule 60% of the marks goes for content, 20% for essay structure/comprehension, and 20 % for understanding; in the marks out of 20 for a single essay, these correspond to 12, 4 and 4 marks respectively. Some of the questions here don't exactly follow that pattern, but could be marked along those lines instead of the finely-divided mark-schemes listed here.

Q1.

Hormones have a major influence on what an animal does,[Bk. 1: 2.9, 5.3.1; Bk. 4: 4.4.2; Bk. 5: 5.2.11] but control is ultimately the responsibility of the nervous system as it, via the motor system, controls muscle contraction.
Hormones affect:
1) signal effects: the stimuli that one animal presents to another (e.g. smell - mice [Bk. 5: 4.3.5], size - most mammals, colour - fish/birds [Bk. 1: 2.5, 2.9], structures - deer/birds, sound - deer/birds/toads/frogs).
2) central effects: the way in which such stimuli are processed (e.g. by altering brain structures during development - rats/birds [Bk. 4: 4.4.2, 4.4.3]).
3) peripheral effects: effects on organs other than the brain affecting the ability of animals to respond (e.g. via stress hormones - mammals [Bk. 5: 5.2.1], reproductive hormones - rats [Bk. 2: 10.3.2] / doves[Bk. 1: 9.2.2] / zebra finches [Bk. 4: 4.4.3], circadian hormones - mammals [Bk. 5:3.9.1]).

Structure:    4 marks
Content:    max. 12 marks
    definition of hormones, etc.    4 marks
    effects and examples    8 marks
    interaction with external stimuli etc.    4 marks
Understanding:    6 marks

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Q2.

There are three main reasons:
1) survival - there is a struggle for existence and only some survive [Bk. 1: 4.3.1, 4.3].
2) developmental factors (e.g. caste - ants [Bk. 4: 4.3.1) / mole rats [Bk. 1:10.4.1], song - zebra finches [Bk. 1: 5.6], hormones - rats [Bk. 1: 5.3.l] / people (infertility) [Bk. 4: 4.5.5]).
3) mate choice (e.g. finding a mate, being chosen by a mate - territories-/displays/competitors (red deer [Bk. 1: 4.3.8], fish/birds [Bk. 1: 9.4], frogs [Bk. 3: 2.2.5-2.2.8]).

Structure:    4 marks
Content:    max. 12 marks
    survival    4 marks
    development    8 marks
    mate choice.    4 marks
    completion/integration    4 marks
Understanding:    4 marks
 

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Q3.

Need to emphasise differences - not just an account of "the synapse".
Differences: e.g. electrical vs. chemical; excitatory vs. inhibitory; different neurotransmitters.
Time: e.g. summation, Hebbian synapse, potentiation.
Mostly Book 2.
Structure:    4 marks
Content:    max. 12 marks
    differences    10 marks
    time related    4 marks
Understanding:    6 marks
 

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Q4.

1st part) The output from one receptor is compared with that of adjacent receptors via a comparator cell. If the receptor in question excites the comparator cell and adjacent receptors inhibit the comparator cell the output of the comparator cell will reflect the balance between inhibition and excitation; it will in effect compare the two types of input. Assuming that the system is wired up appropriately so that equal stimulation of the receptors evokes a nil response from the comparator, then any response from the comparator will mean a luminance discontinuity across the receptors.[Bk. 3: 4.3.2]
2nd part) Largely. Colour: bipolar cells and opponency; motion: the basic motion detector receives input from two receptors in neighbouring retinal positions (delayed inhibition; velocity gradients : detectors add together the responses from neighbouring individual motion detectors which are selective for opposite directions of motion); stereopsis: comparison of the images of the two eyes [Bk. 3: 4.4, 4.5, 4.6].
Structure & Understanding:    4 marks
Content:    max. 12 marks
    luminance discontinuities    10 marks
    other information    10 marks
 

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Q5.

Learning alters the brain in such a way as to create memories which affect future behaviour. Memories also allow interpretation and recognition of stimuli [Bk. 1: 6.1]. There are several types of learning (associative, non-associative and complex [Bk. 1: 6.3]), though whether non-associative learning affects the brain is unclear [Bk. 4: 5.7.1]. Changes in the brain consequent upon learning fit the Hebbian synapse model [Bk. 4: 5.4]. Numerous changes of and to synapses have been reported [Bk. 4: 5.5]. The processes by which these changes come about have been investigated in both the hippocampus following LTP (LTP has many parallels with place learning in the Morris water maze [Bk. 4: 5.7.3]) and the chick following passive avoidance learning [Bk. 4: 5.7.4]. These changes may have a short-term, temporary component, accounting for short-term memory and/or may result in long term, permanent changes, accounting for long-term memory [Bk. 2:11.4; Bk. 4: 5.8].
It is not clear how these changes in individual synapses encode particular memories.

Structure:    4 marks
Content:     12 marks
Understanding:    4 marks
 

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Q6.

This question could possibly be addressed in terms of Tinbergen's four answers [Bk. 1:1.1.1].
Circadian rhythms are those with periods of about a day [Bk. 5: 3.1]. They have been shown to be endogenous, but are usually entrained by a zeitgeber [Bk. 5: 3.2.2, 3.2.3].
In evolutionary terms, extant mammalian species have a circadian rhythm because their ancestors had circadian rhythms and they were more successful than mammals without circadian rhythms.
In functional terms, the rhythm enhances activity at appropriate times of day [Bk. 5: 3.2.2, 3.2.3]. It also permits mating at appropriate times of the year [Bk. 5: 3.9.1].
In developmental terms, the suprachiasmatic nucleus grows in the right place (i.e. just above the optic chiasma) and has connections to other appropriate structures (e.g. via retinohypothalamic tract) and is able to secrete melatonin from the pineal gland [Bk. 5: 3.9.1].
In causal terms, the suprachiasmatic nucleus, entrained by the day night cycle, causes the release of melatonin from the pituitary. Melatonin is a timing hormone which influences reproduction in seasonal breeders [Bk. 5: 3.9.1] and synchrony of internal rhythms in mammals.

Structure:    4 marks
Content:     12 marks
Understanding:    4 marks
 

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Q7.

This question is about direct competition [Bk. 1: 4.3.2] and assessment [Bk. 5: 4.5 -4.8].
Direct competition is where one animal wants exactly the same resource (e.g. food, territory, mate) as another animal, at the same time. Tussles ensue but if the resource is of low value to both or one of the participants then one will leave or flee. If the resource is of high value to both participants (e.g. stags competing for mates) then they may establish their respective resource holding potential (RHP) in a roaring display. One stag will back down if it detects an asymmetry (i.e. that it is weaker). IF neither stag detects an asymmetry, then severe fighting occurs. Toads also use correlated asymmetries to assess the RHP of males in amplexus. They will only attack if they detect an asymmetry in their favour (i.e. they have a lower pitched croak and are therefore bigger). Where a resource is important but neither limited nor permanent (e.g. sunspots in a wood), then an uncorrelated asymmetry (e.g. residence) may be used to resolve the dispute.
Displays have evolved which provide information about RHP to conspecifics. Only in the absence of an asymmetry when the resource is of high value, does direct competition lead to severe injury or death.
Dominance hierarchies could also be mentioned.

Structure:    4 marks
Content:     12 marks
    theory    6 marks
    examples    6 marks
Understanding:    4 marks
 

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Q8.

It is possible to consider the recovery of function and the recovery of structure. Language can be permanently disrupted following brain damage (e.g. Broca's area [Bk. 2: 11.2; Bk. 6: 6.3.3, 6.3.4]), as can memory (e.g. amnesic syndrome [Bk. 2: 11.4]). Arguably, Alzheimer's and Parkinson's diseases are also brain damage and there is no recovery from them [Bk. 6: 3.7.1; Bk. 6: 4.3.2]. Some recovery from stroke and head injuries is possible [Bk. 6: 5.2.1; 5.2.2]. However, if such damage occurs in infancy, then recovery is possible [Bk. 2: 11.3.2; Bk. 6: 5.3]. There is limited axon sprouting [Bk. 6: 5.4.2] and pathway restructuring [Bk. 6: 5.4.3] as well as reversal of oedema [Bk. 6: 5.4.1]. (Intervention to aid recovery could feature in this account (e.g. grafts [Bk. 6: 5.5]).

Structure:    4 marks
Content:     12 marks
Understanding:    4 marks
 

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Q9.

The neurological symptoms of normal ageing (as opposed to pathological ageing) are related to memory (especially short term and working memory, but also prospective and semantic), sensory input and speed of performance. Though highly practiced skills are retained (e.g.chess playing) and wisdom improves. There is little loss of cognitive or other intellectual functions.
Schizophrenia is a psychosis in which the patient experiences life in a disturbed way owing to delusions, hallicunations or misinterpretations. Onset is usually between 16-45 years of age. Pre-senile dementia (early onset Alzheimers) may occur in people in their forties and some of the symptoms are similar. Many though, (memory loss, disorientation, incontinence) are not similar. A major distinction is that the brains of schizophrenics look more or less normal (apart from minor differences (enlargement) of the ventricles and asymmetries between left and right hemispheres) whilst those with Alzheimer's disease are littered with senile plaques and neurofibrillary tangles. The neurotransmitters invoked in these two conditions are different (Alzheimer's: acetylcholine; Schizophrenia: dopamine, serotonin).
There is some overlap in symptoms between schizophrenia and pre-senile dementia but there is no overlap in the biology underlying those symptoms.

Structure:    4 marks
Content:     12 marks
    schizophrenia    6 marks
    ageing    6 marks
Understanding:    4 marks
 

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