Biology Unit 2 - Exam Revision Flashcards

1
Q

Distinction between genes, alleles, and a genome

A

Genes: Basic units of heredity, consisting of DNA sequences that code for proteins, affecting physical and biochemical traits.

Alleles: Different variants of a gene; for example, a gene for flower colour may have a purple allele and a white allele.

Genome: The complete set of genetic instructions for an organism, encompassing all of its genes along with non-coding DNA.

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2
Q

Homologous chromosomes and their gene loci

A

Homologous chromosomes are pairs that contain the same genes at corresponding loci, but may have different alleles (e.g., one is inherited from the mother and the other from the father).

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3
Q

Difference between autosomes and sex chromosomes

A

Autosomes: Non-sex chromosomes that determine traits unrelated to sex (e.g., chromosome pairs 1-22 in humans).

Sex chromosomes: Chromosomes that determine sexual characteristics (e.g., X and Y chromosomes).

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4
Q

Variability in size and number of chromosomes in different organisms

A

E.g, Humans have 46 chromosomes, while fruit flies have 8. The number and structure of chromosomes can vary widely between species, affecting genetic information.

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5
Q

Karyotypes and identification of chromosome abnormalities

A

A karyotype is a comprehensive display of an organism’s chromosomes arranged by size and shape. Karyotypes can be used to identify genetic disorders such as Down syndrome (47, XX or XY +21), characterised by the presence of an extra copy of chromosome 21.

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6
Q

Meiosis and its role in producing haploid gametes from diploid cells

A

Meiosis is a two-staged cell division process (Meiosis I and II) that reduces the chromosome number by half, producing four haploid gametes (sperm or eggs) from one diploid cell.

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7
Q

Significance of crossing over and independent assortment in genetic diversity

A
  • Crossing over allows for the exchange of genetic material between homologous chromosomes during prophase I of meiosis, increasing genetic variation.
  • Independent assortment occurs in metaphase I, where chromosomes are distributed to daughter cells independently of one another, resulting in a mix of maternal and paternal chromosomes in gametes.
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8
Q

Use of symbols to write genotypes

A

Genotypes are represented using symbols, where uppercase letters signify dominant alleles (e.g., A) and lowercase letters signify recessive alleles (e.g., a).

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9
Q

Expression of dominant and recessive phenotypes (including codominance and incomplete dominance)

A

An organism with at least one dominant allele (e.g., AA or Aa) expresses the dominant phenotype, while organisms with two recessive alleles (aa) express the recessive phenotype.

Codominance occurs when both alleles in a heterozygous individual contribute equally to the phenotype (e.g., AB blood type).

Incomplete dominance results in a blended phenotype (e.g., pink flowers from red (RR) and white (WW) parents).

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10
Q

Influence of genetic material, environment, and epigenetic factors on phenotypes

A

Genetic makeup provides the blueprint for traits, but environmental influences (e.g., sunlight, nutrition) and epigenetic modifications (e.g., DNA methylation) can alter gene expression, leading to variations in phenotypes.

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11
Q

Pedigree charts and patterns of inheritance (autosomal and sex-linked)

A

Pedigree charts illustrate the inheritance of traits across multiple generations, allowing examination of autosomal traits (inherited via non-sex chromosomes) and sex-linked traits (associated with genes on sex chromosomes like colour blindness, which is X-linked).

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12
Q

Predicted genetic outcomes for monohybrid crosses

A

Monohybrid crosses consider one trait (e.g., flower colour) and utilise a Punnett square to predict ratios of expected genotypes (1 homozygous dominant: 2 heterozygous: 1 homozygous recessive) and phenotypes in the offspring.

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13
Q

Linked genes vs. independent assortment in inheritance predictions

A

Genes located close together on the same chromosome are said to be linked, leading to fewer recombinant offspring. In contrast, independently assorting genes generate a variety of combinations.

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14
Q

Biological advantages and disadvantages of asexual reproduction

A

Asexual reproduction (e.g., binary fission in bacteria) enables rapid reproduction and colonisation, resulting in large populations. However, it yields little genetic diversity, making populations vulnerable to diseases and environmental changes.

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15
Q

Biological advantages of sexual reproduction, especially in promoting genetic diversity

A

Sexual reproduction leads to increased genetic variability through the mixing of parental genes, which enhances the adaptability of populations in a changing environment and allows for natural selection to act on more diverse traits.

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16
Q

Reproductive cloning technologies and their applications

A

Cloning techniques (e.g, somatic cell nuclear transfer) raise ethical issues but can be employed to save endangered species or for agricultural benefits. However, cloning can lead to reduced genetic diversity in populations.

17
Q

Importance of genetic diversity within a species or population

A

Genetic variability within a population fosters resilience to environmental stresses and enables adaptation to changing conditions, reducing the risk of extinction.

18
Q

Structural, physiological, and behavioural adaptations that enhance survival

A

Structural adaptations: Physical features that enhance survival (e.g., camouflage, specialised teeth).

Physiological adaptations: Internal processes that aid survival (e.g., thermoregulation in mammals).

Behavioural adaptations: Activities or patterns that increase chances of survival (e.g., migration to find food).

19
Q

Survival through interdependencies (e.g., impact of keystone species and top predators)

A

Keystone species play critical roles in maintaining ecological balance (e.g, sea otters controlling sea urchin populations), while top predators regulate prey populations, ensuring ecosystem stability and biodiversity.

20
Q

Contributions of Aboriginal and Torres Strait Islander knowledge regarding species adaptations and interdependencies

A

Traditional ecological knowledge from Aboriginal and Torres Strait Islander peoples provides insights into species co-evolution and sustainable practices, helping to conserve biodiversity and ecosystem health.

21
Q

Difference between primary and secondary data

A

Primary data is direct evidence (e.g., experimental results, field studies), while secondary data involves comprehensive analyses of previously published studies or existing data.

22
Q

Distinguishing opinion, anecdote, and evidence

A

It is essential to distinguish personal opinions and anecdotal evidence from scientifically validated results when forming conclusions about bioethical issues.

23
Q

Validity and authority of data; identifying possible errors or biases

A

Assess the credibility of sources by examining methodology, peer-reviewed status, and potential conflicts of interest, while being mindful of biases which could skew results.

24
Q

Organising, analysing, and evaluating secondary data

A

Effectively compile and dissect secondary data to identify trends, relationships, and discrepancies in scientific literature regarding a bioethical issue.

25
Q

Accurate use of biological concepts and terminology

A

Precision in scientific language is paramount to avoid misinterpretation; familiarity with terms like genotype, allele frequency, and genetic drift is necessary.

26
Q

Clarity, conciseness, and coherence in communication

A

Structure arguments and presentations with clear objectives, logical progression, and concise language to maximise impact and understanding.

27
Q

Use of data representations, models, and theories in explaining concepts

A

Graphical representations (charts, bar graphs, etc.) and models (like Hardy-Weinberg equilibrium) can simplify complex information, making it more accessible.

28
Q

Social, economic, legal, and political factors in bioethical discussions

A

An encompassing view of bioethical issues must consider the broader societal implications, including how legal frameworks, social justice concerns, and economic pressures influence policies and practices.

29
Q

Referencing and acknowledging sources

A

Employ consistent citation styles (e.g., APA, MLA) when documenting sources to uphold academic integrity and support arguments with credible evidence.

30
Q

Identifying bioethical issues in genetics, inheritance, or adaptations

A

Investigate current topics such as genetic modification, cloning ethics, and implications of CRISPR technology, assessing potential benefits and risks.

31
Q

Approaches to bioethics and ethical concepts relevant to the selected issue

A

Consider various ethical frameworks (e.g., utilitarianism – maximising benefits; deontology – adherence to rules) and principles like autonomy, justice, and beneficence when evaluating the moral dimensions of bioethical dilemmas.