You are on page 1of 9
i HAKHAKE | CYORO Rey Reade $CalO# | 20RCE «LCI dads! Age ayy A LOEHY ORK! § Y ely AMOEAE sles A LOERAE 56.0041 pela Ceol pial play — 2020 5253 — Les slSall bulged Jail am gal) ila gl) Shade Anal) Aisa) Ae yall EY Aajatath Ud: Ayal Maa Gay Hyal agle Balad yas yall JAY) Agcy gh Rak th Adal I plat Awe PDR mpl gag Gai NEED ae Seok gl a Gil jo A Bal) a My sb Le AY yan gy Ae cy 3 adh hl al yl Ae 6 Ge 1 ye seats tins ysl isl JS wemeebac@gmail.com : 7s 50 3 4) 05.37.71.48.08 : Sl 05,37.71.48 53/5240 I. Areas of assessment: 1. Spe ic competencies covered by the evaluation According to the pedagogical guidelines and the specific teaching programmes for Life and Earth Sciences at the secondary school, the target competences for Mathematical Science stream ‘A’ enable the learner to: + Acquire knowledge of the transmission of genetic information through sexual reproduction and human genetics, use this knowledge to solve problems related to the transmission of hereditary characteristics/traits and be aware of hereditary diseases so as to take the necessary precautions against diseases; + Acquire basic knowledge of genetic variation with the aim of understanding the importance of selection to improve the quality and profitability of agricultural production and its impact on economic production; + Adopt a scientific approach suitable to address issues related to genetics, genetic and variation; + Use various modes of expression (oral, written and graphic) related to genetics and variation; communicate and present phenomena 2. Content areas areas covered by the evaluation 2.1. First content area: Transmission of genetic information through sexual reproduction and human genetics. This area allows the leamer to acquire knowledge of the transmission of genetic information through sexual reproduction and the statistical laws of the transmission of hereditary characteristics/traits in diploid organisms and human genetics. The study of the transmission of genetic information through sexual reproduction consists of highlighting the role of meiosis and fertilisation in the karyotype stability, and in the recombination and genetic diversity. To achieve that, it is necessary to: + Define meiosis, identify its different phases and show its role in recombination of “alleles (genetic recombination of homologous chromosomes by linkage/crossing-over and chromosomes independent assortment) and therefore deduce the genetic diversity of gametes; + Define fertilisation and show its role in genetic recombination and in genetic diversity of individuals within the same species; + Deal with examples of development cycles in order to show the role of alternation of fertilisation and meiosis in karyotype stability in individuals within the same species from one generation to the next, ‘The study of Mendel’s laws explaining the transmission of hereditary characteristics/traits in diploid organisms consists of: + Formulating the notions of genotype, pure lineage / purebreds (wild type and mutant) and hybridisation; 2020 — 8 SAN 4 npg aS at ED an 8 SEN "Vay hl an Gye JS a) yay Hyd pk ale HEA gan ll YN Shep i AS fl iy a ly aD te 6 O42 Ga ses chtatt ysl iby) 36 leneebac@gmail.com : g's 3! 9s 05.37.71.44.08 : ySil\~ 05,37.71.48.53 [S2ited + Leaming Mendel’s laws and their exceptions through the study of examples of autosomal ‘monohybridism/monohybrid inheritance (dominance and codominance, lethal gene) and sex-linked gene, and dihybridism/dihybrid inheritance (independent and linked genes); + Showing the role of linkage/crossing-over in genetic diversity of generations and in the construction of gene maps. The study of human genetics consists of: + Knowing the methods and the means of studying the transmission of hereditary characteristics/traits in humans (pedigree, karyotypes) and studying the modes of transmission of some hereditary autosomal and sex-linked diseases using pedigree, karyotypes, and gene detection techniques; + Highlighting certain chromosomal abnormalities and their consequences by using karyotypes. 2.2, Second content area: Genetic variation The aim of this content area is to acquire knowledge related to the quantitative study of variation. Quantitative study of genetic variation consists of: + Studying the quantitative characteristics/traits variation across generations (continuous and discontinuous variation) in individuals within a given population by applying principles and statistical techniques, and thus determining the characteristics of continuous and discontinuous variation of hereditary characteristics based on the study of various examples ; + Using graphical representation of continuous and discontinuous variation in order to show these characteristics/traits; + Using quantitative study to determine the characteristics and peculiarities of a population (homogeneity or heterogeneity, pure lineage/ purebreds), and constructing the notion of artificial selection by showing its effectiveness in the selection of purebreds. "2020 — WASH SOS SA eh FRG EI HES GD LT "Vagal yh aa (asl al Daa a My Ra ple fe JY gall JY ASSN ip ASE yah Rly 6 G43 Ua a sl olla 4 sill ys) 56 leneebact@ gmail.com : ys! 518 05.37.71.4408 ; Si — 05.37.71.48.53 [52 II - Organization of notional and methodological areas covered by the evaluation 1.Table of Contents: ‘Area 1 : Transmission of genetic information through sexual reproduction and Human genetics, (Coverage : from 70% to 75%) ‘Sub-areas Content Basic objectives (notional /methodological) | Ll. «© Meiosis phases; ® Describe and recognise the meiosis phases; Transmission | © Karyotypes of diploid ‘Analyse karyotypes of diploid species; of genetic species; Deduce through exploitation of data based information © Role of meiosis and on observation and experimentation: through fertilisation in allelic © Therole of meiosis and fertilisation in sexual recombination/ allelic recombination and in the karyotype reproduction recombination of alleles stability in the same species from a (genetic recombination of homologous chromosomes by linkage/crossing-over and chromosomes independent assortment) and in karyotype stability across generations; Development and chromosome cycles. generation to the next, © The role of meiosis and fertilisation in genetic diversity; Draw diagrams in relation to the meiosis phases, development and chromosome cycles. 1.2. Mendel’s laws of the transmission of hereditary characteristics Jeraits in diploid organisms © Mendel’s laws of the transmission of hereditary characteristics/traits; # Monohybridism/monohybrid cross and dihybridism/dihybrid cross; © Pure lineage and wild type, homozygosity and heterozygosity, hybridisation, test cross, back cross; Punnett squares; * Autosomal heredity (independent of sex) and sex- linked heredity; Dominance, codominance and lethal gene. © Unlinked genes (genes of independent assortment) and linked genes; ‘ Linkage/crossing-over, genetic recombination of homologous chromosomes by linkage/crossing-over and genetic diversity; ‘Analyse and interpret the results ofthe | transmission of a couple of alleles from the study of a specific example (in cases of a sex- linked gene and autosomal gene); Analyse and interpret the results of the transmission of two couples of alleles from the study of a specific example (in cases of ‘two unlinked genes and two linked genes); Draw a diagram of genetic recombination of homologous chromosomes by linkage/crossing-over and independent assortment of homologous chromosomes, according to the example studied; Calculate the distance between linked genes and draw a gene map/gene mapping. “2020— Ua sTSH ed Sad aad gh aS Lat ED ie AS pa gpl te — (as 6 Ay Bnd) Gi aA 2S jel Sy is Ae G4 a phy cAI 5 fil gael 38 Seneebact gmail.com : is 5S) 9.93 05.37.71.4408 : Si 05,37.71.44.53 ISD os ble JY gant J [_* Gene maps. 13. Human | © Notions of pedigree and * Analyse, interpret and explain pedigree and genetics karyotype. karyotype data by inferring/deducing the mode © Hereditary autosomal of transmission of a gene in the case of: diseases. © Hereditary autosomal diseases ; © Hereditary sex-linked © Hereditary sex-linked diseases; diseases. * Analyse, interpret /explain the chromosomal © Chromosomal abnormalities | abnormalities by drawing appropriate diagrams; and their consequences. ‘© Give opinion on the prenatal diagnosis of © Chromosomal interpretation | chromosomal abnormalities based on data of hereditary diseases. exploitation, ‘Area 2: Genetic variation _ Coverage : from 20% to 30% | Sub-areas Content ‘Basie objectives (notional / methodological) Quantitative | * Continuous and [° Determine the distinct characteristics of the study of discontinuous variation of | continuous and discontinuous variation of genetic hereditary hereditary characteristics/traits based on the variation characteristics/traits; study of examples; + Homogeneous and «Use graphs to represent the continuous and the heterogeneous population; | discontinuous variations; * Position and dispersion parameters and their statistical significance; © Notion of pure lineage/purebreds (effective and ineffective selection), «__Asttificial selection. Calculate position and dispersion parameters and deduce their statistical significance; * Deduce/conclude the role of artificial selection in the improvement of agricultural productivity. PRO WPS LW ml nh DOG RAN De ET 1 ty gh an Gia Joe Ml Bal) i Ml gb He AEA gah gS gy A Ng lB py i ee 6 AS Ue ans CHING silyl 36 pleneebacDgmal.com : 21 318 05,37.71.46.08 : SI 05.37.71.48.53 ISD 2. Skills Table Skills areas T ‘Skills ‘Weighting in | (%) Knowledge This section, knowledge retrieval , aims to assess the | Retrieval. degree of mastery of content using the following: | * Multiple Choice Questions (CQ). | + True/false statements. + Matching. 25% + Classification/seriation rearranging. + Short-answer questions (giving definitions, labeling a diagram or a graph, and know theories, laws, scientific terms, facts, signs, etc.) Scientific This Seton, scientific reasoning and communication ip raphic and written modes, aims to assess the degree o Reasoning and | Prfery of skills and competencies: ® Communicatio + Determine and formulate a scientific problem; nin graphic + Use background knowledge, select and organise Ta information in relation to the subject of study; + Link information with acquired knowledge to resolve a scientific problem; + Make/formulate a hypothesis in relation to a scientific problem; + Use knowledge to solve a scientific problem or to explain the phenomena under study; + Suggest appropriate tools to test hypotheses; 0% + Describe and analyse scientific data; 73% + Compare and explain/interpret results; + Infer and generalise the results; * Use principles, laws, models to explain/interpret scientific phenomena and data; + Conduct a synthesis of information and data and turn it into a text or a diagram; * Give an opinion and support it with arguments. + Present a structure or biological and geological phenomena using a diagram. + Turn numerical data into a chart, a graph or a text. + Draw a functional diagram. + Achieve/realise a synthetic flowchart. modes, 72020— YAS Gad an yall il Fai Lats EAN Sm pl LT "Vag pall ae Gui 8 A ad) My Hal pe Be LLY gap BAYH hey 4S 2 Sy ey a 5 pe 6 46 a sil cade 5 ll ile 36 wleneebaet@gmail.com : ys 0 ol 0537.71.48.08 : Sith 05,37.71.44.53 /Sat9d AIAG CHOCO ysl ACOH 1 2ORCE CHO Ag! YA aly NOCH sexta awoch sim nme cons AOE OE vaaseall Sgt 1. Specification table: Knowledge and skills Skills Knowledge | Scientific Reasoning | Total | Scores Retrieval and Communication in | (%) | assigned 25%) graphic and written to each Areas of knowledge ~~ modes 75% content —~ (areas and sub-areas) ~ _ area 1. Transmission | 1.1- transmission of of genetic genetic information information _| through sexual we through sexual | reproduction. e 7 ‘this erase | 0% reproduction | 1.2- Mendel’s laws sete 50% ‘this nT? | 141015 and Human of heredity i? 9 to 90% Ak this. ° pts y areais included in | 75% genetics (70% | transmission of 25% in one of | Sention'! to 75%) characteristics/traits | “wo areas ~ | in diploid organisms. 1,3 Human genetics. 2- Genetic ‘Quantitative study of © 25% to 30% ifthis | variation (25% | genetic variation. area isn’t included in | 25% to 30%) Section 1 to | Sto6pts lo 0% if this area is 30% | included in Section I Total (%) 25% 73% 100% Scores assigned to each Section. Spits 15 pts 20 | 20pts 1/2 2. Design of the National Baccalaureate Exam. TEST SECTIONS Section I (Part I) : Knowledge Retrieval This part, knowledge retrieval, aims to assess the degree of mastery of content using the following: Multiple Choice Questions (MCQ). ‘True/false statements. Matching. Classification/seriation/rearranging. Short-answer questions (give definitions, label a diagram or a graph, and know theories, Jaws, scientific terms, facts, signs, ete.). This part tests the learners’ knowledge in one of the two following content areas: | Scoring | 1. Transmission of genetic information through sexual | reproduction and Human genetics 25% S pts 2. Genetic variation Section II (Part ID) : Scientific Reasoning and Communication in graphic and written modes In case the first area (area 1) is not included | - Exercises in the area 1. 73% 15 pts in part I. Incase the first area _| Exercises in the contents of [ (area 1) is included in | the area 1 not included in 45% to 50% 9 to 10 pts part I. Section I. - One exercise in the area 2. 25% to 30% 5 to 6 pts Note: Section I may include two exercises combining the two areas, and taking into account the scores distribution of those two areas and respecting the scoring of Section I. N.B. Necessary exam tools: In addition to the ID card and the invitation letter for the exam, the candidate must have the following tools: + Pens, pencils, ruler, eraser and a pencil sharpener. + Non-programmable calculator. + Graph paper. 2/2

You might also like