| Literature DB >> 31144570 |
Jennifer S Avena1, Jennifer K Knight1.
Abstract
Problem solving is an integral part of doing science, yet it is challenging for students in many disciplines to learn. We explored student success in solving genetics problems in several genetics content areas using sets of three consecutive questions for each content area. To promote improvement, we provided students the choice to take a content-focused prompt, termed a "content hint," during either the second or third question within each content area. Overall, for students who answered the first question in a content area incorrectly, the content hints helped them solve additional content-matched problems. We also examined students' descriptions of their problem solving and found that students who improved following a hint typically used the hint content to accurately solve a problem. Students who did not improve upon receipt of the content hint demonstrated a variety of content-specific errors and omissions. Overall, ultimate success in the practice assignment (on the final question of each topic) predicted success on content-matched final exam questions, regardless of initial practice performance or initial genetics knowledge. Our findings suggest that some struggling students may have deficits in specific genetics content knowledge, which when addressed, allow the students to successfully solve challenging genetics problems.Entities:
Mesh:
Year: 2019 PMID: 31144570 PMCID: PMC6755211 DOI: 10.1187/cbe.18-06-0093
Source DB: PubMed Journal: CBE Life Sci Educ ISSN: 1931-7913 Impact factor: 3.325
FIGURE 1.Example of a practice question used for problem solving on the content of nondisjunction. Each question in the study had a visual aid, was constructed response, and had a single correct answer.
Content hints
| Content area | Hint |
|---|---|
| Recombination | The map distance between two genes provides information about the chance that recombination will occur between those two genes. |
| Probability | For an autosomal recessive disease, a |
| Gel/pedigree | Males have only one X chromosome and thus only one copy of any DNA sequences on the X chromosome. |
| Nondisjunction | Replicated homologous chromosomes align along the metaphase plate in meiosis I, and sister chromatids align along the metaphase plate in meiosis II. |
Performance on practice problem-solving questionsa
| Content area | Q1 % correct | Q2 % correct | Q3 % correct | |
|---|---|---|---|---|
| All content areas | 553 | 56 | 60 | 60 |
| Recombination | 179 | 38 | 45 | 47 |
| Probability | 122 | 50 | 55 | 52 |
| Gel/pedigree | 127 | 65 | 76 | 76 |
| Nondisjunction | 125 | 76 | 71 | 71 |
Performance at the level of the individual answer for 553 trios of questions (1659 questions total). The number of trios for each content area is represented by n. Practice assignment 2 included the recombination questions; practice assignment 1 included the other three content areas. Across all content areas combined, the Q2 and Q3 percent correct were significantly higher than Q1 (McNemar’s test, p < 0.05), while there was no difference between Q2 and Q3 (McNemar’s test, p > 0.05). For recombination and gel/pedigree, the Q3 percent correct was significantly different from Q1 (McNemar’s test, p < 0.05), while there was no difference in pairwise comparisons between Q1 and Q2 or Q2 and Q3 (McNemar’s test, p > 0.05). For probability and nondisjunction, there was no significant difference in percent correct among Q1, Q2, and Q3 (McNemar’s test, p > 0.05). For Q1, gel/pedigree and nondisjunction had higher performance than probability (OR = 1.9, p < 0.05, and OR = 3.2, p < 0.001, respectively) and also higher than recombination (OR = 3.1, p < 0.001, and OR = 5.2, p < 0.001, respectively); probability had higher performance than recombination (OR = 1.6, p < 0.05).
FIGURE 2.The effect of a hint differs depending on Q1 correctness. (A) Q1 incorrect: the percent of correct answers for Q2 and Q3 is shown for trios in which a hint was taken at Q2 (n = 84 trios) or at Q3 (n = 110 trios). *, p < 0.05; all else NS, p > 0.05 (logistic regression between conditions; McNemar’s test between Q2 and Q3 for each condition). (B) Q1 correct: the percent of correct answers for Q2 and Q3 is shown for trios in which a hint was taken at Q2 (n = 89 trios) or at Q3 (n = 91 trios). There were no significant differences between conditions (logistic regression, p > 0.05) or between Q2 and Q3 (McNemar’s test, p > 0.05).
FIGURE 3.Student-level progression across answer trios in which a hint was taken at Q2. Percent of correct answers is shown with the number of answers in each category (e.g., Q1 incorrect) in parentheses. Arrows indicate the percent of answers that track to the next category. Bolded arrows signify categories of trios that were analyzed for content-specific language use and errors/omissions: trios with Q1 incorrect but Q2 and Q3 correct (011 group) and those with all three answers incorrect (000 group).
FIGURE 4.Student-level progression for answer trios in which a hint was taken at Q3. Percentage of correct answers is shown with the number of answers in each category (e.g., Q1 incorrect) in parentheses. Arrows indicate the percent of answers that track to the next category. Bolded arrows signify categories of trios that were analyzed for content-specific language use and errors/omissions: trios with Q1 and Q2 incorrect but Q3 correct (001 group) and those with all three answers incorrect (000 group).
Presence of language reflecting content in hint criteria, coded only in answers during and after receipt of a hint
| Content area | Student language scored as reflecting content hint if contained: |
|---|---|
| Recombination | Specific mention of map units and/or recombination percentage relevant to the problem |
| Probability | 2/3 as the probability an individual is heterozygous (when known to be unaffected) |
| Gel/pedigree | Description of males as having only one X chromosome or one allele of a gene on the X chromosome |
| Nondisjunction | Description of chromosome alignment before separation (1) and/or timing of homologous chromosome separation (2) and/or timing of sister chromatid separation (3) |
Content errors and omissions codes
| Content code | Description (in an answer, the student does at least one of the following listed for a given code) |
|---|---|
| Recombination | |
| No use of map units | Does not use map units to determine probability |
| Incorrect use of map units | Uses map units in an unconventional manner (e.g., multiplies map units by Mendelian probabilities or considers map units for a double homozygote) |
| Gamete type error | Indicates that the desired gamete is parental versus recombinant (or vice versa)Assigns the probability of a recombinant gamete to the parental gamete (or vice versa) |
| Desired genotype incorrect | Incorrectly states desired genotype for the answer |
| Probability | |
| Genotype/probability misassignment | Misassigns genotype and/or probability (e.g., does not assign 2/3 to an unaffected child of two heterozygote parents with an affected child) |
| No/improper use of product rule | Does not use the probabilities of |
| Inaccurate use of inheritance mode or calculations | Uses wrong mode of inheritanceCombines ideas from multiple modes of inheritance to determine genotypes Uses addition instead of using the product rulePerforms a calculation error |
| Gel/pedigree | |
| No discussion of copy number | Does not discuss number of chromosome copies in males (e.g., one X chromosome, two autosomes) and females (two X chromosomes, two autosomes) |
| No clear use of gel | Uses pedigree, but does not obviously use information in the gel |
| Incomplete inheritance mode | Mentions one or fewer components of a mode of inheritance (i.e., does not consider |
| Nondisjunction | |
| Incorrect chromosome definition/separation rules | Reverses definition of sister chromatids and homologuesReverses separation rules for homologues and sister chromatids |
| Misunderstanding divisions | Does not consider meiotic divisions (I and II) in which error occursDoes not differentiate meiotic divisions I and IIIncorrectly differentiates meiotic divisions I and II based on gamete chromosome number |
| General misunderstanding of meiosis | Incorrectly identifies normally expected chromosome numberAssumes an atypical process or mutation must occur |
FIGURE 5.Presence of content errors and omissions in incorrect answers in four critical content areas in genetics. The number of answers in which each content error/omission code was observed is shown, with overlap in color indicating the presence of multiple errors/omissions within a single answer. Only 000 progression groups are shown for all questions Q1–Q3. In each case, orange shading indicates an error aligned with the hint content.
OLS regression estimates of the association between practice performance and final exam performancea
| Practice-related β (SE) | Practice-unrelated β (SE) | |||
|---|---|---|---|---|
| GCA posttest | Instructor-generated final exam | GCA posttest | Instructor-generated final exam | |
| Model | 1 | 2 | 3 | 4 |
| Practice Q3 correct (%) | 0.24** (0.08) | 0.29*** (0.07) | 0.16*** (0.04) | 0.16** (0.05) |
| Practice Q1 correct (%) | 0.16 (0.08) | 0.06 (0.07) | 0.12** (0.04) | 0.09 (0.05) |
| GCA pretest (%) | 0.32* (0.16) | 0.30* (0.13) | 0.28*** (0.07) | 0.25* (0.10) |
| Adjusted | 0.2697 | 0.3077 | 0.4878 | 0.2767 |
Performance is reported as percent correct. Data reported show only students who completed both practice assignments and all assessments included in analyses (n = 109). Standard error of β (unstandardized beta coefficient) is shown in parentheses. Interpretation example (Practice Q3 correct, model 2): When controlling for practice Q1 performance and GCA pretest, there is a higher final exam performance of 0.29% for each 1% increase in Q3 performance.
*p < 0.05.
**p < 0.01.
***p < 0.001.