1 |
Limits to Cell Size |
1.1.U3 Cell Surface to volume is an important limitation to cell size.
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Outline the activities occurring in the volume and at the surface of the cell.
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Calculate the surface area, volume and SA:V ratio of a cube.
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Explain the benefits and limitations of using cubes to model the surface area and volume of a cell.
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Describe the relationship between cell size and the SA:V ratio of the cell.
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Explain why cells are often limited in size by the SA:V ratio.
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List three adaptations of cells that maximize the SA: volume ratio
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Initial Knowledge audit
SA:V notes
Modeling SA:V with cubes
Cube data
A&B: The unsexiest thing in science (article)
BTB Cube lab
Cube lab data collection form
Iodine into potato cubes lab
Past classes potato lab data
Design a cell lab
Design a cell (old vB version)
SA:V debrief
Limits to cell size CFU |
2 |
Diffusion |
1.4.U1: Particles move across membranes by simple diffusion, facilitated diffusion, osmosis and active transport.
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Describe simple diffusion.
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Explain two examples of simple diffusion of molecules into and out of cells.
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Outline factors that regulate the rate of diffusion.
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Membrane transport (vision learning)
Membrane and distribution (vision learn)
Diffusion virtual simulation
Diffusion across a membrane virtual
Effect of temp on diffusion simulation
Factors affecting the rate of diffusion dry lab
Solute size mini-lab
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3 |
Osmosis |
1.4.U1: Particles move across membranes by simple diffusion, facilitated diffusion, osmosis and active transport.
1.4.A2: Tissues or organs to be used in medical procedures must be bathed in a solution with the same osmolarity as the cytoplasm to prevent osmosis.
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Explain what happens to cells when placed in solutions of the same osmolarity, higher osmolarity and lower osmolarity.
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Outline the use of normal saline in medical procedures.
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Osmolarity in medicine
Modeling tonicity activity
Tonicity practice problems:
Case studies:
Death by osmosis lab
Osmotic changes in RBC lab
Egg osmosis labs:
Review of osmosis
Diffusion and osmosis CFU
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4 |
Measurement Precision and Uncertainty |
1.4.NOS: Experimental design- accurate quantitative measurement in osmosis experiments are essential.
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Define quantitative and qualitative.
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Determine measurement uncertainty of a measurement tool.
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Explain the need for repeated measurements (multiple trials) in experimental design.
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Explain the need to control variables in experimental design
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Measurement slides
Rulers for uncertainty practice
Practice with determining uncertainty
A&B: Visualizing the Uncertainty in Data |
5 |
Estimating Osmolarity |
1.4.S1: Estimation of osmolarity in tissues by bathing samples in hypotonic and hypertonic solutions. Practical 2
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Define osmolarity, isotonic, hypotonic and hypertonic.
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Calculate the percentage change between measurement values.
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Accurately graph mean and standard deviation of data sets.
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Determine osmolarity of a sample given changes in mass when placed in solutions of various tonicities.
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Data Based Questions
Labs: |
6 |
Facilitated Diffusion |
1.4.U1: Particles move across membranes by simple diffusion, facilitated diffusion, osmosis and active transport. |
Scitable ion channel reading
Channel Surfing reading and questions
A&B Vital signs podcast
A&B This Podcast will Kill you CF
Modeling effects of CF lab
Phet membrane channels
Passive transport review
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7 |
Active Transport |
1.4.U1: Particles move across membranes by simple diffusion, facilitated diffusion, osmosis and active transport. |
Active transport yeast lab
Simple co-transport model
CFU: transport proteins |
8 |
Exo and Endocytosis |
1.4.U2: The fluidity of membranes allows materials to be taken into cells by endocytosis or released by exocytosis.
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Describe the fluid properties of the cell membrane and vesicles.
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Explain vesicle formation via endocytosis.
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Outline two examples of materials brought into the cell via endocytosis.
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Explain release of materials from cells via exocytosis.
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Outline two examples of materials released from a cell via exocytosis.
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9 |
Wrap Up and Review |
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