exam questions

Cards (24)

  • Describe why single celled organisms do not need a specialised gas exchange surface (2)
    -       They have a large surface area to volume ratio
    -       Therefore, small volume means short diffusion distances to all organelles
    -       Thus, can rely on simple diffusion, to take in oxygen and remove wastes
  • Explain how the structure of the human lungs enables rapid gas exchange (4) 
    -       Large SA from the many alveoli 
    -       One epithelial cell thick walls of exchange surfaces e.g., capillaries and alveoli creating short diffusion distance
    -      steep concentration gradients maintained by circulation of blood and ventilation 
    -       Extensive capillary network around alveoli provides large SA for gas exchange.
  • Identify 2 properties that make an efficient exchange system and explain how they affect the rate of gas exchange in the lungs (4)
    -       Alveoli increase the surface area of mammalian lungs
    -       The alveolar wall consists of a single layer of flattened epithelium creating a short diffusion distance
    -       It will allow more gas molecules to diffuse across the gas exchange surface
    -       Thereby increasing the rate of diffusion/gas exchange 
     
  • Explain the importance of capillaries in gas exchange (2)
    -       Transports deoxygenated blood high in C02 to the alveoli
    -       Transports oxygenated with low c02 concentration away from the alveoli
    -       This creates a steep concentration gradient for oxygen and c02, facilitating gaseous exchanges 1
  • Determine why animal A does not need a circulation system but animal B does (4)
    -       Both have the same volume 
    -       However, animal A has a larger surface area thus larger SA: V 
    -       So sufficient surface area for diffusion to take place 
    -       Distance to cells in centre of A are shorter than for B, allowing quicker diffusion due to shorter diffusion distance.
  • Give one function of the glycoproteins found in the cell surface membrane (1)
    -       Act as antigens on the cell surface membrane/ allow cell recognition
  • Explain how the structure of a phospholipid molecule contributes to the partial permeability of a cell surface membrane (3)
    -       The phosphate head is polar and fatty acid tails not polar
    -       Allows fat-soluble/non-polar molecules to pass through the membrane 
    -       Polar/ionic molecules cannot pass through phospholipid bilayer
  • Explain how phospholipids form a cell surface membrane (3)
    -       Hydrophilic parts (polar phosphate head) associates with water 
    -       Hydrophobic parts associate with each other but repel water
    -       A bilayer forms with hydrophobic parts pointing in towards the centre and hydrophobic parts on the outside.
  • Explain why the phospholipids are arranged in 2 layers in a cell surface membrane (3)
    -       Hydrophilic region (phosphate head) orientated towards water 
    -       Hydrophobic region away from water- fatty acid tails 
    -       But need the 2 layers as water solution either side of cell membrane
  • Describe the structure of the cell surface membrane (3)
    -       Mainly phospholipids and proteins 
    -       Phospholipids form a bilayer 
    -       Proteins float in the phospholipids and change position 
    -       Proteins may be intrinsic or extrinsic
     
  • Explain why plasma membranes are described as fluid mosaic structures (2) 
    -       Proteins and phospholipids can move around bilayer via diffusion(fluid)
    -       Membranes contain both proteins and phospholipids which are arranged in a scattered pattern- looks like mosaic.
  • State 3 functions of a phospholipid bilayer (3)
    -       Allows cells to maintain different concentration of molecules on either side of the membrane 
    -       Enables membrane to fuse with other membranes or to form vesicles 
    -       Provides flexibility to the membrane
  • Compare and contrast the davson-danielli model of cell surface membrane with the fluid mosaic model (3)
    -       Both contain a phospholipid bilayer 
    -       Globular proteins present in both 
    -       Membrane proteins in fluid mosaic varied in size whereas the proteins are less varied in size in his model.
  • What is the role of cholesterol in cell membranes? (1)
    -       Cholesterol prevents the phospholipid tails from packing too closely together when the temperature decreases to maintain membrane fluidity.
  • Explain why betalain molecules cannot move through intact cell membranes (3)
    -       They are too large to fit through the gaps of phospholipids 
    -       They are also polar so cannot interact with the non-polar phospholipid tails and can’t move through 
    -       Also, no carrier or channel proteins for the belalain molecules to move through.
  • Compare and contrast diffusion and active transport (3) 
    -       Both move molecules through the phospholipid bilayer 
    -       In both molecules can move through proteins 
    -       Diffusion occurs down a conc gradient whereas active transport is against conc gradient
    -       Diffusion is passive so does not require ATP whereas active transport does require ATP.
  • compare and contrast the processes of endocytosis and exocytosis (3)
    -       both involve the use of vesicles 
    -       both involve energy from ATP
    -       endo involved molecules entering cell whereas exo involved molecules leaving the cell
    -       endo involved the formation of new vesicles from the cell surface mem whereas exo involves vesicles fusing with cell mem.
  • Explain why ATP is required for the movements of sodium ions into the cell (2)
    -       Because active transport must occur through carrier proteins
    -       Energy is needed to move sodium ions against their concentration gradients
  • Describe how glucose moves into the cell (2)
    -       Via carrier protein in cell surface membrane
    -       Glucose moves from high to low concentration 
    -       Glucose binds to carrier protein, carrier changed shape to move glucose across membrane
  • Describe how glucose moves into cells by facilitated diffusion (2)
    -       Moves in down its conc gradient without ATP
    -       Moves in via carrier
  • Give 2 differences between endocytosis and exocytosis (2)
    -       Endocytosis allows substances to move in and exocytosis allows substances to leave the cell.
    -       Exo involves vesicles fusing with the cell membrane whereas endo involves the formation of vesicles from the cell surface mem.
  • Describe the function of carrier proteins in a cell surface membrane (4)
    -       Can be used for either facilitated diffusion (from high to low conc) or active transport (against conc gradient) 
    -       Moves charged particles into or out of cell 
    -       Has 2 shapes and ATP required to change shape of protein and move molecules against conc gradient.
  • Describe how glucose enters muscle cells through the cell membrane (2) 
    -       Facilitated diffusion
    -       Via carrier proteins located in membrane
  • Deduce the effect on increasing the concentration of solution surrounding onion, on the change in mass of the onion (3) 
    -       Increased concentration of solution outside, it is stronger (less dilute) than inside of onion 
    -       Therefore, water molecules move down the concentration gradient, from an area of low concentration to high concentration across the partially permeable membrane 
    -       Water moving out means mass of onion will decrease.