Organisms Exchange their Substances with their Environment Flashcards

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1
Q

why do organisms need to exchange substances with their environment?

A

cells need to take in oxygen (for aerobic respiration) and nutrients.
they also need to excrete waste products like carbon dioxide and urea.
most organisms need to stay at roughly the same temperature, so heat needs to be exchanged too.

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2
Q

what is the relationship between the size of animals and their surface area: volume ratio?

A

smaller animals have a higher surface area: volume ratio, whereas larger animals have a smaller surface area: volume ratio.

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3
Q

what two things affect heat exchange?

A

body size and body shape.

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4
Q

how does body size affect heat exchange?

A

the rate of heat loss from an organism depends on its surface area.
if an organism has a large volume, its surface area is relatively small. this makes it harder for it to lose heat from its body.
if an organism is small, its relative surface area is large, so heat is lost more easily. this means smaller organisms need a relatively high metabolic rate, in order to generate enough heat to stay warm.

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5
Q

how does body shape affect heat exchange?

A

animals with a compact shape have a small surface area relative to their volume; this minimises heat loss from their surface.
animals with a less compact shape (have sticky bits out/more gangly) have a larger surface area relative to their volume; this increases heat loss from their surface.

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6
Q

what behavioural and physiological adaptations do organisms have to aid exchange?

A

animals with a high SA: volume ratio tend to lose more water as it evaporates from their surface. some small desert mammals have kidney structure adaptations so that they produce less urine to compensate.
to support their high metabolic rates, small mammals living in cold region need to eat large amounts of high energy foods such as seeds and nuts.
smaller mammals may have thick layers of fur or hibernate when the weather gets really cold.
larger organisms living in hot regions find it hard to keep cool as their heat loss is relatively slow. elephants have developed large flat ears to increase their surface area, allowing them to lose more heat.

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7
Q

what two major adaptations to gas surface exchanges have?

A

they have a large surface area.
they are thin which provides a short diffusion pathway across the gas exchange surface.

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8
Q

how do single-celled organisms exchange gases across their body surface?

A

they absorb and release gases by diffusion through their outer surface.
they have a relatively large surface area, a thin surface and a short diffusion pathway, so there’s no need for a gas exchange system.

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9
Q

how does gas exchange occur in fish?

A

using a counter-current system.
there’s a lower conc. of oxygen in water than in air.
water, containing oxygen, enters the fish through its mouth and passes through the gills. each gill is made of lots of thin plates called gill filaments which give it a big surface area for exchange of gases.
the gill filaments are covered in lots of tiny structures called lamellae, which increase the surface area even more.
the lamellae have lots of blood capillaries and a thin surface layer of cells to speed up diffusion.
blood flows through the lamellae in one direction and water flows over in the opposite direction. this counter-current system maintains a large concentration gradient between the water and the blood. the conc. of oxygen in the water is higher than that in the blood, so as much oxygen as possible diffuses from water into the blood.

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10
Q

how does gas exchange occur in insects?

A

insects have microscopic air-filled pipes called tracheae which they use for gas exchange.
air moves into the tracheae through pores on the surface called spiracles.
oxygen travels down the concentration gradient towards the cells.
the tracheae branch off into smaller tracheoles which have thin permeable walls and go to individual cells. this means that oxygen diffuses directly into the respiring cells; the insect’s circulatory system doesn’t transport oxygen.
carbon dioxide from the cells move down its own concentration gradient towards the spiracles to be released into the atmosphere.
insects use rhythmic abdominal movements to move air in and out of the spiracles.

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11
Q

how does gas exchange occur in dicotyledonous plants?

A

the main gas exchange surface is the surface of the mesophyll cells in the leaf. theyr’e well adapted for their function; they have a large surface area.
the mesophyll cells are inside the leaf. gases move in and out through special pores in the epidermis called stomata.
the stomata can open to allow exchange of gases, and close if the plant is losing too much water.
guard cells control the opening and closing of stomata.

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12
Q

how are insects and plants able to control water loss?

A

insects: if they lose too much water, they close their spiracles using their muscles. they also have waterproof, waxy cuticle all over their body and tiny hairs around their spiracles, both of which reduce evaporation.
plants: a plants’ stomata are usually kept open during the day to allow gaseous exchange. water enters the guard cells, making them turgid which opens the stomatal pore. if a plant starts to get dehydrated, the guard cells lose water and become flaccid, which closes the pore.

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13
Q

what are xerophytic plant adaptations when living in warm, dry or windy habitats where water loss is a problem?

A

stomata sunk in pits that trap moist air, reducing the concentration gradient of water between the leaf and the air. this reduces the amount of water diffusing out of the leaf and evaporating away.
a layer of hairs on the epidermis; which again traps the moist air around the stomata.
curled leaves with the stomata inside, protecting them from wind which helps to increase the rate of diffusion and evaporation.
a reduced number of stomata, so there are fewer places for water to escape.
waxy, waterproofed cuticles on leaves and stems to reduce evaporation.

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14
Q

explain the human gas exchange system.

A

lungs are used for gas exchange in humans.
as you breathe in, air enters the trachea (windpipe).
the trachea splits into two bronchi; one bronchus leading to each lung.
each bronchus then branches off into smaller tubes called bronchioles.
the bronchioles end in small ‘air sacs’ called alveoli.
the ribcage, intercostal muscles and diaphragm all work together to move air in and out.

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15
Q

what is ventilation?

A

this consists of inspiration and expiration.
its controlled by the movements of the diaphragm, internal and external intercostal muscles and ribcage.

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16
Q

explain inspiration.

A

the external intercostal and diaphragm muscles contract.
this causes the ribcage to move upwards and outwards and the diaphragm to flatten, increasing the volume of the thoracic activity (the space where the lungs are).
as the volume of the thoracic cavity increases, the lung pressure decreases to below atmospheric pressure.
air will always flow from an area of higher pressure to an area of lower pressure so air flows down the trachea and into the lungs.
inspiration is an active process and so it requires energy.

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17
Q

explain expiration.

A

the external intercostal and diaphragm muscles relax.
the ribcage moves downwards and inwards and the diagram becomes curved again.
the volume of the thoracic cavity decreases, causing air pressure to increase to above atmospheric pressure.
air is forced down the pressure gradient and out of the lungs.
normal expiration is a passive process and so it doesn’t require energy.

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18
Q

what are two examples of forced expiration?

A

blowing out candles on your birthday cake.
coughing.

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19
Q

explain forced expiration.

A

the external intercostal muscles relax and the internal intercostal muscles contract, pulling the ribcage further down and in. this movement is said to be antagonistic.

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20
Q

where does human gaseous exchange occur?

A

in the alveoli.

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21
Q

what are alveoli made of?

A

a single layer of thin, flat cells called alveolar epithelium.

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22
Q

explain gas exchange in the alveoli.

A

there is a huge number of alveoli in the lungs, which means there’s a big surface area for exchanging oxygen and carbon dioxide.
the alveoli are surrounded by a network of capillaries.
oxygen diffuses out of the alveoli, across the alveolar epithelium and the capillary endothelium (forms the capillary wall) and into haemoglobin in the blood.
carbon dioxide diffuses into the alveoli from the blood, and is breathed out.

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23
Q

what features are present in the alveoli that speed up the rate of diffusion so gases can be exchanged quickly?

A

a thin exchange surface; the alveolar epithelium is only one cell thick and so there’s a short diffusion pathway.
a large surface area; a larger number of alveoli means a larger surface area for gas exchange.

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24
Q

what impact does a steep concentration gradient have on gas exchange in humans?

A

a steep conc. gradient of oxygen and carbon dioxide between the alveoli and the capillaries increases the rate of diffusion.
gases are able to be exchanged quickly.
the conc. gradient is maintained by the flow of blood and ventilation.

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25
Q

what do lung diseases affect in the lungs?

A

they affect both ventilation and gas exchange in the lungs; how well the lungs function.

26
Q

how can doctors diagnose lung diseases?

A

they can carry out tests to investigate lung function.

27
Q

define tidal volume.

A

the volume of air in each breath; usually between 0.4 dm cubed and 0.5 dm cubed for adults.

28
Q

define ventilation rate.

A

the number of breaths per minute, for a healthy person at rest it’s about 15 breaths.

29
Q

define forced expiratory volume1 (FEV1).

A

the maximum volume of air that can be breathed out in 1 second.

30
Q

define forced vital capacity (FVC).

A

the maximum volume of air it is possible to breathe forcefully out of the lungs after a really deep breath in.

31
Q

what equipment is used to measure tidal volume, ventilation rate, (FEV1) and (FVC)?

A

a spirometer.

32
Q

how do we interpret data on risk factors of lung disease?

A

first we describe the data on the graphs, include values from the graph and use the appropriately.
then we draw conclusions from the graph, we do this stating correlations and not causations. just because there’s a correlation does not mean that factor caused the lung disease- there may be other factors.
the look oat other things to consider from the graph; keep information points which can be useful in understanding the risk factors of lung disease.

33
Q

how do we dissect fish gills in bony fish?

A

make sure you are wearing an apron or lab coat.
place chosen fish in a dissection tray or on a cutting board.
gills are located on either side of the fish’s head. they’re protected on each side by a bony flap called an operculum and supported by gill arches.
to remove the gills, push back the operculum and use scissors to carefully remove the gills. cut out each gill arch through the bone at the top and bottom.
looking closely you should see the gill filaments.

34
Q

explain the basics of digestion.

A

the large biological molecules in food are too big to cross cell membranes. this means they can’t be absorbed from the gut into the blood.
during digestion, these large molecules are broken down into smaller molecules by hydrolysis, which can move across cell membranes. This means they can easily be absorbed from the gut into the blood, to be transported around the body for use by the body cells.

35
Q

what is used to break down the biological molecules in food?

A

digestive enzymes.

36
Q

what are digestive enzymes?

A

these are enzymes which are produced by specialised cells in the digestive systems of mammals.
these enzymes are then released into the gut to mix with food.

37
Q

explain the process of carbohydrate digestion.

A

carbohydrates are broken down by amylase and membrane-bound disaccharidases.
amylase is a digestive enzyme that catalyses the conversion of starch into the smaller sugar maltose. this involves the hydrolysis of the glycosidic bonds in starch.
membrane-bound disaccharidases are enzymes that are attached to the cell membranes of epithelial cells lining the ileum. they help to break down disaccharides into monosaccharides. this involves the hydrolysis of glycosidic bonds.

38
Q

where is amylase produced and released into?

A

produced in the salivary glands, which release amylase into the mouth.
and also in the pancreas, which releases amylase into the small intestine.

39
Q

explain the process of lipid digestion.

A

lipids are broken down by lipase with the help of bile salts.
lipase enzymes catalyse the breakdown of lipids into monglycerides and fatty acids. this involves the hydrolysis of the ester bonds in lipids.
bile salts emuslify lipids; this causes the lipids to form small droplets.
once the lipid has been broken down, the monoglycerides and fatty acids stick with the bile salts to form tiny structures called micelles.

40
Q

why are bile salts important in the process of lipid digestion?

A

several small lipid droplets have a bigger surface area than a single large droplet. so the formation of small droplets greatly increases the surface area of lipid that’s available for lipases to work on.

41
Q

where are lipases made?

A

in the pancreas. they work in the small intestine.

42
Q

how are bile salts produced?

A

produced by the liver.

43
Q

what are proteins broken down by?

A

a combination of proteases. these are enzymes that catalyse the conversion of proteins into amino acids by hydrolysing the peptide bonds between amino acids. these proteases are endopeptidases and exopeptidases.

44
Q

define proteases

A

these are enzymes that catalyse the conversion of proteins into amino acids by hydrolysing the peptide bonds between amino acids.

45
Q

what are endopeptidases?

A

they act to hydrolyse peptide bonds within a protein.

46
Q

name and give the functions of two examples of endopeptidases

A

trypsin is an example of an endopeptidase. it is synthesised in the pancreas and secreted into the small intestine.
pepsin is another example. it’s released into the stomach by cells in the stomach lining. pepsin only works in acidic conditions which are provided by hydrochloric acid in the stomach

47
Q

what are exopeptidases?

A

they act to hydrolyse peptide bonds at the ends of protein molecules. they remove single amino acids from proteins.

48
Q

name and give the function plus location of an exopeptidase

A

dipeptidases are exopeptidases that work specifically on dipeptides. they act to separate the two amino acids that make up a dipeptide by hydrolysing the peptide bond between them.
dipeptidases after often located in the cell-surface membrane of epithelial cells in the small intestine.

49
Q

what are the products of digestion?

A

monosaccharides
monoglycerides and fatty acids
amino acids

50
Q

how are monosaccharides absorbed across the ileum epithelium into the bloodstream?

A

glucose is absorbed by active transport with sodium ions via a co-transporter protein.
galactose is absorbed in the same way using the same co-transporter protein.
fructose is absorbed via facilitated diffusion through a different transporter protein.

51
Q

how are monoglycerides and fatty acids absorbed across the ileum epithelium into the bloodstream?

A

micelles help to move monoglycerides and fatty acids towards the epithelium. because micelles constantly break up and reform, they can ‘release’ monoglycerides and fatty acids, allowing them to be absorbed; whole micelles are not taken up to the epithelium.
monoglycerides and fatty acids are lipid-soluble, so can diffuse directly across the epithelial cell membrane.

52
Q

how are amino acids absorbed across the ileum epithelium into the bloodstream?

A

amino acids are absorbed via co-transport.
sodium ions are actively transported out of the ileum epithelial cells into the blood. this creates a sodium ion concentration gradient.
sodium ions can then diffuse from the lumen of the ileum into the epithelial cells through sodium-dependent transporter proteins, carrying the amino acids with them.

53
Q

how is oxygen carried around the body?

A

by haemoglobin

54
Q

what do red blood cells contain?

A

haemoglobin

55
Q

what is haemoglobin?

A

haemoglobin is a large protein with a quaternary structure; its made up of more than one polypeptide chain (four).
each chain has a haem group, which contains an iron ion and gives haemoglobin its red colour.
haemoglobin has a high affinity for oxygen.
oxygen joins to haemoglobin in red blood cells to form oxyhaemoglobin.

56
Q

what is the partial pressure of oxygen?

A

it is the measure of oxygen concentration.
the greater the concentration of dissolved oxygen in cells, the higher the partial pressure.

57
Q

what is the partial pressure of carbon dioxide?

A

it is a measure of the concentration of CO2 in a cell.

58
Q

explain how haemogblobin’s affinity for oxygen varies.

A

it varies depending on the partial pressure of oxygen.
oxygen loads onto haemoglobin to form oxyhaemoglobin where there’s a high partial pressure of oxygen.
oxyhaemoglobin unloads its oxygen where there’s a lower partial pressure of oxygen.
oxygen enters blood capillaries at the alveoli in the lungs. alveoli have a high partial pressure of oxygen so oxygen loads onto the haemoglobin to form oxyhaemoglobin. when cells respire, they use up oxygen; this lowers the partial pressure of oxygen. red blood cells deliver oxyhaemoglobin to respiring tissues, where it unloads its oxygen.
the haemoglobin then returns to the lungs to pick up more oxygen.

59
Q

what does a dissociation curve show?

A

it shows how saturated the haemoglobin is with oxygen at any given partial pressure.

60
Q

why is the dissociation curve ‘s-shaped’?

A

the graph is ‘s-shaped’ because when haemoglobin (Hb) combines with the first O2 molecule, its shape alters in a way that makes it easier for other molecules to join too. but as the Hb starts to become saturated, it gets harder for more oxygen molecules to join. as a result, the curve has a steep bit in the middle where it’s really easy for oxygen molecules to join, and shallow bits at each end where it’s harder. when the curve is steep, a small change in pO2 causes a big change in the amount of oxygen carried by the Hb.

61
Q

explain the Bohr effect

A