Biology Topic 5 Flashcards
(45 cards)
What is interspecific competition?
- When organisms of different species compete with one another for same resources.
- So resources available for both populations are reduced. So both populations will have less energy for growth and reproduction, so the population sizes will be lower for both species.
What is intraspecific competition?
When organisms of the same species compete with each other for the same resources
- The population of a species increases when resources are plentiful. As population increases, there’ll be more organisms competing for the same amount of space and food.
- Eventually resources become limited and population begins to decline.
- Smaller populations means less competition for resources, so population begins to grow again.
- Maximum stable population size that an ecosystem can support = carrying capacity.
Explain how predator and prey population sizes are linked.
- As prey population increases there’s more food for predators, so the predator population grows.
- As predator population increases, more prey is eaten so prey population begins to fall.
- This means less food for the predators, so their population decreases, and so on.
Name some abiotic factors that affect distribution.
Some plants only grow on south-facing slopes in the northern hemisphere, where light intensity is greatest.
Some plants don’t grow near to shoreline because the salt is too saline.
Large trees can’t grow in polar regions because temperature is too low.
Biotic factors that can affect distribution?
Interspecific competition can affect species distribution. If two species are competing but one is better adapted to its surroundings, the less well adapted species will be out-competed and unable to exist alongside better adapted species.
Define niche.
A niche is the role of a species within its habitat, including biotic and abiotic interactions.
Every species has its own unique niche and a niche can only be occupied by one species.
Explain random and non-random sampling.
To avoid bird in your results, the sample should be random. Eg dividing field into grid and using random number generator to select coordinates.
However sometimes necessary to take a non-random sample. Non-random samples can be used in habitats where there’s lots of variety in abiotic features and distribution of species and you want all areas and species to be sampled.
Systematic sampling= type of non-random sampling when samples are taken at fixed intervals often along a line. E.g. quadrats placed along a line called a transect in a sample where abiotic factors gradually change along the transect.
Explain point quadrats
Used to investigate plant populations
- Point quadratic = horizontal bar on two legs with a series of holes at set intervals along its length.
- Pins dropped through holes in frame and every plant that that each pin touches is recorded.
- Number of individuals of each species is recorded in each quadrat.
- Percentage cover= number of pins that touch given species÷ total number of pins x100
- Useful in areas where there’s lots of dense vegetation close to ground
Explain how transects are used
Used to investigate distribution of plant populations
- Line transects- a tape measure is placed along the transect and species that touch the tape measure are recorded.
- Belt transects - data is collected along the transect using fram quadratic placed next to each other.
- Interrupted transects: taking measurements at intervals. E.g. by placing quadratic every 2 metres.
Measuring climate within a habitat?
- Temperature is measured using a thermometer
2.Rainfall is measured using a rain gauge - a funnel attached to a measuring cylinder
- Humidity can be measured using an electronic hygrometer.
- Measuring oxygen availability in a habitat?
- Measuring solar input in a habitat?
- Only neede to be measured in aquatic habitats. The amount of oxygen dissolved in the water is measured using a light sensor.
- Measured using a light sensor
Measuring edaphic factors (soil conditions) in an ecosystem?
pH is measured using indicator liquid - a sample of the soil is mixed with water and an indicator liquid that changes colour depending on pH. The colour is matched against a chart.
Moisture content- the mass of a sample of soil is measured before and after being dried out in an oven at 80-100 degrees Celsius. The difference in mass as percentage of original soil mass = water content of soil.
Measuring topography (shape and features of the Earth’s surface) in a habitat?
Relief (how the height of the land changes across a surface) can be measured by taking height readings using a GPS device at different points across the surface. You can also use contour lines on a map.
Slope angle is measured using a clinometer. A simple clinometer is just a piece of string with a weight on the end attached to the centre of a protractor. You point the flat edge of the protractor up the hill, and read the slope angle of the protractor.
Aspect ( the direction a slope is facing) is measured using a compass.
Difference between primary and secondary succession?
- Primary succession- this happens on newly formed or exposed land e.g. where a volcano has erupted to form a new rock surface, or where sea level has dropped exposing new area of land. There’s no soil or organic material to start, just rock.
- Secondary succession- this happens on land that’s been cleared of all the plants, but where the soil remains, e.g. after forest fire or deforestation.
Describe primary succession
Primary succession starts when species colonise new land surfaces. Seeds and spores are blown by wind and begin to grow. First species to colonise = pioneer species.
The abiotic conditions are hostile e.g. no soil to retain water. Only pioneer species grow because they’re adapted to cope with harsh conditions.
Pioneer species change the abiotic conditions- they die and microorganisms decompose the dead organic material. This forms basic soil.
This makes conditions less hostile so new organisms can move in. Who then die and are decomposed making the soil richer.
Some new species may change the environment so that it becomes less suitable for the previous species.
Describe secondary succession
Secondary in same way as primary, but because there’s already a soil layer it starts at later stage. Pioneer species are therefore larger plants.
At each stage different plants and animals better adapted to conditions move in and out-compete species currently there , so they become the dominant species.
As succession goes on, ecosystem becomes more complex. New species move in alongside existing species, increasing biodiversity.
When ecosystem is supporting largely community it can it won’t change much more. This called the climax community.
Describe the succession of bare rock to woodland.
- Pioneer species colonise the rocks e.g. license grow on and break down rocks, releasing minerals.
- Lichens die and are decomposed to form thin soil. So other species like mosses can grow.
- Larger plants that need more water can move in as the soil deepens.
- Shrubs, ferns and small trees grow, out-competing smaller plants to become dominant species. Diversity increases.
- Finally soil is deep and rich enough to support large trees. They become the dominant species, and the climax community is formed.
Describe role of ATP.
Cell can’t directly fron glucose
During respiration glucose is broken down. This releases energy for ATP which carries energy to where is needed in the cell.
It is synthesised by the phosphorylation of ADP
It is broken down via hydrolysis back into ADP and PI catalysed by ATPase, the releases energy.
ADP and PI are recycled and the process repeats itself
Describe structure of chloroplasts.
Double membrane
Thylakoids have large SA to allow as much light to be absorbed as possible. They’re stacked up in the chloroplast to form granum. The grana are linked together by bits of thylakoid called lamellae. Thylakoid membranes contain lots of ATP synthase to produce ATP in the light dependent reaction.
Chloroplasts contain photosynthetic pigments attached to proteins to form photosystems. Photosystem I = 700nm photosystem II = 680nm
Stroma surrounds thylakoids this is where the light independent reaction takes place.
Describe the light dependent reaction of photosynthesis.
- Light energy excited electrons in chlorophyll.
Light energy is absorbed by PSII.
Light energy excites electrons in chlorophyll making them enter a higher energy level. This causes them to move along the electron transport chain to photosystem I. - As excited electrons from PSII to move along the ETC, they must be replaced. Light energy splits water into protons (H+), electrons and oxygen. This is called photolysis.
- Excited electrons lose energy as they move along ETC. The energy is used to transport H+ into the thylakoids so there is a greater concentration of H+ than the stroma. Protons move down their concentration gradient into the stroma, via ATP synthase. The energy from this movement combines ADP and PI to ATP.
- Light energy absorbed by PSI, exciting electrons to even higher energy level. The electrons are transferred to NADP along with a H+ ion to form NADPH ( reduced NADP).
How does cyclic phosphorylation differ from non cyclic (normal)?
Only uses PSI
Electrons not passed onto NADP, but passed back to PSI via electron carriers.
So ATP is only product produced and in small amounts.
Describe the light independent reaction ( calvin cycle).
- CO2 enters leaf through the stomata and diffuses into the stroma of the chloroplast.
-Here it combines with RuBP, catalysed by RUBISCO. This gives an unstable 6 carbon compound which quickly breaks into two molecules of GP. - Breakdown of ATP from light-indepenent reaction provides energy to convert GP to form GALP. Reaction also needs H+, which comes from NADPH which is recycled to NADP.
- Two molecules of GALP can be used to make a hexose sugar e.g. glucose.
However 5 out of 6 molecules of GALP produced are used to regenerate RuBP. This uses rhe remaining ATP produced by the light dependent reaction.
Investigating photosynthesis using extract of chloroplasts core practical.
- Cut a few leaves into pieces.
- Grind up leaf pieces with chilled isolation solution. Filter the liquid into beaker using funnel lined with muslin cloth. Transfer the liquid into centrifuge tubes and centrifuge at high speed for 10 minutes. This will make the chloroplast gather at bottom of tube in a ‘pellet’.
- Re-suspend pellets in chilled isolation solution. This is your chloroplast extract.
- Set up colorimeter with red filter and zero it using cuvette with pellet and distilled water.
- Set up test tube at a set distance from a lamp. Turn the lamp on.
- Place test tube in rack and add set volume of chloroplast extract and DCPIP and mix.
- Immediately take sample of mixture and add to cuvette. Measure the absorbance every 2 mins for 10 mins. Faster the absorbance decreases the faster the hill reaction as DCPIP is reduced by electrons, losing its blue colour.
- Repeat experiment, ensuring the tubes are exposed to the light source for same amount of time at same distance.
Equation for net productivity?
NPP = GPP - respiration loss