What do we need to understand about food webs - why stable isotopes are important.
What are the rules and properties of these networks?
What are the regulating/control mechanisms within them?
Do these feeding links define important rules of thumb that may be helpful to management?
Strengths of stomach contents data
Strengths
Weaknesses of food web gut contents data
Weaknesses
Alternatives to stomach content analysis
Other approaches: (1) Scat analysis – useful in large animals e.g. mammals, utilises hard structures e.g. otoliths, beaks
Cephalopods from beaks
(2) Fatty acid profiles - some prey have characteristic FA profiles … used as tracers
How do you calculate the trophic level from stomach content analysis?
By looking at the trophic level and the of the diet of known prey in the stomach.
assume: diet fully characterised and quantified (totally made up from the components that you did the calculations with), that the prey TLs correct, and that it reflects the long term mean
Require: long-term diet quantitative data, known prey TPs at the temporal scale of isotopic turnover
What is an isotope?
Isotope = atoms of the same element …differing in atomic weight…identical in chemical properties, and in all physical properties except those determined by the mass of the atom.
Most of the carbon in our bodies is carbon 12, with some C13. This has implications on how it forms and breaks bonds.
How is the data from stable isotope analysis used?
δ𝐻𝑋=[((“Rsample − Rstandard)” )/”Rstandard”] × 1000
International standards
What is isotope fractionation?
Why does fractionation occur as the matter is passed up trophic levels?
Excretion/Respiration: production of metabolites with light isotopes in deamination/transamination (heavy isotopes become concentrated).
Assimilation fractionation: preferential use of heavy isotopes during protein biosynthesis.
Fractionation between diet and consumer assumed constant, level assumed (per ml not % due to the times 1000):
Δdelta 5N = +3.4 ‰ - useful proxy for trophic position
Δdelta 13C = +1.0‰ - good tracer of different sources in the food web.
How would you measure the trophic position of an organism using stable isotope data?
The trophic level of the base plus 15 N of the sample - 15 n of base / 3.4
What are the implications and constraints of working out trophic levels using 15N?
Implications:
Constraints:
Stable isotope proxy of production sources.
How can you work out what a consumer species is eating using C12?
If you know the carbon 12 of the sources, you can work out the ratio of which the carbon in the consumer.
What are the assumptions, constraints and implications of working out the stable isotope proxy of production sources?
Assumptions:
Constraints:
Implications:
What is isotopic routing?
Explain the issue of variability in stable isotope research issues.
Sweeting CJ et al. (2005) Functional Ecology
Looking at Variability among tissues: European seabass (Dicentrarchus labrax) in the lab.
The standard deviation shows samples from the liver are much more variable than that of the muscle.
What variability in different tissues variability when looking at stable isotope data provides an opportunity
Tissues vary in both growth (dilution) and repair (replacement)
Slow tissues integrate any changes over longer periods than fast tissues.
The two tissues may offer proxies at two-time scales in the same consumer
Slow time over tissues will let you know what is going on over longer timescales
Blood or liver is fast turn over, white muscle or sometimes bone is slow turnover
Pinnegar JK et al. 2001 Journal of Fish Biology
relationship in 15N of parasite and its host
Some consumers may do it differently e.g. parasites on fish
For these consumers, apparently 15N <<< 15N diet (but do we know what’s going on?)
Stable isotope research issues
What insights can the timescales stable isotope analysis occurs over give?
Barnes C et al. (2008) Oecologia
Variability within European seabass tissues suggests long term differences in feeding behaviour from individuals.
Significant variability within tissues: not just size, suggests e.g. different feeding strategies.
Dilution – fish keep on growing through there lives,
Stomach content data – last 24 hours
Liver – whats happened over a timescale of say a few weeks
Muscles – give the picture over – say a month
weaknesses of stable-isotope approaches
Weaknesses
Strengths of stable-isotope approaches
strengths
Opportunities of stable-isotope approaches
Opportunities
Compound-specific approaches -
PCA shows great power to discriminate among major production sources in the sea e.g. algae vs terrestrial plants
What essential amino acids can be used as a good indicator of source in compound-specific approaches?
Trophic’ (e.g. glutamic acid) vs ‘source’ (e.g. phenylalanine) amino acid-specific data
By looking at the difference between trophic and source you are getting some indication of the trophic position as they are N15 data but for the individual amino acid.