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Research method

Mesocosm Experiment

A mesocosm experiment holds a simplified piece of an ecosystem — submerged sediment tanks, potted trees, experimental islands or aquaria — under controlled treatments so a process (litter decay, ¹⁵N uptake, fungal inoculum, pH drop) can be measured. It is stronger on mechanism than a field census and weaker on scaling: an 80-day tank or a potted spruce is not a whole lake, forest or century of ocean acidification.

Biogeochemists and restoration ecologists use mesocosms when they need to isolate a driver they cannot independently vary at landscape scale. The design answers 'under this treatment, do production, tracer recovery, growth or mineral structure change?' Its main limitation is that two lakes, LILA islands or Loch Sween thalli cannot be read as a regional carbon budget, and a rate-of-change effect in a tank may not match gradual field ocean acidification.

Studies

4

Findings

4

4 supporting · 0 challenging · 0 qualifying citations

Open tensions

2

Currently

What we know

  1. Submerged-sediment mesocosms with graded deciduous/coniferous litter in a clear lake (Swan) and a dark lake (Laurentian) near Sudbury found that a 25% rise in aromaticity cut bacterial production 14.5%. The dark lake paid a respiratory cost, while the clearer lake was more nutrient-limited and more photo-oxidizing. A two-lake comparison cannot isolate nutrients from light, and the tanks do not measure whole-lake carbon burial over years.
  2. Potted Sitka spruce mesocosms received ¹⁵N on canopies versus soil from February 2013 to March 2014. Canopy N uptake recovered about three times more tracer aboveground and four times more in wood than soil-targeted deposition; needle δ¹⁵N reached about 120‰ versus 38‰. The harvest does not measure whole-forest carbon stocks or prove that canopy uptake changes landscape-scale sequestration.
  3. Soil fungi were sequenced from 8 constructed and 14 natural Everglades tree islands, then four native tree species were grown with live versus sterile inoculum under constrained versus unconstrained water. Diversity and guild mix became similar without actively restoring fungi, but composition along PCo2 still differed. Under flooded (unconstrained) water, live inoculum made that compositional axis matter for trunk diameter; constrained water washed the effect out. Results are from LILA experimental islands and a pot/mesocosm assay, not a landscape planting census.
  4. Live and dead Lithothamnion glaciale thalli were held 80 days in control seawater (pH 8.1), a gradual drop to pH 7.7 (0.05 units per day over 10 days), or an abrupt drop (0.25 units per day over two days from day 52). Bicarbonate (a dissolution marker) was absent in live control thalli but appeared under low and especially abrupt pH. Live algae in stable low pH calcified more by day than they dissolved at night — about twice control daytime rates — without changing photosynthesis or respiration. Dead thalli dissolved faster at low pH and could not buffer. Abrupt-pH calcification was not measured.

Largest unresolved question

These mesocosms do not test one carbon-cycle claim. Litter tanks show aromaticity cutting bacterial production 14.5% with lake-colour differences in respiratory cost versus photo-oxidation. Canopy ¹⁵N recovers 3–4× more tracer in wood than soil targeting but does not scale to forest C stocks. Everglades inoculum effects on trunk diameter appear only under unconstrained flooding. Coralline algae are more sensitive to the rate of the pH drop than to low pH as a level, and live thalli at stable pH 7.7 increased daytime calcification. 'Mesocosms show carbon or OA effects' is not a single result.

Common misconceptions

  • If canopy ¹⁵N recovery is three to four times soil targeting, canopy uptake has been shown to raise landscape carbon sequestration.

    The mesocosms recovered more tracer aboveground and in wood (needle δ¹⁵N ~120‰ versus 38‰). That is a allocation/recovery contrast in potted Sitka spruce, not a measured change in whole-forest carbon stocks.

  • Bicarbonate appearing in live thalli at low pH means the algae are simply dissolving and failing.

    Bicarbonate was a dissolution marker that was absent in live controls and stronger under abrupt pH, but live algae in stable low pH still calcified more by day than they dissolved at night (~twice control daytime rates) without changing photosynthesis or respiration. Rate of pH change, live versus dead, and unmeasured abrupt-pH calcification all matter.

  • If fungal diversity on constructed islands matches natural islands, restoration has rebuilt microbial function.

    Guild mix converged without actively restoring fungi, but composition along PCo2 still differed, and live inoculum affected trunk diameter only under unconstrained flooding. Constrained water washed the growth effect out.

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