Table 2.
process | country and climate | experimental unit | treatments | response variable (method) | RD | ref. |
---|---|---|---|---|---|---|
DE | Australia, semiarid | mesocosms colonized by microorganism | three salt types (sea salt, NaCl and NaHCO3), two salinity levels (1, 10 mS cm−1) | % leaf mass loss (fine leaf bags) fungal biomass (ergosterol measurement) |
↓ — |
[39] |
DE | Australia, semiarid | mesocosms colonized by microorganism | six salt (NaCl) concentrations: (0, 0.05, 0.1, 0.2, 0.5, 1 mS cm−1) | % leaf mass loss (fine leaf bags) | ∩— | [39] |
DE | Spain, semiarid | artificial flow-through stream systems colonized with invertebrates and microorganisms | three salt concentrations (sea salt): 5, 10 and 15 mS cm−1, as repeated pulses of 3 h duration | leaf mass loss (coarse litter bags, Populus nigra) fungal biomass (as ergosterol) biofilm biomass (chlorophyll a) |
↓ ∩ —↓ |
[43] |
DE | Portugal, humid | microcosms conditioned with 5000 fungal conidia | four salinity (NaCl) concentrations: 0, 2.8, 5.7, 11.4 mS cm−1 | leaf mass loss (discs of Quercus robur L.) fungal respiration, growth and sporulation rate (oxygen consumption, counting of conidia) |
↓ ↓ |
[44] |
ME/BP | Argentina, humid | recirculating microcosms with stream colonized glass tiles | salinity (NaCl) pulse (30 min d−1) and press (72 h) exposure with 1.5 mS cm−1, control with no salt addition | biofilm biomass (chlorophyll a concentration) bacterial density (counting) community respiration (oxygen consumption) |
— ↓ ↓ |
[51] |
BP | Germany, humid | microcosm with stream conditioned periphyton | salinity (Na2SO4 and CaCl2) at 2 and 5 mS cm−1, control 0.6 mS cm−1 | biofilm biomass (minimal fluorescence of photosynthesis pigments) | ↑ | [52] |
ME | USA, humid | mesocosms with invertebrate community | three salt types (NaHCO3, MgSO4, NaCl) with six concentrations between 0.07 and 4.4 mS cm−1 | difference between day and night-time DO concentrations (open-system, single-station approach for continuous DO measurement) | ↓ | [53] |