To investigate the effects of the simultaneous occurrence of salt stress and tidal sea-level rise on mangroves, potted Kandelia candel seedlings were treated under deep flooding (flooded 40 cm above the soil surface for 16 h per day, inundating the entire plant) and shallow flooding (flooded just above the soil surface for 8 h per day) at salinity levels of 5, 15, and 25 ppt over 14 months. Deep flooding enhanced stem elongations at all salinity levels but increased stem biomass only at 5 ppt. Deep flooding increased both leaf production and leaf fall; leaf biomass increased at 5 ppt, but decreased at 15 and 25 ppt. Biomass ratios of root/shoot (R/S) of deep flooding treatments were significantly lower than those of shallow flooding treatments. Under deep flooding, superoxide dismutase (SOD) activities did not show significant change between 5 and 15 ppt, but increased at 25 ppt. With increasing salinity level, peroxidase (POD) activities increased, and the difference between shallow and deep flooding was enhanced. Malonaldehyde (MDA) content significantly decreased at 25 ppt with 40 cm flooding, but was not affected by other treatments. These results demonstrated that the growth and physiological responses of K. candel seedlings under deep flooding conditions varied with salinity level; growth was enhanced at low salinity level but inhibited at high salinity level. It is therefore probable that K. candel will shift from downstream to upstream, where the influence of fresher river water resources will ameliorate the effects of increased salinities that accompany deeper tidal flooding in these mangrove ecosystems.
Ecological processing of leaf litter plays important roles in carbon dynamics of mangrove forests. Fate of leaf litter, that is, removal by crabs, microbial decomposition, and tidal export was quantified in two restored Kandelia obovata forests with ages of 24 years and 48 years, respectively, from December 2009 to November 2010. Crab abundance was also investigated to test the role of crabs in leaf litter processing. Daily leaf litter production was 1.064 ± 0.108 g C m−2 day−1 at the 24‐year forest and was 0.689 ± 0.040 g C m−2 day−1 at the 48‐year forest. Annual mean removal of leaf litter by crabs was lower at the 24‐year forest than at the 48‐year forest (0.177 ± 0.046 g C m−2 day−1 vs. 0.220 ± 0.050 g C m−2 day−1), due to a higher crab abundance at the older forest. Microbial decomposition and change in standing stock of leaf litter on the forest floor made a negligible contribution to the annual leaf litter production. Tidal exports of leaf litter were estimated as 0.875 ± 0.090 g C m−2 day−1 and 0.458 ± 0.086 g C m−2 day−1 at the 24‐year and 48‐year forests, respectively, accounting for 82.2% and 66.5% of their daily leaf litter production. Turnover rate of leaf litter was higher at the younger forest (1.7 ± 0.4 day−1) than the older forest (1.2 ± 0.3 day−1). Removal of leaf litter by crabs was higher in warm months while tidal export of leaf litter showed a much less apparent seasonal pattern. Spatial variations of crab removal and tidal export of leaf litter with forest zones were observed within each forest, while microbial decomposition of leaf litter was comparable among the different zones. These indicated that the ecosystem functions of restored mangrove forest could not reach a level equivalent to those of a mature forest even 24 years after restoration.
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