Salt Marshes Mangroves and Wetlands Chapter 5 Salt

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Salt Marshes, Mangroves and Wetlands Chapter 5

Salt Marshes, Mangroves and Wetlands Chapter 5

Salt marshes • Intertidal zone, emergent vegetation • • • Plants have adapted to

Salt marshes • Intertidal zone, emergent vegetation • • • Plants have adapted to saline soils, inundation Salt glands – salt on leaves of Spartina alterniflora High productivity in marsh due to sunlight Peat and sediment accumulation in soil Detritus production high - exported to estuary Habitat complexity is high (shoot density) - refuge from predation • Halophytes – salt-tolerant plants, 600 species in marsh worldwide • Species in NC: Spartina alterniflora, Spartina patens, Salicornia sp. , Juncus roemeranus, Distichilis spicata, Pluchea camphorata (Table 5. 1)

Mangroves • Mangrove – taxonomically, one of eight families of trees, salttolerant, 12 major

Mangroves • Mangrove – taxonomically, one of eight families of trees, salttolerant, 12 major genera worldwide. In Florida (USA): · Avicennia – black mangrove · Rhizophora – red mangrove · Laguncularia – white mangrove · All species grow in loose saline soils in intertidal environments. · "Mangrove" has also been used to describe the whole community of plants and animals where these trees are found (mangrove swamp or forest) · Viviparity – the "propagules" – not seeds, because inside the seeds have germinated already and are ready to sprout • Respiratory roots – pheumatophores stick up out of soil (Avicennia) or are on stilts (prop-roots) in Rhizophora

Latitudinal Zonation • Mangroves: • 29 ºN -- 29 ºS – tropics and subtropics

Latitudinal Zonation • Mangroves: • 29 ºN -- 29 ºS – tropics and subtropics · Mostly 25 ºN -- 25 ºS, but exceptions include: · Black mangroves scrub at 29 ºN (Dog Island, Florida) · 10 -15 ºfurther south in Africa, Australia · 7 º further north in Japan · Salt Marshes · From 25 º N -- 65 º N, and 35 º S -- 60 º S · 38 º N -- 65 º N – no above ground winter biomass due to ice scour · In southern hemisphere, only salt marshes in South America

Regional Zonation • Rainfall, ground water seepage may influence the type of marsh or

Regional Zonation • Rainfall, ground water seepage may influence the type of marsh or mangrove found in a region. • Lots of rainfall = wide band of marsh or mangrove. As salinity decreases, the plant communities change, individual species vary in salinity tolerance • Mangroves – · Rhizophora, Avicennia, Laguncularia (in polyhaline areas) · Typha in oligohaline areas • Salt marshes · Species diversity declines with increased salinity • saline marsh: 6 species plants (Juncus, Spartina, Distichlis) • brackish marsh: 7 • fresh water marsh: 14

Elevation Effects • Different plants can tolerate different amounts of inundation (and salt content).

Elevation Effects • Different plants can tolerate different amounts of inundation (and salt content). • Salt Marsh – Spartina alterniflora – near edge, low elevation. – Juncus roemerianus – higher elevation – Panicum - highest elevation • Mangroves – Trees in mangroves. Rhizophora – Avicennia – Laguncumra

Succession in Marshes · Primary succession – S. alterniflora in SE marshes · In

Succession in Marshes · Primary succession – S. alterniflora in SE marshes · In marshes in N. E. , after disturbance, succession: · Salicornia europea first to colonize (0 -2 yrs) · Distichlis spicata next to invade, vegetatively (2 -3 years) · Juncas or Spartina will out-compete Distichlis (3 -4 years) · Juncas or Spartina will dominate, but outcome depends on elevation. · climax – upland forest

Biological Interactions · Predation and competition may determine local patterns of abundance in both

Biological Interactions · Predation and competition may determine local patterns of abundance in both salt marshes and mangroves: • Juncus gerardi competitively excludes Spartina patens at high marsh/terrestrial zonation boundary. • Distichlis spicata is out-competed by both and is a disturbance fugitive species) (Bertness 1991) Ecology 72: 125 -137 Smith (1987) transplanted propagules of 4 species of mangroves in Australia (high intertidal – high salt, low inundation; low intertidal – low salt, high inundation). Transplanted to zone that was not its "normal" zone – it was zonedominated by Rhizophora racemosa. Although growth and survivorship was greatest in high intertidal, number of individuals was greatest in low intertidal. • • •

Marsh Zonation - caused by physiology? · Physiological tolerance model not supported by field

Marsh Zonation - caused by physiology? · Physiological tolerance model not supported by field studies. • Lab studies suggest that there are opportunities for growth • Multi-factorial experiments on mangroves in which salinity, p. H, redox, soil characteristics, etc. are varied have not been completed • Some support indicated – more data needed

Mangrove Zonation • Tidal Sorting hypothesis – large propagules not able to be transported

Mangrove Zonation • Tidal Sorting hypothesis – large propagules not able to be transported to high intertidal, but take root in low intertidal, high inundation. – Small propagules are not transported to all intertidal areas. • Rhizophora propagules are large and this tree is found in low intertidal; • Avicenna propagules are smaller and found in high intertidal as well as low. • Unfortunately, there are other examples which suggest the opposite is true • This hypothesis not supported by data in literature

Mangrove Seed Predation · Crabs eat many propagules, graspid crabs in particular. · Smith

Mangrove Seed Predation · Crabs eat many propagules, graspid crabs in particular. · Smith (1987, 1988) tethered propagules across intertidal in Australia. • Found inverse relationship between predation rate on propagules and adults in canopy • When protected by cages from crabs, Avicennia propagules grew and survived in areas where adults not normally found • Seed predation probably important!

Competition in Marshes and Mangroves • Mangroves: Smith (1988) tested competition for Ceriops. –

Competition in Marshes and Mangroves • Mangroves: Smith (1988) tested competition for Ceriops. – C. tagal and C. australis were grown in mono and polycultures in salinities 0 -60%. – C. tagal grew better than C. australis at low salinities. – C. australis grew better than C. tagal at high salinities. • Marshes: Bertness & Shumway (1993) – experimentally created bare patches followed succession over four years in a Juncus dominated and Spartina dominated zone – When Spartina removed, Distichlis % cover increases – Spartina % cover is the same, whether Distichlis is removed or not – In high marsh, salt stress inhibits recolonization by Juncus grows back more slowly with other species removed in the unwatered plots. – Removal of other species improves growth of Juncus with the watering and lowering of salt stress. – Alleviating salt stress shifted the nature of interspecific interactions from facilitative to competitive.