The Central and Site Hypotheses of the VCR LTER
Outline
The Central Hypothesis
The central
hypothesis of the VCR LTER is that ecosystem, landscape and successional
patterns are controlled by the relative vertical positions of the land,
sea, and fresh-water table. Large transient and small progressive changes
in the position of these free surfaces result in disturbance of ecosystem
processes and in physiological stresses that may lead to system state change.
Variations in the elevations of these critical surfaces result from local
weather or climate change, such as short-term storm-generated fluctuation
in sea/land levels or long-term sea level rise. Ecological processes, including
species extinctions and invasions that alter rates of erosion and deposition,
also affect the positions of these free surfaces relative to one another.
In many instances, the joint effects of contemporaneous disturbances at
different temporal and spatial scales result in state changes.
The Central Hypothesis as it is applied to the Four Major Research Sites
1. The Megasite (MS)
-
Long-term
progressive and short-term disturbance-driven changes in the intersections
of land, lagoon and water-table free surfaces of the VCR cause changes
in the spatial (10s m to 10s km) organization of VCR ecosystems and shifts
in ecotones.
2. The North Hog Island Chronosequence (HI)
-
Terrestrial vegetation
on coastal barrier islands is limited primarily by the relationship of
the non-parallel land and water table free surfaces. The relative elevation
of the fresh-water table and the magnitude of the reserve of fresh water
available structures the vegetation of the barrier islands.
3. The Hog Island Bay Lagoon and Marshes Site (LM)
-
The type of community and level of productivity
of emergent marsh vegetation on lagoonal marshes is controlled by the relative
elevations of the parallel marsh land free surface and the parallel, oscillatory
lagoon water free surface.
4. The Mainland Marsh Transition Site (MM)
-
The vertical position of the mainland-marsh ecotone is a function
of the interaction of the non-intersecting, sloping free surfaces of the
saline lagoon water, fresh ground water table, and land surface. Within
the ecotone structured by these sloping free surfaces, multiple states
are ordered along a gradient maintained by storm-generated disturbances
against a background of chronic sea level rise. Changes in state along
the gradient are caused by mechanisms which are characteristic of each
change of state (Brinson et al. 1994).
Examples of working sub-hypotheses at each of the Four Major Research Sites
1. Sub-hypotheses at the Megasite (MS)
- The sedimentary layer produced by the 1933 hurricane
that buried then-existing marshes is present throughout Hog Island Bay
and is thickest where sea grass meadows and were extensive before 1933.(Zieman
and Hayden)
- The shorezone of the barrier islands switches from
accretional to erosional with a return period of approximately 80 years.
We further hypothesize that the transition from accretion to erosion patterns
is an Atlantic Coast-wide phenomenon that is caused by changes in winter
storm(s) climate and long-term changes in the subtropical anticyclone of
the North Atlantic. (Hayden and Dolan).
- Seaside vegetation composition
on the barrier islands is a response to winter storm overwash disturbances
(changes in land free surface elevation) and marine flooding; the effects
vary depending on whether sections of the island are erosional or accretional.
(Hayden and Shugart).
- Elevation of the land free surface above
sea and fresh water surfaces are major determinants of the capacity of
an island to support viable populations of vertebrates. Extinctions of
vertebrate populations may result from changes in one or more of these
surfaces. (Dueser, Porter and Moncrief).
- Reworking of regressive
strandplain land free surfaces during the late Holocene transgression produced
a characteristic stratigraphy due to the release of "fines" into
the water column which increased lagoonal turbidity. The "fines"
are preferentially deposited in wave-protected areas, and the marshes of
small watersheds on the lagoon margins. (Oertel)
- Lagoonal waters
are presently light-limited and turbid as the result of both inorganic
and organic (high C/N values) particulate suspension. Increased primary
production by phytoplankton and an increase in macroalgae will reduce organic
turbidity in lagoonal waters. It is further hypothesized that this increase
in clarity will be a key factor in the return of seagrasses to the VCR.
( Zieman and Hayden).
2. Sub-hypotheses at the North Hog Island Chronosequence (HI)
- The depth of the fresh water table below the surface of the
island depends on the elevation of the land above mean sea level. (Kochel,
Hayden, Furman, and Porter)
- In stable or accreting regions of
the islands, species composition of the vegetation is determined by island
elevation, depth to the freshwater table, and variations in water table
elevation due to rainwater input and evapotranspiration losses. (Brinson,
Porter and Hayden)
- In unstable regions of the island, plant species
composition and successional processes are determined by depth to the freshwater
table, climate variations and by the frequency and magnitude of disturbance
from coastal storms. (Young and Hayden)
- Accreting regions of the
islands have landscapes ordered in age from the sea landward. Along this
chronosequence the relative positions of the land and water-table free
surfaces have been in place for periods ranging from less than one year
to about 120 years. Within the chronosequence, autogenic succession accounts
for biogeochemical variations. (Day, Young, Porter, and Shugart)
- Above
and below ground production are limited by proximity to the fresh water
and available nitrogen. (Young and Day)
- Decomposition rate is
a function of soil moisture and thus proximity to the water table. (Day)
- Nutrients (primarily N) are derived from either N-fixation by Myrica
or atmospheric deposition and spatially are a function of exposure to oceanic
influences and soil moisture and thus proximity to the water table. (Young,
Macko and Galloway)
- Utilization of the island landscape by small
mammals varies with age and complexity of the landscape and vegetation
type. (Dueser and Porter)
- Mammalian consumers affect the composition
and structure of vegetation which, in turn alters the rates of change of
free surfaces through alteration of aeolian deposition and evapotranspiration
(Dueser, Young and Porter)
- A change in the mean level of the water
table free surface will result in a change in vegetation composition and
productivity. (Hayden, Porter, Furman, and Young)
3. Sub-hypotheses at the Hog Island Bay Lagoon and Marshes Site (LM)
- Spartina
alterniflora growth form and productivity vary as a function of the
difference between marsh surface elevation and mean sea level. Lowering
the marsh land surface will increase productivity and promote dominance
by the tall form of S. alterniflora. (Zieman and Hayden)
- VCR
Marshes that were buried during the 1933 hurricane are elevated and relatively
flat, and are therefore dominated by the short form of S. alterniflora.
(Zieman and Hayden)
- Hypersaline marshes are restricted to regions
where the marshland-surface is level at elevations between mean high tide
and spring tide. (Zieman)
- Storm-derived marine sediments deposited
below mean high tide level develop a chemistry and texture compatible with
marsh colonization and succession. (Furman and Zieman)
- Reduction
of pore water salinity by infiltration of precipitation and the activitiy
of invertebrates enhances Spartina altinaflora productivity. (Zieman
and D. Smith)
- Exchange of water between ocean and lagoon is accomplished
by a standing tidal wave and tidal currents moving through well-developed
antecedent valleys. The exchange is very efficient, and the resulting lagoonal
water body maintains a relatively constant salinity at 30-32 ppt. Exchange
is determined by water-mass trajectory path, not diffusion of stratified
flows (Oertel).
- Water mass boundaries in lagoons are determined
by differences in current "drag" created by bottom friction and
fluctuating water levels. (Oertel, Porter, and Hayden)
4. Sub-hypotheses at the Mainland Marsh Transition Site (MM)
- The forest to high marsh transition is induced by storm-generated influxes
of saline water that stresses and kills trees, tree mortality is primarily
a result of salt induced water-stress and not water-logging. (Brinson and
Christian)
- Tree mortality allows light penetration to the forest
floor and is followed by replacement of forest by marsh. (Brinson and Christian)
- The transition from organic high marsh to mineral low marsh is facilitated
by erosion of tidal creeks headward and/or along creekbank margins resulting
in subsidence of the surface of the organic high marsh. (Christian, Brinson,
Blum, and Wiberg)
- Increased oxidation of sediment organic matter
contributes to subsidence of the organic high marsh surface. Increased
oxidation is a result of better drainage created by the steeper hydraulic
gradient between the marsh water table and the creek at low tide. (Christian
and Anderson)
- The organic high marsh surface subsides in part
because of decreasing accumulation of below ground organic matter and in
part as a result of decreased allocation of resources for root and rhizome
growth. (Blum and Christian)
- Inundation and salinity by themselves
are insufficient to cause species replacements in organic high marsh communities.
Disturbance due principally to wrack deposition must be involved to maintain
within state heterogeneity (although fire, trampling, and ice scouring
may be additional disturbances). (Christian and Brinson)
- Sediment
deposition on mineral low marsh surfaces is facilitated by the frictional
resistance (i.e., baffling effects) of marsh plants and /or infiltration
of water through the marsh surface on falling tides. Erosion of marsh sediment
is inhibited by the presence of vegetation and sediment particle aggregation
by invertebrate fauna (Wiberg and D. Smith).
- Nutrient transfers
from the mainland into the mainland-marsh tidal creeks depends on the distance
of transport and the number and type of marsh zones through which the flow
must pass. (Macko, Anderson and Blum)