|
|
|
Philosophy |
|
Body of Knowledge |
|
Innovative Methodologies |
|
Management and information transfer |
|
Education/Outreach |
|
|
|
|
Multi/interdisciplinary international
collaboration |
|
Coupled models as integrative tools |
|
Mult-scale (time,space, institutional) analysis |
|
Enhanced understanding of role of higher trophic
levels |
|
|
|
|
Coupled models (trophic, scale, time) to
investigate structure, function and variability |
|
Sampling and technological advances |
|
Retrospective studes of past ecosystem states |
|
Comparative approach among regions |
|
|
|
|
Policy (providing conceptual understanding of
ecosystem function) |
|
Managers (providing tools to incorporate
climate-driven variability) |
|
Communities (enhancing communication on global
ecosystem change and marine sustainability |
|
|
|
|
|
|
|
|
NPZ type |
|
Copepod life cycle type |
|
Larval fish dynamics type |
|
|
|
|
|
|
|
|
|
|
|
|
|
Miller, Lynch, Carlotti, Gentleman, Lewis, 1998 |
|
3-D finite element model and climatology |
|
Individual based model |
|
Growth and reproduction as f (temperature) |
|
Supply to GB from all GoM basins and Scotian
Shelf |
|
Jordan and Georges must be restocked from
upstream sources; role of local production in Wilkinson unresolved |
|
|
|
|
|
|
|
Lynch, Gentleman, McGillicuddy, Davis, 1998 |
|
3D
finite element hydrodynamic model, mean climatological circulation |
|
Advective- diffusive-reactive equation,
stage-based development |
|
Food limitation represented as linear decline
below 150 µgC l-1 |
|
Surface only and depth-averaged transport |
|
Base model has low mortality and abundant food |
|
Spatial and temporal pattersn of Calanus
recruitment in first generation consistent with observations only when
model included food limitation of populations in low chlorophyll GoM in
late winter/early spring |
|
|
|
|
|
McGillicuddy, Lynch, Moore, Gentleman, Davis,
Meise 1998 |
|
McGilluddy, Bucklin et al. papers |
|
|
|
Adjoint data assimilation |
|
3D finite element, climatological circulation |
|
Assuming advective fields correct, calculate
biological terms (R) that fit the observations |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Due to the circulation gyre, the residence time
of water over the Bank is long relative to biological time scales so that
in situ growth rather than lateral exchange is the dominant process
controlling population abundance on the Bank |
|
Fine-scale horizontal exchange causes
significant leakage of nutrients, plankton and fish larvae across the
frontal boundaries of the Bank, thus causing a chronic input and
exchange/loss of nutrients, plankton and fish larvae |
|
Secondary circulation associated with the tidal
mixing fron causes a surface convergence near the well-mixed area boundary,
providing a mechanism for concentrating target species in the tidal front
zone. Transport towards the center of the Bank should be greatest for
plankton in the upper layer of the water column in this zone, or for those
species that undertake vertical migrations. |
|
Periodic vertical migration of zooplankton and
juvenile fish into and out of the sheared bottom-boundary layer can lead to
horizontal movement against the mean flow |
|
|
|
|
|
|
Seasonal density stratification over the
southern flank of the Bank causes prey aggregation in the pycnocline and
increased survival of predator populations |
|
|
|
Differences in phytoplankton abundance and
species composition mediated by differences in water column stability
result in measureable differences in copepod recruitment and growth rates.
This leads to greater abundances in one region over another, due solely to
high growth rates in situ |
|
|
|
Turbulent mixing, generated by wind and tidal
forcing, has a significant impact on rates of ingestion, respiration and
predation; the processes of turbulent mixing and seasonal density
stratification influence predator-prey encounter rates and thus growth and
survival of individual organisms |
|
|
|
|
The residual mean flow is important in
horizontal transport of zooplankton and fish larvae onto and off of Georges
Bank, thus causing major sources and sinks for Bank populations |
|
|
|
The seeding of copepod populations from the Gulf
of Maine during winter has a significant impact on the level of prey
biomass for larval fish during late spring and early summer. A corollary is
that the population genetic makeup of the prey on Georges Bank reflects the
generic makeup of the source populations |
|
|
|
Storms, especially during winter and early
spring, as well as impingement of warm-core rings, can cause large
exchanges/losses of zooplankton and fish larvae from Georges Bank, thus
increasing the apparent mortality rate of Bank populations |
|
|
|
Population size is continuously regulated by
incremental rather than episodic events, i.e. the time scale of the
variability of the driving forces is of the same order as the generation
time of the population. |
|
|
|
|
Predation rather than starvation is the dominant
source of mortality of fish larvae; predation rather than advective
exchange is ths dominant source of mortality of copepods |
|
|