R E S U L T S  

Latest results for the Outdoor Lab Experiments:

Mature Zostera plants (eelgrass) were collected from Middle Marsh, NC in Sept 2002, and returned to the NOAA Beaufort Laboratory for transplanting. Nine plants (each  with 2 shoots) were planted in plastic tubs (Rubbermaid dishpan) filled with sieved quartz beach-sand.  Plants and tubs were placed in an outdoor tank with flow-through seawater, and five different irradiance treatments established using increasing water depths (15cm, 30cm, 50cm, 70cm, and 70cm-Shaded). Measurements were begun on Oct 9, 2002 and are ongoing.  Measurements were taken weekly over the first month, then biweekly until Week 39 (June 2003), with currently monthly sampling intervals.  Light levels between the indoor and outdoor experiments are not directly comparable, however, based on integrated irradiance measures, plants grown at 50cm depth in the outdoor tank received approximately the same amount of light as seedlings grown at the highest light level in the indoor tank.

Table 1: Five irradiance treatments (=depths) used for the outdoor light experiment. Measurements were taken for 2-4 weeks in a) fall = Oct 02, b) winter = Feb 03 and c) spring = Apr 03. Yellow box indicates max light levels seen by plants in the indoor tank.

Fig 2: Plants were grown for the duration of their growth season (orange box = Dec - Jun). Branching with spatial expansion was observed in two shallowest depths (=high irradiance treatments), branching in the other three depths did not result in much areal expansion. Fifteen of 45 plants flowered (33.3%), all at depths except 50cm.


Fig 3: The length of the longest leaf on each surviving plant was measured as a proxy for canopy height.  Leaf growth (linear extension) was greater as depth increased, as the plants attempted to grow towards the higher irradiances near the surface.  Leaf length started to decline at weeks 31-33, corresponding to increased water temperatures in May, which resulted in leaf fragmentation due to increased grazer abundance (isopods, amphipods, and a small gastropod = Bittium).

Fig 4: Leaf area (single surface) was calculated from maximum length x average width. Width was measured on alternative sampling dates on a random subset of 5 plants, with linear interpolation for non-sampled dates. Area is influenced by leaf length, as well as width, which varied with depth, at first decreasing and then increasing again over the growing season. The greatest leaf area was found on the plants in the deeper depths due to the greatly elongated leaves.  Leaf area declined in May for the reasons outlined above.


Fig 5: Plant photosynthesis was measured with an OptiSciences OS-30 PEA (Plant Efficiency Analyzer).  Photosynthetic yield, expressed as a ratio Fv/Fm ranged from 0.6-0.75 in healthy leaves, and fell below 0.5 in leaves that were senescing.  No significant difference in Fv/Fm was observed in the apparently healthy (live) plants across all five depths, indicating acclimation of the photosynthetic apparatus to the ambient light field.  There is a discernable dip in yield (Fv/Fm) at the end of the growing season in June, related to high water temperatures.  Acclimation of these temperate Zostera to the unfavorable summer conditions in NC allows a subset of the population to persist as very stunted individuals until conditions return favorable for growth around December.

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Created and maintained by: Alan Joyner