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Tentative Research Schedule

2004:

Choose sites, sample for basic abundance and biomass information, deploy experiments to measure algal growth rates, sand scour, barnacle growth rates, and oyster growth rates. Photograph experiments monthly, and download temperature dataloggers monthly.

2005:

Continue 2004 experiments. In addition, measure settlement of organisms onto clean ceramic tiles (above the surface) and clean sediment (below the surface).
2006: Continue 2004 and 2005 experiments; harvest and collect all experiments in September.

Stuff on the Beach: Experimental methods and types of data being gathered

We have drawn on an extensive, multi-year database of biota and physical characteristics of 64 sites in Puget Sound to choose the appropriate study sites and generalize our results. All experiments are conducted at 3 replicate beaches with shared geophysical characteristics.

Juvenile Pacific oysters are settled on ceramic tiles in the laboratory and outplanted to each of the 9 experimental beaches, where the tiles are attached to stakes pounded into the sediment. Plates are photographed every 1-2 months and the growth rates of individual oysters are measured from these photographs. The plates also serve as ways to measure natural colonization of other organisms. After approximately 6 months, oysters are sampled for stable isotope analyses (link back to Hypotheses).
Barnacle larvae are allowed to settle on tiles placed in one location (at the Friday Harbor Labs on San Juan Island), then tiles are moved to the experimental beaches and attached to stakes as for the oyster tiles. Barnacle growth is similarly measured from photographs taken every month through the year. Other organisms settling on the barnacle tiles are also quantified.
Chunks of sandstone cobble approximately the size of large local cobbles each had a uniform-size square of grey paint painted onto one flat face, and these rocks (5 per beach) were put out at the experimental beaches. Scouring of the paint off the rock is quantified through time to compare the degree of abrasion experienced by surface-dwelling organisms at each of the 9 beaches..
Small, waterproof temperature dataloggers (TidbiTs, Onset Computer Corporation) are placed at each of the 9 beaches and programmed to log the temperature approximately once every hour. At each beach, separate loggers record the temperature on the surface of the beach (same tidal level as the experiments), buried in the sediment of the beach, and just offshore of the beach. These data will be used to seek correlations between local processes (growth rates, distinct recruitment or mortality events) and temperature, and also to quantify how well nearshore temperatures track those recorded in the middle of Puget Sound by other research groups (e.g. the Washington Department of Ecology; link to their webpage).
 
Rocks with small individuals of the common brown seaweed Fucus gardneri (rockweed) were placed at each of the 9 sites in June 2004, and all the individual plants were marked and measured. Plants are remeasured monthly, and their growth rates compared among sites. This provides a measure of primary productivity.
 
To measure the recruitment of organisms (especially juvenile clams and worms) settling in beach sediments, cores of sterile sediment enclosed in window-screening will be embedded in each beach beginning in Feb. 2005. This cores will be exchanged with new ones each month, so that we can examine seasonal patterns in recruitment as well as patterns along the north-south gradient.
To measure the recruitment of organisms that live on surfaces (e.g. on natural cobbles), we will put out ceramic settling tiles at each beach beginning in Feb. 2005. These will be exchanged with clean ones each month, as for the sediment
Basic information on the abundance and diversity of organisms on each beach are gathered each year at each of the experimental sites. Sampling follows the protocol used by DNR’s SCALE program. Briefly, a 50m line is laid along the beach at 0' tide level. At 10 randomly placed intervals, all the macroscopic organisms on the surface are counted using a 50x50cm quadrat frame, and all the organisms are sieved from a sediment core 15cm deep and 10cm diameter, and identified later in the laboratory.
At 5 additional locations in June of each year, all organisms are collected from the surface and from a sediment core to measure biomasses. Species-specific biomasses are measured by randomly collecting samples of epibiota and large infauna (clams) and returning them to the lab to get wet and dry masses; small infauna biomasses are measured following laboratory identification.