Title
Eelgrass

Scale-dependent and indirect effects of filter feeders on eelgrass: Understanding complex ecological interactions to improve environmental impacts of aquaculture

Oysters and Eelgrass
Funding Sources: USDA Western Regional Aquaculture Center; Taylor Shellfish; Seattle Shellfish
Co-PI’s: Jennifer Ruesink (UW), Sally Hacker (WSU to OSU), Brett Dumbauld (USDA ARS),
Shahid Naeem (Columbia University), Washington Department of Fish and Wildlife
Graduate Students: Lorena Wisehart (WSU to OSU), Heather Tallis (UW), Kirsten Rowell (Arizona)
Image Purpose
We are examining ways that shellfish and aquaculture practices influence water clarity, sediment characteristics, and benthic habitat structure in Washington estuaries. As a rooted, photosynthetic plant, eelgrass responds to the nutrient and light conditions of its environment. Consequently, aquaculture may have indirect, large-scale impacts on eelgrass, in addition to the local disturbance that can occur during harvest operations. To develop best management practices, growers need scientific information on these larger-scale impacts, as well as direct small-scale interactions. This information will allow growers to select among culture techniques and distribute impacts in ways that sustain ecologically-important habitats. Applied on a broader estuarine scale, the study will assist managers in understanding the role of filter feeders and designating areas for aquaculture use.
Eelgrass Primer
One species of eelgrass, Zostera marina, is native to Washington state… at least, it is currently believed to be one species. However, plant morphology (and probably demography) varies dramatically across our study sites. In Willapa Bay, Z. marina occurs at relatively low densities (100 m-2), and plant size is large (up to 2 m). In southern Puget Sound, densities are much higher (800 m-2) and plant size smaller (30 cm). Z. marina occurs worldwide in temperate latitudes. Much of its growth is vegetative. New leaves are produced in the center of the plant, and leaves grow from their base, not at the tip. Leaves on the outside eventually stop growing, die, and fall off. The underground rhizome contains internodes showing where each leaf was attached. New shoots are sometimes produced inside a new leaf, and as the plant continues to grow, these new shoots become branches in the rhizome. In addition to this asexual reproduction (which makes identical genetic copies of the parent shoot), sexual reproduction also occurs through flowering. Flowers are produced on shoots that change their shape dramatically, becoming round-stemmed and elongate. Flowering shoots are terminal; that is, after flowering, a shoot dies. Male flowers release pollen in strings of mucus, and female flowers are pollinated when they encounter this pollen. Seed maturation requires several weeks, during which time the seeds grow, darken in color, and develop a hard seed coat. Most seeds are believed to fall near the parent plant, but they may be transported longer distance if the plant is dislodged before the seeds are ready to fall.
Growth
We use a hole-punching technique to measure the growth rate of eelgrass. This technique takes advantage of the fact that eelgrass leaves grow from the base, and outer leaves stop growing. We use a needle to make two holes just above the leaf sheath. After 3-5 days, we collect these plants and look for the holes. The outer leaves show where the mark was originally placed. On the inner leaves, the holes have moved up as the leaves grew. The “new biomass” is the amount in between the place where the shoot was originally marked and where the holes are now found. In Willapa Bay during the summer, fast-growing leaves extend by 3 cm (1 inch) each day.
Zostera japonica was introduced to Washington state in the 1950s and now occurs widely in north Puget Sound, Willapa Bay, coastal bays of Vancouver Island and mainland British Columbia, and many Oregon estuaries. Its eradication was attempted recently from Humboldt Bay, California. A parallel study to look at the morphology, production, and demography of this species is on-going in collaboration with Jae-Sang Hong, a visiting professor from Inchon University, Korea. Zostera japonica is native to Korea (and elsewhere in Asia) but is in serious decline due to habitat loss and pollution.
Results
1. Lorena Wisehart is in charge of a project to measure seasonal changes in eelgrass in Willapa Bay, as a context for our studies of how shellfish may change conditions for eelgrass. About every two months, the following morphological and demographic attributes are measured at seven locations: Shoot length and width, number of leaves, internode lengths, branching, growth rate, flowering, and recruitment. Lorena is also looking experimentally at whether eelgrass recruitment is affected by oysters, given widespread reports of eelgrass appearing after shellfish are planted.
2. Heather Tallis has coordinated sampling of eelgrass biomass and growth rate across aquaculture beds in Willapa Bay. This study will provide information on the consequences of different aquaculture techniques (dredged ground culture, hand-picked ground culture, and longlines) and frequencies of harvest (some beds are harvested several times a year, whereas others have oysters for up to 3 years between harvests).
3. Undergraduate Nehemiah Richardson has counted thousands of bacteria to understand how microbes in the sediment respond to oysters. These microbes are essential in the nutrient cycling of estuaries, and along with macrobiota determine the conditions for eelgrass.

Baldwin, JR and JR Lovvorn. 1994. Expansion of seagrass habitat by the exotic Zostera japonica and its use by dabbling ducks and brant in Boundary Bay, British Columbia. Mar Ecol Prog Ser 103:119-127

Bigley, RE and JL Barreca. 1982. Evidence for synonymizing Zostera Americana den Hartog with Zostera japonica Aschers. & Graebn. Aquatic Botany 14:349-356.

Bigley, RE and PG Harrison. 1986. Shoot demography and morphology of Zostera japonica and Ruppia maritima from British Columbia, Canada. Aquatic Botany 24:69-82

Churchill, A.C. 1992. Growth characteristics of Zostera marina seedlings under anaerobic conditions. Aquatic Botany 43:379-392.

Dennison, W.C. 1990. Shoot density. pages 61-63 In R. C. Phillips and C. P. McRoy (eds.) Seagrass Research Methods. UNESCO; Paris 210 pp. or Duarte, C. M. and H. Kirkman. 2001. Methods for the measurement of seagrass abundance and depth distribution. Pages 141-153 In F.T. Short and R. G. Coles (eds.). Global Seagrass Research Methods. Elsevier, Amsterdam. 473 pp.

Dennison, WC, RC Aller and RS Alberte. 1987. Sediment ammonium availability and eelgrass (Zostera marina) growth. Marine Biology 94:469-477

Dunton, KH. 1996. Photosynthetic production and biomass of the subtropical seagrass Halodule wrightii along an estuarine gradient. Estuaries 19:436-447

Ewanchuk, PJ and SL Williams. 1996. Survival and re-establishment of vegetative gragments of eelgrass (Zostera marina). Can J Bot 74:1584-1590

Fong, CW, SY Lee and RSS Wu. 2000. The effects of epiphytic algae and their grazers on the intertidal seagrass Zostera japonica. Aquatic Botany 67:251-261

Fourqurean, J.W., J.N. Boyer, M.J. durako, L.N. Hefty and B.J. Peterson. 2003. Forecasting responses of seagrass distributions to changing water quality using monitoring data. Ecological Applications 13(2)474-489

Garcia, E, TC Granata and CM Duarte. 1999. An approach to measurement of particle flux and sediment retention within seagrass (Posidonia oceanica) meadows. Aquatic Botany 65:255-268.

Hahn, DR. 2003. Alteration of microbial community composition and changes in decomposition associated with an invasive intertidal macrophyte. Biol Invasions 5:45-51

Hargrave, BT and NM Burns. 1979. Assessment of sediment trap collection efficiency. Limnology and Oceanography 24:1124-1136

Harrison, PR? 1976. Zostera japonica (Aschers. & Graebn.) in British Columbia, Canada. Syesis 9:359-360

Harrison, PG. 1982a. Spatial and temporal patterns in abundance of two intertidal seagrasses Zostera Americana den Hartog and Zostera marina L. Aq Bot 12:305-320

Harrison, PG. 1982b. Seasonal and year-to-year variations in mixed intertidal populations of Zostera japonica Aschers. & Graeben. and Ruppia maritima L. S.L. Aquatic Bot 14:357-371

Harrison, PG. 1982c. Comparative growth of Zostera japonica Aschers. & Graebn. And Z. marina L. under simulated intertidal and subtidal conditions. Aq Bot 14:373-379

Harrison, PG and RE Bigley. 1982. The recent introduction fo the seagrass Zostera japonica Aschers. & Graebn. to the Pacific Coast of North America. CJFAS 39:1642-1648

Hauxwell, J., J Cebrian, JA Herrara-Silveira, J Ramirez R, A Zaldivar J, N Gomez and N Aranda-Cirerol. 2001. Measuring production of Halodule wrightii: additional evidence suggests clipping underestimates growth rate. Aq Bot 69:41-54

Hemminga, MA and CM Duarte. 2000. Seagrass Ecology. Cambridge Univ Press Holmer, M, FO Andersen, SL Nielsen and HTS Boschker. 2001. The importance of mineralization based on sulfate reduction for nutrient regeneration in tropical seagrass sediments. Aq Bot 71:1-17

Huong, TTL, JE Vermaat, J Terrados, N Van Tien, CM Duare, J Borum and NH Tri. 2003. Seasonality and depth zonation of intertidal Halophila ovalis and Zostera japonica in Ha Long Bay (northern Vietnam). Aq Bot 75:147-157

Iizumi, H, A Hattori and CP McRoy. 1982. Ammonium regeneration and assimilation in eelgrass (Zostera marina L.) beds. Mar Biol 66:59-65

Jones, WB, LA Cifuentes and JE Kaldy. 2003. Stable carbon isotope analysis of sediment derived bacterial fatty acids indicate close coupling in a sub-tropical seagrass dominated system. MEPS 255:15-25

Kaldy, JE and KH Dunton. 2000. Above- and below-ground production, biomass and reproductive ecology of Thalassia testudinum (turtle grass) in a subtropical coastal lagoon. MEPS 193:271-283

Kentula, M. E. and C. D. McIntire. 1986. The autecology and production dynamics of eelgrass (Zostera marina L.) in Netarts Bay, Oregon. Estuaries 9(3):188-199.

Kowalski, JL, HR DeYoe, TC Allison and JE Kaldy. 2001. Productivity estimation in Halodule wrightii: comparison of leaf-clipping and leaf-marking techniques and the importance of clip height. MEPS 220:131-136

Koch, EW. 2001. Beyond light: physical, geological and geochemical parameters as possible submersed aquatic vegetation habitat requirements. Estuaries 24:1-17

Larned, ST. 2003. Effects of the invasive, nonindigenous seagrass Zostera japonica on nutrient fluxes between the water column and benthos in a NE Pacific estuary. MEPS 254:69-80

Lee, K.-S. and KH Dunton. 1999. Inorganic nitrogen acquisition in the seagrass Thalassia testudinum: development of a whole-plant nitrogen budget. L&O 44:1204-1215

Lee, SY, CW Fong and RSS Wu. 2001. The effects of seagrass (Zostera japonica) canopy structure on associated fauna: a study using artificial seagrass units and sampling of natural beds. JEMBE 259:23-50

Lee, SY. 1997. Annual cycle of biomass of a threatened population of the intertidal seagrass Zostera japonica in Hong Kong. Mar Biol 129:183-193

Nomme, KM and PG Harrison. 1991a. A multivariate comparison of the seagrasses Zostera marina and Zostera japonica in monospecific versus mixed populations. Can J Bot 69:1984-1990

Nomme, KM and PG Harrison. 1991b. Evidence for interaction between the seagrasses Zostera marina and Zostera japonica on the Pacific coast of Canada. Can J Bot 69:2004-2010

Olesen, B. and K. Sand-Jensen. 1994. Biomass-density patterns in the temperate seagrass Zostera marina. Mar. Ecol. Prog. Ser. 109:283-291.

Orth, JR. 1997. Effects of nutrient enrichment on growth of the eelgrass Zostera marina in the Chesapeake Bay, Virginia, USA. Mar Biol 44:187-194

Pedersen, MF and J Borum. 1993. An annual budget for a seagrass Zostera marina population. MEPS 101:169-177

Phillips, R. C., C. McMillan and K. Bridges. 1983. Phenology of eelgrass, Zostera marina L., along latitudinal gradients in North America. Aquatic Botany 15:145-156.

Santamaria, L, C Dias and MJM Hootmans. 1994. The influences of ammonium on the growth and photosynthesis of Ruppia drepanensis Tineo from Donana National Park (SW Spain). Hydrobiologia 275/276:219-231

Short, FT and CP McRoy. 1984. Nitrogen uptake by leaves and roots of the seagrass Zostera marina L. Botanica Marina 27:547-555

Thom, R. M. 1990. Spatial and temporal patterns in plant standing stock and primary production in a temperate seagrass system. Botanica Marina 33:497-510.

Thursby, GB and MM Harlin. 1982. Leaf-root interaction in the uptake of ammonium by Zostera marina. Mar Biol 72:109-112

Tomasko, DA and KH Dunton. 1995. Primary productivity in Halodule wrightii: a comparison of techniques based on daily carbon budgets. Estuaries 18:271-278

Van Katwijk, MM, LHT Vergeer, GHW Schmitz and JGM Roelofs. 1997. Ammonium toxicity in eelgrass Zostera marina. MEPS 157:159-173

Van Lent, F, JM Vershuure and MLJ van Veghel. 1995. Comparative study on populations of Zostera marina L. (eelgrass): in situ nitrogen enrichment and light manipulations. JEMBE 185:55-76

Wilson, U.W. and J.B. Atkinson. 1995. Black brant winter and spring-staging use at two Washington coastal areas in relation to eelgrass abundance. The Condor 97:91-98.

UW Biology | University of Washington
Created by Lee McCoy, Updated by Jerome Tichenor, March 19, 2013