Ammophila arenaria

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Authors: Mary Russo, Andrea Pickart, Larry Morse, and Rick Young, Global Invasive Species Team, The Nature Conservancy

A. arenaria
Scientific Name
Ammophila arenaria
(L.) Link
Common Names
European beachgrass, marram

General Description:

Ammophila arenaria is a coarse, perennial grass growing in small tufts connected by deep, tough, extensively creeping rhizomes.

Diagnostic Characteristics:

Ammophila arenaria and A. breviligulata (American beachgrass) can be distinguished by their ligules, those of A. arenaria being thinner and longer ligules (10-30 mm) versus the firmer and shorter ligules (1-3 mm) of A. breviligulata.

Stewardship summary

Ammophila arenaria threatens coastal sand dunes in the eastern and western United States. It displaces native dune species and significantly alters the morphology of dune systems where it invades. Successful management of coastal sand dune elements requires the control of this aggressive species.

The spread of A. arenaria can be controlled through manual removal, but this type of control requires on-going treatment. Control should be emphasized until eradication techniques are refined. Further research is a high priority and is currently being carried out by Humboldt State University, California.

Natural history


Native to the shores of Europe between 30 and 66 degrees north latitude. Introduced to other continents to stabilize drifting sands. In the United States it is found along the west coast.


Ammophila arenaria occurs on coastal sand dunes throughout the world. Along the west coast of the United States, it thrives in areas of active sand movement and most often occupies the windward slopes of exposed dunes. However, it may extend inland for several miles. It grows on well-drained soils with various mineral compositions, including the sands of the Pacific Coast. It tolerates a range of soil pH from 4.5-9.0 and soil temperatures from 10-40° C.[1]


Native habitat. Ammophila arenaria is native to the British Isles and the coasts of the Atlantic Ocean and Baltic and North Seas from 30 to 66 degrees north latitude. It grows most vigorously on mobile and semi-fixed dunes of varying chemical and physical make-up. However, all of the substrates share instability, free drainage, low organic material content, and a homogeneous soil profile.[2]

European Beachgrass plays an important role in the process of dune formation. Young plants become established along the upper beach, often in the lee of driftwood or other beach plant species. As the grass grows taller, wind is deflected upward over the plant. An equilibrium is established between the growth of A. arenaria and sand deposition. The plant causes the wind to slow and sand particles to be deposited. Sand deposition stimulates growth of A. arenaria, which in turn encourages more sand deposition. Too much sand deposition slows growth; too little causes senescence. Thus, sand dune formation is largely determined by the interaction of A. arenaria and wind. Added protection from the wind and sand deposition results in the pattern of new growth to the lee of the existing tussocks.[3][4]

In native habitats, A. arenaria alone makes up the foredune plant community. It also occupies dunes further inland where sand is actively moving. This community is known as "Pure Ammophiletum". As dunes become stabilized by this species, however, other species are able to take hold. This process creates a "Mixed Ammophiletum" community. This mosaic community is typically found on the lee slopes of dunes, mostly on inland, less active slip faces. Occasionally it is found in sheltered areas near the sea. It is an open community with only a moderate amount of bare sand. Since the sand supply is reduced by the fully colonised foredune, the vigour of A. arenaria generally declines in the "Mixed Ammophiletum" community.[3][4]

Non-native habitat A. arenaria has been introduced to stabilize sand on the west coast of the United States since the early 1900s.[5][6][7][8] When planted on disturbed dunes or bare sand, it has initiated dune formation in the manner described above. Rhizome fragments washed along the shore may become buried on the beach, initiating the formation of foredunes.[9] However, the topography and composition of the foredunes differ from those formed by plant species native to the West Coast.[8]

A. arenaria has escaped and become naturalized north of San Francisco [8] and forms extensive stands as far south as Vandenberg Air Force Base, San Luis Obispo county. Before the introduction of European Beachgrass, foredunes in northern California were dominated by Elymus. The foredunes were low and rose above the beach with a gentle slope. Inland from the foredune was a series of dune ridges and swales aligned roughly perpendicular to the coast in the direction of the prevailing onshore winds.

Currently, where dominated by A. arenaria, the foredune topography has changed to a steep slope, and the orientation of the dunes is parallel to the coast. In addition to topographical alterations, A. arenaria replaces the native foredune vegetation, greatly reducing species diversity.[8]

In Oregon, Crook (1979a, 1979b)[6][7] reports that prior to the introduction of European Beachgrass there were no foredunes along the coast. Since its introduction in 1910 near Coos Bay and in 1935 on the Clatsop Plains, A. arenaria has created a foredune and colonized portions of the deflation plains. In addition, it occupies the hummock dunes, the fields of vegetated sand dune mounds occurring inland from the foredune, and the deflation plain. The foredune, as a recent geomorphological feature, has greatly reduced sand supplies to the interior moving dunes and led to their decline.[6][7][10] It has recently been determined that A. breviligulata, native to the dunes of the East Coast and Great Lakes and introduced to Washington and Oregon, is actually more prevalent than A. arenaria in Washington.[11]

Competitive relations:

A study of Pacific Coast beach vegetation [12] revealed that A. arenaria exerts more control over community competition than any other beach dominant. The upper beach and foredune along much of northern California's coast were formerly dominated by Elymus mollis.[8] Research on Elymus and Ammophila ssp. has shown several morphological and physiological differences that may explain the competitive advantage of A. arenaria.

The adaptation of A. arenaria to sand accretion is well known. Ranwell (1959)[1] reports that it can survive 100 cm of sand deposition per year, whereas Elymus mollis can only tolerate 30 cm per year. Increased human disturbance and therefore sand dune destabilization, along the coastline favours A. arenaria.[8]

At Point Reyes, California, Barbour (1977)[13] found that A. arenaria had twice the root density of Elymus at every depth measured from 1-5 m. Differences in root systems may provide A. arenaria greater resistance to drought and more efficient means of tapping soil moisture. In addition, the leaves of A. arenaria inroll during dry periods reducing water loss through transpiration.[2]

Radioactive carbon studies suggest that Ammophila ssp. may have a higher photosynthetic rate than E. mollis during the September to May wet season.[13]

In contrast, Elymus mollis is able to withstand tidal inundation and is tolerant of a wider range of soil salt concentrations. A. arenaria cannot tolerate salt concentrations greater than 1.5-2.0 percent, whereas E. mollis can withstand concentrations of 12 percent or more.[2]


Ammophila arenaria is a stout perennial grass with horizontal and vertical rhizomes. Horizontal rhizomes anchor the young plants and produce new shoots around the parent plant. Vertical rhizomes develop, branching from a horizontal rhizome, as sand accumulates around plants. Several aerial shoots or tillers per node arise from the vertical rhizome to form dense tufts.

Shoots grow most vigorously in spring when leaf production exceeds leaf senescence. In autumn the latter predominates. Growth slows during winter but never ceases entirely.[2] On dune systems in Sweden, the average yearly above ground biomass production is 400 grams per square meter.[14]

A. arenaria is highly adapted to sand accretion. It can withstand burial by as much as one meter per year. Sand burial promotes both leaf elongation and development of vertical rhizomes from axillary buds on the horizontal stems.[1] Internode length of vertical rhizomes varies according to the amount of sand burial and indicates seasonal sand accretion.[2]

Inflorescences are initiated in autumn of the second year after germination and mature in May or June. Flowering occurs from May to August. In Europe, anthesis occurs in July and August [2] but has been reported as early as May.[15] Mature seeds are dispersed in September. Seeds germinate the following spring. Viability of seeds is low. Seedling survival is low as a result of desiccation, burial, and/or erosion.

Reproduction is primarily vegetative by rhizomes. Rhizome fragments are dispersed along the shore by wind and water.[14]

A. arenaria usually invades from the upper beach. There, rhizome fragments of the grass are washed ashore, buried, and sprout. Rapid vertical growth of the grass initiates dune formation, and the grass spreads rapidly in all directions by horizontal rhizomes.


Coastal sand dune systems around the world are threatened by the introduction and establishment of Ammophila arenaria. First, it is able to out-compete native dune plants. Second, it interferes with the natural dynamics of dune systems. In northern California, A. arenaria changes the geomorphology of the foredune community from a gentle slope to a vertical wall which prevents adequate sand movement from beach to interior dunes.[8] In Oregon, it has severely reduced the sand supply from beach to large inland dunes. Along the mid-Atlantic coast of the United States it is known to greatly alter beach profiles and subsequently change the impact and effect of storms on the coastline.[16]

The Northern Foredune Grassland Community described by Holland (1986)[17] has been most severely threatened by the invasion of A. arenaria. This community is restricted to foredunes and is dominated by Elymus mollis. Only two undisturbed examples of this community remain in California, one of which occurs on the North Spit of Humboldt Bay.[17] The most pristine remaining occurrence is at the Lanphere-Christensen Dunes Preserve. In 1963, A. arenaria existed as one small clump 1 km north of the preserve boundary and as several clumps 4 km to the south. By 1984, it occupied 2.2 acres.


Management Requirements:

Control of this introduced species is necessary to protect the limited occurrences of viable natural sand dune systems along our coastlines. Continued control of existing Ammophila arenaria stands and monitoring for new introductions are needed.

Manual removal (digging) controls the spread of A. arenaria but is labor intensive. In one case, complete removal was achieved, but the site was subsequently invaded by other exotic species. In the first year, monthly treatment intervals are suggested; in subsequent years, frequency can be decreased. Monitoring should be conducted to determine if exotic species, such as Carpobrotus, are replacing A. arenaria. Ultimately, re-vegetation with native species should be a standard part of management, once control techniques are refined.

Management Programs:

Management of Ammophila arenaria is being carried out by TNC at the Lanphere-Christensen Dunes Preserve, by Humboldt State University through the Menzies' Wallflower Research Project, by the California Department of Parks at McKenicher State Park, at Vandenberg Air Force Base, and by the Oregon Department of Fish and Wildlife.


  • Andrea Pickart, Habitat Restoration Coordinator Menzies' Wallflower Research Project Lanphere-Christensen Dunes Preserve 6800 Lanphere Road Arcata, CA 95521 (707) 822-6378.
  • James Barry, Resource Protection Division California Dept. of Parks PO Box 2390 Sacramento, CA 95811 (916) 322-8562
  • Charles Bruce, Oregon Dept. of Fish and Wildlife Route 5, Box 325 Corvallis, OR 97330 (503) 757-4186.

Monitoring Requirements:

Biological monitoring should document the long-term spread of A. arenaria and the loss of native habitat. At the Lanphere-Christensen Dunes Preserve (LCDP), monitoring is part of an ongoing eradication program. After the grass has been removed from the preserve, monthly monitoring for newly established plants invading from surrounding areas should be conducted on a continuing basis.

The current method for evaluating the control program at LCDP is through estimates of stand density and size, supported by photodocumentation before treatment and at annual intervals after treatment. Monitoring untreated stands is accomplished by measuring the increase in stand size at four points located at the windward, leeward, and lateral boundaries. Following control, monitoring for new invasion may be accomplished by thorough surveys of the foredune and upper beach each month.

Monitoring Programs:

The current monitoring program involves annual photodocumentation of stands before and after control treatments, and measurement of untreated stands.

Contact: Andrea Pickart, Preserve Manager Lanphere-Christensen Dunes Preserve 6800 Lanphere Road Arcata, CA 95521 (707) 822-6378.


Management Research Programs:

The Habitat Restoration Program of the Menzies' Wallflower Research Project (MWRP) at Humboldt State University, Arcata, California, is currently investigating three methods of A. arenaria control: salt application, use of herbicides, and manual removal. Previous research at LCDP indicates manual removal (digging up plants 10 cm below the surface at repeated intervals) is effective in reducing stand density. An ongoing eradication program has utilized this method with mixed results. Complete eradication has been accomplished on only one stand. The MWRP is implementing an experimental program which increases the frequency and depth of digging to remove the active rhizome bud bank.

Earlier small-scale experiments at the preserve found that a 2% solution of Roundup, applied during anthesis, resulted in 60 to 100% mortality. The MWRP is further refining methods and specifications. Timing of application may be critical.

Salt was believed to be a potential control since A. arenaria has a relatively low tolerance to soil salt (NaCl), although brief to moderate exposure to high salinity may stimulate bud emergence.[18] nfortunately, the use of NaCl to control a weedy species is illegal as it is not registered as a pesticide in the state of California. The use of alternate salts has not been addressed.

Management Research Needs:

Research is needed on the effects of potential control methods including the use of herbicides (Roundup), manual removal, and salt application.

Document Preparation & Maintenance

Edition Date: 88-11-22

Contributing Author(s):

  • MARY J. RUSSO (Revision) [88-08-17]
  • ANDREA PICKART (Revision) [88-09-03]
  • RICK YOUNG (Revision)
  • MARY J. RUSSO (Revision) [88-08-17]
  • ANDREA PICKART (Revision) [88-09-03]
  • RICK YOUNG (Revision)
  • LARRY MORSE (Revision) [95-08-28]

Information sources


  1. Ranwell, D. 1959. Newborough Warren, Anglesey. I. The due system and dune slack habitat. J. Ecology. 47:571-601. 1.0 1.1 1.2
  2. Huiskes, A.H.L. 1979a. Biological flora of the British Isles. J. Ecology 67:363-382. 2.0 2.1 2.2 2.3 2.4 2.5
  3. Willis, A.J., B.F. Folkes, J.F. Hope-Simpson, and E.W. Yemm. 1959b. Braunton Burrows: The dune system and its vegetation. Part II. J. Ecology. 47: 249-288. 3.0 3.1
  4. Willis, A.J., B.F. Folkes, J.F. Hope-Simpson, and E.W. Yemm. 1959a. Braunton Burrows: The dune system and its vegetation. Part I. J. Ecology. 47:1-24. 4.0 4.1
  5. Knudson, H. 1917. A history of the Eureka Coast Guard Station. Humboldt State University Humboldt Collection.
  6. Crook, C.S. 1979b. A system of classifying and identifying Oregon's coastal beaches and dunes. In Fitzpatrick, K.B., (ed.), Articles of the Oregon Coastal Zone Management Association, Inc. Newport, Oregon. 6.0 6.1 6.2
  7. Crook, C.S. 1979a. An introduction to beach and dune physical and biological processes. In Fitzpatrick, K.B. (ed.), Articles of the Oregon Coastal Zone Management Association, Inc. Newport, Oregon. 7.0 7.1 7.2
  8. Barbour, M., and A.F. Johnson. 1977. Beach and dune. In Barbour, M. and J. Major (eds.), Terrestrial vegetation of California. John Wiley and Sons, New York. Pages 223-270. 8.0 8.1 8.2 8.3 8.4 8.5 8.6
  9. Wiedemann, A.M., J. Dennis, and F.S. Smith. 1974. Plants of Oregon coastal dunes. Oregon State University Bookstores, Corvallis, Oregon.
  10. Bruce, C. 1983. Oregon Department of Fish and Wildlife, Corvallis, Oregon. Personal communication.
  11. Wiedemann, A.M. 1988. Evergreen State College, Olympia, Washington. Letter to Andrea Pickart, Preserve Manager, Lanphere-Christensen Dunes Preserve. May 14, 1988.
  12. Barbour, M., T.M. DeJong, and A.F. Johnson. 1976. Synecology of beach vegetation along the Pacific Coast of the United States of America: A first approximation. J. Biogeography. 3:55-69.
  13. Barbour, M. 1977. Management of beach and dune vegetation. Sea Grant Publication, Davis, California. Pp. 27-29; 41-43. 13.0 13.1
  14. Wallen, B. 1980. Changes in structure and function of Ammophila during primary succession. Oikos 34:227-238. 14.0 14.1
  15. Munz, P.A., and D.D. Keck. 1973. A California flora and supplement. Univ. California Press, Berkeley, CA.
  16. Dolan, R., P.J. Godfrey, and W.E. Odum. 1973. Man's impact on the Barrier Islands of North Carolina. American Science 61:152-162.
  17. Holland, R.F. 1986. Preliminary descriptions of the terrestrial natural communities of California. California Department of Fish and Game. 156 pp. 17.0 17.1
  18. Baye, P. 1988. Department of Plant Sciences, University of Western Ontario, Canada. Letter to Andrea Pickart, Preserve Manager, Lanphere-Christensen Dunes Preserve. July 12, 1988.

Additional References

  • Barbour, M.G., T.M. DeJong, and B.M. Pavlik. 1985. Marine beach and dune plant communities. In Chapbot, B. F. and H. A. Mooney, (eds.), Physiological ecology of North American plant communities. Chapman and Hall, New York.
  • Blake, C.T. 1973. Vegetative dune stabilization in North Carolina. Agronomy Information Leaflet. North Carolina Agricultural Extension Service, Beach and Dune Stabilization Series No. 1.
  • Breckon, G.J. and M.G. Barbour. 1974. Review of North American Pacific Coast beach vegetation. Madrono. 22:333-360
  • Cooper, W.S. 1967. Coastal dune of California. Mem. Geol. Soc. of America, Denver, Colorado. No. 104.
  • Cowan, B. 1975. Protecting and restoring native dune plants. Fremontia. 3:3-7.
  • Fowler, T.R. and A. Bernard. 1979. Beach and dune planning and management: an annotated bibliography. In Fitzpatrick, K. B., (ed.), Articles of the Oregon Coastal Zone Management Association, Inc. Newport, Oregon.
  • Gemmell, A.R., P. Greig-Smith, and C.H. Gimingham. 1953. A note on the behavior of Ammophila arenaria (L.) Link in relation to sand dune formation. Trans. Proc. Bot. Soc. Edinborough 36:132-136.
  • Godfrey, P.J. and M.M. Godfrey. 1974. An ecological approach to dune management in the National Recreation Areas of the United States East Coast. Int. J. Biometeor. 18:101-110.
  • Green, D.L. 1965. Developmental history of European beachgrass, Ammophila arenaria (L.) Link: plantings on the Oregon coastal sand dunes. M. A. Thesis, Oregon State University, Corvallis, Oregon.
  • Greig-Smith, P. 1961. Data on pattern within plant communities. II. Ammophila arenaria (L.) Link. J. Ecology 49:703-708.
  • Greig-Smith, P., A.R. Gemmell, and C.H. Gimingham. 1947. Tussock formation in Ammophila arenaria (L.) Link. New Phytology. 46:262-268.
  • Hassouna, M.G., and P.F. Wareing. 1964. Possible role of rhizosphere bacteria in the nitrogen nutrition of Ammophila arenaria. Nature. 202:467-469.
  • Hewett, D.B. 1970. The colonization of sand dunes after stabilization with marram grass (Ammophila arenaria). J. Ecology. 58:653-668.
  • Hitchcock, A.S. 1951. Manual of the grasses of the United States. 2nd edition revised by Agnes Chase, 1971. 2 vols. Dover Publications, Incorporated, New York.
  • Hope-Simpson, J.F., and R.C. Jeffries. 1966. Observations relating to vigour and debility in marram grass [Ammophila arenaria (L.) Link]. J. Ecology 54:271-274.
  • Huiskes, A.H.L. 1977. The natural establishment of Ammophila arenaria from seed. Oikos 29:133-136.
  • Huiskes, A.H.L. 1979b. Damage to marram grass, Ammophila arenaria, by larvae of Meromyxa pratorum (Deptera). Holarctic Ecology 2:182-185.
  • Johnson, A.F. 1974. The rise and fall of Ammophila arenaria. Autecology class paper, University of California at Davis, California.
  • Laing, C. 1958. Studies in the ecology of Ammophila breviligulata: I. Seedling survival and its relation to population increase and dispersal. Bot. Gaz. 119:208-216.
  • Lamb, F.H. 1898. Sand dune reclamation on the Pacific Coast. The Forester 4:141-142.
  • Lindberg, C.A. 1979a. Beach and dune planning and management on the Oregon Coast: a summary of the state-of-the-arts. in Fitzpatrick, K. B., (ed.), Articles of the Oregon Coastal Zone Management Assocation, Inc. Newport, Oregon.
  • Lindberg, C.A. 1979b. Oregon's coastal beaches and dunes: impacts, uses, and management considerations. In Fitzpatrick, K.B. (ed.), Articles of the Oregon Coastal Zone Management Association, Inc. Newport, Oregon.
  • Malloch, B. 1980. A proposal: investigation into methods of control of European beachgrass, Ammophila arenaria (L.) Link. Ecology 230 course paper, University of California at Davis, California.
  • Miller, L.M. 1988. An annotated bibliography of references on Ammophila arenaria (L.) Link. The California Nature Conservancy, 785 Market Street, 3rd Floor, San Francisco, California 94103.
  • Old, K.M., and T.H. Nicolson. 1975. Electron microscopial studies of the microflora of roots of sand dune grasses. New Phytology 74:51-58.
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  • Pavlik, B.M. 1983a. Nutrient productivity relations of the dune grasses Ammophila arenaria and Elymus mollis. I. Blade photosynthesis and nitrogen use efficiency in the laboratory and field. Oecologia. 57:227-232.
  • Pavlik, B.M. 1983b. Nutrient productivity relations of the dune grasses Ammophila arenaria and Elymus mollis. II. Growth and patterns of dry matter and nitrogen allocation as influenced by nitrogen supply. Oecologia. 57:233-238.
  • Pavlik, B.M. 1983c. Nutrient productivity relations of the dune grasses Ammophila arenaria and Elymus mollis. III. Spatial aspects of clonal expansion with reference to rhizome growth and the dispersal of buds. Bull. Torrey Bot. Club. 110:271-279.
  • Ranwell, D. 1960. Newborough Warren, Anglesey. II. Plant associes and succession cycles of the sand dune and dune slack vegetation. J. Ecology 48:117-141.
  • Schmalzer, P.A. 1987. Species biology and potential for controlling four exotic plants (Ammophila arenaria, Carpobrotus edulis, Cortaderia jubata, and Gasoul Crystallinum) on Vandenberg Air Force Base, California. The Bionetics Corp., NASA.
  • Slobodchikoff, C.N., and J.T. Doyen. 1977. Effects of Ammophila arenaria on sand dune arthropod communities. Ecology 48:113-128.
  • Ternyik, W.E. 1979. Dune stabilization and restoration: methods and criteria. In Fitzpatrick, K. B., (ed.), Articles of the Oregon Coastal Zone Management Association, Inc. Newport, Oregon.
  • Tsuriell, D.E. 1974. Sand dune stabilization in Israel. Int. J. Biometeor. 18:89-93.
  • Van Hook, S. 1983. A study of European beachgrass, Ammophila arenaria (L.) Link: control methods and a management plan for the Lanphere-Christensen Dunes Preserve. The Nature Conservancy, San Francisco, California.
  • Webley, D.M., D.J. Eastwood, and C.H. Gimingham. 1952. Development of a soil microflora in relation to plant succession on sand dunes, including the 'Rhizosphere' flora associated with colonizing species. J. Ecology. 40 53:735-745.
  • Willis, A.J. 1965. The influence of mineral nutrients on the growth of Ammophila arenaria. J. Ecology 53:735-745.
  • Willis, A.J., and R.L. Jeffries. 1963. Investigations of water relations of sand dune plants under natural conditions. In A.J. Rutter, and F.H. Whitehead (eds.), The water relations of plants. Blackwell Scientific Publications, Oxford, England. Pp. 168-189.

Original Document

Element Stewardship Abstract; Mary Russo, Andrea Pickart, Larry Morse, and Rick Young, 1988