(Cav.) Trin. ex Steud.
Identity
Unique IDELEMENT_GLOBAL.2.134146
Element CodePMPOA4V010
Record TypeSPECIES
ClassificationSpecies
Classification StatusStandard
Name CategoryVascular Plant
IUCNLeast concern
KingdomPlantae
PhylumAnthophyta
ClassMonocotyledoneae
OrderCyperales
FamilyPoaceae
GenusPhragmites
SynonymsPhragmites communisTrin.
Other Common NamesCana de Indio (ES) common reed (EN) Roseau commun (FR)
Concept ReferenceKartesz, J.T. 1994. A synonymized checklist of the vascular flora of the United States, Canada, and Greenland. 2nd edition. 2 vols. Timber Press, Portland, OR.
Taxonomic CommentsGenerally accepted as an essentially cosmopolitan species; the name Phragmites communis is used for this plant in most older North American literature.
Conservation Status
Rank MethodExpertise without calculation
Review Date2016-05-16
Change Date1988-04-28
Edition Date1993-05-12
Edition AuthorsMarianne Marks (original version), Beth Lapin & John Randall (1993 update), Larry Morse (minor updates 2001).
Range Extent>2,500,000 square km (greater than 1,000,000 square miles)
Number of Occurrences81 to >300
Rank ReasonsNearly cosmopolitan as a presumably native plant in marshes and other wetland habitats on all continents except Antarctica. Additionally, at least in North America, non-native genotypes may have become established in areas not previously supporting Phragmites.
Range Extent CommentsPhragmites australis is found on every continent except Antarctica and may have the widest distribution of any flowering plant (Tucker 1990). It is common in and near freshwater, brackish and alkaline wetlands in the temperate zones world-wide. It may also be found in some tropical wetlands but is absent from the Amazon Basin and central Africa. It is widespread in the United states, typically growing in marshes, swamps, fens, and prairie potholes, usually inhabiting the marsh-upland interface where it may form continuous belts (Roman et al. 1984).
Because Phragmites has invaded and formed near-monotypic stands in some North American wetlands only in recent decades there has been some debate as to whether it is indigenous to this continent or not. Convincing evidence that it was here long before European contact is now available from at least two sources. Niering and Warren (1977) found remains of Phragmites in cores of 3000 year old peat from tidal marshes in Connecticut. Identifiable Phragmites remains dating from 600 to 900 A.D. and constituting parts of a twined mat and other woven objects were found during archaeological investigations of Anasazi sites in southwestern Colorado (Kane & Gross 1986; Breternitz et al. 1986).
There is some suspicion that although the species itself is indigenous to North America, new, more invasive genotype(s) were introduced from the Old World (Metzler and Rosza 1987). Hauber et al. (1991) found that invasive Phragmites populations in the Mississippi River Delta differed genetically from a more stable population near New Orleans. They also examined populations elsewhere on the Gulf coast, from extreme southern Texas to the Florida panhandle, and found no genetic differences between those populations and the one near New Orleans (Hauber, pers. comm. 1992). This increased their suspicion that the invasive biotypes were introduced to the Delta from somewhere outside the Gulf relatively recently.
Phragmites is frequently regarded as an aggressive, unwanted invader in the East and Upper Midwest. It has also earned this reputation in the Mississippi River Delta of southern Louisiana, where over the last 50 years, it has displaced species that provided valuable forage for wildlife, particularly migratory waterfowl (Hauber 1991). In other parts of coastal Louisiana, however, it is feared that Phragmites is declining as a result of increasing saltwater intrusion in the brackish marshes it occupies. Phragmites is apparently decreasing in Texas as well due to invasion of its habitat by the alien grass ARUNDO DONAX (Poole, pers. comm. 1985). Similarly, Phragmites is present in the Pacific states but is not regarded as a problem there. In fact, throughout the western U.S. there is some concern over decreases in the species' habitat and losses of populations.
Occurrences CommentsPerhaps the most widespread plant species on Earth, with numerous large, presumably native stands on all continents except Antarctica. In addition, at least in North America, novel (Eurasian?) genotypes have become widely established along the Atlantic Coast and in scattered inland sites where Phragmites was not previously known historically (Kristin Saltonstall, presentation to Botanical Society of Washington, 5 June 2001).
Threat Impact CommentsIMPACTS (THREATS POSED BY THIS SPECIES)
Phragmites can be regarded as a stable, natural component of a wetland community if the habitat is pristine and the population does not appear to be expanding. Many native populations of Phragmites are "benign" and pose little or no threat to other species and should be left intact. Examples of areas with stable, native populations include sea-level fens in Delaware and Virginia and along Mattagota Stream in Maine (Rawinski 1985, pers. comm. 1992). In Europe, a healthy reed belt is defined as a "homogeneous, dense or sparse stand with no gaps in its inner parts, with an evenly formed lakeside borderline without aisles, shaping a uniform fringe or large lobes, stalk length decreasing gradually at the lakeside border, but all stalks of one stand of similar height; at the landside edge the reeds are replaced by sedge or woodland communities or by unfertilized grasslands" (Ostendorp 1989).
Stable populations may be difficult to distinguish from invasive populations, but one should examine such factors as site disturbance and the earliest collection dates of the species to arrive at a determination. If available, old and recent aerial photos can be compared to determine whether stands in a given area are expanding or not (Klockner, pers. comm. 1985).
Phragmites is a problem when and where stands appear to be spreading while other species typical the of the community are diminishing. Disturbances or stresses such as pollution, alteration of the natural hydrologic regime, dredging, and increased sedimentation favor invasion and continued spread of Phragmites (Roman et al. 1984). Other factors that may have favored recent invasion and spread of Phragmites include increases in soil salinity (from fresh to brackish) and/or nutrient concentrations, especially nitrate, and the introduction of a more invasive genotype(s) from the Old World (McNabb and Batterson 1991; Metzler and Rosza 1987, see GLOBAL RANGE section for further discussion).
Michael Lefor asserts that one reason for the general spread of Phragmites has been the destabilization of the landscape (pers. comm. 1993). In urban landscapes water is apt to collect in larger volumes and pass through more quickly (flashily) than formerly. This tends to destabilize substrates leaving bare soil open for colonization. Watersheds throughout eastern North America are flashier due to the proliferation of paved surfaces, lawns and roofs and the fact that upstream wetlands are largely filled with post-settlement/post agricultural sediments from initial land-clearing operations.
Many Atlantic coast wetland systems have been invaded by Phragmites as a result of tidal restrictions imposed by roads, water impoundments, dikes and tide gates. Tide gates have been installed in order to drain marshes to harvest salt hay, to control mosquito breeding and, most recently, to protect coastal development from flooding during storms. This alteration of marsh systems may favor Phragmites invasion by reducing tidal action and soil water salinity and lowering water tables.
Phragmites invasions may threaten wildlife because they alter the structure and function (wildlife support) of relatively diverse Spartina marshes (Roman et al. 1984). This is a problem on many of the eastern coastal National Fish and Wildlife Refuges including: Brigantine in NJ; Prime Hook and Bombay Hook in DE; Tinicum in PA; Chincoteague in VA; and Trustom Pond in RI.
Plant species and communities threatened by Phragmites are listed in the Monitoring section. Some of these instances are described below:
1. Massachusetts, a brackish pondlet near Horseneck Beach supports the state rare plant MYRIOPHYLLUM PINNATUM (Walter) BSP, which Phragmites is threatening by reducing the available open water and shading aquatic vegetation (Sorrie, pers. comm. 1985).
2. Maryland, at Nassawango Creek, a rare coastal plain peatland community is threatened by Phragmites (Klockner, pers. comm. 1985).
3. Ohio, at the Arcola Creek wetland, phragmites is threatening the state endangered plant CAREX AQUATILIS Wahlenb. (Young, pers. comm. 1985).
Phragmites invasions also increase the potential for marsh fires during the winter when the above ground portions of the plant die and dry out (Reimer 1973). Dense congregations of redwing blackbirds, which nest in Phragmites stands preferentially, increase chances of airplane accidents nearby. The monitoring and control of mosquito breeding is nearly impossible in dense Phragmites stands (Hellings and Gallagher 1992). In addition, Phragmites invasions can also have adverse aesthetic impacts. In Boston's Back Bay Fens, dense stands have obscured vistas intended by the park's designer, Frederick Law Olmstead (Penko, pers. comm. 1993).
As noted above Phragmites is not considered a threat in the West or most areas in the Gulf states.