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Introductory

SPECIES: Typha angustifolia | Narrow-Leaved Cattail
ABBREVIATION : TYPANG SYNONYMS : NO-ENTRY SCS PLANT CODE : TYAN COMMON NAMES : narrow-leaved cattail narrow-leaf cattail narrowleaved cattail TAXONOMY : The currently accepted scientific name for narrow-leaved cattail is Typha angustifolia L. in the family Typhaceae [12]. Typha angustifolia hybridizes with T. latifolia to form T. Xglauca Godron. [14]. LIFE FORM : Graminoid FEDERAL LEGAL STATUS : No special status OTHER STATUS : NO-ENTRY COMPILED BY AND DATE : S. A. Snyder, September 1993 LAST REVISED BY AND DATE : NO-ENTRY AUTHORSHIP AND CITATION : Snyder, S. A. 1993. Typha angustifolia. In: Remainder of Citation

DISTRIBUTION AND OCCURRENCE

SPECIES: Typha angustifolia | Narrow-Leaved Cattail
GENERAL DISTRIBUTION : Narrow-leaved cattail occurs from Nova Scotia south through parts of New England along the coast to southern Florida. It occurs in the Midwest south to southeastern Texas. Scattered populations are found throughout Nebraska and Wyoming, parts of the Intermountain West, and along the Pacific Northwest coast into central California [10]. ECOSYSTEMS : FRES17 Elm - ash - cottonwood FRES28 Western hardwoods FRES37 Mountain meadows FRES39 Prairie FRES41 Wet grasslands FRES42 Annual grasslands STATES : AL AR CA CT DE FL GA IL IN IA KY LA ME MD MA MI MN MS MO MT NE NH NJ NY NC OH OR PA RI SC TN TX UT VT VA WV WI WY MB NB NS ON PQ ADMINISTRATIVE UNITS : ASIS BIBE BICA CACO CALO COLO CUIS CUVA DEVA DINO FIIS GATE GWMP GRTE GUMO GUIS INDU JOTR LAME NERI ROMO SLBE WHSA YELL BLM PHYSIOGRAPHIC REGIONS : 1 Northern Pacific Border 2 Cascade Mountains 3 Southern Pacific Border 5 Columbia Plateau 8 Northern Rocky Mountains 9 Middle Rocky Mountains 10 Wyoming Basin 14 Great Plains KUCHLER PLANT ASSOCIATIONS : K049 Tule marshes K072 Sea oats prairie K073 Northern cordgrass prairie K074 Bluestem prairie K092 Everglades SAF COVER TYPES : 63 Cottonwood 235 Cottonwood - willow SRM (RANGELAND) COVER TYPES : NO-ENTRY HABITAT TYPES AND PLANT COMMUNITIES : Narrow-leaved cattail is listed as a riparian dominance type in the following publication: Riparian dominance types of Montana [31] Some associates of narrow-leaved cattail include sedges (Carex spp.), bulrushes (Scirpus spp.), rushes (Juncus spp.), sphagnum mosses (Sphagnum ssp.), lichens (Cladonia spp.), kalmia (Kalmia spp.), foxtail barley (Critestion jubatum), reed canarygrass (Phalaris arundinaceae), oakleaf goosefoot (Chenopodium glaucum), curled dock (Rumex crispus), panicgrass (Panicum spp.), cottonsedge (Eriophorum spissum), buttonbush (Cephalanthus occidentalis), spiraea (Spiraea spp.), blueberries (Vaccinium spp.), viburnum (Viburnum spp.), chufa flatsedge (Cyperus esculentus), and dwarf huckleberry (Gaylussacia dumosa) [8,28].

VALUE AND USE

SPECIES: Typha angustifolia | Narrow-Leaved Cattail
WOOD PRODUCTS VALUE : NO-ENTRY IMPORTANCE TO LIVESTOCK AND WILDLIFE : Narrow-leaved cattail is eaten by waterfowl and muskrats [24,27]. Muskrats also construct their lodges with cattail, and blackbirds use cattail for perches [31]. Extensive monotypic stands of cattail are usually poor habitat for wildlife [1]. PALATABILITY : NUTRITIONAL VALUE : Food values for leaf litter of the narrow-leaved cattail hybrid, T. Xglauca, have been listed [22]: type time %nitrogen %phosphorus %ash green early July 2.77 0.29 6.55 senesced early Feb. 0.63 0.05 3.89 COVER VALUE : Narrow-leaved cattail provides important cover for muskrats and a variety of waterfowl [4,6,27]. White-tailed deer use cattail for cover [31]. VALUE FOR REHABILITATION OF DISTURBED SITES : Narrow-leaved cattail is used in prairie wetland restoration [17]. It is used to create wetlands for mitigating the effects of wastewater treatment plants and landfills [9]. A shoreline restoration project to provide cover for largemouth bass and other fish determined that rhizome transplants have better survivorship than transplanted greenhouse stock [7]. OTHER USES AND VALUES : Rhizomes are eaten whole or ground into flour. Shoots, seeds, flowers, pollen, and stems are also eaten. Stems and leaves are woven into baskets and rope or used in roofing, bedding, and paper manufacturing [10,15]. Many other uses for narrow-leaved cattail have been documented [21]. MANAGEMENT CONSIDERATIONS : Although narrow-leaved cattail is useful in wetland restoration projects, without control it will form dense stands that eventually outcompete other valuable wildlife food and cover species [4]. It can be controlled with herbicides and through marsh drawdowns or by flooding over freshly cut stubble to reduce oxygen to the rhizomes [15]. A study of the effects of cutting cattail, then flooding the area, showed that stem densities were reduced by 89 percent the first year. When cut a second time, densities were reduced by 99 percent. No fruiting heads or seed germination occured following cutting and flooding [1]. Draining a New Brunswick marsh caused a 36 percent increase in narrow-leaved cattail cover and a 50 percent increase in stem density. However, plant height and basal diameter were reduced by 16.54 percent and 7.14, respectively [30].

BOTANICAL AND ECOLOGICAL CHARACTERISTICS

SPECIES: Typha angustifolia | Narrow-Leaved Cattail
GENERAL BOTANICAL CHARACTERISTICS : Narrow-leaved cattail is an erect, rhizomatous perennial that grows 3 to 6 feet (1-2 m) tall [15]. Its lateral rhizomes, produced at the leaf base, can grow up to 27.6 inches (70 cm) long and 0.8 to 1.6 inches (2-4 cm) in diameter [15]. Its leaves are 2 to 5 feet (0.6-1.5 m) long, very narrow, and flattened [10,12]. Flowers grow on erect stalks, and the fruits are cigar-shaped and 2 to 6 inches (5-15 cm) long. Fruits contain soft, downy seeds [10]. RAUNKIAER LIFE FORM : Helophyte REGENERATION PROCESSES : Cattails reproduce by seed and rhizomes. Their primary means of colonizing is by seed, and once established, colonies are maintained by vegetative reproduction [16]. Seeds are wind pollinated and require moisture, but not oxygen for germination [15]. Laboratory studies have shown that seeds germinate best in water 1 inch (2.5 cm) deep, but can germinate in water as deep as 16 inches (40 cm) [4]. In the field seed germination usually occurs following exposure of mudflats. Narrow-leaved cattail was found in wetland seedbanks that had been drained for more than 70 years [32]. SITE CHARACTERISTICS : Narrow-leaved cattail grows in marshes, wet meadows, fens, estuaries, bogs, ditches, and along lake shores. It is tolerant of saline environments [15,31]. Where T. angustifolia and T. latifolia occur together, T. angustifolia usually colonizes the deeper waters (31.5 in. [80 cm] or more) [16]. In Utah, narrow-leaved cattail occurs in peaty soils of salt marshes and colonizes deep sloughs and sloping marsh perimeters [5]. In Wisconsin, water levels seem to be the most important factor affecting cattail occurrence and establishment [4]. Typha spp. grow best under stable moisture conditions, saturated soil, and water up to 1.5 feet (45 cm) deep. Narrow-leaved cattail can grow in water as deep as 2.5 feet (76 cm) [4]. After establishment, it can tolerate fluctuating water levels including periods of drought and deep flooding. In Wisconsin cattail species usually grow in soils that are fertile and nutrient rich [4]. Narrow-leaved cattail height growth is best in hot temperatures but does not seem to be adversely affected by extreme cold [4]. SUCCESSIONAL STATUS : Facultative Seral Species Narrow-leaved cattail is considered an early to mid-seral species and a dominant in disturbed wetlands [15]. In the absence of disturbance, narrow-leaved cattail dominates marshes in dense, monotypic stands [18]. Under these conditions productivity is lowered because of litter buildup, and narrow-leaved cattail outcompetes other species. Narrow-leaved cattail replaces cordgrass (Spartina spp.) in marshes where coastal wetlands are diked or tidally restricted [2,23]. SEASONAL DEVELOPMENT : Leaves emerge in the spring, flowering is initiated in early to mid-summer, and the greatest clonal growth occurs in the fall [15]. Under good conditions, seeds germinate from May to September [4]. Aerial shoot growth continues into November or until the first freeze when plants go dormant [20]. Development times in a Wisconsin marsh were: April: aerial shoot sprout, new rhizome formation, leaves; May: new shoots; June: spikes formed; July: basal shoots and flower head development; August through September: maturation of flower head [4].

FIRE ECOLOGY

SPECIES: Typha angustifolia | Narrow-Leaved Cattail
FIRE ECOLOGY OR ADAPTATIONS : Cattail rhizomes sprout following fire [4]. POSTFIRE REGENERATION STRATEGY : Rhizomatous herb, rhizome in soil Ground residual colonizer (on-site, initial community)

FIRE EFFECTS

SPECIES: Typha angustifolia | Narrow-Leaved Cattail
IMMEDIATE FIRE EFFECT ON PLANT : Burning topkills narrow-leaved cattail and reduces stem density [1]. Fires that burn into the peat layer can kill cattail [4]. DISCUSSION AND QUALIFICATION OF FIRE EFFECT : The effects of fire on the narrow-leaved cattail hybrid T. Xglauca were determined for a New Brunswick marsh. The marsh was divided into two sections, each containing four blocks of four plots. In each section one block was burned in early and mid-June, one was burned in early and mid-July, and one was burned in mid-August and mid-September. Vegetation was measured the third postfire year. Following each fire, plots were either drained or flooded. On the drained sites T. Xglauca cover, density, and height were least on the plots burned in July. Other burned plots did not differ significantly from the control. On the flooded sites July-burned plots had greater T. Xglauca cover than control plots. Other burned plots did not differ significantly from the control [30]. PLANT RESPONSE TO FIRE : Narrow-leaved cattail will sprout following fire if rhizomes are not consumed [1,4]. For detailed information, refer to the CASE STUDIES FRAME. DISCUSSION AND QUALIFICATION OF PLANT RESPONSE : NO-ENTRY FIRE MANAGEMENT CONSIDERATIONS : Fire can be used to reduce aboveground debris, opening up stands for nesting waterfowl. Burning in winter when rhizomes are buried in ice or in frozen soil usually will not kill cattail. If the objective is to create more open stands for wildlife, burning should be conducted in spring following a relatively dry winter, when the marsh is dry [4]. Cattail marshes are difficult to burn 2 years in a row because accumulated debris is needed for fuel. The thick bases of cattail species are often the last part of the plant to dry out and are difficult to burn. Canada geese, herons, egrets, and other waterfowl use burned marsh areas for feeding and nesting [4]. Draining and burning marshes during July inhibits rapid growth of cattail species. Several fires during summer will release nutrients if a portion of the organic mat is removed [30]. Draining and burning before a thick mat layer forms is necessary for slowing palludification. Fires on nutrient-poor fens can reduce species diversity and create oligotrophic bogs, but on nutrient-rich sites fires will not typically reduce species diversity [30].

FIRE CASE STUDIES

SPECIES: Typha angustifolia | Narrow-Leaved Cattail
CASE NAME : St. Clair National Wildlife Area REFERENCE : Ball, J. P. 1984 [1] SEASON/SEVERITY CLASSIFICATION : The fires were conducted in late winter, possibly in February of the first year and March of the second year. Fires burned over ice and were considered low intensity. STUDY LOCATION : The fires were conducted at the St. Clair National Wildlife Area on the shore of Lake St. Clair in southwestern Ontario. PREFIRE VEGETATIVE COMMUNITY : The principle vegetation was cattail, mostly consisting of Typha Xglauca (a hybrid), although narrow-leaved cattail (T. angustifolia) and common cattail (T. latifolia) were also present. The author states that this marsh contained a "continuum of phenotypes spanning the two parental types" (T. angustifolia and T. latifolia) and assumes that all three entities would respond similarly to treatment. General stand conditions were not given. TARGET SPECIES PHENOLOGICAL STATE : Treatments were applied when Typha spp. stands were dormant. SITE DESCRIPTION : Soils are Rego Humic Gleysols. The study was conducted in a marsh on a lake's edge where water levels were artificially controlled. FIRE DESCRIPTION : A total of 19 circular plots ranging in size from 0.05 to 0.37 acres (0.02-0.15 ha) were burned. Fires were started with propane from a flamethrower and began just after dawn. The temperature was near freezing, and the wind speed was less than 12 miles per hour (20 km/hr). Rate of spread was between 0.6 to 5 miles per hour (1-8 km/hr) and varied with Typha spp. density and wind speed. Flame lengths averaged just over 6 feet (2 m), but sometimes exceeded 21 feet (7 m). Fire intensity was considered low until the frost was melted off vegetation. FIRE EFFECTS ON TARGET SPECIES : Following the fires and spring thawing, the marsh was flooded and reached a maximum depth in April, covering the cattail stubble. No depths were given, but water levels were maintained within 0.8 inches (2 cm) until the end of the growing season. Fires reduced stem density an average of 70 percent compared to control plots. Cattails that survived burning were shorter than controls: 8.9 feet (2.7 m) tall compared to 9.6 feet (2.9 m) tall. No fruiting heads were produced following fires, although some occurred on control sites. No seeds germinated on treated or control sites. No stems occurred at water depths of 30.7 inches (78 cm) following burning. FIRE MANAGEMENT IMPLICATIONS : Fire is an effective tool for opening up dense cattail stands. If marshes are burned in winter, fires are less intense and easier to control. Following burning cattail can be killed by submerging stubble to cut off oxygen to the rhizomes. In this study slow-moving backfires left the shortest stubble and, therefore, water levels did not have to be raised much. However, stubble layers were left under the ice, and if snow builds up on the ice before burning, the stubble layer may be even taller. Under these conditions water levels may not cover the stubble layer enough to kill the cattail. Burning in early winter or early spring might reduce this problem. Burning the same sites year after year may not be feasible because the regrowth is not enough to carry fire.

REFERENCES

SPECIES: Typha angustifolia | Narrow-Leaved Cattail
REFERENCES : 1. Ball, J. P. 1984. Habitat selection and optimal foraging by mallards: a field experiment. Guelph, ON: University of Guelph. 44 p. Thesis. [18071] 2. Barrett, Nels E.; Niering, William A. 1993. Tidal marsh restoration: trends in vegetation change using a geographical information system (GIS). Restoration Ecology. 1(1): 18-28. [20797] 3. Bernard, Stephen R.; Brown, Kenneth F. 1977. Distribution of mammals, reptiles, and amphibians by BLM physiographic regions and A.W. Kuchler's associations for the eleven western states. Tech. Note 301. Denver, CO: U.S. Department of the Interior, Bureau of Land Management. 169 p. [434] 4. Beule, John D. 1979. Control and management of cattails in southeastern Wisconsin wetlands. Tech. Bull No. 112. Madison, WI: Department of Natural Resources. 40 p. [14574] 5. Bolen, Eric G. 1964. Plant ecology of spring-fed salt marshes in western Utah. Ecological Monographs. 34(2): 143-166. [11214] 6. Capen, David E.; Low, Jessop B. 1980. Management considerations for nongame birds in western wetlands. In: DeGraaf, Richard M., technical coordinator. Management of western forests and grasslands for nongame birds: Workshop proceedings; 1980 February 11-14; Salt Lake City, UT. Gen. Tech. Rep. INT-86. Ogden, UT: U.S. Department of Agriculture, Forest Service, Intermountain Forest and Range Experiment Station: 67-77. [17898] 7. Croft, Lisa K.; Haley, Jennifer S.; Paulson, Larry J. 1990. The Lake Mead cover enhancement project: planting native vegetation creates new habitat. In: Hughes, H. Glenn; Bonnicksen, Thomas M., eds. Restoration `89: the new management challange: Proceedings, 1st annual meeting of the Society for Ecological Restoration; 1989 January 16-20; Oakland, CA. Madison, WI: The University of Wisconsin Arboretum, Society for Ecological Restoration: 403-419. [14713] 8. Damman, Antoni W. H.; French, Thomas W. 1987. The ecology of peat bogs of the glaciated northeastern United States: a community profile. Biological Report 85(7.16). Washington, DC: U.S. Department of the Interior, Fish and Wildlife Service, Research and Development, National Wetlands Research Center. 100 p. [9238] 9. Dobberteen, Ross A.; Nickerson, Norton H. 1991. Use of created cattail (Typha) wetlands in mitigation strategies. Environmental Management. 15(6): 797-808. [17431] 10. Elias, Thomas S.; Dykeman, Peter A. 1982. Field guide to North American edible wild plants. [Place of publication unknown]: Outdoor Life Books. 286 p. [21103] 11. Eyre, F. H., ed. 1980. Forest cover types of the United States and Canada. Washington, DC: Society of American Foresters. 148 p. [905] 12. Fernald, Merritt Lyndon. 1950. Gray's manual of botany. [Corrections supplied by R. C. Rollins]. Portland, OR: Dioscorides Press. 1632 p. (Dudley, Theodore R., gen. ed.; Biosystematics, Floristic & Phylogeny Series; vol. 2). [14935] 13. Garrison, George A.; Bjugstad, Ardell J.; Duncan, Don A.; [and others]. 1977. Vegetation and environmental features of forest and range ecosystems. Agric. Handb. 475. Washington, DC: U.S. Department of Agriculture, Forest Service. 68 p. [998] 14. Godfrey, Robert K.; Wooten, Jean W. 1979. Aquatic and wetland plants of southeastern United States: Monocotyledons. Athens, GA: The University of Georgia Press. 712 p. [16906] 15. Grace, James B.; Harrison, Janet S. 1986. The biology of Canadian weeds. 73. Typha latifolia L., Typha angustifolia L. and Typha xglauca Godr. Canadian Journal of Plant Science. 66: 361-379. [17673] 16. Grace, James B.; Wetzel, Robert G. 1982. Niche differentiation between two rhizomatous plant species: Typha latifolia and Typha angustifolia. Canadian Journal of Botany. 60: 46-57. [17683] 17. Jenkins, Robert. 1973. Ecosystem restoration. In: Hulbert, Lloyd C., ed. Third Midwest prai; 1972 September 22-23; Manhattan, KS. Manhattan, KS: Kansas State University, Division of Biology: 23-27. [18794] 18. Kantrud, Harold A. 1990. Effects of vegetation manipulation on breeding waterfowl in prairie wetlands--a literature review. In: Severson, Kieth E., tech. coord. Can livestock be used as a tool to enhance wildlife habitat?: Proceedings, 43rd annual meeting of the Society for Range Managememt; 1990 February 13; Reno, NV. Gen. Tech. Rep. RM-194. Fort Collins, CO: U.S. Department of Agriculture, Forest Service, Intermountain Forest and Range Experiment Station: 93-123. [16001] 19. Kuchler, A. W. 1964. Manual to accompany the map of potential vegetation of the conterminous United States. Special Publication No. 36. New York: American Geographical Society. 77 p. [1384] 20. Linde, Arlyn F.; Janisch, Thomas; Smith, Dale. 1976. Cattail - the significance of its growth, phenology and carbohydrate storage to its control and management. Tech. Bull. No. 94. Madison, WI: Department of Natural Resources. 27 p. [17678] 21. Morton, Julia F. 1975. Cattails (Typha spp.) - Weed problem or potential crop?. Economic Botany. 29: 7-29. [17675] 22. Nelson, Jeffrey W.; Kadlec, John A.; Murkin, Henry R. 1990. Seasonal comparisons of weight loss for two types of Typha glauca Godr. leaf litter. Aquatic Botany. 37(4): 299-314. [17426] 23. Niering, William. 1992. The New England forests. Restoration & Management Notes. 10(1): 24-28. [19731] 24. O'Neil, Ted. 1949. The muskrat in the Louisiana coastal marshes. New Orleans, LA: Louisiana Department of Wildlife and Fisheries, Fish and Game Division, Federal Aid Section. 152 p. [18182] 25. Raunkiaer, C. 1934. The life forms of plants and statistical plant geography. Oxford: Clarendon Press. 632 p. [2843] 26. Stickney, Peter F. 1989. Seral origin of species originating in northern Rocky Mountain forests. Unpublished draft on file at: U.S. Department of Agriculture, Forest Service, Intermountain Research Station, Fire Sciences Laboratory, Missoula, MT; RWU 4403 files. 7 p. [20090] 27. Tilmant, James Thomas. 1975. Habitat utilization by round-tailed muskrats (Neofiber alleni) in Everglades National Park. Arcata, CA: Humboldt State University. 91 p. Thesis. [17793] 28. Ungar, Irwin A. 1984. Autecological studies with Atriplex triangularis willdenow. In: Tiedemann, Arthur R.; McArthur, E. Durant; Stutz, Howard C.; [and others], compilers. Proceedings--symposium on the biology of Atriplex and related chenopods; 1983 May 2-6; Provo, UT. Gen. Tech. Rep. INT-172. Ogden, UT: U.S. Department of Agriculture, Forest Service, Intermountain Forest and Range Experiment Station: 40-52. [8013] 29. U.S. Department of Agriculture, Soil Conservation Service. 1982. National list of scientific plant names. Vol. 1. List of plant names. SCS-TP-159. Washington, DC. 416 p. [11573] 30. Mallik, A. U.; Wein, Ross W. 1986. Response of a Typha marsh community to draining, flooding, and seasonal burning. Canadian Journal of Botany. 64: 2136-2143. [17672] 31. Hansen, Paul L.; Chadde, Steve W.; Pfister, Robert D. 1988. Riparian dominance types of Montana. Misc. Publ. No. 49. Missoula, MT: University of Montana, School of Forestry, Montana Forest and Conservation Experiment Station. 411 p. [5660] 32. Wienhold, C. E.; van der Valk, A. G. 1989. The impact of duration of drainage on the seed banks of northern prairie wetlands. Canadian Journal of Botany. 67(6): 1878-1884. [13799]

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