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Introductory

SPECIES: Typha latifolia | Common Cattail
ABBREVIATION : TYPLAT SYNONYMS : Massula latifolia (L.) Dulac. SCS PLANT CODE : TYLA COMMON NAMES : common cattail cattail broad-leaved cattail soft flag TAXONOMY : The currently accepted scientific name of common cattail is Typha latifolia L. [16,45]. In North America, the cattail family Typhaceae consists of a single genus with three species: Typha latifolia L. - common cattail Typha angustifolia L. - narrow-leaved cattail Typha domingensis Pers. - Dominican cattail The distributions of these species overlap considerably in the contiguous United States. Wherever two species occur together, hybrids are common, especially in habitats with variable water levels [39]. Typha latifolia x T. angustifolia hybrids (T. X glauca Godr.), commonly known as hybrid or glaucus cattail, are especially common in the Midwest and may develop extensive pure stands by rhizomatous growth [3,16]. Common cattail also hybridizes with Dominican cattail. Hybrids are almost always intermediate morphologically between the parental species. This report focuses primarily on common cattail. However, since hybrid cattail is ecologically similar, information on it has been incorporated into some slots. When used, the reader will be alerted that the information pertains specifically to hybrid cattail. LIFE FORM : Graminoid FEDERAL LEGAL STATUS : No special status OTHER STATUS : NO-ENTRY COMPILED BY AND DATE : Ronald Uchytil, March 1992 LAST REVISED BY AND DATE : NO-ENTRY AUTHORSHIP AND CITATION : Uchytil, Ronald J. 1992. Typha latifolia. In: Remainder of Citation

DISTRIBUTION AND OCCURRENCE

SPECIES: Typha latifolia | Common Cattail
GENERAL DISTRIBUTION : Common cattail has a nearly worldwide distribution. It grows in North America, Central America, Great Britain, Eurasia, Africa, New Zealand, Australia, and Japan. In North America it grows in arctic, temperate, subtropical, and tropical regions from central Alaska and northwest Canada to Newfoundland, and south through every province, territory, and state to Mexico and Guatemala [12,30]. ECOSYSTEMS : FRES10 White - red - jack pine FRES11 Spruce - fir FRES13 Loblolly - shortleaf pine FRES14 Oak - pine FRES15 Oak - hickory FRES16 Oak - gum - cypress FRES17 Elm - ash - cottonwood FRES18 Maple - beech - birch FRES20 Douglas-fir FRES21 Ponderosa pine FRES23 Fir - spruce FRES24 Hemlock - Sitka spruce FRES26 Lodgepole pine FRES27 Redwood FRES28 Western hardwoods FRES29 Sagebrush FRES30 Desert shrub FRES31 Shinnery FRES32 Texas savanna FRES33 Southwestern shrubsteppe FRES34 Chaparral - mountain shrub FRES35 Pinyon - juniper FRES36 Mountain grasslands FRES38 Plains grasslands FRES39 Prairie FRES40 Desert grasslands FRES41 Wet grasslands STATES : AL AK AZ AR CA CO CT DE FL GA HI ID IL IN IA KS KY LA ME MD MA MI MN MS MO MT NE NV NH NJ NM NY NC ND OH OK OR PA RI SC SD TN TX UT VT VA WA WV WI WY AB BC LB MB NB NF NT NS ON PE PQ SK YT MEXICO ADMINISTRATIVE UNITS : ACAD AGFO ALPO AMIS APIS ARCH ASIS BADL BIBE BICY BISO BITH BICA CACH CANY CACO CAHA CALO CARE CAMO CHCU CHCH COLO COLM COSW CODA CUGA CUIS CUVA DEWA DINO EFMO EVER FIIS FOBU GATE GWMP GLAC GRCA GRTE GRKO GRSA GRSM HOBE INDU ISRO JELA JECA JODA JOFL LAME LAVO MACA MEVE MORA NATR NABR NERI OBRI OLYM PIRO PIPE PORE PRWI REDW RICH ROMO SAJH SAMO SARA SCBL SLBE THRO TICA VAFO VOYA WHIS WHSA WICA YELL YUCH ZION BLM PHYSIOGRAPHIC REGIONS : 1 Northern Pacific Border 2 Cascade Mountains 3 Southern Pacific Border 4 Sierra Mountains 5 Columbia Plateau 6 Upper Basin and Range 7 Lower Basin and Range 8 Northern Rocky Mountains 9 Middle Rocky Mountains 10 Wyoming Basin 11 Southern Rocky Mountains 12 Colorado Plateau 13 Rocky Mountain Piedmont 14 Great Plains 15 Black Hills Uplift 16 Upper Missouri Basin and Broken Lands KUCHLER PLANT ASSOCIATIONS : K001 Spruce - cedar - hemlock forest K002 Cedar - hemlock - Douglas-fir forest K006 Redwood forest K012 Douglas-fir forest K016 Eastern ponderosa forest K017 Black Hills pine forest K018 Pine - Douglas-fir forest K019 Arizona pine forest K023 Juniper - pinyon woodland K024 Juniper steppe woodland K025 Alder - ash forest K027 Mesquite bosque K028 Mosaic of K002 and K026 K035 Coastal sagebrush K037 Mountain-mahogany - oak scrub K038 Great Basin sagebrush K039 Blackbrush K040 Saltbush - greasewood K041 Creosotebush K045 Ceniza shrub K049 Tule marshes K051 Wheatgrass - bluegrass K055 Sagebrush steppe K056 Wheatgrass - needlegrass shrubsteppe K057 Galleta - three-awn shrubsteppe K058 Grama - tobosa shrubsteppe K059 Trans-Pecos shrub savanna K063 Foothills prairie K064 Grama - needlegrass - wheatgrass K065 Grama - buffalograss K066 Wheatgrass - needlegrass K067 Wheatgrass - bluestem - needlegrass K068 Wheatgrass - grama - buffalograss K070 Sandsage - bluestem prairie K071 Shinnery K074 Bluestem prairie K075 Nebraska Sandhills prairie K078 Southern cordgrass prairie K080 Marl - everglades K081 Oak savanna K082 Mosaic of K074 and K100 K090 Live oak - sea oats K091 Cypress savanna K092 Everglades K093 Great Lakes spruce - fir forest K094 Conifer bog K095 Great Lakes pine forest K096 Northeastern spruce - fir forest K097 Southeastern spruce - fir forest K098 Northern floodplain forest K099 Maple - basswood forest K100 Oak - hickory forest K102 Beech - maple forest K103 Mixed mesophytic forest K104 Appalacian oak forest K106 Northern hardwoods K107 Northern hardwoods - fir forest K108 Northern hardwoods - spruce forest K109 Transition between K104 and K106 K111 Oak - hickory - pine forest K113 Southern floodplain forest K114 Pocosin SAF COVER TYPES : 1 Jack pine 5 Balsam fir 12 Black spruce 13 Black spruce - tamarack 15 Red pine 20 White pine - northern red oak - red maple 25 Sugar maple - beech - yellow birch 26 Sugar maple - basswood 27 Sugar maple 33 Red spruce - balsam fir 35 Paper birch - red spruce - balsam fir 38 Tamarack 42 Bur oak 52 White oak - black oak - northern red oak 53 White oak 55 Northern red oak 60 Beech - sugar maple 63 Cottonwood 82 Loblolly pine - hardwood 95 Black willow 100 Pondcypress 101 Baldcypress 102 Baldcypress - tupelo 103 Water tupelo - swamp tupelo 107 White spruce 108 Red maple 110 Black oak 201 White spruce 204 Black spruce 210 Interior Douglas-fir 218 Lodgepole pine 221 Red alder 222 Black cottonwood - willow 223 Sitka spruce 225 Western hemlock - Sitka spruce 227 Western redcedar - western hemlock 229 Pacific Douglas-fir 230 Douglas-fir - western hemlock 235 Cottonwood - willow 237 Interior ponderosa pine 239 Pinyon - juniper 242 Mesquite SRM (RANGELAND) COVER TYPES : NO-ENTRY HABITAT TYPES AND PLANT COMMUNITIES : Common cattail forms dense, nearly monospecific communities in shallow, freshwater marshes and ponds. It also occurs as a codominant in mixed stands with bulrush (Scirpus acutus, S. californicus) and maidencane (Panicum hemitomon) [5,35]. Publications naming common cattail as a dominant species in riparian and plant community classifications are listed below. Aquatic and semiaquatic vegetation of Utah Lake and its bays [5] Riparian dominance types of Monatana [17] Riparian type community type classification of Utah and southeastern Idaho [33] Plant communities in the marshlands of southeastern Lousiana [35] Plant communities of Voyagers National Park, Minnesota [49]

VALUE AND USE

SPECIES: Typha latifolia | Common Cattail
WOOD PRODUCTS VALUE : NO-ENTRY IMPORTANCE TO LIVESTOCK AND WILDLIFE : Common cattail is generally considered a poor livestock and big game forage [8]. These animals rarely graze common cattail unless upland forage becomes scarce [17]. Common cattail rhizomes and basal portions are an important food of muskrat, nutria, and geese [26,29,30]. For ducks, however, common cattail is of little value as food or cover. It is considered an undesirable weed in marshes managed primarily for ducks [3,24]. The seeds are too small to be an important bird food source, but are eaten by a few species, mainly the green-winged teal, semipalmated sandpiper, and Canada goose, snow goose, and tule goose [30]. PALATABILITY : The palatability of common cattail foliage is low for wild ungulates and livestock [8]. The starchy rhizomes and root stocks are palatable to geese, muskrat, and nutria [26,29]. NUTRITIONAL VALUE : Common cattail's forage value is highest in the early spring, when protein content may reach 15 percent of dry weight. However, its forage quality declines rapidly, and by summer it is usually a poor source of energy and protein [8,40]. COVER VALUE : The structure and density of common cattail stands affect their usefulness as waterfowl nesting cover. Breeding ducks rarely nest in dense cattail stands that cover vast expanses of marsh, but are attracted to wetlands where open water and cattail cover are well interspersed [19]. Murkin and others [31] reported that cattail cover for nesting dabbling ducks was best when open water and common cattail stands covered roughly equal areas. These researchers found that the number of nesting duck pairs increased greatly when large stands were cut in checkerboard patterns to produce a 50:50 water-cover ratio. Common cattail provides favored nesting sites for the red-winged blackbird, yellow-headed blackbird, and marsh wren [26]. In the Horicon Marsh in southeastern Wisconsin, hybrid cattail (T. X glauca) stands were used extensively for nesting by the ruddy duck, redhead, sora, Virginia rail, least and American bittern, and common gallinule [3]. Similarly, the ruddy duck and readhead were the principal duck species nesting in common cattail marshes in Utah [7]. Common cattail provides an excellent hut building material for muskrat [26]. Deer sometimes use common cattail for hiding cover [17]. VALUE FOR REHABILITATION OF DISTURBED SITES : NO-ENTRY OTHER USES AND VALUES : Cattail leaves and stems have been used around the world as bedding, thatching, and matting, and in the manufacture of baskets, boats and rafts, shoes, ropes, and paper. In recent years, cattail has been proposed as a biomass crop for renewable energy [12,30]. Total biomass in southeastern Wisconsin hybrid cattail (T. X glauca) stands reached 15 tons per acre (33.6 t/ha) [3]. Native Americans used common cattail as food. Rhizomes were dried and ground into flour or eaten as cooked vegetables; young stems were eaten raw or cooked; and immature fruiting spikes were eaten after roasting [12,17]. The leaves were woven for matting and the "soft down" from ripe fruiting heads was used as padding and in diapers [30]. MANAGEMENT CONSIDERATIONS : Common cattail is considered a weed on some irrigated agricultural lands and in managed waterfowl production areas. On agricultural lands it invades irrigation canals, farm ponds, and drainage ditches, impeding water flow and increasing siltation [12]. In marshes managed for waterfowl, it often forms dense stands which provide poor nesting habitat [24]. Control measures include: (1) drawdown to reduce cattail and allow the establishment of species preferred by waterfowl, (2) cutting plants below the soil or water surface, (3) crushing, which immediately opens up stands making the surface water available to ducks, (4) spraying with herbicides, (5) burning [see Fire Management Considerations], and (6) cutting, crushing, spraying, or burning in combination with water level manipulation [3,12,22,32]. For best results treatment should take place when carbohydrate reserves are at a minimum. This period, when common cattail is most susceptible to injury, occurs when the pistillate and staminate portions of the spike are lime green and dark green, respectively [3]. Furthermore, because a portion of cattail leaves must protrude above the water surface for normal gas exchange to take place, regrowth following control measures is effectively eliminated if plants are kept completely submerged [3,12]. On marshes where water levels can be manipulated, a combination of drawdown followed by the control treatment and rapid reflooding results in the greatest cattail mortality. Because of increased mobility on ice, winter cutting or burning in northern latitudes is a cost-effective method to remove accumulated litter and thin stands [1]. Farm machinery that could cut cattail but would be difficult to use in marshy habitats can be used on the ice during the winter.

BOTANICAL AND ECOLOGICAL CHARACTERISTICS

SPECIES: Typha latifolia | Common Cattail
GENERAL BOTANICAL CHARACTERISTICS : Common cattail is an erect, rhizomatous, semiaquatic or aquatic, perennial herb. Twelve to sixteen erect, linear, flat, basal leaves arise from each vegetative shoot, which are 0.3 to 0.6 inch (8-15 mm) wide and 3 to 10 feet (1-3 m) tall. The stout rhizomes, which are located 3 to 4 inches (8-10 cm) below the soil surface, grow up to 27 inches (70 cm) in length and are typically 0.2 to 1.2 inches (0.5-3 cm) in diameter [12,30]. Common cattail is monoecious. The inflorescence is a dark brown, cylindrical terminal spike on a stout, 3- to 10-foot (1-3 m) stem. The staminate portion is positioned above the pistillate portion; they are continuous or slightly separated [16,45]. RAUNKIAER LIFE FORM : Geophyte Helophyte REGENERATION PROCESSES : Common cattail reproduces sexually and asexually. Vegetative reproduction occurs through an extensive rhizome system and is responsible for the maintenance and expansion of existing stands. Sexual reproduction via seed dispersal and seedling establishment is responsible for invasion of new areas. Seed production and dispersal: Common cattail is a prolific producer of minute seeds. Each spike may contain 117,000 to 268,000 seeds [47]. At maturity, the spike bursts under dry conditions, releasing the fruits. Each fruit has bristly hairs that aid in wind dispersal. When the fruit comes in contact with water, the pericarp opens rapidly, releasing the seed, which then sinks [12]. In wet weather the fruits often fall to the ground in dense mats [39]. Germination and seedling establishment: Common cattail seeds are capable of germinating immediately after shedding under favorable conditions, but require moist or wet substrates, warm temperatures, low oxygen concentrations, and long day-short night exposures for germination to occur [4,38]. Sifton [38] achieved the highest germination rates (86-89%) at temperatures from 77 to 86 degrees Fahrenheit (25-30 C). Because of the relatively high temperature required for germination, seeds overwinter in northern latitudes, but not necessarily in southern latitudes [27]. In a southeastern Wisconsin marsh, hybrid cattail (T. X glauca) seeds germinated from May through September, with the greatest number of seedlings seen in June and the fewest in September [3]. Following summer marsh drawdown in northwestern Minnesota, common cattail seedlings appeared on moist, vegetation-free areas 10 days after soil exposure [48]. Light, temperature, and oxygen requirements for germination are best met in shallow water or on moist mudflats in vegetation-free areas. Within established common cattail stands, seedlings are practically nonexistent. This is because existing vegetative cover greatly reduces light and temperature for germination, and because cattail leaves and stems may produce allelopathic inhibitors [12,28]. Once established, a single seedling spreads rapidly by rhizomes. In Montana, a single seed planted in a stock tank on April 1, grew into a massive network of clones with 98 aerial shoots and 104 lateral buds by November 1 [47]. Grace and Wetzel [13] reported that 2 years after germination, common cattail may spread over an area of 624 square feet (58 sq m). SITE CHARACTERISTICS : Common cattail grows just about anywhere that soil remains wet, saturated, or flooded most of the growing season [12]. Common habitats include wet meadows, marshes, fens, pond and lake margins, floating bog mats, seacoast estuaries, roadside ditches, irrigation canals, oxbow lakes, and backwater areas of rivers and streams [7,12,17]. It is tolerant of continuous inundation and seasonal drawdowns but is generally restricted to areas where the water depth never exceeds about 2.6 feet (80 cm) [5,13]. It grows mostly in fresh water but also occurs in slightly brackish marshes [12,47]. Along water depth gradients, common cattail often grows upslope of bulrush or open water but downslope of common reed (Phragmites australis), reed canarygrass (Phalaris arundinacea), and willow (Salix spp.) [12,17]. When common cattail and narrow-leaved cattail cooccur, they are frequently segregated by water depth, with common cattail found in shallow water and narrow-leaved cattail in deep water [13]. Soils: Cattail stands produce enormous quantities of litter. Established stands tend to grow on soils with high amounts of organic matter. Common cattail may also grow on fine-textured mineral soils, but the soils often have organic matter incorporated into at least the surface horizons [33]. SUCCESSIONAL STATUS : Facultative Seral Species Common cattail is often a dominant component of early successional stages in wetlands. It rapidly colonizes exposed wet mineral soils, as it produces an extremely high number of seeds, which are dispersed by wind and water. On logged-over black spruce (Picea mariana) lowlands in Ontario, common cattail quickly invades exposed peat and water-filled depressions created by logging machinery [6]. It is also an early seral species occupying the water's edge on floating bog mats [7]. Along oxbow lakes on the Athabaska River in Alberta, Canada, common cattail was abundant only on sites showing evidence of recent flooding. On oxbows with stable water levels, common cattail was replaced by awned sedge (Carex atherodes) and common rivergrass (Scolichloa festucacea), with gradual siltation and organic matter buildup [21]. In some situations where water levels remain constant, common cattail maintains relatively stable communities [17]. SEASONAL DEVELOPMENT : The general pattern of common cattail phenological development includes spring rhizome sprouting and rapid leaf production, early to midsummer flowering, and leaf senescence and new rhizome production in the fall [12]. Timing of sprouting varies with water depth, with deep water shoots sprouting before those in shallow water. Spring growth is usually rapid and sudden, and is almost entirely leaf growth. Along the Athabaska River in northeastern Alberta, Canada, common cattail growth began in late May, and stems reached maximum weight by mid-August. Shoots which began growth in spring showed substantial leaf senescence by late August [21]. Hybrid cattail (T. X glauca) phenology in southeastern Wisconsin was as follows [3]: April - sprout or primary aerial shoot begins growth May - new shoots elongating and growing above the water level June - staminate and pistillate spikes formed, carbohydrate levels in rhizomes at minimum in late June Winter - plants dormant, maximum levels of stored carbohydrates Phenology of common cattail near Gainsville, Florida, was as follows [34]: mid- to late May - flowering June to early August - fruit ripening mid-August to mid-Nov. - sporadic fruit dispersal during low humidity February through May - active growth Nov., Dec., Jan. - dormancy

FIRE ECOLOGY

SPECIES: Typha latifolia | Common Cattail
FIRE ECOLOGY OR ADAPTATIONS : Common cattail rhizomes are buried in the soil and are often under water where they cannot be harmed by the heat of fire. When aboveground foliage is consumed by fire, common cattail quickly initiates new top-growth from these surviving underground regenerative organs. POSTFIRE REGENERATION STRATEGY : Rhizomatous herb, rhizome in soil

FIRE EFFECTS

SPECIES: Typha latifolia | Common Cattail
IMMEDIATE FIRE EFFECT ON PLANT : The effects of fire on common cattail vary with water depth and soil moisture. On flooded sites and on sites with exposed but saturated soils, fire consumes most or all of the aboveground biomass, but underground rhizomes remain undamaged and plants survive [11,41]. When soils become dry because of drought or marshland drainage, fires can burn deep into the organic horizons, consuming the rhizomes and killing the plant [43]. DISCUSSION AND QUALIFICATION OF FIRE EFFECT : NO-ENTRY PLANT RESPONSE TO FIRE : Common cattail quickly sprouts from surviving rhizomes following fires that remove the top-growth. If burned when plants are dormant, new top-growth is initiated in the spring, and annual productivity is not lowered [40,41]. Even following summer fires, plants quickly initiate new growth from surviving underground rhizomes and grow until killed by fall frosts. After an early September fire in Utah, common cattail grew to 1.3 feet (0.4 m) in height before winter dormancy [41]. Hybrid cattail (T. X glauca) stands in New Brunswick, Canada, were burned in spring, summer, or fall in both flooded and drained marshes. Summer burning on drained sites resulted in the greatest reductions in cover, density, and height 3 years after burning. Three years after burning on flooded marsh, hybrid cattail increased in cover but showed little or no change in cover, stem density, or height. Changes in these characteristics 3 years after burning are presented below [24]: control spring summer autumn burned burned burned cover (%) drained marsh 56 54 36 48 flooded marsh 41 44 55 46 stem density/m2 drained marsh 15 14 9 12 flooded marsh 10 10 12 10 plant height (cm) drained marsh 133 126 111 130 flooded marsh 155 165 158 156 DISCUSSION AND QUALIFICATION OF PLANT RESPONSE : NO-ENTRY FIRE MANAGEMENT CONSIDERATIONS : Prescribed burning in late fall, winter, or early spring when plant tops are dry opens up common cattail stands by removing years of accumulated litter. In northern latitudes, winter burning has advantages in that fires can be better directed over ice than open water, as the ice allows for faster movement of men and equipment. Additionally, winter fires are easier to control because they are of lower intensity than fires during warmer months [1]. Annual burning is difficult because more than 1 year of litter is needed to carry fire in cattail stands [1,3]. On marshes where water levels can be controlled, drawdown followed by burning and rapid reflooding kills common cattail if regrowth is kept completely submerged. Following marsh drawdown and burning in Utah, common cattail quickly resprouted and covered areas that were reflooded with up to 8 inches (20 cm) of water. No plants survived, however, on areas flooded with 8 to 18 inches (20-46 cm) of water [32]. When winter burning over ice in southwestern Ontario, Ball [1] found that slow-moving backfires left the shortest cattail stubble which subsequently needed the least amount of water level increase to submerge the stalks. Furthermore, snow buildup over ice can protect the stalks from burning, resulting in tall stubble that is difficult to submerge the following spring. Thus, when using winter burning in conjunction with water level manipulation to control cattail, it is best to burn over ice in early winter before snow accumulation or in early spring after snow melt. In Utah, common cattail was controlled with a combination of burning and cutting. Stands were first cut, then the cut material burned. This made it easier to flood the cut stems, and allowed a second cutting, if needed, to be made very close to the ground [32]. In the Southern High Plains region of Texas, winter burning did not improve common cattail nutritive quality [40].

REFERENCES

SPECIES: Typha latifolia | Common 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. 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] 3. 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] 4. Bonnewell, V.; Koukkari, W. L.; Pratt, D. C. 1983. Light, oxygen, and temperature requirements for Typha latifolia seed germination. Canadian Journal of Botany. 61: 1330-1336. [17671] 5. Brotherson, Jack D. 1981. Aquatic and semiaquatic vegetation of Utah Lake and its bays. Great Basin Naturalist Memoirs. 5: 68-84. [11212] 6. Brumelis, G.; Carleton, T. J. 1989. The vegetation of post-logged black spruce lowlands in central Canada. II. Understory vegetation. Journal of Applied Ecology. 26: 321-339. [7864] 7. Conway, Verona M. 1949. The bogs of central Minnesota. Ecological Monographs. 19(2): 173-206. [16686] 8. Dittberner, Phillip L.; Olson, Michael R. 1983. The plant information network (PIN) data base: Colorado, Montana, North Dakota, Utah, and Wyoming. FWS/OBS-83/86. Washington, DC: U.S. Department of the Interior, Fish and Wildlife Service. 786 p. [806] 9. Eyre, F. H., ed. 1980. Forest cover types of the United States and Canada. Washington, DC: Society of American Foresters. 148 p. [905] 10. 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] 11. Gorenzel, Warner P.; Ryder, Ronald A.; Braun, Clait E. 1981. American coot response to habitat change on a Colorado marsh. Southwestern Naturalist. 26(1): 59-65. [17677] 12. 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] 13. Grace, James B.; Wetzel, Robert G. 1981. Habitat partitioning and competitive displacement in cattails (Typha): experimental field studies. American Naturalist. 118(4): 463-474. [17674] 14. Grace, James B.; Wetzel, Robert G. 1982. Variations in growth and reproduction within populations of two rhizomatous plant species: Typha latifolia and Typha angustifolia. Oecologia. 53: 258-263. [17682] 15. 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] 16. Great Plains Flora Association. 1986. Flora of the Great Plains. Lawrence, KS: University Press of Kansas. 1392 p. [1603] 17. 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] 18. Higgins, Kenneth F.; Kruse, Arnold D.; Piehl, James L. 1989. Effects of fire in the Northern Great Plains. Ext. Circ. EC-761. Brookings, SD: South Dakota State University, Cooperative Extension Service, South Dakota Cooperative Fish and Wildlife Research Unit. 47 p. [14749] 19. 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] 20. 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] 21. Lieffers, V. J. 1983. Growth of Typha latifolia in boreal forest habitats, as measured by double sampling. Aquatic Botany. 15: 335-348. [17670] 22. 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] 23. Lyon, L. Jack; Stickney, Peter F. 1976. Early vegetal succession following large northern Rocky Mountain wildfires. 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Autotoxic feedback in relation to germination and seedling growth in Typha latifolia. Ecology. 49(2): 367-369. [17684] 29. Milne, Robert C.; Quay, Thomas L. 1967. The foods and feeding habits of the nutria on Hatteras Island, North Carolina. Proceedings, Annual Conference of Southeastern Association of Game and Fish Commissions. 20: 112-123. [15302] 30. Morton, Julia F. 1975. Cattails (Typha spp.) - Weed problem or potential crop?. Economic Botany. 29: 7-29. [17675] 31. Murkin, Henry R.; Kaminski, Richard M.; Titman, Rodger D. 1982. Responses by dabbling ducks and aquatic invertebrates to an experimentally manipulated cattail marsh. Canadian Journal of Zoology. 60: 2324-2332. [17669] 32. Nelson, Noland F.; Dietz, Reuben H. 1966. Cattail control methods in Utah. Publication No. 66-2. Salt Lake City, UT: Utah State Department of Fish and Game. 66 p. [17809] 33. Padgett, Wayne G.; Youngblood, Andrew P.; Winward, Alma H. 1989. 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Index

Related categories for Species: Typha latifolia | Common Cattail

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