The Bugwood Network

Spotted Knapweed

J. Story - Montana State University, Western Agricultural Research Center, Corvallis, Montana, USA.

In: Van Driesche, R., et al., 2002, Biological Control of Invasive Plants in the Eastern United States, USDA Forest Service Publication FHTET-2002-04, 413 p.

Pest Status of Weed

Spotted knapweed, Centaurea maculosa Lamarck, is a purple-flowered, herbaceous, perennial weed, living three to five years on average. It infests semiarid range lands in the western United States and roadsides and fields in the eastern part of the country. Infested areas are dominated by the plant, reducing their grazing value and suppressing native plant communities. The plant, originally from Central Asia, has been in North America for over 120 years.

Nature of Damage

Economic damage. Spotted knapweed is a serious problem on rangeland, especially in the western United States. Bucher (1984) estimated that an 800,000 ha infestation in Montana was causing $4.5 million in annual forage losses, and that invasion of 13.6 million ha of vulnerable rangeland in Montana would cost cattle and sheep ranchers $155.7 million of gross revenue annually. Hirsh and Leitch (1996) reported that an 800,000 ha infestation of spotted knapweed, in combination with two knapweeds of minor importance in Montana (diffuse knapweed, Centaurea diffusa Lamarck, and Russian knapweed, Acroptilon repens [L] de Candolle) was causing $14 million in direct negative impacts and $28 million in indirect effects (i.e., reduced regional economy) to the state of Montana. Harris and Cranston (1979) reported that the 30,000 ha infestation in Canada was reducing forage production more than 88%. In the northeastern and northcentral United States, the plant is primarily a problem of roadsides, fields, and waste areas (Hoebeke, 1993); economic impact of the plant in those regions has not been reported.

Ecological damage. Spotted knapweed reduces livestock and wildlife forage (Thompson, 1996; Watson and Renney, 1974), increases surface water runoff and soil sedimentation (Lacey et al., 1989), and lowers plant diversity (Tyser and Key, 1988). Spotted knapweed produces an allelopathic compound that reduces germination of some grass species (Kelsey and Locken, 1987).

Geographical Distribution

Spotted knapweed is native to Europe and western Asia but has become widespread in parts of the United States and Canada. The plant occurs throughout the United States except for Alaska, Texas, Oklahoma, Mississippi, and Georgia (USDA, NRCS, 2001). The plant is a serious invader of rangeland in the Rocky Mountain region. In Montana alone, the plant infests an estimated 1.9 million ha of rangeland and pasture (Lacey, 1989). In Canada, the plant is abundant in British Columbia, and is common in Ontario, Quebec, and the Maritimes (Watson and Renney, 1974).

Background Information On The Pest Plant

Taxonomy

The taxonomy of C. maculosa has been detailed by Dostal (1976) and reviewed by Müller et al. (1988) and Müller (1989). Centaurea maculosa is comprised of several subspecies occurring from western Asia to western Europe. The C. maculosa occurring in North America is a short-lived perennial tetraploid (2n=36) that is considered the same as C. biebersteinii de Candolle subsp. biebersteinii (=C. micranthos Gmelin ex. Hayek), a native of western Asia. However, the most widely distributed C. maculosa in Europe is the biennial diploid (2n=18) C. maculosa spp. rhenana (Boreau) Gugler (Dostal, 1976; Müller et al., 1988; Müller, 1989).

Biology

Spotted knapweed is a purple-flowered, herbaceous weed, 30 to 125 cm tall, with one to 10 upright stems, and a stout taproot (Fig. 1). The plant is a perennial, living an average of three to five years and frequently up to nine years (Boggs and Story, 1987). The flower heads, enclosed by black-tipped bracts, are borne singly at the terminal ends of branches. Seed is shed immediately upon maturation of the seed head. The plant reproduces solely by seed. Seed production ranges from 5,000 to 40,000 seeds/m2 (Sheley et al., 1998). Seeds can survive in the soil for eight or more years (Davis et al., 1993).

The life history of the plant has been described by Watson and Renney (1974). Seed germination occurs in the fall or

Figure 1. Spotted knapweed, Centaurea maculosa Lamarck. (Photo by Jim Story.)
Figure 1. Spotted knapweed,
Centaurea maculosa Lamarck.
(Photo by Jim Story.)
early spring, depending upon moisture availability. Seedlings develop into rosettes; plants that have overwintered as rosettes usually produce floral stems the following summer. Stem elongation occurs in June followed by flowering in July and seed dispersal in August.

Spotted knapweed is adapted to a range of habitats and soil types, but is especially well suited to relatively dry sites (Watson and Renney, 1974). In Europe, the plant is most aggressive in the forest steppe but can form dense stands in more moist areas on well-drained soils including gravel, and in drier sites where summer precipitation is supplemented by runoff (Sheley et al., 1998).

Analysis of Related Native Plants in the Eastern United States

The North American plants most closely related to spotted knapweed include safflower (Carthamus tinctorius L.) and possibly the two “knapweeds,” Centaurea americana and Centaurea rothrockii. Recent evaluations, however, suggest the latter two plants should be treated as Plectocephalus americanus (Nutt.) (Müller-Schärer and Schroeder, 1993). The next closest relatives of spotted knapweed are members of the tribe Cardueae, mainly Carduinae (Cirsium and Cynara [e.g., artichoke]). There are numerous Cirsium species native to North America.

History of Biological Control Efforts in the Eastern United States

Area of Origin of Weed

The native range of the spotted knapweed (tetraploid) occurring in North America is eastern Europe and western Asia (Müller et al., 1989).

Areas Surveyed for Natural Enemies

Surveys were conducted throughout Europe and western Asia for natural enemies.

Natural Enemies Found

Schroeder (1985) listed 38 arthropod species that were known to be associated with spotted knapweed in Eurasia. Of these, 12 species were screened and released in North America against the plant (Table 1).

Table 1. Insects Released in the United States for Biological Control of Spotted Knapweed

Scientific Name Insect Type Plant Part Attcked Where Collected Date of First U.S. Release State/Date of Release in Eastern U.S. and Canada Known Estab. in Eastern U.S. and Canada
Urophora affinis Frauenfeld Fly (Tephritidae) Flower head France, Austria 1973 IN 1997
MD 1983
NY 1983
VA 1986
MN 1990
WI 1991
MI 1994
Quebec 1979
Ontario 1970
 
 
x
x
x
x
x
x
 
Urophora quadrifasciata (Meigen) Fly (Tephritidae) Flower head Former USSR 1980 Quebec 1979
MD 1983
NY 1983
VA 1986
MN 1990
WI 1991
MI 1994
IN 1997
x
x
 
x
x
x
x
x
Terellia virens (Loew) Fly (Tephritidae) Flower head Austria, Switzer. 1992 MN 1994  
Chaetorellia acrolophi White and Marquardt Fly (Tephritidae) Flower head Austria, Switzer. 1992 MN 1996  
Metzneria paucipunctella Zeller Moth (Gelechiidae) Flower head Switzer. 1980 MN 1991
VA 1986

x
Agapeta
zoegana
L.
Moth (Cochylidae) Root Austria, Hungary 1984 IN 1996
MN 1991
WI 1991

x
Pterolonche insperda Staudinger Moth (Pterolon-chidae) Root Hungary 1988 -  
Pelochrista medullana (Staudinger) Moth (Torticidae) Root Austria, Hungary 1984 -  
Cyphocleonus achates (Fahraeus) Weevil (Curculionidae) Root Austria, Romania 1988 IN 1996
MN 1994
 
Bangastemus fausti Reitter Weevil (Curculionidae) Flower head Greece 1990 MN 1992  
Larinus obtusus Gyllenhal Weevil (Curculionidae) Flower head Romania, Serbia 1992 MN 1995  
Larinus minutus Gyllenhal Weevil (Curculionidae) Flower head Greece, Romania 1991 IN 1996
MN 1994
x
x

Host Range Tests and Results

The number of plants included in the test plant list for each of the 12 insect species varied, but averaged around 45 test plant species per insect. Most of the plant species used were from the family Asteraceae, but representative species from one or more other families also were often tested. Particular emphasis was placed on plants in the Asteraceae tribe Cardueae which includes the genus Centaurea. The test plant list for Larinus minutus is presented in Table 2 (Jordan, 1995) because it is fairly representative of the plants tested on all 12 insect species. The only plants of economic importance in North America included in the tests were Carthamus tinctorius L. (safflower), Helianthus annuus L., (common sunflower), and Cynara scolymus L. (globe artichoke). None of the insects oviposited or fed on any of these three plants except for Cyphocleonus achates adults which fed slightly on artichoke. The feeding by C. achates was not of concern, however, because no eggs were laid on the plant. In general, attack by all of the insects was restricted to the genus Centaurea, and usually to the subgenus Acrolophus. There has been no report of attack on non-target species by any of the insects since release, although specific surveys have apparently not been conducted.

Table 2. Test plant list used for Larinus minutus

Family: Asteraceae
  Tribe: Cardueae
    Subtribe: Centaureinae
      Genus: Centaurea
        Subgenus: Acrolophus
          Centaurea arenaria Bieb.
          C. cineraria L.
          C. diffusa Lamarck Europe
          C. diffusa USA
          C. friderici Vis.
          C. maculosa Lamarck Europe
          C. maculosa USA
          C. micranthos S. G. Gmelin
          C. paniculata L.
          C. vallesiaca (D. C.) Jordan
        Subgenus: Calcitrapa
          C. calcitrapa L.
          C. iberica Trev. Sprengel
        Subgenus: Cartholepis
          C. macrocephala Muss.
        Subgenus: Centaurea
          C. ruthenica Lamarck
        Subgenus: Cyanus
          C. cyanus L.
          C. montana L.
        Subgenus: Jacea
          C. jacea L.
          C. nigra L.
          C. nigrescens Willd.
          C. pannonica (Heuffel) Simonkai
          C. phrygia
        Subgenus: Lopholoma
          C. scabiosa L.
        Subgenus: Phalolepis
          C. alba L.
        Subgenus: Psephellus
          C. dealbata Willd.
        Subgenus: Seridia
          C. aspera L.
          C. napifolia
        Subgenus: Solstitiaria
          C. nicaeensis All.
          C. solstitialis L.
      Other genera:
          Acroptilon repens (L.) D.C.
          Carduncellus monspelliensum All.
          Carthamus tinctorius L.
          Cnicus benedictus L.
          Crupina vulgaris Pers.
          Mantisalca salmantica Brig. and Cavillier
          Plectocephalus americanus (Nutt.)
    Subtribe: Carduinae
          Arctium lappa L.
          Carduus acanthoides L.
          C. nutans L.
          Cirsium arvense (L.) Scop.
          C. crassicaule (Greene) Jeps.
          C. creticum
          C. undulatum (Nutt.) Spreng.
          Cynara scolymus L.
          Galactites tomentosa
          Onopordum acanthium L.
          Silybum marianum (L.) Gaertn.
  Tribe: Anthemideae
          Achillea millefolium L.
          Anthemis tinctoris L.
          Artemisia absinthium L.
          Chrysanthemum leucanthemum L.
  Tribe: Astereae
          Aster novi-belgii L.
          Solidago canadensis L.
  Tribe: Calenduleae
          Calendula officinalis L.
  Tribe: Carlineae
          Carlina vulgaris L.
  Tribe: Cichorieae
          Cichorium intybus L.
          Taraxacum officinale Web.
  Tribe: Echinopeae
          Echinops sphaerocephalus L.
  Tribe: Heliantheae
          Helianthus annuus L.
          H. decapetatus L.
          H. tuberosus L.
          Rudbeckia hirta L.
  Tribe: Inuleae
          Inula helenium
          Helichrysum orientale (L.) Gaertn.
  Tribe: Senecioneae
          Senecio jacobaea L.
Family: Caryophyllaceae
          Dianthus superbus
          Silene vulgaris (Moench) Garcke
Family: Chenopodiaceae
          Beta vulgaris L.
Family: Cistaceae
          Helianthemum vulgare Gaertn.
Family: Cruciferae
          Brassica oleracea L.
Family: Dipsacaceae
          Dipsacus fullonum L.
Family: Polygonaceae
          Rumex acetosa L.
Family: Ranunculaceae
          Delphinium elatum L.
Family: Umbelliferae
          Apium graveolens L.
          Daucus carota L.

Releases Made

Of the 12 biological control agent species released against spotted knapweed in the United States, 10 species have been released against spotted knapweed in the eastern United States and five (Table 1) have become established (Hoebeke, 1993; Wheeler, 1995; Mays and Kok, 1996; Wheeler and Stoops, 1996; Lang et al., 1997; Lang, pers. comm.). The root moth, Pelochrista medullana (Staudinger) (Lepidoptera: Tortricidae) and the root moth, Pterolonche inspersa Staudinger (Lepidoptera: Pterolonchidae) were not released in the eastern United States due to insufficient numbers.

Biology and Ecology of Key Natural Enemies

Urophora affinis Frauenfeld (Diptera: Tephritidae)

Urophora affinis is a small (4.5 mm) fly that attacks the flower heads of spotted knapweed (Fig. 2). The fly is distinguished from other knapweed tephritids by the bright yellow spot on its black thorax, the black abdomen, and the light-colored markings on its wings. Collected in France and Austria, the first United States release was made in Montana and Oregon in 1973 (Maddox, 1982).

Figure 2. Urophora affinis Frauenfeld. (Photo by Robert Richard. USDA, APHIS, PPQ.)
Figure 2. Urophora affinis Frauenfeld.
(Photo by Robert Richard. USDA, APHIS, PPQ.)

Larval feeding causes the formation of hard, woody galls in the receptacle tissue. The galls divert plant nutrients, resulting in reduced seed production in both attacked and unattacked seed heads on a plant. Urophora affinis is currently reducing seed production of spotted knapweed in the Pacific Northwest close to the threshold needed to achieve economic control (Harris and Shorthouse, 1996).

Fly larvae overwinter within galls (one larva per gall) and pupate in May, followed by adult emergence in late June and July. Urophora affinis is generally univoltine although a small percentage (approximately 7%) emerge in August and complete a second generation (Zwölfer, 1970; Gillespie, 1983; Story et al., 1992).

Urophora quadrifasciata (Meigen) (Diptera: Tephritidae)

Urophora quadrifasciata is a small (4.5 mm) fly that attacks the flower heads of spotted knapweed (Fig. 3). The fly is distinguished from other knapweed tephritids by its relatively dark body and the dark bands in the shape of the letters “UV” on its wings. The general biology of U. quadrifasciata is similar to that of U. affinis except that U. quadrifasciata forms papery galls in the ovary, attacks larger flower heads than does U. affinis, and is generally bivoltine (Harris, 1980; Gillespie, 1983).

Urophora quadrifasciata was introduced into British

Figure 3. Urophora quadrifasiata (Meigen). (Photo by Robert Richard, USDA, APHIS, PPQ.)
Figure 3. Urophora quadrifasiata (Meigen).
(Photo by Robert Richard, USDA, APHIS, PPQ.)
Columbia in 1972 (Harris, 1980), but not into the United States. However, by the early 1980s, the fly had dispersed into the Pacific Northwest states. Urophora quadrifasciata is now more widely distributed than U. affinis. Urophora quadrifasciata is common in many areas of the northeast and is very abundant in some areas of upstate New York (Blossey, unpub.data). However, U. quadrifasciata numbers remain low in areas where the two Urophora spp. coexist.

Metzneria paucipunctella Zeller (Lepidoptera: Gelechiidae)

Metzneria paucipunctella is a small (9 mm), univoltine moth that attacks the flower heads of spotted knapweed (Fig. 4). The moth is tan with small black spots. Originally collected in Switzerland, the moth was introduced into British Columbia in 1973 (Harris and Myers, 1984). Moths collected from British Columbia were subsequently introduced into the United States in Montana in 1980 (Story et al., 1991a).

Metzneria paucipunctella overwinters as larvae in seed heads. Pupation occurs in May, followed by adult

Figure 4. Metzneria paucipunctella Zeller. (Photo by Robert Richard, USDA, APHIS, PPQ.)
Figure 4. Metzneria paucipunctella Zeller.
(Photo by Robert Richard, USDA, APHIS, PPQ.)
emergence in June and early July. Young larvae feed on developing seeds while older larvae feed on mature seeds and mine the receptacle. Older larvae bind several seeds together with silk webbing, which prevents dispersal of those seeds at maturity. Due to strong intraspecific competition, only one larva survives per seed head (Englert, 1971). Each larva destroys an average of eight seeds per seed head (Story et al., 1991a). Larvae also will attack and destroy other seed head insects, including larvae of the two established seed head flies, Urophora spp. (Story et al., 1991a). Metzneria paucipunctella frequently suffers high overwintering mortality.

Agapeta zoegana L. (Lepidoptera: Cochylidae)

Agapeta zoegana is a small (9 mm), yellow and brown, univoltine moth that attacks the roots of spotted knapweed (Müller et al., 1988) (Fig. 5). Collected in Austria and Hungary, the first United States release of the moth was made in Montana in 1984 (Story et al., 1991b).

Agapeta zoegana overwinters as larvae in roots. Adult emergence occurs from mid-June to early September. Females begin mating the first night after emergence and

Figure 5. Agapeta zoegana L. (Photo by Jim Story.)
Figure 5. Agapeta zoegana L.
(Photo by Jim Story.)
begin laying eggs the following evening. Adults live for nine to 11 days and each female lays an average of 75 eggs (up to 290), mostly within a four-day period. Larvae hatch in seven to 10 days and begin mining in the epidermal tissues of the root crown. Older larvae mine in the cortex and endodermis tissues and several larvae may develop in the same root. Agapeta zoegana has one generation per year. Studies in Montana indicate the moth is reducing the biomass of knapweed at some sites (Story et al., 2000). Analyses by Clark et al. (2001a) suggest that probability of A. zoegana establishment at release sites is affected by soil type and the shape (patchy, continuous or linear) of the weed infestation.

Cyphocleonus achates (Fahraeus) (Coleoptera: Curculionidae)

Cyphocleonus achates is a large (19 mm), gray and black mottled weevil that attacks the roots of spotted knapweed (Fig. 6). Collected in Austria and Romania, the first United States release of the weevil was made in Montana in 1988 (Story et al., 1997).

This univoltine weevil overwinters as larvae in roots. Adults emerge from mid-July to October and live eight to 15 weeks. Each female lays from one to three eggs per day throughout her adult life. Larvae hatch in 10 to 12 days and mine into the root cortex, eventually causing the formation of a conspicuous root gall. Dispersal is slow as adults don’t fly (Stinson et al., 1994).

Figure 6. Cyphocleonus achates (Fahraeus). (Photo by CABI Bioscience.)
Figure 6. Cyphocleonus achates (Fahraeus). (Photo by CABI Bioscience.)

Studies by Clark et al. (2001a) suggest that probability of C. achates establishment at release sites is affected by elevation, the shape (patchy, continuous or linear) of the weed infestation, and the number of years in which releases are made.

Larinus minutus Gyllenhal (Coleoptera: Curculionidae)

Larinus minutus is a small (4.5 mm) univoltine weevil that attacks flower heads of diffuse and spotted knapweed (Jordan, 1995) (Fig. 7). Collected in Greece and Romania, the weevil was introduced into the United States in Montana, Washington, and Wyoming in 1991 (Lang et al., 1996).

Weevils overwinter as adults in soil and become active in early June. Eggs are deposited into freshly opened flower heads during late July through early September. Larvae hatch in about three days and immediately feed downwards

Figure 7. Larinus minutus Gyllenhal. (Photo by Robert Richard, USDA, APHIS, PPQ.)
Figure 7. Larinus minutus Gyllenhal.
(Photo by Robert Richard, USDA, APHIS, PPQ.)
into the flower head, where they eat seeds and pappus hairs. Larval development is completed in about 28 days followed by a short pupation period (one to two weeks; Jordan, 1995). Adult L. minutus emerge from the seed head in late September and October and feed on knapweed leaves for a short period before entering the soil to overwinter.

Larinus minutus has developed large populations on diffuse knapweed in Washington, Montana, and Oregon, but population increase on spotted knapweed has been slow.

Larinus obtusus Gyllenhal (Coleoptera: Curculionidae)

Larinus obtusus is a small (5 mm) univoltine weevil that attacks the flower heads of spotted knapweed (Groppe, 1992). The weevil is slightly larger than L. minutus. Collected in Romania and Serbia, L. obtusus was introduced into the United States in Montana in 1992 (Story, unpub. data). The insect is established in moderate numbers in Montana.

Adult weevils become active in May and June and eggs are deposited into freshly opened flower heads in July. Larvae hatch in about four days and immediately feed downward into the flower head, where they eat seeds and pappus hairs. Larval development is completed in about 17 days followed by a nine-day pupation period. Adults of the new generation emerge from the seed head in late summer, approximately 30 days after egg deposition. Adults feed on knapweed leaves for a short period before entering the soil to overwinter.

Bangasternus fausti Reitter (Coleoptera: Curculionidae)

Bangasternus fausti is a small (4.5 mm) univoltine weevil that attacks the flower heads of spotted knapweed (Sobhian et al., 1992). The weevil, collected in Greece, was introduced into the United States in 1990 (Rees et al., 1995).

Adults become active in May and June and eggs are deposited (usually singly) on the stems or bracts of flower heads that are 3.0 to 3.5 mm in diameter. Females cover eggs with a black, hard material. Eggs hatch in eight to 12 days and larvae tunnel through the stem until they enter the flower head. Larvae from eggs laid on the flower head tunnel directly into the flower head. Once in the flower heads, larvae consume florets and ovules. Adults of the new generation emerge from the seed head in late summer and later enter the soil to overwinter. The period from egg to adult is about 32 days.

Chaetorellia acrolophi White and Marquardt (Diptera: Tephritidae)

Chaetorellia acrolophi is a small (4.5 mm) fly that attacks the flower heads of spotted knapweed (Fig. 8). The fly is distinguished from other knapweed tephritids by having nine black spots on a light-colored thorax, a light-colored abdomen, and light-colored markings on the wings in a “UV” pattern similar to that of U. quadrifasciata. Chaetorellia acrolophi was collected in Austria and Switzerland and introduced into the United States in Montana in 1992 (Story, unpub. data). Establishment rates have been very low in most states.

Chaetorellia acrolophi overwinters as larvae in seed heads.

Figure 8. Chaetorellia acrolophi White and Marquardt. (Photo by CABI Bioscience.)
Figure 8. Chaetorellia acrolophi White and Marquardt. (Photo by CABI Bioscience.)
Pupation occurs in May, followed by adult emergence in June and early July. Eggs are deposited into unopened flower heads from June to July. Larvae hatch in about four days and immediately travel to the center of the flower head, where they burrow into florets. Older fly larvae attack several young seeds, additional florets, and parts of the seed head receptacle. The fly has two generations per year. Larvae and pupae of the first generation of C. acrolophi are white, while second generation larvae and pupae are yellow (Groppe and Marquardt, 1989a).

Terellia virens (Loew) (Diptera: Tephritidae)

Terellia virens is a small (4.5 mm) fly that attacks the flower heads of spotted knapweed (Fig. 9). The fly is distinguished from other knapweed tephritids by its lack of wing markings, its light-colored abdomen, and the faint spots on its light-colored thorax. Terellia virens, collected in Austria and Switzerland, was introduced into the United States in Montana in 1992 (Story, unpub. data). Establishment rates have been very low in most states.

The fly overwinters as larvae in seed heads. Pupation

Figure 9. Terellia virens (Loew). (Photo by CABI Bioscience.)
Figure 9. Terellia virens (Loew).
(Photo by CABI Bioscience.)
occurs in May, followed by adult emergence in June and early July. Eggs are deposited into flower heads that are beginning to open. Larvae hatch in about four days and immediately burrow into young seeds (one larva per seed). Older larvae attack several young seeds and occasionally feed on the seed head receptacle. Terellia virens often has two generations, depending upon fall weather (Groppe and Marquardt, 1989b).

Evaluation of Project Outcomes

Establishment and Spread of Agents

Of the natural enemy species released against spotted knapweed in the eastern United States and Canada, the following have been established: Urophora affinis (Virginia, New York, Pennsylvania, Minnesota, Wisconsin, Michigan, Quebec); Urophora quadrifasciata (Connecticut, Indiana, Maryland, Massachusetts, Michigan, Minnesota, New Hampshire, New Jersey, New York, Pennsylvania, Rhode Island, Vermont, West Virginia, Wisconsin, and Quebec); Metzneria paucipunctella (Virginia); Agapeta zoegana (Minnesota); and Larinus minutus (Indiana, Minnesota) (Hoebeke, 1993; Wheeler, 1995; Wheeler and Stoops, 1996; Mays and Kok, 1996; Lang et al., 1997; Lang, pers. comm.) (Table 1). Except for the two Urophora species, particularly U. quadrifasciata, dispersal of the knapweed agents has been modest. An assessment of the Urophora spp. spread was conducted in Montana (Story et al., 1987).

Suppression of Target Weed

Effects of imported natural enemies on spotted knapweed densities in the eastern United States have not been examined. However, impact information has been collected at sites in the western United States. Studies in Montana indicate that the two Urophora spp. are reducing spotted knapweed seed production by a minimum of 40% (Story et al., 1989), seed reduction by the Urophora spp. is further increased when M. paucipunctella is present (Story et al., 1991a), and A. zoegana is significantly reducing the biomass of spotted knapweed at some sites (Story et al., 2000). Spotted knapweed density is significantly reduced at two sites in western Montana where C. achates is well established (Story, unpub. data). Clark et al. (2001b) reported that spotted knapweed stem density, at 13 sites in Montana and adjacent states where U. affinis and one or both root feeding species of natural enemies (A. zoegana, C. achates) were established, declined from about 15 plants per m2 in 1991 to1993 to seven plants in 1997 to 1998.

Effects on Native Plants

Neither the impact of these released agents on native, non-target plants, nor the recovery of native plant communities as weed densities decline have been examined.

Economic Benefits

The economic benefits of biological control have not been realized yet, even in the west where some agents have been established for more than 15 years. However, given the reductions in knapweed density recently observed at localized infestations in Montana, economic benefits should be measurable in many states in the near future.

Recommendations for Future Work

Because of the large infestations of spotted knapweed in the west and the wide distribution in the north central and eastern United States, extensive redistribution of established biological control agents is required throughout much of the country. For preventative purposes, releases of the agents should be made in all states having only small populations of the weed.

The potential of most of the agents has not yet been realized in the west due to the large size of the infestations and the agents‘ modest rate of population increase. The control agents currently established in the United States are probably capable of reducing spotted knapweed densities in most locations.

There will undoubtedly be locations where the biological control agents are not effective. For example, early observations suggest the current complex of biological control agents in North America may not be effective on knapweed growing at higher elevations (>1,800 m). There are several niches on the plant (e.g., meristem, root collar, stems) that are not being exploited by the current agents in North America. If the need for further agents is deemed necessary, exploration for agents should be concentrated in Asia on tetraploid plants, with some emphasis on those agents attacking the currently unoccupied niches and those occurring at higher elevations.

Evaluation of the agents‘ impact is a priority goal now that some agent populations are reaching high levels at some locations in the west. Evaluation efforts may soon be possible at the smaller infestations in the east, especially in the northcentral states where the root insects, A. zoegana and C. achates, have been introduced.

References

Boggs, K. W. and J. M. Story. 1987. The population age structure of spotted knapweed (Centaurea
     maculosa
) in Montana. Weed Science 35:194-198.

Bucher, R. F. 1984. Potential spread and cost of spotted knapweed on range. MontGuide No. MT8423.
     Montana Cooperative Extension Service, Bozeman, Montana.

Clark, S. E., R. G. Van Driesche, N. Sturdevant, J. Elkinton, and J. P. Buonaccorsi. 2001a. Effects of
     site characteristics and release history on establishment of Agapeta zoegana (Lepidoptera:
     Cochylidae) and Cyphocleonus achates (Coleoptera: Curculionidae), root feeding herbivores
     attacking spotted knapweed, Centaurea maculosa. Biological Control 22: 122-130.

Clark, S. E., R. G. Van Driesche, and N. Sturdevant. 2001b. Effect of root feeding insects on spotted
     knapweed, Centaurea maculosa, stand density. Southwestern Entomologist 2: 129-135.

Davis, E. S., P. K. Fay, T. K. Chicoine, and C. A. Lacey. 1993. Persistence of spotted knapweed
     (Centaurea maculosa) seed in soil. Weed Science 41: 57-61.

Dostal, J. 1976. Centaurea L., pp. 254-301. In Anon. Flora Europaea, Vol. 4. Cambridge University
     Press, Cambridge, United Kingdom.

Englert, W. 1971. Metzneria paucipunctella Zel. (Gelechiidae, Lepidoptera): a potential insect for the
     biological control of Centaurea stoebe L. in Canada, pp. 161-165. In Dunn, P. (ed.). Proceedings of
     the Second International Symposium on Biological Control of Weeds
, October 4-7. Rome, Italy.

Gillespie, R. L. 1983. Bionomics of Urophora affinis Frauenfeld, and U. quadrifasciata Meigen (Diptera:
     Tephritidae) in Northern Idaho. M. S. thesis, University of Idaho, Moscow, Idaho, USA.

Groppe, K. 1992. Larinus obtusus Gyll. (Col: Curculionidae), a Candidate for Biological Control of
     Diffuse and Spotted Knapweed.
CAB International Institute of Biological Control Final Report,
     Silwood Park, Berks, United Kingdom.

Groppe, K. and K. Marquardt. 1989a. Chaetorellia acrolophi White and Marquardt (Diptera: Tephritidae),
     a Suitable Candidate for the Biological Control of Diffuse and Spotted Knapweed in North America.

     CAB International Institute of Biological Control Final Report, Silwood Park, Berks, United Kingdom.

Groppe, K. and K. Marquardt. 1989b. Terellia virens (Loew) (Diptera: Tephritidae), a Suitable Candidate
     for the Biological Control of Diffuse and Spotted Knapweed in North America
. CAB International
     Institute of Biological Control Final Report, Silwood Park, Berks, United Kingdom.

Harris, P. 1980. Establishment of Urophora affinis Frfld. and U. quadrifasciata (Meig.) (Diptera:
     Tephritidae) in Canada for the biological control of diffuse and spotted knapweed. Zeitschrift
     für angewandte Entomologie
89: 504-514.

Harris, P. and R. Cranston. 1979. An economic evaluation of control methods for diffuse and spotted
     knapweed in western Canada. Canadian Journal of Plant Science 59: 375-382

Harris, P. and J. D. Shorthouse. 1996. Effectiveness of gall inducers in weed biological control. The
     Canadian Entomologist 128: 1021-1055.

Harris, P. and J. H. Myers. 1984. Centaurea diffusa Lam. and C. maculosa Lam. s. lat., diffuse and
     spotted knapweed (Compositae), pp. 127-137. In Kelleher, J. and M. Hulme (eds.). Biological
     Control Programmes against Insects and Weeds in Canada 1969-1980
. Commonwealth Agricultural
     Bureau, Slough, United Kingdom.

Hirsch, S. A. and J. A. Leitch. 1996. The impact of knapweed on Montana’s economy. Agricultural
     Economics Report No. 355. North Dakota Agricultural Experiment Station. Fargo, North Dakota,
     USA.

Hoebeke, E. R. 1993. Establishment of Urophora quadrifasciata (Diptera: Tephritidae) and Chrysolina
     quadrigemina
(Coleoptera: Chysomelidae) in portions of eastern United States. Entomological News
     10: 143-152.

Jordan, K. 1995. Host specificity of Larinus minutus Gyll. (Col., Curculionidae), and agent introduced for
     the biological control of diffuse and spotted knapweed in North America. Journal Applied Entomology
     119: 689-693.

Kelsey, R. G. and L. J. Locken. 1987. Phytotoxic properties of cnicin, a sesqiterpene lactone from
     Centaurea maculosa (spotted knapweed). Journal of Chemical Ecology 13: 19-33.

Lacey, C. 1989. Knapweed management - a decade of change, pp. 1-6. In Anon. Proceedings of the
     Knapweed Symposium
. Montana State University, Bozeman, Montana, USA.

Lacey, J. R., C. B. Marlow, and J. R. Lane. 1989. Influence of spotted knapweed (Centaurea maculosa )
     on surface runoff and sediment yield. Weed Technology 3: 627-631.

Lang, R. R., R. D. Richard, and R. W. Hansen. 1997. Urophora affinis and U. quadrifasciata (Diptera:
     Tephritidae) released and monitored by USDA, APHIS, PPQ as biological control agents of spotted
     and diffuse knapweed. The Great Lakes Entomologist 30: 105-113.

Lang, R. F., J. M. Story, and G. L. Piper. 1996. Establishment of Larinus minutus Gyllenhal
     (Coleoptera: Curculionidae) for biological control of diffuse and spotted knapweed in the western
     United States. Pan Pacific Entomologist. 72: 209-212.

Maddox, D. M. 1982. Biological control of diffuse knapweed
     (Centaurea diffusa) and spotted knapweed (Centaurea maculosa). Weed Science 30: 76-82.

Mays, W. T. and L.-T. Kok. 1996. Establishment and dispersal of Urophora affinis (Diptera: Tephritidae)
     and Metzneria paucipunctella (Lepidoptera: Gelechiidae) in southwestern Virginia. Biological Control
     6: 299-305.

Müller, H. 1989. Growth pattern of diploid and tetraploid spotted knapweed, Centaurea maculosa Lam.
     (Compositae), and effects of the root-mining moth Agapeta zoegana (L.) (Lep.: Cochylidae). Weed
     Research
29: 103-111.

Müller-Schärer, H. and D. Schroeder. 1993. The biological control of Centaurea spp. in North America:
     Do insects solve the problem? Pesticide Science 37: 343-353.

Müller, H., D. Schroeder, and A. Gassmann. 1988. Agapeta zoegana (L.) (Lepidoptera: Cochylidae), a
     suitable prospect for biological control of spotted and diffuse knapweed, Centaurea maculosa
     Monnet de la Marck and Centaurea diffusa Monnet de la Marck (Compositae) in North America.
     Canadian Entomologist 120: 109-124.

Müller, H., C. S. A Stinson, K. Marquardt, and D. Schroeder. 1989. The entomofaunas of roots of
     Centaurea maculosa Lam., C. diffusa Lam., and C. vallesiaca Jordan in Europe. Journal of Applied
     Entomology
107: 83-95

Rees, N. E., P. C. Quimby, Jr., G. L. Piper, E. M. Coombs, C. E. Turner, N. R. Spencer, and L. V.
     Knutson. (eds.). 1996. Biological Control of Weeds in the West. Western Society of Weed Science,
     Montana State University, Bozeman, Montana, USA.

Schroeder, D. 1985. The search for effective biological control agents in Europe. Diffuse and spotted
     knapweed, pp. 103-119. In Delfosse, E. (ed.). Proceedings of the VI International Symposium on
     Biological Control of Weeds
. Vancouver, British Columbia, Canada.

Sheley, R. L., J. S. Jacobs, and M. E. Carpinelli. 1998. Distribution, biology, and management of diffuse
     knapweed (Centaurea diffusa) and spotted knapweed (Centeaurea maculosa). Weed Technology 12:
     353-362.

Sobhian, R., G. Campobasso, and P. H. Dunn. 1992. A contribution to the biology of Bangasternus
     fausti
(Col.:Curculionidae), a potential biological control agent of diffuse knapweed, Centaurea
     diffusa
, and its effect on the host plant. Entomophaga 37: 171-179.

Stinson, C. S. A., D. Schroeder, and K. Marquardt. 1994. Investigations on Cyphocleonus achates
     (Fahr.) (Col., Curculionidae), a potential biological control agent of spotted knapweed (Centaurea
     maculosa
Lam.) and diffuse knapweed (C. diffusa Lam.) (Compositae) in North America. Journal of
     Applied Entomology
117: 35-50.

Story, J. M., R. M. Nowierski, and K. W. Boggs. 1987. Distribution of Urophora affinis and U.
     quadrifasciata
, two flies introduced for biological control of spotted knapweed (Centaurea maculosa)
     in Montana. Weed Science 35: 145-148.

Story, J. M., K. W. Boggs, and R. M. Nowierski. 1989. Effect of two introduced seed head flies on
     spotted knapweed. Montana AgResearch 6: 14-17.

Story, J. M., K. W. Boggs, W. R. Good, P. Harris, and R. M. Nowierski. 1991a. Metzneria
     paucipunctella
Zeller (Lepidoptera: Gelechiidae), a moth introduced against spotted knapweed: its
     feeding strategy and impact on two introduced Urophora spp. (Diptera: Tephritidae). Canadian
     Entomologist
123: 1001-1007.

Story, J. M., K. W. Boggs, and W. R. Good. 1991b. First report of the establishment of Agapeta
     zoegana
L. (Lepidoptera: Cochylidae) on spotted knapweed, Centaurea maculosa Lamarck, in the
     United States. Canadian Entomologist 123: 411-412.

Story, J. M., K. W. Boggs, and W. R. Good. 1992. Voltinism and phenological synchrony of Urophora
     affinis
and U. quadrifasciata (Diptera: Tephritidae), two seed head flies introduced against spotted
     knapweed in Montana. Environmental Entomology 21: 1052-1059.

Story, J. M., W. R. Good, and L. J. White. 1997. First report of the establishment of Cyphocleonus
     achates
(Fahraeus) (Coleoptera: Curculionidae) on spotted knapweed, Centaurea maculosa
     Lamarck, in the United States. Canadian Entomologist 129: 373-374.

Story, J. M., W. R. Good, L. J. White, and L. Smith. 2000. Effects of the interaction of the biocontrol
     agent, Agapeta zoegana L. (Lepidoptera: Cochylidae), and grass competition on spotted knapweed.
     Biological Control 17: 182-190.

Thompson, M. J. 1996. Winter foraging responses of elk to spotted knapweed removal. Northwest
     Science
70: 10-19.

Tyser, R. W. and C. H. Key. 1988. Spotted knapweed in natural area fescue grasslands: an ecological
     assessment. Northwest Science 62: 151-160.

USDA, NRCS. 2001. U.S. Department of Agriculture, Natural Resources Conservation Service. PLANTS
     Database. http://plants.usda.gov (accessed in 2001).

Watson, A. K. and A. J. Renney. 1974. The biology of Canadian weeds. Centaurea diffusa and C.
     maculosa
. Canadian Journal of Plant Science 54: 687-701.

Wheeler, A. G. 1995. Urophora quadrifasciata (Diptera: Tephritidae), an introduced seedhead fly new to
     midwestern North America. The Great Lakes Entomologist 28: 235-236.

Wheeler, A. G. and C. A. Stoops. 1996. Establishment of Urophora affinis on spotted knapweed in
     Pennsylvania, with new eastern U.S. records of U. quadrifasciata (Diptera: Tephritidae). Proceedings
     of the Entomological Society of Washington
98: 93-99.

Zwölfer, H. 1970. Investigations on the host-specificity of Urophora affinis Frfld. (Dipt.: Trypetidae).
     Progress Report No. 25. Commonwealth Institute of Biological Control, Silwood Park, Berks, United
     Kingdom.

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