02. Acythopeus cocciniae O'Brien - “Ivy Gourd Leaf Miner”
03. Bagous affinis Hustache - “Hydrilla Tuber Weevil”
04. Bagous hydrillae O'Brien - “Hydrilla Stem Borer”
05. Bangasternus fausti (Reitter) - “Seedhead Weevil”
06. Bangasternus orientalis (Capiomont) - “Yellow Starthistle Bud Weevil”
07. Ceutorhynchus trimaculatus (Fabricius) - “Rosette Weevil”
08. Cyphocleonus achates (Fahraeus) - “Root Boring Weevil” or “Knapweed Root Weevil”
09. Cyrtobagous salviniae Calder and Sands - “Salvinia Weevil”
10. Euhrychiopsis lecontei (Dietz) - “Milfoil Weevil”
11. Eustenopus villosus (Boheman) - “Yellow Starthistle Hairy Weevil”
12. Exapion fuscirostre (Fabricius) - “Seed Feeding Weevil”
13. Exapion ulicis (Forster) - “Gorse Seed Weevil”
14. Gasteroclisus tricostatus (Thunberg)
15. Gymnetron antirrhini (Paykull) - “Seed-gall Weevil”
16. Gymnetron linariae (Panzer) - “Root-gall Weevil”
17. Gymnetron tetrum (Fabricius) - “Mullein Seed Head Weevil”
18. Hadroplontus litura (Fabricius) - “Canadian Thistle Stem Weevil”
19. Heilipodus ventralis (Hustache) - “Argentine Root Boring Weevil”
20. Hylobius transversovittatus (Goeze) - “Root-feeding Weevil"
22. Larinus minutus Gyllenhal - “Seedhead Weevil”
23. Larinus obtusus (Gyllenhal) - “Seedhead Weevil” or “Blunt Knapweed Flower Weevil”
24. Larinus planus (Fabricius) - “Canada Thistle Bud Weevil”
25. Mecinus janthinus Germar - “Stem-boring Weevil”
26. Microlarinus lareynii J. Duval - “Puncturevine Seed Weevil”
27. Microlarinus lypriformis Wollaston - “Puncturevine Stem Weevil”
28. Mogulones cruciger (Herbst) - “Root-feeding Weevil”
29. Nanophyes marmoratus (Goeze) - “Flower Bud Weevil”
30. Neochetina bruchi Hustache - “Chevroned Waterhyacinth Weevil”
31. Neochetina eichhorniae Warner - “Mottled Waterhyacinth Weevil”
32. Neohydronomus affinis Hustache - “Waterlettuce Weevil”
33. Omphalapion hookeri (Kirby) - “Seed-head Feeding Weevil”
34. Oxyops vitiosa Pascoe - “Melaleuca Weevil”
35. Phrydiuchus tau Warner - “Mediterranean Sage Root Crown Weevil”
36. Phytobius leucogaster (Marsham) - “Flower-eating Weevil”
37. Rhinocyllus conicus Frölich - “Flowerhead Weevil”
38. Trichosirocalus horridus (Panzer) - “Thistle Crown Weevil” or “Musk Thistle Rosette Weevil”
1. Acythopeus burkhartorum O'Brien - “Ivy
Gourd Stem Gallmaker”
Species diagnostic characters:
Size:
Small., > 2.0 mm < 4.5 mm
Body shape:
Broad-oval
Predominant color (cuticle):
Reddish black to black
Predominant color (scales):
Gray
Rostral length:
Long
Rostral width:
Slender
Antennal morphology:
Elbowed
Prothoracic collar: Not raised
(side view)
Prothoracic carina(e): Absent
Prothoracic tubercle(s):
Absent
Pronotal depression:
Absent
Elytral carina(e):
Absent
Elytral tubercle(s):
Absent
Elytral spicule(s):
Absent
Mesothoracic epipleuron: Ascending
and visible in dorsal view
Leg color (cuticle):
Black
Leg color (scales):
Gray
Trochanteral shape and length:
Triangular and short
Femoral armature:
Unarmed
Tibial armature of apices: All
with spine
Third tarsus shape:
Bilobed
Vestiture type:
Scales
Vestiture coverage:
Sparse
Waterproof coating:
Absent
Circular scales:
Absent
Erect setae:
Absent
Wax like coating:
Absent
Introduction:
Acythopeus burkhartorum O’Brien is a petiole and tendril galling weevil. To
control ivy gourd, Coccinia grandis (L.) Voigt three natural enemies,
Melittia oedipus Oberthur [Lepidoptera: Sesiidae], Acythopeus
cocciniae O’Brien (Curculionidae) and A. burkhartorum O’Brien were
introduced to the Hawaiian Islands from East Africa. These natural enemies are
being cultured at the Quarantine Laboratory in Guam" (PIER, 2003). In Hawaii two
species of weevils have been released for biological control (Thomas, 1998).
Some regions, including Hawaii, are experimenting with biological control of C. grandis primarily using A.
burkhartorum and A. cocciniae, two nonindigenous weevils, to control
infestations of ivy gourd (Thomas, 1998). The species were described from the
coast of Kenya between Mombasa and Tanzania (O’Brien and Pakaluk,
1998).
Adults live up to 23 months and feed on the leaves causing
holes in the leaves. Eggs are laid singly by inserting them in the young
petioles or tendrils. Eggs hatch in about a week and larval development takes
about three weeks. Pupation takes place within the gall and lasts for three to
four months. Adult feeding on the leaves and larval galling of petioles and
tendrils can cause drying of the leaves and eventual defoliation of vines (Murai
et al., 1998). Currently the species
is under investigation by the USDA for a possible release in Guam and Northern
Mariana Islands for biological control of ivy gourd (USDA, 2004). A. burkhartorum has been field released in
Guam in October 2004 and in Saipan in February 2005. Its field establishment in
Guam on ivy gourd has been confirmed and its establishment in Saipan is yet to
be verified (Reddy and Muniappan, 2005).
Description:
Adults of the ivy gourd stem gallmaker are
small (> 2.0 mm < 4.5 mm long), broad-oval, reddish black to black,
moderately convex weevils. The dense coarse punctures each have a recumbent
scale, which does not conceal the finely reticulate somewhat shining body. The
venter is equally punctate with similar scales. The rostrum is strongly curved
and strongly punctate in the stout basal three fourths, and the apex is markedly
attenuate and finely punctate. There are neither spots nor bands formed by the
pale setae. The small pygidium is visible and vertical. The legs are moderately
stout with the femora and most clavate (not strongly swollen) and unarmed. The
tibiae are straight with a small, indistinct, apical, inner
tooth.
Host Plant:
Ivy gourd, Coccinia grandis (L.)
Voigt
Bibliography:
Murai, K., M. Chan and T. Culliney. 1998. Host range
studies of two African Acythopeus
spp. (Coleoptera: Curculionidae), potential biocontrol agents of ivy gourd, Coccinia grandis (Cucurbitaceae). Plant
Pest Control Branch, Hawaii Department of Agriculture.
19pp.
O'Brien, C.W. and J. Pakaluk. 1998. Two new species of
Acythopeus Pascoe (Coleoptera: Curculionidae: Baridinae) from Coccinia
grandis (L.) Voigt (Cucurbitaceae) in Kenya. Proceedings of the Entomological Society of
Washington 100 (4):
764-774.
PIER (Pacific Island Ecosystems at Risk). 2003. Coccinia
grandis. Summary: Ecology,
synonyms, common names, distributions (Pacific as well as global), management
and impact information. Available from:
http://www.hear.org/pier/species/coccinia_grandis.htm [Accessed 2 August
2005].
Reddy, G.V.P. and R. N. Muniappan. 2005. Biological control
of the ivy gourd, Coccinia grandis
(Cucurbitaceae) in the Mariana Islands. Annual Meeting of Entomological Society
of America. Oral presentation (18 December 2005), Fort Lauderdale,
Florida.
Thomas, P.A, 1998. Ivy gourd. Hawaiian Ecosystems At Risk,
(HEAR). Summary: Information on
ivy gourd in Hawaii. Available from: http://www.hear.org/ivygourd/index.html
[Accessed 2 August 2005].
USDA (United States Department of Agriculture). 2004. Field
release of Acythopeus burkhartorum
(Coleoptera: Curculionidae), a non-indigenous weevil for control of ivy gourd,
Coccinia grandis (Cucurbitaceae), in
Guam and Northern Mariana Islands. Environmental Assessment. USDA-APHIS, PPQ,
Riverdale, MD. 12pp.
2. Acythopeus cocciniae O'Brien - “Ivy
Gourd Leaf Miner”
Species
diagnostic characters:
Size: Minute to small., < 2.0
mm to < 4.5 mm
Body shape:
Narrow-oval
Predominant color (cuticle):
Black
Predominant color (scales): Gray
or white
Rostral length:
Long
Rostral width:
Slender
Antennal morphology:
Elbowed
Prothoracic collar: Not raised
(side view)
Prothoracic carina(e): Absent
Prothoracic tubercle(s):
Absent
Pronotal depression:
Absent
Elytral carina(e):
Absent
Elytral tubercle(s):
Absent
Elytral spicule(s):
Absent
Mesothoracic epipleuron: Ascending
and visible in dorsal view
Leg color (cuticle):
Black
Leg color (scales):
Gray
Trochanteral shape and length:
Triangular and short
Femoral armature:
Unarmed
Tibial armature of apices: All
with spine
Third tarsus shape:
Bilobed
Vestiture type:
Scales
Vestiture coverage:
Sparse
Waterproof coating:
Absent
Circular scales:
Present
Erect setae:
Absent
Wax like coating:
Absent
Introduction:
Acythopeus cocciniae O’Brien is a leaf-mining weevil, native to East Africa.
The species was described from the coast of Kenya between Mombasa and Tanzania
(O’Brien and Pakaluk, 1998). Adults live up to 200 days and feed on the leaves
causing numerous holes in the lamina. Eggs are laid singly by insertion into the
lamina of ivy gourd leaves. Eggs hatch in about eight days and larvae mine the
leaves for nine to ten days. Pupation takes place within the mine and lasts for
15 days. Adult feeding and larval mining can cause drying of the leaves and
eventual defoliation of the ivy gourd vines (USDA, 2003). O’Brien and Pakaluk
(1998) reported that this insect occurs only on ivy gourd. Some regions,
including Hawaii, are experimenting with biological control primarily using A. burkhartorum and A. cocciniae, two nonindigenous weevils, to
control infestation of ivy gourd (Thomas, 1998). These biological control agents
are being cultured at the Quarantine Laboratory in Guam (PIER,
2003).
Description:
Adults of the ivy gourd leaf miner are
minute to small (< 2.0 mm to < 4.5 mm long), narrow-oval, moderately
convex weevils, black with several small white spots of circular scales. At the
base of the thorax (when not worn away) are three small white spots formed by
shinglelike oval scales. A large white spot is found on the side of the body
between the thorax and elytra, visible even in dorsal view. The venter of the
thorax is coarsely punctate, and each puncture has a large recumbent grayish
white scale. The venter of the abdomen is very sparsely punctate, each puncture
with a fine pale seta, and the surface is smooth and shining. The rostrum is
strongly curved throughout and strongly punctate in the basal half. The apical
half is moderately attenuate and moderately coarsely punctate. The very small
pygidium is visible and vertical. The legs are moderately stout with the femora
moderately swollen and unarmed. The tibiae have a small, rather distinct,
apical, inner tooth.
Host Plant:
Ivy gourd, Coccinia grandis (L.)
Voigt
Bibliography:
O’Brien, C.W. and J. Pakaluk. 1998. Two new species of
Acythopeus Pascoe
(Coleoptera: Curculionidae: Baridinae) from Coccinia grandis (L.) Voigt
(Cucurbitaceae) in Kenya. Proceedings of the Entomological Society of
Washington, 100 (4): 764-774.
PIER (Pacific Island Ecosystems at Risk). 2003. Coccinia
grandis. Summary: Ecology,
synonyms, common names, distributions (Pacific as well as global), management
and impact information. Available from:
http://www.hear.org/pier/species/coccinia_grandis.htm [Accessed 2 August
2005].
Thomas, P.A. 1998. Ivy gourd. Hawaiian Ecosystems At Risk,
(HEAR). Summary: Information on
ivy gourd in Hawaii. Available from: http://www.hear.org/ivygourd/index.html
[Accessed 2 August 2005].
USDA (United States Department of Agriculture). 2003. Field
release of Acythopeus cocciniae
(Coleoptera: Curculionidae), a non-indigenous leaf-mining weevil for control
of ivy gourd, Coccinia grandis
(Cucurbitaceae), in Guam and Saipan. Environmental Assessment. USDA-APHIS, PPQ,
Riverdale, MD. 16pp.
3.
Bagous
affinis Hustache - “Hydrilla Tuber
Weevil”
Species
diagnostic characters:
Size: Medium-sized., > 4.5 mm
< 10.0 mm
Body shape:
Elongate-oval
Predominant color (cuticle): Dark
brown to black
Predominant color (scales):
Brown
Rostral length: Moderately
short
Rostral width:
Slender
Antennal morphology:
Elbowed
Prothoracic collar: Weakly raised
(side view)
Prothoracic carina(e): Absent
Prothoracic tubercle(s):
Absent
Pronotal depression:
Present
Pronotal depression orientation:
Longitudinal
Elytral carina(e):
Absent
Elytral tubercle(s):
Present
Elytral spicule(s):
Absent
Mesothoracic epipleuron: Not
ascending and not visible in dorsal view
Leg color (cuticle): Dark
brown
Leg color (scales):
Brown
Trochanteral shape and length:
Triangular and short
Femoral armature:
Unarmed
Tibial armature of apices: All
with spine
Third tarsus shape: Heart shaped,
apically emarginate
Vestiture type:
Scales
Vestiture coverage: Dense and
complete
Waterproof coating:
Present
Type of waterproof coating:
Clear
Circular scales:
Present
Erect setae:
Absent
Wax like coating:
Absent
Introduction:
Bagous affinis Hustache was originally described from India and Pakistan
and was first released in Florida in 1987. Buckingham (1988) reported the
release of B. affinis in south Florida in April 1987 by the United
States Army Corps of Engineers in a preliminary effort to control hydrilla. The
species failed to establish in Florida and Texas (Coombs et al., 2003). Eggs are roughly
spherical with a creamy white color. Eggs are laid usually on dead vegetation on
the ground, e.g. plant stems, moist wood, etc in areas with annual dry
periods, separate from periods of inundation by flooding or heavy rains. Annual
drawdowns of water can serve the same purpose. Each female can lay up to 650
eggs in her life time. Eggs hatch in 3-4 days, and emerging larvae can crawl and
search for the underground tubers, which they enter to feed on and to take
shelter after burrowing through the soil (PMIS, 2003). The larvae feed inside
subterranean turions or tubers of Hydrilla verticillata (L.f.) Royle
during low water conditions. This results in reduced sprouting of the tubers
(Godfrey and Anderson, 1994). The host range of B. affinis was
studied in a quarantine laboratory to determine if the weevil would be safe for
release in the United States as a biological control agent. Thirty-nine plant
species (20 families) were tested with larvae and feeding was observed on only
six species. In India and Pakistan this weevil species was taken only on
hydrilla even though some of the other tested plants were present (Buckingham
and Bennett, 1996).
Description:
Adults of the hydrilla tuber weevil are
dark brown to black, occasionally gray in color, and have a relatively
streamlined body. Body medium-sized (> 4.5 mm < 10.0 mm long),
elongate-oval and robust. Rostrum moderately short, 0.83 × as long as pronotum.
Head weakly convex, swelling beside eyes very weak; eyes moderately convex.
Antennae inserted laterally at apical 1/3, scape long, slender and subclavate.
Pronotum weakly transverse, 0.92 × as long as broad. Prosternal sulcus deep,
broad, scarcely narrowed at apical constriction. Scutellum large. Elytra
subparallel behind humeri. Meso- and metasternum with punctures not forming
large concavities, mesosternal process large. Abdominal sternum 1 with median
impression shallow, broad, basal only; convex in apical 2/3, not continued on
sternum 2. Intraspecific variation: declivital calli (tubercles) of elytral
interval 5 vary from moderately developed and subquadrate, to weak and scarcely
evident; color varies from black and gray to brown and whitish tan (O’Brien and
Pajni, 1989).
Host Plant:
Hydrilla, Hydrilla verticillata
(L.f.) Royle
Bibliography:
Buckingham, G.R. 1988. Reunion in Florida –
Hydrilla, a weevil, and a fly. Aquatics 10: 19-25.
Buckingham, G.R. and C.A. Bennett. 1996. Host range studies
with Bagous affinis (Coleoptera: Curculionidae) an Indian weevil that
feeds on hydrilla tubers. Tektran, USDA-ARS.
Coombs, E., J. Balciunas and P. McEvoy. 2003. Current
status in each state of all 100 agents approved for release in the continental
USA. Biological control of invasive plants in the United States. Corvallis, OR.,
Oregon University Press.
Godfrey, K.E. and L.W.J. Anderson. 1994. Feeding by Bagous affinis (Coleoptera:
Curculionidae) inhibits germination of hydrilla tubers. Florida Entomologist
77(4): 480-488.
O’Brien, C.W. and H.R. Pajni. 1989. Two Indian
Bagous weevils (Coleoptera: Curculionidae), tuber feeders of Hydrilla
verticillata (Hydrocharitaceae), one a potential biocontrol agent in
Florida. Florida Entomologist 72: 462-468.
PMIS (Plant Management Information System). 2003. Noxious
and nuisance plant information system, ver. 5.3. Developed by Cofrancesco et al., (Cds and Web based. Available
from: http://el.erdc.usace.army.mil/pmis/ [Accessed 14 April
2006].
4.
Bagous
hydrillae O'Brien - “Hydrilla Stem
Borer”
Species diagnostic characters:
Size: Small to medium-sized., >
2.0 mm to < 10.0 mm
Body shape:
Elongate-oval
Predominant color (cuticle): Dark
brown
Predominant color (scales): Brown
mottled with tan and white
Rostral length: Moderately
short
Rostral width: Moderately
narrow
Antennal morphology:
Elbowed
Prothoracic collar: Raised (side
view)
Prothoracic carina(e): Absent
Prothoracic tubercle(s):
Present
Pronotal depression:
Present
Pronotal depression orientation:
Longitudinal
Elytral carina(e):
Absent
Elytral tubercle(s):
Present
Elytral spicule(s):
Absent
Mesothoracic epipleuron: Not
ascending and not visible in dorsal view
Leg color (cuticle): Black to
reddish brown
Leg color (scales):
Brown
Trochanteral shape and length:
Triangular and short
Femoral armature:
Unarmed
Tibial armature of apices: All
with spine
Third tarsus shape: Heart shaped,
apically emarginate
Vestiture type:
Scales
Vestiture coverage: Dense and
complete
Waterproof coating:
Present
Type of waterproof coating:
Earthen
Circular scales:
Present
Erect setae:
Absent
Wax like coating:
Absent
Introduction:
Bagous hydrillae O’Brien is native to Australia and was released first in
the United States in Florida in 1991 (PMIS, 2003). The weevil has since been
released at numerous sites in Florida and Texas (Center et al., 2000) but had failed to
establish (Coombs et al., 2003). At
the time of this writing (2006) no established populations have been confirmed.
A number of experiments were conducted in South Florida to determine the growth
and development of B. hydrillae on hydrilla (Wheeler and
Center, 1997).
Adults can be found on growing submersed hydrilla as well
as on pieces of hydrilla that wash up on the shoreline. Adults feed externally
on leaf and stem tissues on drying or submersed hydrilla. Eggs are laid within
stem tissues, usually at the leaf node (i.e. where the leaves attach).
There are three larval instars, each lasting from 3 to 4 days. Larval feeding
subsequently fragments the stem, which floats to the shoreline where the 3rd
instar larvae exit and eventually pupate within the soil or drying hydrilla.
Pupation usually takes place under relatively dry conditions. The pupa does not
form any protective covering such as a cocoon and is therefore referred to as
naked. The pupal period lasts in 3 to 4 days depending on appropriate
temperature (PMIS, 2003). The life cycle of B. hydrillae requires
17-21 days. Adults spend daylight time below the surface of the water where they
crawl about, feed, and oviposit on the hydrilla stems. They emerge from the
water and usually fly at dusk. Adults can live 60-80 days (Center et al.,
2000).
Description:
Adults of the hydrilla stem borer are
dark brown with a distinctly mottled appearance. The rostrum is moderately
short, 0.83 × as long as the pronotum. The body is relatively slender, small to
medium-sized (> 2.0 mm to < 10.0 mm long) elongate-oval and strongly
covered with dense, granulate scales. The usual earthen coating may be absent in
some recently emerged adult specimens. The antennae are inserted near the apical
1/4th of the rostrum. The sulcus of the prosternum is moderately broad, deep and
biangulate. The combination of reddish brown antennal scape and funicle and that
of the basal 1/2 of the femora and the complete tibiae and tarsi (especially the
femoral color) is diagnostic for the species. In many individuals 2-4 pale spots
can be seen towards the rear of the elytra.
Host Plant:
Hydrilla, Hydrilla verticillata
(L.f.) Royle.
Bibliography:
Center, T.D., F.A. Dray and V.V. Vandiver, Jr. 2000.
Biological Control with Insects: The hydrilla stem weevil. SS AGR 138. Institute
of Food and Agricultural Sciences, University of Florida. Revised May 2002.
Available from: http://edis.ifas.ufl.edu [Accessed on 17 December
2002].
Coombs, E., J. Balciunas and P. McEvoy. 2003. Current
status in each state of all 100 agents approved for release in the continental
USA. Biological control of invasive plants in the United States. Corvallis, OR.,
Oregon University Press.
PMIS (Plant Management Information System). 2003. Noxious
and nuisance plant information system, ver. 5.3. Developed by Cofrancesco et al., (Cds and Web based. Available
from: http://el.erdc.usace.army.mil/pmis/ [Accessed 14 April
2006].
Wheeler, G.S. and T.D. Center. 1997. Growth and development
of the biological control agent Bagous
hydrillae as influenced by hydrilla (Hydrilla verticillata) stem quality.
Biological Control 8 (1): 52-57.
5. Bangasternus fausti (Reitter) -
“Seedhead Weevil”
Species diagnostic characters:
Size: Small., > 2.0 mm < 4.5
mm
Body shape: Elongate-oval
Predominant color (cuticle):
Brown
Predominant color (setae): Brown
to white
Rostral length:
Short
Rostral width: Broad
Antennal morphology:
Elbowed
Prothoracic collar: Raised (side
view)
Prothoracic carina(e): Absent
Prothoracic tubercle(s):
Absent
Pronotal depression:
Absent
Elytral carina(e):
Absent
Elytral tubercle(s):
Absent
Elytral spicule(s):
Absent
Mesothoracic epipleuron: Not
ascending and not visible in dorsal view
Leg color (cuticle):
Black
Leg color (setae): Brown to
white
Trochanteral shape and length:
Triangular and short
Femoral armature:
Unarmed
Tibial armature of apices: All
with spine
Third tarsus shape:
Bilobed
Vestiture type:
Setae
Vestiture coverage: Dense, in
bands or patches
Waterproof coating:
Absent
Circular scales:
Absent
Erect setae:
Present
Wax like coating:
Absent
Introduction:
Bangasternus fausti (Reitter) is native to northern Greece and was released in
the United States in 1991 (Rees et
al., 1996). The weevil has been established in a number of States including
California, Colorado, Minnesota, Montana, Nebraska, Oregon, South Dakota, Utah,
Washington, and Wyoming as part of a program to control spotted and diffuse knapweed
(Centaurea stoebi Lam. [formerly maculosa] and C. diffusa Lam.) (Lang, 1997., Coombs et al., 2003). It is not known how B.
fausti will interact with other seedhead infesting biological control
agents. Early concerns about the potential of B. fausti displacing
Urophora affinis [Diptera: Tephritidae] have yet to be realized. Under
favorable conditions weevil density can increase dramatically allowing the
collection of large numbers of weevils for redistribution. Adult weevils emerge
from the seedheads as well as ground litter in May and early June. Oviposition
may occur 1-2 weeks after adult emergence. Eggs are oval, yellowish, and covered
with a black egg-cap. The eggs hatch in 8-12 days and the larvae then mine into
the knapweed seedhead and begin feeding. Larvae are white, legless, C-shaped
grubs with brown head capsules that reach a length of approximately 8 mm. Each
larva tunnels into the stem or bur. After this, it tunnels into the seedhead and
feeds. Larvae consume up to 95% of the seeds in a head (Rees et al.,
1996). Pupation occurs inside the seedhead. Adults may be found feeding on
spotted or diffuse knapweed foliage in the spring and in the summer on the
flowers. The white pupae are found inside a cell in the seedhead. The period
from egg to adult is about 32 days and species is univoltine.
Description:
Adults of the
seedhead weevil are small (> 2.0 mm <
4.5 mm long), mottled white or gray and brown with a short, cone shaped blunt
snout that appears to have been cut off (Lang, 1997). It has a distinct pair of
raised ridges in front of the fore coxae. Dorsal setae are bifid and suberect to
recumbent. The two claws on each tarsus are asymmetrical, one of each shorter
than the other.
Host Plants:
Diffuse knapweed, Centaurea diffusa
Lam.; spotted knapweed, C. stoebi Lam. (formerly maculosa); purple starthistle, C.
calcitrapa L.; squarrose knapweed, C. squarrosa Roth; and yellow
starthistle, C. solstitialis L.
Bibliography:
Coombs, E., J. Balciunas and P. McEvoy. 2003. Current
status in each state of all 100 agents approved for release in the continental
USA. Biological control of invasive plants in the United States. Corvallis, OR.,
Oregon University Press.
Lang, R.F. (1997). Bangasternus fausti. Biological control. A guide to natural enemies in North
America, Cornell University. Available:
http:www.nysaes.cornell.edu/ent/biocontrol/weedfeeders/bangasternus_fausti.html
[Accessed 2 August 2005].
Rees, et. al.,
(1996). Biological Control of Weeds in the West, Western Society of Weeds
Science, in Cooperation With USDA ARS, MT
Department of Ag, and MT State Univ., Color World Printers, Bozeman
MT.
6.
Bangasternus orientalis (Capiomont) - “Yellow Starthistle Bud
Weevil”
Species
diagnostic characters:
Size:
Medium-sized., > 4.5 mm < 10.0 mm
Body
shape: Elongate-oval
Predominant color (cuticle): Dark brown to black
Predominant color (setae): Yellowish to whitish
Rostral
length: Short
Rostral
width: Broad
Antennal
morphology: Elbowed
Prothoracic collar: Raised (side
view)
Prothoracic carina(e): Absent
Prothoracic tubercle(s): Absent
Pronotal
depression: Absent
Elytral
carina(e): Absent
Elytral
tubercle(s): Absent
Elytral
spicule(s): Absent
Mesothoracic epipleuron: Not ascending and not visible in
dorsal view
Leg color
(cuticle): Reddish brown
Leg color
(setae): Brown
Trochanteral shape and length: Triangular and
short
Femoral
armature: Unarmed
Tibial
armature of apices: All with spine
Third
tarsus shape: Bilobed
Vestiture
type: Setae
Vestiture
coverage: Dense, in bands of patches
Waterproof coating: Absent
Circular
scales: Absent
Erect
setae: Present
Wax like
coating: Absent
Introduction: Bangasternus orientalis
(Capiomont) was imported from northern Greece (PMIS, 2003). It is native to
southern Eurasia and the Mediterranean Basin. The weevil was first introduced in
the United States in 1985 in California, Idaho, Oregon, and Washington and now
is established in these States (Coombs et
al., 2003). Adult weevils emerge from their overwintering sites in May and
can be seen on yellow starthistle from May through early July. A female may lay
up to 470 eggs, which are laid in spring to summer. The eggs are deposited on
leaves or stems below the young unopened buds and are covered with a black
tar-like secretion by the female. The female glues eggs to the leaf and the
coating prevents desiccation. Larvae, after hatching burrow into the leaf and up
to the developing bud. They feed on the developing seeds and tissue of the disk.
Usually 40-60% of the seeds in a head are consumed (Maddox et al., 1991), however, seed destruction
can range from 30-100% depending on the size of the head (Pitcairn, 1996).
Pupation occurs within the seed heads in chambers formed from damaged and
undamaged seeds. Adults exit from the pupal chambers in the heads in late summer
and overwinter outside the host plant. The weevil has one generation per year.
Adults can live approximately 2 months. The cooler climates including coastal,
higher elevations and latitudes are unfavorable to this weevil.
Description:
Adults of
the yellow
starthistle bud weevil are medium-sized
(> 4.5 mm < 10.0 mm long) and are elongate-oval in shape. The adult color
varies from dark brown to black with a reddish tinge. The adult body is usually
covered with yellowish to whitish hairs, with a somewhat mottled appearance. The
rostrum is straight, 1.6 to 1.9 times longer than wide and strongly constricted
at the base. Antennae are attached near the middle of the rostrum, the scape is
shorter than the funicle, and the club is distinct and is wide in the middle and
narrow apically and basally. The pronotum and elytra are clothed with bifid
setae. The prosternum has a pair of raised ridges in front of the fore coxae
which form a deep groove for receiving the rostrum. Legs are thick, the femora
are unarmed but the tibiae possess a minute apical spine. Two claws are present,
one side shorter than the other. The center of the first abdominal segment is
depressed somewhat in males, however, it is flat in
females.
Host Plants: Yellow starthistle,
Centaurea solstitialis L. Host plants are restricted to the
closely related genera of Cardumcellus, Carthamus, and
Centaurea.
Bibliography:
Coombs, E., J. Balciunas and P. McEvoy. 2003. Current
status in each state of all 100 agents approved for release in the continental
USA. Biological control of invasive plants in the United States. Corvallis, OR.,
Oregon University Press.
Maddox, D.M., D.B.Joley, A. Mayfield, and B.E. Mackey.
1991. Impact of Bangasternus
orientalis (Coleoptera: Curculionidae) on achene production of Centaurea solstitialis (Asterales:
Asteraceae) at a low and high elevation site in California. Environmental
Entomology 20: 335-337.
Pitcairn, M. 1996. Yellow starthistle control methods:
biological control. California Exotic Plant Council. Proceedings paper.
1-4.
PMIS (Plant Management Information System). 2003. Noxious
and nuisance plant information system, ver. 5.3. Developed by Cofrancesco et al., (Cds and Web based. Available
from: http://el.erdc.usace.army.mil/pmis/ [Accessed 14 April 2006].
7.
Ceutorhynchus
trimaculatus (Fabricius) - “Rosette
Weevil”
Species
diagnostic characters:
Size: Small., > 2.0 mm < 4.5 mm
Body shape: Broad-oval
Predominant color (cuticle): Black
Predominant color (scales): White
Rostral length: Long
Rostral width: Slender
Antennal morphology: Elbowed
Prothoracic collar: Raised (side view)
Prothoracic carina(e): Absent
Prothoracic tubercle(s): Present
Pronotal depression: Present
Pronotal depression orientation: Longitudinal
Elytral carina(e): Absent
Elytral tubercle(s): Absent
Elytral spicule(s): Absent
Mesothoracic epipleuron: Ascending and visible in dorsal
view
Leg color (cuticle): Dark brown
Leg color (setae): Brown
Trochanteral shape and length: Triangular and
short
Femoral armature: Toothed
Tibial armature of apices: All lack
spine
Third tarsus shape: Bilobed
Vestiture type: Scales
Vestiture coverage: Dense and
complete
Waterproof coating: Absent
Circular scales: Present
Erect setae: Absent
Wax like coating: Absent
Introduction:
Ceutorhynchus
trimaculatus (Fabricius) is native to
Europe and northern Africa (Bolt et al., 1980). This weevil was studied
in depth as a candidate for biological control (Kok et al., 1982., Kok and McAvoy, 1983).
The species can be employed against Italian thistle and other Carduus
species in North America (Goeden, 1974). The weevil has been considered a pest
of artichoke, safflower crops and also has been found to be a potential predator
of flowers and seeds of Italian and slender thistles (Bolt et al., 1980;
Kok et al., 1982). The species has one generation per year. Adults emerge
at the end of April and feed on the leaves of new rosettes or mature plants for
three to four weeks. At the end of May, adults enter the soil to aestivate.
Adults gradually become active again in autumn and feed on the leaves of young
rosettes. Oviposition starts in November and continues through March or April.
Larvae feed gregariously by boring into leaf buds or growing tips, and moving
down into the crown. Pupation occurs in the soil (Boldt and Campobasso, 1981;
Kok and McAvoy, 1983)
Description:
Adults of the rosette weevil are small
(> 2.0 mm < 4.5 mm long) in size,
stout, broad-oval, and black, with distinct maculae and vittae formed by
coarse, elongate-oval white scales. The body is rather densely clothed with
black, tan, and a few white, scale like setae and patches of imbricate, white
scales. The thorax has a small, median, basal, white macula and the sides are
white with a pair of large, anterior, dorsolateral, white maculae. The base of
the thorax is broadly rounded and the apex is strongly narrowed. The dorsum has
a pair of subacute, basolateral tubercles. The elytra are strongly striate
(grooved) with subcontiguous, large, deep, strial punctures. The intervals are
more or less flattened throughout, except on the declivity where they form a
broad callus on intervals 3-8. At the basal third angling forward to just behind
the scutellum, the white scales form an interrupted maculate vitta. A transverse
white fascia is present in front of the declivity and merges with the white
elytral apex. The rostrum is long, curved, narrowly cylindrical, coarsely
punctured, and densely clothed with suberect coarse setae. The rostrum is
sharply constricted basally at its attachment to the head. The antennae are dark
brown to yellowish and the funicle is seven-segmented. The eyes are round and
moderately convex, with a broad shallow depression between them on the frons.
The prosternum is deeply, narrowly sulcate. The legs are stout with strongly
clavate femora, each with a large acute tooth. The tibiae are stout, sinuate and
possess a small apical tooth on the inner margin. The tarsi (feet) are wide with
the third segment strongly bilobed. The tarsal claws are free, subapproximate
and long.
Host Plants:
Thistles, Carduus spp.
and Cirsium spp.
Bibliography:
Boldt, P.E. and G. Campobasso. 1981. Biology of two
weevils, Ceutorhynchus trimaculatus and Trichosirocalus horridus,
on Carduus spp. in Europe. Environmental Entomology 10:
691-696.
Bolt, P.E., G. Campobasso, and E.
Colonnelli. 1980. Paleartic distribution and
host plants of Ceutorhynchus trimaculatus and Trichosirocalus
horridus (Coleoptera: Curculionidae). Ann. Entomol. Soc. America 73:
694-698.
Goeden, R. 1974. Comparative survey of the phytophagous
insect faunas of Italian thistle, Carduus pycnocephalus, in southern
California and southern Europe relative to biological weed control. Environ.
Entomol. 3: 464-474.
Kok, L.T. and T.J. McAvoy. 1983. Biological studies of
Ceutorhynchus trimaculatus (Coleoptera: Curculionidae), a thistle rosette
weevil. Canadian Entomologist 115: 927-932.
Kok, L., T.J. McAvoy, G. Johnson, and P. Dunn. 1982.
Further studies on Ceutorhynchus trimaculatus F. as a candidate for the
biological control of Carduus species. Crop Protection 1:
67-74.
8. Cyphocleonus achates (Fahraeus) - “Root
Boring Weevil”
or “Knapweed Root
Weevil”
Species
diagnostic characters:
Size: Large., > 10.0 mm
Body shape: Elongate, broad-oval
Predominant color (cuticle): Black
Predominant color (setae): Strongly mottled, bicolored or
tricolored
Rostral length: Moderately long
Rostral width: Broad
Antennal morphology: Elbowed
Prothoracic collar: Not raised (side
view)
Prothoracic carina(e): Absent
Prothoracic tubercle(s): Present
Pronotal depression: Present
Pronotal depression orientation:
Transverse
Elytral carina(e): Absent
Elytral tubercle(s): Present
Elytral spicule(s): Absent
Mesothoracic epipleuron: Not ascending and not visible in
dorsal view
Leg color (cuticle): Black
Leg color (setae): White
Trochanteral shape and length: Triangular and
short
Femoral armature: Unarmed
Tibial armature of apices: All with
spine
Third tarsus shape: Bilobed
Vestiture type: Setae
Vestiture coverage: Dense and
complete
Waterproof coating: Absent
Circular scales: Absent
Erect setae: Absent
Wax like coating: Absent
Introduction:
Cyphocleonus achates (Fahraeus) is native to Austria, Greece, Hungary, and
Romania. The first release of the weevil in the United States occurred in 1988
in Montana to control spotted and diffuse knapweed, Centaurea spp. (PMIS,
2003). Then, species was released in Arizona, California, Colorado, Idaho,
Minnesota, Montana, Nebraska, Nevada, Oregon, South, Dakota, Utah, Washington,
and Wyoming to control spotted and diffuse knapweed; and is established on Centaurea diffusa Lam. in Montana,
Nevada, and Oregon, but failed to establish in California, Colorado, Wyoming and
Washington. The species was also released to control Centaurea jaceae × nigra (L.) and Centaurea stoebi (Coombs et al., 2003). In Canada, the species is
widely distributed in British Columbia on spotted and large diffuse knapweed
plants (Harris, 2005).
Adults emerge from mid-July to early September with peak
emergence at about mid-August. Adults spend most of their life (about 10 weeks)
on the root crown, just below the surface. They climb up to the tops of plants
on sunny, warm days in search of a mate. Larvae hatch in 10 to 12 days and begin
to tunnel into the root’s central vascular tissue where they complete their
development. Unlike other knapweed weevils, C. achates has four larval
instars. By the fourth instar, larvae are large, white and C-shaped.
Cyphocleonus achates overwinter as larvae in the root. Mature larvae
cause a gall in the root giving the root a swollen appearance. They pupate in
the gall during the onset of warmer spring temperatures. New adults appear after
about two weeks of pupation by chewing their way out of the root gall. Evidence
of larval damage is a wide tunnel, abundant frass, and a swollen root gall
(caused by the third and fourth instars). The species has one generation per
year (PMIS, 2003; Harris, 2005).
Description:
Adults of the root boring weevil are large
(> 10.0 mm long) in size, elongate, broad-oval with a distinct tan-brown and
white, banded and spotted pattern on the thorax and elytra. The recumbent white
scale like setae are much coarser and denser than the moderately coarse
tan-brown setae. The white setae nearly or completely conceal the body, but the
brown setae are less dense, and visible among them are flattened shining black
tubercles. The rostrum is moderately long, broadly flattened and has two broad,
deep, sublateral grooves on the basal two thirds. Three broad carinae are
visible in this area. The apical third is flattened and densely punctate under
the dense, white, scale like setae. The legs and venter are covered with dense,
white, and a few brown, recumbent, scale like setae, mixed with some erect, fine
setae. The eyes are broad-oval. The prosternum is not sulcate, but has a pair of
swellings just in front of the coxae. The tibiae have a moderate-sized, inner,
apical tooth. The tarsal claws are large, approximate, connate (basally fused),
and symmetrical.
Host Plants:
Diffuse knapweed, Centaurea diffusa
Lam. and spotted knapweed, C. stoebi Lam. (formerly maculosa) and
C. jaceae × nigra
(L.).
Bibliography:
Coombs, E., J. Balciunas and P. McEvoy. 2003. Current
status in each state of all 100 agents approved for release in the continental
USA. Biological control of invasive plants in the United States. Corvallis, OR.,
Oregon University Press.
Harris, P. 2005. Classical biological control of weeds,
established biological control agent. Cypocleonus achates (Fahr.). Root-core
feeding weevil. Available from:
http://res2.agr.ca/lethbridge/weedbio/agents/acypach_e.htm [Accessed on 17 April
2006).
PMIS (Plant Management Information System). 2003. Noxious
and nuisance plant information system, ver. 5.3. Developed by Cofrancesco et al., (Cds and Web based. Available
from: http://el.erdc.usace.army.mil/pmis/ [Accessed 14 April
2006].
9.
Cyrtobagous salviniae Calder and Sands -
“Salvinia Weevil”
Species
diagnostic characters:
Size: Minute to small., < 2.0 mm to < 4.5
mm
Body shape: Round-oval
Predominant color (cuticle): Black [in mature
individuals]
Predominant color (cuticle): Brown [in teneral
individuals]
Predominant color (scales): Metallic
gold
Rostral length: Long
Rostral width: Slender
Antennal morphology: Elbowed
Prothoracic collar: Not raised (side
view)
Prothoracic carina(e): Absent
Prothoracic tubercle(s): Absent
Pronotal depression: Absent
Elytral carina(e): Absent
Elytral tubercle(s): Present
Elytral spicule(s): Absent
Mesothoracic epipleuron: Not ascending and not visible in
dorsal view
Leg color (cuticle): Reddish brown
Leg color (setae): Gray
Trochanteral shape and length: Triangular and
short
Femoral armature: Unarmed
Tibial armature of apices: All with
spine
Third tarsus shape: Linear
Vestiture type: Scales
Vestiture coverage: Sparse
Waterproof coating: Present
Type of waterproof coating: Clear
Circular scales: Absent
Erect setae: Absent
Wax like coating: Absent
Introduction: Cyrtobagous salviniae Calder and Sands is native to South America, and was first
reported in the United States by Kissinger in 1966 as Cyrtobagous
singularis Hustache, the only species of the genus known at that time. The
sibling species (C. salviniae) was described as a new species in
1985, and the different host association clearly demonstrated the reason for
control of the weed in Australia following lack of control in Fiji (see Room,
et al., 1981; Forno et al., 1983 and Calder and Sands, 1985 for a
complete history of this problem). Biology of the weevil was studied in its
native habitat of South America by Forno et al., 1983, who found that teneral
adults are light brown when they first emerge, but as they mature they darken to
black in 5 days. Adults are sub-aquatic and can be found beneath young leaves,
within leaves or in the roots of Salvinia. Adults of this tribe,
Stenopelmini, respire, when resting or feeding below the water surface, with the
aid of air bubbles, a plastron (a specialized physical gill), or air trapped
from plant stems. The preoviposition stage is 6-14 days. Eggs are laid singly in
stem cavities made by the adult using its rostrum and apical mouthparts.
Oviposition took place only when Salvinia was in contact with the water.
Females laid one egg every 2-5 days over a 60 day study period. Larvae feed on
young terminal buds and enter the leaf bud tunneling inside after 3-14 days of
surface feeding. The average developmental time for larvae is 23 days at 25.5°C.
Pupation takes place in a cocoon in contact with living plants. Most cocoons are
found below the leaves or within the root mass.
Description: Adults of the salvinia weevil are minute to small (< 2.0
mm to < 4.5 mm long) in size, round-oval, shining black, and convex. The body
is covered with a clear, shellac-like, waterproof coating through which the
scattered, small, round, metallic gold, recumbent scales are clearly visible.
The thorax lacks punctures. However, the elytra have large, very coarse, deep,
strial punctures, which are broader than the convex elytral intervals. The
rostrum is nearly straight and strongly swollen at, and in front of, the
antennal insertion. The antennae and legs are reddish brown. The antennae are
shining and glabrous basally, with only the apical half of the club setose. The
inner surface of the femora and tibiae, the entire tarsi and the venter of the
mesosternum, metasternum, and the basal two segments of the abdomen are
completely covered with a grayish, velvet-like hydrofuge pubescence. The femora
are moderately clavate, and the tibiae are nearly straight, with a minute (but
visible) tooth on the inner apical surface. The tarsi are linear with the last
segment longer than segments 1-4 together. The tarsal claws are free,
approximate and very long.
Plant Hosts: Salvinia; Salvinia minima Baker, and S.
molesta D.S. Mitchell.
Bibliography:
Calder, A.A. and D.P.A. Sands. 1985. A new Brazilian
Cyrtobagous Hustache (Coleoptera: Curculionidae) introduced into
Australia to control salvinia. J. Aust. Entomol. Soc. 24:
57-64.
Forno, I.W., D.P.A. Sands and W. Sexton. 1983.
Distribution, biology and host specificity of Cyrtobagous singularis
Hustache (Coleoptera: Curculionidae) for biological control of Salvinia
molesta. Bull. Ent. Res. 73: 89-95.
Room, P.M., I.W. Forno and M.F.J. Taylor. 1984.
Establishment in Australia of two insects for biological control of the floating
weed Salvinia molesta. Bull. Entomol. Res. 74:
505-516.
10.
Euhrychiopsis lecontei (Dietz) -
“Milfoil Weevil”
Species
diagnostic characters:
Size: Minute to small., < 2.0 mm to < 4.5
mm
Body shape: Elongate, broad-oval
Predominant color (cuticle): Brown to black
Predominant color (scales): Strongly mottled, bicolored or
tricolored
Rostral length: Short
Rostral width: Slender
Antennal morphology: Elbowed
Prothoracic collar: Raised (side
view)
Prothoracic carina(e): Absent
Prothoracic tubercle(s): Present
Pronotal depression: Present
Pronotal depression orientation:
Longitudinal
Elytral carina(e): Absent
Elytral tubercle(s): Absent
Elytral spicule(s): Absent
Mesothoracic epipleuron: Ascending and visible in dorsal
view
Leg color (cuticle): Orange
Leg color (scales): Gray
Leg color (setae): Brown
Trochanteral shape and length: Triangular and
short
Femoral armature: Unarmed
Tibial armature of apices: All lack
spine
Third tarsus shape: Bilobed
Vestiture type: Scales
Vestiture coverage: Dense and
complete
Waterproof coating: Present
Type of waterproof coating: Clear
Circular scales: Present
Erect setae: Absent
Wax like coating: Absent
Introduction:
Euhrychiopsis lecontei (Dietz) is a weevil endemic to North America (Newman et
al., 1997). This aquatic weevil species is being used as a biological
control agent for Eurasian watermilfoil, Myriophyllum spicatum L. Both adults and
larvae feed on Eurasian watermilfoil. This genus is currently monotypic, since a
second species, E. albertanus Brown, has been synonymized.
The two species appeared to be very different externally, but a study showed
that the external morphological differences were the result of a cline in color
and size from east to west in the USA and Canada and that the male genitalia
were identical in more than 20 populations studied (Tamayo, et al., 1999). The species is highly specific to
watermilfoils. Of over 200 females tested with watermilfoils and other native
plants, only 3 eggs were laid on nonwatermilfoils (Solarz and Newman, 1996). The
weevil spends most of its time under water except when overwintering. Females lay eggs singly on the meristem
of watermilfoil plants. The larvae feed on the meristem and burrow through the
stem cortex (Newman et al., 1996). The development time at 70-75°F on
Eurasian watermilfoil averaged 4 days for the egg stage, 13 days for the larval
stage, and 10-13 days for the pupal stage (Sheldon and O’Bryan, 1996). In New
England, this species takes about 30 days for development from egg to adult
stage and there are three generations per summer. The adults of the third
generation leave a lake in the fall and fly to overwinter in terrestrial leaf
litter. In the spring the adults fly back to the lake where they mate, lay eggs
and complete their life cycle. Because of its very small size, this species is
difficult to detect, and the current range of the weevil in North America is not
completely known. However, this species has been found in the United States in
Connecticut, Illinois, Iowa, Massachusetts, Michigan, Minnesota, New York,
Vermont, Washington, Wisconsin, and in Canada in Alberta, British Columbia, and
Saskatchewan.
Description:
Adults of the milfoil weevil are minute to
small (< 2.0 to < 4.5 mm long) in size, brown to black (mottled with
whitish or greenish to yellowish markings) and rather strongly convex. The body
is covered with hydrofuge scales completely concealing the cuticle in most
specimens. Typically, pale scales cover the suture and margins of the elytra,
and the midline and margins of the thorax, and form various maculae on the rest
of the elytra. Some western forms are nearly all black, with only a whitish
median macula and whitish margins as well. The dorsum of the thorax is undulate
and has a pair of lateromedian blunt processes behind the middle. The elytra are
striate (grooved) with evenly convex intervals, but the strial punctures are
often not visible due to the dense coating of scales. The rostrum is rather
short, nearly straight, and broadly cylindrical, and coated with hydrofuge
(satin like) scales except near the apex. The antennae are reddish yellow. The
funicle is six segmented. The eyes are round and strongly bulging with the frons
distinctly, broadly depressed between them. The prosternum is not sulcate. The
legs are long with the femora unarmed and moderately expanded to the apex. The
tibiae are nearly straight, apically expanding and lacking apical teeth. The
tarsi are long, with long fine sparse setae (setae as long as or longer than the
diameter of a tarsal segment). The last tarsal segment on the hind tarsi is
longer than the second and third segments together. The tarsal claws are free,
widely separated and moderately long.
Host Plants:
Eurasian watermilfoil (Myriophyllum
spicatum L.) and North American watermilfoils particularly northern
watermilfoil (M. sibiricum =
exalbescens).
Bibliography:
Newman, R.M., K.L. Holmberg, D.D. Biesboer and B.G. Penner.
1996. Effects of a potential biocontrol agent, Euhrychiopsis lecontei, on
Eurasian watermilfoil in experimental tanks. Aquatic Botany 53:
131-150.
Sheldon, S.P. and L.M. O’Bryan. 1996. Life history of the
weevil Euhrychiopsis lecontei, a potential biological control agent of
Eurasian watermilfoil. Entomological News 107: 16-22.
Solarz, S.L. and R.M. Newman. 1996. Oviposition specificity
and behavior of the watermilfoil specialist Euhrychiopsis
lecontei. Oecologia 106: 337-344.
Tamayo, M., C.W. O’Brien, R.P. Creed Jr., C.E. Grue, and K.
Hamel. 1999. Distribution and
classification of aquatic weevils (Coleoptera: Curculionidae) in the genus Euhrychiopsis in Washington State.
Entomological News 110: 103-112.
11. Eustenopus villosus (Boheman) - “Yellow
Starthistle Hairy Weevil”
Species
diagnostic characters:
Size: Medium-sized., > 4.5 mm < 10.0
mm
Body shape: Broadly oblong-oval
Predominant color (cuticle): Brown
Predominant color (setae): Brown to gray or
white
Rostral length: Long
Rostral width: Slender
Antennal morphology: Elbowed
Prothoracic collar: Raised (side view)
Prothoracic carina(e): Absent
Prothoracic tubercle(s): Present
Pronotal depression: Present
Pronotal depression orientation:
Longitudinal
Elytral carina(e): Absent
Elytral tubercle(s): Absent
Elytral spicule(s): Absent
Mesothoracic epipleuron: Not ascending and not visible in
dorsal view
Leg color (cuticle): Brown
Leg color (setae): Brown to gray
Trochanteral shape and length: Triangular and
short
Femoral armature: Unarmed
Tibial armature of apices: All with
spine
Third tarsus shape: Bilobed
Vestiture type: Setae
Vestiture coverage: Dense and
complete
Waterproof coating: Absent
Circular scales: Absent
Erect setae: Present
Wax like coating: Absent
Introduction:
Eustenopus villosus (Boheman) was introduced from Greece into California for
the biological control of yellow starthistle by the USDA-ARS in 1990. The insect
was established near Grass Valley (Nevada County) and Camino (El Dorado County)
in 1990 and Atlas Peak (Napa County), Potter Valley (Mendocino County), and
Round Mountain (Shasta County) in 1991 (Villegas, 2004). This species is also a
proven successful biological control agent for yellow starthistle in Arizona,
California, Idaho, Oregon, and Washington (Coombs et al., 2003). The species was
established readily in most areas of California, however, preferred the hotter
interior parts of the state over cooler climate (coastal, higher elevations and
latitudes) (Woods, 1998). In addition, high moisture and humidity may also be
unfavorable to this species.
The species has one generation per year, and adults
overwinter in the organic matter and litter at the base of previous-year stands
of yellow starthistle and emerge to feed on young and unopened buds as
temperatures warm up in May and June. Unlike other yellow starthistle natural
enemies, this damage can be very extensive and readily noticeable. The weevils
mate on top of the buds and the females lay individual eggs inside feeding holes
on the sides of mature buds from late May through July depending on the area in
California (Villegas, 2004). In about three days eggs hatch and the larvae begin
to feed on the developing seeds and receptacle tissues. After about two weeks,
larvae pupate in the pupal chambers. In another two weeks adult emerge and feed
on developing small flower heads.
Description:
Adults of the yellow starthistle hairy
weevil are medium-sized (> 4.5 mm < 10.0 mm long) and are broadly
oblong-oval in shape. The body color is light brown immediately upon eclosion
but turns dark brown later. The elytra and upper thorax are covered with very
long erect to suberect hairs which give it a hairy or fuzzy appearance. There
are two white stripes running along the entire length of the third and fourth
intervals and an even broader stripe on the margins of the ninth and tenth
intervals of the elytra. The snout is quite long, 2-3 mm in length and nearly
straight to weakly curved. The antennae are attached near the middle of the
snout, strongly elbowed, and distinctly clubbed. Males are smaller than females
(PMIS, 2003).
Host Plant: Yellow
starthistle, Centaurea solstitialis L.
Bibliography:
Coombs, E., J. Balciunas and P. McEvoy. 2003. Current
status in each state of all 100 agents approved for release in the continental
USA. Biological control of invasive plants in the United States. Corvallis, OR.,
Oregon University Press.
PMIS (Plant Management Information System). 2003. Noxious
and nuisance plant information system, ver. 5.3. Developed by Cofrancesco et al., (Cds and Web based. Available
from: http://el.erdc.usace.army.mil/pmis/ [Accessed 14 April
2006].
Villegas, B. 2004. Releases of the Hairy Weevil, Eustenopus
villosus, in California During 2000. California Department of Food and
Agriculture. Available from:
http://www.cdfa.ca.gov/phpps/ipc/biocontrol/annuals/2000annual/2000-28-euvi-rels.htm
[Access on 17 April 2006].
Woods, D.M. (Ed.). 1998. Biological Control Program Annual
Summary, 1997. California Department of Food and Agriculture, Plant Health and
Pest Prevention Services, Sacramento, California. 85pp.
12.
Exapion fuscirostre (Fabricius) - “Seed
Feeding Weevil”
[Type Species of
Exapion]
Species
diagnostic characters:
Size:
Small., > 2.0 mm < 4.5 mm
Body
shape: Elongate, Pear-shaped
Predominant color (cuticle): Black to reddish
brown
Predominant color (setae): White
Rostral
length: Moderately long
Rostral
width: Slender
Antennal
morphology: Straight
Prothoracic collar: Not raised (side
view)
Prothoracic carina(e): Absent
Prothoracic tubercle(s): Absent
Pronotal
depression: Present
Pronotal
depression orientation: Longitudinal
Elytral
carina(e): Absent
Elytral
tubercle(s): Absent
Elytral
spicule(s): Absent
Mesothoracic epipleuron: Not ascending and not visible in
dorsal view
Leg color
(cuticle): Brown
Leg color
(setae): Brown
Trochanteral shape and length: Rectangular and moderately
long
Femoral
armature: Unarmed
Tibial
armature of apices: All lack spine
Third
tarsus shape: Bilobed
Vestiture
type: Scales like setae
Vestiture
coverage: Dense and complete
Waterproof coating: Absent
Circular
scales: Absent
Erect
setae: Absent
Wax like
coating: Absent
Introduction: Exapion fuscirostre (Fabricius) was
introduced from Italy to the United States in 1964 and has established in both
coastal and Sierran broom (Julien, 1992). There are high populations of E. fuscirostre in the coastal mountains,
however, only small populations survive on Sierran plants. This is probably due
to mortality in pods exposed to high temperature (Julien, 1992). The seed feeding weevil is specific to scotch broom, Cytisus scoparius (L.) and will not feed
or develop on French broom (Andres, 1979). The weevil has become established in
California (widespread, > 50% of host range), Oregon (widespread, > 50% of
host range), and Washington (limited in host range, recovered in < 50% of
host range) (Coombs et al., 2003).
Adults feed on stems, while larvae feed on developing seeds inside pods. Despite
a 60% reduction in seed production at some sites, the weevil has a limited
impact on scotch broom (Rees et al.,
1996).
Description:
Adults of the seed feeding weevil are small (> 2.0 mm
< 4.5 mm long), elongate, pear-shaped, black to reddish brown, with pale
reddish antennae. The tarsi are dark reddish black to black. The body is covered
with coarse scale like setae. The primary dorsal color is brown to brassy brown,
due to the moderately coarse setae. The elytra have a pair of broad white
stripes of coarse scale like setae curving from the shoulders to the apex where
they connect with broad lateral white marginal stripes. The pleural area of the
thorax has similar white coarse scale like setae that also cover most of the
underside. The eyes are large, strongly convex and bulge outward on the small
head. The base of the thorax has a median elongate deep glabrous furrow, visible
as a short black line. The weakly curved rostrum is moderately long in both
sexes and is glabrous and shining black. The antennae are straight, and inserted
basally on the sides of the strongly expanded rostrum. The legs are long and
moderately slender. The femora are subclavate and the nearly straight tibiae are
expanded markedly from the base to the widened apex, which lacks any evident
teeth. The basal segment, of the hind tarsus of the male only, has a stout
ventral tooth. The tarsal claws are free, widely separated, basally toothed and
long.
Host Plant:
Scotch broom, Cytisus scoparius
(L.)
Bibliography:
Andres, L.A. 1979.
Biological control ‑ will it solve the broom problem? Fremontia 7(3):
9‑11.
Coombs, E., J. Balciunas and P. McEvoy. 2003. Current
status in each state of all 100 agents approved for release in the continental
USA. Biological control of invasive plants in the United States. Corvallis, OR.,
Oregon University Press.
Julien, M.H.
1992. Biological control of weeds:
A world catalogue of agents and their target weeds. C.A.B. International.
Third Edition. CSIRO, ACIAR, Australia. 186pp.
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, USDA/ARS, Montana Dept.
Agric., Montana State University, Bozeman, MT.
13.
Exapion ulicis (Forster) - “Gorse Seed Weevil”
Species
diagnostic characters:
Size: Minute to small., < 2.0 mm to < 4.5 mm
Body shape: Broad, Pear-shaped
Predominant color (cuticle): Reddish black to
black
Predominant color (setae): Whitish to golden
Rostral length: Moderately long
Rostral width: Slender
Antennal morphology: Straight
Prothoracic collar: Not raised (side view)
Prothoracic carina(e): Absent
Prothoracic tubercle(s): Absent
Pronotal depression: Present
Pronotal depression orientation:
Longitudinal
Elytral carina(e): Absent
Elytral tubercle(s): Absent
Elytral spicule(s): Absent
Mesothoracic epipleuron: Not ascending and not visible in
dorsal view
Leg color (cuticle): Black to reddish
black
Leg color (setae): Gray
Trochanteral shape and length: Rectangular and moderately
long
Femoral armature: Unarmed
Tibial armature of apices: All lack
spine
Third tarsus shape: Bilobed
Vestiture type: Scale like setae
Vestiture coverage: Dense and complete
Waterproof coating: Absent
Circular scales: Absent
Erect setae: Absent
Wax like coating: Absent
Introduction:
Exapion ulicis (Forster) feeds only on gorse, Ulex europaeus L. The species was selected in the
early 1920’s for research to determine its effectiveness as a biological control
agent. In the United States, it was released in 1926, 1949, 1951, and 1952 but
failed to establish. The gorse seed weevil was again brought into the United
States in 1953 from France (Holloway and Huffaker, 1957). Establishment was
finally successful after its release in Hawaii in 1953 (PMIS, 2003). Now this
species is established in California (widespread, > 50% of host range),
Oregon (widespread, > 50% of host range), Hawaii, and Washington (limited in
host range < 50% of host range) (Coombs et al., 2003). The species tends to do
better in open, sunny pastures and hillsides. Bronzing of foliage can be found
during summer, and conspicuous holes in flowers are made by adults searching for
oviposition sites. Females after chewing hole(s) lay eggs singly or in clusters
of up to 20 inside young green gorse pods. Larvae are white, squat, legless
grubs (2-5 mm long) with a very small, brown head. Pupae are found inside the
seed pod, and the newly formed pupae are white. As the pupae develop further,
their color generally changes to gray. Development from egg to adult takes
approximately 16 weeks. The eggs take 4 weeks to hatch, the larvae take 6-8
weeks to pupation, and pupae take 4 weeks to complete development within the
pods. The species is univoltine. When the pods are opened adult weevils are
released to feed on the spines and flowers (Cowley, 1983), sometimes defoliating
large plants. In California, the weevil has been successful only partially in
controlling gorse (Amme, 1983).
Description: Adults
of the gorse seed weevil are minute to small (< 2.0 mm to < 4.5 mm long),
rather broad, pear-shaped, reddish black to black weevils, which are densely
clothed with whitish to golden, often shining metallic, scale like setae. The
primary color is grayish white at low magnification. The elytra appear to be
striped due to the pale color of the setae on the broad intervals versus the
blackish narrow stripes of the striae (grooves) and their punctures. The base of
the thorax has a median small round shallow glabrous pit, which is scarcely
visible among the dense scale like setae. The eyes are large, strongly convex
and bulge outward on the relatively small head. The evenly curved, moderately
long, male rostrum and very long, female rostrum are glabrous and shining black.
The straight reddish brown antennae are inserted basally on the side of the
moderately expanded rostrum. The front legs are pale reddish, while the other
legs are dark colored with black femora and reddish black tibiae. The femora are
strongly clavate, while the tibiae are nearly straight and expanded markedly
from the base to the widened apex, which lacks any evident teeth. Male tarsi
lack a ventral tooth. The tarsal claws are free, widely separated, basally
toothed and moderately long.
Host Plant: Gorse,
Ulex europaeus L.
Bibliography:
Amme, D. 1983. Gorse control at Jughandle State Reserve:
resource restoration and development. Unpublished manuscript. The Nature
Conservancy, California Field Office, 785 Market Street, 3rd Floor, San
Francisco.
Coombs, E., J. Balciunas and P. McEvoy. 2003. Current
status in each state of all 100 agents approved for release in the continental
USA. Biological control of invasive plants in the United States. Corvallis, OR.,
Oregon University Press.
Cowley, J.M. 1983. Life cycle of Apion ulicis and gorse seed attack
around Auckland, New Zealand. N.Z. J. Zool. 10: 83-86.
Holloway, J.K. and C.B. Huffaker. 1957. Establishment of
the seed weevil, Apion ulicis for
suppression of gorse in California. J. Econ. Entomol. 50:
498-499.
PMIS (Plant Management Information System). 2003. Noxious
and nuisance plant information system, ver. 5.3. Developed by Cofrancesco et al., (Cds and Web based. Available
from: http://el.erdc.usace.army.mil/pmis/ [Accessed 14 April
2006].
14. Gasteroclisus tricostatus
(Thunberg)
Species
diagnostic characters:
Size: Medium-sized., > 4.5 mm < 10.0
mm
Body shape: Elongate-oval
Predominant color (cuticle): Dark brown to
black
Predominant color (scales): Strongly mottled, bicolored or
tricolored
Predominant color (setae): Gray
Rostral length: Moderately long
Rostral width: Slender
Antennal morphology: Elbowed
Prothoracic collar: Not raised (side
view)
Prothoracic carina(e): Present
Prothoracic tubercle(s): Absent
Pronotal depression: Absent
Elytral carina(e): Absent
Elytral tubercle(s): Absent
Elytral spicule(s): Absent
Mesothoracic epipleuron: Not ascending and not visible in
dorsal view
Leg color (cuticle): Dark brown
Leg color (setae): Gray
Trochanteral shape and length: Triangular and
short
Femoral armature: Unarmed
Tibial armature of apices: All with
spine
Third tarsus shape: Bilobed
Vestiture type: Scales and setae
Vestiture coverage: Dense, in bands or
patches
Waterproof coating: Absent
Circular scales: Absent
Erect setae: Absent
Wax like coating: Present
Introduction:
In the United States, the original colonies were brought in
the quarantine in 1999 from Pietermaritzburg, South Africa, to control the
serious weed pest, Madagascar ragwort, Senecio madagascariensis Poir. This
distinctive weevil was reared in the quarantine for 2-3 years in Hawaii. The
larvae develop in the stems of the host plant. The weevil was discarded in the
quarantine because it was not successful in controlling the weed (Bernarr
Kumashiro, pers. comm.). The weevil is regarded as a successful biological
control agent of Madagascar ragwort in its native habitats in South Africa,
therefore, further study is needed to know its biology, ecology and
effectiveness under field conditions. Currently, the species is considered
without a common name.
Description: Adults of this
medium-sized (> 4.5 mm < 10.0 mm long) weevil are quite slender and
elongate-oval. Freshly emerged and carefully handled specimens are coated with a
dense wax like secretion, both orange-brown and white in places on the
body. The pleural area of the
prothorax is separated from the dorsum by a pair of angled longitudinal carinae
separating them from each other.
The pleural area is strongly impressed and visible in dorsal view and
usually coated with a dense white colored wax-like secretion. The addition of a
median longitudinal prothoracic carina to the two lateral carinae explains the
specific name, tricostatus and these
are not to be found on any other North American weevil species. The elytra are
narrowed apically and these are produced as two widely separated variously acute
processes.
Host
Plant: Madagascar regwort, Senecio madagascariensis
Poir.
15. Gymnetron antirrhini
(Paykull) - “Seed-gall Weevil”
Species
diagnostic characters:
Size: Small., > 2.0 mm < 4.5 mm
Body shape: Broad-oval
Predominant color (cuticle): Black
Predominant color (setae): Brown
Rostral length: Moderately long
Rostral width: Slender
Antennal morphology: Elbowed
Prothoracic collar: Not raised (side view)
Prothoracic carina(e): Absent
Prothoracic tubercle(s): Absent
Pronotal depression: Absent
Elytral carina(e): Absent
Elytral tubercle(s): Absent
Elytral spicule(s): Absent
Mesothoracic epipleuron: Not ascending and not visible in
dorsal view
Leg color (cuticle): Black
Leg color (setae): Brown
Trochanteral shape and length: Triangular and
short
Femoral armature: Toothed
Tibial armature of apices: All with
spine
Third tarsus shape: Bilobed
Vestiture type: Setae
Vestiture coverage: Dense and
complete
Waterproof coating: Absent
Circular scales: Absent
Erect setae: Present
Wax like coating: Absent
Introduction: The
native range of Gymnetron antirrhini Paykull extends from North
Africa to the northern limit of yellow toadflax, Linaria vulgaris P.Mill., however, it is
scarce in southwestern Europe. The species was accidentally introduced into
North America after 1900, especially through infested ornamental plants. The species is established in Canada
with apparently stable host preferences for narrow-leaved or broad-leaved
dalmatian toadflax or yellow toadflax. A "strain" of G. antirrhini
presumably more host-specific to dalmatian toadflax was approved for release in
the United States in 1995. In Washington State the species was reported to be
equally abundant on narrow-leaved dalmatian and yellow toadflax, but not on
broad-leaved dalmatian toadflax. Broad-leaved dalmatian toadflax is attacked
locally in Saskatchewan (Smith, 1959) and broad-leaved dalmatian toadflax
populations of both weevils from Yugoslavia, released in 1993, are surviving in
British Columbia. The yellow-toadflax population was released in Alberta and
Saskatchewan in 1957 and is now established across Canada (Harris and Gassmann,
2005). The larvae develop inside the fruit, and adults feed on leaves, buds and
stems. Harris (1961) concluded that G. antirrhini is the most important
agent for biological control of Linaria vulgaris P.Mill. in the eastern
provinces of Canada, British Columbia, and the northwestern United
States.
Description: Adults
of the seed-gall weevil are small (> 2.0 mm < 4.5 mm long) in size,
broad-oval in shape, black in color with a strongly attenuate and weakly curved
rostrum, The rostrum is nearly straight, but curved downward at the antennal
insertion, due to the strong attenuation of the rostrum apicad of the insertion.
The rostrum is 2/3 to 3/4 as long as the pronotum. The elytral striae are 1/2 to 2/3 as wide as the
intervals. The femora are equal
sized and each have a minute tooth. The eltra and prothorax are covered densely
with mainly erect to suberect dark colored setae. Each egg is a flattish oval,
0.49 x 0.27 mm long and is inserted into a round hole and usually covered by a
yellow secretion. Larvae are about 2-5 mm long, legless, and C-shaped when
viewed from the side. They are creamy-white in color with a tan head
capsule.
Host Plants: Snapdragon, Antirrhinum majus L.; lesser snapdragon, A.
orontium L.; dwarf
snapdragon, Chaenorrhinum minus., dalmatian toadflax, Linaria
dalmatica L. Mill.,
L. genistifolia L., L. repens (L.) Miller, L.
tourneforti (Poir); and
yellow toadflax, L. vulgaris P.Mill.
Bibliography:
Harris, P. 1961. Control of toadflax by Brachypterolus
pulicatius (L.) (Coleoptera: Nitidulidae) and Gymnetron antirrhini
(Paykull.) (Coleoptera: Curculionidae) in Canada. Canadian Entomologist 93:
977-981.
Harris, P. and A. Gassmann. 2005. Classical biological
control of weeds, established biocontrol agents. Gymnetron antirhini Paykull and G. netum Germar Seed-gall Weevils.
Available from http://res2.agr.ca/lethbridge/weedbio/agents/agymnet_e.htm
[Accessed 18 April 2006].
Smith, J.M. 1959. Notes on insects, especially Gymnetron
spp. (Coleoptera: Curculionidae), associated with toadflax, Linaria
vulgaris Mill. (Scrophulariaceae), in North America. Canadian Entomologist
91: 116-121.
16. Gymnetron linariae
(Panzer) - “Root-gall Weevil”
Species
diagnostic characters:
Size: Small., > 2.0 mm < 4.5 mm
Body shape: Broad-oval
Predominant color (cuticle): Black
Predominant color (setae): Whitish gray
Rostral length: Long
Rostral width: Slender
Antennal morphology: Elbowed
Prothoracic collar: Not raised (side view)
Prothoracic carina(e): Absent
Prothoracic tubercle(s): Absent
Pronotal depression: Present
Pronotal depression orientation:
Longitudinal
Elytral carina(e): Absent
Elytral tubercle(s): Absent
Elytral spicule(s): Absent
Mesothoracic epipleuron: Not ascending and not visible in
dorsal view
Leg color (cuticle): Black
Leg color (setae): Gray
Trochanteral shape and length: Triangular and
short
Femoral armature: Toothed
Tibial armature of apices: All with
spine
Third tarsus shape: Bilobed
Vestiture type: Setae
Vestiture coverage: Dense and
complete
Waterproof coating: Absent
Circular scales: Absent
Erect setae: Absent
Wax like coating: Absent
Introduction:
Gymnetron linariae (Panzer) which is native to Europe was approved for
release in the United States in 1995 (Hansen, 1998). Several releases have been
made in western Canada and the United States; small populations may be
established in Canada, but only one confirmed establishment in Wyoming has been
reported on Linaria genistifolia L.
in the United States (Coombs et al.,
2003). The species appears in late spring. After feeding for several weeks on
toadflax shoots, adults mate and females oviposit on roots. Eggs are deposited
singly in small pockets chewed (into the root tissue) by the female and covered
with excrement. Most eggs are laid in the root crown area. After hatching,
larvae feed inside galls formed on the roots and their development with three
instars, takes two to three months. Also pupation occurs within the galls during
summer. Newly emerged adults may remain within the galls and enter diapause,
while others may emerge and feed on toadflax shoots for 7-14 days before
returning to the soil to overwinter. There is one generation known to occur in a
year (Jordan, 1994; Hansen, 1998).
Description:
The adults of the root-gall weevil are
small (> 2.0 mm < 4.5 mm long), with dark brown to pale brown tarsi and
antennae. They have a strongly curved rostrum, clearly attenuate towards the
apex and as long as the pronotum. The lack of erect setae readily separates this
species from the other Gymnetron. It possesses only whitish gray,
recumbent, scale like setae on the prothorax and elytra. The margins of the
pronotum are strongly, unevenly rounded near the middle. The femora are
moderately swollen and have a minute inner tooth, easily missed due to the
coarse long scale like setae, which often conceal it. Larvae are small, legless,
and C-shaped. They are creamy-white in color with a yellowish head
capsule.
Host
Plants:
Yellow
dalmatian, Linaria vulgaris P.Mill., dalmatian toadflax Linaria genistifolia L. (= L.
dalmatica L.Mill.).
Bibliography:
Coombs, E., J. Balciunas and P. McEvoy. 2003. Current
status in each state of all 100 agents approved for release in the continental
USA. Biological control of invasive plants in the United States. Corvallis, OR.,
Oregon University Press.
Hansen, R. 1998. Gymnetron Linariae Panzer (Coleoptera:
Curculionidae). USDA-APHIS-PPQ, Forestry
Science Lab, Montana State University, MT. Available from
http://www.nysaes.cornell.edu/ent/biocontrol/weedfeeders/gymnetron_linariae.html
[Accessed 18 April 2006].
Jordan, K. 1994. Gymnetron linariae. Panzer (Col.,
Curculionidae), a candidate for biological control of dalmatian and yellow
toadflax in North America. Intl. Inst. of Biol. Control European Station Final
Report. 37pp.
17.
Gymnetron tetrum (Fabricius) - “Mullein Seed Head Weevil”
Species
diagnostic characters:
Size:
Small:. > 2.0 mm < 4.5 mm
Body
shape: Broad, round-oval
Predominant color (cuticle): Black
Predominant color (setae): Brassy metallic
Rostral
length: Long
Rostral
width: Slender
Antennal
morphology: Elbowed
Prothoracic collar: Not raised (side view)
Prothoracic carina(e): Absent
Prothoracic tubercle(s): Absent
Pronotal
depression: Present
Pronotal
depression orientation: Longitudinal
Elytral
carina(e): Absent
Elytral
tubercle(s): Absent
Elytral
spicule(s): Absent
Mesothoracic epipleuron: Not ascending and not visible in
dorsal view
Leg color
(cuticle): Black
Leg color
(setae): Gray
Trochanteral shape and length: Triangular and
short
Femoral
armature: Toothed
Tibial
armature of apices: All with spine
Third
tarsus shape: Bilobed
Vestiture
type: Setae
Vestiture
coverage: Dense and complete
Waterproof coating: Absent
Circular
scales: Absent
Erect
setae: Present
Wax like
coating: Absent
Introduction:
Gymnetron tetrum
(Fabricius) was in the United States before 1876 when it was reported from
Pennsylvania as a European introduction by LeConte and Horn (O’Brien Pers.
Comm.). Blatchley and Leng (1916)
indicated its range from Canada and
New England to Iowa, north of Georgia and Arkansas. The species has been
reported in Montana, Washington, and California where it controls Verbascum thapsus L. and it has been
accidentally introduced into western Canada. It feeds on the seeds and has been
found effective in reducing seed production throughout its range. As an
introduction, and movement by man, the weevil has no natural range in the New
World. The larvae feed on seeds and other tissues in the seed capsules. Larvae
are able to destroy all seeds in a capsule; however, usually not all seed
capsules are infested. Gross and Werner (1978) reported that up to 50 percent of
seeds may be destroyed by the larval feeding of this species. The species
oviposits in the flowers, and the developing larvae effectively
destroy most of the seeds (Reinartz, 1984). However, weevil activity
is confined largely to the first few weeks of the flowering season.
Weevils are primarily found on larger plants within a
population.
Description:
Adults of mullein seed head weevil are
broad, round-oval and flattened above. They are small (> 2.0 mm < 4.5 mm
long) in size. The erect and recumbent, dense pubescence nearly conceals the
shining black body. The setae and scalelike setae often have a brassy metallic
color. The rostrum is straight and very strongly attenuate, and nearly as long
as or longer than the pronotum. The erect to suberect pubescence is equally
dense on the basal half of the rostrum, the legs, and the underside of the body.
The femur of the front leg is toothed strongly only in the males. The femora are
strongly dilated and toothed.
Host Plant: Flannel
mullein/common mullein/flannelplant, Verbascum thapsus
L.
Bibliography:
Gross, K.L. and P.A. Werner. 1978. The biology of Canadian
Weed. 28, Verbascum thapsus L. and V. blattaria L. Can. J. Plant Sci. 58:
401-413.
Reinartz, J.A. 1984. Life history variation of common
mullein (Verbascum thapsus). I. Latitudinal differences in population
dynamics and timing of reproduction. Journal of Ecology 72:
897–912.
18. Hadroplontus litura (Fabricius) - “Canadian
Thistle Stem Weevil”
[Type Species of
Hadroplontus]
Species
diagnostic characters:
Size: Small., > 2.0 mm < 4.5 mm
Body shape: Broad-oval
Predominant color (cuticle): Dark
gray
Predominant color (scales): White
Rostral length: Long
Rostral width: Slender
Antennal morphology: Elbowed
Prothoracic collar: Raised (side
view)
Prothoracic carina(e): Absent
Prothoracic tubercle(s): Present
Pronotal depression: Absent
Elytral carina(e): Absent
Elytral tubercle(s): Absent
Elytral spicule(s): Present
Mesothoracic epipleuron: Ascending and visible in dorsal
view
Leg color (cuticle): Dark brown
Leg color (scales): White
Leg color (setae): Brown
Trochanteral shape and length: Triangular and short
Femoral armature: Toothed
Tibial armature of apices: All lack spine
Third tarsus shape: Bilobed
Vestiture type: Scales
Vestiture coverage: Dense and complete
Waterproof coating: Absent
Circular scales: Present
Erect setae: Absent
Wax like coating: Absent
Introduction:
Hadroplontus litura (Fabricius) is
a stem boring weevil which is native to Atlantic Europe (southern France to
southern Scandinavia), and was introduced to Canada in 1965 and to the United
States in the early 1970s to control Canada thistle (Evans, 1993). The species
is established in the provinces of
Alberta, British Columbia, Nova Scotia, Ontario, and Saskatchewan (Harris,
2005). In California and Colorado it failed to establish on Cirsium
arvense. However, it established
in Idaho, Nebraska, North Dakota, Oregon, Virginia, Utah, Washington, and
Wyoming (Coombs et al., 2003). One of the major constraints
in the widespread use of this species as a biological control agent for Canada
thistle was the inability to collect adults for mass redistribution. Females can
lay a group of 1-5 eggs in small cavities in the leaf tissues or in the mid vein
on the underside of the young leaf. Eggs are deposited from March or April until
mid-May, generally until plants are about 5 cm tall, after this time the plant
becomes undesirable for egg laying. Each female lays an average of 120 eggs,
generally on the smaller younger shoots. The newly hatched larvae mine the
tissues of the leaf toward the main vein. Older larvae mine the stem, root
crown, and root. There are three larval instars. Larvae are whitish, grub-like,
and pointed at the rear end. The larvae leave the plant at the end of the third
instar to pupate in an oval cocoon of soil particles about 4-6 mm in diameter.
Adults can be found in the field from August until the following May or June,
and, in some areas, July. Adults overwinter in the soil litter and can even
tolerate spring flooding. There is only one generation per year (PMIS, 2003).
The weevils can be found in habitats with disturbed areas, where thistle density
is high and not affected by grazing, mowing, flooding or even
herbicides.
Description:
Adults of the
Canadian thistle stem weevil are small (>
2.0 mm < 4.5 mm long) in size. The underside is white and the back is dark
gray with a yellowish white cross at the center of the wings. This and other
disruptive white patterns make the weevil almost invisible on the soil (Harris,
2005). They have a long snout and a white haired T-shaped marking on their back
which is quite prominent.
Host Plants:
Canada
thistle, Cirsium arvense
(L.) Scop., and Carduus defloratus
L.
Bibliography:
Coombs, E., J. Balciunas and P. McEvoy. 2003. Current
status in each state of all 100 agents approved for release in the continental
USA. Biological control of invasive plants in the United States. Corvallis, OR.,
Oregon University Press.
Evans, E.W. 1993. Biological control agents for Utah weeds:
Ceutorhynchus litura, a stem-mining
weevil of Canada thistle. Fact sheet No. 92. Utah State University, Extension
Entomology. 1-4.
Harris, P. 2005. Classical biological control of weeds,
established biological control agents. Hadroplontus litura F. Stem Weevil.
Available from: http://res2.agr.ca/lethbridge/weedbio/agents/aceutlit_e.htm
[Accessed 17 April 2006].
PMIS (Plant Management Information System). 2003. Noxious
and nuisance plant information system, ver. 5.3. Developed by Cofrancesco et al., (Cds and Web based. Available
from: http://el.erdc.usace.army.mil/pmis/ [Accessed 14 April 2006].
19. Heilipodus ventralis
(Hustache) - “Argentine Root Boring Weevil”
Species
diagnostic characters:
Size: Medium-sized to large., > 4.5 mm to > 10.0
mm
Body
shape: Elongate-oval
Predominant color (cuticle): Dark
brown
Predominant color (scales): Brown
Rostral
length: Long
Rostral
width: Slender
Antennal
morphology: Elbowed
Prothoracic collar: Not raised (side view)
Prothoracic carina(e): Absent
Prothoracic tubercle(s): Present
Pronotal
depression: Present
Pronotal
depression orientation: Longitudinal
Elytral
carina(e): Absent
Elytral
tubercle(s): Present
Elytral
spicule(s): Absent
Mesothoracic epipleuron: Not ascending and not visible in
dorsal view
Leg color
(cuticle): Reddish brown
Leg color
(scales): Brown
Trochanteral shape and length: Triangular and
short
Femoral
armature: Toothed
Tibial
armature of apices: All with spine
Third
tarsus shape: Bilobed
Vestiture
type: Scales
Vestiture
coverage: Dense, in bands or patches
Waterproof coating: Absent
Circular
scales: Absent
Erect
setae: Absent
Wax like
coating: Absent
Introduction:
Heilipodus ventralis (Hustache) was named as a potential biological control
agent of poisonous native weeds (perennial snakeweeds) of rangelands of the
southern United States in the genus Gutierrezia (Cordo et al.,
1999). These authors also recorded the life history and ecology of H.
ventralis in Argentina and discussed its potential as a biological
control agent for snakeweed in North America. Adult weevils emerge from the
taproots in early summer and lay eggs mostly in the crown near the soil line.
The larvae tunnel down to the taproots where they pupate. They may overwinter in
the taproots of the snakeweed and pupate in the spring. A generation usually
requires one year, however, some individuals probably require two growing
seasons. No predators or parasitoids have been recorded on this
species.
Heilipodus ventralis
occurs in climatic zones of Argentina that
they are very similar to much of the area infested by Gutierrezia in North America. This type
of infestation apparently does not occur, or is rare, in northern Argentina,
which is climatically more similar to the southern range of Gutierrezia in central and northern
Mexico. Also, the northern area infested by Gutierrezia in Wyoming and Montana is
colder than that of the most southern areas of Argentina where H.
ventralis occurs (Chubut Province) (Cordo et al., 1999).
H. ventralis would appear to have a reasonable chance for reducing
the present abundance of snakeweeds in North America. Trials in quarantine at
Temple, Texas showed that the insect was sufficiently host specific for
introduction and it was released in New Mexico and Texas in May and August
1998.
Description: The
adults of the Argentine root boring weevil are medium-sized to large (> 4.5
mm to > 10.0 mm long) in size. Males and females are very similar in shape,
although females are usually a little larger than the males. Hustache (1938)
described H. ventralis from Argentina and it is known only from
Argentina and Paraguay (Wibmer and O’Brien, 1986). Adults are dark brown in
color with white, yellow, and dark spots that make the insect inconspicuous in
its habitat at the base of the host plants. The most obvious character for
separating the sexes is the shape of the two tibial teeth of the forlegs; in the
male, the proximal tooth is much shorter than the distal tooth; in the female,
the difference in length of the tibial teeth is minimal. Also, the color of the
leg (cuticle) is reddish brown and the color of scales on the leg is
brown.
Host Plants:
Perennial snakeweeds: Broom snakeweed,
Gutierrezia sarothrae (Pursh) Britton; and Rusby, and sticky snakeweed,
G. microcephala (De-Candolle).
Bibliography:
Cordo, H.A., C.J. DeLoach and D.H. Habeck. 1999. Biology of
Heilipodus ventralis (Coleoptera: Curculionidae), an Argentine weevil for
biological control of snakeweeds (Gutierrezia spp.) in the United States.
Biological Control 15:
210-227.
Hustache, A. 1938.
Curculionides nouveaux de l’ Amérique méridionale, que se trouvent dans le
Deutsches Entomologisches Institut 3ieme note. Arb. Morph. Tax. Ent. Berlin-Dahlem, 5(4):
334-349.
Wibmer, G.J. and C.W. O’Brien. 1986. Annotated checklist of
weevils (Curculionidae sensu lato) of South America (Coleoptera:
Curculionoidea). Mem. Am. Entomol. Inst. 39: 563pp.
20. Hylobius
transversovittatus (Goeze) - “Root-feeding Weevil”
Species
diagnostic characters:
Size:
Large., > 10.0 mm
Body
shape: Elongate-oval
Predominant color (cuticle): Reddish
black
Predominant color (scales): White
Predominant color (setae): Pale
Rostral
length: Long
Rostral
width: Slender
Antennal
morphology: Elbowed
Prothoracic collar: Not raised (side view)
Prothoracic carina(e): Absent
Prothoracic tubercle(s): Present
Pronotal
depression: Present
Pronotal
depression orientation: Longitudinal
Elytral
carina(e): Absent
Elytral
tubercle(s): Present
Elytral
spicule(s): Absent
Mesothoracic epipleuron: Not ascending and not visible in
dorsal view
Leg color
(cuticle): Reddish black
Leg color
(setae): Pale
Trochanteral shape and length: Triangular and
short
Femoral
armature: Toothed
Tibial
armature of apices: All with spine
Third
tarsus shape: Bilobed
Vestiture
type: Scales and setae
Vestiture
coverage: Dense, in bands or patches
Waterproof coating: Absent
Circular
scales: Absent
Erect
setae: Absent
Wax like
coating: Absent
Introduction:
Hylobius
transversovittatus (Goeze) is native to
Europe and was introduced in the United States in 1992 to control purple
loosestrife (Malecki et al., 1993). This species has been released in
numerous states in the United States (Coombs et al., 2003). After that, releases were
made in Ohio, Indiana, Illinois, Iowa, Michigan, Wisconsin, South Dakota,
Colorado and Montana. Colonization of this introduced species appears to have
been successful (Blossey et al., 1994). Within two years after their
release, 18 of the 19 releases in nine States and two Canadian Provinces showed
initial establishment or colonization (Hight et al., 1995; Piper 1996).
The species occurs in all purple loosestrife habitats, except for permanently
flooded areas. Experiments have shown that adults and larvae can survive
extended submergence depending on prevailing temperature. However, excessive
flooding prevents access by the adult weevil and eventually kills developing
larvae.
Most of the adults emerge in spring from soil or soil litter and are
nocturnal. They usually feed on new leaves of purple loosestrife. Damaged leaves
show symptoms of adult feeding on leaf edges. Peak activity is reported from
June to August. Eggs are laid singly and each female can lay up to 200 eggs in
her life span. A female can lay 1-3 eggs daily into the plant stem or near a
root. After hatching, larvae start mining down to the roots where they feed on
root tissues. Larval development is completed in 1-2 years. Mature larvae form a
pupation chamber in the upper part of the root. Larvae can hibernate at
different stages of maturity. Adults usually emerge between July and October and
may live for several years (Kok et
al., 1992; Malecki et al., 1991).
Description:
Adults of the root-feeding weevil are large (>
10.0 mm long) in size, and are similar in appearance to Heilipodus, but
are less convex above and have two distinct, undulate, transverse bands of white
strap like scales on the back. The rest of the surface has much sparser, much
finer scales and setae, which do not cover the reddish black body color. The
body punctures, especially those on the thorax, are very coarse and very deep,
and each puncture has either a strap like scale or more often a seta projecting
from it. The rostrum is long and evenly curved. The femora of all legs have a
strongly developed acute tooth and the tibiae have only a single, strong, inner,
apical tooth.
Host Plant:
Purple loosestrife, Lythrum
salicaria L.
Bibliography:
Blossey, B., D. Schroeder, S.D. Hight and R.A. Malecki
(1994). Host specificity and environmental impact of the weevil Hylobius
transversovittatus, a biological control agent of purple loosestrife
(Lythrum salicaria), Weed Sci. 42: 128-133.
Coombs, E., J. Balciunas and P. McEvoy. 2003. Current
status in each state of all 100 agents approved for release in the continental
USA. Biological control of invasive plants in the United States. Corvallis, OR.,
Oregon University Press.
Hight, S.D., B. Blossey, J. Laing and R. DeClerck-Floate.
1995. Establishment of insect biological control agents from Europe against
Lythrum salicaria in North America. Environ. Entomol. 24:
967-977.
Kok, L.T., T.J. McAvoy, R.A. Malecki, S.D. Hight, J.J. Drea
and J.R. Coulson. 1992. Host specificity tests of Hylobius transversovittatus Goeze
(Coleoptera: Curculionidae), a potential biological control agent of purple
loosestrife, Lythrum salicaria L.
(Lythraceae). Biological Control 2: 1-8.
Malecki, R.A., B. Blossey, S.D. Hight, D. Schroeder, L.T.
Kok and J.R. Coulson. 1993. Biological control of purple loosestrife: A case
study for using insects as control agents, after rigorous screening, and for
integrating release strategies with research. BioScience 43:
680-686.
Malecki, R.A., S.D. Hight, L.T. Kok, D. Schroeder and J.R.
Coulson. 1991. Information for the preparation of an environmental assessment.
Plant Protection and Quarantine, APHIS, USDA. 79pp.
Piper, G.L. 1996. Biological control of the wetlands weed
purple loosestrife (Lythrum salicaria) in the Pacific northwestern United
States. Hydrobiologia 34: 291-294.
21. Larinus curtus (Hochhut)
- “Flower Weevil”
Species
diagnostic characters:
Size:
Small., > 2.0 mm < 4.5 mm
Body
shape: Broad-oval
Predominant color (cuticle): Black
Predominant color (setae): Gray, Metallic, bronzed
Rostral
length: Moderately short
Rostral
width: Broad
Antennal
morphology: Elbowed
Prothoracic collar: Not raised (side view)
Prothoracic carina(e): Absent
Prothoracic tubercle(s): Absent
Pronotal
depression: Absent
Elytral
carina(e): Absent
Elytral
tubercle(s): Absent
Elytral
spicule(s): Absent
Mesothoracic epipleuron: Not ascending and not visible in
dorsal view
Leg color
(cuticle): Dark reddish brown
Leg color
(setae): Gray to bronze
Trochanteral shape and length: Triangular and
short
Femoral
armature: Unarmed
Tibial
armature of apices: All with spine
Third
tarsus shape: Bilobed
Vestiture
type: Setae
Vestiture
coverage: Dense and complete
Waterproof coating: Absent
Circular
scales: Absent
Erect
setae: Absent
Wax like
coating: Absent
Introduction: Larinus curtus (Hochhut) was introduced
from Greece into California, Idaho, Oregon, and Washington from 1992 to 1994 by
the USDA-ARS for the biological control of yellow starthistle, Centaurea solstitialis (Villegas, 2004).
The species is established in California, Idaho, Oregon, and Washington (Coombs
et al., 2003). The insect likes to
live in cool climates particularly at higher elevations and latitudes and near
the coastal areas. This weevil oviposits inside open flowers of a yellow
starthistle and the larvae feed directly on the seeds. A single larva can
consume most of the seeds in the seedheads of yellow starthistle. Larval
development may be completed in 17-20 days. Pupation occurs in damaged seeds and
the pupal period is completed in 4-5 days. Adults feed on the plants from late
June to early August. They overwinter away from their host plants. The species
has one generation per year (PMIS, 2003).
Description:
Adults of the
flower weevil are small (> 2.0 mm < 4.5 mm long) in size. Adult-body with entire underside densely covered with
multiradiate setae divided to their bases. Rostrum moderately short and stout,
gradually widening from base to apex, coarsely rugose; frons with punctures
merging in short sulci in places. Pronotum subconical, with sides in basal half
nearly straight, moderately converging at the anterior. Anterior margin of
pronotum behind eyes straight, not forming rounded prominences (postocular
lobes). Elytra at base noticeably wider than pronotum, usually narrowing from
base to apex. Pubescence of dorsal surface noticeably raised. Legs usually
reddish brown, rarely femora black. Fore tibia lacking sharp granules on inner
margin; in females, without large, very broad, nearly lobe-shaped prominence
adjacent to the sharp, narrow and long mucro.
Host Plant:
Yellow starthistle, Centaurea
solstitialis L.
Bibliography:
Coombs, E., J. Balciunas and P. McEvoy. 2003. Current
status in each state of all 100 agents approved for release in the continental
USA. Biological control of invasive plants in the United States. Corvallis, OR.,
Oregon University Press.
PMIS (Plant Management Information System). 2003. Noxious
and nuisance plant information system, ver. 5.3. Developed by Cofrancesco et al., (Cds and Web based. Available
from: http://el.erdc.usace.army.mil/pmis/ [Accessed 14 April
2006].
Villegas, B. 2000. Releases of the flower weevil, Larinus curtus, for the biological
control of yellow starthistle in California in 2000. CDFA Biological Program
Annual Report 2000.
22. Larinus minutus Gyllenhal
- “Seedhead Weevil”
Species
diagnostic characters:
Size:
Small to medium-sized., > 2.0 mm < 10.0 mm
Body
shape: Broad-oval
Predominant color (cuticle): Black
Predominant color (setae): Gray
Rostral
length: Moderately short
Rostral
width: Moderately broad
Antennal
morphology: Elbowed
Prothoracic collar: Not raised (side view)
Prothoracic carina(e): Absent
Prothoracic tubercle(s): Absent
Pronotal
depression: Absent
Elytral
carina(e): Absent
Elytral
tubercle(s): Absent
Elytral
spicule(s): Absent
Mesothoracic epipleuron: Not ascending and not visible in
dorsal view
Leg color
(cuticle): Pale reddish brown
Leg color
(setae): Gray
Trochanteral shape and length: Triangular and
short
Femoral
armature: Unarmed
Tibial
armature of apices: All with spine
Third
tarsus shape: Bilobed
Vestiture
type: Setae
Vestiture
coverage: Dense and complete
Waterproof coating: Absent
Circular
scales: Absent
Erect
setae: Absent
Wax like
coating: Absent
Introduction:
Larinus minutus Gyllenhal was proven to be host specific and was imported
from Greece for release in the United States and Canada in 1991 (Lang, 1997). On
diffuse knapweed, Centaurea diffusa
Lam., the species is established in California, Colorado, Montana, Nebraska,
Nevada, Oregon, Utah, Washington, and Wyoming while on squarrose knapweed, C. virgata Lam., the species is established
in California and Utah (Coombs et
al., 2003). This weevil species is considered to be the most impressive
biological control agent against diffuse knapweed. The insect has a significant
impact on the plant growth and density in the Pacific Northwest (Story and
Piper, 2001).
Adults are strong fliers and disperse throughout the entire knapweed
patch in several years. They spend the winter in plant litter within the
knapweed patch. Adults are active in the field from May or June until August.
Mating occurs continuously during this 11-week period. Adults feed on the leaves
(including rosette leaves in the spring), outer stem tissue and flowers, prior
to laying eggs (Lang, 1997). Eggs are deposited in the seedhead between the
pappus hairs. Up to five eggs are clustered; the number of eggs laid per female
ranges between 28 and 130. Eggs hatch three days later and the newly hatched
larvae feed on the pappus hairs, then move downward to consume seeds, and
partially the receptacle. Feeding lasts about four weeks as larvae go through
three instars. The number of L. minutus larvae a seedhead can support
depends on the size of the seedhead and the knapweed species. The larva
constructs a pupal chamber (partly from seed coats) attached to the flower base
and pupate there. New adults emerge and feed on foliage and flowers before
moving to overwintering sites at the base of the plants.
Description: Adults of the seedhead weevil
are small to medium-sized (> 2.0 mm < 10.0 mm long), black in color, have a moderately short robust snout and
are a soft seed-feeder like the Terellia virens (Loew) [Diptera: Tephritidae] and
Larinus obtusus. Eggs are elongate, yellow and are often clustered in the
seedhead between pappus hairs. Larvae are typical white, legless, C-shaped grubs
with brown head capsules which undergo through three larval instars and reach a
length of approximately 8 mm. Pupae are about 6 mm long, and white, turning
brown shortly before emergence and generally resemble the adult weevil. Tibiae
are always reddish brown, usually light reddish brown; femora more or less
infuscate but at least the middle and hind femora always are with a brownish
tint. The underside of the head and postocular area are clothed with bi-and
tri-radiate scales, sides of meso-and meta-thorax with numerous such scales.
Legs covered with long semierect hair-like setae or hairs. Inner margin of the
fore tibia in female with shorter obtuse or bifurcate tooth adjacent to and not
more than half as long as mucro. The aedeagus has a membraneous, nonsclerotized
dorsal surface. The body narrower, usually parallel-sided in middle part, and
often more or less shining; the pronotum and elytra have longer, more strongly
raised and uniform pubescence, often producing no distinct maculae on the elytra
(Korotyaev, Pers. Comm.).
Host Plants: Spotted
knapweed; Centaurea stoebi Lam. (formerly maculosa), diffuse knapweed, C.
diffusa Lam., and squarrose knapweed, C. virgata Lam.
Bibliography:
Coombs, E., J. Balciunas and P. McEvoy. 2003. Current
status in each state of all 100 agents approved for release in the continental
USA. Biological control of invasive plants in the United States. Corvallis, OR.,
Oregon University Press.
Lang, R.F. 1997. USDA-APHIS-PPQ, Bozeman Biocontrol
Facility, Forestry Sciences Laboratory, Montana State University, Bozeman, MT
59717. Available from:
http://www.nysaes.cornell.edu/ent/biocontrol/weedfeeders/larinus_minutus.html
[Accessed 19 April 2006].
Story, J.M. and G.L. Piper. 2001. Status of biological
control efforts against spotted and diffuse knapweed, 11-16pp. In L.
Smith (ed.), the First International Knapweed Symposium of the Twenty-First
Century, Idaho.
23. Larinus obtusus
(Gyllenhal) - “Seedhead Weevil”
or “Blunt
Knapweed Flower Weevil”
Species
diagnostic characters:
Size:
Small to medium-sized., > 2.0 mm < 10.0 mm
Body
shape: Broad-oval
Predominant color (cuticle): Black
Predominant color (setae): Gray
Rostral
length: Moderately long
Rostral
width: Moderately broad
Antennal
morphology: Elbowed
Prothoracic collar: Not raised (side view)
Prothoracic carina(e): Absent
Prothoracic tubercle(s): Absent
Pronotal
depression: Absent
Elytral
carina(e): Absent
Elytral
tubercle(s): Absent
Elytral
spicule(s): Absent
Mesothoracic epipleuron: Not ascending and not visible in
dorsal view
Leg color
(cuticle): Black and brown
Leg color
(scales): Gray
Trochanteral shape and length: Triangular and
short
Femoral
armature: Unarmed
Tibial
armature of apices: All with spine
Third
tarsus shape: Bilobed
Vestiture
type: Setae
Vestiture
coverage: Dense, in bands or patches
Waterproof coating: Absent
Circular
scales: Absent
Erect
setae: Absent
Wax like
coating: Present
Introduction:
(Gyllenhal) is native
to Europe. It was approved as a biological control agent for release in the
United States in 1993 (Lang, 1999) against spotted knapweed, Centaurea stoebi Lam. (formerly maculosa) and meadow knapweed, C. jacea × nigra L. On meadow knap weed, the
species is established in Wyoming, Washington, Oregon, and Montana while on
spotted knapweed, it is established in California and Oregon (Coombs et al., 2003).
Adults of this species spend winter in soil litter, at or
near the base of plants. Overwintering adults appear at the end of May and reach
peak population levels during early July. Adults feed heavily on the foliage and
flowers prior to mating and laying eggs. Females oviposit among the inner
florets of newly opened flower heads throughout their 5 to 6 month lifespan.
Occasionally adults may hibernate a second time and live a second season. Eggs
hatch in 3 to 6 days and larvae begin feeding on pappus hair and developing
seeds. More than one larva can occupy a seedhead. Larvae develop through three
instars over a 4 to 6 weeks period, pupating in chambers constructed from
cemented seeds and pappus hairs (Norman et al., 1996). The pupal period
generally lasts 9 days. Adults emerge in late July and early August through
holes chewed in the tops of the pupal chambers and vigorously feed on foliage
before moving to overwintering sites in the soil. The species has one generation per
year.
Description:
Adults of the
seedhead weevil are small to medium-sized
(> 2.0 mm < 10.0 mm long), black-gray in color, and with a prominent
bulbous snout. The weevils newly emerged from the seedhead are lighter gray in
color and have a yellowish wax-like coating, appearing and fuzzy on their setae
and bodies. The older weevils lose this coating, turning darker and sometimes
become completely black in appearance. It is a soft seed feeder. Eggs are
yellowish, oval to round. Larvae are white, legless, C-shaped grubs with brown
head capsules. Pupae are also white, they turn brown shortly before emergence.
The femora and tibiae are black, occasionally apices of tibiae and femora
reddish brown. Underside of entire body with simple hairs, all except head and
postocular area without bi-or triradiate scales, and sides of thorax without or
with few such scales. Legs covered with short recumbent or subrecumbent (on
tibiae) hair-like scales. Inner margin of fore tibia in female with large,
broad, irregular-shaped tooth adjacent to and 2/3 as long as mucro. The aedeagus
with sclerotized dorsal area depressed along midline. Body more robust, often
nearly oval, always matte; pronotum and elytra with short recumbent narrow seta
like scales, elytra always with distinct mottled
pattern.
Host Plants:
Spotted knapweed, Centaurea stoebi
(formerly maculosa)., and meadow
knapweed, C. jacea × nigra L.
Bibliography:
Coombs, E., J. Balciunas and P. McEvoy. 2003. Current
status in each state of all 100 agents approved for release in the continental
USA. Biological control of invasive plants in the United States. Corvallis, OR.,
Oregon University Press.
Lang, R.F. 1999. Larinus obtusus (Coleoptera:
Curculionidae). USDA-APHIS, PPQ. Bozeman Biological Control Facility. Forestry
Science Laboratory, Montana State University. Available from:
http://www.nysaes.cornell.edu/ent/biocontrol/weedfeeders/larinus_obtusus.html
[Accessed 20 April 2006].
Norman. R, et.
al,. 1996. Biological Control of
Weeds in the West, Western Society of Weed Science, in cooperation with
USDA, ARS, Mt, Dept. of Ag, and Mt State Univ., Color World Printers, Mt,
Fed.
24. Larinus planus
(Fabricius) - “Canada Thistle Bud Weevil”
Species
diagnostic characters:
Size:
Medium-sized., > 4.5 mm < 10.0 mm
Body
shape: Elongate-oval
Predominant color (cuticle): Black
Predominant color (setae): White
Rostral
length: Moderately long
Rostral
width: Slender
Antennal
morphology: Elbowed
Prothoracic collar: Not raised (side view)
Prothoracic carina(e): Absent
Prothoracic tubercle(s): Absent
Pronotal
depression: Absent
Elytral
carina(e): Absent
Elytral
tubercle(s): Absent
Elytral
spicule(s): Absent
Mesothoracic epipleuron: Not ascending and not visible in
dorsal view
Leg color
(cuticle): Dark brown
Leg color
(setae): White
Trochanteral shape and length: Triangular and
short
Femoral
armature: Unarmed
Tibial
armature of apices: All with spine
Third
tarsus shape: Bilobed
Vestiture
type: Setae
Vestiture
coverage: Dense, in bands or patches
Waterproof coating: Absent
Circular
scales: Absent
Erect
setae: Absent
Wax like
coating: Absent
Introduction:
Larinus planus (Fabricius) was accidentally introduced to the
Northeastern United States from Europe and the flower-head weevil preferred
feeding on Canada thistle, but also fed on native Cirsium species
(McClay, 1990). However, this adventives species became established in the
United States in the 1960s (White, 1972). It has been released in British
Columbia (IPMnet News, 1995), and is being redistributed from the northeast into
other ecoregions of the United States. Certain unexpected ecological effects of
distributing this exotic weevil for biological control of Canada thistle have
been discussed, including its preferred attack on native thistles (Louda and
O’Brien, 2001). The species significantly reduces the seed production of an
endangered native thistle in Colorado,
which reproduces by seed, and has had relatively little effect on Canada thistle
in the same area, which propagates equally well with rhizomes. (Louda and
O’Brien, 2001). The weevil overwinters in the adult stage in soil litter. The
females lay eggs by drilling a hole into the side of an unopened bud. Usually a
single egg is laid in the hole, however, if more than one egg is laid only one
larva can survive. Larvae feed on the seed tissues and other flower parts.
Pupation occurs in a cocoon made inside the bud. Average egg to adult
development in the field is 38 days.
Description:
Adults of the Canada thistle bud weevil
are medium-sized (> 4.5 mm < 10.0 mm long), elongate-oval with a
moderately distinct, white and black, spotted pattern on the elytra, and white
margins on the thorax, formed by moderately coarse recumbent white setae. The
setae conceal the shining black body partially. The rostrum is moderately long,
slender, and evenly, weakly curved. It is not dorsally flattened and is
carinate, not sulcate. The eyes are broadly oval. The prosternum is not sulcate.
The tibiae have a small, inner, apical tooth. The tarsal claws are large,
approximate, connate (basally fused) and symmetrical.
Host Plants: Canada
thistle, Cirsium arvense, C. palustre with occasional
records from other small headed Cirsium spp., including endangered
species, Carduus spp., Galactites spp., Serratula spp.
Bibliography:
IPMnet News. 1995. Consortium for International Crop
Protection. Integrated Plant Protection Center, Oregon State University,
Corvallis.
Louda, S.M. and C.W. O’Brien. 2001. Unexpected ecological
effects of distributing the exotic weevil, Larinus planus (F.), for the
biological control of Canada thistle. Conservation Biology 16:
717-727.
McClay, A.S. 1990. The potential of Larinus planus
(Coleoptera: Curculionidae), an accidentally introduced insect in North America,
for biological control of Cirsium arvense (Compositae). Proceedings of
the VII International Symposium on Biological Control of Weeds, pp. 173-179.
In E.S. Delfosse (ed.), Instituto
Sperimentale per la Patologia Vegetale Ministero dell’ Agricoltura e delle
Foreste.
White, J.C. 1972. A European Weevil, Larinus
carlinae Oliver, collected in Maryland. Cooperative Economic Insect Report
22: 418pp.
25. Mecinus janthinus Germar
- “Stem-boring Weevil”
Species
diagnostic characters:
Size:
Small., > 2.0 mm < 4.5 mm
Body
shape: Elongate-oval
Predominant color (cuticle): Metallic
blue
Predominant color (setae): Bronze to gray
Rostral
length: Long
Rostral
width: Slender
Antennal
morphology: Elbowed
Prothoracic collar: Not raised (side
view)
Prothoracic carina(e): Absent
Prothoracic tubercle(s): Absent
Pronotal
depression: Absent
Elytral
carina(e): Absent
Elytral
tubercle(s): Absent
Elytral
spicule(s): Absent
Mesothoracic epipleuron: Not ascending and not visible in
dorsal view
Leg color
(cuticle): Black
Leg color
(setae): Gray
Trochanteral shape and length: Triangular and
short
Femoral
armature: Toothed
Tibial
armature of apices: All with spine
Third
tarsus shape: Bilobed
Vestiture
type: Setae
Vestiture
coverage: Sparse
Waterproof coating: Absent
Circular
scales: Absent
Erect
setae: Absent
Wax like coating: Absent
Introduction:
Mecinus janthinus Germar was approved for release in the United States in
1995-1996. Its native range extends from central and southern Europe to the
former southern USSR (Hoffmann, 1959). Field releases have been made at sites in
western Canada and the western United States (Coombs et al., 2003). The early results with
M. janthinus on dalmatian toadflax are extremely encouraging. On
dalmatian toadflax, Linaria genistifolia
Mill., the weevil species is established in Colorado, Idaho, Montana,
Oregon, Washington, and Wyoming while on yellow toadflax, L. vulgaris Mill, the species is
established in Wyoming only (Coombs et
al., 2003).
Adults usually emerge in late spring or
early summer and feed on toadflax leaves and stems, and may live for several
weeks to about a month. Females chew holes in toadflax and oviposit singly into
each hole, with approximately 2-100 eggs per stem (DeClerck-Floate and Miller,
2002). The newly emerged larvae begin feeding within toadflax stems, creating
tunnels that increase in size and length as the larvae mature. Wilted shoots can
be observed resulting from larval feeding. Larval development is completed in
about a month, and mature larvae construct a cell within the mined stem where
pupation occurs. Pupal development is completed in several weeks. Adults remain
within pupal cells and overwinter there. The species has one generation per year
(Jeanneret and Schroeder, 1992).
Description:
Adults of stem-boring weevil are small (>
2.0 mm < 4.5 mm long) in size, elongate-oval, very slender, and have a
pronounced long strongly curved snout. The head, thorax and appendages are
black, except for the brownish tarsi. The wing covers are metallic bluish with
parallel sides. The front femur of the male is strongly toothed while that of
the female is smooth. This small, elongate thin weevil is not likely to be
confused with any other biological control agents (native species in North
America). The typical legless larvae are creamy-white in color with a
light-brown head capsule, and appear C-shaped when viewed from the
side.
Host Plants:
Dalmatian toadflax, Linaria
genistifolia Mill. (formerly L.
dalmatica Mill)., and yellow toadflax L. vulgaris Mill.
Bibliography:
Coombs, E., J. Balciunas and P. McEvoy. 2003. Current
status in each state of all 100 agents approved for release in the continental
USA. Biological control of invasive plants in the United States. Corvallis, OR.,
Oregon University Press.
DeClerck-Floate and V. Miller. 2002. Overwintering
mortality of and host attack by the stem-boring weevil, Mecinus janthinus Germar, on dalmatian
toadflax (Linaria dalmatica (L.)
Mill) in western Canada. Biological Control 24: 65-74.
Hoffmann, A. 1959. Coléoptères (Curculionidae)
(Tribu des Mecinni). Faune de France, 62.
Lechevalier, Paris. 1264-1327.
Jeanneret, P. and D. Schroeder. 1992. Biology and host
specificity of Mecinus janthinus Germar (Col.: Curculionidae), a
candidate for the biological control of yellow and Dalmatian toadflax,
Linaria vulgaris (L.) Mill. and Linaria dalmatica (L.) Mill.
(Scrophulariaceae), in North America. Biocontrol Sci. and Technol. 2: 25-34.
26. Microlarinus lareynii J. Duval -
“Puncturevine Seed Weevil”
Species
diagnostic characters:
Size:
Small., > 2.0 mm < 4.5 mm
Body
shape: Elongate-oval
Predominant color (cuticle): Reddish
brown
Predominant color (setae): Gray
Rostral
length: Short
Rostral
width: Broad
Antennal
morphology: Elbowed
Prothoracic collar: Not raised (side
view)
Prothoracic carina(e): Absent
Prothoracic tubercle(s): Absent
Pronotal
depression: Absent
Elytral
carina(e): Absent
Elytral
tubercle(s): Absent
Elytral
spicule(s): Absent
Mesothoracic epipleuron: Not ascending and not visible in
dorsal view
Leg color
(cuticle): Brown
Leg color
(setae): Gray
Trochanteral shape and length: Triangular and
short
Femoral
armature: Unarmed
Tibial
armature of apices: All with spine
Third
tarsus shape: Bilobed
Vestiture
type: Setae
Vestiture
coverage: Dense and complete
Waterproof coating: Absent
Circular
scales: Absent
Erect
setae: Present
Wax like
coating: Present
Introduction:
Microlarinus lareynii J. Duval was released for the first time on pucturevines
in the United States in 1961, after the weevils’ importation from Italy
(Huffaker et al., 1983; PMIS, 2003).
In the early summer months of the same year they were released in Clark County,
Nevada, and Stanislaus County, California. Subsequent releases were carried out
in Arizona, California, Colorado, Utah, and Washington. On puncturevine, Tribulus terrestris L., the weevil
species is established in Arizona, California, Colorado, Florida, Kansas,
Nebraska, Oklahoma, Oregon, Texas, and Utah while establishment failed in Idaho,
Wyoming, and Washington (Coombs et
al., 2003). Adult weevils
overwinter in the debris near the host plants. Adults can be found on several non-host
plant species, probably in search of water. After excavating a pit in the side
of a seedpod, the female weevil oviposits in this pit, covering the eggs with a
fecal cement to prevent desiccation. The larvae on eclosion bore into the seed,
where they feed. Total time for the life cycle in summer is usually 22 days.
Probably, there are three generations of this species in California (PMIS,
2003).
Description:
Adults of the puncturevine seed weevil are similar to the
puncturevine stem weevil. The adult is a small (> 2.0 mm < 4.5 mm long)
reddish-brown weevil. The species can be distinguished by its broader
elongate-oval shape, the broader less attenuate rostrum, and symmetrically round
eyes. The body is clothed densely with fine erect setae and slightly coarse
recumbent setae, which do not completely conceal the reddish-brown body color,
except on the sides of the thorax and parts of the elytra. The apical lateral
margins of the prothorax lack ocular lobes, and possess very strong postocular
vibrissae (a cluster of long dense setae). The prosternum (underside with front
legs) is not sulcate medially. The tarsal claws are small, connate (basally
fused), approximate, and symmetrical.
Host Plants:
Puncturevine, Tribulus terrestris
L., and Jamaica feverplant, Tribulus cistoides L.
Bibliography:
Coombs, E., J. Balciunas and P. McEvoy. 2003. Current
status in each state of all 100 agents approved for release in the continental
USA. Biological control of invasive plants in the United States. Corvallis, OR.,
Oregon University Press.
Huffaker, C.B., J. Hamai and R.M. Nowierski. 1983.
Biological control of puncturevine, Tribulus terrestris in California after
twenty years of activity of introduced weevils. Entomophaga 28(4):
387-400.
PMIS (Plant Management Information System). 2003. Noxious
and nuisance plant information system, ver. 5.3. Developed by Cofrancesco et al., (Cds and Web based. Available
from: http://el.erdc.usace.army.mil/pmis/ [Accessed 14 April 2006].
27.
Microlarinus lypriformis Wollaston -
“Puncturevine Stem Weevil”
Species
diagnostic characters:
Size:
Minute., < 2.0 mm
Body
shape: Elongate-oval
Predominant color (cuticle): Reddish
brown
Predominant color (setae): Gray
Rostral
length: Short
Rostral
width: Slender
Antennal
morphology: Elbowed
Prothoracic collar: Not raised (side
view)
Prothoracic carina(e): Absent
Prothoracic tubercle(s): Absent
Pronotal
depression: Absent
Elytral
carina(e): Absent
Elytral
tubercle(s): Absent
Elytral
spicule(s): Absent
Mesothoracic epipleuron: Not ascending and not visible in
dorsal view
Leg color
(cuticle): Brown to black
Leg color
(setae): Gray
Trochanteral shape and length: Triangular and
short
Femoral
armature: Unarmed
Tibial
armature of apices: All with spine
Third
tarsus shape: Bilobed
Vestiture
type: Setae
Vestiture
coverage: Dense and complete
Waterproof coating: Absent
Circular
scales: Absent
Erect
setae: Present
Wax like
coating: Present
Introduction: The
puncturevine stem weevil, Microlarinus lypriformis Wollaston is a native
of Europe. The first release of this species in 1961 in the United States was of
specimens imported from Italy (Andres, 1978; PMIS, 2003). The subsequent
releases were made in Nevada, California Arizona, Colorado, Utah, and
Washington. On puncturevine, Tribulus
terrestris L., the weevil is established in Arizona, California, Colorado,
Florida, Kansas, Nevada, Nebraska, New Mexico, Oklahoma, Oregon, Texas, and
Utah, however, no establishment occurred in Idaho, Wyoming, and Washington
(Coombs et al., 2003). The weevils
are widespread in most areas in which they have become established, although in
colder climates or mountain areas the cold temperatures have prevented
establishment which is favored by warm temperature in areas associated with mild
winters. Eggs are laid in pits chewed in the root crowns and the stems. The
larvae mine the stems and roots and are very similar to those of M.
lareynii. They pupate in the stems. Adults emerge from the exit holes in
the stems and root crowns, and feed on stems and leaves. There are a number of
generations of this species in a year. Their biology on puncturevine was studied
under laboratory and insectory conditions in California. The eggs hatch in 2 to
3 days. The young larvae tunnel directly into the pith, where they initially
confine their feeding. As the larvae mature, they also feed on the vascular
tissues and inner cortex. Larvae tunnel 1-12 cm during their development, which
lasts 27-28 days. Pupation occurs in open tunnels or in cells enlarged from
smaller tunnels. The pupal stage lasts 4-5 days. The adults emerge from circular
holes chewed mainly in the upper surfaces of stems, branches and crowns
(Kirkland and Goeden, 1978).
Description:
Adults of the puncturevine stem weevil are
similar to those of the puncturevine seed weevil. The puncturevine stem weevil
can be distinguished by its minute size (< 2.0 mm long), more slender
elongate-oval shape, the relatively slender distinctly attenuate rostrum, and
narrower asymmetrical oval eyes. The body is densely clothed with fine erect
setae and slightly coarse recumbent setae, which do not completely conceal the
reddish brown body color, except on the sides of the thorax and much of the
sides of the elytra. The apical lateral margins of the prothorax lack postocular
lobes, and possess very long postocular vibrissae (a cluster of dense setae).
The prosternum (underside with the front legs) is not sulcate medially. The
tarsal claws are small, connate (basally fused), approximate, and
symmetrical.
Host Plants:
Puncturevine, Tribulus terrestris
L., Jamaica feverplant, Tribulus cistoides L., and
Kallstroemia spp.
Bibliography:
Andres, L.A. 1978. Biological control of puncturevine, Tribulus terrestris (Zygophyllaceae):
post introduction collection records of Microlarinus spp. (Coleoptera:
Curculionidae). Proceedings of the 4th International Symposium on Biological
Control of Weeds, Gainesville, FL. 132-136.
Coombs, E., J. Balciunas and P. McEvoy. 2003. Current
status in each state of all 100 agents approved for release in the continental
USA. Biological control of invasive plants in the United States. Corvallis, OR.,
Oregon University Press.
Kirkland, R.L. and R.D. Goeden. 1978. Biology of Microlarinus lypriformis (Col.:
Curculionidae) on puncturevine in southern California. Annals of Entomol. Soc.
America 71(1): 65-69.
PMIS (Plant Management Information System). 2003. Noxious
and nuisance plant information system, ver. 5.3. Developed by Cofrancesco et al., (Cds and Web based. Available
from: http://el.erdc.usace.army.mil/pmis/ [Accessed 14 April
2006].
28. Mogulones cruciger
(Herbst) - “Root-feeding Weevil”
Species
diagnostic characters:
Size: Small., > 2.0 mm < 4.5 mm
Body shape: Broad-oval
Predominant color (cuticle): Black
Predominant color (scales): Strongly mottled, bicolored or
tricolored
Rostral length: Long
Rostral width: Slender
Antennal morphology: Elbowed
Prothoracic collar: Raised (side
view)
Prothoracic carina(e):Absent
Prothoracic tubercle(s): Absent
Pronotal depression: Present
Pronotal depression orientation: Longitudinal
Elytral carina(e): Absent
Elytral tubercle(s): Absent
Elytral spicule(s): Present
Mesothoracic epipleuron: Ascending and visible in dorsal
view
Leg color (cuticle): Dark Brown
Leg color (setae): Brown
Trochanteral shape and length: Triangular and
short
Femoral armature: Toothed
Tibial armature of apices: All lack
spine
Third tarsus shape: Bilobed
Vestiture type: Scales
Vestiture coverage: Dense, in bands or
patches
Waterproof coating: Absent
Circular scales: Absent
Erect setae: Absent
Wax like coating: Absent
The eggs are laid in a cavity gnawed in
the petiole of rosette leaves, in the petiole of stem leaves nearest the crown,
and in the shoot base and in the root crown. After oviposition the female covers
the cavity with frass. The larvae are white with a light brown head capsule and
development is completed in three instars. The larvae consume all parts of the
root, including the central core and root crown, and if this food is
insufficient they may feed on any tissue of hound’s tongue. Full-grown larvae
leave the roots and construct a pupal chamber from soil particles, in which they
pupate. Pupation is completed within two weeks. Most of the adults emerge in the
spring. Adults may live 12-14 months and sex ratio is almost equal. Most adults
emerge in April-May. They later feed on the leaves and mate within 14 days
(DeClerck-Floate and Harris, 2005).
Description:
Adults of
root-feeding weevil are small (> 2.0 mm < 4.5 mm long) in size,
broad-oval in shape, black body and body
scales are strongly mottled, bicolored or tricolored. The center of the wing
covers has a white cross that gives the species its name (DeClerck-Floate and
Harris, 2005).
Host Plants:
Hound’s tongue, Cynoglossum
officinale L., and C. cheirifolium L.
Bibliography:
Andreas E. J. and M. Schwarzlaender. 2004. Seven years
after its release in Canada: Is it safe to introduce the houndstongue root
weevil, Mogulones cruciger, in the United States? Talk Presented at the
Entomological Society of America. Available from:
http://esa.confex.com/esa/2004/techprogram/paper_17422.htm [Accessed 21 April
2006].
DeClerck-Floate R. and P. Harris. 2005. Classical
biological control of weeds established biocontrol agent. Mogulones cruciger (Herbst), root
feeding weevil. Available from:
http://res2.agr.ca/lethbridge/weedbio/agents/amogcruc_e.htm [Accessed 21 April
2006].
29. Nanophyes marmoratus
(Goeze) - “Flower Bud Weevil”
Species
diagnostic characters:
Size:
Minute to small., < 2.0 mm to < 4.5 mm
Body
shape: Broad-oval
Predominant color (cuticle): Black and reddish
yellow
Predominant color (setae): Strongly mottled, bicolored or
tricolored
Rostral
length: Long
Rostral
width: Slender
Antennal
morphology: Elbowed
Prothoracic collar: Not raised (side
view)
Prothoracic carina(e): Absent
Prothoracic tubercle(s): Absent
Pronotal
depression: Absent
Elytral
carina(e): Absent
Elytral
tubercle(s): Absent
Elytral
spicule(s): Present
Mesothoracic epipleuron: Not ascending and not visible in
dorsal view
Leg color
(cuticle): Yellowish brown
Leg color
(setae): Brown
Trochanteral shape and length: Rectangular and moderately
long
Femoral
armature: Unarmed
Tibial
armature of apices: All lack spine
Third
tarsus shape: Bilobed
Vestiture
type: Setae
Vestiture
coverage: Moderately sparse, in bands or patches
Waterproof coating: Absent
Circular
scales: Absent
Erect
setae: Absent
Wax like
coating: Absent
Introduction:
Nanophyes marmoratus (Goeze) is widely distributed in Europe and Western
Siberia. It was introduced from Germany, and first released in New York and
Minnesota in 1994. In Canada, the species is established in Manitoba (Harris,
2005). In the United States, it is established in California, Colorado, Idaho,
Michigan, Montana, New Jersey, New York, Oregon, and Washington (Coombs et al., 2003).
After
hibernation adults begin feeding on the young leaves of small pre-flowering host
plants. After flowering, adults move to the flower spikes and feed on the
receptacle and ovaries of the developing flower buds (Blossey, 2002). These
unopened flower buds are located primarily in the upper portion of the flower
spike. Flower buds damaged by adult feeding are often aborted or excised. Eggs
are deposited singly in the tip of unopened flower buds. A female may lay two
eggs per day with 60-100 eggs in her life span (PMIS, 2003; Harris, 2005). A
single larva develops in a flower bud where it consumes the stamens, petals and
ovary. Most buds drop before larval development is complete, but development
continues, even in water, as the buds float. Pupation occurs in the lower
portion of the bud where a pupation chamber is constructed from frass that
accumulated during larval feeding. The emerging adults feed on the leaves before
beginning hibernation. There is only one generation per year (PMIS,
2003). The weevil prefers habitats without
prolonged flooding for its development.
Description:
Adults of the flower bud weevil are minute
to small (< 2.0 mm to < 4.5 mm long), black with variously placed light
colored patches, on the elytra and pronotum. The legs are yellowish brown,
sometimes with black knees (apices of femora). Both sexes have a long, very
slender, slightly curved snout. The elbowed antennae separate this genus from
the Apioninae, the only other group which also possesses the rectangular
moderately long trochanter.
Host Plants:
Purple loosestrife, Lythrum salicaria
L.
Bibliography:
Blossey, B. 2002. Purple loosestrife. In Biological Control
of Invasive Plants in the Eastern United States. R.V. Driesche, B. Blossey, M.
Hoddle, S. Lyon and R. Reardon (eds.). USDA, Forest Service.
149-157.
Coombs, E., J. Balciunas and P. McEvoy. 2003. Current
status in each state of all 100 agents approved for release in the continental
USA. Biological control of invasive plants in the United States. Corvallis, OR.,
Oregon University Press.
Harris, P. 2005. Classical
biological control of weeds, established biocontrol agents. Nanophyes marmoratus (Goeze), flower
feeding weevil. Available from:
http://res2.agr.ca/lethbridge/weedbio/agents/ananmar_e.htm [Accessed 21 April
2006].
PMIS (Plant Management Information System). 2003. Noxious
and nuisance plant information system, ver. 5.3. Developed by Cofrancesco et al., (Cds and Web based. Available
from: http://el.erdc.usace.army.mil/pmis/ [Accessed 14 April
2006].
30. Neochetina bruchi
Hustache - “Chevroned Waterhyacinth Weevil”
Species
diagnostic characters:
Size:
Small., > 2.0 mm < 4.5 mm
Body
shape: Broad-oval
Predominant color (cuticle): Gray to
brown
Predominant color (scales): Brown
Rostral
length: Long
Rostral
width: Slender
Antennal
morphology: Elbowed
Prothoracic collar: Not raised (side
view)
Prothoracic carina(e): Absent
Prothoracic tubercle(s): Absent
Pronotal
depression: Absent
Elytral
carina(e): Present
Elytral
carina(e) position: Posterior half of elytra on sutural
interval
Elytral
tubercle(s): Absent
Elytral
spicule(s): Absent
Mesothoracic epipleuron: Not ascending and not visible in
dorsal view
Leg color
(cuticle): Cinnamon
Leg color
(scales): Brown
Trochanteral shape and length: Triangular and
short
Femoral
armature: Unarmed
Tibial
armature of apices: All with spine
Third
tarsus shape: Bilobed
Vestiture
type: Scales
Vestiture
coverage: Dense and complete
Waterproof coating: Present
Type of
waterproof coating: Earthen
Circular
scales: Present
Erect
setae: Absent
Wax like
coating: Absent
Introduction:
Neochetina bruchi Hustache is native to South America. All members of this genus are
semi-aquatic, spending much of their time on or in aquatic plants of the family
Pontederiaceae. The chevroned waterhyacinth weevil was introduced in Florida in
1974 and was released in Alabama, California, Louisiana, and Texas in following
years (PMIS, 2003) to control waterhyacinth, Eichhornia crassipes (Mart.) Solms.
Adult females chew holes in the lamina or petiole of the
leaf and deposit a single egg in each hole. Eggs may be deposited around the
edges of adult feeding scars. It has been reported that chevroned waterhyacinth
weevils prefer to lay eggs in the tender central leaves or ligules surrounding
the leaf bases. Eggs hatch within 7-10 days at 75°F. A single female may
oviposit more than 400 eggs during her lifetime, with more than 90% of the eggs
deposited within a single one-month period (Center et al., 2002; PMIS, 2003). Essentially,
the larvae are "worm-like", bearing no legs or prolegs, with only small
enlargements with setae (small hairs) where legs would be found normally. The
larvae are usually white or cream-colored with a yellow-orange head. The larvae
typically are found feeding within the bases of leaves and petioles, entering
the apex of the stem, when mature, where they destroy the apical bud. Pupae are
creamy white and are enclosed within a cocoon which is formed among the lateral
rootlets below the water surface.
Description:
Adults of the chevroned waterhyacinth
weevil are small (> 2.0 mm < 4.5 mm long) in size, similar in appearance
to the mottled waterhyacinth weevil, and can be distinguished from it by the
color and pattern of scales on the wing covers (i.e. elytra). The
chevroned waterhyacinth weevil is usually gray to brown with a distinct lighter
brown to tan chevron (crescent-shaped marking) on the wing covers. Although the
chevron can be seen distinctly in most individuals, it is absent in others.
Therefore, the glabrous dark raised lines (sutural carinae) present on the
elytra are used as a primary difference to separate the species. In the
chevroned waterhyacinth weevil the lines are shorter in length and located
behind the midline of the wing covers. Another subtle character is the nature of
the shallow grooves or striae running the length of the elytra; for the mottled
waterhyacinth weevil the striae are relatively "coarse" as opposed to the "fine"
striae present on the chevroned waterhyacinth weevil. O’Brien (1976) revised the
genus Neochetina and added three new species with all six species are
included in the key to species.
Host Plant: Waterhyacinth, Eichhornia crassipes (Mart.)
Solms.
Bibliography:
Center, T.D., M.P. Hill, H. Cordo and M.H. Julien. 2002.
Waterhyacinth. In Biological Control of Invasive Plants in the Eastern United
States. R.V. Driesche, B. Blossey, M. Hoddle, S. Lyon and R. Reardon (eds.).
USDA, Forest Service. 41-64.
O’Brien, C.W. 1976. A taxonomic revision of the new world
subaquatic genus Neochetina (Coleoptera: Curculionidae: Bagoini). Ann.
Entomol. Soc. America 69: 165-174.
PMIS (Plant Management Information System). 2003. Noxious
and nuisance plant information system, ver. 5.3. Developed by Cofrancesco et al., (Cds and Web based. Available
from: http://el.erdc.usace.army.mil/pmis/ [Accessed 14 April
2006].
31. Neochetina eichhorniae
Warner - “Mottled Waterhyacinth Weevil”
Species
diagnostic characters:
Size:
Small., > 2.0 mm < 4.5 mm
Body
shape: Broad-oval
Predominant color (cuticle):
Gray-black
Predominant color (scales): Brown
Rostral
length: Long
Rostral
width: Slender
Antennal
morphology: Elbowed
Prothoracic collar: Not raised (side
view)
Prothoracic carina(e): Absent
Prothoracic tubercle(s): Absent
Pronotal
depression: Absent
Elytral
carina(e): Present
Elytral
carina(e) position: Anterior half of elytra on sutural
interval
Elytral
tubercle(s): Absent
Elytral
spicule(s): Absent
Mesothoracic epipleuron: Not ascending and not visible in
dorsal view
Leg color
(cuticle): Dark brown
Leg color
(scales): Brown
Trochanteral shape and length: Triangular and
short
Femoral
armature: Unarmed
Tibial
armature of apices: All with spine
Third
tarsus shape: Bilobed
Vestiture
type: Scales
Vestiture
coverage: Dense and complete
Waterproof coating: Present
Type of
waterproof coating: Earthen
Circular
scales: Present
Erect
setae: Absent
Wax like
coating: Absent
Introduction:
Overseas surveys were conducted in South
America in the 1960’s to identify organisms that feed on waterhyacinth,
Eichhornia crassipes (Mart.) Solms. in its native range. Three agents
were identified including two weevil species in the genus Neochetina. The
mottled waterhyacinth weevil, Neochetina
eichhorniae Warner, was introduced in Florida in 1972 and was released in
Alabama, California, Louisiana, and Texas in the following few years (Perkins,
1973). Currently, the mottled waterhyacinth weevil is well distributed
throughout most of the range of waterhyacinth in the United States (PMIS,
2003).
Studies in most of the United States showed that adults of this species
are reproductive all year, without producing distinct generations. However, in
Florida, females of this weevil undergo a reproductive quiescence during the
winter. Reproduction may begin again, usually after the month of December. Eggs
are laid singly in the leaf epidermis and hatch in 7-17 days, depending on
temperature. A larva completes its development in 36-90 days and has three
instars. Larvae feed and develop in the petioles. Pupation lasts for 7-9 days at
81°F (Center et al., 2002; PMIS,
2003). A generation is completed in 70-140 days, based on temperature, depending
on the time of the year.
Description:
Adults of the mottled waterhyacinth weevil
are small (> 2.0 mm < 4.5 mm long) in size and are similar in appearance
to the chevroned waterhyacinth weevil. The dark, widely distributed mottled
appearance is in contrast to the chevroned waterhyacinth weevil, which, in most
individuals, has a distinct, lighter brown to tan chevron (crescent-shaped
marking) on the wing covers. The dark, glabrous, sutural, raised lines (short
carinae) present on the elytra are used as a primary difference to separate the
species. In the mottled waterhyacinth weevil, these lines are longer and located
forward of the midline of the wing covers. Another subtle character is the
nature of the shallow grooves or striae running the length of the elytra. In the
chevroned waterhyacinth weevil, the striae are relatively "fine" as opposed to
the "coarse" striae present on the mottled waterhyacinth weevil (O’Brien,
1976).
Host Plant:
Waterhyacinth, Eichhornia crassipes
(Mart.) Solms.
Bibliography:
Center, T.D., M.P. Hill, H. Cordo and M.H. Julien. 2002.
Waterhyacinth. In Biological Control of Invasive Plants in the Eastern United
States. R.V. Driesche, B. Blossey, M. Hoddle, S. Lyon and R. Reardon (eds.).
USDA, Forest Service. 41-64.
O’Brien, C.W. A taxonomic revision of the new world
subaquatic genus Neochetina. Annals
of the Entomological Society of America 69(2): 165-174.
Perkins, B.D. 1973. Potential for waterhyacinth management
with biological agents. Proc. Tall Timbers Conf. Ecol. Anim. Control Habitat
Manage. 4: 53-64.
PMIS (Plant Management Information System). 2003. Noxious
and nuisance plant information system, ver. 5.3. Developed by Cofrancesco et al., (Cds and Web based. Available from:
http://el.erdc.usace.army.mil/pmis/ [Accessed 14 April 2006].
32. Neohydronomus affinis
Hustache - “Waterlettuce Weevil”
Species
diagnostic characters:
Size:
Minute to small., < 2.0 mm to < 4.5 mm
Body
shape: Elongate-oval
Predominant color (cuticle): Dark
brown
Predominant color (scales): Strongly mottled, bicolored or
tricolored
Rostral
length: Moderately long
Rostral
width: Slender
Antennal
morphology: Elbowed
Prothoracic collar: Not raised (side
view)
Prothoracic carina(e): Absent
Prothoracic tubercle(s): Absent
Pronotal
depression: Absent
Elytral
carina(e): Absent
Elytral
tubercle(s): Absent
Elytral
spicule(s): Absent
Mesothoracic epipleuron: Not ascending and not visible in
dorsal view
Leg color
(cuticle): Brown
Leg color
(scales): Strongly mottled, bicolored or tricolored
Trochanteral shape and length: Triangular and
short
Femoral
armature: Unarmed
Tibial
armature of apices: All with spine
Third
tarsus shape: Bilobed
Vestiture
type: Scales
Vestiture
coverage: Dense and complete
Waterproof coating: Present
Type of
waterproof coating: Earthen
Circular
scales: Present
Erect
setae: Absent
Wax like
coating: Absent
Introduction:
Neohydronomus affinis Hustache is native to South America. It was first released
as a biological control agent of waterlettuce in Florida in 1987 (Coombs et al., 2003). It is being used
presently for the management of waterlettuce populations in Florida, Louisiana,
and Texas (PMIS, 2003), and is established in these states (Coombs et al., 2003). Waterlettuce weevils are
weak fliers. The species superficially resembles a number of other small weevils
feeding on aquatic plants, e.g. Stenopelmus sp., which has a 7 segmented
funicle and Tanysphyrus sp., which has the claw segment of the tarsi not
extended beyond the bilobed third segment. Adults can be found on any
non-submerged portion of the waterlettuce plant. Usually, adults are found in
the grooves on the underside of the leaves or within the spongy leaf tissue.
Female weevils lay cream-colored, sub-spherical eggs within
a small hole (0.5 mm diameter) cut into the upper surface of the leaf near the
leaf edge. Larvae are very minute, yellowish, relatively featureless grubs. The
posterior end of the larva appears "cut-off" as though someone took a hatchet to
it. The larvae commonly mine the leaves although sometimes they can be observed
on the leaf surface (Dray and Center, 2003). Mines are seen more often in the
thinner outer 1/3 of the waterlettuce leaf and are not nearly so obvious in the
thicker central and basal portions of the leaf. Mature larvae are usually more
than 3 mm long. Pupation occurs within the mine galleries created by the
larvae.
Description:
Adults of waterlettuce weevil are minute
to small (< 2.0 mm to < 4.5 mm long) stout, covered loosely with scales
that vary from whitish through blue-gray to brown. Some populations are
unicolored, others are marked by one or smaller to large subtriangular spots on
the anterior mid-dorsum of the elytra (often forming a "Smiley" face-like
caricature). These weevils are weak fliers and superficially resemble a number
of other small weevils feeding on aquatic plants, notably Stenopelmus sp.
and Tanysphyrus sp., from which they can be distinguished on the basis of
snout structure and appearance of the tarsal claws (O’Brien and Wibmer,
1989).
Host Plants: Waterlettuce, Pistia stratiotes
L.
Bibliography:
Coombs, E., J. Balciunas and P. McEvoy. 2003. Current
status in each state of all 100 agents approved for release in the continental
USA. Biological control of invasive plants in the United States. Corvallis, OR.,
Oregon University Press.
Dray, A.F. and T.D. Center. 2002. Waterhyacinth. In
Biological Control of Invasive Plants in the Eastern United States. R.V.
Driesche, B. Blossey, M. Hoddle, S. Lyon and R. Reardon (eds.). USDA, Forest
Service. 65-75.
O’Brien, C.W. and G.J. Wibmer. 1989. Revision of the
Neotropical genus Neohydronomus Hustache (Coleoptera: Curculionidae). The
Coleopts. Bull. 43: 291-304.
PMIS (Plant Management Information System). 2003. Noxious
and nuisance plant information system, ver. 5.3. Developed by Cofrancesco et al., (Cds and Web based. Available
from: http://el.erdc.usace.army.mil/pmis/ [Accessed 14 April
2006].
33. Omphalapion hookeri
(Kirby) - “Seed-head Feeding Weevil”
Size:
Minute to small., < 2.0 mm to < 4.5 mm
Body
shape: Pear-shaped
Predominant color (cuticle): Black, metallic
blue
Predominant color (setae): Brassy
metallic
Rostral
length: Long
Rostral
width: Slender
Antennal
morphology: Straight
Prothoracic collar: Not raised (side
view)
Prothoracic carina(e): Absent
Prothoracic tubercle(s): Absent
Pronotal
depression: Present
Pronotal
depression orientation: Longitudinal
Elytral
carina(e): Absent
Elytral
tubercle(s): Absent
Elytral
spicule(s): Absent
Mesothoracic epipleuron: Not ascending and not visible in
dorsal view
Leg color
(cuticle): Black
Leg color
(setae): Brassy metallic
Trochanteral shape and length: Rectangular and moderately
long
Femoral
armature: Unarmed
Tibial
armature of apices: All lack spine
Third
tarsus shape: Bilobed
Vestiture
type: Setae
Vestiture
coverage: Dense, in bands or patches
Waterproof coating: Absent
Circular
scales: Absent
Erect
setae: Absent
Wax like
coating: Absent
Introduction: Omphalapion hookeri (Kirby) (formerly Apion hookeri) is originally from Europe
and was released against scentless chamomile, Matricaria perforate Mérat and was recovered at different
localities in western Canada between 1992 and 1997 (Hinz and McClay, 2000). The
species is established in British Columbia,
Alberta, Saskatchewan, and Manitoba (McClay and DeClerck-Floate, 1999). Eggs
are white, later turn brown, 0.4 × 0.3 mm long, and are laid in the tubular
flowers. They are aggregated and preferentially laid in apical heads, which
produce the most seeds. The eggs hatch in 5-12 days. Larvae feed in tubular
florets and pupate in the seeds. Development takes 4-5 weeks. Pupation takes
place in the seed chamber in a cell of chewed plant fragments. Adults emerge in
7-14 weeks. Newly emerged adults feed and mate in the Fall, however, there is no
oviposition in this season. Males do not survive the winter. However, females
resume feeding in the Spring. Oviposition is delayed until a week after the
first flower buds appear in June. The species is univoltine in nature (Harris
and McClay, 2005).
Description:
Adults of
seed-head feeding weevil are minute to small
(< 2.0 mm < 4.5 mm) in size and pear-shaped. The species has a domed
prothorax strongly medially rounded at the sides, a visibly tapered rostrum,
protruding eyes and no wing cover pattern. Striae are relatively wide and deep,
and the intervals are broad and coarsely shallowly punctuate. The setae are brassy metallic and rather
fine. The male body color is brassy black and 1.6-2.0 mm long, while the female
is metallic blue, blue-green or purple, although they may appear black if
greased and ranges in size from 1.9-2.4 mm long. The larva is white, legless,
curved and found in the seedheads.
Host Plants:
Scentless chamomile Matricaria
perforate Mérat, M.
maritime L., Anthemis
cotula L., A. arvensis
L., and Chrysanthemum
leucanthemum L.
Bibliography:
Harris, P. and A. McClay. 2005. Classical biological
control of weeds, established biocontrol agents. Omphalapion hookeri Kirby, seed-head
weevil. Available from:
http://res2.agr.ca/lethbridge/weedbio/agents/aomphook_e.htm [Accessed 24 April
2006].
Hinz, H.L. and A. McClay. 2000. Ten years of scentless
chamomile: prospects for the biological control of a weed of cultivated land. In
Proceedings of the X International Symposium on Biological Control of Weeds 4-14
July 1999, N.R. Spencer (ed.), Montana State University, Montana.
537-550.
McClay, A. and R. DeClerck-Floate. 1999. Establishment and
early effects of Omphalapion hookeri
(Kirby) (Coleoptera: Apionidae) as a biological control agent for scentless
chamomile, Matricaria perforata Mérat
(Asteraceae). Biological Control 14: 85-95.
34.
Oxyops vitiosa Pascoe - “Melaleuca
Weevil”
Species
diagnostic characters:
Size:
Medium-sized., > 4.5 mm < 10.0 mm
Body
shape: Broad-oval
Predominant color (cuticle): Dark brown to
gray
Predominant color (scales): Pale gray
Rostral
length: Short
Rostral
width: Broad
Antennal
morphology: Elbowed
Prothoracic collar: Not raised (side
view)
Prothoracic carina(e): Present
Prothoracic tubercle(s): Absent
Pronotal
depression: Present
Pronotal
depression orientation: Longitudinal
Elytral
carina(e): Present
Elytra
carina(e) position: Entire length of elytra
Elytral
tubercle(s): Present
Elytral
spicule(s): Present
Mesothoracic epipleuron: Not ascending and not visible in
dorsal view
Leg color
(cuticle): Brown
Leg color
(scales): White
Trochanteral shape and length: Triangular and
short
Femoral
armature: Unarmed
Tibial
armature of apices: All with spine
Third
tarsus shape: Bilobed
Vestiture
type: Scales
Vestiture
coverage: Dense and complete
Waterproof coating: Absent
Circular
scales: Absent
Erect
setae: Absent
Wax like
coating: Absent
Introduction:
Oxyops vitiosa Pascoe is native to Australia and was originally described
from Queensland, in 1870. The tree, known as melaleuca or the paperbark tree,
was imported from Australia in 1906 and later planted extensively to drain the
Everglades. Specimens of this weevil species were field released at several
sites in Florida in 1997 to control melaleuca, Melaleuca
quinquenervia (Cavanilles) S.T. Blake. As
of March 1998, eight populations had become established in South Florida (Coombs
et al., 2003).
Adults feed, mate, and lay eggs on or near young leaves and
subsequently cover them with feces. A single female can lay up to 500-1000 eggs
in her life span (Cuda et al., 2004).
Oviposition occurs mainly during the daylight hours from September to March in
Florida (Center et al., 2000). The
eggs hatch in 6-10 days. Larvae are "slug-like", covered with a slimy and oily
exudate, and with feces which remains attached at the anus and strings out and
often forms long coiled filaments. The oil and feces sequester poisons from the
host plant, which help protect the larvae from predation. They feed externally
on young leaves, which is very uncommon in weevils. When they are done feeding,
mature larvae burrow into the soil to fashion an oily cell in which to pupate.
The adult weevil emerges in 2-3 weeks and lives for up to 9 months. The life
cycle from egg to adult is about 48 days.
Description:
Adults of the melaleuca weevil are
medium-sized (> 4.5 mm < 10.0 mm long), dark brown and gray, usually with
a rather distinct, dark brown, quadrate macula in the middle of the back
(elytra). The macula is actually the result of a decrease in both the size and
density of the pale gray scales covering the body, exposing the darkened surface
of the body in the area of the macula. Adults are broad-oval and stout bodied
with a short broad snout, which is slightly longer than broad. They have four
strongly developed and two weakly developed tubercles in a pair of lines on
their back.
Host Plants:
Melaleuca, paperbark tree, "the tree from
hell", cajeput tree, (Melaleuca quinquenervia (Cavanilles) S.T.
Blake.
Bibliography:
Center, T.D., T.K. Van, M.B. Rayachhetry, G.R. Buckingham,
F.A. Dray, S. Wineriter, M.F. Purcell, and P.D. Pratt. 2000. Field colonization
of the melaleuca snout beetle (Oxyops
vitiosa) in south Florida. Biological Control 19:
112-123.
Coombs, E., J. Balciunas and P. McEvoy. 2003. Current
status in each state of all 100 agents approved for release in the continental
USA. Biological control of invasive plants in the United States. Corvallis, OR.,
Oregon University Press.
Cuda, J., S.A. Wineriter, G.R. Buckingham, T.D. Center and
K.T. Gioeli. 2004. Melaleuca snout beetle. Available from:
http://creatures.ifas.ufl.edu/beneficial/melaleuca_weevil.htm [Accessed 24 April
2006].
35. Phrydiuchus tau Warner -
“Mediterranean Sage Root Crown Weevil”
Species
diagnostic characters:
Size:
Small., > 2.0 mm < 4.5 mm
Body
shape: Broad-oval
Predominant color (cuticle): Black
Predominant color (setae): Strongly mottled, bicolored or
tricolored
Rostral
length: Long
Rostral
width: Moderately slender
Antennal
morphology: Elbowed
Prothoracic collar: Raised (side
view)
Prothoracic carina(e): Absent
Prothoracic tubercle(s): Present
Pronotal
depression: Present
Pronotal
depression orientation: Longitudinal
Elytral
carina(e): Absent
Elytral
tubercle(s): Present
Elytral
spicule(s): Present
Mesothoracic epipleuron: Not ascending and not visible in
dorsal view
Leg color
(cuticle): Dark brown
Leg color
(setae): Strongly mottled, bicolored or tricolored
Trochanteral shape and length: Triangular and
short
Femoral
armature: Toothed
Tibial
armature of apices: All lack spine
Third
tarsus shape: Bilobed
Vestiture
type: Setae
Vestiture
coverage: Dense, in bands or patches
Waterproof coating: Absent
Circular
scales: Absent
Erect
setae: Absent
Wax like
coating: Absent
Introduction: Phrydiuchus
tau Warner is native to Europe and was
introduced in Oregon in 1971 against Mediterranean sage, Salvia aethiopis
L. The species is now established at several locations in California, Colorado,
Idaho, and Oregon (Coombs et al.,
2003). This weevil feeds on the roots and crown during its larval stage and on
the foliage and flowering shoots during its adult stage. Plants are greatly
weakened or die under heavy feeding. The insect is readily available for
distribution, or may be collected at previously established locations. The
species can be transferred to new sites in cool, dry, storage containers with
ample food (Wilson et al., 1994).
Establishment of the weevil is favored on warm, dry, southern exposed slopes.
This weevil has been successful in some areas, but may be ineffective in others.
Utilizing the weevil with good perennial grass management has shown the most
success. The weevil will feed also on meadow sage, but with little effect on the
plants.
Description: Adults of the Mediterranean
sage root crown weevil are small (> 2.0 mm < 4.5 mm long), stout, broad-oval, black, covered with dense checkered
patches of white, black and reddish setae. It has a large median white t-shaped
mark at the base of the wing covers. The snout is long and moderately slender,
often hidden from view in a groove on the underside of the body. The adult
weevil is easily identified, by the characteristic white "T" on the
back.
Host Plant: Mediterranean sage,
Salvia aethiopis L.
Bibliography:
Coombs, E., J. Balciunas and P. McEvoy. 2003. Current
status in each state of all 100 agents approved for release in the continental
USA. Biological control of invasive plants in the United States. Corvallis, OR.,
Oregon University Press.
Wilson, L.M., J.P. McCaffrey, and C.E. Coombs. 1994.
Biological control of Mediterranean sage. Collection and redistribution of the
Mediterranean root crown weevil. Pacific Northwest Extension Bulletin
473.
36. Phytobius leucogaster
(Marsham) - “Flower-eating Weevil”
Species
diagnostic characters:
Size:
Small., > 2.0 mm < 4.5 mm
Body
shape: Broad-oval
Predominant color (cuticle): Black, reddish
brown
Predominant color (scales): Strongly mottled, bicolored or
tricolored
Rostral
length: Long
Rostral
width: Slender
Antennal
morphology: Elbowed
Prothoracic collar: Not raised (side
view)
Prothoracic carina(e): Absent
Prothoracic tubercle(s): Present
Pronotal
depression: Present
Pronotal
depression orientation: Longitudinal
Elytral
carina(e): Absent
Elytral
tubercle(s): Absent
Elytral
spicule(s): Absent
Mesothoracic epipleuron: Ascending and visible in dorsal
view
Leg color
(cuticle): Brown to black
Leg color
(scales): Strongly mottled, bicolored or tricolored
Trochanteral shape and length: Triangular and
short
Femoral
armature: Unarmed
Tibial
armature of apices: All lack spine
Third
tarsus shape: Bilobed
Vestiture
type: Scales
Vestiture
coverage: Dense and complete
Waterproof coating: Absent
Circular
scales: Present
Erect
setae: Absent
Wax like
coating: Absent
Introduction: Phytobius leucogaster
(Marsham) can be found in lakes pools and ditches and can tolerate brackish
water. This species was recorded from spiked water-milfoil Myriophyllum
spicatum L. and whorled water-milfoil M. verticillatum L. The
flower-eating weevil has been reported from three distinct areas in North
America. These include the northeastern United States (Connecticut,
Massachusetts, New York, and Vermont), upper midwestern United States (Michigan,
Minnesota, Wisconsin, Illinois, and Iowa), and western Canada/northwestern
United States (Alberta, British Columbia, Idaho, Colorado, Saskatchewan, and
Washington) (O'Brien and Wibmer 1982; Creed and Sheldon 1994). The weevil
completes all life stages fully submersed and the larvae are stem miners. Very
limited information is available on the biology of this species in the United
States and Canada.
Description: Adults of the flower-eating weevil are small (> 2.0 mm
< 4.5 mm long), moderately elongate, strongly broad-oval, black, and reddish
brown, with one or a few small pale spots, on a black and brown hydrofuge (satin
like) scale coating, which completely conceals the cuticle of the body. The body
is convex and lacks evident setae. The thorax is truncate apically, with a pair
of small acute tubercles, and has a pair of acute strongly developed lateral
tubercles behind the middle. The dorsum is mainly black with a median, basal,
sublinear, impressed, white spot and the side margins are white. The elytra are
black and brown with a distinctive, postscutellar, sutural, white spot and often
with a similar, subapical, sutural, white spot.
Host Plants: Spiked water-milfoil, Myriophyllum spicatum L., and
whorled water-milfoil, M. verticillatum L.
Bibliography:
Creed, R.P. and S.P. Sheldon. 1994. Aquatic weevils
(Coleoptera, Curculionidae) associated with northern watermilfoil
(Myriophyllum sibiricum) in Alberta, Canada. Entomological News 105:
98-102.
O'Brien, C.W. and G.J. Wibmer. 1982. Annotated checklist of
the weevils (Curculionidae sensu lato) of North America, Central America,
and the West Indies (Coleoptera: Curculionidae). Mem. Am. Entomol. Inst. 34:
382pp.
37. Rhinocyllus conicus
Frölich - “Flowerhead Weevil”
Species
diagnostic characters:
Size:
Medium-sized., > 4.5 mm < 10.0 mm
Body
shape: Elongate-oval
Predominant color (cuticle): Black
Predominant color (setae): Strongly mottled, bicolored or
tricolored
Rostral
length: Short
Rostral
width: Broad
Antennal
morphology: Elbowed
Prothoracic collar: Not raised (side
view)
Prothoracic carina(e): Absent
Prothoracic tubercle(s): Absent
Pronotal
depression: Absent
Elytral
carina(e): Absent
Elytral
tubercle(s): Absent
Elytral
spicule(s): Absent
Mesothoracic epipleuron: Not ascending and not visible in
dorsal view
Leg color
(cuticle): Dark brown
Leg color
(setae): Gray
Trochanteral shape and length: Triangular and
short
Femoral
armature: Unarmed
Tibial
armature of apices: All with spine
Third
tarsus shape: Bilobed
Vestiture
type: Setae
Vestiture
coverage: Dense, in bands or patches
Waterproof coating: Absent
Circular
scales: Absent
Erect
setae: Present
Wax like
coating: Present
Introduction:
Rhinocyllus conicus Frölich was introduced from Europe into California in the
early 1970’s for biological control of weedy thistles (Turner et al.,
1987) after its establishment on naturalized thistle in Canada. Since then it
has been introduced and redistributed widely within North America to control
Carduus nutans L., and less widely to control C.
acanthoides L., C. crispus L., C.
pycnocephalus L., and Silybum marianum (L.). The larvae of this
weevil species feed primarily within the flowerheads of Carduus,
Cirsium, Onoprodum, and Silybum thistles in the subtribe
Carduinae (Zwölfer and Harris, 1984). This is an introduced weevil species that
oviposits on the bracts of thistle heads and whose larvae feed in the
receptacle, destroying the seed. In 1969 the weevil was released in Montana
(Rees, 1977) and Virginia (Surles et al., 1974). The species is now well
established in several states of the United States (Trumble and Kok, 1982;
Roduner et al., 2003).
Each female lays 100 to 200 eggs on
the bracts of thistle heads. Eggs hatch in 6 to 9 days and newly hatched larvae
feed through the bracts into the receptacle. Developing larvae feed on the
receptacle and the young seeds, reducing or preventing the production of viable
seeds. There are four larval instars which together last about 4 to 6 weeks.
Pupation occurs in a black oval cell inside the thistle head, and requires
another 7 to 10 days. Adults emerge from seed heads in July and August in more
northern locations and in June and July in Texas. They remain inactive during
the summer and then hibernate through the winter. The following spring adults
emerge from winter shelters to lay eggs on the developing buds. There is one
generation per year.
Description:
Adults of the flowerhead weevil are
medium-sized (> 4.5 mm < 10.0 mm long). They are elongate-oval, with an
indistinct spotted pattern of white, and non-descript brown, recumbent, fine to
moderately coarse setae. At most, the setae only partially conceal the shining
black body. The thorax and elytra are very densely, moderately coarsely
punctuate and frequently covered with a yellowish wax-like exudation. The
rostrum is short, very broad, and broadly sulcate, with the side margins of the
sulcus subcarinately raised and has a fine, but evident, median, longitudinal
carina. The eyes are very narrowly oval. The prosternum is not sulcate. The
tibiae have a very small, inner, apical tooth. The tarsal claws are small,
approximate, connate (basally fused) and symmetrical.
Host Plants: Carduus,
Cirsium, Onoprodum, and Silybum
thistles.
Bibliography:
Rees, N.E. 1977. Impact of Rhinocyllus conicus on
thistles in southwestern Montana. Environ. Entomol. 6:
839-842.
Roduner, M., G. Cuperus, P. Mulder, J. Stritzke and M.
Payton. 2003. Successful biological control of the musk thistle in Oklahoma
using the musk thistle head weevil and the rosette weevil. Am. Entomol. 49:
112-120.
Trumble, J.T. and L.T. Kok. 1982. Integrated pest
management techniques in thistle suppression in pastures of North America. Weed
Res. 22: 345-359.
Turner, C.E., R.W. Pemberton and S.S. Rosenthal. 1987. Host
utilization of native Cirsium thistles (Asteraceae) by the introduced
weevil Rhinocyllus conicus (Coleoptera: Curculionidae) in California.
Environ. Entomol. 16: 111-115.
Zwölfer, H., K.E. Frick and L.A. Andres. 1971. A study of
the host plant relations of European members of the genus Larinus (Col.:
Curculionidae). Common Wealth Institute of Biological Control Technical Bulletin
14: 97-143.
38. Trichosirocalus horridus
(Panzer) - “Thistle Crown Weevil”
or “Musk Thistle Rosette Weevil”
Species
diagnostic characters:
Size:
Small., > 2.0 mm < 4.5 mm
Body
shape: Broad-oval
Predominant color (cuticle): Reddish brown,
black
Predominant color (scales): Gray
Predominant color (setae): Strongly mottled, bicolored or
tricolored
Rostral
length: Long
Rostral
width: Slender
Antennal
morphology: Elbowed
Prothoracic collar: Raised (side
view)
Prothoracic carina(e): Absent
Prothoracic tubercle(s): Present
Pronotal
depression: Absent
Elytral
carina(e): Absent
Elytral
tubercle(s): Present
Elytral
spicule(s): Present
Mesothoracic epipleuron: Not ascending and not visible in
dorsal view
Leg color
(cuticle): Dark brown
Leg color
(setae): Brown
Trochanteral shape and length: Triangular and
short
Femoral
armature: Toothed
Tibial
armature of apices: All lack spine
Third
tarsus shape: Bilobed
Vestiture
type: Scales and setae
Vestiture
coverage: Dense, in bands or patches
Waterproof coating: Absent
Circular
scales: Absent
Erect
setae: Present
Wax like
coating: Present
Introduction: Trichosirocalus horridus (Panzer) is considered to be a native of south and central
Europe. This species was introduced from Italy to the United States in 1970-1972
for quarantine testing. After testing, the species was approved for field use in
1974 to control musk thistle,
Carduus nutans L. (Kok, 1986). The
species is now established in several states from Virginia to Washington (Kok
and Mays, 1991; Coombs et al., 2003).
In Oregon, the species was released to control Italian plumeless thistle, Carduus pycnocephalus L. in 1994,
however, the weevil did not establish (Coombs et al., 2003), but it did establish in
Virginia. The species is likely to be the most effective biological control
agent for the control of plumeless thistle in Ontario and Quebec and of nodding
thistle in cool summer regions (Kok, 2002).
This winter-active weevil, which produces hundred of eggs per female, has
great potential as a control agent of nodding (musk) thistle too. In spring
newly emerged adults feed extensively for several weeks before seeking shelter
in the ground litter. They remain in a state of rest for the majority of the
summer. Mating starts in late summer and females deposit eggs by making
punctures on the underside of the leaf, and along the midrib and primary veins.
Eggs are deposited singly or in clusters of as many as 2000 per female.
Incubation lasts 13 days. Upon emergence, larvae move down the petiole toward
the growth point. They feed within the stem-root junction for 40-164 days,
depending on temperature. Overwintering can occur in this stage. Larvae pupate
in the soil next to the host root, with pupation lasting about 18 days. Adult
usually emerge in late June and early July, start feeding on foliage briefly,
and then aestivate for the remainder of the summer. They become active again in
September until colder weather arrives.
Description:
Adults of the thistle crown weevil are
small (> 2.0 mm < 4.5 mm long), stout, broad-oval, and reddish brown and
black, with indistinct maculate vittae (stripes) formed by a waxy coating on
recumbent short-oval scales. The body is also covered moderately densely with
scattered, long, erect, white, black, and reddish brown, scale like setae. The
thorax has white transverse fasciae (transverse elongate marks) behind the apex
and behind the middle, and a median, longitudinal, narrow vitta, all formed by
moderately dense, white, short-oval, recumbent scales.
Host Plants: In
Europe this weevil species attacks the genera Carduus, Cirsium,
Silybum, and Onopordum, however, most frequently it feeds on
Carduus nutans.
Bibliography:
Coombs, E., J. Balciunas and P. McEvoy. 2003. Current
status in each state of all 100 agents approved for release in the continental
USA. Biological control of invasive plants in the United States. Corvallis, OR.,
Oregon University Press.
Kok, L.T. 2002. Plumeless thistle (Curled thistle, Bristly
thistle). In: Biological Control of Invasive Plants in the Eastern United
States. USDA Forest Service Publication FHTET, (ed. Van Driesche R. et al.,
2002). 413pp.
Kok, L.T. 1986. Impact of Trichosirocalus horridus
(Coleoptera: Curculionidae) on Carduus thistles in pastures. Crop Protection 5:
214-217.
Kok, L.T and W.T. Mays. 1991. Successful biological control
of plumless thistle, Carduus
acanthoides L. [Campanulatae: Asteraceae (=Compositeae)], by Trichosirocalus horridus (Panzer)
(Coleoptera: Curculionidae) in Virginia. Biological Control 1: 197-202.