Pest Management Guidelines |
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| Management of Turf Pests | ![]() |
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By: Dr. Wallace Mitchell, Emeritus Professor,
Dept. of Entomology
University of Hawaii at Manoa
MANAGEMENT OF TURFGRASS INSECT AND MITE
PESTS
Hawaii has fewer pests of turfgrasses than the mainland United
States. Experience on various crops from the mainland U. S. has
shown that the use of chemical pesticides has been reduced
between 25-50% with an IPM program. Brief discussions of the
insect and mite pests of turfgrasses in Hawaii are presented.
Both federal and state laws and regulations concerning the sale
and use of pesticides are continually changing. Pesticides
mentioned in the various sections of this document were
registered in Hawaii for application to turfgrass when this
report was prepared. The mention of trade names does not
constitute an endorsement. It is the responsibility of the user
to make sure label directions are followed precisely.
Insects and mites are soft-bodied, invertebrate organisms that
have lived on earth for more than 300 million years. They are
better adapted than humans to exist on earth. Insects vary in
size from 0.01 inch to over 10 inches in length. they can be
found from below sea level (Death Valley) to the top of the
highest mountains and in the air to 6,000 feet or more. Most
insects are not harmful to man and in fact are very beneficial.
Less than one percent of the insects known to man are considered
pests. Being cold blooded organisms, activity of insects and
mites is controlled by temperature and humidity. Cool
temperatures slow down all activities, including feeding,
reproduction, etc. Activities of mites and insects increase with
increasing temperatures up to a certain point. Extremely high or
low temperatures are lethal. Each insect and mite species has an
optimum range of temperatures for their biological activities.
Turfgrass insect and mite pests occupy a specific part of the
turfgrass environment, namely leaves, stems, thatch and soil. The
mild temperatures in Hawaii allow insects and mites to be active
throughout the year although there may be some seasonal variation
in population size.
A turfgrass manager should familiarize himself with the basic
biological and ecological knowledge of the insect and mite pests.
Good pest management depends upon correct identification of pests
and the injury they produce. The manager should know about their
behavior, growth and development, life stages causing damage, and
food preference. In addition, he must understand environmental
factors, such as humidity, temperature, soil type, location etc.
that affect pest populations growth.
GENERAL BIOLOGY OF INSECTS AND MITES
Adult insects may be recognized by being segmented and having a
body divided into three sections, the head, thorax and abdomen.
The head contains structures to monitor the environment, antennae
(1 pair that contains sensory hairs, cells, etc.), compound eyes,
simple eyes, and mouthparts that are adapted for sucking plant
juices or chewing plant tissue. The thorax contains appendages
for locomotion, 3 pairs of legs, and may be wingless or have one
or two pairs of wings. The abdomen is the terminal end of the
insects body and the last segment contains structures for
reproduction, ovipositor in the female and claspers in the male.
Insects possess structures for the five senses common with man,
sight, touch, smell, taste, and hearing. Adult moths and
butterflies do not damage turfgrass while adult billbugs, chinch
bugs and mealy bugs will feed on turfgrasses.
Mites are relatives of insects but differ greatly. They have only
one body region that is sac-like. Antennae and wings are lacking.
Adult forms usually have simple eyes and four pairs of legs.
Mouthparts are called chelicerae, not mandibles, and are adapted
for sucking plant juices.
All insects and mites develop from eggs that are deposited by the
female on or in plant tissue or near a food source and conditions
suitable for development. This stage of the life cycle is
resistant to most pesticides. Size, color, ornamentation, and
placement of eggs differs greatly and is characteristic for each
species. Eggs do not damage turfgrasses.
Upon hatching from the egg, growth and development of insects and
mites are accomplished in distinct steps or a series of molts, in
which the exoskeleton (outer shell) is shed and renewed. They
change in form and size as they grow. The amount of change varies
from group to group. This change is called metamorphosis. Two
basic types, simple and complete, are found in insects. Stages
between molts are called instars. Growth ceases with the adult
stage.
Immature forms that hatch from eggs of insects with simple
metamorphosis are called nymphs. Nymphs resemble the adults
except in size, body proportions, and the development of wings.
Wings are developed externally during the early instars (stages)
and compound eyes are present. There is no prolonged non-feeding
stage prior to the last molt. Nymphs generally live in the same
habitat and feed on the same food as adults. Chinch bugs,
mealybugs, grasshoppers, cockroaches, stink bugs, termites, etc.
all develop with simple metamorphosis.
Eggs of insects with complete metamorphosis hatch into a
worm-like stage, the larva. Larvae of insects vary in form, some
have legs or are legless, some lack a well developed head.
Mouthparts of larvae may be different than the adult
(caterpillars have chewing types while the adult butterflies and
moths have sucking mouthparts). Food habits of the immature forms
may be similar (bill bugs or snout beetles) or different than the
adults. Larvae do not have compound eyes. Wing development is
internal. Larvae molt and pass through several instars,
increasing in size and often changing in color. The larva is the
most damaging stage in the development of insects having complete
metamorphosis and is the primary target of a pest management
program. After the last larval instar, the insect changes into a
pupa. Pupae do not move about, are inactive and do not feed. The
pupa may be enclosed in a special cell or protective covering,
which may be a hibernaculum, cocoon, or formed by the last larval
skin, the puparium. The pupal stage is highly active,
biologically for all larval tissues are broken down and
reconstructed into adult tissues. Wings develop externally. The
pupal stage is difficult to kill with pesticides for it does not
feed or come in contact with pesticidal sprays. Moths,
butterflies, beetles, flies, wasps, and bees develop through
complete metamorphosis.
Turfgrass problems can result from causes other than insects.
Careful observation should be made of areas exhibiting injury.
Other causes of turf injury may be improper irrigation, improper
fertilizer practices, excess accumulation of thatch, poor root
system, detrimental weather conditions, improper mowing height,
improper selection of turfgrass cultivar, oil or fuel spills,
pesticide injury and acid or basic soil reaction. Many of these
conditions are discussed in more detail in the section on
turfgrass management.
When examining turfgrass, look for signs of insect or mite injury
such as; thin grass stands, discolored, twisted or withered leaf
blades, dying or dead patches, chewed or frayed leaf blades, and
the presence of webbing or frass (fecal pellets) in the grass.
The presence of large numbers of bufo toad or bird droppings
indicate feeding on insects and a turfgrass problem may be
developing. Small mounds or burrows also indicate the presence of
turfgrass pests or predators in the damaged area. Inspect the
zone between the healthy and damaged turfgrass.
In IPM we encourage the use of all pest control tactics in an
integrated unified program. Pesticides are not eliminated as a
tactic, but are used in a precise manner only when needed. There
are many alternatives to chemical pesticides and all should be
considered.
Damage to turfgrass is done by feeding of adult and/or immature
forms. The type of injury is closely associated with the type of
mouthparts. Insects with chewing mouthparts have laterally moving
mandibles that tear off pieces of plant tissue and those with
sucking mouthparts have the parts modified into a beak through
which the plant sap is sucked. Mites also suck juices from the
plant. Some pests feed only at night. Unless special effort is
made to find the pest they may go undetected for some time.
Most turfgrass injury from mites or insects can be prevented by
regular inspections of the areas and immediate remedial action.
Insects and mites damage may be recognized by defoliation,
yellowing, twisted growth, shortening of the internodes,
stunting, browning and bleaching of leaves or dieback of the
turfgrass. Early detection of such symptoms may prevent rapid
buildup of insect pest populations when conditions are optimum.
PESTS
In Hawaii there are ten arthropod invertebrate pests of
turfgrasses. Five are larvae of moths or butterflies (Order:
Lepidoptera). One is a snout beetle or bill bug (Order:
Coleoptera). One is a mealybug (Order: Homoptera). Early workers
have erroneously called the mealybugs scale insects (i.e.
Rhodesgrass scale). One is a scale insect (Homoptera). One new
pest of St. Augustinegrass which has only recently (August 1990)
been reported in the state is a chinch bug (Order:Hemiptera). One
species of mite (Order:Acarina) is a pest of bermudagrass. Each
of these will be covered separately.
MOTHS AND BUTTERFLIES
Order: Lepidoptera
KEY PESTS GRASS WEBWORM (GWW)
Herpetogramma licarsisalis (Walker) (Family: Pyralidae)
is the most serious pest of turfgrasses in Hawaii. It was first
reported in 1967 feeding on Kikuyu grass, Pennisetum
clandestinumHchst. ex Chiov., (Davis, 1969). It was infesting
pasture grasses and then spread to turfgrasses.
DAMAGE
Larvae damage turf by feeding on grass blades and crowns. Their
presence is noticed by the feeding injury (ragged blades), green
fecal pellets, and the conspicuous amounts of webbing on the
surface leading to holes into the thatch. Feeding occurs at
night. During the day larvae may be found near the base of the
grass curled up. When disturbed, they become active and move
rapidly away. Larvae are usually shiny green when feeding and
brownish when unfed. The larvae live in silken tunnels near the
soil line. The first indication of damage is usually the ragged
appearance of turfgrass, although it is still green. After a
period of time, with continued feeding, large brown patches
appear. These patches may coalesce into larger areas.
HOST RANGE
Larvae of the GWW will damage pasture grasses and are considered
serious pests of Sunturf bermudagrass, Cynodon magennisii
Hurcombe. Davis (1968) reported larvae feeding on 13 other
grasses in Hawaii (Table 1), including all the important
bermudagrasses. Host preference studies by Murdoch and Tashiro
(1976) with Sunturf bermudagrass; common bermudagrass, C.
dactylon (L.) Pers.; Tifway bermudagrass, C. dactylon x C.
transvaalensis Burtt-Davey; Tifway bermudagrass C. dactylon x C.
transvaalensis Burtt-Davey; FB-137 bermudagrass, C. sp. showed
the least feeding injury on common and Tifway bermudagrasses.
Feeding injury spread more rapidly on the fine textured grasses
than on coarse textured ones. Reinert and Busey (1983) reported
on resistance of several bermudagrass selections to the tropical
sod webworm, Herpetogramma phaeopteralis Guenee, not found in
Hawaii, but closely related to the GWW. In their studies common
bermudagrass and the FB-119 selection had less feeding injury.
DESCRIPTION OF THE LIFE STAGES
Reports on the biology of the GWW have been published by Champ
(1955), Davis (1969), Tashiro (1976, 1977,1987) and Marsden.
(1979a.)
Adult
Moths are gregarious and often found clustered on vegetation.
They are attracted to lights and may be a nuisance around the
home when populations are high. The moth is nearly a uniformly
light brown in color with small dark dots scattered about the
wings. Wing span is about 0.75 inches when at rest in the field.
Fully expanded wings reach 0.94 inches and the body is about 0.5
inches long. When at rest, the insect is triangular in shape.
Preovipositional period varied from 3 to 6 days. Egg production
averaged 249 per female with a maximum of 557. Mating and
oviposition occurs at night. Adult longevity averaged 13.1 and
13.5 days for male and female moths, respectively.
Egg
Females usually deposit their eggs on the upper surface of a
leaf, along the midrib near the base of the blade. Eggs are flat,
elliptical and laid singly or in masses overlapping each other
like shingles. Newly deposited eggs are creamy white and as
Table 1. Host range of Herpetogramma licarsisalis in Hawaii.
Host common name |
Host scientific name |
Narrow-leaved carpetgrass |
Axonopus affinis Chase |
Californiagrass (paragrass) |
Brachiaria mutica (Forsk) |
Stargrass |
Chloris divaricata R. Br. |
Bermudagrasses |
Cynodon spp. Rich |
Henry's crabgrass |
Digitaria adscendens H. B. K. |
Pangolagrass |
Digitaria decumbens Stent |
Goosegrass (wiregrass) |
Eleusine indica (L.) Gaertn. |
Centipedegrass |
Eremochloa ophiuroides (Munro) Hack |
Torpedograss (Wainakugrass) |
Panicum repens L. |
Hilograss |
Paspalum conjugatum Berg. |
Panama paspalum |
Paspalum fimbriatum H. B. K. |
Seashore paspalum |
Paspalum vaginatum Sw. |
Kikuyugrass |
Penniseturn clandestinum Hochst ex Choiv. |
Rattailgrass |
Sporobolus africanus (Poir.) |
| St. Augustinegrass (buffalograss) | Stenotaphrum secundatum (Walt.) Kuntz |
development of the embryo progresses, change in
color from light yellow to orange. Just prior to hatching, the
black head of the larva is visible through the chorion (egg
shell). Egg development ranges from 4 to 6 days. Hatching of the
egg takes place at night. Eggs have been collected on grasses up
to 4000 feet elevation.
Larva
There are 5 larval instars in the development of the GWW. The
first instar, with a black head capsule, does not eat the
chorion. It is translucent and amber colored until feeding
begins. It then changes to light green as a result of the
ingested plant material. All other instars have brown head
capsules. Larger larvae are various shades of color from brown to
green, depending upon the quantity of fresh food ingested. The
body of larger non-feeding larvae are mostly brown and may have a
rose tint over most of the body. The prothoracic shield (above
the first pair of legs) is lighter brown than the head capsule
and each segment of the body has a ring of dark brown spots. Many
of the brown spots bear 1 to 3 conspicuous setae (hairs). First
instar larvae are about 0.04 inch long and the mature larvae (5th
instar) are nearly one inch. Larvae feed at night and hide in the
thatch near the surface of the soil during daylight. First and
second instar larvae feed on the upper surface of the blades
leaving the lower surface intact. Third to fifth instars notch
and eat entire leaves and spin large quantities of silk webbing.
Larval development averages 14.3 days. Prior to pupation, the
fifth instar larva becomes quiescent, slightly shorter in length,
and constructs a silken sheath (hibernaculum), covered with
insect excrement and plant debris. Pest management tactics are
applied against the larval stage.
Pupa
GWW pupation takes place within the hibernaculum. Pupae at first
are creamy white color, then change to light brown and finally
dark brown. Sex of the pupae can be determined. The average
length of the pupae is about 0.4 inch. Duration of the pupal
stage averages 7.3 days. Adults emerge from the pupal stage at
night. Pesticides are ineffective against this stage of
development. Natural control factors affect this stage of
development.
At 24. 5° C (76.1° F) the total duration from egg hatching to
adult emergence averaged 21.7 days. If the temperature was 30° C
(86° F), the period was shortened to 16 days. Tashiro (1976)
estimated that the optimum temperature for development of the GWW
was slightly above 31° C (87.8° F).
MONITORING METHODS
A simple, rapid, accurate method of measuring the population of
GWW larvae in turfgrass is essential for a pest management
program. Several techniques have been tried. One of the earliest
was a sprinkling can application of one gallon of water
containing either pyrethrins or a detergent over an area of one
sq. yd. The number of larvae rising to the surface within a ten
minute period were counted (Anon., 1981; Niemczyk, 1981). Plywood
boards 0.5 x 12 x 24 inches were placed on the turfgrass in the
late afternoon, left overnight, and GWW larval counts taken the
following morning. Nocturnal feeding larvae came to the surface
to feed and remained, since the board excluded light (Mitchell
and Murdoch, 1974). Visual ratings of larval feeding within a
randomly selected area (2 sq. ft.), replicated 4 or 5 times, have
been used to estimate GWW damage. Researchers' visual ratings of
GWW feeding in the turfgrass plots were averaged.
Tashiro et al. (1983) made comparisons of the boards, sprinkling
can and submergence of an area with water alone and water
containing either pyrethrins or a detergent. For submergence
tests, three metal rings (each 8 in. in diameter and 8 in high)
were compared to a rectangular metal frame 3 x 12 x 24 in. The
metal forms, with the bottom edge tapered to a cutting edge, were
forced through the turfgrass into the soil at randomly selected
areas. Four liters of liquid were applied to each frame, allowed
to stand for 10 minutes with continuous counting of the larvae
coming to the surface. Number of larvae surfacing was compared
with larval counts under the boards. Research indicated more than
one gallon of liquid irritant per treated area may be needed to
completely saturate the turf.
Liquid irritants tested were water alone, water with 0.0002%
(v/v) pyrethrins and water with 0.25% (v/v) liquid detergent. The
detergent used was a mixture of anionic and nonionic surfactant
plus ethyl alcohol (Joy, Procter and Gamble Co.).
Use of liquid irritants resulted in higher counts per unit area
of turf. Approximately 3 times more larvae were forced to the
surface within the 10 min. period than were found under plywood
boards left overnight on the same turfgrass plots. Boards were
31% as efficient as pyrethrins and 25% as efficient as detergent
Complete submergence with standing water for 10 min. was more
effective than sprinkling solutions over the surface or utilizing
boards.
To obtain accurate counts, continuous observation of the treated
area for 10 min. was necessary. Not all larvae were forced to the
surface within a 5 min. period but some larvae forced to the
surface early reenter the turf before 10 min. period is up. It is
recommended that a metal form, circular in shape (6 in. high and
20 in. diameter), be used as a sampling frame. Four liters of
water containing either 0.0015% pyrethrins or 0.25% detergent is
poured within the frame and the number of larvae coming to the
surface within ten minutes counted. The process is replicated 3
to 5 times. The Lawn armyworm (LAW), fiery skipper (FS), and
black cutworm (BCW) larvae responded to liquid irritants in the
same manner as the GWW. Short (1990) recommended mixing one fluid
ounce of detergent in two gallons of water and drenching a 4 sq.
ft. area with the solution. If no larvae are observed coming to
the surface, examine other suspect areas and repeat.
ACTION (THRESHOLD) LEVELS
The action or threshold level is when the pest population or
turfgrass damage level has reached the point that a decision must
be made whether or not to treat with an insecticide. The decision
will depend upon the population of pest per unit area, the vigor
and condition of the turf, and the intended use of the turf.
Decision to treat is purely subjective, as pest populations are
so dependent upon available moisture, temperature and vigor of
turfgrass. Pests in Hawaii are active throughout the year, but
become inactive if the temperature goes below 61° F. Threshold
levels for more valuable greens and tees will be lower than for
fairway and rough areas.
A visual rating of 10% or greater damage to bermudagrass turf,
with the presence of lepidopterous larvae, is considered the
level at which a pest management control tactic (insecticide)
must be applied (Mitchell and Murdoch, 1974). Grass webworm
larval counts of 5 per 2 sq. ft. plot indicated that more
frequent observations were needed to determine the impact. An
average of 10 GWW larvae per 2 sq. ft. is considered the action
level at which a pest management tactic must be considered. These
action levels are a beginning and can be finely tuned with
experience.
Bowen (1980) in California recommended control measures be
initiated if pest populations exceeded 5 cutworms, 10 skipper
larvae, 15 sod webworms, or 9 billbug larvae per square yard of
turfgrass.
BIOLOGICAL CONTROL
A number of parasites and predators attack various stages of the
GWW in Hawaii. Several of these beneficial organisms were
purposely introduced for other lepidopterous pests, others
arrived accidentally. Pathogenic organisms attacking the GWW have
not been reported to date in Hawaii.
Egg Parasite
Davis (1969) reported an accidentally introduced small wasp,
Trichogramma sp., parasitized up to 96% of the GWW eggs from sea
level to 2,000 feet (610 meters) elevation. An average of two
parasites emerged from each GWW egg. The parasite was
mis-identified as T. semifumatum.
Larval Parasites
Three parasitic wasps and one fly have been recorded attacking
GWW larvae (Table 2). Adult tachinid flies, Eucalatoria armigera,
have been observed, in a wide range of field conditions, to be an
effective parasite. The ichneumonid wasp, Cremastus
flavo-orbitalis also ranked high in parasite emergences.
A single Chalcid wasp was reported parasitizing the GWW pupa.
Data on the impact of the larval and pupal parasites is meager.
Both invertebrate and vertebrate predators have been recorded
feeding on GWW larvae. The bigheaded ant, Pheidole megacephala
(Fab.) (Family: Formicidae) was the most common insect. Avian
predators included the cattle egret, Bubulcus ibis L.; the
mynah bird, Acridothermes tristis tristis (L); the Brazilian
cardinal, Paroaria coronata (Latham) and the Pacific golden
plover, Pluvialis dominica fulva (Gmelin). Head capsules of the
GWW have been found in the droppings of the giant toad, Bufo
marinus (L.). The impact of these predators on GWW populations is
not known.
Table 2. Grass webworm larval and pupal parasites.
| Scientific name | Order | Family | ||
| Larval Parasites | ||||
| Casinaria infesta (Cress) | Hymenoptera | Ichneumonidae | ||
| Cremastus (= trathala ) flavo-orbitalis Cam. | Hymenoptera | Ichneumonidae | ||
| Meteorus laphygmae Viereck | Hymenoptera | Braconidae | ||
| Eucelatoria armigera (Coq.) | Diptera | Tachinidae | ||
| Pupal Parasites | ||||
| Brackymeria sp. | Hymenoptera | Chalcidae |
Biocontrol agents are effective in some
situations. Accurate observations on the impact of beneficial
organisms are essential in making the decision whether or not to
apply additional pest management tactics on the GWW population.
CULTURAL CONTROL
Some of the cultivars of bermudagrass have shown differences in
feeding injury by GWW larvae (Murdoch and Tashiro, 1976, Tashiro,
1976 and Reinert and Busey, 1983a) . Future genetic selections of
bermudagrass may show resistance to GWW feeding. Good management
practices, fertilization, irrigation, aeration, etc., which
produces healthy turfgrass, allows the turf a better chance of
recovery from GWW damage. Mowing at 1.5 inches and reduced use of
nitrogen fertilizer has been recommended in Florida (Short,
1990). Short recommended using water insoluble (slow release) N
and controlling thatch.
CHEMICAL CONTROL
Insecticidal control is the first line of defense when there is a
sudden widespread increase of defoliation by GWW or other
turfgrass pests. There is no alternative but to depend upon a
recommended insecticide. A number of insecticides for application
to turfgrasses have been registered by the EPA and the Hawaii
Department of Agriculture for use in Hawaii (Table 3). Even
though a pesticide may be registered for turfgrass on the
mainland U. S., it may not be used in Hawaii unless it is
registered in Hawaii.
Insecticides are compounds that kill insects through their
chemical action. All insecticides must be considered hazardous
chemicals in handling, storage, application and post-application
use. Pesticide users must understand the label to be sure that
the pesticide is registered for use in Hawaii for turfgrass and
for the particular site and pest in question. Directions for use,
clean up, safety, precautions, storage, disposal, and symptoms of
poisoning and emergency procedures should be clearly understood.
For example, diazinon, and organic phosphate insecticide, CANNOT
BE USED ON GOLF COURSES AND SOD FARMS, but may be used by
homeowners on their lawns. The federal and state regulations
change frequently and one must follow directions on the latest
label. Information on the insecticides may be obtained from the
basic manufacturer or his representative in Hawaii, University of
Hawaii Extension Service, and Hawaii Department of Agriculture,
Pesticide Division. Any problems with spills or accidents should
be reported to the State Departments of Agriculture and Health,
Occupational Safety and Health (OSHA).
Proper timing of a pesticide application directed against the
most vulnerable stage is necessary for effective GWW control and
may reduce the number of applications necessary per season. The
most commonly used formulations are emulsifiable concentrates
(EC), wettable powders (WP), soluble powders (SP), and granules
(G). Granular formulations were more effective in reaching the
crown of the grasses at the soil level and lasted longer than
emulsifiable concentrates. Soluble powders and emulsifiable
concentrates were easier to mix, apply, and in some instances
more effective than the WP formulations. Pesticides selected
should be biodegradable, nonphytotoxic, have a low leaching
potential and a low mammalian toxicity. Extreme care should be
taken in the selection of a pesticide to be applied to turf or
pasture grasses for grazing cattle, horses or pets in order to
reduce pesticide residue hazard.
Insecticides registered in Hawaii for control of turfgrass pests
are listed in Table 3. Registrations for use are changing daily,
so one should read and understand the label before applying the
material to turfgrass. The insecticide selected must be
registered for application to turfgrass in golf courses. If there
is any question as to whether it can or cannot be used, check
with the DOA, basic manufacturer or their representative. New
materials may be added and present registrations may be withdrawn
at any time by EPA, DOA, and the basic manufacturer.
Table 3. Insecticides registered for turfgrass insect control on
golf courses in Hawaii.å
Common name Trade name(s) |
Use* |
Classification** |
Biorational: |
||
Bacillus thuringiensis Dipel, Thuricide |
I |
G |
Carbamates: |
||
Bendiocarb Turcam |
I |
G |
Carbaryl Sevin 80S |
I |
G |
Organic Phosphates: |
||
Acephate |
Orthene Turf, Tree and |
|
Ornamantal spray I |
G |
|
Chlorpyrifos |
Dursban 50W I |
G |
Ethion |
Ethion 8 EC I, A |
R |
Isofhenfos |
Oftanol 2 I |
G |
Methomyl |
Lannate I |
R |
Trichlorfon |
Dylox 80 I |
G |
Synthetic Pyrethoids: |
||
Fluvalinate MavrikAquaflow |
I. A |
G |
*Use: I = insecticide, A = acaricide, N =
nematocide:
**Classification: G = general use, R = restricted use
BE SURE TO READ THE LABEL BEFORE APPLYING PESTICIDES
Other insecticides that have been suggested for sod webworms and
army worms in Florida are acephate, bendiocarb, Bacillus
thuringiensis var. kurstaki, ethion, methomyl and trichlorfon
(Short 1990, Reinert 1976, 1983a). These materials have not been
tested against lepidopterous pests in Hawaii.
For the GWW and other lepidopterous larvae, chlorpyrifos
(Dursban) emulsifiable concentrate or granular formulations and
carbaryl (Sevin) soluble powders, wettable powders, and granular
formulations have been very effective. Check the label for the
rate of application. Treatments should be applied in the evening
or late afternoon and not watered in. Repeat the treatment if
necessary. Chlorpyrifos is normally tightly sorbed onto the
organic matter in the thatch and in the soil so that leaching is
not a problem.
OCCASIONAL PESTS LAWN ARMYWORM (LAW) Spodoptera
mauritia (Boisduval) [Family: Noctuidae]
The LAW was first discovered in Hawaii in 1953 (Pemberton, 1953)
and like the GWW is established on all islands. LAW is not known
to occur in the continental United States. During the sixties it
was the most important pest of turfgrass and in recent years the
populations have stabilized, apparently due to actions of
parasites and predators. Information on the biology and ecology
of the LAW have been published by Tanada and Beardsley (1958),
Marsden (1979b) and Tashiro (1987).
DAMAGE
The larval stage or caterpillar damages the turfgrass by feeding
on the blade, crowns and stems. Young larvae may feed on the
blades during daylight hours and the grass shows a silvering at
the tips. Watch for this sign of feeding damage. As the larvae
increase in size they eat all the leaves and stems in their path
and greener portions of the crown leaving only the tough old
runners. Damaged areas take on a brown, dried up appearance.
Active infestations are characterized by having a sharply defined
advancing front between defoliated and green undamaged turf. With
large active populations the front may move as much as one foot
each night. Normally the denuded area spreads out from around the
bases of buildings or trees and shrubs where eggs have been
deposited. Older larvae feed at night and hide in the grass
during the day.
HOST RANGE
In Hawaii LAW damage was most severe to bermudagrass lawns.
Tanada and Beardsley (1958) believed the large recorded host
range may have been confusion in larval identification of other
species of Spodoptera. They conducted host range and preference
studies. LAW larvae have been reported to feed on sedges
(Firnbristylis tenera Roemer and Schultes), two week old
sugarcane seedlings and several grass species (Table 4). In the
Orient the insect sometimes caused injury to rice. Survival of
LAW larvae on these hosts ranged from 72 to 100 per cent in
various tests.
DESCRIPTION OF THE LIFE STAGES
Descriptions of the life stages and the biology of the LAW have
been published by Fletcher (1956), Marsden (1979a), Tanada and
Beardsley (1958) and Tashiro (1987).
Adult
Moths are nocturnal and commonly attracted to lights. Adults are
common grayish brown with a wingspan of 1.2 to 1.6 inches. Males
are slightly smaller (1.31.5 inch wingspan) and more vividly
marked than the females. The forewing of the male has a white
diagonal mark in the anterior median area of the upper surface of
the wing between the whitish or buff-colored orbicular spot and
the dark bean-shaped spot. The female is slightly larger (1.4-1.6
inch wingspan) than the male and this area is dull grayish-brown
and not much different from adjacent areas of the forewing. The
dark bean-shaped spot is well defined. The hind wings of both
sexes
Table 4. Host Range of Spodoptera mauritia in Hawaii
Common Name |
Scientific Name |
Bermudagrass |
Cynodon spp. |
McCoy grass |
Cyperus gracilis R. Br. |
Kyllinga |
Cyperus kyllingia Endl. |
Nutgrass |
Cyperus rotundus L. |
Henry's Crabgrass |
Digitaria adscendens H.B.K. |
Wiregrass |
Eleusine indica (L.) Gaertn. |
Dallisgrass |
Paspalum dilatatum Poir. |
Napiergrass |
Pennisetum purpurem Schumach. |
Bristly Foxtail |
Setaria verticillata (L.) |
Buffalograss,St.Augustine Grass |
Stenotaphrum secundatum (Walt.) Ktze. |
Manilagrass |
Zoysia matrella (L.) Merr. |
are pale with darker areas along the outer
margins. The dorsum of the thorax is covered with greyish to
reddish brown scales.
Adults mate within a day after emergence from the pupa and start
to lay eggs about 4 days later. Oviposition begins shortly after
dusk and is usually completed before midnight When fed sugared
water adults lived for 9-14 days.
Egg
Females usually deposit their eggs on the foliage of shrubs and
small trees. Females rarely deposited their eggs on grass. Wooden
and concrete structures, especially near outdoor lights allowed
to burn in the evening or near a window from which light
emanated, were used as ovipositional sites.
Eggs are deposited in flat, felt-like masses, elongate-oval in
outline, covered with light brown hairs from the tip of the
females abdomen. The eggs are not visible unless the female is
old and her abdominal hairs are exhausted, the last egg masses
may be nearly naked. Each egg mass consists of several layers and
may contain 600, 700 or more eggs. Eggs are light tan or greenish
with a pearly luster and as development progresses turn to grey
or dark tan prior to hatching. Eggs are circular, flattened and
sculptured with fine lines. Eggs hatch within 3-5 days.
Larva
Caterpillars of the LAW have 7 or 8 instars in their development.
First instar larvae are pale green, about 0.05 inch long, emerge
from the eggs and spin a silken thread to reach the ground. First
to third instar larvae remain predominantly green as soon as
feeding begins. As the larvae continue to grow, they become
brownish with a pair of pale stripes down their backs. Patterns
and stripes are present in the fifth to seventh or eighth
instars. Mature larvae are 1.5 inches long with a pair of
prominent jet black marks on each body segment, with exception of
the first thoracic and terminal segments, toward the center of
the body inside the longitudinal yellow stripes. Spiracles are
black. Development takes approximately 28 days.
Pupa
Pupation occurs in a loosely formed silken cocoon containing
dirt, plant material and larval webbing. The pupa is normally
found in the soil or grass debris at the base of the turf. It is
reddish brown when fully hardened. Pupal period lasts from 10-14
days.
The entire life cycle takes approximately 42 days depending upon
the temperature and humidity. Adult moths have a preovipositional
period of nearly 4 days, eggs hatch in 3 days, larval period
lasts 28 days and the pupal period averages 11 days.
MONITORING METHODS
Methods for monitoring LAW populations are the same as described
for the GWW. The use of liquid irritants or flooding the sample
area with water forced the larvae to come to the surface. The
liquid irritants were more efficient than the boards left
overnight.
ACTION LEVELS
Larval populations of LAW have been low probably due to the
impact of predators, parasites and pathogenic organisms. A
general level of 5 LAW larvae per square yard indicates an
increasing population and a pest management tactic should be
considered. With more experience the action level may be fine
tuned and more accurate.
BIOLOGICAL CONTROL
In Hawaii a number of natural enemies have made an impact on
populations of LAW. Several of these beneficial organisms were
introduced for other lepidopterous pests and others arrived
accidentally with the host.
Microorganisms
A polyhedrosis virus attacking LAW was reported by Bianchi
(1957). The virus has been observed in both young (second to
fourth instar) and older larvae. The viral infection was most
likely introduced by the insect. Tanada and Beardsley (1957) and
Tanada (1960) described the virus as Borrelinavirus sp. The virus
could infect all larval stages but was more pathogenic to the
younger than older larvae.
A microsporidian, Nosema spp., was found in LAW eggs. The
microsporidian was highly infectious but its impact on LAW
populations has not been determined. A fungus and bacterial
disease of LAW has been reported in Australia (Smith 1933) and
Sri Lanka (Hudson 1920). Neither of these two microorganisms has
been reported in Hawaii. Some of the microorganisms may show
promise in microbial control of the LAW.
Egg Parasites
Two species of parasitic wasps, (Telenomus nawai Ashmead [Family:
Scelionidae] and Trichogramma minutum Riley [Family:
Trichogrammatidae]) attack LAW eggs. Parasitism of eggs ranged
from 20 to 80 per cent. The heavy covering of hair and several
layers of eggs appeared to hinder the egg parasites.
Egg-larval Parasites
The braconid wasp, Chelonus texanus (Cresson) was observed
ovipositing in LAW eggs. The parasitoid was introduced into
Hawaii from Texas to control Laphygma exempta (Walk.) (Bianchi
1944). The wasp larva emerges from fifth or sixth instar LAW
larvae and pupates in a silken cocoon in ground litter. Thirty
days are needed for completion of development from oviposition to
emergence of the adult wasp.
Larval Parasites
LAW caterpillars attacked by braconid wasps are killed usually
before they are half grown. One of the most important parasites
of LAW larvae is Apantales marginiventris (Cress.). It was reared
from early instar LAW larvae. The parasitoid larvae emerges from
the hosts fourth instar caterpillar and forms a white cocoon,
usually found on a grass blade. The life cycle of A.
marginiventrus is completed is 12-18 days.
Three species of tachinid flies, Chaetogaedia monticola (Bigot),
Achaetoneura archippivora (Williston) and Eucelatoria armigera
(Coq.) have been found parasitizing LAW larvae. When parasitized
by one of these flies the host is killed in the pupal or last
larval stage. The emergence of the parasitoid in the later
instars allows the larvae to do contribute materially to the
damage of turfgrass before they die.
Predators
Both invertebrate and vertebrate predators have been observed in
Hawaii feeding on LAW larvae or pupae. Two species of ants,
Monomorium floricola Jordan and Pheidole megacephala (Fab.)
attack LAW egg masses. The big-headed ant, P. megacephala has
also attacked LAW larvae. Three species of coccinellid (ladybird)
beetles, Orcus chalybeus (Boisd.) larvae and adults, and only
adults of Cryptolaemus montrouzieri Mulsant and Scymnus roepkei
Fluiter were feeding on eggs of LAW. Although data is lacking,
other insects, such as lacewings larvae and wasps may also attack
LAW larvae in the grass.
The major vertebrate predators of LAW larvae are the giant toad,
Bufo marinus (L.), and the Indian mynah bird, Acridotheres
tristis (L.). The toad is believed to be a valuable predator
because its nocturnal feeding habits coincide with those of
mature LAW larvae. In other parts of the world ducks, storks,
cranes, herons, egrets, chickens and crows have been reported to
be effective predators of the LAW.
The biocontrol agents are effective in some situations. Accurate
observations on the impact of these natural control agents is
essential in making the decision whether or not to apply an
insecticide on the LAW population.
CULTURAL CONTROL
One of the simplest methods is to brush off egg masses on
ceilings and walls of buildings. Mow grass properly. Avoid the
buildup of thatch and remove it when it is excessive. Larvae tend
to hide in the thatch. Fertilize turfgrass properly for the
increase in succulence of grass encourages an increase in insect
attack
CHEMICAL CONTROL
The insecticides suggested for GWW control are also effective in
controlling LAW. The biorational, Bacillus thuringiensis var.
kurstaki spores, is an effective larvicide. It is harmless to
humans and safe to the environment. Its activity decreases with
exposure to strong sunlight and extreme temperatures. Refer to
the label for instructions on dosage rates, application
information and precautions. An area treated with granular
formulations should be watered down following application.
Evening treatments are preferred and repeat applications may be
necessary.
POTENTIAL PEST FIERY SKIPPER (FS) Hylephila
phyleus (Drury) [Family: Hesperiidae]
The skipper butterfly was first discovered in Hawaii in 1970
(Kawamura and Funasaki 1971), has the potential to cause
significant damage to turfgrass during warm periods. It is found
on all islands with the exception of Lanai. The common name,
fiery skipper, is due to the bright orange and brownish color and
erratic, skipping flight pattern of the adults.
DAMAGE
Larvae are seldom seen and the first evidence of damage are small
isolated round spots where single larvae have devoured the grass
blades. The circular spots are 1-2 inches in diameter. These
spots may coalesce into larger areas.
HOST RANGE
Larvae will feed on all common lawn grasses but appears to prefer
bermudagrasses (Cynodon spp.), bentgrasses (Agrostis spp.),
crabgrasses (Digitaria adscendens) and St. Augustine grass
(Stenotaphrum secundatum).
DESCRIPTION OF LIFE STAGES
Biology of the fiery skipper in Hawaii has been published by
Tashiro and Mitchell (1985) and Tashiro (1987).
Adult
Adults are more commonly seen flying about visiting flowers of
lantana, honeysuckle, clover and other plants to feed on nectar.
The FS has a wingspan of 1.0 inch or slightly larger. Males are
predominantly bright orange-yellow above and pale yellow with
black spots on the underside of front and hind wings. Females are
predominantly dark brown with orange-yellow spots on the upper
wing surface and similar coloration of the males on the
undersurface of the wings.
Egg
Hemispherical eggs are deposited singly on the upper surface of
the grass blades. Freshly deposited eggs are pearly white and as
development continues change to powdery blue, then greenish blue
within 1-2 days. Just prior to hatching the egg becomes nearly
white again and the black head of the larva is visible through
the chorion. Egg development may take 3-5 days.
Larva
Larvae are seldom seen since they remain concealed in lightly
woven silken tubes in the thatch area. There are five larval
instars in the development of FS. First instar larvae are pale
greenish in color with a granular appearing surface over the
body. The first two body segments behind the head are smaller
than the rest, appearing as a strongly constricted neck. The
"neck" is a distinguishing characteristic for all FS
larval instars. The head is strongly constricted in the neck area
and a black narrow shield over the prothorax is evident. The head
is black and mottled or striped with brown and the body is
covered with short setae for all five instars. Later instars the
body becomes yellowish-brown to grayish-brown with a faint median
longitudinal stripe. FS larvae are approximately 1.0 inch in
length. Just prior to pupation the body becomes rigidly straight
(prepupa). First instar larvae notch the edges of the blade and
later instars consume the whole leaf. Third to the fifth instar
larvae spin large quantities of strong silk webbing. Larval
development at 81-84° F is completed in about 15.5 days
Pupa
Pupation often occurs in grass near the surface of the soil in a
loosely woven cocoon covered with leaf litter debris. If debris
is not available the pupa may be free in the grass-root zone.
Young pupae have a light green head and thorax, and a light tan
abdomen. As development progresses the pupa turns brownish-yellow
with a conspicuous black dorsal line and is covered with rather
thick bristly hairs. Pupae of FS are about 0.7 inch long. Pupal
development at 81-84°F is completed within 7.6 days.
Development from egg to adult takes 48 days when reared at 75°F
and fed bermudagrass. When reared at 81-84°F it took only 23
days.
MONITORING METHODS
Methods for monitoring FS populations are the same as described
for the GWW. Larvae have been observed under boards as well as
being forced to the surface with the use of irritating liquids.
ACTION LEVELS
Larval populations of FS have been low and present in few
situations. We do not know the reason for such low populations
but believe it must be due to environmental conditions and the
impact of parasites or predators. Because of the low populations
in Hawaii, action levels have not been developed for FS. Ten FS
larvae per square yard as suggested by Bowen (1990) in California
may be a starting point.
BIOLOGICAL CONTROL
Information on natural enemies of FS is lacking for Hawaii. In
California a braconid wasp, Apanteles spp., and an ichneumonid
wasp, Amblyteles sp., attack the larvae and pupae, respectfully.
CULTURAL CONTROLS
Mow, fertilize and manage the turfgrass properly. Avoid the build
up of thatch and remove it when it is excessive. Thatch provides
a haven for the larvae to hide in and their populations may
increase. Good management practices for good healthy turf
requires fewer insecticide applications.
CHEMICAL CONTROL
Insecticide treatments may not be needed if the FS populations
continue to remain low. The insecticides suggested for GWW and
LAW are also effective in controlling FS. Refer to the label for
rates of application, precautions and directions for use.
Granular formulations should be watered down to move the toxicant
down into the thatch and grass at the surface of the soil. Apply
the pesticides in the evening or late afternoon. Repeat
treatments may be necessary.
POTENTIAL PEST BLACK CUTWORM (BCW): Agrotis
ipsilon (Hufnagel) [Family: Noctuidae]
Occasionally a larva of this noctuid moth will come to the
surface of the turfgrass when monitoring for the key pests.
Although the insect has been recorded in Hawaii since 1879, it
has not developed into a serious pest of turfgrass but has the
potential for serious outbreaks. It is also called the greasy
cutworm.
DAMAGE
The common name describes the larval habits. Larvae feed at night
on the leaves and crown of the turfgrass and may cut off plants
near the soil surface. They may cut off one plant, not feed, move
to an adjacent plant and repeat the process. During daylight the
larvae hide in the thatch, ground litter or burrow into the soil.
HOST RANGE
In Hawaii is has been a serious pest of many garden vegetable
crops by cutting the seedlings off at or below the ground level.
It has damaged sugarcane and corn. It was recorded feeding on
Sunturf bermudagrass, Cynodon magennissii Hurcombe experimental
plots at Waimanalo. In particular situations it probably will
attack other bermudagrass cultivars as well as other lawn
grasses. They also feed on some weeds i.e. purslane, Portulaca
oleracea L.. In California it feeds on dicondra and white clover.
DESCRIPTION OF LIFE STAGES
Descriptions of the developmental stages are published by
Zimmerman (1958), Rings (1977) and Tashiro (1987).
Adult
Moths are dark grey to black or brown. Antenna of the male is
pectinate and filiform for the female. In the forewing is a black
reniform spot and a black bar extending toward the tip of the
wing. The hind wings are nearly white, veins prominent without a
medial band. Adults are active at night. Wingspan of the adults
is about 1.0 inch. Adults are attracted to lights, especially
black light. Adults may live 30 days.
Egg
Freshly laid eggs are naked, creamy white in color, dome shaped
with a small circular depression at the upper pole from which
radiate ridges down the sides to the base. As development
progresses the eggs darken to tan, gray, dark brown and black
before hatching. Eggs are deposited on the surfaces of leaves or
stems near the soil surface. Eggs may be deposited singly or
close together in a batch. Development takes 2-4 days.
Larva
Like other lepidopterous pests, IPM programs are directed against
the worm stage. The larvae are nearly a uniform dark greasy gray
to black in color and paler underneath. Spiracles are black. The
head and dorsal part of the segment behind the head is brown.
Conspicuous tubercles appear as rows of brown dots. The larva
molts five times in its development. Mature larvae are 1.75
inches long. The larvae actively feed at night and hide during
the day in the thatch or beneath the soil or plant debris at the
surface of the soil. Young larvae feed on the grass blades and
later instars tunnel under the soil, cutting off the plants and
pulling them down into the burrow. With crowded conditions the
larvae are cannibalistic. Larval development takes 28-30 days.
Pupa
Pupation takes place in an earthen cell below the surface of the
soil. It is about 0.75 inch long, medium brown color, with a dark
dorsal band at the apex of abdominal segments 4 to 7. At the tip
of the abdomen are two large tapering spines. The spines are
black at the base and pale at the tip. Pupal development takes
10-14 days.
The entire life cycle from egg to adult may take from 40-48 days.
MONITORING METHODS
Methods for monitoring BCW populations are the same as described
for the GWW. Liquid irritants or flooding the area forced the
larvae to the surface to be counted.
ACTION LEVELS
Larval populations of the BCW have been low in our turfgrass
experiments probably due to the impact of parasites and predators
and environmental conditions. Because of the low populations
action levels for BCW have not been ascertained. As a starting
point an artificial control measure may be necessary if the
larval population reaches 5 per square yard.
BIOLOGICAL CONTROL
A number of parasites and predators of the BCW have been recorded
for Hawaii (Zimmerman 1958). Invertebrate parasites and predators
of BCW are presented in Table 5. The invertebrate organisms
attack both the larvae and pupae. Information on vertebrate
predators is lacking. The mynah and other birds, the giant toad
probably consume BCW larvae when feeding in the turfgrass. Data
on the impact of these beneficial organisms is lacking.
Table 5. Invertebrate parasites and predators of BCW in Hawaii
Parasites |
||
Diptera |
Tachinidae |
Archytas cirphis Curran |
Chaetogaedia monticola |
||
(Bigot) |
||
Eucelatoria armigera (Coq) |
||
Hymenoptera |
Braconidae |
Chelonus texanus Cresson |
Meteorus laphygmae Viereck |
||
Eulophidae |
Euplectrus plathypenae |
|
Howard |
||
Ichneumonidae |
Hyposoter exiguae (Viereck) |
|
Pseudamblyteleskoebeli |
||
(Swezey) |
||
Pterocormusrufiventris |
||
(Bruelle) |
||
Predator |
||
Coleopteraa |
Carabidae |
Calosoma blaptoides |
tehuacanum (Lapouge) |
CULTURAL CONTROLS
Mow the grass properly. Avoid the buildup of thatch and remove it
when it becomes excessive. Larvae will hide in the thatch.
CHEMICAL CONTROL
The insecticides suggested for GWW and LAW are also effective for
the BCW. Products containing Bacillus thuringiensis var.
kurstaki, carbaryl, chlorpyrifos or trichlorfon are suggested for
BCW application. Refer to the label instructions on proper
application, dosage rates, and precautions. The biorational
compound B. thuringiensis is a larvicide.
POTENTIAL PEST BAGWORM (BW): Brarachycyttarus
possibly griseus de Joannis
The bagworm was found in Kaneohe, Oahu in 1984. The common name
"bagworm" is due to the bag-like silken case covered
with pieces of grass in which the larva and adult female live
(Heu et al. 1984).
DAMAGE
Similar to other lepidopterous pests, the larva is the damaging
stage. The larvae chew off the blades of grass. Ragged appearance
of the grass may be noticeable but the first evidence will most
likely be the conical silken case hanging from branches of
shrubs, buildings, or other structures. Large numbers of bags are
often noticeable.
HOST RANGE
This is a new pest to Hawaii, and the host range is not well
known. The larvae have been recorded feeding on bermudagrass,
Hilograss (Paspalum conjugatum), foxtail (Setaria spp.), Natal
redtop (Rhynchelytrum repens (Wild.) C. E. Hubb.), Desmodium sp.,
sensitive plant, (Mimosa pudica L.), green kyllinga (Kyllinga
brevifolia Rottb.), and purple nutsedge (Cyperus rotundus L.). It
has also been able to complete its life cycle on Citrus spp.,
Nishiki juniper, lima beans and Spanish needle (Bidens pilosa
L.).
DESCRIPTION OF LIFE STAGES
Adult
Male bagworm moths have well developed, grey colored wings and
are about 0.2 inch long. Females are slightly longer than the
male, wingless, legless, lacking eyes, antennae, and mouthparts.
The females remain in the silken case made while it was a larva.
The female attracts the male, probably with a pheremone, mating
takes place without leaving the bag. Shortly after mating she
lays several hundred eggs within the silken case and then dies.
Egg
The eggs are deposited within the silken case. They hatch and the
young larvae crawl out of the bag, construct their own conical
silken case that is carried upright.
Larva
The bagworm larva carries the silken case with it as it moves
about. The bag protects the larva. As the larva matures, the
surrounding bag increases in size and is positioned beneath the
body while the larva clings to a surface with its thoracic legs.
A mature larva case may be nearly 0.5 inch long.
Pupa
Pupation takes place within the silken case.
The life cycle is completed in approximately 11 weeks.
MONITORING METHODS
Monitoring methods have not been developed. First evidence of a
population is usually the silken bags hanging form the grass
stems, vegetation, or buildings surrounding the turfgrass area.
ACTION LEVELS
Action levels have not been developed. The populations have not
been sufficiently damaging to turfgrasses to warrant a research
program.
BIOLOGICAL CONTROL
No information is known about beneficial organisms attacking this
insect.
CULTURAL CONTROLS
Brushing the silken cases from buildings may provide a measure of
control.
CHEMICAL CONTROLS
With the present population pressures, control with chemicals has
not been researched. The insecticides suggested for GWW should be
effective against bagworm larvae.
BEETLES
Order: Coleoptera
OCCASIONAL PEST HUNTING BILLBUG (HBB).
Sphenophorus venatus vestitusChittenden [Family: Cucurlionidae]
This snout beetle was first reported in Hawaii in 1960 infesting
zoysiagrass. It has been reported from all islands with the
exception of Lanai.
DAMAGE
First symptoms of hunting billbug damage are regular elongated or
round areas of brown dead or dying grass. The turf can easily be
pulled by hand and the root system appears to be cut off.
Presence of the legless, white grub of the billbug near the
border of dead and healthy grass will confirm the diagnosis.
Young larvae feed on the stolons, crowns and new leaf buds. Older
larvae attack the roots and runners to a depth of 3 inches or
more. Adults and larvae damage turfgrass.
HOST RANGE
Billbug damage has been observed in lawns, turfgrasses and
pasture grasses in Hawaii. Serious infestations have been in
bermudagrasses of greens and tees. The list of hosts for Hawaii
are presented in Table 6. Kikuyugrass pastures at 2,500-3,500
feet elevation on the island of Hawaii were damaged by the HBB
(La Plante, 1967). Weevils were also damaging sugarcane and corn
seedlings. Literature reports St. Augustinegrass, centipedegrass,
crabgrass, signal grass, barnyardgrass (Echinochloa crusgalli
(L.) Beauv.), leatherleaf fern and Pensacola bahiagrass (Paspalum
notatum Flugge) as hosts. In Hawaii, zoysiagrass and bermudagrass
cultivars were most seriously damaged.
The host range of the HBB is given in Table 6 below.
Table 6. Host range of the hunting billbug in Hawaii.
Common name |
Scientific name |
Bermudagrass |
Cynodon spp. |
Manieniegrass (Common bermuda) |
Cynodon dactylon (L.) Pers. |
Yellow nutsedge |
Cyperus esculentus (L.) |
Kikuyugrass |
Pennisetum clandestinum Hochst ex Chiov. |
Sugarcane |
Saccharum officinarum L. |
Corn |
Zea mays L. |
Manilagrass |
Zoysia matrella (L.) Merr. |
Japanese lawngrass |
Zoysia japonica Steud. |
Biologies and descriptions of the HBB have been published by
Woodruff (1966), Marsden (1979c), Tashiro (1987) and
Johnson-Cicalese (1990).
DESCRIPTION OF LIFE STAGES
Adult
The adult weevil is dark reddish brown in color about 0.4 inch
long. A slightly curved beak at the front of the head bears a
pair of stout mandibles for chewing grass stems and blades. When
disturbed, the adults will feign death for short periods of time.
Adults can fly and may live 6 months or longer.
Egg
Females bite a small hole in the stem, leaf or crown of the grass
and then deposit a small, white elongate egg in the slit. Eggs
are deposited singly and hatch in 3-7 days depending upon
temperature.
Larva
The larva or grub is legless, dirty white in color with a brown
head. Mature grubs are about 0.4 inch in length. Upon hatching,
the young grubs hollow out the stem and fill the space with
frass. As the larva increases in size, the stem can no longer
conceal it, and the grub feeds on the crown and moves to the
roots. Mature larvae may be found in the crown, just below the
thatch or just below the soil surface to a depth of 3 inches.
Larval development takes from 3-5 weeks.
Pupa
Pupation takes place in an earthern cell in the soil. Development
to the adult stage takes from 7-10 days.
The entire life cycle may take from 27-55 days depending upon the
temperature.
MONITORING METHODS
A standard monitoring method has not been developed for the HBB
because of its secretive habits. Turfgrass should be examined for
irregular or circular brown spots of dying grass. These spots
should be examined more closely for the presence of adult or
larval HBB. First instar larvae are concealed inside the stem and
easily missed. Frequent examination of suspect areas would find
the later larval instars that are outside the stems. The use of
irritating liquids forces a few adults to the surface but the
legless grubs do not respond like the GWW, LAW and BCW larvae. If
adult HBB are noticed crawling along walkways, curbs or paved
areas, they are indicative of a potential problem.
ACTION LEVELS
Because of the cryptic habits of HBB, if 1 or more grubs per
square foot are found, the turfgrass should be treated. Spot
treatment may be all that is necessary.
BIOLOGICAL CONTROL
In Hawaii the billbugs appear to be free from many of the
beneficial organisms. Mitchell (1966) reported adults killed by
the fungus, Beauvaria bassiana (Bals.) Vuill. This disease
attacks many insect species if conditions are optimum. A braconid
parasite, Bracon sp. nr. sphenophori Mues. was released in 1968
(Chong, 1968). A mymarid egg parasite, Patassion calendrae
(Gahan) had multiple releases in 1929, 1963, and 1967 (Bianchi,
1968). Neither one has been recovered to confirm establishment.
Scats of the giant toad, Bufo marinus, have contained large
numbers of HBB adults (Habeck, 1962). Some HBB were alive in the
fecal droppings. The toad feeds at night on HBB, GWW, LAW, and
BCW.
CHEMICAL CONTROL
Insecticide applications are suggested because the HBB is free of
effective parasites or predators. For effective control, the
chemical must reach the larvae which are located in or below the
thatch or under the surface of the soil. Most researchers suggest
pretreatment irrigation of the area to soak the thatch layer and
the upper surface of the soil. The wetting of the area will
insure better penetration of the toxicants to the depth of the
roots and the zone where adult and larval HBB exist. Post
treatment irrigation is recommended when granular formulations
are applied. Products containing chlorpyrifos, carbaryl,
ethoprop, isofenphos, propoxur or trichlorfon have been suggested
for HBB control in Florida (Short, 1982). Refer to the label to
be sure the chemical is registered for the site and HBB control
MEALYBUGS
Order: Hemiptera Suborder: Homoptera
Mealybugs are small elongate, oval, soft-bodied insects with well
developed legs. They damage plants by sucking the juices from
them. Their bodies are often covered with waxy secretions.
Mealybugs produce honeydew which is attractive as food for other
insects.
OCCASIONAL PESTS:
RHODESGRASS MEALYBUG: (RGMB): Antonina graminis (Maskell)
[Family: Pseudococcidae] .
The Rhodesgrass mealybug has been misnamed Rhodesgrass scale. The
insect has been in Hawaii since 1910 and occasionally develops
troublesome infestations in turfgrasses. It is found on all
islands.
DAMAGE
Rhodesgrass mealybug damage to grasses is difficult to see
because the insects are small and located at the bases of the
grass stems and under old leaf sheaths. Active infestations
produce large quantities of honeydew, a sweet sticky secretion
that is highly attractive to honeybees, ants and other insects.
Bee activity in the grass or being stung while walking barefoot
in the grass are often the first indications of the development
of a mealybug population. Closer examination of the turfgrass
will reveal small, reddish, globular insects enclosed in white
felt-like waxy masses, near the bases of the stems and under old
leaf sheaths. Larger populations of RGMB cause the infested grass
to become unsightly and weak in appearance. The bases of the
infested plants, including crowns, leaf axils, etc., appear to be
covered with tufts of cotton. Injury is most severe during
extended hot, dry periods.
HOST RANGE
The insect has a worldwide distribution and has been reported
infesting over 100 species of grasses. In Hawaii, it has been
recorded on sugarcane, bermudagrasses, caribgrass (Eriochloa
polystachaya (H. B. K.) Hitch), torrid panicgrass (Panicum
torridum Guad.), Paspalum spp., rhodesgrass (Chloris gayana
(Kunth.)) and pineapple roots (Zimmerman, 1948).
DESCRIPTION OF THE LIFE STAGES
Adult
The small mealybug adults are inside the white, cottony, waxy
secretion that the insect produces. All adults are females.
Reproduction is by parthenogenesis, and males are unknown. The
adult is a globular, dark purplish, reddish-brown, saclike body
about 0.125 inch diameter. Mealybugs are found clustered about
the bases of the plants. Mealybug feed by sucking plant sap
through a long, hair-like proboscis which is inserted into the
tissue of the grass plant.
Egg
Females give birth to living young (nymphs or crawlers).
Elongate, cream colored eggs can be seen if dissected from a
female.
Nymph or Crawler
Young, larvae, nymphs or crawlers, are produced in large numbers
by the female. They are minute, flat, brownish insects with
well-developed legs and antennae. The infestation is spread in
the turfgrass by these tiny crawlers moving from plant-to-plant.
Crawler and adult feeding cause cells to collapse and reduce
vigor of the plant. Once the crawlers have started to feed they
become sessile, loose their appendages, become saclike and look
like adult females but are smaller in
size.
The life cycle from crawler to reproductive adult may take as
much as 45-50 days depending upon the temperature.
MONITORING METHODS
A standardized monitoring method for RGMB has not been developed.
If white cottony masses are observed in the turfgrass and there
is considerable activity of honeybees and ants feeding on the
honeydew there is most likely an infestation developing. Further
close inspection of the turfgrass is suggested.
ACTION LEVELS
We do not have an action level for RGMB. If people are being
stung, by bees feeding on the honeydew, as they walk across the
turf a pest management tactic is suggested.
BIOLOGICAL CONTROL
In Hawaii one encyrtid parasite, Anagyrus antoninae Timberlake,
has been recorded attacking RGMB. The parasite has effectively
controlled RGMB populations in some situations. Failures have
probably been due to parasite mortalities from insecticide
applications.
CULTURAL CONTROLS
Grass mowed at l.5 inches or more is less prone to injury than
grass that has been cut shorter. Proper irrigation and
fertilization aides in preventing damage Do not spread grass
clippings from an infested area to uninfested areas.
CHEMICAL CONTROL
Insecticidal control has not been very effective because of the
waxy secretions protecting the mealybug. In Florida malathion in
combination with volck oil has been reported to give satisfactory
control. In Hawaii the insecticides suggested for GWW control
have also prevented population increases of RGMB. Timing of the
insecticide application is important to contact the crawler
stages.
SCALE INSECTS
Order: Hemiptera Suborder: Homoptera
The pest of turfgrass is an armored scale. They are generally
small, flat disc like organisms without legs and antennae. They
live under a scale (armor) formed of wax secretions of the insect
and cast skins of immatures. The scales vary in shape, size and
color. Scale insects also produce honeydew.
POTENTIAL PEST
BERMUDAGRASS SCALE (BGS). Odonaspis ruthae Kotinsky [Family:
Diaspididae]
This insect was first discovered in Hawaii in 1910 (Zimmerman
1948). It is also called Ruth's scale. It may be found wherever
bermudagrass is found.
DAMAGE
In Hawaii, the scale seldom causes serious damage to bermudagrass
but is most injurious when the turf is under stress. Adults and
immatures suck plant juices from the plant and may reduce
vitality and growth of turf. Heavily infested turfgrass takes on
a brown, dry appearance and new growth is retarded. The scale
does well in shade and heavily thatched turf.
HOST RANGE
As the common name implies, the host range is limited to
bermudagrass and its hybrids.
DESCRIPTION OF THE LIFE STAGES
Adult
The adult scale (0.06 inch long) is oyster or clam-shaped and
chalky white found beneath the leaf sheaths, clustered around the
nodes and occasionally on the leaves. Scales have not been
reported on the roots.
Egg
Eggs are deposited by females under their oyster-shaped scale.
Nymphs or Crawlers
These are the active mobile stage in the life cycle. Crawlers
move out from beneath the scale and spread the infestation. They
soon settle down, loose their legs, insert their piercing sucking
mouthparts into the grass, start to feed and become sessile. In
molting they loose their appendages, secrete the waxy covering
and remain there for several months before producing eggs and
repeating the life cycle.
MONITORING METHODS
Methods for monitoring have not been developed. Close examination
of the turf for the white oyster or clam-shaped scales will
indicate the presence of the scale.
ACTION LEVEL
The scale has not developed into sufficient populations to
determine an action level.
BIOLOGICAL CONTROL
As with the mealybug only a single encyrtid wasp, Adelencyrtus
odonaspidis Fullaway, has been recorded parasitizing BGS. Data on
its effectiveness is lacking.
CULTURAL CONTROL
Keep the turfgrass in a healthy condition. Do not spread grass
clippings from an infested area into uninfested areas.
CHEMICAL CONTROL
Infestations in Hawaii have not required pesticide applications.
The insecticides suggested for GWW control should also be
effective for control of this pest. Timing of the application is
important so that the crawlers come in contact with the
insecticide. The waxy covering protects the scale from the
sprays, therefore an adjuvant or volck oil may be incorporated
into the spray to overcome this problem.
SOUTHERN CHINCH BUG
Order: Hemiptera Suborder: Heteroptera
OCCASIONAL PEST
SOUTHERN CHINCH BUG (SCB). Blissus insularis Barber [Family:
Lygaeidae]
The southern chinch bug is an recent arrival in Hawaii. If was
found infesting St. Augustinegrass in Nuuanu Valley in August
1990. Under certain conditions this insect may be a limiting
factor in the culture of St. Augustinegrass and its cultivars.
DAMAGE
Both adults and nymphs suck juices from the turfgrass. They
insert their needle-like mouthparts, suck sap and in the process
inject saliva that interferes with water conducting system of the
plant. Damage begins as patches of yellowing grass which later
turn brown. If the grass is under stress and the yellowing
continues to spread the grass may be killed. Activity is greatest
in hot, open areas. Shaded areas are not usually damaged unless
the SCB populations are very large. By parting the grass runners,
adults and nymphs can be seen crawling through the loose debris
on the surface of the soil.
HOST RANGE
Its major host is St. Augustinegrass, Stenotaphrum secundatum.
Other grasses in close proximity to St. Augustinegrass that have
been slightly damaged by SCB are zoysiagrass, centipedegrass,
bahiagrass, and bermudagrass. Some selections of St. Augustine
grass are resistant to SCB.
DESCRIPTION OF THE LIFE STAGES:
Adult
Adults are 0.2 inch long, black with shiny wings that are held
flat over the back. The white wing covers are marked with a black
triangular patch at the middle of their outer margin. Legs are
reddish to reddish yellow. Fully winged (macropterous) and short
winged (brachypterous) adults may be found in the population.
Egg
Eggs are deposited in the leaf sheaths and in the ground on
roots. The eggs are nearly cylindrical, are three or four times
longer than broad, whitish when freshly deposited. As development
progresses the color changes to yellow and a deep red prior to
hatching. Egg development takes about 2 weeks.
Nymph
There are five wingless instars in the development of SCB. The
first two instars are red in color, with a white band on the
first two abdominal segments. The basic color changes from red to
orange in the third instar, orange brown in the fourth and black
in the fifth instar. Wing pads are visible in the fifth instar.
Nymphal development takes 30 days or longer depending upon
temperature. The complete life cycle from egg to reproductive
adult may take 6-8 weeks.
MONITORING METHODS
Sampling methods described for sampling the GWW are effective for
SCB. Flooding of an area with water or irritating liquids will
force the adults and nymphs to the surface to be counted. Ten
minutes of continuous counting is advised.
ACTION LEVELS
Action levels for the SCB have not been developed for Hawaii.
Populations have been scarce and limited to the island of Oahu.
Reinert (1982) recommended treatment if 22-28 SCB were observed
per square foot.
BIOLOGICAL CONTROL
The infestation is so recent in Hawaii, no information is
available on beneficial organisms here. One biorational,
Beauvaria bassiana, and a number of parasites and predators have
been recorded elsewhere (Tashiro 1987).
CULTURAL CONTROL
St Augustinegrass is the preferred host for the SCB. A number of
varieties have shown resistance to chinch bug feeding.
Publications by Busey and Coy (1988), Busey and Center (1987),
Busey (1990), discuss the vulnerability of St. Augustinegrass and
the genetics of resistance. Floratam and accessions FA 108 and TX
33 have exhibited resistance to SCB feeding. We do not know if
the cultivars of St. Augustine grass being sold commercially in
Hawaii are tolerant to SCB feeding. Control of thatch will reduce
SCB numbers. Reduced amounts of nitrogen should result in less
chinch bug problems.
CHEMICAL CONTROL
To preserve any beneficial organisms spot treatment of the
damaged area and a ten foot swath surrounding it is suggested.
Refer to the label for directions on dosage rates, application
methods, precautions etc. Insecticides containing chlorpyrifos,
ethion, ethoprop, isofenphos or propoxur are suggested.
Irrigation of the turf prior to application will allow the
pesticide to reach the SCB below the thatch and at the surface of
the soil. In some area phosphate resistance has developed in the
SCB (Reinert and Portier, 1983). We do not know if a phosphate
resistant population of chinch bugs is present in Hawaii.
Resistant cultivars is the best control of SCB.
BERMUDAGRASS MITE
Order Acarina
OCCASIONAL PEST
BERMUDAGRASS MITE (BGM).Eriophyes cynodoniensis Sayed [Family:
Eriophyidae]
This eriophyid mite, also called the bermudagrass stunt mite, was
first detected in Hawaii in 1966. It has spread to all islands.
It can be a serious pest of bermudagrasses under certain
conditions. It is a more frequent problem in grasses under stress
and in new plantings.
DAMAGE
Damage is characterized by a yellowing of the tips of the leaves,
a turning upward and inward of the leaves and shortening of the
internodes and a rosetting or tufting of the grass (Kerr and
Brogdon, 1968). When rosettes are numerous the area looks clumped
without internodes. Walking over the area the turf feels lumpy.
With heavy infestations the grass turns brown and dies. Adults
and immatures suck plant juices.
HOST RANGE
As the name implies, the host range is limited to bermudagrasses
and the cultivars or hybrids. Cultivars have varying degrees of
resistance to feeding by the mite.
DESCRIPTION OF THE LIFE STAGES
Adult
Adults of the mite are extremely small and with difficulty can be
seen with a 10X hand lens magnifier. They are worm like, creamy
white to yellow in color and have four legs near the head end.
They are found behind the leaf sheath sucking plant sap.
Eggs
Eggs are spherical, transparent to opaque white and deposited
singly or in groups behind the leaf sheaths.
Nymphs
Nymphs resemble the adults in being microscopic in size, about
twothirds the size of the adults, longer than broad with two pair
of legs at the head end. The nymphs may be observed behind the
leaf sheath sucking plant sap. Upon hatching the nymphs molt
twice (2 instars) and molt again into a sexually mature adult.
All stages of development may be found behind the leaf sheath.
Major means of dispersal are by wind, grass clippings and riding
on other insects or birds. During warm weather the life cycle of
the BGM may only take 5-10 days.
MONITORING METHODS
Look for tufted or rosetted plants. With the aide of a dissecting
microscope pull away the leaf sheath from the stem and examine
the inside of the sheath for eggs, nymphs and adults.
ACTION LEVELS
An action level has not been developed for BGM in Hawaii. If
damage continues to increase and the turf show evidence of
decline, thinning etc. a pest management tactic must be
considered.
BIOLOGICAL CONTROL
Information on parasites or predators of BGM in Hawaii is nil.
Two predacious mites, Neocunoxoides andrei (Baker and Hoffman)
[Family: Cunaxidae] and Stenotarsonemus spirifex (Marchal)
[Family: Tarsonemidae] have been reported reducing BGM
populations in Florida and Arizona, respectively (Butler 1963.
Johnson 1975).
CULTURAL CONTROL
Several cultivars, Midiron, Tifdwarf, Tifgreen 328, Tifway 419
exhibited degrees of resistance to BGM (Reinert 1982, 1985). New
selections are currently being developed. The normal maintenance
operation, mowing, may spread the mite on clippings to uninfested
areas. Reduce mowing height.
CHEMICAL CONTROL
Insecticidal control of the mite with chlorpyrifos has been
erratic in Hawaii. The insecticide-miticide, fluvalinate is
recommended in Florida. Reinert and Cromroy (1981), Reinert
(1985) and Butler (1963) have reported on BGM resistant cultivars
and the effectiveness of various miticides.