Spot the Difference

Large numbers of different spotted larvae have recently been observed in many mungbean crops. The spotted larvae of the bean pod borer remains a significant pest of mungbeans yet the spotted fungus eating ladybird larvae poses no threat to crops.

In recent years, significant populations of bean podborer larvae (Maruca vitrata) have been reported in crops as far west as Surat. This is a considerable distance west of their normal range which is in coastal and sub coastal regions, with occasional incursions onto the Darling Downs.

Large bean pod borer

As a rule, pod borer activity is much higher in wetter seasons, with populations in excess of 100 per square metre recorded in the summer of 2011/12. Despite a slow start to the wet season of 2012/13, podborers are now present in many mungbean crops, albeit in not as high numbers as last year and not as far inland.

The cool and rainy weather also favours the larvae of the fungus-eating ladybird Illeis galbula. Recent weather conditions favour the growth of fungi that they (adults and larvae) feed on, including sooty mould and powdery mildew. 

Fungus eating ladybird larvae and adult

Fungus eating larvae are readily differentiated from bean podborer larvae by the six rows of black spots, a bright yellow head, and legs that splay out sideways from the body. Podborer larvae have 4 rows (2 main rows) of black spots, a black or brown head, and legs held under the body. Fungus-eating ladybirds are found on the leaves, whereas podborer larvae feed in flowers and pods

Fungus-eating ladybird larvae can easily be distinguished from predatory ladybirds, as their basal colour is white, whereas predatory ladybird larvae are usually black with orange bands. The adults are instantly recognizable as they are bright yellow with black markings, whereas the predatory ladybird adults are orange with black markings.

Predatory ladybird larvae

Note that an emergency use permit (PER 14020 – valid to 31 May 2013) has been secured for the use of Altacor (chlorantraniliprole) against bean podborer in mungbeans, at the rate of 70 g/100L plus a non-ionic surfactant at 125g ai/100L.

This product gives good residual caterpillar control but has no impact on predatory or fungus-eating ladybirds, or any other beneficial insects.

Article by Hugh Brier

Images by Joe Wessels

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Soybean stem fly outbreak in soybean crops

An estimated 4,000 ha of soybeans near Casino in Northern NSW have been affected to varying degrees by soybean stem fly (Melanagromyza sojae) , a pest rarely seen in damaging numbers in Australia. Damage in many Casino crops is confounded by the presence of charcoal rot, a disease which blocks the plant’s vascular (xylem and phloem) tissue and causes similar damage – leaf wilting and plant death.

 

Stem fly damage in soybeans near Casino, NSW

Soybean stem fly have also been reported this summer in the Clarence valley, but not yet in damaging levels. The only previously documented Australian outbreak of significance was in early vegetative soybeans in the Mackay region in 2009.
 
While soybean stem fly occurs in Australia it is more common in Africa and Asia, where it is a common pest of soybeans.  Literature suggests that stem fly activity is favoured by warm temperatures, high rainfall and high humidity.
 
Management of this pest is difficult as the damaging larval stage feeds inside the petioles and stems. Consequently its presence is usually not detected until plants display noticeable symptoms such as leaf wilting and death. Following is more information about this pest, its lifecycle and the damage it causes.
 
What are soybean stem flies?

Adult flies are shiny black and about 2mm long and look very similar to the bean fly (Ophiomyia phaseoli) which is a major pest of navy bean seedlings. The damaging stage is the white larvae (maggot) which feeds inside the stem. Soybean stem fly larvae can be distinguished from other bean fly species by the “blunt, somewhat atrophied (shrunken) central horn” in each posterior spiracle. The pale brown pupae are cylindrical in shape with rounded ends.

 

Stemfly larvae burrows into soybean stems   

 

                              Adult stem fly

The soybean stem fly inserts eggs on the underside of young leaves. Ovipositing sites present as pale pinprick spots when infested leaves are held up to the light. Upon emergence the larva mines through the leaf tissue towards the mid vein. From here it works its way down the leaf petiole into the stem where it feeds on the pith. Before pupation, which takes place inside the stem, the larva makes an exit hole for the emergence of the adult, through the stem’s xylem and phloem tissue. It is this damage to plants vascular tissue that affects the plant’s growth and reduces yield. The larval stage takes 8-11 days and the pupal stage lasts 6-12 days (depending on temperature).

Several generations can develop in the soybean crop and it is possible that successive generations in the infested crops have built to damaging levels.

 

 Stemfly pupae

Damage symptoms

Infected stems are often red inside (sometimes pale) and a distinct zig-zag tunnel may be observed – with maggots or pupae inside. Apart from the exit holes, the soybean plants will initially appear healthy on the outside. Large infestations (3 or more maggots per plant) may cause wilting and may even cause plant death, especially in younger plants particularly if damage occurs in the plant’s hypocotyl (basal stem) region. In the Casino outbreak, damage symptoms in earlier-planted crops were manifested rapidly throughout infested crops in as little as 4-7 days. In many later-planted crops, significant stem fly activity has been observed (in dissected plants), but damage symptoms have yet to be manifested.

 

Dissected soybean stem reveals feeding tunnels leading to exit hole. These are not obvious until stems are dissected

Overseas literature suggests 20-30% yield reductions when crops are infested in the early vegetative stage. Damage causes reduced pod and seed set. If leaves wilt or die during podfill, as in the current outbreak, it is likely that significant yield losses will occur due to reduced seed size. However, many of the Casino crops are also affected  by charcoal rot, a disease which blocks the plant’s vascular (xylem and phloem) tissue and this causes similar damage to stem fly with leaf wilting, plant death and reduced seed size.

Note – do not confuse stem fly with the larvae of etiella (lucerne seed webmoth) (Etiella behrii) and lucerne crown borer (Zygrita diva) which also feed inside the stems and make reddish feeding tunnels. These larvae are much bigger, have well defined head capsules, and in the case of larger etiella larvae, are green with pink stripes. Lucerne crown borer is a common pest of soybeans. Plants infested by crown borer only die when fully-developed crown borer larvae ‘ringbark’ stems internally prior to pupation.

 Typical charcoal rot lesion on soybean

Management

No chemicals are registered for the control of soybean stem fly in Australia. However a emergency use permit was recently secured for dimethoate @ 800mL/ha (permit number 14121, valid until 31 May 2013). However by the time significant leaf damage symptoms (wilting/death) are observed, it may be too late to prevent yield loss. As well, prophylactic spraying of dimethoate at the 800mL/ha rate will flare mites, silverleaf whitefly and helicoverpa. More sustainable management options will be explored for future seasons.

 

Sticky traps, such as this one used in nothern NSW, can indicate the presence of adult stem flies

In Asia, where stem fly is a recurring problem, a number of soybean varieties have some resistance to stem fly. In the Casino outbreak, significant damage has been reported in all commercial cultivars.
 
Biological control
There has been no research done in Australia on soybean stem fly or its natural enemies, but the indiscriminate use of broad spectrum insecticides will kill beneficial insects attacking stem fly (and other pests).

While stem fly larvae are seemingly well protected from natural enemies as they feed inside stems, significant parasitism by tiny wasps has been recorded in Africa and Asia. Soybean stem fly parasitism has also been observed in infested crops at Casino. The identity of these wasps has yet to be determined but it is possible they are keeping stem fly in check in most years.

 Soybean stem fly wasp parasite (2.5 mm).

Please report any suspected soybean stem fly infestations to:

Hugh Brier DAFF Kingaroy 0741 600 740 or 0428 188 069 (hugh.brier@daff.qld.gov.au)
Natalie Moore NSW DPI 02 6640 1637 natalie.moore@industry.nsw.gov.au
Or contact your local agronomist
When assessing suspected infestations, also inspect the crop’s root development and look for charcoal rot symptoms.

 

 

Article by Hugh Brier and Kate Charleston

Images by L. Gaynor, Natalie Moore, Joe Wessels and Hugh Brier

 

Post script comment

 Reports are coming in from agronomists in the Richmond Valley of new instances of damage (leaf death) in stem fly infested crops with healthy root systems. However the recent rain does seem to be easing symptoms in other crops as they are better able to meet their water demands despite damage to vascular tissue in the stems, be it due to stem fly, charcoal rot or earlier water logging.
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Mealybug outbreak found on the Darling Downs

DAFF Queensland entomologists have confirmed a small outbreak of Solenopsis mealybug (Phenacoccus solenopsis) on a cotton property west of Dalby on the Darling Downs.

This is the same species of mealybug that affected cotton crops in Emerald and the Burdekin in 2010 and more recently in the South Burnett.

When infested at the early development stage, plants often exhibit distorted terminal growth and crinkled and bunchy leaves. In severe cases plant death will occur. Late season cotton crop infestations can cause squares and small bolls to drop, as well as fewer, smaller and deformed bolls and premature crop senescence. Mealybug also produce honeydew which can contaminate cotton lint and promote the growth of sooty mould fungi that reduces photosynthesis.

  

Methods of spread
How the mealybug outbreak on the Darling Downs started is not known but it is important to avoid spreading this pest onto other properties.

Localised movement of mealybug occur when juveniles (crawlers) move from infected fields to adjacent healthy crops. The waxy coating on the mealybug crawlers also facilitates passive transport of the insect by sticking onto equipment, other insects (e.g. bees), birds, animals or people. Small crawlers are also readily transported by wind and rain or in water in irrigation channels. Long-distance movement through the transport of infested plants is also possible.

Management of mealybugs
There are no insecticides registered for the control of mealybug in cotton. However there are a number of management options that can reduce infestations and the overall impact of this pest.
 
·         Mealybug multiply on different hosts and may initially breed on weeds before migrating to cotton crops
·         Weeds in and around fields should be removed.
·         Do not throw uprooted weeds into water channels.
·         The removal of affected plants at the early stage of infestation may reduce mealybug numbers in the rest of the crop.
·         Avoid physical contact with infested plants as mealybug easily adhere to clothing and implements.
·         Practice good farm hygiene and clean all equipment that has been in affected fields.
·         Natural enemies such as cryptolaemus and other lady beetles and lacewings play vital role in keeping mealybug under control
·         Consider using the ‘softer’ insecticides that are used in control of other insect pests to conserve natural enemies of mealybugs.
 
Lessons learnt from previous outbreaks

While you can still find mealybug in Emerald, infestations are not nearly as severe as in 2010.

A good farm hygiene program, which includes weed management has been implemented on most properties and has resulted in a decrease of this pest.

Natural enemies have also proven to be important in reducing mealybug numbers. In some instances, these beneficial insects have been so abundant and effective that they have decimated local mealybug populations. Ladybirds, lacewings, spiders and cockroaches are some of the important predators of mealybug. A parasitoid of mealybug, Aenasius bambawalei, first found in a cotton field in Byee in 2012 is also providing control of this pest. 

Cryptolaemus lady birds are important predators of mealybug

Flaring mealybug populations

The use of insecticides targeting other pests can have a major impact on mealybug numbers in the crop.

In 2012, a conventional cotton crop in the Byee area was severely affected by mealybug infestations. However an adjacent crop, had very low numbers of mealybug. The main management difference between the crops was the use of insecticides.
 
The crop with high mealybug numbers was sprayed with seven different insecticides targeting; tipworm, helicoverpa, aphids and green vegetable bugs.
 
Mealybug were observed from flowering onwards and were present throughout the season with numbers increasing progressively.  Mealybug numbers only declined towards the end of the season when insecticides were no longer applied and beneficial insect numbers increased within the crop. 

This case study clearly illustrates that insecticides, especially broad spectrum chemistries, can have a detrimental effect on those beneficial insects that keep mealybug in check.

Sooty mould is a result of honeydew excreted by mealybug

Observations made this season in Emerald suggest that continuous high temperatures may promote breeding of mealybug and hence contribute to outbreaks.

 
Please report any infestations of mealybug to Dr Moazzem Khan (07 4688 1310) or Kristy Byers (07 4688 1535)
 
For more information about mealybug, please refer to previous Beatsheet articles by selecting mealybug in the ‘categories’ section.
 
Thanks to Damien Sippel from BGA Agriservices for providing the information about flaring of mealybug.
 
 
 
 
 
 
 
 
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Etiella outbreak in vegetative soybeans on the Darling Downs

Etiella (Etiella behrii) larvae have been observed in significant numbers (up to 10 larvae per square metre) in vegetative soybean crops in the Cecil Plains/ Pampas regions of the Darling Downs, and in low numbers (<1/sqm) in a DAFF soybean trial at Kingaroy.

These infestations are likely due to the current hot and dry seasonal conditions which historically favour increased etiella activity in other susceptible summer hosts, especially peanuts.
Damage of the magnitude observed to date is most likely not economically significant. This assertion is based on field experience with other pests damaging stems and buds in vegetative soybeans. Preliminary trials suggest larvae can’t be controlled effectively with current pesticides because of their sheltered feeding sites inside buds and stems.

Signs of an Etiella infestation in soybeans

Larvae are attacking terminals and axilliary buds and are also tunnelling in the stems. This feeding behaviour has been documented previously in peanuts but not to date in soybeans.
This season is certainly not the first time Etiella has infested vegetative soybeans. However, the low number of records suggests that either their damage has been either attributed to other pests, or the level of damage has been insufficient to trigger a closer examination to determine the pest responsible.
This season Etiella damage has been reported from crops at late podfill, although mostly at sub-economic levels. Etiella are a major pest of late podfill peanuts as etiella damage to pods greatly increases aflatoxin levels in harvested peanut seed.
The first readily visible etiella damage symptoms in vegetative soybeans are dead buds and terminals, but with few to no external signs of the tunnelling inside the stem. Dissection of infested plants from the infested crops revealed small larvae inside damaged terminals/buds, and larger larvae tunnelling in stems, feeding mainly on pith tissue.
Microscopic examination of dead buds/terminals suggests that damage to the plant’s vascular tissue as larvae tunnel towards the pith is responsible for the death of these structures. Not all damaged bud/terminal sites had subsequent tunnelling, suggesting that not all small larvae survive on vegetative soybeans.
Etiella tunnels have a brown discolouration and contain larval frass (poo). In contrast, undamaged pith tissue is almost white.

Etiella damage symptoms visible in the field, and that of similar species.

Etiella damage symptoms visible in the field, and that of similar species.

What impact might the infestations have on crop yields?

Soybeans can compensate for considerable axilliary bud damage but replacement buds and subsequent pods are often set lower on the plants, making for more difficult harvesting. It is unclear whether the etiella damage witnessed so far this season will result in lower pod set.
Extensive stem tunnelling may make the plants more brittle and prone to snapping off when being sampled vigorously with a beat sheet. Experience with other stem-tunnelling pests suggests this does not necessarily lead to lodging of the crop at or prior to harvest.

 

Identifying Etiella and distinguishing it from other pests causing similar symptoms in vegetative soybeans (across all soybean growing regions)

Small etiella larvae are cream with a dark head. Larger larvae (reaching 12 mm in length) are typically pale green with pink stripes and a dark red band behind the head.

Helicoverpa and grass blue butterfly larvae can kill terminals and axilliary buds, but don’t tunnel in stems. Grass blue feeding often results in the windowing of terminal and more-fully expanded leaves. Grass blue butterfly larvae are short (12 mm long) and slug like, while Helicoverpa are brown or green, with a parallel body, a pale stripe along their flanks, and characteristic pale striations on their back.
Helicoverpa damage to stems is usually coincidently inflicted when large larvae (on the outside of the stems) are targeting the plant’s axilliary buds. Such damage can have a major impact on yield, particularly if stems are severed and tops of the plant are lost.

Soybean moth larvae can attack vegetative terminals, but don’t tunnel in the stems. Larvae feed inside the leaves in leaf mines, which appear as translucent tan-coloured tissue. Soybean moth larvae reach 7 mm in length and are grey green in colour.

Legume and cotton webspinners web and fold leaves together. Legume webspinner is common in coastal soybeans but is rarely seen in more-inland crops. Outbreaks of cotton webspinners in soybeans are extremely rare but severe leaf damage (shredding) has been occasionally observed in seedling soybeans.

Zygrita or lucerne crown borer (Zygrita diva) larvae commonly tunnel in the stem’s pith, but tunnels originate from oviposition sites in the plant stem, not from the axilliary buds. Tunnels made by Zygrita are similar in appearance to etiella tunnels with a brown discolouration. Zygrita larvae are cream with a distinct thickening behind the head. They can reach 12 mm in length and are devoid of pink stripes and ventral prolegs. Zygrita only inflict economic damage if they pupate prior to pods reaching physiological maturity. This is because just prior to pupation, larvae ‘ringarbark’ the stem from the inside in order to plug the pupal chamber in the lower stem.

Soybean stemfly (Melanagromyza sojae) larvae have been reported tunnelling in soybean stems only in the Mackay region. The 5 mm long larvae are typical fly maggots and are translucent cream with no legs.

Etiella and other caterpillar species that will cause damage to soybeans similar to that being seen in association with Etiella.

Etiella and other caterpillar species that will cause damage to soybeans similar to that being seen in association with Etiella.

Managing Etiella in vegetative soybeans

Etiella is a problematic pest, largely because of its concealed feeding behaviour, in this instance inside plant stems, buds and terminals. In vegetative soybeans, it is unclear what level of etiella activity would warrant control. As a rule of thumb, the threshold guidelines recommend action if greater than 25% terminal loss for terminal-attackers such as larvae of the grass blue.

For helicoverpa, published data (Rogers 2010) show that vegetative soybeans can tolerate up to 6-7 larvae/m2 with no yield loss, but above this level, severe yield loss is experienced due to damage to axilliary buds and plant stems. It should be noted that helicoverpa are 10 times heavier than etiella when fully grown. Consequently it would be reasonable to assume the crop could tolerate considerably more etiella per square metre without yield loss.

There are no threshold guidelines for stem tunnelling, although observations with lucerne crown borer suggest no yield loss unless vascular tissue is damaged, which is not occurring to any significant effect with etiella. Plant samples will be taken this year to compare yields of infested and un-infested plants.

Caterpillar pests and damage to soybeans.

Caterpillar pests and damage to soybeans.

Monitoring for the pest is difficult. To establish the level of larval activity, damaged terminals and axilliary buds and adjoining stem sections have to be dissected to detect hidden larvae. This is best done under a microscope as young (early instar) larvae may be only 1-2 mm long. As well, it is very easy to damage larvae when dissecting plants.

Note that vegetative soybeans are frequently also infested with grass blue butterfly, soybean moth, helicoverpa, and Zygrita, so correct identification of the pest/s inflicting damage is important.
In southern states, the timing of influxes of etiella moths into crops are monitored with pheromone or light traps, or with sweep nets, and susceptible crops (lentils) sprayed before egg lay with a SP pesticide (deltamethrin or esfenvalerate).

In northern Australia, blanket use of this approach in vegetative soybeans would be very risky as it would flare mites, whitefly and helicoverpa.

An alternative approach could be to apply a pesticide with trans-laminar activity while larvae are still inside axilliary buds and terminal leaves, and before they tunnel into the stems. This approach would require close monitoring to detect moth flights to get the timing right. Ideally, any pesticide used to this effect would be very selective so not to flare other pests. Monitoring for eggs is not really practical as they are difficult to spot, being small, laid singly, often laid in sheltered sites (e.g. under bracts) and not brightly coloured.
Preliminary results from a test strip of soybeans sprayed with a product registered in soybeans, and with trans-laminar activity, suggested at best only 33% control of etiella larvae. Given this unacceptably low level of control, it is doubtful whether targeting larvae is economically viable. Granted some larvae in the test strip had already commenced tunnelling, but this would very likely also be the case in commercial crops.

Conclusions

Etiella infestations in vegetative soybeans have most likely occurred in previous seasons but have only been reported recently because scouts are now better trained, and because of higher than usual etiella activity. The latter may be an artefact of the current hot and dry seasonal conditions which are linked to increased etiella activity in other susceptible summer hosts such as peanuts.
Concerns have been raised regarding the pest’s impact in seedling crops. While small plants might be at greater risk, one would have thought that severe etiella damage would have been previously reported. It may be that larger plants with more axilliary bud sites are more attractive to ovipositing etiella moths.
Control is likely to be difficult. Monitoring for moths plus the availability of highly selective pesticides with trans-laminar activity targeting small larvae still in axilliary buds may be a viable option in the future. However the efficacy of this approach has yet to be proven and further research is required. Initial results suggest at best mediocre control of larvae with current chemistry.
Panic spraying with SP’s targeting etiella moths may or may not be effective, but would certainly trigger outbreaks of mites, whitefly and helicoverpa.
As well, the impact of etiella damage in vegetative soybeans has yet to be quantified. In the majority of seasons it is likely that the damage is of no economic consequence and that spraying would be a waste of money, even if pestides did give effective control.
The author is very keen to receive any reports of significant etiella activity in vegetative soybeans to better document this season’s outbreak and to evaluate possible management options.
If you suspect etiella activity in your soybeans, please contact Hugh Brier DAFF Kingaroy on 0741 600 740, or Mobile 0428 188 069, or Email hugh.brier@daff.qld,gov.au. The postal address for samples is: Attention: Hugh Brier, C/- PO Box Kingaroy Q4610.

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Rutherglen bugs in cotton – cause for concern?

Contributors: Susan Maas (CRDC), Lewis Wilson (CSIRO)

There are currently reports of high numbers of Rutherglen bugs (RGB) in cotton across a number of growing regions (Downs, Namoi, Gwydir), and questions being asked about whether this pest can cause damage to reproductive cotton.
This season has seen large spring migrations of RGB into cropping areas from Emerald to the Liverpool Plains. Although the immigrations seem to have slowed now, the populations being seen in cotton may be the result of local movement from weeds or crop hosts (e.g. canola, sunflowers).

Rutherglen bug adult (top) and nymph (bottom). Photo: Keith Power.

Rutherglen bug (Nysius vinitor) is a native species, adults are 3-4 mm long, mottled grey-brown-black, and have clear wings folded flat over the back. Nymphs are wingless, with a reddish-brown, pear-shaped body. Rutherglen bugs breed on a wide range of native and weed hosts, building up to large numbers in inland areas when winter and spring rainfall allows the growth of native herbs and weeds. In spring, as the hosts start to dry off, large numbers of adult bugs will move into the eastern cropping areas, migrating on the winds associated with storm fronts. In summer, these migration events stop, and by mid February females cease producing eggs and populations tend to decline going into autumn.

 

Better known as a pest of grain crops (sunflowers, sorghum, canola, safflower), RGB is not considered a pest of cotton. RGB damage to seedling cotton, and other crops, has been observed occasionally, particularly under hot, dry conditions. The damage to seedling crops is caused by large numbers of bugs sucking on the small plants, with sustained feeding pressure causing seedlings to wilt and die. This sort of damage can occur in autumn or summer.
Seedling crops at greatest risk are those adjacent to weed hosts, stubbles of canola, sorghum or sunflower, or planted directly into the stubble of these crops (e.g. maize into canola stubble).

Lodged sorghum head sprouting. This fallen seed was supporting a population of Rutherglen bug adults and nymphs.

Nymphs are able to survive for some time on fallen seed and will walk from stubbles, following cultivation or from drying weeds into neighbouring crops. Often damage is confined to the edges of the fields. The movement of RGB nymphs into seedling crops can be managed with border sprays.

 

Because RGB has not been considered a pest of cotton, there is little known about its capacity to cause damage. Luckily, there is one published study of RGB in cotton in Australia, and a little work in the US on a similar species (False Chinch Bug, Nysius raphanus) which provides some guidance.

The Australian study (Chinajariyawong, Walter and Harris, 1989) showed that neither adults nor nymphs caused any damage to squares (including damage to anthers, ovaries or stamina columns). These studies also found that RGB survival on cotton was quite short and there was no reproduction; cotton is not a good host. Given this information, it is unlikely that populations of RGB will persist in cotton and increase as a result of reproduction (as happens in sunflower and sorghum). The US study showed a similar result, with high numbers of False Chinch Bug causing no reduction in the number of fruit set.

If extremely high bug numbers are found in cotton, monitoring plant growth and fruiting will indicate if there is accumulating crop damage. Look for damage to terminals (wilting, blackening), and cut open fruit to check for blackened stamens in squares and staining of the seeds in young bolls. Monitoring techniques for cotton plant damage can be found in the Cotton Pest Management Guide 2012-13 p 51 (http://www.cottoncrc.org.au/industry/Publications/Pests_and_Beneficials). Continue to monitor for other causes of reduced retention.

There are no products registered for control of Rutherglen bugs in cotton. While some products in cotton may provide incidental control it is important to consider the impact on beneficials and the likelihood of future impacts, including the inadvertent resistance pressure on aphids, and the risk of flaring other pests such as mites and silverleaf whitefly. Refer to the IRMS and always follow label directions.

As with IPM for all cotton pests and diseases, it is important to have good farm hygiene that includes removal of weeds that the pest may use as hosts. In the case of RGB, particularly mat-like weed growth (e.g. pigweed, sowthistle, capeweed, fleabane and cudweed).

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Helicoverpa and midge management in sorghum

As crops come into head and start to fill grain, sorghum midge and helicoverpa will start to infest crops. Making a decision about when control is warranted is made somewhat easier with the availability of economic threshold calculators now available on the Beatsheet Blog (http://thebeatsheet.com.au/sampling-2/); or use the ready reckoners in this article.

MANAGEMENT OF SORGHUM MIDGE

How to count for midge
Often the first midge seen are caught in spiders webs in the field – a sign that midge are active. Generally, peak midge activity occurs between 9 and 11 am, and this is the best time to look. However changes in weather can bring midge into a field from surrounding areas (Johnson grass, earlier sorghum crops) at any time of day. Midge numbers can vary widely both within a crop and between plants, this makes the thorough sampling critical to estimate midge abundance.

Sorghum heads are most attractive to midge at mid flower. It is not uncommon to see double or triple the number of midge on panicles at early-mid flower compared with the end of flowering. At lower midge densities, adult flies will move around and lay almost exclusively on the flowering portion of the panicle.

Midge flies are only 1-2 mm long, and it is very easy to underestimate midge numbers if you are not careful. The easiest way to ‘get your eye in’ is to look at the top half of mid flowering panicles and look for MOVEMENT of the small red flies against a still sorghum panicle looking from side on and slightly above side on one section of the sorghum panicle at a time. Keep your eyes focused over a couple of branches of florets for several seconds at a time to detect female midge walking around the branch or bobbing up and down probing their ovipositor into each floret. On windy days you may have to hold each head still and shelter the panicle with your body before examining each panicle.

Monitor for midge over 10 metres of row in at least 4 different locations in your crop. Use the average midge density in the economic threshold calculator or ready reckoner.

Female sorghum midge laying eggs in sorghum floret.

As the season progresses, you may also start to see the black midge parasitoid, Eupelmus spp . Whilst it can be present in reasonably large numbers, this parasitoid does not occur early enough to prevent midge from causing damage. It can also be confused with midge, so be sure to look for the reddish abdomen of the midge, not just little black ‘flies’.

Managing midge in sorghum
Insecticides only kill the adult midge as they move about the crop and do not kill the eggs or hatched larvae that are already present inside the sorghum florets. While midge adults only live for one day, they do most of their egg laying (and subsequent damage to the crop) in the morning.
It is possible to calculate theoretical yield loss estimates for a particular crop senario (see table). These yield loss estimates are based on extensive field trials that determined the average yield losses per midge per day on different rated midge hybrids. The on-line calculator uses the data you enter to determine if the potential yield loss is greater than the cost of control.

Economic value of midge damage for a range of sorghum midge ratings.

The yield loss estimates in the table assume that spraying results in a 100% kill and that there is no midge damage prior to chemical application. It also assumes that you will receive the same average midge pressures over 4-5 days. In reality research has shown that one well timed insecticide for midge (put on from panicle emergence and before midge even enter the crop) will still only prevent 70-80% damage protection in lower rated sorghum hybrids. In 8 rated hybrids, yield losses can be reduced by over 90% with this spray timing.

Implications of midge control for other pests (helicoverpa and Rutherglen bug)
Often a spray for midge (synthetic pyrethroid) will be combined with a virus application for helicoverpa. Whilst the synthetic pyrethroid will have efficacy against midge and Rutherglen bug, it will devastate beneficial insect population. As a result, there may be implications for the ongoing control of helicoverpa populations in the crop. Larvae that survive a spray are more likely to go on and cause damage to maturing grain following a pyrethroid application because predators and parasitoids that might have otherwise killed them will be much less abundant. Because of the depletion of beneficial insects, another potential downside of midge and Rutherglen bug control with pyrethroids is the flaring of aphids which may cause stickiness issues at harvest.

HELICOVERPA MANAGEMENT IN SORGHUM

NPV infected, and killed helicoverpa larva.

Virus is the most commonly used control option for helicoverpa in sorghum. It is highly effective, and has the benefit of preserving beneficials, which then contribute to the suppression of surviving helicoverpa and aphids in the crop. To determine whether the helicoverpa infestation is likely to cause significant economic loss, use the threshold calculator, or the ready-reckoner below.

Economics of helicoverpa damage to sorghum.

Recommendations for the use of low volume aerial applications of Vivus Max in sorghum have recently been revised, and it is worth highlighting them. Whilst most NPV use in sorghum would have been without an additive, the revised recommendation for low volume applications suggests the inclusion of an additive. Recommendations for the use of NPV applied at higher volumes (by ground) have not changed, and there is no evidence that the inclusion of an additive is required to get high levels of efficacy.

Low water application volumes (down to 10 L per hectare) can be used successfully with Vivus Max with benefits in terms of timely application and being able to get over large areas of crop quickly and in wet conditions. However, low volumes increase the risk of poor coverage, particularly through droplet evaporation.
The inclusion of Optimol is recommended in low volume applications at a rate of 1 L/ha. In other words, 9 L water per hectare + 1 L Optimol per hectare + Vivus Max*

(* Important Note: Vivus Max + Optimol at 10 L per hectare in sorghum is subject to APVMA approval – expected March 2013)

For information on the activity of Optimol, go to the AgBitech website. www.agbitech.com

Posted in economic thresholds, helicoverpa, Sorghum, Sorghum midge | Leave a comment

Management of Rutherglen bug in seedling crops, sorghum and sunflower – updated

Since early November, large numbers of Rutherglen bug (RGB) have been migrating into cropping regions from northern NSW through to Central Queensland. Whilst the exact origin of the bugs is unknown, it is likely that they are being carried on storm fronts from inland regions where they have bred up over winter and spring on native host plants that are now drying off. Given how widespread the infestations are, it is unlikely that local weed hosts are driving the populations being seen in crops this season.

Rutherglen bug adult (top) and late instar nymph (bottom). Photo: Keith Power.

RGB damage to seedling crops

Large numbers of RGB are affecting seedling establishment, simply by weight of numbers feeding on the emerging seedlings. In some instances the seedling crops are invaded by large numbers of RGB nymphs walking out of weedy fallows into establishing crops. Ploughing a deep furrow between the seedling crop and the source of RGB, or a border spray may be sufficient to prevent ongoing infestation.

RGB damage to sorghum

Sorghum is vulnerable to RGB from flowering to soft dough. Research has shown that sorghum crops infested during flowering will fail to set seed, and infestations at milky dough stage will result in seed covered in small, dark feeding wounds.

Developing grain affected by RGB feeding is light in weight, with poor germination. Under wet conditions, fungal and bacterial infections further degrade RGB-damaged grain, infecting through feeding wounds on the seed.

Developing sorghum head showing signs of RGB damage; undeveloped seed, and spotting on developing seed.

Monitor for RGB in sorghum crops from booting to milky dough. This sampling can be done at the same time as checking for Helicoverpa. Shake the sorghum head into a bucket and count the number of RGB present. Repeat for at least 10 heads from across the field and average the RGB count. RGB infestations can vary greatly between heads. Take samples from the earliest flowering sections of the field as these will incur damage first.

Female RGB start laying eggs once grain fill starts and they have fed on the protein in the developing seed. Nymphs will emerge, and populations start to increase rapidly within 10 days. First instar nymphs have orange-reddish abdomens and do not feed on the developing seed. Late instar nymphs have developing wingbuds and are browner in colour (see picture at top of page).

The management recommendations for RGB in sorghum are:

  • Flowering – Milky dough:control warranted if more than 20 bugs per head
  • Soft dough: 20-25 bugs per head
  • Hard dough – physiological maturity: RGB have no impact on yield at this stage.

These thresholds were derived from trials done in irrigated and non-irrigated plots. RGB infestations did not significantly increase the yield loss in moisture stressed plots, but there was a significant difference in the yield of the irrigated and moisture stressed plots. In other words, the impact of RGB was insignificant in terms of impact on yield, compared with the impact that moisture stress had on yield.

These preliminary thresholds provide a broad guide for a range of sorghum prices. To work out a threshold for your specific situation, use a potential yield loss of 20% for these RGB numbers. For example, if you have 20 bugs per head at flowering then the potential yield loss will be 20%. With a sorghum price of $200/t, then a 20% yield loss will cost $40/ha. In this example, clearly it is an economic proposition to treat the infestation to prevent yield loss.

RGB damage to sunflower

Large numbers of RGB adults congregating on a sunflower bud. Kingaroy December 2012. M.Miles.

In sunflower there are two critical periods during which RGB control may be necessary to prevent crop loss:

  • Budding: bugs congregrate on the upper stem and bud. Bug feeding on the stem behind the head may cause the stem to wither and the bud droop. These heads do not continue to develop and set seed normally.
  • Flowering and seed fill: eggs are laid in the florets when they open, and nymphs emerge in about a week and start feeding on developing seeds.

Adult numbers are often minor in comparison with the size of the population once nymphs start to emerge. Preventing the subsequent population of nymphs is the key driver of RGB control prior to petal drop.

Feeding on developing seeds causes yield loss, and a loss of oil content and quality of grain.

Reinfestation is a real possibility, with continuing influxes of RGB into crops through November – January. It is likely that spring crops will require multiple sprays to keep populations below threshold and prevent the build up of large populations of nymphs through the grain filling stage. Being very clear on what critical stages need to be protected will enable better targeting of RGB populations.

Thresholds for spring (early) sunflower:

  • Budding: 10 bugs per head
  • Flowering – seed fill: 20-25 bugs per head

The aim of RGB control is to prevent adults from laying eggs and having large populations of nymphs present, feeding on maturing grain. This is why the thresholds are low, it is not related to the direct damage the adults are causing, but to the potential for a subsequent population feeding on the developing seed.

Thresholds for late sunflowers are higher, reflecting the lower potential for large increases in the size of the population. From about February on, RGB stop laying eggs and start to go into a reproductive diapause (resting stage) through winter.

Late sunflower crop thresholds (January – April):

  • Budding: 20-25 RGB per bud
  • Flowering – seed fill: 50 RGB per head

Making decisions about the control of RGB in sunflower

Synthetic pyrethroids (SP) are the only really effective available option for controlling RGB. Synthetic pyrethroids are extremely disruptive to natural enemies, and spraying for RGB may increase the survival of Helicoverpa larvae that would have otherwise been controlled by predatory bugs, beetles and parasistoids. If Helicoverpa are present, consider including NPV. Bees are also killed by synthetic pyrethroids. Note that the permit for indoxacarb (Steward®) has now lapsed.

Critical periods – targeting control.

The first critical period for protecting sunflowers is budding when the RGB congregate on the stems behind the head. At this stage the population will be made up entirely of adults. The development of the bud can be severely affected by the feeding of large numbers of RGB. Under dry conditions, RGB damage is greater than under conditions with adequate moisture. Continued influxes of adults into the crop will require ongoing monitoring from budding through to flowering.

Wilting sunflower bud in a field heavily infested with RGB.

The second critical stage is just prior to petal drop. From about petal drop, when the florets are opening on the face of the flower, RGB will start to lay eggs between the florets. It is critical that RGB adults are controlled before they can lay eggs for two key reasons:

  1. the resulting nymph population can be many times larger than the adult population (one RGB female can lay up to 400 eggs);
  2. once the sunflower heads starts to turn down it is extremely difficult to get good control of RGB feeding on the developing seed.

Ongoing monitoring is essential post spray.

Posted in Rutherglen bug, Sorghum, Sunflower | Leave a comment

An economic threshold calculator for Helicoverpa in chickpeas

 

Calculating the economics of control is critical to making a decision about if and when Helicoverpa populations in chickpeas require treatment. This season, for the first time, growers and agronomists have access to an on-line calculator to help them make these decisions. The calculator overcomes the need to try and remember the formulas in the field. Best of all, the calculator can be used off-line on most mobile devices, so it is available when you need to make the decision in the field. Some of the features of the calculator include:

  • Calculation of average larval density per square metre
    • Input checking data (number of larvae) and row spacing
  • Calculate an economic threshold for your specific situation
    • Input costs of control and crop value
  • Recalculate the economic threshold for a specific cost:benefit ratio

The Helicoverpa in chickpea threshold calculator is available on the Beatsheet Blog – find it under the “Economic Threshold Calculators – NEW!!” tab at the top of the page.

The calculator can be used on-line, and users with the latest browser versions of Internet Explorer (9+), Chrome, Firefox or Safari, the calculator can also be used offline. This means that after using the calculator on-line, you will still be able to access and use them offline without an internet connection. The other way to determine a current economic threshold is to use the ‘ready reckoner’ table below. When making decisions about Helicoverpa control in chickpeas, these are key considerations:

  • Larvae do not damage buds and flowers, yield loss starts to accumulate when pods are damaged as they set and fill. This means control can be delayed until pod set to minimise the chance of needing a second treatment before the crop matures. An exception to this ‘rule’ would be if control is applied to a population of small-medium larvae during late flowering to remove them so they are more easily controlled and not in the crop when it reaches pod set.
  • Use a beatsheet to sample chickpeas. Using a stick that is a metre long to ‘beat’ the crop simplifies the estimate of larval density. Watch the short Youtube video on how to use a beatsheet in chickpeas.

  • Try to make an assessment of the H. amigera  and H. punctigera numbers in the crop. This is particularly important if you are attempting to control medium to large larvae as H. armigera may be less susceptible to some older products (e.g. synthetic pyrethroids).  You may recall a recent article on the Beatsheet by Dr Lisa Bird on the results of resistance testing over summer – the level of resistance to synthetic pyrethroids had increased over previous seasons.On the Downs this season, the population of Helicoverpa in crops is made up of both H. armigera and H. punctigera. Take this into account when making a decision about which product to use.

For a more detailed discussion of Helicoverpa management in chickpeas, the formulas for calculating an economic threshold, and background information on how the thresholds were devised you can read previous posts on the Beatsheet Blog. http://thebeatsheet.com.au/category/chickpeas/

Posted in helicoverpa | Leave a comment

Research developments in Solenopsis mealybug management and boll rot in cotton.

Solenopsis mealybug (Phenacoccus solenopsis) was first identified at Emerald and the Burdekin during the 2009-10 cotton growing season. This sucking pest causes leaf distortion, stunting and reduced boll size and number. Heavy infestations can lead to plant death. Solenopsis mealybugs also produce a honeydew which affects photosynthesis and leads to sooty mould development on lint. This pest has the potential to significantly reduce yield.

 

Several chemical trials for the control of solenopsis mealybug were conducted this past season. Field trials took place in both Emerald and Byee at the late crop stage. (Unfortunately the Emerald trial was inconclusive due to heavy rain and storm activity which impacted on the mealybug population there).

Field trials indicate that many insecticides have little impact on the mealybug population although some reduced numbers by up to 60%. Unfortunately these chemicals had a heavy impact on beneficials. This loss of beneficial activity in the crop allows mealybugs to thrive unchecked and this results in greater crop damage. This was clearly evident in one crop of conventional cotton which was sprayed five times throughout the growing season with disruptive chemicals. As a result mealybug numbers increased rapidly at boll opening stage resulting in significant sooty mould on open bolls.

Results from the field trials also determined that insecticides used for the control of other cotton insect pests were not effective in controlling late season infestations of mealybug.  This, together with other trial results led researchers to conclude that insecticides may not be the answer for mealybug infestations. Beneficials remain the best management option for mealybug control in the later stages of the season. Key predators associated with mealybug control include green lacewings, Cryptolaemus lady beetles (pictured below), other lady beetles including three banded, transverse and Hippodamia.

Other observations made during the season also indicated that pre-planting operations such as herbicide applications, pupae busting and insecticide treated seed reduced early mealybug influx. This is important when considering options for fields which have a previous history of mealybug infestation.

New mealybug parasitoid

A key development this season was the discovery of a previously undetected parasitoid of mealybug in the Byee trial field. This parasitoid was identified by John LaSalle (CSIRO) as Aenasius bambawalei. Another beneficial, a hyperparasitoid (which develops within the already established parasitoid), Prochiloneurus Silvestri was also recorded at this location. The parasitoid has been recorded on P. solenopsis in India and Pakistan, and may have been introduced at the same time. Observations on the level of parasitism during the latter part of the season, remained relatively low (<10%). Further research on Aenasius bambawalei is planned for the coming 2012/13 cotton season.

The female parasitoid is pictured below (left) and a healthy (top) and a parasitised mealybug (bottom) in the right hand image.

 

Boll rot bacterium

In addition to the Solenopsis research, the cotton pest team also examined a number of damaged bolls from across cotton growing regions. These damaged bolls were found to contain a bacterium, Pantoea agglomerans. This wasthe first time this bacterium was identified to be associated with boll rot in Australian cotton. Three species of fly, which potentially play a role in introducing the bacterium into the bolls, were also identified. All three species of fly were found in unsprayed Bollgard cotton, var. 71BRF, in Kingaroy where 80% of the bolls were rotten. A major concern with this boll rot is that, from the outside, medium to large size bolls looked normal but once bolls were cut open, all locules were damaged and maggots were found inside.

 

Article summarised by Kristy Byers

For any further information please contact DAFF Entomologist Dr Moazzem Khan on (07) 4688 1310.

Posted in Cotton, mealybugs | Leave a comment

Whitefly resistance monitoring in Cotton

Results for 2011-12

Monitoring for resistance in Silverleaf whitefly, collected in the 2011-12 cotton season, is now complete. Results show that resistance exists for Admiral® and bifenthrin (e.g. Talstar®) in horticulture but not in cotton while SLW remain susceptible to Pegasus® and Movento®

In total 17 collections were made from Emerald, St George, Theodore, Moree and Narrabri for resistance monitoring. Whitefly were not collected from the Darling Downs due to very low numbers this season. Testing was conducted against the four registered insecticides, Admiral® (pyriproxyfen), Pegasus® (diafenthiuron), Movento® (spirotetramat) and Bifenthrin (e.g. Talstar®).

The 2011-12 season was generally a low pressure year with the exception of the Moree region. Whitefly were generally below action thresholds in the Emerald, Burdekin, Biloela, Theodore and Darling Downs regions. Low to moderate whitefly pressure at St George resulted in approximately 15% of fields being treated with insecticide. Suppression of low-moderate infestations was achieved by using Pegasus® or Admiral® (many growers had purchased Admiral® the previous season and wanted to use it rather than hold old stock on farm).  

Moree had very high pressure with almost all irrigated cotton treated for SLW with some fields requiring more than one application. This was due to unfavourable crop development caused by flooding as well as late season whitefly migrations. Insecticides used included Admiral®, Pegasus®, Movento® and/or Talstar®.

Admiral® remains the cornerstone of effective management of high density infestations. After five years of monitoring, resistance levels remain susceptible in cotton dominated regions, however high levels of resistance exist in Bowen and the Burdekin due to intensive usage for fruit and vegetable production.

SLW remain susceptible to Pegasus® and Movento®. These products are useful options for whitefly management from a resistance perspective. As these products are also registered for aphid control consideration should include both pests as there is a high risk of developing resistance. The best way to avoid developing resistance is to minimise the use of any one mode of action group.

Bifenthrin (eg Talstar®)has elevated resistance factors in cotton and this has been confirmed as resistance in one sample from St George. Bifenthrin is generally not recommended as a product for SLW management except for circumstance where late season pest abundance may warrant its use just prior to defoliation. The earlier use of bifenthrin for SLW is not recommended as it has marginal efficacy and is highly disruptive to beneficial insects and often results in subsequent re-flaring of SLW numbers within weeks of application.

No changes have been made to the Insecticide Resistance Management Strategy for the 2012-13 season. That means that a maximum of one application of Admiral® may be used in a season. Resistance risks should be avoided by rotating products of different modes of action.

Thank you to Geoff Cornwell, Chris Monsour and Gail Spargo for collecting whitefly for the resistance monitoring project and to Jamie Street, Steve Madden and Rob Hones for assisting in locating whitefly for collection. This is a CRDC funded project.

For more information on SLW, including how to check for parasitism, please refer to previous blogs. You can find these under the categories on the right hand side of the blog. You can also find a guide to recognising parasitism – under Resources at the top of the Beatsheet page. Or contact Zara Hall, DAFF field crops entomology Toowoomba, 07 46881436.

Article by Zara Hall

Posted in Cotton, Silverleaf whitefly | Leave a comment
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