The effects of temperature and photoperiod on the morphology of the egg-pod of the Australian plague locust (Chortoicetes terminifera Walker,Orthoptera: Acrididae)

Chortoicetes terminifera can detect absolute differences of both temperature and photo-period, as well as the directional change of these parameters. Insects subjected to long-day conditions, or to an increase in photo-period during development lay long straight pods, whereas those subjected to short days or to a decrease in photoperiod during development lay short pods, which are usually curved and/or laid obliquely. Temperature does not affect oviposition behaviour at long photoperiod, but at medium and short photoperiod, high temperature or an increase in temperature promotes the production of long pods, whereas low temperature or a decrease in temperature stimulates the production of short pods. When temperature and photoperiod change in opposite directions, the effects of photoperiod override those of temperature. The significance of these findings is discussed in relation to egg development and survival.     

Levels of ecdysteroids in diapause and non-diapause eggs of the Australian plague locust,Chortoicetes terminifera (Walker)

The levels of ecdysteroids during embryogenesis in Chortoicetes terminifera were measured by radioimmunoassay. Soon after laying, eggs laid by females reared under non-diapause conditions contained three times as much as those laid by females reared under diapause inducing conditions. In eggs incubated at 32°C which did not enter diapause there was a sharp rise in ecdysteroid levels which coincided with the formation of the first-instar cuticle, but this did not occur in eggs incubated at 20°C even though they developed and hatched normally. Comparisons are made with previous results in other locust species and the possible role of ecdysteroids in embryonic diapause is discussed.     

Aerial treatment of the Australian plague locust, Chortoicetes terminifera (Orthoptera: Acrididae) with Metarhizium anisopliae (Deuteromycotina: Hyphomycetes)

Between October 1999 and April 2000, nearly 4000 ha of nymphal bands and adult swarms of Chortoicetes terminifera (Walker) were aerially treated using a ULV oil formulation of strain FI-985 of Metarhizium anisopliae var. acridum. During the mild weather (maxima 22-30 degrees C) of spring (October), there was little change in nymphal bands during the first week but at all doses between 25-100 g (1-4 x 10(12) conidia) ha(-1), the bands rapidly declined 9-12 days after treatment reaching > 90% mortality by 14 days. Metarhizium persisted for some time as there was 50% mortality of locusts fed vegetation collected from the treated blocks seven days after treatment. Persistence was confirmed by the high mortality of bands that invaded from untreated areas and of nymphs that hatched on the plot five to seven days after treatment, though mortality was then delayed until early in the third week. During summer (January), temperatures were high (maxima 36-42 degrees C), and at all doses between 25 and 125 g (1-5 x 10(12) conidia) ha(-1), there was a rapid decline seven to ten days after treatment. By 12-14 days, there was a > 90% decline in numbers in most blocks which was confirmed by helicopter surveys two weeks after treatment that found very few adults within or near treated areas. Mortality was delayed in the high dose where there were blockages of spray equipment during treatment. The clear demonstration that Metarhizium can suppress small local populations of C. terminifera led to the limited operational use of Metarhizium on an organic farm and in a National Park where nearly 2500 ha of bands and swarms were treated. Continued research is needed to develop a commercially viable product so that Metarhizium can form a significant part of a programme of integrated pest management of locusts in Australia.     

Chromosome organisation in the Australian plague locust,Chortoicetes terminifera

In Chortoicetes terminifera, G-banding, produced by the trypsin treatment of air-dried slides followed by Giemsa staining, leads to light staining gaps at the secondary constrictions on autosomal pair 6 and regions proximal to the centromere on the long arms of pair 4. The variable short arms of two of the three smallest pairs were usually flared and lightly stained after treatment. In contrast to the relatively minor response of the normal chromosome set to G-banding, the large supernumerary chromosomes of C. terminifera show a spectacular series of dark bands alternating with lightly stained gaps. Two G-band variants of the B-chromosome were found in a laboratory stock. These patterns of G-banding are discernable both at mitosis in adults and embryos of both sexes and at all stages of male meiosis. Some regions which are gaps after G-banding appear as dark bands after C-banding. Consequently the supernumerary chromosome is mainly darkly stained with C-banding. In addition the centromeres and some telomeres are C-banded along with narrow interstitial bands and polymorphic heterochromatic blocks. — C-banding was not always successful, the technique often yields a mixture of G- and C-banding. The disparity of banding between the normal complement and the B-chromosome implies that whatever the source of origin of the B it has undergone spectacular changes in organisation since its origin.     

Chromosome organisation in the Australian plague locust Chortoicetes terminifera

In Chortoicetes terminifera 45 independently-occurring B-chromosomes were tested and 23 distinct banding variants were detected with either G- or C-banding; six types were found more than once. In particular the Type I banding morph was detected 12 times indicating that individuals carrying this type may be under a different regime of selection compared with individuals bearing other types of banding morph; or the Type I may be subjected to a higher rate of meiotic drive in either or both sexes than other types. Also the Type I appeared to be obviously related to four other banding morphs whereas most types were not obviously related to any other banding morphs, but a few were similar in banding pattern to one or two other types. Three types of B-chromosomes were found in three or more different populations. A relatively high frequency of the Type I banding morph was found in one population, which was probably mainly composed of non-migratory individuals, and also in a laboratory-raised population. The most likely mechanisms for small changes in the banding sequence of the B-chromosomes are three-break insertions which are often indistinguishable from inversions. Rearrangements which add or delete bands, or sequences of bands, to or from B-chromosomes are probably the result of exchanges which are now known to take place in rare individuals with two B-chromosomes. The most distal region of all the banding morphs of the B-chromosome in C. terminifera, plus a short interstitial region in some types, is not late-replicating and has the banding characteristics of euchromatin. The rest of the chromatin of the B-chromosomes is heterochromatic and is the latest replicating heterochromatin in the whole genome. It consists of G-bands, which are also deeply stained with C-banding, and alternating G-interbands, which in turn are stained grey with C-banding. Both of these staining combinations are seen in heterochromatin of the normal complement. The heterochromatin of the B-chromosomes is condensed throughout 1st meiotic prophase in the male and in all somatic interphase nuclei where it can be quickly detected using the G-banding technique. The B-chromosome has a relatively constant, acrocentric morphology with a tendency to increase of length of the long arm as band numbers increase. Isochromosomes of the long arm have been seen only in laboratoryraised embryos. From egg pods with significantly fewer than expected B-chromosomes it is strongly suggested that more than one male may fertilize the eggs in a single pod.     

Variation in diapause potential and strength in eggs of the Australian plague locust, Chortoicetes terminifera (Walker) (Orthoptera: Acrididae)

Samples of eggs of Chortoicetes terminifera were incubated under 3 temperature regimes which would allow non-diapause eggs to develop about 50% and so take them beyond the diapause stage. Even so, many more eggs entered diapause when reared at 20°C for 3 weeks than at 32°C for 1 week. By collecting and incubating eggs at intervals after laying in autumn, diapause potential or strength of eggs at different stages of development was estimated. For eggs in pre-diapause, the proportion in diapause after rearing was used to estimate diapause “potential”; for those in diapause, the proportion was used to estimate diapause “strength”. At laying, eggs varied greatly in their potential to enter diapause. However, those with lower potential at laying often increased their potential during the pre-diapause stage so that by the time diapause was reached diapause strength varied but over a lesser range. In all eggbeds, diapause strength decreased by 7–9 weeks after laying; little or none remained by mid-winter.These variations in diapause potential and diapause strength seem to reflect how much the temperature threshold for development during diapause is increased above that for non-diapause. Both diapause potential and strength may reflect the value of some factor whose level at laying is determined by the environment experienced by the parents but which changes subsequently.     

Behavioural phase polyphenism in the Australian plague locust (Chortoicetes terminifera)

Swarming and the expression of phase polyphenism are defining characteristics of locust species. Increases in local population density mediate morphological, physiological and behavioural changes within individuals, which correlate with mass marching of juveniles in migratory bands and flying swarms of adults. The Australian plague locust (Chortoicetes terminifera) regularly forms migratory bands and swarms, but is claimed not to express phase polyphenism and has accordingly been used to argue against a central role for phase change in locust swarming. We demonstrate that juvenile C. terminifera express extreme density-dependent behavioural phase polyphenism. Isolated-reared juveniles are sedentary and repelled by conspecifics, whereas crowd-reared individuals are highly active and are attracted to conspecifics. In contrast to other major locust species, however, behavioural phase change does not accumulate across generations, but shifts completely within an individual''s lifetime in response to a change in population density.     

Fat body changes in a locust,Chortoicetes terminifera (Walker) (Orthoptera: Acrididae), parasitized by a nemestrinid fly

The fat body of Chortoicetes terminifera (Walker) (Orthoptera: Acrididae) parasitized by Trichopsidea oestracea (Westwood) (Diptera: Nemestrinidae) was hypertrophied and showed extensive cytological and functional changes. Lipid content (as a percentage of dry weight) was significantly higher in parasitized locusts. Regression of lipid content against parasitoid weight was quadratic in female hosts and linear (negative) in male hosts. The fatty acid composition of C. terminifera was not affected by parasitization. Parasitized male locusts had lower body weight than nonparasitized males and contained less soluble protein. Results indicated that egg development was inhibited in parasitized female locusts. These conditions may be related to changes in the host's fat body.     

Eight polymorphic microsatellite loci for the Australian plague locust, Chortoicetes terminifera

Few population genetics studies have been carried out on major locust species. In particular, an understanding of the population genetic structure of the Australian plague locust, Chortoicetes terminifera, is lacking. We isolated and characterized eight polymorphic microsatellite loci in C. terminifera, and described experimental conditions for polymerase chain reaction multiplexing and genotyping these loci. The number of alleles per locus ranged from 11 to 29 and the expected heterozygosity ranged from 0.797 to 0.977. One locus was found to be X-linked. Results of cross-taxon amplification tests are reported in four species of the Oedipodinae subfamily.     

Effect of Insecticide Usage on Parasitism of Chortoicetes terminifera (Walker) (Orthoptera: Acrididae)

Parasitism of adult Chortoicetes terminifera by Trichopsidea oestracea Westwood and Blaesoxipha rufipes (Macquart) was assessed to discern any effect of chemical control during an outbreak in the 1995–96 season in eastern New South Wales. In the Moree and Gunnedah regions the effects of ground control of bands and aerial control of bands and swarms on parasitism were compared with untreated controls. In the Hunter region only the effect of ground control of bands could be measured. Within both the Moree and Gunnedah regions there were no differences in parasitism rates by either T. oestracea or B. rufipes which could be attributed to chemical control. Parasitism by T. oestracea was significantly higher in the Hunter region than in all treatments in the Moree and Gunnedah regions, except untreated sites in the Gunnedah region. Parasitism by T. oestracea was significantly higher in the Gunnedah region than in the Moree region. Regional differences in parasitism by T. oestracea are attributed to intrinsic climatic and landuse differences between the regions rather than coincident regional differences in insecticide usage. There were no treatment or regional differences in parasitism by B. rufipes. Parasitism levels recorded during the study were atypically low, a fact attributed to a severe drought which preceded the outbreak. Emigration of C. terminifera took place during the study but is not considered to have affected trends in parasitism.     

The role of pressure in controlling the entry of water into the developing eggs of the Australian plague locust Chortoicetes terminifera (Walker)

The normal internal hydrostatic pressure and the additional pressure necessary to rupture the egg shell was measured in the eggs of Chortoicetes terminifera, Newly laid white eggs burst at c 0.15 kg cm^-2, but after external tanning the chorion withstands c 0.5 kg cm^-2 when removed from its tanned foam ‘corset’ and 1.0 kg cm^-2 if left embedded in the egg pod material. Older eggs with formed cuticles often withstand 2.0 kg cm^-2 but yield at rather lower pressures if they develop ‘pin-holes’. As the OP of the egg contents always exceeds 7.7 kg cm^-2 the rigidity of the wall is clearly insufficient to permit the generation of high hydrostatic pressures capable of preventing water entry during the non-absorbing phases of development. Real hydrostatic pressures are lower than 0.06 kg cm^-2 in the young intact egg and reach only c 0.5 and 0.3 kg cm^-2, respectively, during the absorptive and post-absorptive phases of development. Several events contribute to the sigmoid form of the water uptake curve. Water is at first excluded by a permeability barrier associated with the chorion. Absorption is delayed until the yolk is completely enclosed by the serosal cell layer. After undergoing cleavage, the yolk is then rapidly mobilized to furnish precursors for cuticle synthesis; in consequence, the internal OP rises from δ 0.76d?K to 0.93d?K despite the massive inflow of water which is governed by the osmotic gradient. At blastokinesis the serosa becomes detached from the cuticle; cuticle deposition and yolk mobilization are halted, the OP falling rapidly to cδT 0.53d?K. The bulk entry of water then ceases. Any excessive hydrostatic pressures which develop later are relieved by the formation of self-sealing ‘pin-holes’.     

Evidence from traditional and new technologies for northward migrations of Australian plague locusts (Chortoicetes terminifera) (Walker) (Orthoptera: Acrididae) to western Queensland

Abstract The development of recent infestations of the Australian plague locust (Chortoicetes terminifera) (Walker) (Orthoptera: Acrididae) has been traced using traditional survey data combined with information from several modern technologies including simulation of windborne transport trajectories, direct observation with entomological radar and satellite imagery. The results indicate that migration from spring generations in the southern and eastern parts of the species range, including agricultural areas, to the summer rainfall areas in arid western Queensland (Qld) has contributed to the development of infestations on several occasions. Migration from swarm populations in New South Wales to western Qld in November and December 1999 contributed to a rapid population increase that, over a sequence of generations, led to the major infestation of agricultural areas in March and April 2000. There is evidence that northward migrations also occurred in 1995, 1997 and 2000. These contributed to the early summer populations in Qld, but did not result in large migrations to the south in autumn. These observations suggest that a pattern of exchange migration across much of the geographical range of the species between regions of winter and summer rainfall characterizes the spatial dynamics of this species. This pattern appears to be adaptive and suggests migration in C. terminifera is sustained by contemporary natural selection.     

Indigestibility of plant cell wall by the Australian plague locust, Chortoicetes terminifera

The plant cell wall may play an important role in defence against herbivores since it can be both a barrier to, and nutrient diluter of, the easily digested cell contents. The aim of this study was to investigate the digestibility of the cell wall of three grasses, Triticum aestivum L., Dactyloctenium radulans (R. Br.) Beauv., and Astrebla lappacea (Lindl.) Domin, by the Australian plague locust, Chortoicetes terminifera Walker (Orthoptera: Acrididae, Acridinae) as determined by the Van Soest method [ Van Soest PJ, Robertson JB & Lewis BA (1991) Methods for dietary fiber, neutral detergent fiber, and nonstarch polysaccharides in relation to animal nutrition. Journal of Dairy Science 74: 3583–3597]. Determination of plant cell wall digestion by locusts required a precise methodological procedure to determine both the exact intake and the concentration of cell wall in the diet and the faeces. Plant cell wall determination is affected by the particle size distribution of the dried plant material. All three grasses differed in the percentage of cell wall per gram dry matter and the proportions of hemicellulose, cellulose, and acid‐detergent sulphuric lignin within the cell wall. The locust was unable to digest the cell wall of any of the grasses. Thus, plant cell walls are a mechanical barrier hindering locusts assimilating nutrients. That is, access, rather than nutrient concentration per se, may be limiting nutrient factor.     

Analysis of the development of major plagues of the Australian plague locust Chortoicetes terminifera (Walker) using a simulation model

The development and decline of all the past major plagues of Chortoicetes terminifera in Australia has been analysed using all available locust data and a simulation model to estimate the course of events for periods when few locusts were reported. The model is based on the developmental biology of the locust and includes methods of estimating the duration of egg, nymphal and adult development and uses a pasture growth index and potential night displacement index to assess likely survival and migration. The analysis shows that five of the six plagues originated in the arid interior, where good spring and summer rain allowed two or three consecutive generations of successful breeding, before emigration to the agricultural country occurred in the late summer or early autumn. This is contrary to the idea held previously that most plagues developed from local breeding in established outbreak areas in the agricultural belt. The applications of these results, to improve population monitoring and control strategy by suggesting the best timing for surveys and when control would have most effect, are discussed.