Wing Abnormality in Locustana pardalina

Nature ◽  
1937 ◽  
Vol 139 (3509) ◽  
pp. 197-197 ◽  
Author(s):  
T. F. DREYER
Keyword(s):  
1956 ◽  
Vol 33 (1) ◽  
pp. 174-185
Author(s):  
BRYN M. JONES

1. A brain-ventral head gland system operates in embryos of Locustana pardalina and Locusta migratoria. 2. The initiation of growth and differentiation on the termination of diapause in the egg of pardalina takes place before the ventral head glands are formed. 3. Maximal activity in the ventral head glands coincides with the retraction of the epidermis from the cuticle. 4. Embryos, dissected out of the egg, were kept alive in aerated sterile Ringer's solution for up to 2 weeks during which time they progressed in their development. 5. If post-katatrepsis embryos are ligatured between the thorax and abdomen before a ‘critical’ period the moult is limited to the thorax. If ligatured immediately behind the head, the body fails to moult. 6. Since on the termination of diapause in the egg of pardalina mitosis begins before the formation of the ventral head glands, it is suggested that in locust embryos these glands are exclusively concerned with the retraction of the epidermis from the cuticle. 7. It is suggested that the uptake of water by the egg of pardalina in stretching the cells stimulates a growth factor which, although present throughout the diapause phase, is only capable of initiating mitosis after the diapause phase has come to an end.


1946 ◽  
Vol 36 (3) ◽  
pp. 343-371 ◽  
Author(s):  
J. J. Matthée

The theory of phases, Uvarov (1921), had the object of explaining the interrelationship between different forms ofLocusta migratoriaandLocustana pardalina. This theory has been accepted by most entomologists working on locust problems. Authors such as Faure (1923 and 1932), Johnston and Maxwell-Darling (1931) and later a series of others including Hussein and Ramchandra Rao, proved and confirmed the truth of Uvarov's theory.


1956 ◽  
Vol 33 (4) ◽  
pp. 685-696
Author(s):  
BRYN M. JONES

1. Secretory activity of the ventral head glands in embryos of Locustana pardalina and Locusta migratoria is necessary for inducing the moult and controlling subsequent events in late development. 2. Continued secretory activity of the glands for a period after the moult is required for further progress in development. 3. The development hormone released by the glands activates in turn the pleuropodial glands. The latter, in order to become fully functional, also require the continued secretory activity of the endocrine glands for a period after the moult. 4. The enzyme-substrate system responsible for the formation of melanin does not become active until the development hormone is liberated. However, the system was present in the egg beforehand in an inactive state and it is suggested that it is held in check by an inhibiting influence. 5. The amount of melanin deposited appears to be correlated with the amount of development hormone released.


Nature ◽  
1948 ◽  
Vol 162 (4110) ◽  
pp. 226-227 ◽  
Author(s):  
J. J. MATTHÉE

Agronomy ◽  
2021 ◽  
Vol 11 (11) ◽  
pp. 2212
Author(s):  
Roger Price

Regular and often intense outbreaks of the brown locust, Locustana pardalina (Walker), in the semi-arid Nama Karoo region of South Africa present a formidable pest control problem. Outbreak patterns over a 64-year period (1941–2005) were reviewed indicating a very high frequency of outbreak years with regular ‘plague’ periods being experienced, while a more detailed analysis of the numbers of locust targets controlled during a 22-year period (1983–2005) described the intensity and scale of the outbreaks. The operational constraints associated with the traditional ground-based control strategy employed against the thousands of individual roosting brown locust hopper band and swarm targets in the Karoo are discussed. A brief review of laboratory and field trials of alternative methods of controlling the brown locust, such as insecticide baits, barrier treatments and the Green Muscle® myco-insecticide, as an alternative to broad-spectrum pyrethroid insecticides are described. In addition, alternative control strategies to the current ‘Commando’ system of ground-based control operations are discussed. The recommendation is for a modernised and technology-equipped integrated brown locust management strategy (IPM), combining ground and aerial tactics that will have the flexibility and the capacity to deal effectively with outbreaks. The integrated management strategy should focus on ground-based control of hopper bands and fledgling swarms in the Upper and eastern Karoo, while outbreaks over most of the Central Karoo and arid Bushmanland areas should be left to fledge and coalesce into large-sized swarms that could then be targeted by spray aircraft as they migrate along their known swarm flight paths. The introduction of electronic reporting and GIS mapping technologies for brown locust campaign management is essential.


It is known that the hoppers (or immature forms) of certain species of locusts, in the solitary phase, bear a marked colour resemblance to the immediate environment in which they are living. They are, for example, green when living among fresh green vegetation, light brown on sand, speckled greyish white on white limestone rocks, and so on. Faure (1932) conducted a series of experiments with Locustana pardalina (Walk.) and Locusta migratoria subspecies migratorioides R. and F. in South Africa. His object was to discover whether there was only a coincidence between the prevailing coloration of the hoppers of these two species and that of their environment, or whether a genuine colour adaptation is involved. He isolated a number of young hoppers, of the same stock, placing each insect in a separate wooden box, provided with a sliding glass lid and reared it to the adult instar. The wood of each box was painted on the inside with ordinary commercial oil paints and, when dry, the latter were compared with the coloured plates of Ridgway (1912) and named according to the tints which they resembled most closely. The experiments of Faure were done out of doors, and he recorded the general coloration assumed by each locust during and at the end of the experiments, noting them as “good”, “fair”, “slight” or “none”, according to the degree of resemblance their coloration bore to that of the insides of the boxes. He obtained a majority of “good” or “fair” resemblances on white, black, grey, yellow and brown backgrounds in the boxes, and one striking resemblance on a black and white striped background. No resemblance occurred when confined in boxes painted green, pink, blue, or with black and orange stripes. Faure also carried out some other experiments on a smaller scale, such as using glass lids of the colours resembling those of the walls of the boxes, but these, as he states, were, on the whole, inconclusive. He brought forward evidence, however, of great importance as regards the production of green hoppers. These, he found, did not result in response to a green background and were only produced in the presence of a moist atmosphere and an abundance of succulent food. He further showed that the green colour-producing substance was spectroscopically very different from chlorophyll, and prepared extracts showed none of the characteristic fluorescence. The present paper describes experiments which have been made with a view to determining the relation between the general coloration of the hoppers and the wave-lengths of the effective colours forming different backgrounds.


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