The Cytochemistry of an Unusual Type of Proteinaceous Globule in Reserve Tissues of Aphodius constans Duft. (Col., Scarabaeidae)1

1970 ◽  
Vol 1 (4) ◽  
pp. 315-320
Author(s):  
Reinhold Charpentier

AbstractMorphological, cytochemical and developmental studies were undertaken of a new "double" type of proteinaceous globules in fat body and haemolymph of Aphodius constans Duft. The homogeneous globules first appear in the late first instar or the early second instar larva—i.e. earlier than in other insects. In the middle of the third instar the central region of the globules begins to differentiate into a core, much resembling the polyhedron of a nuclear insect virus. The cores are, however, not a pathological phenomenon, but constitute normal reserve substances, present in all individuals, especially in the prepupa, the pupa and the early adult. Both the core and the periphery of the "double" globules, as well as "empty" globules from second and third instar larvae, contain proteins and ribonucleic acid, although the cytochemical reactions of the core was always the most intense. Neither lipids, carbohydrates, desoxyribonucleic acids nor uric acid are deposited inside the globules. There is no membrane around the globules.

1968 ◽  
Vol 100 (2) ◽  
pp. 202-206 ◽  
Author(s):  
Louis F. Wilson

AbstractThe willow beaked gall midge, Mayetiola rigidae (Osten Sacken), is univoltine in Michigan. Adults emerge from bud galls on Salix discolor Mühl. and other willows on mornings of warm days in early April. Eggs are laid singly on or near the buds of the host. Head capsule measurements indicate three larval instars. The last two instars each possess a spatula. The first-instar larva emerges in late April and penetrates the soft bud tissues. The gall begins to develop at the beginning of the second instar in mid-May. The third instar appears in early July and continues to enlarge the gall until fall. Prior to overwintering, the larva lines the inner chamber of the gall with silk and constructs one to seven silken septa across the passageway. Pupation occurs in mid-March. The gall deforms the stem and occasionally a galled branch dies or breaks off.


1988 ◽  
Vol 19 (3) ◽  
pp. 381-391 ◽  
Author(s):  
Anders N. Nilsson

AbstractA lectotype is designated for Agabus setulosus (J. Sahlberg, 1895), a rare rheophilous dytiscid known mainly from northern Fennoscandia. The larval instars are described for the first time, based on material from northern Sweden. The first-instar larva is characterized by the presence of two dorsal spines on each femur and a pair of mediodorsal setae on last abdominal segment; both characters are seemingly unique among Agabus. The third instar differs from all other Palaearctic Agabus species in the complete sclerotization of the ring-like abdominal segment 6. The biology of A. setulosus is described from a Swedish population; semivoltine life cycle with overwintering eggs laid in summer followed by adult overwintering prior to breeding is suggested.


Zootaxa ◽  
2010 ◽  
Vol 2658 (1) ◽  
pp. 38 ◽  
Author(s):  
MARIANO C. MICHAT ◽  
YVES ALARIE ◽  
CHRIS H. S. WATTS

The first-instar larva of Neobidessodes Hendrich & Balke (through the hypogaeic species N. limestoneensis (Watts & Humphreys)) and the third-instar larva of Hydroglyphus Motschulsky (through H. balkei Hendrich) (Dytiscidae: Bidessini) are described and illustrated in detail for the first time, including detailed morphometric and chaetotaxic analyses of the cephalic capsule, head appendages, legs, last abdominal segment and urogomphi. A cladistic analysis including 51 characters and 32 hydroporine taxa is performed, which supports the inclusion of both genera in the tribe Bidessini based on the absence of the primary pore ABc on the last abdominal segment. The third instar of H. balkei is characterized by the absence of secondary setae on the urogomphi and anterior secondary setae on the coxa, and the presence of 8–9 secondary setae on the mesofemur. On the other hand, the first instar of N. limestoneensis bears 14 lamellae clypeales on the anteroventral margin of the nasale. This species has evolved several morphological characters that are probably associated with its hypogaeic existence, including a lightly sclerotized body, relatively longer cephalic capsule and mandibles, a strongly reduced occipital foramen, absence of stemmata, and short claws. However, primary chaetotaxy apparently has remained as a very conservative expression of the phenotype.


1968 ◽  
Vol 100 (2) ◽  
pp. 184-189 ◽  
Author(s):  
Louis F. Wilson

AbstractThe taxonomic status of Rhabdophaga sp. cannot be determined until a complete revision of the genus occurs. Rhabdophaga sp. on Salix discolor Mühl. is univoltine in Michigan. Adults emerge in mid-April, and shortly afterward deposit numerous eggs on the setaceous undersurface of emerging willow leaves; larval eclosion occurs between 1 and 2 weeks later. Head capsule measurements reveal three larval instars. The first-instar larva bores into the stem until it reaches the pith. Gall development begins about mid-June shortly after the second instar appears. The third-instar larva overwinters in the gall and the pupa appears in early April. The prolate gall is found on the proximal ends of young willow shoots; heavily galled shoots usually die.


1976 ◽  
Vol 108 (8) ◽  
pp. 815-821 ◽  
Author(s):  
K. P. Lim ◽  
R. K. Stewart

AbstractDevelopment of P. pallipes, from egg to emerged larva, in the tarnished plant bug lasts 24.49 ± 2.38 days at 25 °C/16 h and 20 °C/8 h and 77 ± 5% R.H. with 16 h illumination.Eggs of P. pseudopallipes need 72–96 h to hatch under the above-cited regime. At least three distinct larval stages can be recognized without special staining procedures. The first instar larva is a caudate-mandibulate type. The second larval stage is acaudate and lives in the host haemocoele. The third larval stage is also acaudate and emerges from the host. The pupa is an exarate type diapausing in a cocoon. P. pseudopallipes is an arrhenotokous species. The longevity of the adults in the laboratory is about 16 days. The adult oviposits into the host abdomen.Survival of diapausing pupae is better at 16 h photophase than at 8 h photophase.


2012 ◽  
Vol 155 (2-3) ◽  
pp. 193-208
Author(s):  
Bernhard J. van Vondel

The third instar larvae of Haliplus fortescueensis Watts & McRae, 2010, H. halsei Watts & McRae, 2010, H. pilbaraensis Watts & McRae, 2010 and H. pinderi Watts & McRae, 2010 are described, together with the first instar larva of H. halsei Watts & McRae, 2010. A key to the six known third stage larvae of Australian Haliplidae is given and notes are given on subgeneric placement of the species.


1989 ◽  
Vol 79 (3) ◽  
pp. 381-391 ◽  
Author(s):  
Peter T. Bailey

AbstractPelidnoptera nigripennis (F.) is a parasitoid of the millipedes Ommatoiulus spp. in Portugal. It is univoltine. The adults lay eggs on their hosts during the spring in southern Portugal, and the first-instar larva penetrates through the soft tissue of the millipede. The parasitoid spends the summer as a firstinstar larva, kills the host during the autumn when in the third instar and overwinters in the pupal stage. P. nigripennis occurs in habitats of low bushes, but not in open grasslands. The female searches for prey by day. The maximum rate of parasitism recorded in this study was 20%. In laboratory specificity studies, 15 species of millipedes from five families were exposed to P. nigripennis, but only julid millipedes were successfully parasitized. Synchronization of the life-cycle in the laboratory with the seasons of the southern hemisphere was achieved by inducing pupation five months prematurely after cooling to 10°C.


1966 ◽  
Vol 57 (1) ◽  
pp. 121-136 ◽  
Author(s):  
U. S. Srivastava ◽  
S. B. Agarwal

Anjeerodiplosis peshawarensis Mani is a serious pest in North India of the fruit of the country fig (Ficus carica), which is its only known host. The midges are abundant, hovering under the host tree in the mornings and at dusk, and breed throughout the year, except in the summer from April until the July rains. In this period newly formed fruits are not infested, but in other months scarcely 30 per cent, of the fruits remain free from attack.Eggs are laid in fruits when they one week old, succulent, and of the size of a pea. The eggs are minute, hyaline, unsculptured, oval and pedicellate and occur in bundles of 16. Incubation takes three days in September and March and five days in December and January. In laboratory tests, average viability in January was found to be about 83 per cent.The entire larval period is passed inside the figs, each of which may contain 200–300 larvae. There are four larval instars, which differ in size according to Dyar's law and in morphology. The first-instar larva is devoid of cuticular outgrowths and does not show spiracles; the second and third instars have nine pairs of spiracles and possess characteristic spines, warts and tubercles; the fourth instar develops the sternal spatula. The entire larval period lasts three weeks from the middle of August to October and four weeks in January and February. From the middle of April until the July rains, fourth-instar larvae remain inside the figs. When the larval period is three weeks, the first and second instars together and the third and fourth instars separately last about a week.Full-grown fourth-instar larvae bore out of the fruit and drop to the ground, where they jump for some time with the aid of their sternal spatula. They finally pupate in the soil without forming a cocoon but become covered in a protective case composed of soil particles that adhere to the larval skin. Early fourth-instar larvae, which do not have a sternal spatula, if taken from the fruits, may also successfully pupate, and the pupal period is normal. This period is 10–15 days between July and November and 25–26 days in January and February. It is shortest (10 days) in the rainy season, when both temperature and humidity are high.The pupa is obtect, creamy white and bears poorly developed cephalic horns and bristles, well developed thoracic horns and many spines and cuticular outgrowths. Mortality in the pupal stage is between 15 and 30 per cent.Emergence of the adults invariably occurs in the early hours of the day. Two or three days before emergence, the protective case becomes detached piecemeal. Males emerge before females. The ratio of males to females on the day of emergence is 1:2 between March and December and 2:3 in January and February. Copulation starts soon after emergence and lasts from 60 to 90 seconds.There is considerable overlapping of generations. On the basis of the time required for completion of the life-cycle in different months, it is calculated that seven generations are completed in a year.


1956 ◽  
Vol 47 (1) ◽  
pp. 23-42 ◽  
Author(s):  
A. Milne

The Garden Chafer, Phyllopertha horticola (L.), has three larval instars, the third ending in hibernation, which gives way to a prepupal stage. The development cycle occupies 12 months and only one generation is present in the soil at any time. From a study extending over five years, 1948 to 1952, the cycle from egg to adult in the English Lake District may be outlined as follows:—At the earliest, oviposition starts in the latter half of May. In soil 3½ in. deep, eggs are laid at an average depth of 1½ in. (range ¾ to 2½ in.). Other authors report that where the soil is sufficiently deep, the maximum egg depth may extend to four inches in the Lake District and even eight inches elsewhere. The eggs are spaced about a quarter of an inch apart (max. 1 in.), each in a tiny earthen cavity, all more or less directly below the point where the female enters the soil. Incubation of the individual egg averages five weeks.The first instar occupies individually about three weeks on the average; the second instar about four weeks; and the third instar, up to the beginning of hibernation, eight to ten weeks. On the average also, first-instar larvae begin to appear in a population about the first week of July, second instars about the fourth week of July, third instars about the fourth week of August, and the earliest hibernators about the third week of October. Except for a few stragglers occasionally in early December, the entire population is generally hibernating by the end of November. The hibernation is a true diapause.A detailed description of the method of feeding is given. The larva consumes plant roots which it obtains by tunnelling through the soil. Since its natural habitat is pasture land, grass roots are the main food. It probably also eats invertebrate carrion occurring by chance in its path. The first and second larval instars are given over to growth, the third and final is occupied mainly in storing up fat-body. This store has to suffice for maintenance during the remainder of development and also for the entire egg or sperm production.On hatching, the larvae feed at about 1½ inches (¾ to 2½ in.) depth in the soil, i.e., at egg-level. As they grow, however, they ascend until latterly, as third instars, they are feeding about ½ inch (¼ to 1 in.) from the surface. This progressive rise is probably dictated by the increasing need for a more copious food supply. With the possible exception of a very prolonged drought, weather has no effect on the level at which larvae feed.Larvae hibernate at 2 inches (0·8 to 3·8 in.) below the surface of soil 4 inches (2·3 to 6·0 in.) deep, i.e., well above the “ pan ” (gravel bed, or rock). In other localities other authors have recorded hibernation at the same as well as greater depth in deeper soils. The existing data are insufficient to show what governs the choice of depth in the soil.On the average, prepupation begins in a population about the end of March and, individually, lasts between three and four weeks; pupation begins in the third week of April and lasts about four weeks. The pupa lies inside the last larval exuvium in the hibernation cell. Sex can easily be discerned in the pupa. There are always rather more males than females in a field population, considerably more in some years. Pupal sex ratios ranged from 1·13 to 1·89. On the average, male pupation precedes female by one day or a little more.Behaviour after the splitting of the pupal skin is the same in male and female. At first, for about four days (1 to 7), the adult remains motionless in the hibernation cell. Then, alternately burrowing and resting, it ascends to the base of the sward in about two days (¼ to 4). At the sward base it now halts for about two days (½ to 6) before emerging into activity upon the sward surface for the first time; this halt of two days may be prolonged by one or more days if weather is unsuitable when a beetle is ready to become active. In toto, given no weather hindrance, the individual transit from cell to sward surface usually occupies rather more than one week (7·7 days, range 6·0 to 8·5). On the average, the first active beetles are seen in the last week of May but may be as early as the third week of May or as late as the second week of June, according to the weather. The male precedence over females in development is maintained from pupation onwards, hence the first males are always active upon the sward at least one day before the first females.It takes some considerable time for all the individuals in a population to accomplish the change from any one particular stage of development to the next. There are, however, never more than two successive stages in the soil at the same time. The period of overlap of two stages in the population fluctuates widely (8 to. 41 days) from step to step in the development cycle. This is the result of the seasonal rise and fall in the soil temperature, and of diapause. The overlap, which is really a measure of range of developmental age among individuals, contracts to the minimum (8 days) as the population approaches maturity. This facilitates mating.


Author(s):  
M. Locke ◽  
J. T. McMahon

The fat body of insects has always been compared functionally to the liver of vertebrates. Both synthesize and store glycogen and lipid and are concerned with the formation of blood proteins. The comparison becomes even more apt with the discovery of microbodies and the localization of urate oxidase and catalase in insect fat body.The microbodies are oval to spherical bodies about 1μ across with a depression and dense core on one side. The core is made of coiled tubules together with dense material close to the depressed membrane. The tubules may appear loose or densely packed but always intertwined like liquid crystals, never straight as in solid crystals (Fig. 1). When fat body is reacted with diaminobenzidine free base and H2O2 at pH 9.0 to determine the distribution of catalase, electron microscopy shows the enzyme in the matrix of the microbodies (Fig. 2). The reaction is abolished by 3-amino-1, 2, 4-triazole, a competitive inhibitor of catalase. The fat body is the only tissue which consistantly reacts positively for urate oxidase. The reaction product is sharply localized in granules of about the same size and distribution as the microbodies. The reaction is inhibited by 2, 6, 8-trichloropurine, a competitive inhibitor of urate oxidase.


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