Molecular genetics of Drosophila alpha-actinin: mutant alleles disrupt Z disc integrity and muscle insertions

We have isolated a Drosophila melanogaster alpha-actinin gene and partially characterized several mutant alleles. The Drosophila protein sequence is very similar (68% identity) to those of chicken alpha-actinin isoforms, but less closely related (30% identity) to Dictyostelium alpha-actinin. The gene is within subdivision 2C of the X chromosome, coincident with 15 lethal (1)2Cb mutations. At least four alleles, l(1)2Cb1, l(1)2Cb2, l(1)2Cb4, and l(1)2Cb5 are interrupted by rearrangement breakpoints and must be null. In all four cases, hemizygous mutants complete embryogenesis and do not die until the second day of larval growth, signifying that either the role of alpha-actinin in nonmuscle cells is redundant or that a distinct and only distantly related gene encodes the non-muscle isoform. Allelic but less severely affected fliA mutants are apparently due to point mutations, and develop into adults having thoracic muscle abnormalities. EM of mutant muscles reveals that Z discs and myofibrillar attachments are disrupted, whereas epithelial "tendon" cells are less affected. We discuss these phenotypes in the light of presumed in vivo alpha-actinin functions.     

DNA insertion mutagenesis in a Pseudomonas aeruginosa R plasmid.

The transposons Tn501 and Tn7 were used to obtain transfer-deficient (Tra^?) and carbenicillin-sensitive (Cb^s) mutants of the narrow-host-range R plasmid R91-5 of Pseudomonas aeruginosa. In cells that are harboring R91-5 together with an unrelated transposon-donor plasmid and that have undergone 50–75 cell divisions (established donors), both transposons induced a very high frequency (87–93%) of mutations affecting Tra and Cb^r. However, when transconjugants inheriting the transposon are immediately assayed for mutations (recent transposition events) there is a marked difference in the yield of mutants. Although both transposons generated Cb^s mutants at the same frequency (0.1%), Tn7 induced Tra^? mutants at a frequency of 59% as compared to 0.23% by Tn501. Some Tra^? mutants induced by both transposons were leaky but retransfer tests showed that this was not due to reversion. Both transposons showed considerable specificity when mutations affecting transfer-related functions such as sensitivity to donor-specific phage, inhibition of the replication of phage G101, and entry exclusion were compared. Thirty-seven percent of the Tra^? mutants induced by Tn501 were also Cb^s. These double mutants were leaky with respect to all the properties tested and selection for Cb^r revertants restored Tra⁺ simultaneously. A number of hypotheses were considered as explanations including the possibility that tra (transfer genes) and bla (the β-lactamase gene for carbenicillin resistance) are closely linked in R91-5, that tra formed a number of operons with one of them encompassing bla, and the possible creation of a new promoter in the bla gene which impeded tra expression. Both transposons generated a high frequency (81–86%) of deletions of the bla gene as judged by nonrevertibility.     

Aldehyde oxidase cross-reacting material in the Aldox n,cin, mal,and lxd mutants of Drosophila melanogaster

Rocket immunoelectrophoresis was used to estimate aldehyde oxidase cross-reacting material (AO-CRM) in larval hemolymph and adult fly extracts in mutants with reduced AO enzymatic activity. Hemolymph of larvae homozygous for Aldox ⁿ, which is a mutation of the presumed structural gene for AO, contains 30% of the wild-type CRM. The demonstration of AO-CRM in Aldox ⁿ larval hemolymph is surprising since this genotype has been reported to lack CRM. By contrast, adult Aldox ⁿ flies lack detectable CRM. The other AO-deficient mutants that were examined are cin, mal, and lxd; each has appreciable levels of CRM in both larval hemolymph and adult extracts. Detection of CRM in these mutants helps to clarify conflicting reports in the literature.This research was supported by a grant from the Natural Sciences and Engineering Research Council of Canada to L.W.B.     

Neuron-Type Specific Functions of DNT1, DNT2 and Spz at the Drosophila Neuromuscular Junction

Retrograde growth factors regulating synaptic plasticity at the neuromuscular junction (NMJ) in Drosophila have long been predicted but their discovery has been scarce. In vertebrates, such retrograde factors produced by the muscle include GDNF and the neurotrophins (NT: NGF, BDNF, NT3 and NT4). NT superfamily members have been identified throughout the invertebrates, but so far no functional in vivo analysis has been carried out at the NMJ in invertebrates. The NT family of proteins in Drosophila is formed of DNT1, DNT2 and Spätzle (Spz), with sequence, structural and functional conservation relative to mammalian NTs. Here, we investigate the functions of Drosophila NTs (DNTs) at the larval NMJ. All three DNTs are expressed in larval body wall muscles, targets for motor-neurons. Over-expression of DNTs in neurons, or the activated form of the Spz receptor, Toll ^10b, in neurons only, rescued the semi-lethality of spz ² and DNT1 ⁴¹ , DNT2 ^e03444 double mutants, indicating retrograde functions in neurons. In spz ² mutants, DNT1 ⁴¹ , DNT2 ^e03444 double mutants, and upon over-expression of the DNTs, NMJ size and bouton number increased. Boutons were morphologically abnormal. Mutations in spz and DNT1,DNT2 resulted in decreased number of active zones per bouton and decreased active zone density per terminal. Alterations in DNT function induced ghost boutons and synaptic debris. Evoked junction potentials were normal in spz ² mutants and DNT1 ⁴¹ , DNT2 ^e03444 double mutants, but frequency and amplitude of spontaneous events were reduced in spz ² mutants suggesting defective neurotransmission. Our data indicate that DNTs are produced in muscle and are required in neurons for synaptogenesis. Most likely alterations in DNT function and synapse formation induce NMJ plasticity leading to homeostatic adjustments that increase terminal size restoring overall synaptic transmission. Data suggest that Spz functions with neuron-type specificity at the muscle 4 NMJ, and DNT1 and DNT2 function together at the muscles 6,7 NMJ.     

Analysis of Skeletal Muscle Defects in Larval Zebrafish by Birefringence and Touch-evoke Escape Response Assays

Zebrafish (Danio rerio) have become a particularly effective tool for modeling human diseases affecting skeletal muscle, including muscular dystrophies^1-3, congenital myopathies^4,5, and disruptions in sarcomeric assembly^6,7, due to high genomic and structural conservation with mammals⁸. Muscular disorganization and locomotive impairment can be quickly assessed in the zebrafish over the first few days post-fertilization. Two assays to help characterize skeletal muscle defects in zebrafish are birefringence (structural) and touch-evoked escape response (behavioral).Birefringence is a physical property in which light is rotated as it passes through ordered matter, such as the pseudo-crystalline array of muscle sarcomeres⁹. It is a simple, noninvasive approach to assess muscle integrity in translucent zebrafish larvae early in development. Wild-type zebrafish with highly organized skeletal muscle appear very bright amidst a dark background when visualized between two polarized light filters, whereas muscle mutants have birefringence patterns specific to the primary muscular disorder they model. Zebrafish modeling muscular dystrophies, diseases characterized by myofiber degeneration followed by repeated rounds of regeneration, exhibit degenerative dark patches in skeletal muscle under polarized light. Nondystrophic myopathies are not associated with necrosis or regenerative changes, but result in disorganized myofibers and skeletal muscle weakness. Myopathic zebrafish typically show an overall reduction in birefringence, reflecting the disorganization of sarcomeres.The touch-evoked escape assay involves observing an embryo''s swimming behavior in response to tactile stimulation^10-12. In comparison to wild-type larvae, mutant larvae frequently display a weak escape contraction, followed by slow swimming or other type of impaired motion that fails to propel the larvae more than a short distance¹². The advantage of these assays is that disease progression in the same fish type can be monitored in vivo for several days, and that large numbers of fish can be analyzed in a short time relative to higher vertebrates.     

Effects of food availability on larval development in the slipper limpet Crepidula onyx (Sowerby)

Effects of food availability on the larval survival and development of Crepidula onyx were studied in four experiments by feeding the larvae with different concentrations of the chrysophyte Isochrysis galbana and by starving the larvae for different periods of time. Food concentration had a clear impact on the survival, growth and development time of C. onyx veligers. Larval development occurred only at 10⁴ cells ml⁻¹ and higher algal concentrations. No shell increment was detected in the veligers cultured for 12 days at 10² cells ml⁻¹I. galbana or the blank control. At 10³ cells ml⁻¹, there was only a slight increase in shell length over 12 days. At 10⁴ cells ml⁻¹, about 40% of the larvae became competent in 18 days. At 10⁵ and 10⁶ cells ml⁻¹, more than 90% of the larvae reached competence in 7 days. Initial starvation negatively affected the larval development, but the sensitivity differed among parameters measured on day 5: lower survivorship was detected only for larvae that had suffered 3 days or longer initial starvation, whereas one-day initial starvation caused shorter shells and lower percentage of competent larvae. Three days of continuous feeding was required for 50% of the larvae to reach competence. After feeding for 3 days, most larvae could become competent to metamorphose even under starvation. The time of starvation was also critical: larvae that suffered 1-day food deprivation in the first 2 days of larval release had shorter shells and lowered percent competent larvae than those that suffered the same length of food deprivation in later stages of development. Our study thus indicates that both food concentration and short-term starvation have detrimental effects on the larval development of this species, and that once the larva has consumed certain amount of food, starvation may induce metamorphosis.     

Variations in larval growth and metabolism of an estuarine shrimp Palaemonetes pugio during toxicosis by an insect growth regulator

1. Exposure of the estuarine shrimp, Palaemonetes pugio, to a juvenile hormone analogue (⩾8 μg methoprene 1⁻¹) throughout larval development inhibited successful completion of metamorphosis.2. Methoprene exposure retarded growth in early larval stages and postlarvae, but enhanced growth in premetamorphic larvae.3. Respiration rates of early larvae were elevated by methoprene exposure, but not so older larvae or post larvae.4. Lower net growth efficiency (K₂ values) in methoprene-exposed early larvae suggests that increased metabolic demands reduced assimilated energy available for growth.5. Modifications in O:N ratios of premetamorphic larvae and postlarvae suggest that methoprene altered substrate utilization patterns during metamorphosis.     

Caterpillar color patterns are determined by a two‐phase melanin gene prepatterning process: new evidence from tan and laccase2

SUMMARY The larval color patterns in Lepidoptera exhibit splendid diversity, and identifying the genes responsible for pigment distribution is essential to understanding color‐pattern evolution. The swallowtail butterfly, Papilio xuthus, is a good candidate for analyzing marking‐associated genes because its body markings change dramatically at the final molt. Moreover, the silkworm Bombyx mori is most suitable for identification of lab‐generated color mutants because genome information and many color mutants are available. Here, we analyzed the expression pattern of 10 melanin‐related genes in P. xuthus, and analyzed whether these genes were responsible for Bombyx larval color mutants. We found that seven genes correlated strongly with the stage‐specific larval cuticular markings of P. xuthus, suggesting that, compared with Drosophila, more genes showed marking specificity in lepidopteran larvae. We newly found that the expression of both tan and laccase2 is strongly correlated with the larval black markings in both P. xuthus and B. mori. The results of F2 linkage analysis and mutant analysis strongly suggest that tan is the responsible gene for Bombyx larval color mutant rouge, and that tan is important in emphasizing black markings of lepidopteran larvae. Detailed comparison of temporal and spatial expression patterns showed that larval cuticular markings were regulated at two different phases. Marking‐specific expression of oxidizing enzymes preceded the marking‐specific expression of melanin synthesis enzymes at mRNA level, which is the reverse of the melanin synthesis step.     

Photoresponses of second-instar Chaoborus larvae

The diel vertical migration of Chaoborus larvae varies with larval instar. Although light is involved in the control of vertical migration the contribution of larval photoresponses is unknown. In order to describe ontogenetic changes in larval photoresponses we measured photoresponses of second-instar Chaoborus punctipennis larvae in the laboratory. The response spectrum of these larvae had peaks in sensitivity at 420 and 620 nm with a wide plateau of lower sensitivity from 460 to 600 and 640 to 680 nm. Dark adapted larvae were positively phototactic at intensities from 10^?7 to 10¹ Wm^?2 at 420 nm. The level of response decreased somewhat above 10^?4 Wm^?2, and above 10^?2 Wm^?2 a small proportion of larvae shifted to a negative phototaxis. At 420 nm the threshold intensity was about 10^?7 Wm^?2 for positive phototaxis and 10^?2 Wm^?2 for negative phototaxis. Light adaptation increased the threshold intensity for positive phototaxis. The differences in larval photoresponses between second- and fourth-instar larvae suggests that the young instars are adapted to the photoenvironment of the water column and older larvae are adapted to avoid the water column except at very low light intensities. These predictions match the diel distribution of these larvae.     

Sequential developmental programmes for retractor muscles of a caenogastropod: reappraisal of evolutionary homologues

Evolutionary changes in the development of shell-attached retractor muscles in gastropods are of fundamental importance to theories about the early evolution and subsequent diversification of this molluscan class. Development of the shell-attached retractor muscle (columellar muscle) in a caenogastropod has been studied at the ultrastructural level to test the hypothesis of homology with the post-torsional left retractor muscle (larval velar retractor) in vetigastropod larvae. The vetigastropod muscle has been implicated in the generation of ontogenetic torsion, a morphogenetic twist between body regions that is important to theories about early gastropod evolution. Two shell-attached retractor muscles develop sequentially in the caenogastropod, Polinices lewisii, which is a pattern that has been also identified in previous ultrastructural studies on a vetigastropod and several nudibranch gastropods. The pattern may be a basal and conserved characteristic of gastropods. I found that the first-formed retractor in larvae of P. lewisii is comparable to the larval velar retractor that exists at the time of ontogenetic torsion in the vetigastropod, Haliotis kamtschatkana. However, the post-metamorphic columellar muscle of P. lewisii is derived exclusively from part of the second-formed muscle, which is comparable to the second-formed pedal muscle system in the vetigastropod. I conclude that the post-metamorphic columellar muscle of P. lewisii, is not homologous to the larval velar retractor of the vetigastropod, H. kamtschatkana.     

Larval size relative to larval feeding, cannibalism of larvae, egg or adult female size and larval–adult setal patterns among 13 phytoseiid mite species

Phytoseiid mite larvae vary in size and feeding type. We compared larval size to feeding by larvae, cannibalism of larvae by adult females, egg and adult female size and the setae lengths of larvae and adults among 13 species. There was no relationship between size of larvae and either feeding by larvae or cannibalism of larvae by adult female mites. Correlations were highest between larval size as measured by idiosoma plus extended leg lengths and adult female size of idiosoma plus extended leg lengths (r²=0.746), while next highest was larval idiosoma length and adult female idiosoma length (r²=0.662) and then larval idiosoma length and egg length (r²=0.579). Based on idiosoma length, Phytoseiulus persimilis had the largest larvae (non-feeding) among species and Euseius finlandicus had the smallest larvae (obligatory feeding). However, based on idiosoma length plus extended leg length, obligatory feeding larvae (on pollen or mites) of E. finlandicus and Euseius hibisci were largest and facultative feeding larvae (on mites) of Neoseiulus californicus and obligatory feeding larvae (on mites) of Galendromus occidentalis were the smallest. Among species with non- or facultative feeding larvae, Amblyseius andersoni and Neoseiulus barkeri had larger larvae and Typhlodromus pyri and Neoseiulus fallacis had smaller larvae when leg lengths were included in larval size. Setae lengths of larvae versus adult females (after adjustment for body sizes) showed high correlation for j6 (r²=0.942) and s4 (r²=0.854), but low correlation for larval Z4 versus adult female Z4 (r²=0.084) or Z5 (r²=0.063). Overall, larval morphological traits were most closely correlated to traits of other life stages, although for setae there were some exceptions. Differences in the functions of setae j6, s4 and Z4 in the larva versus adult female are discussed.     

EVOLUTIONARY LOSS OF LARVAL FEEDING: DEVELOPMENT,FORM AND FUNCTION IN A FACULTATIVELY FEEDING LARVA,BRISASTER LATIFRONS

Species with large eggs and nonfeeding larvae have evolved many times from ancestors with smaller eggs and feeding larvae in numerous groups of aquatic invertebrates and amphibians. This change in reproductive allocation and larval form is often accompanied by dramatic changes in development. Little is known of this transformation because the intermediate form (a facultatively feeding larva) is rare. Knowledge of facultatively feeding larvae may help explain the conditions under which nonfeeding larvae evolve. Two hypotheses concerning the evolutionary loss of larval feeding are as follows: (1) large eggs evolve before modifications in larval development, and (2) the intermediate form (facultatively feeding larva) is evolutionarily short-lived. I show that larvae of a heart urchin, Brisaster latifrons, are capable of feeding but do not require food to complete larval development. Food for larvae appears to have little effect on larval growth and development. The development, form, and suspension feeding mechanism of these larvae are similar to those of obligate-feeding larvae of other echinoids. Feeding rates of Brisaster larvae are similar to cooccurring, obligate-feeding echinoid larvae but are low relative to the large size of Brisaster larvae. The comparison shows that in Brisaster large egg size, independence from larval food, and relatively low feeding rate have evolved before the heterochronies and modified developmental mechanisms common in nonfeeding echinoid larvae. If it is general, the result suggests that hypotheses concerning the origin of nonfeeding larval development should be based on ecological factors that affect natural selection for large eggs, rather than on the evolution of heterochronies and developmental novelties in particular clades. I also discuss alternative hypotheses concerning the evolutionary persistence of facultative larval feeding as a reproductive strategy. These hypotheses could be tested against a phylogenetic hypothesis.     

A field study of potential ecological costs of resistance by ‘stem ducking’ in tall goldenrod,Solidago altissima

Culex quinquefasciatus Say (Diptera: Culicidae) is an abundant urban mosquito that is the vector of filariasis. Breeding in septic tanks, where there are very high levels of bacterial food, it is likely to have a different reaction to crowding compared with other mosquitoes. To test for the presence and type of crowding effects, four larval densities of C. quinquefasciatus varying from 0.4 to 3.2 larvae ml^?1 of water were reared in tubes. Mortality was found to greatly increase at densities above 0.8 larvae, whereas larval duration increased even above 0.4 larvae ml^?1. Changing the water in the tubes daily gave a small (but significant) response in reducing mortality and larval duration. However, when larvae kept at a low density shared the same water with larvae at high density, there was no chemical influence on their growth rate and mortality. The effect of crowding was primarily due to physical disturbances between larvae. When larvae were kept at a high density in the same volume of water, but in shallow trays with a large surface area and therefore much less contact between them, mortality was the same as for the lowest density. There was still, however, a significant increase in larval duration from 8.6 days at 0.4 larvae ml^?1 to 12.1 days at 3.2 larvae ml^?1. It is therefore concluded that the larvae respond to physical rather than chemical factors by prolonging larval development and having some increase in mortality.     

Influence of tannic acid and Cry1Ac toxin of Bacillus thuringiensis on larval survival, growth, and development of Helicoverpa armigera

Helicoverpa armigera (Hübner) (Lepidoptera: Noctuidae) causes huge economic losses in cotton production around the world. Tannin, one of the important secondary substances in cotton plants, can increase the δ‐endotoxin activity of Bacillus thuringiensis ssp. kurstaki. The mechanism of interaction between tannin and Bt toxin on H. armigera is unclear. We investigated the interaction between tannic acid and Cry1Ac toxin in H. armigera, and monitored survival, growth, and development during the larval period after treating the larvae with four concentrations of Cry1Ac toxin (0, 2, 8, and 14 μg^?1) alone or in combination with four concentrations of tannic acid (0, 0.5, 1, and 2 mg g^?1). Mortality of larvae treated with both tannic acid and Cry1Ac was higher than the mortality of larvae treated with tannic acid or Cry1Ac alone. Mortality was 47.5 and 51.5% in larvae treated with 14 μg g^?1 Cry1Ac alone or 2 mg g^?1 tannic acid alone, respectively. In contrast, larval mortality was 75% when treated with the mixture of 14 μg g^?1 Cry1Ac and 2 mg g^?1 tannic acid, suggesting that a mixture of the two enhanced the effectiveness of each one alone. The developmental time of larvae treated with the combination of tannic acid and Cry1Ac was significantly longer than when they were treated with Cry1Ac or tannic acid alone. Larval weight, pupal weight, and pupation rate were also significantly reduced in larvae treated with both toxins, compared with the larvae treated with either toxin alone. These results showed that the interactive effect of tannic acid and Cry1Ac on larval growth inhibition is additive, and that tannic acid improves Cry1Ac toxicity to insects. Tannic acid used in combination with B. thuringiensis might potentially reduce overall insecticide use, thus delaying development of insecticide resistance.     

Larval Starvation to Satiation: Influence of Nutrient Regime on the Success of Acanthaster planci

High density populations of the crown-of-thorns seastar, Acanthaster planci, are a major contributor to the decline of coral reefs, however the causes behind periodic outbreaks of this species are not understood. The enhanced nutrients hypothesis posits that pulses of enhanced larval food in eutrophic waters facilitate metamorphic success with a flow-on effect for population growth. The larval resilience hypothesis suggests that A. planci larvae naturally thrive in tropical oligotrophic waters. Both hypotheses remain to be tested empirically. We raised A. planci larvae in a range of food regimes from starvation (no food) to satiation (excess food). Algal cell concentration and chlorophyll levels were used to reflect phytoplankton conditions in nature for oligotrophic waters (0-100 cells ml^-1; 0-0.01 μg chl a L^-1), natural background levels of nutrients on the Great Barrier Reef (GBR) (1,000-10,000 cells ml^-1; 0.1-1.0 μg chl a L^-1), and enhanced eutrophic conditions following runoff events (100,000 cells ml^-1; 10 μg chl a L^-1). We determine how these food levels affected larval growth and survival, and the metamorphic link between larval experience and juvenile quality (size) in experiments where food ration per larvae was carefully controlled. Phytoplankton levels of 1 μg chl a L^-1, close to background levels for some reefs on the GBR and following flood events, were optimal for larval success. Development was less successful above and below this food treatment. Enhanced larval performance at 1 μg chl a L^-1 provides empirical support for the enhanced nutrients hypothesis, but up to a limit, and emphasizes the need for appropriate mitigation strategies to reduce eutrophication and the consequent risk of A. planci outbreaks.     

VENOM FROM THE ECTOPARASITIC WASP Habrobracon hebetor ACTIVATES CALCIUM‐DEPENDENT DEGRADATION OF Galleria mellonella LARVAL HEMOCYTES

Ectoparasitoids inject venom into hemolymph during oviposition. We determined the influence of envenomation by the parasitoid, Habrobracon hebetor, on the hemocytes of its larval host, Galleria mellonella. An increase in both intracellular Са²⁺ content and phospholipase C activity of the host hemocytes was recorded during 2 days following envenomation by the parasitoid. The decreased hemocyte viability was detected 1, 2, and 24 h after the envenomation. Injecting of the crude venom (final protein concentration 3 μg/ml) into the G. mellonella larvae led to the reduced hemocyte adhesion. The larval envenomation caused a decrease in transmembrane potential of the hemocytes. These findings document the suppression of hemocytic immune effectors in the parasitized host larvae.     

The action of theI(1)npr-1 + locus on theDrosophila glue geneSgs-3 is cell-autonomous

The 2B5 chromosomal locus inDrosophila contains a gene,I(1)npr-1 ⁺, whose product required intrans for the expression of the larval salivary gland-specific geneSgs-3. We have addressed the question as to whether this factor acts in a cell-autonomous manner or not. This was made possible by the use of a transformant strain that makes anSgs-3-E. coli β-galactosidase (lacZ) fusion protein, under the control of anSgs-3 promoter, allowing the cellular examination of gene expression by a histochemical assay for enzyme activity. Using genetic methods, larvae that were mosaic for the loss of function mutationl(l)npr-1 were generated. The expression of theSgs-3-lacZ fusion gene was assayed histochemically in such larvae. Our results strongly indicate a cell-autonomous requirement for the product ofl(1)npr-1+. This is in contrast to another factor, the hormone ecdysterone, which is also required forSgs-3 expression, but acts in a non-autonomous manner     

Replication in Drosophila chromosomes

Prolongation of larval life in Drosophila melanogaster, by growing wild type larvae at lower temperature, or in animals carrying the X-linked mutation giant is known to result in a greater proportion of nuclei in salivary glands showing the highest level of polyteny. We have examined by autoradiography the patterns of ³H-thymidine incorporation during 10 min or 1 min pulses in salivary gland polytene chromosomes of older giant larvae and of wild type late third instar larvae of D. melanogaster grown since hatching either at 24 ° C or at 10 ° C. The various patterns of labelling and their relative frequencies are generally similar in glands from the warm-(24 ° C) or cold (10 ° C)-reared wild type larvae, except the interband (IB) labelling patterns which are very frequent in the later group but rare in the former. The IB type labelled nuclei in cold-reared wild type larvae show labelling ranging from only a few puffs/interbands labelled to nearly all puffs/interbands labelled. In warm-reared wild type larvae, very low labelled IB patterns are not seen. In older giant larvae, the ³H-thymidine labelling patterns are in most respects similar to those seen in cold-reared wild type larvae. In 1 min pulsed preparations from all larvae, the IB patterns are relatively more frequent than in corresponding 10 min pulsed preparations. No nuclei with the continuous (2C or 3C) type of labelling pattern, with all bands and interbands/puffs labelled, were seen in 1 min pulsed preparations from cold-reared wild type or in giant larvae, and only a few nuclei in 1 min pulsed preparations from warm-reared wild type larvae exhibited the 2C labelling pattern. Analysis of silver grain density on specific late replicating sites in late discontinuous (1D) type labelled nuclei suggests that the rate of DNA synthesis per chromosomal site is not different at the two developmental temperatures. It is suggested that correlated with the prolongation of larval life under cold-rearing conditions or in giant larvae, the polytene replication cycles are also prolonged. It is further suggested that the polytene S-period in these larvae is longer due to a considerable asynchrony in the initiation and termination of replication of different sites during a replication cycle.