The relationship between radiation-induced and transposon-induced genetic damage during Drosophila spermatogenesis

The combined effect of transposon mobility and X-rays on X-linked recessive lethals and dominant lethals was measured in the germ line of F₁ male hybrids in the P-M system of hybrid dysgenesis. X-linked lethal mutation rate was measured in the chromosome derived from the P-strain father of the M × P cross. Mutations induced in irradiated dysgenic males were compared to those of unirradiated males, as well as to irradiated nondysgenic males derived from M × M crosses. Three four-day broods of sperm were tested for both X-linked lethals and dominant lethals. X-linked lethal mutation rate in dysgenic control males was 6.38%, 6.36% and 4.55% in broods 1, 2 and 3 respectively, thus showing a decrease in older males. The mutation rate in the same broods of irradiated, nondysgenic control males was 3.66%, 4.46% and 6.38%, respectively. The rate obtained in dysgenic irradiated males was 10.33, 11.16 and 7.97 in the same 3 broods. These results demonstrate that when X-rays and P element mobility were and 7.97 in the same 3 broods. These results demonstrate that when X-rays and P element mobility were combined as a source of mutagenesis, a strickly additive effect on genetic damage was observed in the first two broods of sperm which represent primarily mature sperm and spermatids respectively. The third brood, representing mostly spermatocytes showed a less than additive effect, probably due to germinal selection. In contrast, the induction of dominant lethals showed a clearly synergistic effect in the last two Broods of sperm tested, when X-rays and transposon mobility were combined. The X-ray component of dominant lethlity in brood 1, representing mostly mature spermatozoa, was negative, indicating a lower than expected lethality induced by X-irradiation in the presence of P element mobility. The X-ray-induced component of dominant lethality, was expressed as the per cent of embryo lethality after adjusting the results obtained with each brood of sperm from nondysgenic and dysgenic males to their respective unirradiated controls. These values were 32.3%, 30.5% and 64.7% for brood 1, 2 and 3 respectively from nondysgenic males, and 14.1%, 56.1% and 71.4% for the same broods from dysgenic males. Thus the differential effect of X-rays in sperm broods 1, 2 and 3 was −18.2, +25.6 and +6.7% respectively. These results suggest that the synergistic effect may be due to the common component of X-ray and P element-induced genetic damage, namely chromosome breaks, and that the interaction of these lesions resulted in a greater than additive number of of unrestitude chromosome breaks and nonviable chromosomal rearrangements.     

Hyperthermia of male Drosophila melanogaster meiocytes induces abnormalities in both paternal and maternal sex chromosome sets of the offspring

Nondisjunction and loss of sex chromosomes caused by exposure of male Drosophila melanogaster to heat shock (HS) (37 degrees C for 1 h) has been studied to determine the role of mutation l(1)ts403 (sbr10) in the control of chromosome segregation during cell division. Hyperthermia of males at the pupal stage has been demonstrated to increase the number of offspring with abnormalities of not only paternal, but also maternal sex chromosome sets. According to the criterion used, there is a temperature-sensitive period of spermatogenesis, which presumably coincides with meiosis. Phenotypes of some individuals correspond to the presence of two sex chromosomes of obtained from the same parent. The frequency of abnormal chromosome sets in the offspring of male carriers of the sbr10 mutation is about two times higher than in the offspring of males without this mutation.     

X-ray-induced mutation spectra of different germ-cell stages of Drosophila males with a double marked Y-chromosome and either a normal X-or a ring-X-chromosome (author's transl)

Different germ-cell stages of Drosophila males with a double marked Y-chromosome and either a normal X- or a ring-X chromosome were irradiated with X-rays, inducing the following aberrations: chromosome loss, chromosome gain (XYX-females), partial Y loss and isochromosomes of the Y-chromosome.Doses of 520 rad in spermatocytes and spermatids and 2600 rad in sperm, produced the same effect in these stages with regard to the chromosome loss in the males with a normal X, and the following results were obtained: (a) The partial Y loss in postmeiotic stages is small in comparison with spermatocytes in both stocks. This could mean that in spermatocytes this aberration is determined by exchange processes which can only be induced and/or detected in premeiotic stages. (b) In spermatocytes and mature sperm of males with a ring-X chromosome, the chromosome loss was 2.9 times greater than in those with a normal X. In spermatids of the males with a ring-X the rate of loss was only 1.5 times greater. In spermatocytes of either males with a ring-X or a normal X a similar high rate of isochromosomes could be induced. However, in spermatids and mature sperm the rate of induction of isochromosomes was found to be very small. These results seem to indicate that in mature sperm the rejoining of breaks in the Y-chromosome takes place before, and in the X-chromosome usually after the replication. If in post-meiotic stages of Drosophila the X- and Y-chromosomes existed as chromatid-like subunits then in spermatids these should behave as a structural unit.In sperm we were able to induce similar frequencies of individuals with a single isochromosome type in all body cells as of individuals with two types of isochromosomes (isochromosome mosaics). This result seems to indicate that after irradiation of sperm one of the first two division nuclei is lethal in an proportion of the zygotes.     

Sex-ratio depression as a brood-pattern criterion of radiation damage inDrosophila melanogaster

The results of analyses of the brood variance in the relative frequency of females to males in the progeny ofD. melanogaster males having structurally-normal chromosomes, not only established that there is a brood-curve of sex-ratio depression in the progeny of irradiated males, but also revealed that there was a curve of sex-ratio change in successive broods of offspring from unirradiated males even though the ratio of females to males in the total progeny was 1 : 1. The brood curve of sex-ratio change in both series of control males tended to be bimodal, with an increasing frequency of female offspring during the first five or six days, followed by a progressive decrease until about the 12th day, than subsequently an increase until about the 15–16th days, with perhaps again a decrease in the latest (17–24d) broods. The bimodality of the curve appeared to be the consequence of a complex relationship between brood-size, brood-rank and sex-ratio change. Following irradiation of the males with 3000r of X-rays, the incidence of female offspring decreased linearly for the first eight days, with a low of 44.32% in the 6–8d broods. This was followed by an abrupt return to a 1 : 1 sex-ratio in the 9th day and subsequent (10–24d) broods. The recovery of 50% female offspring in the 9th-day brood was interpreted as supporting evidence for the thesis that this brood was derived from cells that had been spermatogonia at the time of irradiation of the parental males. Supported by Research Grant GM 15009-01 from the Public Health Service (U.S.).     

Induction of MGE 412 Transpositions in Spermatogenesis of Drosophila Males Separately by Heat and Cold Shock

Effects of temperature treatment (heavy heat shock, HHS; heat shock, HS; and cold shock, CS) on the daily productivity of treated males in different spermatogenesis stages have been studied in isogenic line 51 of Drosophila melanogaster. The average productivity was shown to substantially decrease in all cases. The sum of the HS and CS contributions to this decrease was nearly equal to the HHS (the combined HS and CS) contribution, i.e., these contributions were almost additive. The temperature treatments did not kill mature sperm. In the control, mating productivity of day 1 exceeded that of the next day at least by 10–20%. Each day, most sperm in matings was new, i.e., matured during that day. Transposition induction of MGE 412was studied at four spermatogenesis stages after HS and CS. Both temperature treatments were effective but CS had a more pronounced inducing effect. Most temperature-induced transpositions occurred at stage III (meiosis) and IV (spermiogenesis). The day rates of transpositions at different stages were estimated. After HS at the meiosis stage, = 0.11 events per initial MGE copy per sperm per day of mating, which is approximately equal to the previous estimates after HHS. After CS at the meiosis stage, = 0.51. The transposition hot sites (including the previously known 43B and 97DE as well as a number of new sites) were detected. The lists of transpositions after CS completely included the corresponding lists after HS, which suggests similarity of induction mechanisms underlying CS and HS.     

Effect of constant light on male sterility in the cotton leafworm Spodoptera littoralis

Females of the cotton leafworm (Spodoptera littoralis) reared in long day conditions (LD 16:8 h) and mated to males kept throughout the whole period of development in continuous light (LL) oviposit very small numbers of mostly sterile eggs. It was found that in control males reared from the first larval instar in long day conditions there was a large accumulation of euperene sperm bundles in their testes on day 1 after imaginal moult. On day 10 of adult life the number of the sperm bundles was very small. In males kept from the first instar in continuous light there was also high number of sperm bundles on day 1 after imaginal moult but it did not decrease significantly on day 10 as was observed in controls. Transfer of different developmental stages of S. littoralis from long day conditions to continuous light resulted in a big difference in the density of eupyrene sperm bundles in their testes. In control insects reared through the whole of their development in long day conditions there was a significant decrease in the density of eupyrene sperm bundles on day 10 of adult life. By contrast, in males in continuous light, regardless of their developmental stage when transferred, there was either no change in density of sperm bundles in day 10 adults or there was a significant increase in comparison with day 1 adults. The highest density of eupyrene sperm bundles was observed in day 10 adults when they were transferred to continuous light shortly before moulting to the last instar (as day 4 larvae in the last stadium or day 1 pupae). Generally, the density of eupyrene sperm bundles on day 10 of adult development was about 2–2.5 times higher in males in continuous light then those under long day conditions. The results presented here indicate that the last larval instar and the pupa are the stages most sensitive to constant light treatment, which greatly reduces the amount of eupyrene sperm bundles released from the testes.     

Mating and role of seminal receptacles in the reproductive biology of the spider crab Maja squinado (Decapoda, Majidae)

The reproductive biology of the spider crab Maja squinado was analyzed based on monthly samples from an 18-month study carried out in Galicia (NW Spain) and laboratory experiments holding primiparous and multiparous females in captivity with and without males. The seminal receptacles of adult females were analyzed and their relationship with the presence and developmental stage of the eggs and the gonad maturity stage was determined. Gonad maturation in primiparous females began one or two months after the pubertal moult. Females having gonads in an advanced stage of development made their appearance in December and the first spawning took place in mid-winter or early spring. The percentage of ovigerous females from March to September was ∼75%. As the incubation period progressed, the ovaries became mature again in order to carry out the next spawning. Under experimental conditions the breeding cycle started earlier in multiparous females, during their second yearly cycle, than in primiparous ones. After mating, female spider crabs store sperm in seminal receptacles and this sperm is used in the fertilization of eggs immediately prior to spawning. The analyses of seminal receptacles consisted of the estimation of fullness and the number of differentiated sperm masses. The number of masses ranged between 0 and 6 in field samples (median for females with stored sperm=1) and was positively correlated with fullness. Differences in colour and volume of individual masses showed that, at least in some cases, females carried out successive matings with long intervals in between. This storage mechanism allowed females to fertilize successive broods without remating (as was also shown under experimental conditions). Juvenile females from shallow waters did not have developed seminal receptacles which indicated that mating was not possible until the onset of maturity. Postpubertal females in shallow waters (August to October), including animals participating in aggregations, always showed empty receptacles. The seasonality of receptacle fullness showed that mating involved hard-shelled females and occurred in deep water during the autumn migration from juvenile habitats or in the wintering habitats, during the last stages of gonad maturation (November to February). After fertilization ovigerous females continued to store sperm, but the volume was lower than in non-ovigerous females. Mating may occur in ovigerous females, particularly in the final period of incubation, because in females with broods almost ready to hatch, both new and older sperm masses were seen in the receptacles (distinguished by colour and size). The fullness of the receptacles decreased both in ovigerous and non-ovigerous females in the final phase of the annual breeding cycle (August–October), however, some sperm was still available. In the laboratory, mating was observed, and no courtship nor postcopulatory guarding was recorded. The analysis of receptacles from laboratory experiments indicated that primiparous and multiparous females showed differences in the seasonality of mating in the first phase of the breeding cycle (September–January), related to differences in the timing of gonad maturation and hatching. Mating occurred in the final stages of gonad maturation, a short time before hatching, and matings were detected in ovigerous females. Multiple matings were also evident, to a greater extent than in the field, probably due to the higher availability of males. Females underwent over four successive spawnings in the laboratory without having to recopulate, and the incubation lasted on the average from 40 to 58 days (∼18 and 16°C respectively) and the mean duration between hatching and the next spawning was 3.4 days. It is estimated that most females carry out three successive spawnings during the annual cycle.     

Induction of MGE 412 transposition individually by heat and cold shock in spermatogenesis in Drosophila males

Effects of temperature treatment (heavy heat shock, HHS; heat shock, HS; and cold shock, CS) on the daily productivity of treated males in different spermatogenesis stages have been studied in isogenic line 51 of Drosophila melanogaster. The average productivity was shown to substantially decrease in all cases. The sum of the HS and CS contributions to this decrease was nearly equal to the HHS (the combined HS and CS) contribution, i.e., these contributions were almost additive. The temperature treatments did not kill mature sperm. In the control, mating productivity of day 1 exceeded that of the next day at least by 10-20%. Each day, most sperm in matings was new, i.e., matured during that day. Transposition induction of MGE 412 was studied at four spermatogenesis stages after HS and CS. Both temperature treatments were effective but CS had a more pronounced inducing effect. Most temperature-induced transpositions occurred at stage 3 (meiosis) and 4 (spermiogenesis). The day rates of transpositions at different stages were estimated. After HS at the meiosis stage, lambda = 0.11 events per initial MGE copy per sperm per day of mating, which is approximately equal to the previous estimates after HHS. After CS at the meiosis stage, lambda = 0.51. The transposition hot sites (including the previously known 43B and 97DE as well as a number of new sites) were detected. The lists of transpositions after CS completely included the corresponding lists after HS, which suggests similarity of induction mechanisms underlying CS and HS.     

Hyperthermia of male <Emphasis Type="Italic">Drosophila melanogaster</Emphasis> meiocytes induces abnormalities in both paternal and maternal sex chromosome sets of the offspring

Nondisjunction and loss of sex chromosomes caused by exposure of male Drosophila melanogaster to heat shock (HS) (37°C for 1 h) has been studied to determine the role of mutation l(1)ts403 (sbr ¹⁰) in the control of chromosome segregation during cell division. Hyperthermia of males at the pupal stage has been demonstrated to increase the number of offspring with abnormalities of not only paternal, but also maternal sex chromosome sets. According to the criterion used, there is a temperature-sensitive period of spermatogenesis, which presumably coincides with meiosis. Phenotypes of some individuals correspond to the presence of two sex chromosomes of obtained from the same parent. The frequency of abnormal chromosome sets in the off-spring of male carriers of the sbr ¹⁰ mutation is about two times higher than in the offspring of males without this mutation.     

Multiple morphs of sperm were required for the evolution of the Sex Ratio trait in Drosophila

In Sex Ratio males of D. subobscura Y sperm degenerate. Nevertheless, Sex Ratio males can produce as many offspring as non-Sex Ratio males. In order to find an explanation for the high number of offspring of Sex Ratio males we analysed spermatogenesis and sperm storage in females. Because D. subobscura has two morphs of sperm, short and long sperm, we studied the relationship of sperm heteromorphism to the Sex Ratio trait in this species. Spermatids of both lengths developed simultaneously in the testes. The first mature sperm produced by a young male were nearly all short sperm. This result indicates that short cysts need less time to mature than long cysts. Thus in a given time more short cysts than long cysts can mature. In the testes of Sex Ratio males more short cysts and fewer long cysts were formed than in the tests of non-Sex Ratio males. Thus in a unit time Sex Ratio males can produce as many or more sperm than non-Sex Ratio males. Females mated to Sex Ratio males had more sperm in their storage organs than those which were mated to non-Sex Ratio males. From the transferred sperm females stored selectively more long than short sperm after mating to a Sex Ratio male than after mating to a non-Sex Ratio male. The effect of the high amount of sperm in Sex Ratio males is twofold: the loss of Y sperm is compensated, and probably in nature a second copulation is prevented by the complete filling of the female storage organs. From these results we conclude that the development and persistence of the Sex Ratio trait in natural populations depends on the presence of sperm heteromorphism.     

Genetic factors affecting normal growth of testes inDrosophila hydei

Summary A marked growth in the length of testes ofDrosophila hydei males occurred during pupal development. This growth continued over the first 8 days of adult life and in the young adults sperm were not produced until the testes increased approximately threefold in length to about 28 mm. The length of testes is correlated with genetic factors on the X and Y chromosomes. In males lacking a Y chromosome (X/O) or the short arm (Y^S) of the Y chromosome (X/Y^L) the testes were about half the length of testes of control males (X/Y) or double Y males (X/Y/Y). Males with deletions of the distal Y^L chromosome arm had testicular lengths equivalent to the controls. Males with short testes (X/O and X/Y^L) showed disruptions to spermatogenesis at meiosis and an absence of normal spermatid elongation. Reduction of active ribosomal RNA genes on the X chromosome in X/O caused an increased expression ofbobbed (bb) and a corresponding reduction in length of testes. Severelybobbed X/O males had very few cysts of spermatogonia and these cysts did not develop into primary spermatocytes.     

Multiple paternity in viviparous kelp rockfish, <Emphasis Type="Italic">Sebastes atrovirens</Emphasis>

Analysis of multilocus microsatellite genotypes revealed multiple paternity for all of the seven viable broods of larvae produced by kelp rockfish, Sebastes atrovirens (Jordan and Gilbert 1880), held jointly in a large aquarium tank (n = eight females and eight males). Only two of the eight experimental males were identified as fathers, and alleles not found in any of the captive males were present in all seven broods, demonstrating paternity by wild males external to the experiment. Thus, all of the females mated with one or more males prior to capture, confirming that female kelp rockfish are capable of storing sperm and controlling the overall timing of egg fertilization. These results highlight the potential for a paternal influence on larval quality through female mate choice and sperm competition.     

Function of the nuclear receptor FTZ‐F1 during the pupal stage in Drosophila melanogaster

The nuclear receptor βFTZ‐F1 is expressed in most cells in a temporally specific manner, and its expression is induced immediately after decline in ecdysteroid levels. This factor plays important roles during embryogenesis, larval ecdysis, and early metamorphic stages. However, little is known about the expression pattern, regulation and function of this receptor during the pupal stage. We analyzed the expression pattern and regulation of ftz‐f1 during the pupal period, as well as the phenotypes of RNAi knockdown or mutant animals, to elucidate its function during this stage. Western blotting revealed that βFTZ‐F1 is expressed at a high level during the late pupal stage, and this expression is dependent on decreasing ecdysteroid levels. By immunohistological analysis of the late pupal stage, FTZ‐F1 was detected in the nuclei of most cells, but cytoplasmic localization was observed only in the oogonia and follicle cells of the ovary. Both the ftz‐f1 genetic mutant and temporally specific ftz‐f1 knockdown using RNAi during the pupal stage showed defects in eclosion and in the eye, the antennal segment, the wing and the leg, including bristle color and sclerosis. These results suggest that βFTZ‐F1 is expressed in most cells at the late pupal stage, under the control of ecdysteroids and plays important roles during pupal development.     

The ontogeny of the female reproductive system in the parasitic castrator pea crab Calyptraeotheres garthi: Implications for its mating system

The knowledge of the mating system of pea crabs is still fragmentary as it remains dubious whether females copulate in the juvenile and free‐living ‘hard’ or in the obligatory symbiotic stages (adult stage ‘V’ or intermediate stages II to IV). To discriminate between these two possibilities, we analysed the female seminal receptacles, vagina and opercula, and the sperm content in different stages of the pea crab Calyptraeotheres garthi. Our histology and scanning electron microscopy results revealed that in the hard stage the seminal receptacle is simple without secretory epithelia, and vagina and opercula are not controlled by musculature. In stages II to IV, the seminal receptacles, vagina, and opercula are under development and these structures reach maturity in stage V. These results suggest that females become receptive in stage V and not during predating stages. We found no spermatozoa in SR of ‘hard’ and stage II to IV females while these structures were loaded of sperm in most stage V, indicating that females start to mate in stage V. Our results support the notion that males of C. garthi roam among hosts in search for sedentary stage V females, as predicted by Baeza and Thiel's ( 2007 ) model of mating systems for symbiotic crustaceans. Nevertheless, we failed to reveal whether females mate repeatedly: the accumulation of sperm in larger females might indicate occurrence of multiple copula or a high variability in male sperm transfer.     

X-ray-induced recombination during oogenesis in the silkworm (Bombyx mori L.)

Summary The physical induction of recombinational events has been studied in the female silkworm (Bombyx mori), in which crossing-over does not normally occur. Female silkworms heterozygous in the trans type of two egg-color genes,pe (V-0.0) andre (V-31.7), received a single dose of X-rays (1000 R) at various developmental stages. Then they were crossed to marked males homozygous for both genes. The results indicated that X-rays increase the occurrence of recombinational events in silkworm females from first instar larvae to late stage pupae. The spontaneous frequency of exchange type recombinants in the control series was 2.5 x 10^–5, while after irradiation the frequency of these recombinants was up to 38.8 x^10–5. The sensitive stage to X-ray-induced recombinational events was late stage larvae from fourth to fifth instar. Exchange (cross-over) type recombinants were about three times more frequent than interchange types among the 122 recombinants recovered. The biological significance of the present finding is discussed.     

Production of mosaic lethals in different germ cell stages of drosophila by N-methyl-N'-nitro-N-nitrosoguanidine.

The delayed effect of N-methyl-N'-nitro-N-nitrosoguanidine (MNNG) was studied in Drosophila melanogaster by the proportion of mosaic progeny produced after this treatment. Following injection of the chemical into wild type males, complete and mosaic sex-linked recessive lethals were scored by the Muller-5 method, in five successive broods representing the different stages of spermatogenesis. All broods showed significant increase over the control in the frequencies of complete lethals with gradual decrease in mutation rate from the post-meiotic stages to the pre-meiotic ones. In the case of mosaic lethals, too, the post-meiotic stages were generally more sensitive; but the increase over the control was significant only for the mature spermatozoa. The extension of the experiment to F4 generation showed that a mosaic F1 female may produce further mosaic progeny. The production of lethal mutations in successive generations after treatment with MNNG supports the view that chemically induced instabilities can be transmitted as such over several generations.     

Sperm maturation and male tactic-specific differences in ejaculates in the plainfin midshipman fish Porichthys notatus

Using the plainfin midshipman fish Porichthys notatus, a species with alternative reproductive tactics (ARTs), we investigated how sperm maturation shapes sperm competitive abilities. We compared sperm performance and morphology before and after final sperm maturation by sampling sperm from the testes and stripped ejaculates of guarders and sneakers. In accordance with sperm competition risk theory, ejaculates from sneaker males had three times as much sperm as ejaculates from guarder males and sneaker males produced faster swimming sperm than guarder males, but this was only the case after final sperm maturation had occurred. Additionally, fully mature sperm found in ejaculates had larger heads and midpieces than sperm found in the testes. These results emphasize the important role played by non-sperm components of an ejaculate in mediating sperm performance and potentially also morphology.     

The developmental strategy of an idiobiont ectoparasitoid, Dendrocerus carpenteri : influence of variations in host quality on offspring growth and fitness

Dendrocerus carpenteri (Curtis) (Hymenoptera: Megaspilidae) is a solitary hyperparasitoid, which attacks prepupal and pupal stages of hymenopteran parasitoids inside mummified aphids. The larva feeds externally on the host, which is envenomed by the female at oviposition. To evaluate the influence of variations in host quality on the growth, development and fitness of D. carpenteri, we varied the size and developmental stage of the primary parasitoid host (Aphidius ervi Haliday), which was reared on different instars of pea aphid [Acyrthosiphon pisum (Harris)] and English grain aphid [Sitobion avenae (F.)]. Within each kind of host, females eclosed from the relatively larger mummies, while males eclosed from the smaller mummies. Host size and hyperparasitoid size were correlated, and females were larger than males. In hyperparasitoids developing on prepupal and pupal hosts, development time from oviposition to adult eclosion was proportional to size; females required more time for development than males. The mean relative growth rate was the same in males and females and increased with host quality, as predicted by the growth model of Mackauer and Sequeira (1993) for idiobiont parasitoids. Larvae developing on late-pupal stages and pharate adults of A. ervi were unable to consume sclerotized host tissues; they were smaller and needed more time for development. The average number of mature eggs at eclosion was six, except in females developing on suboptimal hosts, which contained only one egg or none. Egg volume was correlated with female size, possibly reflecting differences in larval ontogeny. We provide equations describing the relationship between host quality as indexed by hind-tibia length of the mummified aphid and adult body size in terms of dry mass, development time and mean relative growth rate of D. carpenteri. We discuss the usefulness of host size as a proxy of host quality for idiobiont parasitoids, and provide examples of exceptions. Received: 14 December 1997 / Accepted: 23 July 1998     

Temperature‐dependent development of the European larch bark beetle,Ips cembrae

The temperature‐dependent development of the European larch bark beetle, Ips cembrae, was studied under long‐day conditions L:D 16:8 at three temperature regimes, 15°C, 20°C and 25°C, using the sandwich plate method. By observing the individual developmental progress, we calculated the developmental times and lower developmental thresholds of one entire generation and various ontogenetic stages. The mean developmental time of one generation was about 120, 64 and 37 days at 15°C, 20°C and 25°C, respectively. The egg stage comprised about 9% of the total development or about 16% of the pre‐imaginal development. The larval stages took about 39% of the entire and about 66% of the pre‐imaginal development. The pupal stage needed about 11% of the total or about 18% of the pre‐imaginal development. The lower developmental threshold for one generation was 11.2°C. The egg stage had the highest lower developmental threshold of 12.0°C, the pupa the lowest of 9.8°C and the total larval stages showed a value of 11.2°C. The thermal requirements for I. cembrae have never been studied in detail before. The results will be a valuable contribution for monitoring and risk assessment models to estimate the beetle's phenology and its potential impacts on forest ecosystems under changing climate conditions.