Journal of insect physiology最新文献

{"title":"Basking improves but winter warming worsens overwinter survival in the linden bug","authors":"Jan Rozsypal","doi":"10.1016/j.jinsphys.2024.104655","DOIUrl":"10.1016/j.jinsphys.2024.104655","url":null,"abstract":"<div><p>The present study investigates the effects of rare winter basking behavior (observed in wild populations of the Linden bug, <em>Pyrrhocoris apterus</em>) and the effects of winter warming (predicted by climate models) on overwinter survival and physiology of <em>P. apterus</em>. The insects were exposed to scenarios simulating basking and winter warming in the laboratory. Part of the insects were exposed to real winters under semi-natural conditions in the field for comparison. The results show a clear positive effect of winter basking, implying that basking behavior is critical for overwinter survival in <em>P. apterus</em>. In contrast, winter warming was found to have a strong negative effect on overwinter survival, potentially representing a threat to central European populations of <em>P. apterus</em>. Physiological parameters (mass, water content, SCP, energy reserves) measured in this study cannot fully explain all the results. Further study is needed to better understand the mechanisms behind the positive effects of winter basking and the negative effects of winter warming on overwintering <em>P. apterus</em>.</p></div>","PeriodicalId":16189,"journal":{"name":"Journal of insect physiology","volume":"156 ","pages":"Article 104655"},"PeriodicalIF":2.2,"publicationDate":"2024-06-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141296259","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Influence of temperature on the photoperiodic time measurement and on the induction of Trichogramma telengai progeny diapause: The separation of the two effects","authors":"Sergey Ya. Reznik,&nbsp;Natalia D. Voinovich","doi":"10.1016/j.jinsphys.2024.104654","DOIUrl":"https://doi.org/10.1016/j.jinsphys.2024.104654","url":null,"abstract":"<div><p>Thermal effects on photoperiodic time measurement and accumulation of inductive photoperiods have been studied in many insect species whereas the influence of temperature on the last step of the photoperiodic response, the induction of diapause, received less attention from researchers. We investigated thermal modification of the maternal photoperiodic response in <em>Trichogramma telengai</em> (Hymenoptera: Trichogrammatidae). Even a single long-night photoperiod experienced by females of this minute egg parasitoid immediately before oviposition causes a substantial increase in larval diapause incidence in the progeny. This feature allows separation of the thermal effects on different steps of the diapause-inducing photoperiodic response. Laboratory experiments showed that the temperature of the last scotophase (when the final decisive photoperiodic time measurement occurs) caused an inverted U-shaped diapause-inducing response similar to that observed in some other long-day insects. The temperature of the last photophase (when progeny diapause is induced) had a positive linear effect that has not been reported for the induction of winter diapause in any long-day insect. Most probably, such a thermal response is not a specific seasonal adaptation but a direct consequence of the influence of temperature on the rate of metabolism.</p></div>","PeriodicalId":16189,"journal":{"name":"Journal of insect physiology","volume":"155 ","pages":"Article 104654"},"PeriodicalIF":2.2,"publicationDate":"2024-05-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141095395","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Habituation leads to short but not long term memory formation in mosquito larvae","authors":"Martin Dessart,&nbsp;Claudio R. Lazzari,&nbsp;Fernando J. Guerrieri","doi":"10.1016/j.jinsphys.2024.104650","DOIUrl":"10.1016/j.jinsphys.2024.104650","url":null,"abstract":"<div><p>In animals, memory allows to remember important locations and conserve energy by not responding to irrelevant stimuli. However, memory formation and maintenance are metabolically costly, making it worthwhile to understand the mechanisms underlying different types of memory and their adaptive value. In this study, we investigated the memory persistence of <em>Aedes aegypti</em> mosquito larvae, after habituation to a visual stimulus. We used an automated tracking system for quantifying the response of mosquito larvae to the passage of a shadow, simulating an approaching predator. First, we compared different retention times, from 4 min to 24 h, and found that mosquito larvae only exhibited memory capabilities less than 3 h after training. Secondly, we investigated the role of inter-trial intervals in memory formation. In contrast to other aquatic invertebrates, mosquito larvae showed no long-term memory even at long inter-trial intervals (i.e., 5 min and 10 min). Our results are discussed in relation to the ecological constraints.</p></div>","PeriodicalId":16189,"journal":{"name":"Journal of insect physiology","volume":"155 ","pages":"Article 104650"},"PeriodicalIF":2.2,"publicationDate":"2024-05-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141080631","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Tracheal hyperallometry and spatial constraints in a large beetle","authors":"Tomer Urca ,&nbsp;Gal Ribak ,&nbsp;Eran Gefen","doi":"10.1016/j.jinsphys.2024.104652","DOIUrl":"10.1016/j.jinsphys.2024.104652","url":null,"abstract":"<div><p>Insects exchange respiratory gases with their environment through their gas-filled tracheal system, a branched tracheal tree extending from segmental openings and terminating at fine tissue penetrating tracheoles. It was shown that the tracheal volume increases hyperallometrically with insect body size (<span><math><mrow><msub><mi>M</mi><mi>b</mi></msub></mrow></math></span>), both interspecifically and across developmental stages. In this study, we used the sixfold <span><math><mrow><msub><mi>M</mi><mi>b</mi></msub></mrow></math></span> variation in adult <em>Batocera rufomaculata</em> <!-->(Cerambicidae; Coleoptera) examining the allometry of adult tracheal volume (<span><math><mrow><msub><mi>V</mi><mrow><mi>tr</mi></mrow></msub></mrow></math></span>). We further explored the effect of sex and sexual maturity on tracheal gas conductance, testing the hypotheses that (i) larger body size and (ii) egg volume in gravid females would result in lower safety margins for tracheal oxygen transport due to structural restriction. We report a hyperallometric tracheal growth in both sexes of adult <em>B. rufomaculata</em> <!-->(mean mass exponent of 1.42 ± 0.09), similar in magnitude to previously reported values. Tracheal gas conductance was independent of <span><math><mrow><msub><mi>M</mi><mi>b</mi></msub></mrow></math></span> and reproductive state, but was significantly higher in females compared with males. We suggest that females may have pre-adapted a higher tracheal conductance required for the higher flight power output while gravid. Lack of compliant air sacs and rigid trachea may explain how gravid females retain their <span><math><mrow><msub><mi>V</mi><mrow><mi>tr</mi></mrow></msub></mrow></math></span>. However, we show that <span><math><mrow><msub><mi>V</mi><mrow><mi>tr</mi></mrow></msub></mrow></math></span> outgrows thoracic dimensions with increased <em>B. rufomaculata</em> <!-->size. Hyperallometric growth of the giant cerambycid thoracic trachea could explain the previously reported hypometric scaling of flight muscles in <em>B. rufomaculata</em>, and the compromised long-distance flight performance of larger compared with smaller conspecifics.</p></div>","PeriodicalId":16189,"journal":{"name":"Journal of insect physiology","volume":"155 ","pages":"Article 104652"},"PeriodicalIF":2.2,"publicationDate":"2024-05-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141080632","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Hemolin increases the immune response of a caterpillar to NPV infection","authors":"Liqiong Yan,&nbsp;Arina Nur Faidah,&nbsp;Lili Sun,&nbsp;Chuanwang Cao","doi":"10.1016/j.jinsphys.2024.104651","DOIUrl":"10.1016/j.jinsphys.2024.104651","url":null,"abstract":"<div><p>Hemolin, a member of the immunoglobulin superfamily, plays a crucial role in the immune responses of insects against pathogens. However, the innate immune response of Hemolin to baculovirus infection varies among different insects, and the antiviral effects of Hemolin in <em>Hyphantria cunea</em> (HcHemolin) remain poorly understood. Our results showed that <em>HcHemolin</em> was expressed throughout all developmental stages, with higher expressions observed during pupal and adult stages of <em>H. cunea</em>. Additionally, <em>HcHemolin</em> was expressed in reproductive and digestive organs. The expression levels of the <em>HcHemolin</em> were induced significantly following <em>H. cunea</em> nucleopolyhedrovirus (HcNPV) infection. The susceptibility of <em>H. cunea</em> larvae to HcNPV decreased upon silencing of <em>HcHemolin</em>, resulting in a 40% reduction in median lifespan compared to the control group. The relative growth rate (RGR), the relative efficiency of consumption rate (RCR), the efficiency of the conversion of ingested food (ECI), and efficiency of the conversion of digested food (ECD) of silenced <em>H. cunea</em> larvae were significantly lower than those of the control group. Immune challenge assays showed that the median lifespan of treated <em>H. cunea</em> larvae was two-fold longer than the control group after HcNPV and HcHemolin protein co-injection. Therefore, we propose that HcHemolin plays a crucial role in regulating the growth, development, and food utilization of <em>H. cunea</em>, as well as in the antiviral immune response against HcNPV. These findings provide implications for the development of targeted nucleic acid pesticides and novel strategies for pollution-free biological control synergists for HcNPV.</p></div>","PeriodicalId":16189,"journal":{"name":"Journal of insect physiology","volume":"155 ","pages":"Article 104651"},"PeriodicalIF":2.2,"publicationDate":"2024-05-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141065666","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Impact of climate change on the reproductive diapause and voltinism of the carrot weevil, Listronotus oregonensis","authors":"Annie-Ève Gagnon,&nbsp;Gaétan Bourgeois","doi":"10.1016/j.jinsphys.2024.104653","DOIUrl":"10.1016/j.jinsphys.2024.104653","url":null,"abstract":"<div><p>The impacts of climate change on the development of insects are of great concern due to potential alterations in population dynamics and pest pressure. The carrot weevil, <em>Listronotus oregonensis</em>, is a major agricultural pest, and its development is influenced by temperature and photoperiod. In this study, our aim was to investigate the impact of temperature increases on the voltinism and reproductive diapause of the carrot weevil under field conditions and bioclimatic models. Field observations were conducted over two growing seasons using structures that allowed for temperature increases. The developmental stages of the carrot weevil, including female reproductive status, oviposition and larval stage, were monitored weekly to measure the proportion of individuals undergoing an additional generation. Concurrently, bioclimatic models were used to simulate the probability of a second generation under current (1981–2010) and future (2041–2070) climates, considering a lower and a higher change in emission scenarios. Results showed that rising temperatures led to an increase in the proportion of carrot weevils undergoing inhibition of the reproductive diapause and a higher number of eggs laid in the field. The models indicated a substantial rise in the probability of a second generation developing, from 24% to 37% to 62%–99% under current and future climates, respectively. These findings demonstrate the potential for significant alterations in carrot weevil population dynamics, resulting in increased pest pressure on crops. Further research is needed to fully understand the implications of these findings and to develop effective adaptation measures to mitigate the negative impacts of global warming on insect populations and agriculture.</p></div>","PeriodicalId":16189,"journal":{"name":"Journal of insect physiology","volume":"155 ","pages":"Article 104653"},"PeriodicalIF":2.2,"publicationDate":"2024-05-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141054209","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Chemical defence of a centipede (Clinopodes flavidus)","authors":"Bojan M. Mitić ,&nbsp;Vesna B. Jovanović ,&nbsp;Marina M. Todosijević ,&nbsp;Margret Eckhard ,&nbsp;Ljubica C. Vasiljević ,&nbsp;Vele V. Tešević ,&nbsp;Ljubodrag V. Vujisić","doi":"10.1016/j.jinsphys.2024.104649","DOIUrl":"10.1016/j.jinsphys.2024.104649","url":null,"abstract":"<div><p>Chemical substances are of utmost importance for the biotic interactions between animals and their predators/parasites; many of these semiochemicals are emitted for defence purposes. One of the most deterrent and toxic biogenic substances we know of is hydrogen cyanide, which can be stored by certain insects, millipedes, centipedes and arachnids in the form of stable and less volatile molecules. The aim of this study was to analyse the biology and chemistry of such a defence mechanism in a geophilomorph centipede (Chilopoda). The cyanogenic secretion of <em>Clinopodes flavidus</em> is discharged from the ventral glands, whose glandular units are located in the space between the cuticle and the trunk muscles and do not extend deep into the segment. In addition to hydrogen cyanide, the ventral secretion contains 2-methylpentanoic acid, benzaldehyde, benzoyl cyanide, 2-methyl branched C-9 carboxylic acid (tentatively identified as 2-methyloctanoic acid), methyl 2-phenylacetate, benzoic acid and mandelonitrile as well as four major proteins with a molecular weight of 150, 66.2, 59 and 55 kDa. The correlation between the presence of ventral glands and guarding with the female’s ventral side facing away from the eggs and young indicates a functional link between these two traits. We hope that the specificity of the chemical composition of the ventral secretion could serve as a criterion for chemotaxonomy and that the analysis of more species will help to clarify the phylogenetic relationships within the Geophilomorpha.</p></div>","PeriodicalId":16189,"journal":{"name":"Journal of insect physiology","volume":"155 ","pages":"Article 104649"},"PeriodicalIF":2.2,"publicationDate":"2024-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140957678","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Evidence of plasticity, but not evolutionary divergence, in the thermal limits of a highly successful urban butterfly","authors":"Angie Lenard,&nbsp;Sarah E. Diamond","doi":"10.1016/j.jinsphys.2024.104648","DOIUrl":"10.1016/j.jinsphys.2024.104648","url":null,"abstract":"<div><p>Despite the generally negative impact of urbanization on insect biodiversity, some insect species persist in urban habitats. Understanding the mechanisms underpinning the ability of insects to tolerate urban habitats is critical given the contribution of land-use change to the global insect decline. Compensatory mechanisms such as phenotypic plasticity and evolutionary change in thermal physiological traits could allow urban populations to persist under the altered thermal regimes of urban habitats. It is important to understand the contributions of plasticity and evolution to trait change along urbanization gradients as the two mechanisms operate under different constraints and timescales. Here, we examine the plastic and evolutionary responses of heat and cold tolerance (critical thermal maximum [CT_max] and critical thermal minimum [CT_min]) to warming among populations of the cabbage white butterfly, <em>Pieris rapae</em>, from urban and non-urban (rural) habitats using a two-temperature common garden experiment. Although we expected populations experiencing urban warming to exhibit greater CT_max and diminished CT_min through plastic and evolutionary mechanisms, our study revealed evidence only for plasticity in the expected direction of both thermal tolerance traits. We found no evidence of evolutionary divergence in either heat or cold tolerance, despite each trait showing evolutionary potential. Our results suggest that thermal tolerance plasticity contributes to urban persistence in this system. However, as the magnitude of the plastic response was low and comparable to other insect species, other compensatory mechanisms likely further underpin this species’ success in urban habitats.</p></div>","PeriodicalId":16189,"journal":{"name":"Journal of insect physiology","volume":"155 ","pages":"Article 104648"},"PeriodicalIF":2.2,"publicationDate":"2024-05-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140957671","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Temperature influences desiccation resistance of bumble bees","authors":"Jamieson C. Botsch ,&nbsp;Jesse D. Daniels ,&nbsp;Jelena Bujan ,&nbsp;Karl A. Roeder","doi":"10.1016/j.jinsphys.2024.104647","DOIUrl":"10.1016/j.jinsphys.2024.104647","url":null,"abstract":"<div><p>Ongoing climate change has increased temperatures and the frequency of droughts in many parts of the world, potentially intensifying the desiccation risk for insects. Because resisting desiccation becomes more difficult at higher temperatures and lower humidity, avoiding water loss is a key challenge facing terrestrial insects. However, few studies have examined the interactive effects of temperature and environmental humidity on desiccation resistance in insects. Such studies on bees (Hymenoptera: Apoidea: Anthophila) are especially rare, despite their ecological and economic importance. Here, we crossed temperature (20, 25, and 30 °C) with humidity (&lt;5, 50, &gt;95 % RH) manipulations and measured time to mortality, water loss rates, and the water content at mortality of bumble bees (<em>Bombus impatiens</em>). We found that both higher temperature and lower humidity increased water loss rates, while warmer temperatures reduced survival time and lower humidity decreased water content at mortality. Additionally, we observed large intraspecific variation in water balance traits between colonies, and larger individuals survived longer and could tolerate more water loss before mortality. This study raises important questions about the mechanisms underpinning water loss in bumble bees and suggests that frequent access to nectar may be especially important for bumble bees’ water balance and survival in a warming and drying climate.</p></div>","PeriodicalId":16189,"journal":{"name":"Journal of insect physiology","volume":"155 ","pages":"Article 104647"},"PeriodicalIF":2.2,"publicationDate":"2024-05-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140866460","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Cellular dynamics of host − parasitoid interactions: Insights from the encapsulation process in a partially resistant host","authors":"Samuel Gornard,&nbsp;Florence Mougel,&nbsp;Isabelle Germon,&nbsp;Véronique Borday-Birraux,&nbsp;Pascaline Venon,&nbsp;Salimata Drabo,&nbsp;Laure Kaiser","doi":"10.1016/j.jinsphys.2024.104646","DOIUrl":"10.1016/j.jinsphys.2024.104646","url":null,"abstract":"<div><p><em>Cotesia typhae</em> is an eastern African endoparasitoid braconid wasp that targets the larval stage of the lepidopteran stem borer, <em>Sesamia nonagrioides</em>, a maize crop pest in Europe<em>.</em> The French host population is partially resistant to the Makindu strain of the wasp, allowing its development in only 40% of the cases. Resistant larvae can encapsulate the parasitoid and survive the infection. This interaction provides a very interesting frame for investigating the impact of parasitism on host cellular resistance. We characterized the parasitoid ovolarval development in a permissive host and studied the encapsulation process in a resistant host by dissection and histological sectioning compared to that of inert chromatography beads. We measured the total hemocyte count in parasitized and bead-injected larvae over time to monitor the magnitude of the immune reaction. Our results show that parasitism of resistant hosts delayed encapsulation but did not affect immune abilities towards inert beads. Moreover, while bead injection increased total hemocyte count, it remained constant in resistant and permissive larvae. We conclude that while <em>Cotesia</em> spp virulence factors are known to impair the host immune system, our results suggest that passive evasion could also occur.</p></div>","PeriodicalId":16189,"journal":{"name":"Journal of insect physiology","volume":"155 ","pages":"Article 104646"},"PeriodicalIF":2.2,"publicationDate":"2024-05-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140849895","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}