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1.
Micron ; 183: 103656, 2024 08.
Article in English | MEDLINE | ID: mdl-38759450

ABSTRACT

A trichobothrium is a complex sensory organ, which usually consists of a long, slender mechanoreceptive seta (trich), which is situated in a cuplike depression in the cuticle (bothrium). Nabidae (Hemiptera: Heteroptera: Cimicomorpha), also called damsel bugs, are a relatively small family within which two subfamilies, Nabinae and Prostemmatinae, are distinguished. Trichobothria are present in the number of one to seven pairs located laterally on the scutellum of adult representatives of Prostemmatinae. This feature is commonly used to distinguish this subfamily from Nabinae. Trichobothria are also found on the abdominal tergites of Prostemmatinae nymphs. Similar sensilla have been observed in adult representatives of Nabinae, but their homology has not yet been confirmed. During morphological studies on Nabidae, conducted using scanning electron microscopy, we noticed sensilla resembling trichobothria on the heads of these insects. This discovery prompted us to examine the presence of these structures in damsel bugs more carefully. Imagines of fifteen species of both subfamilies were analysed using a scanning electron microscope. The results present data on the distribution and micromorphology of the trichobothria in damsel bugs. A pair of dorsal and ventral cephalic trichobothria were observed in all of the examined species of subfamily Nabinae. These sensilla were not found on the heads of Prostemmatinae. The results of studies on scutellar trichobothria confirmed the previously known data regarding their occurrence in Prostemmatinae. Moreover, our research showed the presence of these sensory structures in all of the examined Nabinae species: one pair of trichobothria in Arachnocorini, Carthasini, Gorpini and Nabini, and two pairs in Stenonabini. The presence of abdominal trichobothria was shown in Nabini and Stenonabini. In the remaining studied tribes of Nabinae and in the subfamily Prostemmatinae, the presence of structures that could undoubtedly be considered abdominal trichobothria was not found.


Subject(s)
Heteroptera , Microscopy, Electron, Scanning , Sensilla , Animals , Heteroptera/anatomy & histology , Heteroptera/ultrastructure , Sensilla/ultrastructure , Female , Male , Nymph/ultrastructure , Nymph/anatomy & histology
2.
Zhongguo Xue Xi Chong Bing Fang Zhi Za Zhi ; 34(2): 179-182, 2022 Feb 23.
Article in Chinese | MEDLINE | ID: mdl-35537840

ABSTRACT

OBJECTIVE: To investigate the morphological characteristics of Dermatophagoides farinae at different developmental stages. METHODS: The cultured D. farinae was isolated, and the external morphological features of mites at various developmental stages were observed using scanning electron microscopy (SEM), including egg, larva, nymph and adult stages. RESULTS: The D. farinae egg appeared a long oval shape, and the larval mites had three pairs of legs. The nymph had four pairs of legs and underdeveloped genital pores containing genital setae and anal setae, and adult mites appeared long and oval in shape, with decorative patterns on epidermis, and had four pairs of legs. In male adult mites, remarkable thickening of the leg I and thicker and longer leg III than the leg IV were seen, and ventral genital regions were found between the basal segments of legs III and IV; the anus was surrounded by a circular peri-anal ring, with a pair of anal suckers and anal setae within the ring. In the female adult mites, slender legs III and IV with an equal length were seen, and a "λ-shape" genital hole was observed on the ventral surface, with a crescent-like genital plate in the anterior part, and the anus appeared a longitudinal slit. CONCLUSIONS: An SEM observation of the external morphology of D. farinae provides understandings of the morphological characteristics of D. farinae, which is of great significance for the classification and identification.


Subject(s)
Dermatophagoides farinae , Mites , Animals , Electrons , Female , Larva/anatomy & histology , Male , Microscopy, Electron, Scanning , Nymph/ultrastructure
3.
Elife ; 102021 02 23.
Article in English | MEDLINE | ID: mdl-33620311

ABSTRACT

Using serial block-face scanning electron microscopy, we report on the internal 3D structures of the brown planthopper, Nilaparvata lugens (Hemiptera: Delphacidae) at nanometer resolution for the first time. Within the reconstructed organs and tissues, we found many novel and fascinating internal structures in the planthopper such as naturally occurring three four-way rings connecting adjacent spiracles to facilitate efficient gas exchange, and fungal endosymbionts in a single huge insect cell occupying 22% of the abdomen volume to enable the insect to live on plant sap. To understand the muscle and stylet movement during phloem sap-sucking, the cephalic skeleton and muscles were reconstructed in feeding nymphs. The results revealed an unexpected contraction of the protractors of the stylets and suggested a novel feeding model for the phloem sap-sucking.


Since the 19th century, scientists have been investigating how the organs of insects are shaped and arranged. However, classic microscopy methods have struggled to image these small, delicate structures. Understanding how the organs of insects are configured could help to identify new methods for controlling pests, such as chemicals that target the mouthparts that some insects use to feed on plants. Most insects that feed on the sap of plants suck out the nutrient via their stylet bundle ­ a thin, straw-like structure surrounded by a sheath called the labium. As well as drying out the plant and damaging its tissues, the stylet bundle also allows the insect to transmit viruses that cause further harm. To investigate these mouthparts in more detail, Wang, Guo et al. used a method called SBF-SEM to determine the three-dimensional structure of one of the most destructive pests of rice crops, the brown planthopper. In this technique, a picture of the planthopper was taken every time a thin slice of its body was removed. This continuous slicing and re-imaging generated thousands of images that were compiled into a three-dimensional model of the brown planthopper's whole body and internal organs. Previously unknown features emerged from the reconstruction, including a huge cell in the planthopper's abdomen which is full of fungi that provide the nutrients absent in plants. Next, Wang, Guo et al. used this technique to see how the muscles in the labium and surrounding the stylet move by imaging planthoppers that were frozen at different stages of the feeding process. This revealed that when brown planthoppers bow their heads to eat, the labium compresses and pushes out the stylet, allowing it to pierce deeper into the plant. This is the first time that the body of such a small insect has been reconstructed three-dimensionally using SBF-SEM. Furthermore, these findings help explain how brown planthoppers and other sap-feeding insects insert their stylet and damage plants, potentially providing a stepping stone towards identifying new strategies to stop these pests from destroying millions of crops.


Subject(s)
Hemiptera/ultrastructure , Imaging, Three-Dimensional , Animals , Feeding Behavior , Female , Hemiptera/growth & development , Microscopy, Electron, Scanning , Mouth/ultrastructure , Nymph/growth & development , Nymph/ultrastructure , Phloem
4.
Ticks Tick Borne Dis ; 12(1): 101572, 2021 01.
Article in English | MEDLINE | ID: mdl-33068841

ABSTRACT

Females, nymphs, and larvae of Ixodes silvanus n. sp. collected from birds and from the vegetation in northwestern Argentina (Yungas Phytogeographic Province) are described herein. The new species belongs to the subgenus Trichotoixodes (Acari: Ixodidae). The female is diagnosed by a combination of the following characters: scutum with setae moderately long and more numerous in central field, fewer and moderately long setae on lateral fields, and inconspicuous setae in anterior field; basis capituli subtriangular dorsally; porose areas large and irregular in shape, lacking distinct margins; auriculae with straight edges diverging posterolaterally and ending with small blunt processes; hypostome narrow and pointed with dental formula 4/4 in the anterior third, then 3/3 and 2/2 near the base; coxae I with two spurs, sub-equal in size, internal slightly slimmer than external. The nymph is diagnosed by notum with numerous and long setae, ventral surface covered by numerous whitish setae, scutum with short scapulae and few and shallow punctations, setae on scutum few, short and irregularly distributed, basis capituli sub-triangular dorsally with posterior margin straight, cornua large and directed postero-laterally, auriculae large and projected laterally, lateral margin of basis capituli above auriculae with a lateral and triangular projection, hypostome pointed with dental formula 3/3 in the anterior third and then 2/2, and coxa I with two short, sub-equal, triangular spurs. The diagnostic characters of the larva are: basis capituli dorsally sub-triangular with lateral angles acute and posterior margin straight, auriculae as large triangular lateral projections, hypostome with apex bluntly pointed and dental formula 3/3 in the anterior third and then 2/2, coxa I with two short, sub-equal, triangular spurs, and pattern of dorsal and ventral body setae. This new species is phylogenetically related to Ixodes brunneus, Ixodes turdus and Ixodes frontalis, and the principal hosts for all its parasitic stages are birds.


Subject(s)
Ixodes/anatomy & histology , Ixodes/classification , Animals , Argentina , DNA, Ribosomal Spacer/analysis , Electron Transport Complex IV/analysis , Female , Ixodes/growth & development , Ixodes/ultrastructure , Larva/anatomy & histology , Larva/classification , Larva/growth & development , Larva/ultrastructure , Microscopy , Microscopy, Electron, Scanning , Nymph/anatomy & histology , Nymph/classification , Nymph/growth & development , Nymph/ultrastructure , Phylogeny , RNA, Ribosomal, 16S/analysis
5.
Micron ; 139: 102931, 2020 12.
Article in English | MEDLINE | ID: mdl-33007471

ABSTRACT

Human ectoparasites, including lice, have been recovered from a wide range of archaeological materials. The human head louse, Pediculus humanus capitis, has been identified from mummies and sediments for decades. Louse eggs are the body part most commonly encountered and therefore the most frequently quantified. Typically, several types of microscopy are applied for egg documentation. For studies in which quantification of infestation is a goal, counting is done with the naked eye or with the aid of handheld lenses. For determination and stage classification, stereomicroscopy is commonly used. For more detailed examination of microstructure, light microscopy, scanning electron microscopy (SEM), and confocal laser scanning microscopy (CLSM) can be employed. In most reports, researchers use two or more techniques to accomplish interrelated goals. Automontage microscopy is used to document prehistoric arthropods with good success. Herein, we report the results of a combination of SEM and automontage microscopy to document lice and eggs recovered from South American mummies. This combined approach allows for simultaneous examination of internal and external characteristics. Thirty automontage composite images of 2 adult lice and 16 eggs showed that egg internal morphologies were easily examined showing the within-egg anatomy of emergent nymphs. SEM imaging of 9 lice and 129 eggs was completed. In the case of two adults and several eggs, SEM imaging was accomplish after automontage image capture of the same specimens. This one-to-one image comparison of SEM and automontage shows that transmitted light of automontage reveals egg internal structures and details of the adult lice. SEM allows for high magnification examination of egg, nymph and adult microstructures. We conclude that automontage imaging followed by SEM results in efficient graphic documentation of rare louse specimens.


Subject(s)
Archaeology/methods , Microscopy, Electron, Scanning/methods , Microscopy/methods , Pediculus/ultrastructure , Animals , Ectoparasitic Infestations/parasitology , Female , Humans , Male , Mummies/parasitology , Nymph/ultrastructure , Ovum/ultrastructure , Pediculus/anatomy & histology
6.
J Insect Sci ; 20(4)2020 Jul 01.
Article in English | MEDLINE | ID: mdl-32809023

ABSTRACT

The male accessory glands (MAGs) in insects are pair(s) of internal reproductive organs that produce and secrete the plasma component of seminal fluid. In various insects, MAG size is important for male reproductive success because the fluid provides physiologically active substances and/or nutrients to females to control sperm as well as female reproductive behaviors. Although the MAG epithelial cells in most insect species are standard mononucleate cells, those in some insect taxa are binucleate due to incomplete cytokinesis (e.g., Drosophila [Fallén] [Diptera: Drosophilidae]) or cell fusion (e.g., Cimex [Linnaeus] [Hemiptera: Cimicidae]). In the case of Drosophila, the apicobasal position of the two nuclei relative to the epithelial plane changes from vertical to horizontal after nutrient intake, which allows the volume of the MAG cavity to expand effectively. On the other hand, in the case of Cimex, the positions of the two nuclei do not change apicobasally in response to feeding, but their position relative to the proximodistal axis varies depending on the tubular/spherical organ morphology. Here, we report that the MAG of the benthic water bug Aphelocheirus vittatus (Matsumura) (Hemiptera: Aphelochiridae) shows binucleation in all epithelial cells. Despite the phylogenetically close relationship between Aphelocheirus and Cimex, the MAG cells in Aphelocheirus showed a Drosophila-like apicobasal change in the position of the two nuclei in response to feeding. Furthermore, the cytological processes during binucleation are more similar to those in Drosophila (incomplete cytokinesis) than to those in Cimex (cell fusion). These results indicate that the physiological role and mechanism of binucleation in MAG cells changed during the evolution of Hemiptera.


Subject(s)
Hemiptera/anatomy & histology , Hemiptera/growth & development , Animals , Genitalia/anatomy & histology , Genitalia/growth & development , Genitalia/ultrastructure , Hemiptera/ultrastructure , Male , Microscopy, Confocal , Microscopy, Electron, Transmission , Nymph/anatomy & histology , Nymph/growth & development , Nymph/ultrastructure
7.
Arthropod Struct Dev ; 58: 100976, 2020 Sep.
Article in English | MEDLINE | ID: mdl-32791436

ABSTRACT

The horned gall aphid, Schlechtendalia chinensis, inhabits the productive species of Chinese gallnuts, which have economic value. Aphid wax glands are crucial for the survival of the insects, since the secreted waterproofing wax is important to protect the aphids from predators, pathogens and honeydew contamination. In this study, we investigated the structure of wax glands and their role in different aphid stages using light and electron microscopy. Our results show that aphids of all stages except the newly hatched fundatrix possess six parallel dorsal lines and have a total of 56 wax gland plates. Although no wax glands occur on the dorsum of the newly hatched fundatrix (first instar), the glands do appear once a fundatrix enters the second instar. The wax gland plate is composed of 2-22 polygonal depressions, each of which corresponds to a secretory cell covered by cuticle. The wax glands of this aphid belong to the class 1 glands, which are formed by epidermal secretory cells. The structure of the wax glands varies in the different stages and these changes may be adaptive to the changeable microenvironments in which the aphids live.


Subject(s)
Aphids/anatomy & histology , Animals , Aphids/growth & development , Aphids/ultrastructure , China , Exocrine Glands/anatomy & histology , Exocrine Glands/ultrastructure , Female , Male , Microscopy , Microscopy, Electron, Scanning , Microscopy, Electron, Transmission , Nymph/anatomy & histology , Nymph/growth & development , Nymph/ultrastructure , Waxes/metabolism
8.
Ticks Tick Borne Dis ; 11(5): 101497, 2020 09.
Article in English | MEDLINE | ID: mdl-32723643

ABSTRACT

Ornithodoros cerradoensis n. sp. is described from field-collected and laboratory reared nymphs, males, females, and larvae parasitizing the rodents Cavia aperea and Thrichomys sp. in the Brazilian Savannah. This new species is morphologically and genetically related with the Ornithodoros talaje group and can be separated from other Neotropical species using the following combination of characters: larva with 18 pairs of setae on dorsum (seven anterolateral, four central and seven posterolateral), hypostome with median dentition 2/2; adults provided with large mammillae; dorsal disks surrounded by bulked marginal ridges delimiting barely pebbled areas; three disks in the anterolateral file, and median disk not merging with the posteromedian file. Feeding assays in the laboratory demonstrated that (1) larvae of O. cerradoensis are slow-feeders (∼6 days), (2) first nymphal instar (N1) molts to second instar (N2) without feeding, and (3) N2 and third nymphal instar (N3) engorge rapidly (minutes). With the exception of Ornithodoros hasei nymphs that depict flattened bodies, O. cerradoensis N1, N2, and N3 highly resemble homologous instars of other species in O. talaje sensu lato, therefore are not suitable for morphological comparisons within the group. In addition to morphological signature of larvae and adults that separate this new species; results of cross-mating attempts between O. cerradoensis and Ornithodoros guaporensis a morphologically and phylogenetically closely related species that also parasitizes rodents in the Brazilian Savannah; a Principal Component Analysis using larval characters; and a phylogenetic analysis using mitochondrial markers, support O. cerradoensis as an independent lineage within the Ornithodorinae.


Subject(s)
Host-Parasite Interactions , Ornithodoros/classification , Rodentia/parasitology , Animals , Brazil , DNA, Ribosomal/analysis , Female , Grassland , Guinea Pigs/parasitology , Larva/growth & development , Larva/ultrastructure , Male , Microscopy, Electron, Scanning/veterinary , Nymph/growth & development , Nymph/ultrastructure , Ornithodoros/growth & development , Ornithodoros/ultrastructure , Phylogeny , RNA, Ribosomal, 16S/analysis
9.
Arthropod Struct Dev ; 58: 100952, 2020 Sep.
Article in English | MEDLINE | ID: mdl-32540512

ABSTRACT

Kissing bugs (Hemiptera: Reduviidae: Triatominae) are able to bend their rod-like maxillae while searching for blood vessels in the tissue of their vertebrate hosts. Little is known about the working mechanisms of these bending movements and the distal opening of the food channel. We compared the morphological structure of the stylets (mandibles and maxillae) of four triatomine species and analyzed the feeding process of Dipetalogaster maxima (Uhler, 1894). The maxillae of triatomine bugs are interlocked by a tongue-and-groove system, allowing longitudinal sliding. While penetrating the host tissue, the animals perform rapid alternate back and forth movements of the maxillae. The resistance of the surrounding tissue pushes the asymmetric apex of the maxillae away from its straight path, i.e., if one individual maxilla is protracted alone, its tip curves inwards, and the other maxilla follows. Once a blood vessel is tapped, the spine-like tip of the left maxilla splays outwards. Apically, each of the maxillae features an abutment, the left one exhibiting a notch that presumably facilitates splaying. The mechanical interaction of the two maxillary abutments enables the distal opening of the food channel but might also support the movements of the maxillary bundle attributable to different bending moment distributions.


Subject(s)
Triatominae/anatomy & histology , Triatominae/physiology , Animals , Feeding Behavior , Female , Male , Maxilla/anatomy & histology , Maxilla/physiology , Maxilla/ultrastructure , Mouth/anatomy & histology , Mouth/physiology , Mouth/ultrastructure , Nymph/anatomy & histology , Nymph/physiology , Nymph/ultrastructure , Panstrongylus/anatomy & histology , Panstrongylus/growth & development , Panstrongylus/physiology , Panstrongylus/ultrastructure , Rhodnius/anatomy & histology , Rhodnius/growth & development , Rhodnius/physiology , Rhodnius/ultrastructure , Species Specificity , Triatoma/anatomy & histology , Triatoma/growth & development , Triatoma/physiology , Triatoma/ultrastructure , Triatominae/growth & development , Triatominae/ultrastructure
10.
J Insect Physiol ; 123: 104052, 2020.
Article in English | MEDLINE | ID: mdl-32259526

ABSTRACT

Insect cuticular lipids are a complex cocktail of highly diverse cuticular hydrocarbons (CHCs), which form a hydrophobic surface coat to maintain water balance and to prevent desiccation and penetration of exogenous substances. Fatty acid elongases (ELOs) are key enzymes that participate in a common CHC synthesis pathway in insects. However, the importance of ELOs for CHC synthesis and function remains understudied. Using transcriptomic data, we have identified seven ELO genes (LmELO1-7) in the migratory locust Locusta migratoria. We determined their tissue-specific and temporal expression profiles in fifth instar nymphs. As we are interested in cuticle barrier formation, we performed RNA interference against LmELO7, which is mainly expressed in the integument. Suppression of LmELO7 significantly decreased its expression and caused lethality during or shortly after molting. CHC quantification by GC-MS analysis indicated that suppression of LmELO7 resulted in a decrease in total CHC amounts. By consequence, CHC deficiency reduced desiccation resistance and enhanced cuticle permeability in LmELO7-suppressed L. migratoria. Interestingly, LmELO7 expression is induced at low air humidity. Our results indicate that LmELO7 plays a vital role in the production of CHCs and, hence, cuticle permeability. Induction of LmELO7 expression in drought conditions suggests a key role of this gene in regulating desiccation resistance. This work is expected to help developing new strategies for insect pest management based on CHC function.


Subject(s)
Animal Shells/physiology , Fatty Acid Elongases/genetics , Hydrocarbons/metabolism , Insect Proteins/genetics , Locusta migratoria/physiology , Animal Shells/ultrastructure , Animals , Fatty Acid Elongases/metabolism , Female , Insect Proteins/metabolism , Locusta migratoria/genetics , Locusta migratoria/growth & development , Locusta migratoria/ultrastructure , Male , Microscopy, Electron, Transmission , Nymph/genetics , Nymph/growth & development , Nymph/physiology , Nymph/ultrastructure
11.
Ticks Tick Borne Dis ; 11(3): 101385, 2020 05.
Article in English | MEDLINE | ID: mdl-32014466

ABSTRACT

A new argasid (Argasidae) tick is herein described based on morphology and molecular data obtained from larvae parasitizing Octodon degus and from ticks collected inside burrows in northern Chile. Unfed laboratory-reared larvae were mounted in slides for morphometrical and morphological analyses. Larvae of Ornithodoros octodontus n. sp. share morphological traits with Ornithodoros quilinensis and Ornithodoros xerophylus, two species associated with rodents in the Argentinean Chaco. However, a longer hypostome with two rows of 21 and 22 denticles each one, and conspicuous leaf-shaped anal plates separate O. octodontus. While nymphal stages of O. octodontus lack cheeks and possess a micromammillated dorsal integument, adults have cheeks and exhibit markedly irregular mammillae along their dorsal surface. Phylogenetic analyses of neotropical Argasidae based on mitochondrial 16S rDNA sequences point that O. octodontus forms a monophyletic group with O. xerophylus and an unidentified Ornithodoros sp. from Bolivia, all of them associated with burrow-dweller rodents. Ornithodoros aragaoi and Ornithodoros davisi, two rare species collected once only in the Peruvian Andean Plateau during 1955 are morphologically closely related with adults and nymphs of O. octodontus. Biological observations of O. octodontus revealed autogenic females. For the moment, subgeneric classification of this new species depends on further biological studies. The fauna of ticks occurring in Chile is now represented by 22 species, 11 belonging to the Argasidae family.


Subject(s)
Octodon , Ornithodoros/classification , Rodent Diseases/parasitology , Tick Infestations/veterinary , Animals , Chile , Female , Larva/anatomy & histology , Larva/classification , Larva/growth & development , Larva/ultrastructure , Male , Microscopy, Electron, Scanning/veterinary , Nymph/anatomy & histology , Nymph/classification , Nymph/growth & development , Nymph/ultrastructure , Ornithodoros/anatomy & histology , Ornithodoros/growth & development , Ornithodoros/ultrastructure , Tick Infestations/parasitology
12.
Neotrop Entomol ; 48(6): 1046-1057, 2019 Dec.
Article in English | MEDLINE | ID: mdl-31664684

ABSTRACT

The predatory stink bugs are well known by their behavior, but the knowledge of the immature morphology and their natural history are scarce. Studies on predatory stink bugs are important to better understand their evolution and their use as biological controllers. Here, we describe the morphology of egg and the five nymphal instars of Oplomus catena (Drury, 1782), using optical and scanning electron microscopy. In general, O. catena immatures are very distinctive from other Asopinae species already studied. The egg is black, with short aero-micropylar processes and similar to those described for Stiretrus species. The nymphs can be diagnosed by the abdominal plates very large and bright blue. The color polymorphism of adults is fully illustrated, and four color patterns are proposed. The natural history of the species is described based on field and laboratory observations. The known prey of the species is reviewed and new preys are reported. The morphological and biological traits here described are discussed in order to better understand the biological role of predatory stink bugs.


Subject(s)
Color , Heteroptera/anatomy & histology , Nymph/anatomy & histology , Ovum/ultrastructure , Animals , Brazil , Female , Male , Microscopy, Electron, Scanning , Nymph/ultrastructure , Phenotype , Polymorphism, Genetic
13.
J Med Entomol ; 56(5): 1260-1269, 2019 09 03.
Article in English | MEDLINE | ID: mdl-31329909

ABSTRACT

The genus Belminus Stål, 1859 is distinguished by markedly entomophagous species. This genus is a poorly studied group of the Triatominae (Jeannel, 1919), which includes hematophagous species that are vectors of Trypanosoma cruzi (Chagas, 1909), the etiological agent of Chagas disease. This study reports for the first time the description of the antennal sensilla of Belminus corredori (Galvão & Angulo, 2003), Belminus herreri (Lent & Wygodzinsky, 1979), and Belminus ferroae (Sandoval, Pabón, Jurberg & Galvão, 2007) nymphs and adults throughout scanning electron microscopy and optical microscopy. Nine morphological types of sensilla were identified in the three species, including bristles I and II, trichobothria, tapered hairs, thin-walled trichoid, thick-walled trichoid, basiconic, campaniform, and coeloconica sensilla. The analysis of the most abundant types of sensilla and their distribution in nymphs and adults shows similarities with the antennal phenotypes described in other Triatominae. Quantitative differences showed the important phenotypic plasticity of this morphological trait in the genus and allowed for the separation of the species in both sexes. These differences were associated with sexual dimorphism and wing condition (macropterous and brachypterous). The role of the antennal phenotype in sexual behavior, its usefulness as a taxonomic tool, and its relationship with the dispersal capacity of these species are discussed.


Subject(s)
Sensilla/anatomy & histology , Triatominae/anatomy & histology , Animals , Female , Male , Microscopy , Microscopy, Electron, Scanning , Nymph/anatomy & histology , Nymph/growth & development , Nymph/ultrastructure , Phenotype , Sensilla/ultrastructure , Triatominae/growth & development , Triatominae/ultrastructure
14.
Environ Entomol ; 48(2): 410-418, 2019 04 03.
Article in English | MEDLINE | ID: mdl-30759210

ABSTRACT

The scale insect, Ericerus pela Chavannes, shows a typical sexual dimorphism. Males and females are different not only in morphology, but also in their ability to secrete wax and ecological adaptability. Here we report the morphological and structural characteristics of wax glands on E. pela females and males. The differences in wax glands and wax secretion between females and males reflect their different needs for living habitats and different ecological strategies. Sciophilous male nymphs are with five types of wax glands, and the wax glands on the dorsum secrete a layer of wax filaments plausibly for protection against direct light irradiation. On the other hand, five types of wax glands were found on the abdomen of females. Heliophilous female nymphs hardly secrete any wax, but the wax glands located along the spiracle on the abdomen may help this insect to breathe. Female adults secrete wax filaments on eggs to protect them from predators and prevent themselves from sticking to each other. In summary, males appear to secreted wax for creating a shaded niche that fits their sciophilous life style, whereas females are likely to adopt an ecological strategy with thickened epidermis for heliophilous acclimatization and overwintering.


Subject(s)
Exocrine Glands/ultrastructure , Hemiptera/physiology , Hemiptera/ultrastructure , Sex Characteristics , Waxes/metabolism , Adaptation, Biological , Animals , Biological Evolution , Female , Male , Nymph/metabolism , Nymph/ultrastructure
15.
Exp Appl Acarol ; 76(3): 413-419, 2018 Nov.
Article in English | MEDLINE | ID: mdl-30302626

ABSTRACT

A new species of co-endangered tick, Ixodes heathi n. sp., is described from specimens of the nymph collected on the critically endangered mountain pygmy possum (Burramys parvus Broom) from the alpine region of Victoria, Australia. Its biology is discussed along with strategies for its conservation.


Subject(s)
Conservation of Natural Resources , Endangered Species , Ixodes/anatomy & histology , Ixodes/classification , Life History Traits , Marsupialia/parasitology , Animals , Female , Ixodes/growth & development , Ixodes/ultrastructure , Male , Microscopy, Electron, Scanning , Nymph/anatomy & histology , Nymph/classification , Nymph/growth & development , Nymph/ultrastructure , Victoria
16.
Arthropod Struct Dev ; 47(5): 529-541, 2018 Sep.
Article in English | MEDLINE | ID: mdl-29885492

ABSTRACT

Pharate 1st instar nymphs enclosed in the embryonic cuticle, referred to as pronymphs, were studied in a froghopper Aphrophora pectoralis Mats. (Aphrophoridae) and the leafhoppers Oncopsis flavicollis (L.), Populicerus populi (L.), Alebra wahlbergi (Boh.), Igutettix oculatus (Lindb.), and Scenergates viridis (Vilb.) (Cicadellidae). The species vary in the relative length of the pronymphal antennae and details of sculpturing of the cephalic region. No egg bursting structures were observed, except small denticles on the crown region of S. viridis pronymphs. Rudimentary mandibular and maxillary stylets of a pronymph are external, short, tubular appendages containing tips of the corresponding nymphal stylets, whose more basal parts develop inside of the head. Casting off of the embryonic cuticle results in the nymphal stylets being passively pulled out and assuming a close-set parallel orientation. Once the sheaths of unsclerotized cuticle secreted by the peripodial epithelium and enveloping each developing stylet have been cast off with the exuviae, the bare stylets become squeezed and interlocked into a functional bundle. The roles of the maxillary plates, clypeus, labrum, and labium in the stylet bundle assembly are discussed. The process repeats after each molt.


Subject(s)
Hemiptera/growth & development , Animals , Hemiptera/anatomy & histology , Hemiptera/ultrastructure , Metamorphosis, Biological , Microscopy, Electron, Scanning , Nymph/growth & development , Nymph/ultrastructure , Pupa/growth & development , Pupa/ultrastructure
17.
Zhongguo Xue Xi Chong Bing Fang Zhi Za Zhi ; 31(5): 513-515, 2018 Aug 29.
Article in Chinese | MEDLINE | ID: mdl-31713381

ABSTRACT

OBJECTIVE: To observe the morphological characteristics of live Carpoglyphus lactis at different stages of life cycle and its ultrastructure. METHODS: The live C. lactis specimens were isolated from longan pulp, and firstly rinsed with double distilled water under a light microscope to make slide preparation by the conventional manner, and then were made into scanning electron microscope (SEM) specimens. The specimens were observed under SEM for the ultrastructure characteristics at different developmental stages including egg, larva, nymph and adult (male and female) . RESULTS: The SEM photographs showed that the egg was oval and milky. The larva had three pairs of legs, without genital setae, preanal seta and coxal rod, and there was no trace of genital growth. The nymph had four pairs of legs, genital seta and preanal seta, whereas the genital area was looked still under-developed. The male adult had a conical gnathosoma and a pair of external verticals which were longest setae at the dorsal idiosoma, whereas the other dorsal setae were all short rhabdoid. At the ventral idiosoma, there was an aedoeagus which was like a bent cube, and the top was straight forward. The external sacral setae and post anal were longest setae. The female adult's genital plates were a composite of plastron and cutex inner root, covering the genital tract, and a hole of anus and a pair of anal setae were located at posterior of idiosoma. CONCLUSIONS: The morphological characteristics and ultra-structure of C. lactis at different stages of life cycle can be vividly observed under SEM, which provides the morphological bases for further study of the relation between parasitism and disease.


Subject(s)
Acaridae , Microscopy, Electron, Scanning , Acaridae/ultrastructure , Animals , Female , Larva/ultrastructure , Male , Nymph/ultrastructure , Ovum/ultrastructure
18.
Arthropod Struct Dev ; 46(6): 777-787, 2017 Nov.
Article in English | MEDLINE | ID: mdl-29042213

ABSTRACT

Trombidiform mites are characterized by the presence of several paired glands in the anterior body portion united by a common conducting duct (podocephalic canal). Apart from the acinous (salivary) glands the podocephalic system includes a pair of tubular coxal glands (CGs) responsible for osmoregulation. The aim of the present study was to figure out how functional changes of acinous glands reflect on the corresponding CG. For this purpose, the anatomy and fine structure of the CG were analyzed in two mite species, Bakericheyla chanayi and Ornithocheyletia sp. (Cheyletidae), which have a different composition of their single acinous gland. The results showed that in both species the CG lacks a filtering saccule. It is composed of the proximal and distal tubes and leads into a cuticle-lined excretory duct. Both tubes demonstrate a similar species-specific fine structure. They are characterized by an extensive system of apical membrane invaginations (internal canals) associated with numerous large mitochondria. Local areas of modified internal canals were regularly observed in both species. They contain structures resembling those constituting filtering slit diaphragms of other animals. In O. sp., CG cells in addition demonstrate features characteristic of protein-like secretion. Apparently this correlates with the loss of true salivary glands in this species, as its acinous gland was previously assumed as silk producing. Contrary to this, the CG of B. chanayi shows no kind of granulation, which coincides with the presence of a salivary portion in its complex acinous gland. The microtubule-rich intercalary cells at the base of the excretory duct were associated with special muscles presumably regulating the dilation of the duct lumen. These cells might represent a basic feature common to different types of podocephalic glands.


Subject(s)
Mites/ultrastructure , Animals , Exocrine Glands/ultrastructure , Extremities , Female , Finches/parasitology , Host-Parasite Interactions , Male , Microscopy, Electron, Transmission , Mites/growth & development , Nymph/growth & development , Nymph/ultrastructure , Russia , Songbirds/parasitology
19.
Exp Appl Acarol ; 72(4): 339-365, 2017 Aug.
Article in English | MEDLINE | ID: mdl-28852943

ABSTRACT

Stylostomes (feeding tubes) of Hirsutiella zachvatkini (Schluger) (Trombiculidae), feeding on bank voles [Myodes glareolus (Schreber)], and of Trombidium holosericeum (L.) (Trombidiidae), feeding on larvae of Stenodemini sp. (Heteroptera, Miridae), were studied by TEM methods and on semi-thin sections. The stylostome of H. zachvatkini is a homogeneous structure of low electron density and without strict margins. It extends within the concave host epidermis, undergoing hyperplasia and hyperkeratosis. TEM does not reveal any obvious stratification in the stylostome walls. The cheliceral movable digits are moved apart by 5-6 µm and tightly applied/adhered to the stylostome substance. A local area beneath the open end of the stylostome canal is not empty but contains a nearly homogeneous substrate, which can pass into the central stylostome canal. The latter is mostly free of contents. In contrast to H. zachvatkini, larvae of T. holosericeum form a root-like stylostome chaotically branching within the clear space underneath the host cuticle free of tissue elements. Tubules of the distal stylostome branches become progressively thinner and disappear blindly. As in H. zachvatkini, the stylostome walls of T. holosericeum are devoid of stratification but show moderate to high electron density. The cheliceral movable digits are moved apart by the same distance, as in H. zachvatkini, and tightly applied to the stylostome substance. The lumen of the central canal is either electron lucent, in the distal portions, or filled with a fine granular or homogeneous substrate of low electron density in the proximal portions forming a type of ampoule. This study shows that Trombiculidae and Trombidiidae share similar initial stages of stylostome formation but the resultant stylostome of each family is distinctly different.


Subject(s)
Arvicolinae/parasitology , Heteroptera/parasitology , Mites/ultrastructure , Animals , Heteroptera/growth & development , Host-Parasite Interactions , Larva/growth & development , Larva/physiology , Larva/ultrastructure , Microscopy, Electron, Transmission , Mites/growth & development , Mites/physiology , Nymph/growth & development , Nymph/physiology , Nymph/ultrastructure , Species Specificity , Trombiculidae/growth & development , Trombiculidae/physiology , Trombiculidae/ultrastructure
20.
J Econ Entomol ; 110(3): 1179-1186, 2017 06 01.
Article in English | MEDLINE | ID: mdl-28334370

ABSTRACT

The climbing abilities of two bed bug species, Cimex lectularius L. and Cimex hemipterus (F.), were determined by evaluating their escape rates from smooth surface pitfall traps using four commercial bed bug monitors (Verifi Bed Bug Detector, ClimbUp Insect Interceptor, BlackOut Bed Bug Detector, and SenSci Volcano Bed Bug Detector). All detectors were used in the absence of lures or attractants. Unlike C. lectularius, adult C. hemipterus were able to escape from all traps. On the other hand, no or a low number nymphs of both species escaped, depending on the evaluated traps. Examination of the vertical friction force of adults of both species revealed a higher vertical friction force in C. hemipterus than in C. lectularius. Scanning electron microscope micrograph observation on the tibial pad of adult bed bugs of C. hemipterus showed the presence of a greater number of tenent hairs on the tibial pad than on that of adult C. lectularius. No tibial pad was found on the fourth and fifth instars of both species. Near the base of the hollow tenent hairs is a glandular epithelium that is better developed in adult C. hemipterus than in adult C. lectularius. This study highlights significant morphological differences between C. lectularius and C. hemipterus, which may have implications in the monitoring and management of bed bug infestations.


Subject(s)
Bedbugs/physiology , Insect Control , Animals , Bedbugs/anatomy & histology , Bedbugs/growth & development , Bedbugs/ultrastructure , Biomechanical Phenomena , Extremities/anatomy & histology , Female , Male , Microscopy, Electron, Scanning , Motor Activity , Nymph/anatomy & histology , Nymph/growth & development , Nymph/physiology , Nymph/ultrastructure , Species Specificity
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