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256 results for “sensilla”
Fig. 8 in Antennal sensillum morphology and electrophysiological responses of olfactory receptor neurons in trichoid sensilla of the diamondback moth (Lepidoptera: Plutellidae)
Fig. 8. Traces of the response spikes of the olfactory receptor neurons (ORNs) in class A trichoid sensilla of female Plutella xylostella in response to various green leaf volatiles. Each trace shows the extracellular signals for a period of 5 s. The scale bar indicates the stimulation for 0.1 s with corresponding test stimulus.
Fig. 9 in Antennal sensillum morphology and electrophysiological responses of olfactory receptor neurons in trichoid sensilla of the diamondback moth (Lepidoptera: Plutellidae)
Fig. 9. Traces of the response spikes of the olfactory receptor neurons (ORNs) in class D trichoid sensilla of female Plutella xylostella in response to geraniol and (±)-linalool. Each trace shows the extracellular signals for a period of 5 s. The scale bar indicates the stimulation for 0.1 s with corresponding test stimulus.
Fig. 1 in Antennal sensillum morphology and electrophysiological responses of olfactory receptor neurons in trichoid sensilla of the diamondback moth (Lepidoptera: Plutellidae)
Fig. 1. The length (triangles) and diam (squares) of each flagellar subsegment of the antennae of female (A) and male (B) diamondback moth, Plutella xylostella. Data obtained from 3 females and 5 males.
Fig. 5 in Antennal sensillum morphology and electrophysiological responses of olfactory receptor neurons in trichoid sensilla of the diamondback moth (Lepidoptera: Plutellidae)
Fig. 5. Detailed surface morphology of the sensilla trichodea (A, B, C and D) and sensilla chaetica (A, B and E) of the antennae of Plutela xylostella.
Figure 4 in Antennal sensilla of two species of Gymnetis MacLeay, 1819 (Coleoptera: Scarabaeidae: Cetoniinae)
Figure 4 Gymnetis holosericea, female, antenna. Distal lamella, outer and inner sides (A, B), medial lamella, outer and inner sides (C, D), proximal lamella, outer and inner sides (E, F). White dotted line showing the posterior homogeneous area, black dotted line showing the anterior heterogeneous area. Sensilla chaetica (Ch), sensilla trichodea (T). Scale = 200 µm.
Figure 6 in Antennal sensilla of two species of Gymnetis MacLeay, 1819 (Coleoptera: Scarabaeidae: Cetoniinae)
Figure 6 Gymnetis rufilateris, female antenna.Distal lamella, outer and inner sides (A, B), medial lamella, outer and inner sides (C, D), proximal lamella, outer and inner sides (E, F). White dotted line showing the posterior homogeneous area, black dotted line showing the anterior heterogeneous area. Scale = 200 µm.
Figure 1 A-E in Setae and sensilla in the Iberian Myrmeleon Linnaeus, 1767 larvae (Insecta, Neuroptera: Myrmeleontidae)
Figure 1 A-E. SEM images of Iberian Myrmeleon larvae. A: Myrmeleon hyalinus: complete body, lateral view. B: M. formicarius: complete body, ventral view. C: M. hyalinus: head setae, dorsal view. D: M. almohadarum: thoracic setae, dorsal view. E:M. gerlindae: abdominal setae, dorsal view.Abbreviations: ant: antenna; brst: bristles; digs: digging setae; grs: sensilla placodea; inb: inner jaws bristles; lp: labial palp; op: odontoid process; ph: plumose hairs; sb: sensilla basiconica; sco: sensilla coeloconica; st: sensilla trichodea; stmt: stemmata; Tsp: thoracic setiferous process.
Figure 7 in Sensilla of the Western Flower Thrips, Frankliniella occidentalis (Pergande) (Thysanoptera, Thripidae)
Figure 7 Types of sensilla in Frankliniella occidentalis tail: (A) short sensilla trichodea (SST), (B) long sensilla basiconica (L-SB), (C,E) long sensilla chaetica (LSC), (D,F), short sensilla chaetica (ShSC).
Figure 6 in Sensilla of the Western Flower Thrips, Frankliniella occidentalis (Pergande) (Thysanoptera, Thripidae)
Figure 6 Types of sensilla in Frankliniella occidentalis wings: (A) long sensilla chaetica (LSC), (B) sensilla trichodea (ST), (C) long sensilla basiconica (LSB).
Figure 5 in Sensilla of the Western Flower Thrips, Frankliniella occidentalis (Pergande) (Thysanoptera, Thripidae)
Figure 5 Types of sensilla in Frankliniella occidentalis mouthparts: (A) short sensilla trichodea (SST), (B) long sensilla basiconica (LSB), (C) finger sensilla basiconica (FiSB), (D) long sensilla basiconica (L-SB), (E) sensilla ear washing buob-shaped (SEWB), and (F) sensilla mamillary (SM).
Figure 2 in Sensilla of the Western Flower Thrips, Frankliniella occidentalis (Pergande) (Thysanoptera, Thripidae)
Figure 2 Types of sensilla in Frankliniella occidentalis antennae: (A) finger sensilla basiconica (FSB), (B) angle sensilla basiconica (ASB), (C) long sensilla basiconica (LSB), (D) sensilla mamillary (SM), (E) trichodea sensilla (TSB) and (F) fork sensilla basiconica (FOSB).
Figure 1 in Identification and description of the antennal sensilla of Liogenys suturalis (Coleoptera: Scarabaeidae)
Figure 1 Proximal lamella of Liogenys suturalis. A) Outer (proximal) side, female. B) Outer side, detail of sensilla trichodea, female; C) Inner (distal) side, female. D) Inner (distal) side, male. E) Inner side, groove detail, female. F) Inner side, detail of sensilla coeloconica I, female. G) Inner side, groove detail with several sensilla auricilica, male.
Figure 3 in Identification and description of the antennal sensilla of Liogenys suturalis (Coleoptera: Scarabaeidae)
Figure 3 Distal lamella of Liogenys suturalis. A–B) Inner (proximal) side, female (rigth) and male (left). C–D) Outer (distal) side, female (rigth) and male (left). E) Outer side, surface detail, female. F) Inner side, sensilla detail, male. Black dotted line showing posterior area (ventral area when antennae distended) with sensilla placodea, s. coeloconica, and s. auricilica; otherwise the anterior area (dorsal area when antennae distended) has a reticulated surface with some s. trichodea. au, sensilla auricilica; c1, s. coeloconica I; c2, s. coeloconica II; p1, s. placodea I; p2, s. placodea II.
Fig. 3 in Ultrastructure of the antennal sensilla of Alabama argillacea (Hübner, 1823) (Lepidoptera: Erebidae)
Fig. 3. Photomicrographs of Alabama argillacea antennal (A and B) sensilla coeloconica, (C and D) sensilla auricillica, and (E and F) sensilla styloconica. (A) Three close s. coeloconica; (B) s. coeloconica details, showing spines around a coniform structure in the center; (C) s. auricillica with more open side edges; (D) s. auricillica with more closed side edges in the center; (E) s. styloconica seen laterally; (F) s. styloconica showing two coniform structures in the apical extremity. Abbreviations: S co, s. coeloconica; S Aur, s. auricillica; S Sty, s. styloconica.
Figure 5. Sensilla basiconica type 1 in Sexual dimorphism in antennal sensilla of Parthenium beetle Zygogramma bicolorata
Figure 5. Sensilla basiconica type 1 (SB1) (a); sensilla basiconica type 2 (SB2) (b); magnified view of the tip of SB-2 (c) in Z. bicolorata.
Figure 2 in Sexual dimorphism in antennal sensilla of Parthenium beetle Zygogramma bicolorata
Figure 2. Sensilla trichodea (ST1, ST2), sensilla chaetica (SCh), and sensilla basiconica (SB1 and SB2) of Z. bicolorata.
Figure 1 in Sexual dimorphism in antennal sensilla of Parthenium beetle Zygogramma bicolorata
Figure 1. Whole view of antenna in Zygogramma bicolorata (11 antennomeres). Sc - scape, P - pedicel, F - flagellomere.
Confirmation of Basitarsal Compound Slit Sensilla (BCSS) in scorpion genera Chaerilus and Scorpiops (Arachnida: Scorpiones)
<p><span>Basitarsal Compound Slit Sensilla (BCSS) are a cluster of mechanosensory structures, collectively composed of striated, curved, successive slits located at the prodistal end of basitarsus, forming into a fan-shaped configuration. It can efficiently detect and amplify substrate-borne micro-vibrational signals at a certain frequency range which cause slit deformation (Wang et al., 2019), being most sensitive to surface Rayleigh waves and crucial for locating the vibration source (but requires sensilla on multiple legs) (Brownwell & Farley, 1979). This structure, to my knowledge, has only been formally reported in three species, <em>Androctonus australis </em>(Linnaeus, 1758), <em>Heterometrus silenus</em> (Simon, 1884) and <em>Smeringurus mesaensis </em>(Stahnke, 1957) (Barth & Wadepuhl, 1975; Brownwell & Farley, 1979; Wang et al., 2019). The present work constitutes an informal observation (out of curiosity) of BCSS across 3 genera, confirming its presence (with different forms) in two of those genera.</span></p> <p><span>BCSS was confidently confirmed in all <em>Scorpiops</em> and <em>Chaerilus</em> species examined (see figures on subsequent pages). There appeared to be some interspecific differences (e.g., the proximal boundary that delineates the sensillar area) within the same genus, but I have not confirmed if those differences are stable and non-overlapping (i.e., diagnostic). Sensilla are closely associated with specific ecological adaptions which shape their phenotypic configurations. One of the most famous sensilla in scorpions is the trichobothrium, which serves as an important diagnostic character for many distinct lineages. Similarly, the constellation array on the externodistal surface of pedipalp fixed finger was also found to be diagnostic in some vaejovids. It is interesting to note the different configurations of slit sensilla between genera <em>Scorpiops</em> and <em>Chaerilus</em>, where in <em>Chaerilus</em> a long, accessory slit sensillum was always present external to the main sensillar area (on or near its boundary). Occasionally, several short striations (sensilla?) were also observed on the joint tubercle between the basi- and telotarsi. Unfortunately, due to the magnification constraint: I was not able to examine genera <em>Langxie</em> and <em>Qianxie</em> (both with highly slender basitarsi); I was not able to confidently identify the striation in genus <em>Olivierus</em> albeit observing a similar depression at the same location (BCSS of the much smaller species of <em>Scorpiops</em> (<em>S. jendeki</em> and <em>S. kovariki</em>) and <em>Chaerilus</em> were even more conspicuous).</span></p>
Figure 7 in Morphology of the antennal sensilla of two species of Hoplopyga Thomson, 1880 (Coleoptera, Scarabaeidae, Cetoniinae)
Figure 7 Hoplopyga albiventris, antenna female (left: A, C, E, G, I) and male (right: B, D, F, H, J). (dl) distal lamella; (ex) outer side; (in) inner side; (md) medial lamella; (pl) proximal lamella. Scale = A, C, E, F, I, J: 100 Μm; B, D, G, H: 200 Μm.
Figure 2 in Morphology of the antennal sensilla of two species of Hoplopyga Thomson, 1880 (Coleoptera, Scarabaeidae, Cetoniinae)
Figure 2 Hoplopyga liturata, antennal lamella of female (left:A, C, E, G,I) and male (right: B, D, F, H, J). (dl) distal lamella; (ex) outer side; (in) inner side; (md) medial lamella; (pl) proximal lamella. Scale = A, B, C, D, E, F, J: 100 Μm; G, H, I: 200 Μm.
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