Antennular sensilla of the brine shrimp, Artemia salina.

1. Scanning electron microscopy was used to characterize the external morphology of setae found on the antennules of adults and nauplii of the brine shrimp, Artemia salina (L.). The permeability of the antennular setae was studied by means of Slifer's crystal violet method. 2. Each antennule of an adult brine shrimp possessed a terminal cluster of sensory setae. Within a cluster there were two morphologically distinct kinds of sensilla, here designated type 1 and type 2. Three type 1 sensilla were observed on every antennule examined. The number of type 2 sensilla per antennule was usually four or five. 3. Type 1 sensilla of adults were 43 to 80 micrometer long and simple in external morphology. They were widest at the base, decreased in diameter gradually, and terminated as a finely tapered tip. No pores were resolved by scanning electron microscopy. 4. Type 2 sensilla of adults were shorter (shaft length, 12 to 23 micrometer) and displayed a single pore at the tip (average pore diameter, 0.4 micrometer). In thin section they were seen to possess a distinctive articular specialization of the cuticle at the base of the seta. 5. Dye penetration experiments indicated that type 2 sensilla were permeable to aqueous crystal violet, whereas type 1 sensilla were not. 6. The antennular setae of nauplii resembled type 1 sensilla in general shape, in being impermeable to crystal violet, and in lacking a terminal pore and basal articular specialization. Moreover, a total of three setae was normally present on each naupliar antennule, and the same number of type 1 sensilla was found on each adult antennule examined. If the three naupliar setae represent a developmental stage in the formation of three adult sensilla, available observations suggest that the larval setae are developmentally related to type 1, rather than to type 2 adult sensilla.     

Ultrastructure and functional organization of mouthpart sensory setae of the spiny lobster Panulirus argus: new features of putative mechanoreceptors

In comparison with other decapods, the Caribbean spiny lobster Panulirus argus has little diversity in the external morphology of the setae on the mouth apparatus. In mouthpart areas that frequently touch food items only two types of setae can be distinguished: simple setae and cuspidate setae. Simple setae are by far more numerous. The ultrastructural data presented here show that both types of seta are bimodal, in that they both contain mechano- and chemosensory cells as indicated by morphological features. The morphological features divide the sensory cells into three types: type 1, which has a mechanosensory appearance; type 2, which has a chemosensory appearance; and type 3, which is believed to be a mechanoreceptor due to desmosomal connections to a scolopale. All three cell types were found in all examined setae. In an earlier study the simple setae were found to contain two types of mechanosensors: bend-sensitive cells and displacement-sensitive cells. The morphological arrangement of the outer dendritic segment described in the present study cannot explain this division. Instead, it is suggested that the difference in sensitivity is caused by a differential arrangement of their stretch-sensitive ion channels. This hypothesis also provides an explanation for the earlier observation that only bend cells respond to changes in osmolarity.     

The pedipalp of Pseudocellus pearsei (Ricinulei, Arachnida) - ultrastructure of a multifunctional organ

Ricinulei possess movable, slender pedipalps with small chelae. When ricinuleids walk, they occasionally touch the soil surface with the tips of their pedipalps. This behavior is similar to the exploration movements they perform with their elongated second legs. We studied the distal areas of the pedipalps of the cavernicolous Mexican species Pseudocellus pearsei with scanning and transmission electron microscopy. Five different surface structures are characteristic for the pedipalps: (1) slender sigmoidal setae with smooth shafts resembling gustatory terminal pore single-walled (tp-sw) sensilla; (2) conspicuous long, mechanoreceptive slit sensilla; (3) a single, short, clubbed seta inside a deep pit representing a no pore single walled (np-sw) sensillum; (4) a single pore organ containing one olfactory wall pore single-walled (wp-sw) sensillum; and (5) gustatory terminal pore sensilla in the fingers of the pedipalp chela. Additionally, the pedipalps bear sensilla which also occur on the other appendages. With this sensory equipment, the pedipalps are highly effective multimodal short range sensory organs which complement the long range sensory function of the second legs. In order to present the complete sensory equipment of all appendages of the investigated Pseudocellus a comparative overview is provided.     

Morphology and distribution of antennal sensilla of the tarnished plant bug,Lygus lineolaris (Palisot de beauvois) (Hemiptera: Miridae)

Sensilla on the antennae of adult and last-instar nymphs of the tarnished plant bug, Lygus lineolaris (Hemiptera: Miridae), were examined with light, scanning and transmission electron microscopy. Six different types were identified in adult females and males and 5 types in last-instar nymphs: types 1 and 4 are sensilla trichodea, 2 and 3 are sensilla chaetica, and 5 and 6 are sensilla basiconica. Type 1 are located at distal region of terminal segment and type 2 are located at distal regions of proximal 3 segments in both adults and nymphs. Type 3 is present on all segments, more numerous on scape and pedicel and less abundant on distal third and fourth segments in both adult and nymphal stages. Types 4 and 6 are absent on the scape and present on the distal 3 antennal segments in adults, but they are present only on the distal-most antennal segment in nymphs. Type 5 sensilla are present only on second antennal segments in adults and are absent in nymphs. Sexual dimorphism is observed in total numbers: there are significantly more type(s) 3, 4, 5 and 6 sensilla in adult males than adult females. Types 1, 4 and 5 are multiporous with thin cuticle, branched dendrites and pore tubules which suggests an olfactory function. These sensilla have 3, 3 and 2 neurons, respectively. The type 6 sensillum has an apical pore and pores in the cuticular wall, and is innervated by 5 nerve cells with unbranched dendrites. Sensillar types 2 and 3 have thick cuticle, a single apical pore and nerve cells with unbranched dendrites. Type 2 has 1 neuron and type 3 has 2 chambers and 2 nerve cells.     

Show me your tenent setae and I tell you who you are – Telling the story of a neglected character complex with phylogenetic signals using Leiodidae (Coleoptera) as a case study

The tarsal setae in 97 species of Leiodidae and eight outgroups were examined using SEM imaging and dissections. Modified adhesive setae present in males are referred to as “male tenent setae” (MTS). In most cases, dilated tarsomeres were associated with MTS, which were always present on the protarsi and sometimes the mesotarsi. MTS are reported for the first time on the mesotarsi of Leptodirini and on the metatarsi in two genera of Sogdini. Contrary to reports in the literature, the reduction in the number of the MTS bearing mesotarsomeres is considered a derived condition. Both sexes of Leptinus (Platypsyllinae) have modified setae (referred to as tenent setae in the literature), probably related to their specialised association with mammals, and a patch of MTS was recognized for the first time among those modified setae among males. Four main types of MTS are recognised: (1) a plesiomorphic discoidal type that has a shaft with a round cross-section and maintains a similar diameter throughout its length until forming the expanded discoidal terminal plate; (2) a minidiscoidal type, similar to discoidal but with a relatively small terminal plate, found in Cholevinae; (3) a conical type, present in Leiodinae (excluding Estadiini) where the shaft increases in diameter until forming the terminal plate; and (4) a spatulate type, where an even wider terminal plate has a lateral projection, derived from the conical form and synapomorphic for the leiodine tribes Pseudoliodini, Scotocryptini, and possibly Agathidiini.     

The modality of the dominance signal in snapping shrimp (Alpheus heterochaelis) and the corresponding setal types on the antennules

Previous behavioural experiments showed that snapping shrimp lacking lateral antennular filaments, i.e. without chemosensory aesthetascs, lose the ability to distinguish between conspecifics that are inexperienced in fighting and former winners. A chemosensory dominance signal was assumed to be present, although other receptors unique to the lateral filaments may have been responsible for the behavioural changes. In the present study, the antennules of snapping shrimp were examined for differences between the lateral and medial antennule filaments to identify the modality of the dominance signal. We found six different types of setae and two types of pores. A new probably bimodal setal type is described, the broad long simple seta. Only the chemosensory aesthetascs and their associated hydrosensory companion setae are unique to the lateral filament. Thus we conclude that the dominance signal is chemical, because a hydrodynamic signal would be also received by the simple setae distributed on both filaments.     

The modality of the dominance signal in snapping shrimp (Alpheus heterochaelis) and the corresponding setal types on the antennules

Previous behavioural experiments showed that snapping shrimp lacking lateral antennular filaments, i.e. without chemosensory aesthetascs, lose the ability to distinguish between conspecifics that are inexperienced in fighting and former winners. A chemosensory dominance signal was assumed to be present, although other receptors unique to the lateral filaments may have been responsible for the behavioural changes. In the present study, the antennules of snapping shrimp were examined for differences between the lateral and medial antennule filaments to identify the modality of the dominance signal. We found six different types of setae and two types of pores. A new probably bimodal setal type is described, the broad long simple seta. Only the chemosensory aesthetascs and their associated hydrosensory companion setae are unique to the lateral filament. Thus we conclude that the dominance signal is chemical, because a hydrodynamic signal would be also received by the simple setae distributed on both filaments.     

Ultrastructure of tarsal sensilla and other integument structures of two Pseudocellus species (Ricinulei, Arachnida)

Ricinuleids are one of the least investigated groups of Arachnida. In particular, knowledge of their ultrastructure is poor. Observations of the distal tarsomeres of ricinuleids show differences in their shape and equipment of surface structures. Legs I and II are used by the Ricinulei to explore their surroundings with tentative movements. The tarsomeres of these legs show similarities in shape and surface structures that distinguish them from those of legs III and IV. In this study, 11 different structures of the tarsomere surfaces of two cave-dwelling species, Pseudocellus pearsei and P. boneti from México, were investigated for the first time with scanning and transmission electron microscopy and discussed regarding their possible function: 1) a single treelike ramifying seta resembles a no pore single-walled (np-sw) sensillum; 2) setae occurring in a small number and possessing a bipartite shaft represent terminal pore single-walled (tp-sw) sensilla. The surface of the proximal half of the shaft shows small branches. The distal half has a smooth surface; 3) long setae with conspicuous longitudinal lamellae show characteristics of chemoreceptive wall pore single-walled (wp-sw) sensilla; 4) frequent small wp-sw sensilla with flat and irregular lamellae; 5) very short wp-sw sensilla occurring solitary or in groups; 6) a few short setae with smooth surface correspond to wp-sw sensilla; 7) a single short clubbed seta articulating in a flat pit is considered to be a np-sw sensillum; 8) common long setae with a pointed tip show characteristics of mechanoreceptive np-sw sensilla; 9) ventral setae with adhesive and mechanosensory function are accompanied by multicellular "class III" glands; 10) slit organs with mechanoreceptive function; and 11) dome-like tubercles with no indication of sensorial function. Several of these sensilla form a sensory field on the dorsofrontal surface which is particularly pronounced on the distal tarsomeres of legs I and II.     

Morphology and distribution of setae on the antennules of the Caribbean spiny lobster Panulirus argus reveal new types of bimodal chemo-mechanosensilla

This study describes the morphology and distribution of setae on the lateral and medial flagella of the antennules of the spiny lobster Panulirus argus in an effort to identify antennular chemoreceptors in addition to the well-studied aesthetasc chemosensilla. Setae were examined using light and electron microscopy, and their distribution on flagellar annuli was analyzed. We identified ten setal types based on external morphology: hooded, plumose, short setuled, long simple, medium simple, short simple, aesthetasc, guard, companion, and asymmetric setae, with the last four types being unique to the "tuft" located on the distal half of the lateral flagellum. The three setal types whose ultrastructure was examined--hooded, long simple, and medium simple setae--had characteristics of bimodal (chemo-mechanoreceptive) sensilla. The antennules have four distinct annular types based on their setal complement, as shown by cluster analysis. This basic distribution of non-tuft setal types is similar for both lateral and medial flagella. Annuli in the tuft region have tuft setal types superimposed on a basic organization of non-tuft setal types. These results show that the antennules possess a diverse set of setae, that these setae have a highly ordered arrangement on the antennules, that at least four (and probably many more) of these setal types are chemosensilla, and suggest that most antennular chemosensilla are bimodally sensitive.     

Mechanical functions of setae from the mouth apparatus of seven species of decapod crustaceans

The mouthpart setae of seven species of decapods were examined with macro-video recordings and scanning electron microscopy. The general mechanical (nonsensory) functions of the different mouthparts are described and an account of their setation is given. This offers the possibility to determine the mechanical functions of the different types of setae. Pappose setae do not participate in food handling but in general make setal barriers. Plumose setae likewise do not contact food objects but assist in current generation. Papposerrate setae are rare but they were seen to assist in pushing food particles into the mouth. Serrulate setae are very common and mainly participate in gentle food handling and grooming. Serrate setae are used for more rough food manipulation and grooming. The roughest shredding, tearing, and manipulation of prey items are handled by the cuspidate setae. Simple setae seem to be divided into two populations with very different functions. On the maxillipeds of Panulirus argus they are used for shredding, tearing, and holding the food objects, but on the basis of maxilla 2 of three other species they appear to have very little mechanical influence and only when handling small prey items. The functional scheme seems to be consistent within the Decapoda.     

Cytology of various antennal setae in a troglobitic Mysidacea (Crustacea)

Summary The various antennal setae can be differentiated from each other by the number and the type of their dendrites and by the cuticular structure of their external parts; these features correspond to functional differences. Moreover, the work revealed differences in relation to the corresponding setae of a marine Mysidacea previously studied by Guse (1978). Various hypotheses linking the ultrastructural differences to those that characterize the environments in which these two species live can be put forward.Abbreviations A1, A3 simple setae A1, A3 - An antenna - B1, B2 setulate setae B1, B2 - Bi bifid seta - bp bending plane - c1, c2, c3 type 1, 2, or 3 cilia (outer dendritic segments) - cu cuticle - d1, d2, d3 type 1, 2, or 3 dendrites (inner dendritic segments) - ec enveloping cell - g Golgi apparatus - h helically arranged cuticle - md microtubule doublet - n nucleus - p apical pore - r ciliary root - s setules - sc scolopale - scc scolopale cell - Si sickle-shaped seta - sm small seta - st stopper - t extracellular matter tube     

Ultrastructure of sensory cells on the mantle tentacles of the gastropod Notoacmea scutum

Previous studies have indicated that the mantle margin of the gastropod mollusc Notoacmea scutum is sensitive to chemical, photic, and mechanical stimulation. Here, the ultrastructure of sensory cells on the mantle tentacles of N. scutum is examined by transmission electron microscopy to determine if morphological types of sensory cells can be correlated with known sensory capabilities. The sensory cells of the mantle tentacles are found to be ciliated, primary receptors with subepithelial nuclei. The ciliated sensory endings are concentrated at the tip of the tentacles, but also occur in smaller numbers along the shaft. Ultrastructural differences between cilia form the basis of distinguishing two types of sensory ending. Type 1 sensory endings, which are over 90% of the endings, bar unusual cilia that typically are filled with an electron-dense material. Type 2 sensory endings bear cilia that have a 9 + 2 arrangement of longitudinal elements and thus more closely resemble previously reported sensory cilia of molluscs.     

Morphology and distribution of antennular setae of scyllarid lobsters (Scyllarides aequinoctialis, S. latus, and S. nodifer) with comments on their possible function

Abstract. Lateral flagella of the antennules of scyllarid lobsters were examined for setal morphology and distribution via scanning electron microscopy. Setal distribution patterns were mapped directly for 3 regions of the antennule ( base, tuft , and tip ) and analyzed for differences: (1) between left and right antennules, (2) between males and females within a species, and (3) among species by comparing counts of setae per annulus in the ventral tuft region only. Six types of antennular setae were identified based on their external morphology: aesthetases, simple, modified simple, asymmetric, hemi-plumose, and toothbrush setae. These different types were organized in a clear pattern over the ventral and dorsal surfaces of the lateral flagella of the antennule. Aesthetase, asymmetric, modified simple, and hemi-plumose setae were found only on annuli in the tuft region between the distal and proximal ends of the flagellum. Simple setae were found on all annuli of all regions of the antennule, and toothbrush setae were mainly concentrated on all annuli of the base region and on proximal annuli of the tuft region . All species of scyllarids examined had the same general pattern of setal distribution and no differences were found between left and right, or male and female antennules. Similar setae located on the lateral antennules of species from the families Nephrophidae and Palinuridae (clawed and spiny lobsters) have been previously described as chemo- and/or mechanoreceptive for use in distance chemoreception (i.e., detection and orientation to olfactory stimuli). Based on work on clawed and spiny lobsters, we predict that the aesthetases on slipper lobsters have a chemoreceptive function and that simple and toothbrush setae may have a bimodal chemo- and mechanoreceptive function.     

Seasonal dynamics of Callibaetis willineri (Ephemeroptera, Baetidae) associated with Eichhornia azurea (Pontedericeae) in Guaraná Lake of the Upper Paraná River, Brazil

The micro-anatomy of the cephalon is described in the troglobic asellotan isopod Craseriella anops from the Nohoch Nah Chich anchialine cave system in southeast Mexico. The cephalon is entirely covered by cuticular scales bordered by marginal spines. The anterior end of the cephalon is bordered by a carina that is wider medially. The isopod is eyeless. The distal seventh portion of the cephalon is characterized by the presence of two sutures and six setae. A suture is found on each side of the distal margin of the cephalon.Each suture is bordered by microtrichs. Two simple setae with a sensory hair, articulated on the base by a socket, are found one on each side of each of the sutures. Two additional setae, similar in shape and size, occur medially on the cephalon. A terminal pore is absent on the sensory hairs of all setae. These setae are suggested to be mechanoreceptors that provide directional sensitivity and enhance the sensibility of turbulent motion, viscosity and changes of hydrostatic pressure.     

革螨跗感器的结构和功能

本文进一步研究了:④厩真厉螨截肢前后的爬行行为,表明第1对足其感觉功能;②用古拉广厉螨分别截各对足驱避反应的对比试验,见到只有当截去第1对足跗节时失去嗅觉功能,而截去第Ⅱ、Ⅲ、Ⅳ对足时,各组都仍有嗅觉功能;⑤对格氏血厉螨、厩真厉螨、毒厉螨和鼠颚毛厉螨进行涂漆前后的驱避试验,显示当跗感器被涂满封闭,则嗅觉功能消失;④以0.5%结晶紫或龙胆紫液染色的截肢标本,观察了厩真厉螨、毒厉螨、格氏血厉螨、古拉广厉螨及尾足螨股一种螨,足Ⅰ跗节末端凹窝中,至少都存在两类感毛,钝钉型感毛和长而尖的刚毛型感毛;⑤厩真厉螨雌螨和幼螨跗感器的钝钉毛分别为8根和5根,另外各有2根短而尖的毛,分别测定了长度,描述了形态特点;⑥透射电镜观察厩真厉螨、毒厉螨等的跗感器钝钉毛,毛外围有表皮壁,壁上有很多微孔,内有中心腔,腔内有树突。属化感器——嗅觉器;⑦电生理技术研究,当用氨和醋酸的气体刺激厩真厉螨、毒厉螨的离体足Ⅰ时,均产生明显的应激电位差,充分证明足Ⅰ辩节有嗅觉功能。     

Antennal sensilla of female Trichogramma nubilale (Ertle and Davis) (Hymenoptera : Trichogrammatidae) and comparisons with other parasitic Hymenoptera

We describe the external morphology and relative positions of antennal sensilla of female Trichgramma nubilale (Hymenoptera : Trichogrammatidae) by scanning electron microscopy (SEM), and compared the results with 11 similar studies representing 15 species and 8 families within the parasitic Hymenoptera. There are 6 morphologically and structurally distinct structures on female T. nubilale antennae, which are probably sensilla, and one seta and one campaniform-like structure that may have a sensory function. Sensilla pore numbers and positions suggests that the multiporous grooved basiconica (MPG) C, multiporous pitted (MPP) trichodea A and the MPP placodea A have an olfactory function, whereas the MPP trichodea C have a gustatory function. The lack of pores and the presence of a basal socket suggests a mechanoreceptor function for aporous (AP) trichodea B, and the uniporous pitted (UPP) trichodea D, although, the latter also have a minute pore or dimple at the sensillar apex. Positions and numbers of these sensilla, setae and campaniform-like structures were consistent in all the specimens examined. These analyses suggest that antennal sensilla types and relative positions are highly conserved within the genus Trichogramma, and there are broad similarities within the parasitic Hymenoptera.     

Antennal sensilla on cave species of Australian Paratemnopteryx cockroaches (Blattaria : Blattellidae)

The external morphology and distribution of antennal sensilla of cave-dwelling Australian cockroaches, Paratemnopteryx stonei (Races B and C), P. howarthi and P. sp. nov. (Blattaria : Blattellidae), are described using scanning electron microscopy. Eight major types of sensilla were found. Long and medium-length sensilla chaetica are deeply grooved mechano and contact chemo-receptors with a terminal pore; the long type forms 5–11% and the medium-length 7–22% of all sensilla. Sensilla trichodea type 1 are very slender, non-porous, and form 43–60% of all sensilla. Sensilla trichodea type 2 are stouter, shorter and have wall pores; they form 5–14% of the sensilla. Sensilla basiconica type B are very short, non-porous, inflexible-socket receptors that are known to be hygro- and thermo-receptors; they comprise less than 0.6% of the sensilla. Sensilla basiconica type Gl are short, grooved and have a terminal pore; they form 5–11% of all sensilla. Type G2 are longer with indications of a terminal pore and form 7–10% of the sensilla. Sensilla basiconica type P are short with wall pores, and they form 3–9% of the sensilla. Total sensillar numbers ranged from 5700–8900 for P. stonei, depending on the race and sex, 6950–9950 for P. sp. nov. and 11,700-15,100 for the smaller and possibly more epigean-related P. howarthi. Females had 700–3150 fewer sensilla than males. Comparisons are made between Paratemnopteryx and common epigean cockroaches in relation to sensillar types and numbers.