Statocysts of hydromedusae

The statocysts of Leptomedusae are formed as a depression in the velum. They are lined on the inside towards the distal part of the velum by thin epithelium and towards the proximal part by ciliated sensory cells. Lithocytes are present in the centre. The concretion contains calcium sulphate and in some cases, calcium phosphate is also present in addition to some membranous material. The statocysts of Narcomedusae arise from the exumbrellar nerve ring as free sensory clubs. They have a proximal basal cushion of sensory cells from the centre of which arises a sensory club (Aegina) or a sensory papilla carrying a sensory club (Solmissus). The sensory club has an axial strand of endodermal cells covered by ciliated sensory cells. Some of the endodermal cells have a concretion. While the statocysts of Leptomedusae are totally ectodermal, those of Narcomedusae are ecto-endodermal in origin. The sensory cilia of Leptomedusae, especially those present on the sensory cells adjacent to the lithocyte, run close and parallel to the lithocyte membrane. In Narcomedusae the sensory cilia of the basal cusion and sensory papilla are tall and strong. Ciliary rootlets are missing in the sensory cilia of Leptomedusae and in the sensory club of Narcomedusae but they are strongly developed in the cilia of basal cusion and sensory papilla. The cilia have 9+2 filament content. A ring of stereocilia surrounds the kinocilium of the sensory club cells. Mechanism of statocyst function is discussed.     

Evolution of sensory systems

Sensory systems evolve and enable organisms to perceive their sensory Umwelt, the unique set of cues relevant for their survival. The multiple components that comprise sensory systems — the receptors, cells, organs, and dedicated high-order circuits — can vary greatly across species. Sensory receptor gene families can expand and contract across lineages, resulting in enormous sensory diversity. Comparative studies of sensory receptor function have uncovered the molecular basis of receptor properties and identified novel sensory receptor classes and noncanonical sensory strategies. Phylogenetically informed comparisons of sensory systems across multiple species can pinpoint when sensory changes evolve and highlight the role of contingency in sensory system evolution.     

An unusual mechanosensitive cell in a crustacean exteroceptor

The ultrastructure and mechanosensitivity of a sensory organ in a terrestrial isopod are investigated. The mechanosensitivity of this sensory organ is demonstrated. Seven sensory cells are observed; one of them displays unusual ultrastructural features, a lamellar ciliary root and a tubular body-like structure. The six other sensory cells are similar to usual chemosensitive cells. No sensory cell presents the characteristic cytological features of crustacean mechanosensitive exteroceptors.     

Ultrastructural investigation of the nuchal organs ofPygospio elegans (Polychaeta). I. Larval nuchal organs

The structural differentiation of the nuchal organs during the post-embryonic development ofPygospio elegans is described. The sensory organs are composed of two cell types: ciliated cells and bipolar primary sensory cells, constituting the nuchal ganglion, which is associated with both the sensory epithelium and the brain. Since the sensory neurons are largely integrated into posterolateral parts of the cerebral ganglion, the nuchal organs are primary presegmental structures. The microvilli of the ciliated cells form a cover over the cuticle with a presumed protective function. An extracellular space extends between cuticle and sensory epithelium. The distal dendrites of the sensory cells terminate in sensory bulbs, bearing one modified sensory cilium each that projects into the olfactory chamber, embedded within the secretion of the ciliated cells. During development, the nuchal organs increase in size. This is accompanied by a shift in position, an expansion of the sensory area, and secretory activity of the ciliated cells. The nuchal ganglion differentiates into three nuchal centres forming three distinct sensory areas around the ciliated region. Each nuchal complex reveals two short nuchal nerves comprising the sensory axons, which enter the posterior circumesophageal connective. The sensory cells lying in the brain exhibit neurosecretory activity; the sensory cilia enlarge their surface area by dilating and branching. Nuchal organs accomplish the basic structural adaptions of chemoreceptors and show structural analogies to arthropod olfactory sensilla; thus, there is every reason to suppose chemoreceptor function.     

Sensory receptors of the rosette organ of Gyrocotyle rugosa

The fine structure of three sensory receptors of the rosette organ of Gyrocotyle rugosa, is described. The Type I sensory receptors, localised towards the edge of both upper and lower surfaces, are characterized by a long cilium embedded in a bulb containing two electron-dense collars and several mitochondria. The Type II sensory receptors, larger than Type I, are located on the upper surface of the rosette and have a long cilium and a ciliary rootlet. They also have two electron-dense collars and one or two mitochondria. The sensory cilia of both types are characterized by 9 + 2 axonemes. The Type III sensory receptors, localised on the under surface, lack a sensory cilium but have a ciliary rootlet and are enclosed in the tegument and musculature; there is a complicated three-dimensional spherical lattice of microfibrils associated with the rootlet. The sensory bulbs contain large numbers of membrane bound vesicles and neurotubules. A function is postulated for each of the three types of sensory receptors.     

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.     

SENSORY DIRECTIONALS FOR PIZZA: A DEEPER ANALYSIS

This paper presents a set of analyses on sensory directional attributes used to rate experimentally designed pizza products. Consumers may or may not know the 'optimal' sensory level of attributes for pizza, so that the usefulness of the sensory directional varies by attribute. Furthermore, the sensory magnitude of each sensory directional attribute varies, as shown by the slope (B) relating the two attributes (Sensory Magnitude = A + B (Directional Rating)). The study incorporated sensory directionals into evaluation of products varied according to an experimental design. The optimal product emerging from the design does not necessarily exhibit a sensory directional profile where all attributes are 'on target', nor does a product whose sensory attributes are all on 'target' exhibit the highest level of liking.     

Transformation of sensory organs by mutations of the cut locus of D. melanogaster

The identities of two types of sensory organs in the body wall of Drosophila, namely the external sensory organs and the chordotonal organs, are under genetic control. Embryonic lethal mutations in the cut gene complex transform the external sensory organs into chordotonal organs. The neurons, as well as the support cells forming the external sensory structures, change their morphological and antigenic characteristics to those of chordotonal organs, providing genetic evidence that these two types of sensory organs are homologous. Similar transformations of external sensory organs are observed in adult mosaic flies. Analysis of mosaic larvae and flies suggests that the cut gene function is required either in or near external sensory organs in order for them to acquire their correct identity.     

明视人听词分类任务时的视皮层激活——跨感觉通道的新证据

近期的脑成像研究在盲人等感官缺陷被试者身上发现了感觉替换现象,即传统上认为仅对单一感觉通道刺激反应的皮层区域也参与其他感觉通道的信息加工．类似的效应在感觉剥夺(蒙住眼睛)的明视人被试中也被观察到,提示脑内可能预存着多感觉交互作用的神经通路．通常认为,上述神经通路在常态的人脑中是以潜伏形式存在的,只有当感觉剥夺时才显露出来或得到加强．但是,感觉剥夺是否是该类神经通路发挥作用的必要条件,已有的研究尚缺乏确切的证据．采用统计力度较强的实验设计,给未蒙眼明视人被试听觉呈现一组名词,要求其对听到的每一个词语做出是人工物体还是自然物体的语义判断．对同步采集的功能磁共振信号进行统计分析,观察到视皮层脑区有显著激活．这些结果表明,跨感觉通道的神经通路在未实施感觉剥夺的条件下依然能够显示出来,因而在常态人脑中也不是完全以潜伏形式存在的．上述研究为建立多感觉交互作用神经机制的具体理论模型提供了一个约束条件．     

Response Properties of a Sensory Hair Excised from Venus''s Flytrap

Multicellular sensory hairs were excised from the leaf of Venus's flytrap, and the sensory cells were identified by a destructive dissection technique. The sensory layer includes a radially symmetrical rosette of 20–30 apparently identical cells, and the sensory cells are organized in a plane normal to the long axis of the sensory hair. The sensory cells were probed with intracellular glass electrodes. The resting membrane potential was about -80 mv, and the response to a mechanical stimulus consisted of a graded response and an "action potential." The action potential appears to be similar to the action potential which propagates over the surface of the leaf. In the absence of stimulation, the upper and lower membranes of a single sensory cell behave in an electrically symmetrical fashion. Upon stimulation, however, the upper and lower membranes become electrically asymmetrical. Limiting values for the response asymmetry were calculated on the hypothesis of an electrical model consistent with the histology of the sensory cells.     

Sensory bias as an explanation for the evolution of mate preferences

The sensory bias model of sexual selection posits that female mating preferences are by-products of natural selection on sensory systems. Although sensory bias was proposed 20 years ago, its critical assumptions remain untested. This paradox arises because sensory bias has been used to explain two different phenomena. First, it has been used as a hypothesis about signal design, that is, that males evolve traits that stimulate female sensory systems. Second, sensory bias has been used as a hypothesis for the evolution of female preference itself, that is, to explain why females exhibit particular preferences. We focus on this second facet. First, we clarify the unique features of sensory bias relative to the alternative models by considering each in the same quantitative genetic framework. The key assumptions of sensory bias are that natural selection is the predominant evolutionary mechanism that affects preference and that sexual selection on preferences is quantitatively negligible. We describe four studies that would test these assumptions and review what we can and cannot infer about sensory bias from existing studies. We suggest that the importance of sensory bias as an explanation for the evolution of female preferences remains to be determined.     

Development and evolution of inner ear sensory epithelia and their innervation

The development and evolution of the inner ear sensory patches and their innervation is reviewed. Recent molecular developmental data suggest that development of these sensory patches is a developmental recapitulation of the evolutionary history. These data suggest that the ear generates multiple, functionally diverse sensory epithelia by dividing a single sensory primordium. Those epithelia will establish distinct identities through the overlapping expression of genes of which only a few are currently known. One of these distinctions is the unique pattern of hair cell polarity. A hypothesis is presented on how the hair cell polarity may relate to the progressive segregation of the six sensory epithelia. Besides being markers for sensory epithelia development, neurotrophins are also expressed in delaminating cells that migrate toward the developing vestibular and cochlear ganglia. These delaminating cells originate from multiple sites at or near the developing sensory epithelia and some also express neuronal markers such as NeuroD. The differential origin of precursors raises the possibility that some sensory neurons acquire positional information before they delaminate the ear. Such an identity of these delaminating sensory neurons may be used both to navigate their dendrites to the area they delaminated from, as well as to help them navigate to their central target. The navigational properties of sensory neurons as well as the acquisition of discrete sensory patch phenotypes implies a much more sophisticated subdivision of the developing otocyst than the few available gene expression studies suggest.     

Roles for short-term synaptic plasticity in behavior.

Short-term synaptic plasticity is phylogenetically widespread in ascending sensory systems of vertebrate brains. Such plasticity is found at all levels of sensory processing, including in sensory cortices. The functional roles of this apparently ubiquitous short-term synaptic plasticity, however, are not well understood. Data obtained in midbrain electrosensory neurons of Eigenmannia suggest that this plasticity has at least two roles in sensory processing; enhancing low-pass temporal filtering and generating phase shifts used in processing moving sensory images. Short-term synaptic plasticity may serve similar roles in other sensory modalities, including vision.     

Absence of rapid sensory adaptation in neocortex during information processing states

One prominent feature of sensory responses in neocortex is that they rapidly adapt to increases in frequency, a process called "sensory adaptation." Here we show that sensory adaptation mainly occurs during quiescent states such as anesthesia, slow-wave sleep, and awake immobility. In contrast, during behavior-ally activated states, sensory responses are already adapted. For instance, during learning of a behavioral task, when an animal is very alert and expectant, sensory adaptation is mostly absent. After learning occurs, and the task becomes routine, the level of alertness lessens and sensory adaptation becomes robust. The primary sensory thalamocortical pathway of alert and expectant animals is in the adapted state, which may be required for adequate sensory information processing.     

A matter of focus: monoaminergic modulation of stimulus coding in mammalian sensory networks

Although the presence of neuromodulators in mammalian sensory systems has been noted for some time, a groundswell of evidence has now begun to document the scope of these regulatory mechanisms in several sensory systems, highlighting the importance of neuromodulation in shaping feature extraction at all levels of neural processing. The emergence of more sophisticated models of sensory encoding and of the interaction between sensory and regulatory regions of the brain will challenge sensory neurobiologists to further incorporate a concept of sensory network function that is contingent on neuromodulatory and behavioral state.     

Combination of non-specific cholinesterase histochemistry and immunofluorescence staining for the study of the sensory innervation of skin and muscle

Summary In the present study we describe the application of the non-specific cholinesterase (nChE) histochemical method for the detection of encapsulated sensory nerve endings prior to immunofluorescence staining of the sensory nerve fibres. The nChE staining of Schwann-derived structures surrounding sensory terminals allowed us to identify unequivocally the sensory corpuscles in the skin and the muscle proprioceptors (muscle spindles and Golgi tendon organs) in longitudinal sections of muscle tissue. The nChE staining of sensory nerve endings and immunofluorescence-labelled nerve fibres and their terminals could be viewed and photographed in the same section using appropriate filters. Since nChE activity persists in terminal Schwann cells for a long time after loss of the sensory axons, this combined enzyme- and immunohistochemical approach is also useful for experimental studies involving denervation and re-innervation of sensory nerve endings.     

Head sensory organs of Halobiotus stenostomus (Eutardigrada, Hypsibiidae)

The structure and arrangement of sensory organs in the tardigrade Halobiotus stenostomus (Richters 1908) have been studied using transmission and scanning electron microscopy techniques. The sensory organs found on the head of H. stenostomus are as follows: the circumoral sensory field, cephalic papillae, anterolateral and posterolateral sensory fields, and suboral sensory region. Four types of ciliated receptor structures are described in the sensory fields. The lateral sensory fields contain two types of receptor endings, dense and lucent, which differ in the presence or absence of a collar and in the structure of the outer dendrite segment. Two more types of receptor endings, ultrastructurally differing from the lateral sensory field receptors, are located in the suboral sensory region. Receptors with an asymmetric collar have been found, and a receptor ending without a collar is described for the first time in tardigrades. Unlike in other species studied, the sensory organs of H. stenostomus lack the lymph cavity surrounding the outer receptor segment. Similarity and differences in the ultrastructure of receptors between H. stenostomus and other species of Eutardigrada and Heterotardigrada are discussed.     

RELATIONSHIP BETWEEN SENSORY AND INSTRUMENTAL TEXTURE PROFILE ATTRIBUTES

Texture relationships were studied using both sensory and instrumental texture profile analysis (TPA) techniques to evaluate twenty-one food samples from a wide variety of foods. High linear correlations were found between sensory and instrumental TPA parameters for hardness (r = 0.76) and springiness (r = 0.83). No significant correlations were found between sensory and instrumental TPA parameters for cohesiveness and chewiness. Logarithmic transformations of data improved correlations between sensory attributes and their instrumental corollaries. The correlation between sensory hardness and the logarithm of instrumental hardness was improved to r=0.96. The correlation between the logarithm of both sensory and instrumental springiness was improved to r=0.86. The correlation between the logarithms of both sensory and instrumental chewiness was improved to r=0.54, which was significant at P<0.05.     

Comparative ultrastructure of juvenile and adult nuchal organs of an annelid (Polychaeta: Opheliidae)

Opheliid nuchal organs are composed of ciliated cells, retractor muscles, and sensory cells. The perikarya of sensory cells are located in the posterior portion of the brain, and their distal processes extend along the body wall, as the nuchal nerve, and terminate just anterior to the ciliated region. The nuchal nerve of the juvenile is composed of 30–35 dendrites; the adult nuchal nerve has 35–40 dendrites. The ends of the sensory dendrites form sensory bulbs which are clustered around the olfactory chamber, and each bulb bears a modified cilium. Sensory cilia lose their axonemes and extend as microvillous-like structures into the olfactory chamber. Supportive cells delineate approximately the posterior and dorsal portions of the chamber with sensory bulbs forming the remaining ventral and anterior portions. On the lateral aspect of the chamber, cuticular matrix extends into it, and in this area supportive cells bear microvilli which extend into the matrix. The adult nuchal organ is larger than that of the juvenile, and the sensory portion of the olfactory chamber wall is expanded. Expansion of the sensory area is apparently the result of size increase in sensory bulbs and by intrusion of supportive cells between sensory bulbs.     

Sensory activity affects sensory axon development in C. elegans

The simple nervous system of the nematode C. elegans consists of 302 neurons with highly reproducible morphologies, suggesting a hard-wired program of axon guidance. Surprisingly, we show here that sensory activity shapes sensory axon morphology in C. elegans. A class of mutants with deformed sensory cilia at their dendrite endings have extra axon branches, suggesting that sensory deprivation disrupts axon outgrowth. Mutations that alter calcium channels or membrane potential cause similar defects. Cell-specific perturbations of sensory activity can cause cell-autonomous changes in axon morphology. Although the sensory axons initially reach their targets in the embryo, the mutations that alter sensory activity cause extra axon growth late in development. Thus, perturbations of activity affect the maintenance of sensory axon morphology after an initial pattern of innervation is established. This system provides a genetically tractable model for identifying molecular mechanisms linking neuronal activity to nervous system structure.