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Observations on the leg receptors ofCiniflo (Araneida: Dictynidae)
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/jcp.1030540209openalex-snapshot
Initiation of spike potentials in contact chemosensory hairs of insects. III. D.C. stimulation and generator potential of labellar chemoreceptor of calliphora
inferredcites →https://doi.org/10.1002/jez.1401650205openalex-snapshot
Proprioceptor distribution and properties in Limulus walking legs
inferredcites →https://doi.org/10.1002/jez.1401750106openalex-snapshot
Structure and function of tarsal sensilla in the spider Araneus diadematus
inferredcites →https://doi.org/10.1002/jmor.1050580108openalex-snapshot
The slit sense organs of spiders
inferredcites →https://doi.org/10.1002/jmor.1051320306openalex-snapshot
Chemosensitive hairs in spiders
inferredcites →https://doi.org/10.1007/978-1-4684-7155-7_6openalex-snapshot
Responses of Olfactory and Gustatory Receptor Cells in Insects
inferredcites →https://doi.org/10.1007/978-3-663-01719-6_26openalex-snapshot
Basics of the Generation of Receptor Potentials in Epidermal Mechanoreceptors of Insects
inferredcites →https://doi.org/10.1007/978-3-663-01719-6_27openalex-snapshot
Measurements on the Ionic Milieu of the Receptor Terminal in Mechanoreceptive Sensilla of Insects
inferredcites →https://doi.org/10.1007/bf00298488openalex-snapshot
The fluid pressure pumps of spiders (Chelicerata, Araneae)
inferredcites →https://doi.org/10.1007/bf00302624openalex-snapshot
Ein einzelnes Spaltsinnesorgan auf dem Spinnentarsus: seine Erregung in Abh�ngigkeit von den Parametern des Luftschallreizes
inferredcites →https://doi.org/10.1007/bf00307218openalex-snapshot
Die Feinstruktur der Sinneshaare auf den Cerci von Gryllus bimaculatus Deg. (Saltatoria, Gryllidae)
inferredcites →https://doi.org/10.1007/bf00310298openalex-snapshot
Mechanorezeptive Strukturen der antennalen Haarsensillen der Baumwollwanze Dysdercus intermedius Dist.
inferredcites →https://doi.org/10.1007/bf00324812openalex-snapshot
Die Feinstruktur der tarsalen Schmeckhaare der Fliege Phormia terraenovae Rob.-Desv.
inferredcites →https://doi.org/10.1007/bf00330916openalex-snapshot
The structure of the terminal sensilla on the maxillary palps of Locusta migratoria (L.), and changes associated with moulting
inferredcites →https://doi.org/10.1007/bf00331842openalex-snapshot
Der sensorische Apparat der Spaltsinnesorgane (Cupiennius salei Keys., Araneae)
inferredcites →https://doi.org/10.1007/bf00340548openalex-snapshot
Trichobothrien, ein Ferntastsinnesorgan bei Webespinnen (Araneen)
inferredcites →https://doi.org/10.1007/bf00341332openalex-snapshot
Untersuchungen �ber den Geruchssinn der Spinnenart Cupiennius salei keyserling
inferredcites →https://doi.org/10.1007/bf00375785openalex-snapshot
The hydraulic interaction between prosoma and opisthosoma in Amaurobius ferox (Chelicerata, Araneae)
inferredcites →https://doi.org/10.1007/bf00376004openalex-snapshot
Some comments on the hydrostatic system of spiders (Chelicerata, Araneae)
inferredcites →https://doi.org/10.1007/bf00389906openalex-snapshot
Quelques données sur l'ultrastructure de récepteurs gustatifs de l'antenne de la fourmi Camponotus vagus scop. (Hymenoptera, Formicinae)
inferredcites →https://doi.org/10.1007/bf00406229openalex-snapshot
Beiträge zur kenntnis der hautsinnesorgane und hautdrüsen der cheliceraten und der augen der ixodiden
inferredcites →https://doi.org/10.1007/bf00407436openalex-snapshot
Untersuchungen über das „Tarsalorgan” der spinnen
inferredcites →https://doi.org/10.1007/bf00589698openalex-snapshot
On the mode of action of blue light on the products of photosynthesis in Chlorella vulgaris
inferredcites →https://doi.org/10.1007/bf00589702openalex-snapshot
Mehrfach innervierte Mechanorezeptoren (Trichobothrien) bei Spinnen
inferredcites →https://doi.org/10.1007/bf00655871openalex-snapshot
Observations on the leg receptors ofCiniflo (Araneida: Dictynidae)
inferredcites →https://doi.org/10.1007/bf00696148openalex-snapshot
Electrophysiological studies of gustation in lepidopterous larvae
inferredcites →https://doi.org/10.1007/bf00696631openalex-snapshot
Die Physiologie der Spaltsinnesorgane
inferredcites →https://doi.org/10.1007/bf00697661openalex-snapshot
Die Physiologie der Spaltsinnesorgane
inferredcites →https://doi.org/10.1007/bf01379293openalex-snapshot
An electrophysiological survey of joint receptors in the walking legs of the scorpion,Paruroctonus mesaensis
inferredcites →https://doi.org/10.1007/bf02960371openalex-snapshot
Das Gehör- und Geruchsorgan der Spinnen
inferredcites →https://doi.org/10.1016/0010-406x(62)90061-0openalex-snapshot
Responses of cuticular sense organs of the lobster, Homarus vulgaris (crustacea)—I. Hair-peg organs as water current receptors
inferredcites →https://doi.org/10.1016/0010-406x(62)90160-3openalex-snapshot
Responses of cuticular sense organs of the lobster, Homarus vulgaris (crustacea)—II. Hair-fan organs as pressure receptors
inferredcites →https://doi.org/10.1016/0010-406x(65)90254-9openalex-snapshot
Neuromuscular transmission in a spider and the effect of calcium
inferredcites →https://doi.org/10.1016/0010-406x(66)90562-7openalex-snapshot
Observations on a proprioceptive system in the legs of the scorpion hadrurus hirsutus
inferredcites →https://doi.org/10.1016/0010-406x(68)90590-2openalex-snapshot
Observations on a redescribed crustacean cuticular sense organ
inferredcites →https://doi.org/10.1016/0022-1910(57)90039-2openalex-snapshot
Electrophysiological studies of arthropod chemoreception—II
inferredcites →https://doi.org/10.1016/0022-1910(72)90070-4openalex-snapshot
Differential sensitivity of insect chemoreceptors to alkali cations
inferredcites →https://doi.org/10.1016/0022-1910(72)90092-3openalex-snapshot
Mechanism of stimulation of insect taste cells by organic substances
inferredcites →https://doi.org/10.1016/0022-1910(72)90137-0openalex-snapshot
Interactions between ions and receptor membrane in insect taste cells
inferredcites →https://doi.org/10.1016/0022-1910(74)90215-7openalex-snapshot
The specificity of the labellar chemoreceptors of the blowfly and the response to natural foods
inferredcites →https://doi.org/10.1016/0300-9629(73)90567-7openalex-snapshot
Structure and physiology of the patella-tibia joint receptors in scorpion pedipalps
inferredcites →https://doi.org/10.1016/b978-1-4831-9849-1.50052-9openalex-snapshot
HYDROCARBON INHIBITION OF PRIMARY CHEMORECEPTOR CELLS
inferredcites →https://doi.org/10.1016/s0040-8166(73)80037-0openalex-snapshot
The morphology of spider sensilla i. mechanoreceptors
inferredcites →https://doi.org/10.1016/s0040-8166(73)80038-2openalex-snapshot
The morphology of spider sensilla II. chemoreceptors
inferredcites →https://doi.org/10.1016/s0040-8166(73)80053-9openalex-snapshot
The ultrastructure of chemoreceptor sensilla in Ciniflo (Araneida, Arachnida)
inferredcites →https://doi.org/10.1017/s0025315400015654openalex-snapshot
Movement receptors in decapod Crustacea
inferredcites →https://doi.org/10.1038/212520a0openalex-snapshot
Oscillographic Analysis of some Proprioceptors in the Scorpion Heterometrus fulvipes
inferredcites →https://doi.org/10.1038/241286a0openalex-snapshot
Retention of Pacemaker Activity in Mammalian Myocardial Cells recovered from Liquid Nitrogen
inferredcites →https://doi.org/10.1038/newbio241286a0openalex-snapshot
Mechanotransduction in Insect Neurones
inferredcites →https://doi.org/10.1073/pnas.60.4.1296openalex-snapshot
Electrophysiological responses of the chemoreceptors of the blowfly to sodium salts of fatty acids.
inferredcites →https://doi.org/10.1085/jgp.42.2.393openalex-snapshot
ELECTRICAL ACTIVITY IN THE CHEMORECEPTORS OF THE BLOWFLY
inferredcites →https://doi.org/10.1085/jgp.44.1.105openalex-snapshot
Electrical Characteristics of Insect Mechanoreceptors
inferredcites →https://doi.org/10.1085/jgp.45.3.487openalex-snapshot
Electrophysiological Studies of a Water Receptor Associated With the Taste Sensilla of the Blowfly
inferredcites →https://doi.org/10.1085/jgp.50.2.337openalex-snapshot
Stimulation of the Salt Receptor of the Blowfly
inferredcites →https://doi.org/10.1085/jgp.50.2.351openalex-snapshot
Stimulation of the Salt Receptor of the Blowfly
inferredcites →https://doi.org/10.1085/jgp.50.2.359openalex-snapshot
Stimulation of the Salt Receptor of the Blowfly
inferredcites →https://doi.org/10.1086/278464openalex-snapshot
Observations on Hearing and Smell in Spiders
inferredcites →https://doi.org/10.1093/aesa/58.6.909openalex-snapshot
Electron Microscopy of the Contact Chemoreceptors of the Stable Fly, Stomoxys calcitrans (Diptera: Muscidae)1
inferredcites →https://doi.org/10.1093/icb/12.3.419openalex-snapshot
Evolution of Social Behavior in Spiders (Araneae; Eresidae and Theridiidae)
inferredcites →https://doi.org/10.1098/rspb.1973.0042openalex-snapshot
The fine structure of the PD proprioceptor of Cancer pagurus . I. The receptor stand and the movement sensitive cells
inferredcites →https://doi.org/10.1098/rspb.1973.0043openalex-snapshot
The fine structure of the PD proprioceptor of Cancer pagurus II. The position sensitive cells
inferredcites →https://doi.org/10.1101/sqb.1965.030.01.010openalex-snapshot
A Proposed Transducing Mechanism for a Multiply-Innervated Mechanoreceptor (Trichobothrium) in Spiders
inferredcites →https://doi.org/10.1101/sqb.1965.030.01.011openalex-snapshot
An Insect Mechanoreceptor: Part I: Fine Structure and Adequate Stimulus
inferredcites →https://doi.org/10.1126/science.122.3166.417-aopenalex-snapshot
Physiology of a Primary Chemoreceptor Unit
inferredcites →https://doi.org/10.1146/annurev.en.20.010175.002121openalex-snapshot
Structure of Cuticular Mechanoreceptors of Arthropods
inferredcites →https://doi.org/10.1163/002829672x00095openalex-snapshot
Tarsal Taste Discrimination in the Blowfly, Calliphora Vicina Robineau-Desvoidy
inferredcites →https://doi.org/10.1242/jeb.29.2.220openalex-snapshot
The Response Of A Sense Organ To A Harmonic Stimulus
inferredcites →https://doi.org/10.1242/jeb.31.1.127openalex-snapshot
An Organ for Proprioception and Vibration Sense in Carcinus Maenas
inferredcites →https://doi.org/10.1242/jeb.36.1.102openalex-snapshot
Unidirectional Movement Fibres from a Proprioceptive Organ of the Crab, Carcinus Maenas
inferredcites →https://doi.org/10.1242/jeb.36.2.423openalex-snapshot
The Hydraulic Mechanism of the Spider Leg
inferredcites →https://doi.org/10.1242/jeb.40.1.137openalex-snapshot
Electrical Responses from Dually Innervated Tactile Receptors on the Thorax of the Crayfish
inferredcites →https://doi.org/10.1242/jeb.56.2.509openalex-snapshot
An Analysis of the Types of Sensory Unit Present in the PD Proprioceptor of Decapod Crustaceans
inferredcites →https://doi.org/10.1242/jeb.60.1.223openalex-snapshot
Analysis of the Electrophysiological Responses of the Trochanteral Hair Receptors of the Cockroach
inferredcites →https://doi.org/10.1242/jeb.60.2.275openalex-snapshot
Electrophysiological Responses of the Terminal Sensilla on the Maxillary Palps Of Locusta Migratoria (L.) To Some Electrolytes and Non-Electrolytes
inferredcites →https://doi.org/10.1515/znb-1962-0419openalex-snapshot
Notizen: Ableitung der Rezeptorpotentiale und Nervenimpulse einzelner Cuticula-Senillen bei Insekten
inferredcites →https://doi.org/10.5962/bhl.title.6849openalex-snapshot
The physiology of insect senses
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.11646/zootaxa.4407.4.1zenodo-depositor-declared
Five new cave-dwelling species of Hemirrhagus Simon 1903 (Araneae, Theraphosidae, Theraphosinae), with notes on the generic distribution and novel morphological features
inferred← citeshttps://doi.org/10.1002/(sici)1097-0029(19971215)39:6<506::aid-jemt5>3.0.co;2-bopenalex-snapshot
Functional morphology of insect mechanoreceptors
inferred← citeshttps://doi.org/10.1002/jemt.10137openalex-snapshot
Peripheral synaptic contacts at mechanoreceptors in arachnids and crustaceans: Morphological and immunocytochemical characteristics
inferred← citeshttps://doi.org/10.1002/jez.1402130209openalex-snapshot
Alteration of locomotor behavior in wolf spiders carrying normal and weighted egg cocoons
inferred← citeshttps://doi.org/10.1002/neu.480150506openalex-snapshot
Proprioceptor distribution and control of a muscle reflex in the tibia of spider legs
inferred← citeshttps://doi.org/10.1007/978-1-4899-2519-0_39openalex-snapshot
Distribution and Innervation of Cuticular Sense Organs in the Scorpion, Heterometrus Fulvipes
inferred← citeshttps://doi.org/10.1007/978-3-319-25492-0_2openalex-snapshot
A Spider’s Sense of Touch: What to Do with Myriads of Tactile Hairs?
inferred← citeshttps://doi.org/10.1007/978-3-642-70348-5_12openalex-snapshot
Spider Proprioception: Receptors, Reflexes, and Control of Locomotion
inferred← citeshttps://doi.org/10.1007/978-3-642-70348-5_7openalex-snapshot
Mechano- and Chemoreceptive Sensilla
inferred← citeshttps://doi.org/10.1007/bf00053308openalex-snapshot
Chemoreception in four species of water mites (Acari: Hydrachnida): behavioural and morphological evidence
inferred← citeshttps://doi.org/10.1007/bf00229202openalex-snapshot
Are the funnel-canal organs the ?campaniform sensilla? of the shore crab, Carcinus maenas (Decapoda, Crustacea)?
inferred← citeshttps://doi.org/10.1007/bf00297489openalex-snapshot
The organization of plurisegmental mechanosensitive interneurons in the central nervous system of the wandering spider Cupiennius salei
inferred← citeshttps://doi.org/10.1007/bf00312129openalex-snapshot
Fine structure of scorpion trichobothria (Arachnida, Scorpiones)
inferred← citeshttps://doi.org/10.1007/bf00312156openalex-snapshot
Proprioceptors and sensory nerves in the legs of a spider, Cupiennius salei (Arachnida, Araneida)
inferred← citeshttps://doi.org/10.1007/bf00606240openalex-snapshot
The release of attack and escape behavior by vibratory stimuli in a wandering spider (Cupiennim salei keys.)
inferred← citeshttps://doi.org/10.1007/bf00655871openalex-snapshot
Observations on the leg receptors ofCiniflo (Araneida: Dictynidae)
inferred← citeshttps://doi.org/10.1007/bf00656830openalex-snapshot
Lyriform slit sense organs and muscle reflexes in the spider leg
inferred← citeshttps://doi.org/10.1007/bf00993303openalex-snapshot
Hair regeneration during moulting in the spiderCiniflo similis (Araneae, Dictynidae)
inferred← citeshttps://doi.org/10.1007/bf01342636openalex-snapshot
Tactile hairs and the adjustment of body height in wandering spiders: Behavior, leg reflexes, and afferent projections in the leg ganglia
inferred← citeshttps://doi.org/10.1007/s00049-010-0062-2openalex-snapshot
Chemoreceptors distribution and relative importance of male forelegs and palps in intersexual chemical communication of the wolf spider Pardosa astrigera
inferred← citeshttps://doi.org/10.1007/s00265-002-0547-2openalex-snapshot
The spider and fly revisited: ploy-counterploy behavior in a unique predator-prey system
inferred← citeshttps://doi.org/10.1007/s00359-004-0497-4openalex-snapshot
Arthropod touch reception: structure and mechanics of the basal part of a spider tactile hair
inferred← citeshttps://doi.org/10.1007/s00359-010-0527-3openalex-snapshot
Jumping kinematics in the wandering spider Cupiennius salei
inferred← citeshttps://doi.org/10.1007/s00359-012-0729-yopenalex-snapshot
Behavioral response to antennal tactile stimulation in the field cricket Gryllus bimaculatus
inferred← citeshttps://doi.org/10.1007/s00359-014-0965-4openalex-snapshot
Spider joint hair sensilla: adaptation to proprioreceptive stimulation
inferred← citeshttps://doi.org/10.1007/s003590050043openalex-snapshot
Wind-sensitive interneurones in the spider CNS ( Cupiennius salei ): directional information processing of sensory inputs from trichobothria on the walking legs
inferred← citeshttps://doi.org/10.1007/s00435-019-00442-8openalex-snapshot
Morphology of putative chemosensory setae in males of the spider genus Ariadna Audouin (Araneae, Synspermiata, Segestriidae)
inferred← citeshttps://doi.org/10.1007/s11756-024-01737-yopenalex-snapshot
Comparative stereo scanning studies on sense organs of some terrestrial spiders at Assiut, Egypt
inferred← citeshttps://doi.org/10.1016/b978-0-12-415919-8.00001-xopenalex-snapshot
The Sensory and Behavioural Biology of Whip Spiders (Arachnida, Amblypygi)
inferred← citeshttps://doi.org/10.1016/j.asd.2021.101027openalex-snapshot
Variation of cleaning organ structures and setae of pedipalp tarsus in the family Phrynidae (Arachnida: Amblypygi)
inferred← citeshttps://doi.org/10.1016/j.ydbio.2007.11.003openalex-snapshot
Evolutionary changes in sensory precursor formation in arthropods: Embryonic development of leg sensilla in the spider Cupiennius salei
inferred← citeshttps://doi.org/10.1016/s0003-3472(80)80133-3openalex-snapshot
Trall-following behaviour in two species of wolf spiders: Sensory and etho-ecological concomitants
inferred← citeshttps://doi.org/10.1046/j.1365-2435.2002.00686.xopenalex-snapshot
Influence of venom availability on a spider's prey‐choice behaviour
inferred← citeshttps://doi.org/10.1080/03014223.1979.10428352openalex-snapshot
The feeding behaviour of New Zealand Dolomedes species (Araneae: Pisauridae)
inferred← citeshttps://doi.org/10.1098/rstb.1999.0370openalex-snapshot
Dynamics of arthropod filiform hairs. V. The response of spider trichobothria to natural stimuli
inferred← citeshttps://doi.org/10.1111/j.1365-2435.2006.01103.xopenalex-snapshot
Olfactory information saves venom during prey‐capture of the hunting spider Cupiennius salei (Araneae: Ctenidae)
inferred← citeshttps://doi.org/10.1242/jeb.066811openalex-snapshot
Silk secretion from tarantula feet revisited: alleged spigots are probably chemoreceptors
inferred← citeshttps://doi.org/10.1523/jneurosci.19-01-00298.1999openalex-snapshot
Peripheral Synapses at Identified Mechanosensory Neurons in Spiders: Three-Dimensional Reconstruction and GABA Immunocytochemistry
inferred← citeshttps://doi.org/10.22376/ijpbs.2017.8.2.b59-65openalex-snapshot
Ultrastructural and electrophysiological study of the sensilla on the pedipalps and forelegs of oxyopesrufisternum (araneae: oxyopidae).
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