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Sense organs in Pycnogonida: A review

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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/(sici)1097-0029(19971215)39:6<506::aid-jemt5>3.0.co;2-bopenalex-snapshot
Functional morphology of insect mechanoreceptors
inferredcites →https://doi.org/10.1002/(sici)1097-0029(19991215)47:6<428::aid-jemt6>3.0.co;2-popenalex-snapshot
Arthropod sensilla: Morphology and phylogenetic considerations
inferredcites →https://doi.org/10.1002/jmor.1052220105openalex-snapshot
Microscopic anatomy of pycnogonida: I. Cuticle, epidermis, and muscle
inferredcites →https://doi.org/10.1002/jmor.10779openalex-snapshot
Persisting stemma neuropils in Chaoborus crystallinus (Diptera: Chaoboridae): Development and evolution of a bipartite visual system
inferredcites →https://doi.org/10.1002/zoos.201200016openalex-snapshot
Chilean and Subantarctic Pycnogonida collected by the “Huinay Fjordos” Expeditions 2005-2011
inferredcites →https://doi.org/10.1007/978-1-4613-2743-1_10openalex-snapshot
Photoreceptor Structures and Vision in Arachnids and Myriapods
inferredcites →https://doi.org/10.1007/978-3-642-60725-7_10openalex-snapshot
Ecdysteroids in Pycnogonids: Hormones and Interspecific Allelochemicals
inferredcites →https://doi.org/10.1007/bf00220161openalex-snapshot
The postantennal organ: A specialized unicellular sensory input to the protocerebrum in apterygotan insects (Collembola)
inferredcites →https://doi.org/10.1007/bf00277623openalex-snapshot
Die augen der Araneae
inferredcites →https://doi.org/10.1007/bf00307299openalex-snapshot
The morphology of the Limulus visual system
inferredcites →https://doi.org/10.1007/bf00332499openalex-snapshot
The fine structure of a nauplius eye
inferredcites →https://doi.org/10.1007/bf00342937openalex-snapshot
The fine structure of the visual system of Lycosa (Araneae: Lycosidae)
inferredcites →https://doi.org/10.1007/bf01999135openalex-snapshot
Zur Ultrastruktur der seitlichen Sinnesorgane am Augenhügel vonAnoplodactylus pygmaeus (Pycnogonida)
inferredcites →https://doi.org/10.1007/bf02367135openalex-snapshot
The eyes of a “nobody”,Anoplodactylus petiolatus (Pantopoda; Anoplodactylidae)
inferredcites →https://doi.org/10.1007/s004410050543openalex-snapshot
Central projections of Tömösváry's organ in Lithobius forficatus (Chilopoda, Lithobiidae)
inferredcites →https://doi.org/10.1016/0166-2236(90)90069-mopenalex-snapshot
From cornea to retinal image in invertebrate eyes
inferredcites →https://doi.org/10.1016/j.asd.2006.06.002openalex-snapshot
The organization and evolutionary implications of neuropils and their neurons in the brain of the onychophoran Euperipatoides rowelli
inferredcites →https://doi.org/10.1016/j.asd.2006.06.003openalex-snapshot
Structure and development of onychophoran eyes: What is the ancestral visual organ in arthropods?
inferredcites →https://doi.org/10.1016/j.asd.2006.08.004openalex-snapshot
The frontal eyes of crustaceans
inferredcites →https://doi.org/10.1016/j.asd.2007.06.003openalex-snapshot
Comments on the eyes of tardigrades
inferredcites →https://doi.org/10.1016/j.asd.2012.09.001openalex-snapshot
How do mandibles sense? – The sensory apparatus of larval mandibles in Palaemon elegans Rathke, 1837 (Decapoda, Palaemonidae)
inferredcites →https://doi.org/10.1016/j.asd.2015.07.005openalex-snapshot
Arthropod eyes: The early Cambrian fossil record and divergent evolution of visual systems
inferredcites →https://doi.org/10.1016/j.cub.2013.01.026openalex-snapshot
Molecular Timetrees Reveal a Cambrian Colonization of Land and a New Scenario for Ecdysozoan Evolution
inferredcites →https://doi.org/10.1016/j.ympev.2014.08.001openalex-snapshot
A transcriptome approach to ecdysozoan phylogeny
inferredcites →https://doi.org/10.1016/s0020-7322(97)00017-2openalex-snapshot
Comparative morphogenesis of sensilla: A review
inferredcites →https://doi.org/10.1016/s0065-2806(07)34001-0openalex-snapshot
Medium Flow-Sensing Hairs: Biomechanics and Models
inferredcites →https://doi.org/10.1016/s0065-2881(08)60073-5openalex-snapshot
The Biology of Pycnogonida
inferredcites →https://doi.org/10.1017/s0025315410002067openalex-snapshot
SEM description of the first larval instar ofAchelia assimilis(Pycnogonida: Ammotheidae)
inferredcites →https://doi.org/10.1038/nature08742openalex-snapshot
Arthropod relationships revealed by phylogenomic analysis of nuclear protein-coding sequences
inferredcites →https://doi.org/10.1038/ncomms3314openalex-snapshot
Correction: Corrigendum: Cancer cells that survive radiation therapy acquire HIF-1 activity and translocate toward tumour blood vessels
inferredcites →https://doi.org/10.1038/ncomms3485openalex-snapshot
Arthropod fossil data increase congruence of morphological and molecular phylogenies
inferredcites →https://doi.org/10.1071/is16050openalex-snapshot
Testing species delimitation with larval morphology: scanning electron microscopy analysis of protonymphon larvae of two closely related sea spiders, Pallenopsis patagonica (Hoek) and Pallenopsis yepayekae Weis*
inferredcites →https://doi.org/10.1080/10236247309386912openalex-snapshot
Ultrastructure of the Photoreceptors in the Pycnogonid species,Nymphon gracile(Leach), andPycnogonum littorale(Strom)
inferredcites →https://doi.org/10.1080/10236247909378576openalex-snapshot
The response of the PycnogonidsNymphon gracileleach andPycnogonum littorale(Strom) to light stimuli of different wavelength and intensity
inferredcites →https://doi.org/10.1093/acprof:oso/9780199581139.001.0001openalex-snapshot
Animal Eyes
inferredcites →https://doi.org/10.1093/acprof:oso/9780199682201.001.0001openalex-snapshot
Structure and Evolution of Invertebrate Nervous Systems
inferredcites →https://doi.org/10.1093/chemse/bjq096openalex-snapshot
Organization of Deutocerebral Neuropils and Olfactory Behavior in the Centipede Scutigera coleoptrata (Linnaeus, 1758) (Myriapoda: Chilopoda)
inferredcites →https://doi.org/10.1101/lm.5.1.11openalex-snapshot
Evolution, Discovery, and Interpretations of Arthropod Mushroom Bodies
inferredcites →https://doi.org/10.1111/j.1096-0031.1998.tb00331.xopenalex-snapshot
The Phylogeny of the Extant Chelicerate Orders
inferredcites →https://doi.org/10.1111/j.1096-3642.1978.tb02090.xopenalex-snapshot
Experiments on food preference and chemical sense in Pycnogonida
inferredcites →https://doi.org/10.1111/j.1439-0469.1980.tb00726.xopenalex-snapshot
Beiträge zur Morphologie und Embryologie des vorderen Kdrperabschnitts (Cephalosoma) der Pantopoda Gerstaecker, 1863: Entstehung und Struktur des Zentralnervensystems
inferredcites →https://doi.org/10.1111/j.1439-0469.2004.00284.xopenalex-snapshot
Pycnogonid affinities: a review
inferredcites →https://doi.org/10.1111/j.1463-6395.1996.tb01261.xopenalex-snapshot
Fine Structure of the ‘Slit Organs’ of the Pycnogonid Anoplodactylus petiolatus (Anoplodactylidae)
inferredcites →https://doi.org/10.1111/j.1469-7793.1998.499bk.xopenalex-snapshot
Intracellular calcium clearance in Purkinje cell somata from rat cerebellar slices
inferredcites →https://doi.org/10.1111/pala.12105openalex-snapshot
Origins and early evolution of arthropods
inferredcites →https://doi.org/10.1113/jphysiol.1984.sp015312openalex-snapshot
Receptive fields of cricket giant interneurones are related to their dendritic structure.
inferredcites →https://doi.org/10.1134/s1063074007030029openalex-snapshot
Larvae of three sea spider species of the genus Nymphon (Arthropoda: Pycnogonida) from the White Sea
inferredcites →https://doi.org/10.1146/annurev-ento-112408-085342openalex-snapshot
Physical Ecology of Fluid Flow Sensing in Arthropods
inferredcites →https://doi.org/10.1186/1742-9994-10-40openalex-snapshot
Looking like Limulus? – Retinula axons and visual neuropils of the median and lateral eyes of scorpions
inferredcites →https://doi.org/10.1186/1742-9994-7-29openalex-snapshot
Invertebrate neurophylogeny: suggested terms and definitions for a neuroanatomical glossary
inferredcites →https://doi.org/10.1186/s12862-015-0422-1openalex-snapshot
Serotonin-immunoreactivity in the ventral nerve cord of Pycnogonida – support for individually identifiable neurons as ancestral feature of the arthropod nervous system
inferredcites →https://doi.org/10.1186/s12915-014-0059-3openalex-snapshot
Dissecting a neuron network: FIB-SEM-based 3D-reconstruction of the visual neuropils in the sea spider Achelia langi (Dohrn, 1881) (Pycnogonida)
inferredcites →https://doi.org/10.1186/s12983-016-0182-9openalex-snapshot
The visual system of harvestmen (Opiliones, Arachnida, Chelicerata) – a re-examination
inferredcites →https://doi.org/10.1186/s12983-017-0192-2openalex-snapshot
From egg to “no-body”: an overview and revision of developmental pathways in the ancient arthropod lineage Pycnogonida
inferredcites →https://doi.org/10.1371/journal.pone.0030474openalex-snapshot
Wiring a Periscope – Ocelli, Retinula Axons, Visual Neuropils and the Ancestrality of Sea Spiders
inferredcites →https://doi.org/10.1371/journal.pone.0044799openalex-snapshot
Ketamine Decreases Resting State Functional Network Connectivity in Healthy Subjects: Implications for Antidepressant Drug Action
inferredcites →https://doi.org/10.1371/journal.pone.0095435openalex-snapshot
The ‘Ventral Organs’ of Pycnogonida (Arthropoda) Are Neurogenic Niches of Late Embryonic and Post-Embryonic Nervous System Development
inferredcites →https://doi.org/10.15298/invertzool.01.1.02openalex-snapshot
Fine morphology of larvae of sea spiders (Arthropoda: Pycnogonida) from the White Sea
inferredcites →https://doi.org/10.2307/1535715openalex-snapshot
NOTES ON THE HABITS OF PYCNOGONIDS
inferredcites →https://doi.org/10.2307/j.ctv1dp0v2hopenalex-snapshot
Arthropod Brains
inferredcites →https://doi.org/10.24199/j.mmv.2014.72.07openalex-snapshot
A reassessment of the pycnogonid genus Stylopallene (Arthropoda, Callipallenidae) with description of a new genus
inferredcites →https://doi.org/10.3109/10520296009114740openalex-snapshot
A Copper Sulfate-Silver Nitrate Method for Nerve Fibers of Planarians
inferredcites →https://doi.org/10.3109/10520296209117750openalex-snapshot
Application of Betchaku's Silver Technic to the Nervous System of A Marine Gastropod,Aplysia californica
inferredcites →https://doi.org/10.3897/zse.90.7520openalex-snapshot
Common littoral pycnogonids of the Mediterranean Sea
inferredcites →https://doi.org/10.5281/zenodo.16194459openalex-snapshot
Pycnogonida from the Althorpe Islands, South Australia
inferredcites →https://doi.org/10.5281/zenodo.16543727openalex-snapshot
Facts and theories concerning the insect head
inferredcites →https://doi.org/10.5962/bhl.title.10504openalex-snapshot
Die pantopoden des golfes von Neapel und der angrenzenden meeres abschnitte
inferredcites →https://doi.org/10.5962/bhl.title.28283openalex-snapshot
A contribution to the embryology and phylogeny of the pycnogonids ...
inferredcites →https://doi.org/10.5962/bhl.title.8208openalex-snapshot
Contribution to the embryology and phylogeny of the Pycnogonids

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.5852/ejt.2022.851.1999zenodo-depositor-declared
Sea spiders (Arthropoda: Pycnogonida) collected during the Madibenthos Expedition from Martinique shallow waters
inferred← citeshttps://doi.org/10.1002/jmor.21038openalex-snapshot
The (not very) typical protonymphons of Pycnogonum litorale
inferred← citeshttps://doi.org/10.1002/jmor.21308openalex-snapshot
Anatomical changes in postembryonic development of Pycnogonum litorale
inferred← citeshttps://doi.org/10.1002/spp2.1515openalex-snapshot
New insights into the sea spider fauna (Arthropoda, Pycnogonida) of La Voulte‐sur‐Rhône, France (Jurassic, Callovian)
inferred← citeshttps://doi.org/10.1007/s00300-020-02636-zopenalex-snapshot
Analyzing drivers of speciation in the Southern Ocean using the sea spider species complex Colossendeis megalonyx as a test case
inferred← citeshttps://doi.org/10.1007/s10158-018-0222-6openalex-snapshot
A study of the role of vision in the foraging behaviour of the pyrrhocorid bug Antilochus conquebertii (Insecta; Hemiptera; Pyrrhocoridae)
inferred← citeshttps://doi.org/10.1016/j.asd.2019.06.002openalex-snapshot
The visual system of Thelyphonida (whip scorpions): Support for Arachnopulmonata
inferred← citeshttps://doi.org/10.1016/j.asd.2021.101048openalex-snapshot
The origin and evolution of the euarthropod labrum
inferred← citeshttps://doi.org/10.1093/jcbiol/ruy012openalex-snapshot
Mechanoreceptors and chemoreceptors in pycnogonids (Arthropoda: Pycnogonida)
inferred← citeshttps://doi.org/10.1146/annurev-vision-121820-074736openalex-snapshot
The Diversity of Eyes and Vision
inferred← citeshttps://doi.org/10.1186/s12915-021-01212-zopenalex-snapshot
The visual pathway in sea spiders (Pycnogonida) displays a simple serial layout with similarities to the median eye pathway in horseshoe crabs
inferred← citeshttps://doi.org/10.1186/s12983-019-0316-yopenalex-snapshot
Combining morphological and genomic evidence to resolve species diversity and study speciation processes of the Pallenopsis patagonica (Pycnogonida) species complex
inferred← citeshttps://doi.org/10.1186/s12983-022-00459-8openalex-snapshot
A microCT-based atlas of the central nervous system and midgut in sea spiders (Pycnogonida) sheds first light on evolutionary trends at the family level
inferred← citeshttps://doi.org/10.1186/s40851-023-00223-8openalex-snapshot
Epimorphic development in tropical shallow-water Nymphonidae (Arthropoda: Pycnogonida) revealed by fluorescence imaging
inferred← citeshttps://doi.org/10.55730/1300-0179.3201openalex-snapshot
A new pycnogonid species from Türkiye: Anoplodactylus gullukensis n. sp. (Pycnogonida, Phoxichilidiidae), with an identification key to the Turkish species of the genus
inferred← citeshttps://doi.org/10.70675/11b4a7c9z313dz4a69z8a38z23d43c86e314openalex-snapshot
Biodiversité et histoire évolutive des Pycnogonides (Arthropoda, Pycnogonida)
inferred← citeshttps://doi.org/10.7717/peerj.17766openalex-snapshot
New insights into the Devonian sea spiders of the Hunsrück Slate (Arthropoda: Pycnogonida)
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