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sensory organs

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Journal Article
Published: 03 August 2023
Journal of the Geological Society (2023) 180 (5): jgs2023-019.
... being completely eaten up. Moreover, the large-eyed trilobite Nileus , which has a similar size and morphology to Ordosaspis , had a theoretical preying rate less than 1/20 of that of Ordosaspis , indicating that the eye is an important sensory organ in trilobites. The increased predation pressure may...
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Journal Article
Journal: Paleobiology
Published: 01 May 2010
Paleobiology (2010) 36 (2): 303–317.
... or absence of macroscopic sense organs in specific Cambrian taxa (e.g., Zhang and Shu 2007 ). Various papers have discussed, on genetic and developmental grounds, the potential existence of sensory cells, sensilla, and organs in ancestral Metazoa and Bilateria ( Knoll and Carroll 1999 ; Erwin 2005...
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Journal Article
Journal: Paleobiology
Published: 01 August 2022
Paleobiology (2022) 48 (3): 397–419.
... sensory organs, nervous systems, and brains (e.g., Chen et al. 1999 ; Shu et al. 2003 ; Paterson et al. 2011 ; Ma et al. 2012 ; Schoenemann and Clarkson 2013 , 2017 ; Tanaka et al. 2013 ; Cong et al. 2014 ; Strausfeld 2015 ). Panarthropods (arthropods and their relatives), possessing a diversity...
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Journal Article
Journal: Elements
Published: 01 August 2009
Elements (2009) 5 (4): 235–240.
... microscopy techniques, including electron holography, reveal the complex interplay between the physical and magnetic properties and biological functions of ferrimagnetic nanocrystals in bacteria. although some information is now available about magnetic sensory systems in more complex organisms, much further...
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Conceptual framework for motion paleoecology (based on Fig. 2 in Nathan et al. 2009), including potential sources of paleontological evidence. Three components—motion capacity, navigation capacity, and internal state—focus on the individual organism. These components dynamically interact with each other and the external biotic and abiotic environment to produce a movement path. The internal state is the “why move” component, which determines if and why the organism is ready to move, such as hunger or the desire to mate. This can be assumed by comparison with modern relatives or analogs and may occasionally be preserved as “frozen behavior.” Navigation capacity is “where to move,” and reflects the organism's sensory capabilities. Fossil sense organs and sensory abilities can be directly observed or inferred from morphologic correlates or phylogeny. Motion capacity is “how to move” and reflects the functional capabilities for movement, determined from morphologic analysis of both potential tracemakers and the trace, as well as comparison with modern forms. The result of the interactions of the three factors with each other and the external environment is the movement path, the potentially preserved burrow, track, trail, etc. Movement itself can also alter the external environment, such as through bioturbation or resource depletion, as well as lead to changes in the internal state.
Published: 01 June 2012
or analogs and may occasionally be preserved as “frozen behavior.” Navigation capacity is “where to move,” and reflects the organism's sensory capabilities. Fossil sense organs and sensory abilities can be directly observed or inferred from morphologic correlates or phylogeny. Motion capacity is “how to move
Journal Article
Published: 01 September 2007
Journal of Paleontology (2007) 81 (5): 1031–1043.
... of teeth, an anteriorly arched shape of the premaxilla, a lateral rostral bone participating in the orbital margin, parietals separated in the midline by small bones, the insertion of the basisphenoid region of the braincase into a posterior area on the parasphenoid, and an ethmoidal sensory canal running...
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Journal Article
Published: 01 April 2000
Bulletin of the Seismological Society of America (2000) 90 (2): 312–323.
... selection. This evolutionary pattern has been termed exaptation ( Gould and Vrba, 1982 ). For a seismic-escape response to develop in this fashion, an organism would need to combine an existing escape, panic, or “exit from the burrow” behavioral pattern with one or more appropriate sensory inputs to trigger...
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Journal Article
Journal: Paleobiology
Published: 01 June 2012
Paleobiology (2012) 38 (3): 459–473.
... or analogs and may occasionally be preserved as “frozen behavior.” Navigation capacity is “where to move,” and reflects the organism's sensory capabilities. Fossil sense organs and sensory abilities can be directly observed or inferred from morphologic correlates or phylogeny. Motion capacity is “how to move...
FIGURES
Journal Article
Published: 01 July 2004
Geological Magazine (2004) 141 (4): 541.
... from convergent evolution in the unrelated desert plants of a New World cactus and a Kenyan spurge. And that’s just a sample. But more intriguingly, many of the sensory organs of widely different organisms have also evolved independently, sometimes many times over. The camera-like eye is a classic...
Journal Article
Published: 01 November 2003
Geological Magazine (2003) 140 (6): 727–728.
... is the reluctance to consider the ethology of extinct animals and the real possibility of changing levels of intelligence that might be mediated in part by the evolution of more complex sensory organs, especially olfaction and vision. This is not to say, however, that some of the current investigators...
Journal Article
Published: 01 March 2023
Journal of Paleontology (2023) 97 (2): 454–476.
...María E. Arnaudo; Michelle Arnal Abstract The study of the cranial endocast provides valuable information to understand the behavior of an organism because it coordinates sensory information and motor functions. In this work, we describe for the first time the anatomy of the encephalon of an early...
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Journal Article
Journal: PALAIOS
Published: 01 February 2005
PALAIOS (2005) 20 (1): 3–26.
... data add to morphofunctional information obtained from fossil organisms and indicate that predation occurred at different levels of the water column with: (1) endobenthic predators (diverse priapulid fauna) feeding near the sediment-water interface; (2) epibenthic predators/scavengers (almost...
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Journal Article
Published: 01 March 2014
Journal of Paleontology (2014) 88 (2): 309–330.
... and the ability of the organism to shift to a higher or lower bedding surface. The chaotic pathways and lack of recognizable patterns in Helminthoidichnites implies that sensory systems were not being used extensively in the construction of the burrows. This may imply that organisms had poor sensory skills...
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Journal Article
Published: 01 January 2012
Journal of Paleontology (2012) 86 (1): 19–24.
... and other arthropods ( Clarkson et al., 2006 ; Lee et al., 2011 ), the sensory organs of fossil invertebrates have been little studied ( Plotnick et al., 2010 ). In this paper we will show that one such organ, the tympanal ears of insects, not only has high preservation potential, but is of major...
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Journal Article
Published: 01 July 2014
Journal of Paleontology (2014) 88 (4): 652–663.
.... Revan A. Ho A. 2012 . Evolution of the brain and sensory organs in Sphinsciformes: new data from the stem penguin Paraptenodytes antarcticus . Zoological Journal of the Linnean Society, London , 166 : 202...
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Journal Article
Published: 31 January 2005
Canadian Journal of Earth Sciences (2005) 42 (1): 25–36.
... far anterior in the blunt head and the dentition consists of a series of small, equal-sized and slender conical teeth on the jaw borders. Canals and pit-lines of the sensory organs in the skull are wide and easily discernible; the maxilla and the tail share a modified palaeonisciform shape. The scales...
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Journal Article
Published: 01 February 1991
Jour. Geol. Soc. India (1991) 37 (2): 105–108.
... experience. the presence of Divinity became almost palpable and I knew that life in the universe was not just an accident based on random processes. This knowledge came to me directly - poetically . .. It was not perceptible by the sensory organs, but it was there nevertheless - an unseen dimension behind...
Journal Article
Journal: Paleobiology
Published: 01 August 2007
Paleobiology (2007) 33 (3): 469–493.
... indentation in most living siphonate gastropods is associated with organs that produce a narrow anterior inhalant current of water. Associated sensory organs detect both the concentration and direction of chemical cues released by distant food, enemies, or mates ( Lindberg and Ponder 2001 ). Inhalant streams...
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Journal Article
Published: 01 July 2020
Journal of Paleontology (2020) 94 (4): 773–787.
... on organic remains with the placoderms. A detailed lithological description of the enclosing rocks and a taphonomic description of the ichthyofauna are also provided. The 2010 Stratigraphic Chart of the Devonian deposits of Belarus was used as the stratigraphic basis. The presence of the genus Actinolepis...
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Journal Article
Published: 01 May 2021
Journal of Paleontology (2021) 95 (3): 601–612.
... are covered with specialized sensilla and slit organs that perform thermosensory, hygrosensory, gustatory, olfactory, mechanosensory, and proprioceptive functions (Talarico et al., 2006 ). The long length of the second leg makes it particularly well suited for sensory purposes; modern ricinuleids tap...
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