Helostoma temminckii are known for a "kissing" behavior, which is often used in intraspecific interactions, and an unusual cranial morphology that is characterized by an intramandibular joint (IMJ). The IMJ is located within the lower jaw and aids in generating the eponymous kissing movement. In other teleost linages the IMJ is associated with the adoption of a substrate-grazing foraging habit. However, because of anatomical modifications of the gill-rakers, Helostoma has been considered a midwater filter-feeding species. We offered midwater, benthic, and attached food to Helostoma, Betta, and two "true" osphronemid gouramis, to ask: (1) how do food capture kinematics differ in different foraging contexts; and (2) are Helostoma feeding kinematics distinct when compared with closely related anabantoids that lack an IMJ? For all anabantoid species except Helostoma, benthic prey were captured using a greater contribution of effective suction relative to midwater prey, though Helostoma was rarely willing to feed in the midwater. Helostoma individuals produced relatively less suction than other species regardless of the food type. Helostoma produced a much larger gape and more premaxillary protrusion than other species, but also took longer to do so. We suggest that the jaw morphology of Helostoma facilitates an extremely large mouth-gape to enhance substrate-scraping. The large amplitude mouth-opening that characterizes substrate-feeding may represent a functional trade-off, whereby the enhanced ability to procure food from the substrate is accompanied by a concomitant reduction in the ability to produce suction.
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http://dx.doi.org/10.1002/jez.1749 | DOI Listing |
Animals (Basel)
April 2021
Department of Ichthyology and Biotechnology in Aquaculture, Institute of Animal Science, Warsaw University of Life Sciences, Ciszewskiego 8, 02-786 Warsaw, Poland.
Accessory respiratory organs (AROs) are a group of anatomical structures found in fish, which support the gills and skin in the process of oxygen uptake. AROs are found in many fish taxa and differ significantly, but in the suborder Anabantoidei, which has a labyrinth organ (LO), and the family Clariidae, which has a dendritic organ (DO), these structures are found in the suprabranchial cavity (SBC). In this study, the SBC walls, AROs, and gills were studied in anabantoid (, , ) and clariid (, ) fishes.
View Article and Find Full Text PDFMitochondrial DNA
March 2016
a Heilongjiang River Fisheries Research Institute, Chinese Academy of Fishery Sciences , Harbin , People's Republic of China .
The kissing gourami (Helostoma temminkii) belongs to the Labyrinth fishes (Perciformes: Anabantoidei), which exhibits a wide variety of behavioral traits. In this study the complete mitogenome of H. temminkii was determined to be 16,740 bp in length.
View Article and Find Full Text PDFJ Exp Zool A Ecol Genet Physiol
November 2012
Mathematical & Natural Sciences, Arizona State University, Phoenix, AZ, USA.
Helostoma temminckii are known for a "kissing" behavior, which is often used in intraspecific interactions, and an unusual cranial morphology that is characterized by an intramandibular joint (IMJ). The IMJ is located within the lower jaw and aids in generating the eponymous kissing movement. In other teleost linages the IMJ is associated with the adoption of a substrate-grazing foraging habit.
View Article and Find Full Text PDFJ Comp Physiol A
September 1998
School of Biological Sciences, University of Kentucky, Lexington 40506-0225, USA.
Fish hearing specialists (e.g., goldfish, holocentrids, clupeoids, mormyrids) have evolved specialized structures (e.
View Article and Find Full Text PDFJ Neurophysiol
October 1997
Departments of Ophthalmology, New York University Medical Center, New York, New York 10016, USA.
The same set of stimuli and analytic methods that was used to study the dynamics of horizontal cells () was applied to a study of the response dynamics and signal processing in amacrine cells in the retina of the kissing gourami, Helostoma rudolfi. The retina contains two major classes of amacrine cells that could be identified from their morphology: C and N amacrine cells. C amacrine cells had a two-layered dendritic field, whereas N cells had a monolayered dendritic field.
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