Intertidal burrows of the air-breathing eel goby, Odontamblyopus lacepedii (Gobiidae: Amblyopinae)
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2008Page views
1,111ASFA keyword
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Abstract
Odontamblyopus lacepedii inhabits burrows in mudflats and breathes air at the surface opening. Investigations of the intertidal burrows using resin casting demonstrated a highly branched burrow system. The burrows are composed primarily of branching patterns of interconnected tunnels and shafts that communicate into two to seven surface openings. Bulbous chambers (i.e., dilated portions of the burrow) at branching sections of the tunnels or shafts are common features of the burrow. The presence of these chambers accords the fish adequate space to maneuver inside the burrow, and thus constant access to the surface. The combination of all burrow characteristics and previously reported variability in air breathing patterns are ostensibly of selective value for aerial predator avoidance during air breathing in O. lacepedii.
Suggested Citation
Gonzales, T. T., Masaya, K., & Ishimatsu, A. (2008). Intertidal burrows of the air-breathing eel goby, Odontamblyopus lacepedii (Gobiidae: Amblyopinae). Ichthyological Research , 55(3), 303-306. https://doi.org/10.1007/s10228-008-0042-5
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ArticleISSN
1341-8998; 1616-3915Koleksi
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Air breathing of aquatic burrow-dwelling eel goby, Odontamblyopus lacepedii (Gobiidae: Amblyopinae)
(Company of Biologists, 2006)Odontamblyopus lacepedii is an eel goby that inhabits both coastal waters and intertidal zones in East Asia, including Japan. The fish excavates burrows in mudflats but, unlike the sympatric amphibious mudskippers, it does not emerge but stays in the burrows filled with hypoxic water during low tide. Endoscopic observations of the field burrows demonstrated that the fish breathed air in the burrow opening; air breathing commenced 1.3 h following burrow emersion, when water PO2 was ∼2.8 kPa, with an air-breathing frequency (fAB) of 7.3±2.9 breaths h–1 (mean ± s.d., N=5). Laboratory experiments revealed that the fish is a facultative air breather. It never breathed air in normoxic water (PO2=20.7 kPa) but started bimodal respiration when water PO2 was reduced to 1.0–3.1 kPa. The fish held air inside the mouth and probably used the gills as gas-exchange surfaces since no rich vascularization occurred in the mouth linings. As is known for other air-breathing fishes, fAB increased with decreasing water PO2. Both buccal gas volume (VB) and inspired volume (VI) were significantly correlated with body mass (Mb). At a given Mb, VI was nearly always equal to VB, implying almost complete buccal gas renewal in every breathing cycle. A temporal reduction in expired volume (VE) was probably due to a low aerial gas exchange ratio (CO2 elimination/O2 uptake). Air breathing appears to have evolved in O. lacepedii as an adaptation to aquatic hypoxia in the burrows. The acquisition of the novel respiratory capacity enables this species to stay in the burrows during low tide and extends the resident time in the mudflat, thereby increasing its chances of tapping the rich resources of the area.
