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Relevant bibliographies by topics / Mugilogobius

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Academic literature on the topic 'Mugilogobius'

Author: Grafiati

Published: 4 June 2021

Last updated: 5 February 2022

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Journal articles on the topic "Mugilogobius"

1

Gee, J., and P. Gee. "Aquatic surface respiration, buoyancy control and the evolution of air-breathing in gobies (Gobiidae: Pisces)." Journal of Experimental Biology 198, no. 1 (January 1, 1995): 79–89. http://dx.doi.org/10.1242/jeb.198.1.79.

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The role of a buccal gas bubble, held while performing aquatic surface respiration (ASR; ventilating the gills with surface water during hypoxia), was examined in benthic, intertidal Australian gobies (Favonigobius tamarensis, F. exquisitus, Pseudogobius olorum, Chlamydogobius sp., Mugilogobius paludis, Cryptocentroides cristatus and Arenigobius bifrenatus). Analyses of the forces of lift and weight of the head and body during ASR indicate a hydrostatic role for the bubble. During ASR, lift from the bubble was sufficient to provide neutral or positive buoyancy to the head, anchoring the mouth at the water surface. A buoyancy role was confirmed by experiments demonstrating the ability of some species to alter bubble volume, to compensate either for different body positions or for water densities (salinities). Use of the bubble for aerial respiration by Cryptocentroides, Mugilogobius, Chlamydogobius and Arenigobius was confirmed in hypoxia by the presence of blood-filled capillaries in the buccal subepithelium (mean airblood barrier less than 30 µm) in areas of the buccal cavity that contacted the bubble. Blood-filled capillaries were rare or absent in normoxia in all species except Mugilogobius. Cutaneous respiration was inferred from the presence of blood-filled capillaries in the dermis and epidermis of emersed portions of the head in Mugilogobius, Chlamydogobius and Arenigobius. The buccal bubble has respiratory and hydrostatic roles and there is support for the hypothesis that ASR and the buoyancy regulation (air-gulping) required to perform it effectively are prerequisite steps in the evolution of air-breathing in these gobies.

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2

Iwata, K., and M. Kajimura. "Functional ureagenesis in a gobiid fish, Mugilogobius abei." Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology 124 (August 1999): S62. http://dx.doi.org/10.1016/s1095-6433(99)90246-5.

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3

Cai, Lei, Ren Huang, Lu-Jun Yu, and Jian-Jun Li. "Complete mitochondrial genome of Mugilogobius chulae (Perciformes: Gobiidae)." Mitochondrial DNA Part A 27, no. 6 (January 28, 2015): 4054–55. http://dx.doi.org/10.3109/19401736.2014.1003840.

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4

Iwata, K., M. Kajimura, and T. Sakamoto. "Functional ureogenesis in the gobiid fish Mugilogobius abei." Journal of Experimental Biology 203, no. 24 (December 15, 2000): 3703–15. http://dx.doi.org/10.1242/jeb.203.24.3703.

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To examine the transition to ureogenesis, the gobiid fish Mugilogobius abei was immersed in 2 mmol l(−)(1) NH(4)HCO(3) or a (15)N-labelled ammonia solution [1 mmol l(−)(1) ((15)NH(4))(2)SO(4), pH 8.0] for 4–8 days. When exposed to 2 mmol l(−)(1) NH(4)HCO(3) or (15)N-labelled ammonia solution for 4 days, the rate of urea excretion increased to seven times that of the control (in 20 % synthetic sea water) and remained at this level for 4 days. The proportion of nitrogen excreted as urea reached 62 % of total nitrogen excretion (ammonia-N + urea-N). (15)N-enrichment of the amide-N in glutamine in the tissues of fish exposed to (15)N-labelled ammonia was virtually the same as that of ammonia-N: i.e. approximately twice that of urea-N in the excreta and the tissues. Glutamine contents and glutamine synthetase activities in the liver and muscle increased greatly following exposure to ammonia. Urea and citrulline contents in the muscle and whole body of the exposed fish increased significantly, whereas uric acid contents remained unchanged. Carbamoyl phosphate synthetase III (CPSase III) mRNA expression and CPSase III activity were detected in the muscle, skin and gill, but levels were negligible in the liver. Furthermore, all other ornithine-urea cycle (O-UC) enzymes were also detected in muscle, skin and gill. Thus, M. abei clearly shows the transition from ammoniotely to ureotely under ammonia-loading condition and is able to produce urea mainly via the O-UC operating in multiple non-hepatic tissues as a means for ammonia detoxification.

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5

THACKER, CHRISTINE E. "Phylogenetic placement of the European sand gobies in Gobionellidae and characterization of gobionellid lineages (Gobiiformes: Gobioidei)." Zootaxa 3619, no. 3 (February 28, 2013): 369–82. http://dx.doi.org/10.11646/zootaxa.3619.3.6.

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The Mediterranean, northeastern Atlantic, and inland freshwaters of Europe and the Ponto-Caspian region host a distinct fauna of gobiiform fishes, including the sand gobies (Pomatoschistus Gill and related genera), all of which have been clas-sified in the most diverse goby group, the family Gobiidae. Recent molecular phylogenetic analyses have suggested that the sand gobies are not gobiids, and are instead part of their sister clade Gobionellidae (Thacker and Roje 2011). Phylo-genetic analysis of Pomatoschistus in the context of both gobiid and gobionellid taxa indicates that Pomatoschistus is part of Gobionellidae, specifically the Mugilogobius lineage. Gobionellidae includes 93 genera, which are arrayed into four lineages (Stenogobius, Mugilogobius, Periophthalmus and Northern Pacific). These lineages exhibit variation in charac-ters of the jaw and suspensorium, including the shapes and relative positions of the palatine, quadrate, and ectopterygoid. The observations of the palatopterygoid complex in Gobionellidae of Harrison (1989) and Larson (2001) are supported and augmented. Gobionellidae generally exhibit suspensoria that are overall more elongated and gracile than those of go-biids: the palatine/ectopterygoid pair features a very short (Periophthalmus lineage) or elongate, pointed palatine (Mugi-logobius, Northern Pacific, and Stenogobius lineages), with a relatively slender ectopterygoid and a short quadrate articulation. In Gobiidae, the palatine extends about halfway along the length of the ectopterygoid, and the ectopterygoid generally features a large, flat articulation with the quadrate. Suspensoria of Pomatoschistus and relatives are similar to those of other taxa in the Mugilogobius lineage. Placement of Pomatoschistus and relatives in Gobionellidae rather than Gobiidae is significant in that it indicates that sand gobies are not closely related to other European gobies, and has impli-cations for any comparative evolutionary or biogeographic studies.

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6

Mukai, Takahiko, Makiko Kajimura, and Katsuya Iwata. "Evolution of a Ureagenic Ability of Japanese Mugilogobius Species (Pisces: Gobiidae)." Zoological Science 17, no. 4 (May 2000): 549–57. http://dx.doi.org/10.2108/0289-0003(2000)17[549:eoauao]2.0.co;2.

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7

Iwata, K., T. Sakamoto, I. Iwata, E. Nishiguchi, and M. Kajimura. "High ambient ammonia promotes growth in a ureogenic goby, Mugilogobius abei." Journal of Comparative Physiology B 175, no. 6 (July 5, 2005): 395–404. http://dx.doi.org/10.1007/s00360-005-0001-7.

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8

Henmi, Yumi, Yuya Okada, and Gyo Itani. "Occasional utilization of crustacean burrows by the estuarine goby Mugilogobius abei." Journal of Experimental Marine Biology and Ecology 528 (July 2020): 151383. http://dx.doi.org/10.1016/j.jembe.2020.151383.

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9

CHENG, Zhang, Xiang-Ping NIE, Fang WANG, and Kai-Bin LI. "CLONING AND SEQUENCE ANALYSIS OF P450 1A1 IN MUGILOGOBIUS ABEI." Acta Hydrobiologica Sinica 33, no. 4 (August 5, 2009): 782–88. http://dx.doi.org/10.3724/sp.j.1035.2009.40782.

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10

Kajimura, Makiko, Katsuya Iwata, and Hideharu Numata. "Diurnal nitrogen excretion rhythm of the functionally ureogenic gobiid fish Mugilogobius abei." Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology 131, no. 2 (February 2002): 227–39. http://dx.doi.org/10.1016/s1096-4959(01)00503-6.

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Books on the topic "Mugilogobius"

1

Larson, H. K. A revision of the gobiid fish genus Mugilogobius (Teleostei: Gobioidei) and its systematic placement. Perth, W.A: Western Australian Museum, 2001.

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