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Artículos de revistas sobre el tema "Fishes Fishes Fishes Oxygenases"

Autor: Grafiati

Publicado: 4 de junio de 2021

Última modificación: 10 de febrero de 2022

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1

Scarabotti, Pablo A., M. Julieta Parma, Javier A. López y Romina Ghirardi. "Dermal lip protuberances associated with aquatic surface respiration in juveniles of the piscivorous characid Salminus brasiliensis (Actinopterygii: Characidae)". Neotropical Ichthyology 7, n.º 3 (septiembre de 2009): 459–64. http://dx.doi.org/10.1590/s1679-62252009000300013.

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Some South American freshwater fishes can improve their capability of aquatic surface respiration (ASR) by developing dermal lip protuberances in the lower jaw. This adaptation was thought to be limited to omnivorous or herbivorous fishes. The present work provides the first evidence that juveniles of a piscivorous characid, Salminus brasiliensis, develop dermal lip protuberances during periods of hypoxia in floodplain ponds of the Salado River, in Argentina. The protuberance of S. brasiliensis involves dermal portions of both jaws exhibiting lateral lobes on the sides of the mouth arranged in the vertical plane. Water dissolved oxygen concentrations less than or equal to 1.05 mgl-1 were associated with a remarkable increase in lip protuberance. The lateral lobes of the protuberance in this species may limit the access of water to the anterior portion of the mouth which is positioned nearer to the oxygenated surface water during ASR. Finally, ASR, complemented with the development of dermal lip protuberances, can be considered a valuable strategy to survive in hypoxic environments, even for carnivorous fishes with elevated oxygen requirements.

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2

Barske, Lindsey, Peter Fabian, Christine Hirschberger, David Jandzik, Tyler Square, Pengfei Xu, Nellie Nelson et al. "Evolution of vertebrate gill covers via shifts in an ancient Pou3f3 enhancer". Proceedings of the National Academy of Sciences 117, n.º 40 (21 de septiembre de 2020): 24876–84. http://dx.doi.org/10.1073/pnas.2011531117.

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Whereas the gill chambers of jawless vertebrates open directly into the environment, jawed vertebrates evolved skeletal appendages that drive oxygenated water unidirectionally over the gills. A major anatomical difference between the two jawed vertebrate lineages is the presence of a single large gill cover in bony fishes versus separate covers for each gill chamber in cartilaginous fishes. Here, we find that these divergent patterns correlate with the pharyngeal arch expression of Pou3f3 orthologs. We identify a deeply conserved Pou3f3 arch enhancer present in humans through sharks but undetectable in jawless fish. Minor differences between the bony and cartilaginous fish enhancers account for their restricted versus pan-arch expression patterns. In zebrafish, mutation of Pou3f3 or the conserved enhancer disrupts gill cover formation, whereas ectopic pan-arch Pou3f3b expression generates ectopic skeletal elements resembling the multimeric covers of cartilaginous fishes. Emergence of this Pou3f3 arch enhancer >430 Mya and subsequent modifications may thus have contributed to the acquisition and diversification of gill covers and respiratory strategies during gnathostome evolution.

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3

Farmer, Colleen. "Did lungs and the intracardiac shunt evolve to oxygenate the heart in vertebrates?" Paleobiology 23, n.º 3 (1997): 358–72. http://dx.doi.org/10.1017/s0094837300019734.

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Traditional wisdom of the evolution of lungs in fishes is that lungs arose when gill ventilation was hindered by an aquatic habitat that was low in oxygen. This scenario has been buttressed primarily by a proposed correlation between extant air-breathing fishes and hypoxic habitats, as well as by the fact that early vertebrate fossils were found in sediments believed to indicate a semi-arid environment. There are problems with this scenario, yet it retains a dominant influence on how the evolution of aerial respiration is viewed. This paper presents a new hypothesis for lung evolution that is more consistent with the fossil record and physiology of extant animals than the traditional scenario; I propose that lungs evolved to supply the heart with oxygen. The primitive vertebrate heart was spongy in architecture and devoid of coronary support, obtaining oxygen from luminal blood. By supplying oxygen to this tissue, lungs may have been important in ancient fishes for sustaining activity, regardless of environment. Furthermore, this function for lungs may have influenced cardiovascular adaptations of tetrapods because their divided cardiovascular system isolates the right side of the heart from pulmonary oxygen. I propose that three innovations compensate for this isolation: In extant amphibians oxygen-rich blood from cutaneous and buccal respiration enters the right side of the heart; in chelonians and lepidosaurs the intracardiac shunt washes oxygen-rich blood into the right side of the heart; in mammals, birds, and perhaps in crocodilians, support of the heart by coronary vasculature eliminates this problem.

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4

Hemal, Shahrear, Md Shahab Uddin, Md Saif Uddin, Bhaskar Chandra Majumdar, Md Golam Rasul y Md Tariqul Alam. "Present status and problems of fish seed marketing in Sylhet district, Bangladesh". Research in Agriculture Livestock and Fisheries 4, n.º 1 (30 de abril de 2017): 45–54. http://dx.doi.org/10.3329/ralf.v4i1.32405.

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Correction: On 3rd May 2017, the PDF was replaced with a correction on page 51. In the figure at the top of page 51, Channel 6 was added.This study was conducted to explore the present status and problems of fish seed marketing system in Sylhet district, Bangladesh. Data were collected through questionnaire interview from the selected areas during April to September 2016. Brood fishes were collected from wild sources as well as hatchery produced brood fishes also used for seed production. Good length, weight and age of brood fishes were selected for spawning and induced breeding. In nursery, hatchlings were reared for 30-40 days and 37.7% nursery owner practiced single cycle production/year where the average stocking density of seed was found 24.65±3.94 g/decimal (mean±SD). Six different fish seed marketing channels were identified where hatchery owners, nursery owners, forias (retailer) and fish farmers were main stakeholders. The highest (6520 Tk/day) and lowest (355 Tk/day) average income were found in hatchery owner and fish farmer, respectively. Oxygenated bag, big aluminum bowl/container and plastic barrels with continuously agitate the water were used for seed transportation. Maximum 17.67% seed mortality was noticed in hatchery owner and minimum 5.67% in fish farmers. Late breeding season, lack of capital, lack of technical knowledge on hatchery operation and management, poor transport facilities, high transportation cost, high labor cost, lack of training and high price of spawn are identified as some major problems.Res. Agric., Livest. Fish.4(1): 45-54, April 2017

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5

Turcu, Adina F., Aya T. Nanba y Richard J. Auchus. "The Rise, Fall, and Resurrection of 11-Oxygenated Androgens in Human Physiology and Disease". Hormone Research in Paediatrics 89, n.º 5 (2018): 284–91. http://dx.doi.org/10.1159/000486036.

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The 11-oxyandrogens, particularly 11-ketotestosterone, have been recognized as a biologically important gonadal androgen in teleost (bony) fishes for decades, and their presence in human beings has been known but poorly understood. Today, we recognize that 11-oxyandrogens derive from the human adrenal glands and are major bioactive androgens, particularly in women and children. This article will review their biosynthesis and metabolism, abundance in normal and pathologic states, and potential as biomarkers of adrenal developmental changes and disease. Specifically, 11-oxyandrogens are the dominant active androgens in many patients with 21-hydroxylase deficiency.

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6

Cao, Jun y Xiuzhu Cheng. "Transcriptome-Based Identification and Molecular Evolution of the Cytochrome P450 Genes and Expression Profiling under Dimethoate Treatment in Amur Stickleback (Pungitius sinensis)". Animals 9, n.º 11 (28 de octubre de 2019): 873. http://dx.doi.org/10.3390/ani9110873.

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Cytochrome P450s (CYPs) are a family of membrane-bound mono-oxygenase proteins, which are involved in cell metabolism and detoxification of various xenobiotic substances. In this study, we identified 58 putative CYP genes in Amur stickleback (Pungitius sinensis) based on the transcriptome sequencing. Conserved motif distribution suggested their functional relevance within each group. Some present recombination events have accelerated the evolution of this gene family. Moreover, a few positive selection sites were identified, which may have accelerated the functional divergence of this family of proteins. Expression patterns of these CYP genes were investigated and indicated that most were affected by dimethoate treatment, suggesting that CYPs were involved in the detoxication of dimethoate. This study will provide a foundation for the further functional investigation of CYP genes in fishes.

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7

Janssens, B. J., J. J. Childress, F. Baguet y J. F. Rees. "Reduced enzymatic antioxidative defense in deep-sea fish". Journal of Experimental Biology 203, n.º 24 (15 de diciembre de 2000): 3717–25. http://dx.doi.org/10.1242/jeb.203.24.3717.

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Oxygen, while being an obligate fuel for aerobic life, has been shown to be toxic through its deleterious reactive species, which can cause oxidative stress and lead ultimately to cell and organism death. In marine organisms, reactive oxygen species (ROS), such as the superoxide anion and hydrogen peroxide, are generated within respiring cells and tissues and also by photochemical processes in sea water. Considering both the reduced metabolic rate of nektonic organisms thriving in the deep sea and the physico-chemical conditions of this dark, poorly oxygenated environment, the meso- and bathypelagic waters of the oceans might be considered as refuges against oxidative dangers. This hypothesis prompted us to investigate the activities of the three essential enzymes (superoxide dismutase, SOD; catalase, CAT; glutathione peroxidase, GPX) constitutive of the antioxidative arsenal of cells in the tissues of 16 species of meso- and bathypelagic fishes occurring between the surface and a depth of 1300 m. While enzymatic activities were detected in all tissues from all species, the levels of SOD and GPX decreased in parallel with the exponential reduction in the metabolic activity as estimated by citrate synthase activity. In contrast, CAT was affected neither by the metabolic activity nor by the depth of occurrence of the fishes. High levels of metabolic and antioxidative enzymes were detected in the light organs of bioluminescent species. The adjustment of the activity of SOD and GPX to the decreased metabolic activity associated with deep-sea living suggests that these antioxidative defense mechanisms are used primarily against metabolically produced ROS, whereas the maintenance of CAT activity throughout all depths could be indicative of another role. The possible reasons for the occurrence of such a reduced antioxidative arsenal in deep-sea species are discussed.

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8

Mucha, Stefan, Lauren J. Chapman y Rüdiger Krahe. "The weakly electric fish, Apteronotus albifrons, actively avoids experimentally induced hypoxia". Journal of Comparative Physiology A 207, n.º 3 (10 de marzo de 2021): 369–79. http://dx.doi.org/10.1007/s00359-021-01470-w.

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AbstractAnthropogenic environmental degradation has led to an increase in the frequency and prevalence of aquatic hypoxia (low dissolved oxygen concentration, DO), which may affect habitat quality for water-breathing fishes. The weakly electric black ghost knifefish, Apteronotus albifrons, is typically found in well-oxygenated freshwater habitats in South America. Using a shuttle-box design, we exposed juvenile A. albifrons to a stepwise decline in DO from normoxia (> 95% air saturation) to extreme hypoxia (10% air saturation) in one compartment and chronic normoxia in the other. On average, A. albifrons actively avoided the hypoxic compartment below 22% air saturation. Hypoxia avoidance was correlated with upregulated swimming activity. Following avoidance, fish regularly ventured back briefly into deep hypoxia. Hypoxia did not affect the frequency of their electric organ discharges. Our results show that A. albifrons is able to sense hypoxia at non-lethal levels and uses active avoidance to mitigate its adverse effects.

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9

Lehnert, S. J., K. A. Christensen, W. E. Vandersteen, D. Sakhrani, T. E. Pitcher, J. W. Heath, B. F. Koop, D. D. Heath y R. H. Devlin. "Carotenoid pigmentation in salmon: variation in expression at BCO2-l locus controls a key fitness trait affecting red coloration". Proceedings of the Royal Society B: Biological Sciences 286, n.º 1913 (16 de octubre de 2019): 20191588. http://dx.doi.org/10.1098/rspb.2019.1588.

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Carotenoids are primarily responsible for the characteristic red flesh coloration of salmon. Flesh coloration is an economically and evolutionarily significant trait that varies inter- and intra-specifically, yet the underlying genetic mechanism is unknown. Chinook salmon ( Oncorhynchus tshawytscha ) represents an ideal system to study carotenoid variation as, unlike other salmonids, they exhibit extreme differences in carotenoid utilization due to genetic polymorphisms. Here, we crossed populations of Chinook salmon with fixed differences in flesh coloration (red versus white) for a genome-wide association study to identify loci associated with pigmentation. Here, the beta-carotene oxygenase 2-like ( BCO2-l ) gene was significantly associated with flesh colour, with the most significant single nucleotide polymorphism explaining 66% of the variation in colour. BCO2 gene disruption is linked to carotenoid accumulation in other taxa, therefore we hypothesize that an ancestral mutation partially disrupting BCO2-l activity (i.e. hypomorphic mutation) allowed the deposition and accumulation of carotenoids within Salmonidae. Indeed, we found elevated transcript levels of BCO2-l in white Chinook salmon relative to red. The long-standing mystery of why salmon are red, while no other fishes are, is thus probably explained by a hypomorphic mutation in the proto-salmonid at the time of divergence of red-fleshed salmonid genera (approx. 30 Ma).

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10

Carr, H. Sorayya, Alwyne Wheeler y Andrew K. G. Jones. "Fishes". Journal of Field Archaeology 17, n.º 4 (1990): 496. http://dx.doi.org/10.2307/530016.

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11

Swift, Camm C., Alwyne Wheeler y Andrew K. G. Jones. "Fishes". Copeia 1991, n.º 1 (7 de febrero de 1991): 270. http://dx.doi.org/10.2307/1446285.

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12

Vanatian, Bertha. "What Do Fishes Know About Fishes?" Annals of Improbable Research 9, n.º 4 (1 de julio de 2003): 7. http://dx.doi.org/10.3142/107951403782226021.

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13

Costantini, Marco, Stuart A. Ludsin, Doran M. Mason, Xinsheng Zhang, William C. Boicourt y Stephen B. Brandt. "Effect of hypoxia on habitat quality of striped bass (Morone saxatilis) in Chesapeake Bay". Canadian Journal of Fisheries and Aquatic Sciences 65, n.º 5 (1 de mayo de 2008): 989–1002. http://dx.doi.org/10.1139/f08-021.

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Eutrophication-induced hypoxia may affect both benthic and pelagic organisms in coastal systems. To evaluate the effect of hypoxia on pelagic striped bass (Morone saxatilis), we quantified the growth rate potential (GRP) of age-2 and age-4 fish in Chesapeake Bay during 1996 and 2000 using observed temperature, dissolved oxygen, and prey abundance information in a spatially explicit bioenergetics modeling framework. Regions of the Bay with bottom hypoxia were generally areas with high quality habitat (i.e., GRP > 0 g·g–1·day–1), primarily because prey fish were forced into warm, oxygenated surface waters suitable for striped bass foraging and growth. In turn, by concentrating fish prey above the oxycline and removing bottom waters as a refuge, hypoxia likely enhanced striped bass predation efficiency and contributed to the recovery of striped bass during the mid-1990s, a time when the striped bass fishery also was closed. This short-term positive effect of hypoxia on striped bass, however, appears to have been counterbalanced by a long-term negative effect of hypoxia in recent years. Ultimately, hypoxia-enhanced predation efficiency, combined with an abundance of striped bass due to restricted harvest, appears to be causing overconsumption of prey fishes in Chesapeake Bay, thus helping to explain poor growth and health of striped bass in recent years.

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14

Fialho, Clarice Bernhardt. "Viviparous Fishes". Neotropical Ichthyology 4, n.º 4 (diciembre de 2006): 462. http://dx.doi.org/10.1590/s1679-62252006000400012.

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15

DE CAPRONA, M. DOMMINIQUE CRAPON y BERND FRITZSCH. "African fishes". Nature 350, n.º 6318 (abril de 1991): 467. http://dx.doi.org/10.1038/350467b0.

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16

MEYER, AXEL, THOMAS D. KOCHER y ALLAN C. WILSON. "African fishes". Nature 350, n.º 6318 (abril de 1991): 467–68. http://dx.doi.org/10.1038/350467c0.

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17

Smyth, Amanda. "Little Fishes". Wasafiri 28, n.º 2 (junio de 2013): 66–68. http://dx.doi.org/10.1080/02690055.2013.758992.

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18

Eastman, Joseph T. y Arthur L. DeVries. "Antarctic Fishes". Scientific American 255, n.º 5 (noviembre de 1986): 106–14. http://dx.doi.org/10.1038/scientificamerican1186-106.

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19

Bell, Michael A. "Darwin's fishes". Trends in Ecology & Evolution 19, n.º 6 (junio de 2004): 298. http://dx.doi.org/10.1016/j.tree.2004.03.004.

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20

Patterson, Colin. "Bony Fishes". Short Courses in Paleontology 7 (1994): 57–84. http://dx.doi.org/10.1017/s2475263000001264.

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Bony fishes or osteichthyans comprise two main monophyletic groups: the actinopterygians (rayfins, including the staples of the fish market and aquarium) and sarcopterygians (lobefins, fringefins or tasselfins, including lungfishes, coelacanths, and, perhaps unexpectedly or inconveniently, all land vertebrates or tetrapods). In the broadest terms, the two groups have similar histories, each with beginnings in the late Silurian or earliest Devonian, each with a primary radiation in the late Devonian and Mississippian, a secondary radiation in the Mesozoic, and a major Tertiary radiation, and each with an extant diversity of roughly 25,000 species (Nelson, 1994, p. 2). The remainder of this course (eight topics) is devoted to sarcopterygians, so I shall give almost all my space to the other half of bony fish diversity, the actinopterygians.

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21

SUZUKI, RYO. "Fishes, Pisces." Kagaku To Seibutsu 23, n.º 11 (1985): 742–48. http://dx.doi.org/10.1271/kagakutoseibutsu1962.23.742.

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22

Horn, Michael H. y Robin N. Gibson. "Intertidal Fishes". Scientific American 258, n.º 1 (enero de 1988): 64–70. http://dx.doi.org/10.1038/scientificamerican0188-64.

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23

Bernardi, Giacomo, Marina L. Ramon, Yvette Alva-Campbell, John E. McCosker, Giuseppe Bucciarelli, Lauren E. Garske, Benjamin C. Victor y Nicole L. Crane. "Darwin's fishes: phylogeography of Galápagos Islands reef fishes". Bulletin of Marine Science 90, n.º 1 (1 de enero de 2014): 533–49. http://dx.doi.org/10.5343/bms.2013.1036.

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24

Krajewski, João Paulo. "How do follower reef fishes find nuclear fishes?" Environmental Biology of Fishes 86, n.º 3 (13 de octubre de 2009): 379–87. http://dx.doi.org/10.1007/s10641-009-9533-0.

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25

Barton, Douglas G. y Mark VH Wilson. "Taphonomic variations in Eocene fish-bearing varves at Horsefly, British Columbia, reveal 10 000 years of environmental change". Canadian Journal of Earth Sciences 42, n.º 2 (1 de febrero de 2005): 137–49. http://dx.doi.org/10.1139/e05-001.

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The Eocene Horsefly locality in British Columbia has yielded many fossil fishes, insects, and plants. Its varved sediments make it ideal for study of temporal changes in environment and fish morphology. Several intervals of diatomaceous varves indicate a deep, stratified lake setting. Earlier studies focused on morphological and taphonomic change during the 700-year H2 interval and morphological change during the 10 000-year H3 interval. The present study uses taphonomy as an index for environmental change during the ten millennia represented by H3, comparing taphonomic changes with the morphologic changes found earlier. The H3 interval records deposition in deep water, indicated by dominance of the fish genera Amyzon and Eohiodon. Quiet water conditions are indicated by minimal fin disarticulation. Hypoxia at the time of fish death is confirmed by open mouths of most fish specimens, while cool water on the lake floor prevented full flotation of fish carcasses. Water depth, temperature, and oxygenation fluctuated during H3 deposition. Periods of cooler, deeper, more hypoxic water are indicated by greater numbers and size of Amyzon specimens and by less disarticulation of skull and abdominal bones. Periods of warmer, shallower, more oxygenated waters are indicated by more disarticulation, less fin tetany, smaller fish specimens, and greater diversity of species. Correlations between the taphonomic changes and morphological changes in A. aggregatum are weak. Therefore, the morphological changes are not easily explained as ecophenotypic or short-term evolutionary responses to changes in physical lake conditions.

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26

P., Arturo Acero, Juan José Orellana Amador y Juan Jose Orellana Amador. "Marine Fishes of Los Cobanos: Fishes of El Salvador". Copeia 1988, n.º 2 (18 de mayo de 1988): 505. http://dx.doi.org/10.2307/1445900.

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27

Kizer, Kenneth W. "Coral Reef Fishes". Wilderness & Environmental Medicine 13, n.º 4 (diciembre de 2002): 278. http://dx.doi.org/10.1580/1080-6032(2002)013[0278:br]2.0.co;2.

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28

Reinthal, Peter N., Graham Bell-Cross y John L. Minshull. "Fishes of Zimbabwe". Copeia 1989, n.º 3 (8 de agosto de 1989): 809. http://dx.doi.org/10.2307/1445530.

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29

Etnier, David A., Henry W. Robison y Thomas M. Buchanan. "Fishes of Arkansas". Copeia 1989, n.º 3 (8 de agosto de 1989): 815. http://dx.doi.org/10.2307/1445535.

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30

Robins, C. Richard, Margaret M. Smith y Phillip C. Heemstra. "Smiths' Sea Fishes". Copeia 1987, n.º 3 (5 de agosto de 1987): 816. http://dx.doi.org/10.2307/1445686.

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31

Smith, C. Lavett, John R. Paxton y William N. Eschmeyer. "Encyclopedia of Fishes". Copeia 1996, n.º 1 (2 de febrero de 1996): 235. http://dx.doi.org/10.2307/1446971.

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32

Coburn, Miles y Maurice Kottelat. "European Freshwater Fishes". Copeia 1998, n.º 4 (30 de diciembre de 1998): 1116. http://dx.doi.org/10.2307/1447371.

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33

Grande, Lance y John G. Maisey. "Discovering Fossil Fishes". Copeia 1997, n.º 3 (1 de agosto de 1997): 639. http://dx.doi.org/10.2307/1447577.

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34

Nelson, Joseph S., Melanie L. J. Stiassny, Lynne R. Parenti y G. David Johnson. "Interrelationships of Fishes". Copeia 1997, n.º 3 (1 de agosto de 1997): 647. http://dx.doi.org/10.2307/1447582.

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35

Kynard, Boyd E. y Robert M. McDowall. "Diadromy in Fishes". Estuaries 12, n.º 3 (septiembre de 1989): 208. http://dx.doi.org/10.2307/1351827.

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36

Reis, Roberto E. "Catalog of Fishes". Copeia 2000, n.º 3 (agosto de 2000): 904–6. http://dx.doi.org/10.1643/0045-8511(2000)000[0904:br]2.0.co;2.

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37

Stevenson, Duane E. "FISHES OF ALASKA". Copeia 2003, n.º 1 (febrero de 2003): 202–4. http://dx.doi.org/10.1643/0045-8511(2003)003[0202:]2.0.co;2.

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38

Ferraris, Carl J. "FISHES OF LAOS". Copeia 2003, n.º 1 (febrero de 2003): 216–17. http://dx.doi.org/10.1643/0045-8511(2003)003[0216:]2.0.co;2.

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39

Etnier, David A. "Fishes of Alabama". Copeia 2006, n.º 2 (mayo de 2006): 321–22. http://dx.doi.org/10.1643/0045-8511(2006)6[321:foa]2.0.co;2.

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40

Pinion, Sheila. "Following the fishes". Lancet Child & Adolescent Health 2, n.º 4 (abril de 2018): 241. http://dx.doi.org/10.1016/s2352-4642(18)30077-4.

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41

Groff, Joseph M. "Neoplasia in fishes". Veterinary Clinics of North America: Exotic Animal Practice 7, n.º 3 (septiembre de 2004): 705–56. http://dx.doi.org/10.1016/j.cvex.2004.04.012.

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42

Meunier, François J. y Mireille Gayet. "Interrelationships of fishes". Geobios 30, n.º 3 (enero de 1997): 446. http://dx.doi.org/10.1016/s0016-6995(97)80206-9.

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43

Watanabe, Tasuku y Tadaaki Moritomo. "Phagocytes of fishes". Developmental & Comparative Immunology 21, n.º 1 (enero de 1997): 64. http://dx.doi.org/10.1016/s0145-305x(97)87954-2.

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44

Lockwood, Stephen J. "Fishes in Estuaries". Fisheries Research 58, n.º 3 (noviembre de 2002): 410–12. http://dx.doi.org/10.1016/s0165-7836(02)00167-4.

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45

Blaber, Stephen J. M. "Fishes in Estuaries". Fish and Fisheries 3, n.º 4 (diciembre de 2002): 360–61. http://dx.doi.org/10.1046/j.1467-2979.2002.00100.x.

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46

Patnaik, B. K., N. Mahapatro y B. S. Jena. "Ageing in Fishes". Gerontology 40, n.º 2-4 (1994): 113–32. http://dx.doi.org/10.1159/000213582.

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47

Elliott, Mike. "Tropical Estuarine Fishes". Journal of Fish Biology 62, n.º 4 (abril de 2003): 983–84. http://dx.doi.org/10.1046/j.1095-8649.2003.00080.x.

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48

Prince, Jean. "Sharks and fishes!" 5 to 7 Educator 2009, n.º 49 (enero de 2009): xvi—xvii. http://dx.doi.org/10.12968/ftse.2008.8.1.31919.

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49

Davenport, John. "Ecomorphology of fishes". Journal of Experimental Marine Biology and Ecology 209, n.º 1-2 (febrero de 1997): 309–10. http://dx.doi.org/10.1016/s0022-0981(96)02620-2.

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50

Borko, Hilda, Dan Liston y Jennifer A. Whitcomb. "Apples and Fishes". Journal of Teacher Education 58, n.º 5 (noviembre de 2007): 359–64. http://dx.doi.org/10.1177/0022487107309977.

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