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Journal articles on the topic 'Snook ecology'

Author: Grafiati

Published: 4 June 2021

Last updated: 3 February 2022

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1

Ault, E., S. Webb, and D. Cox. "Offshore behavioral contingent of an estuarine fish population, common snook Centropomus undecimalis." Marine Ecology Progress Series 669 (July 8, 2021): 175–89. http://dx.doi.org/10.3354/meps13692.

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Research that identifies behavioral contingents, portions of a population that exhibit alternate life history strategies or habitat preferences, can provide a better understanding of a species’ resilience to disturbances, changes in environmental factors, and harvest. Sightings of the estuarine-dependent common snook Centropomus undecimalis at offshore reef areas throughout the year in southeast Florida prompted an investigation to determine whether a contingent of the snook population remains offshore year-round and if they can contribute to the inshore population. This study employed underwater visual observations, specimen collections, and acoustic telemetry over 7 yr to document and describe the snook that utilize offshore habitat. Fish were observed in groups of up to 225 individuals, 20.4 km from an inlet, and in waters up to 36.6 m deep. Snook were present in 79.4% of dive surveys conducted on artificial reefs but only in 18.4% of surveys on natural reefs. Acoustic telemetry showed that many fish remained offshore for multiple years. Most sampled fish (89.1%) were spawning capable, with some classified as actively spawning (15.8%). Reports of snook using offshore reefs occur elsewhere, including southwest Florida and the Florida Keys, indicating that this contingent behavior may not be unique to southeast Florida. Evaluating these occurrences and identifying potential triggers that prompt snook to leave the estuary for an offshore environment can aid in determining how the offshore contingent affects the overall population.

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2

Boucek, Ross E., Mariajesus Soula, Felipe Tamayo, and Jennifer S. Rehage. "A once in 10 year drought alters the magnitude and quality of a floodplain prey subsidy to coastal river fishes." Canadian Journal of Fisheries and Aquatic Sciences 73, no. 11 (November 2016): 1672–78. http://dx.doi.org/10.1139/cjfas-2015-0507.

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Disturbances that alter cross-habitat food web linkages can lead to whole-scale changes to aquatic systems. In coastal rivers of the Everglades (Florida, U.S.A.), increases in rainfall inundate adjacent floodplains, providing habitat for floodplain fish and macroinvertebrate species. In the dry season, rainfall decreases and floodplains dry, forcing floodplain prey into these river systems. These prey provide a prey subsidy for an estuarine predator, the common snook (Centropomus undecimalis). In 2011, severe drought impacted the region, likely affecting this prey subsidy. In this study, we ask (i) did the 2011 drought affect the magnitude and composition of floodplain prey subsidies to the common snook? and (ii) if species composition changed, were there energetic differences between the pre- and post-disturbance prey species? Results showed that 1 year after the drought, subsidies to the common snook decreased by 75%. On top of that decrease in overall flux, diet composition of the common snook switched from floodplain fishes to drought-tolerant floodplain macroinvertebrates. Lastly, energetic analyses showed that these postdrought macroinvertebrate prey subsidies had 43% less calories than floodplain fishes. Our findings illustrate the importance of considering not only the biomass that transfers from one food web to the next, but also how the species composition of the subsidy may affect incorporation into recipient food webs.

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3

Taylor, R. G., H. J. Grier, and J. A. Whittington. "Spawning rhythms of common snook in Florida." Journal of Fish Biology 53, no. 3 (September 1998): 502–20. http://dx.doi.org/10.1111/j.1095-8649.1998.tb00998.x.

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4

Grier, H. J., and R. G. Taylor. "Testicular maturation and regression in the common snook." Journal of Fish Biology 53, no. 3 (September 1998): 521–42. http://dx.doi.org/10.1111/j.1095-8649.1998.tb00999.x.

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5

Tavares, L. E. R., and J. L. Luque. "Community ecology of metazoan parasites of the later juvenile common snook Centropomus undecimalis (Osteichthyes: Centropomidae) from the coastal zone of the state of Rio de Janeiro, Brazil." Brazilian Journal of Biology 64, no. 3a (August 2004): 523–29. http://dx.doi.org/10.1590/s1519-69842004000300015.

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Between April and December 2000, seventy-nine specimens of Centropomus undecimalis from Angra dos Reis, coastal zone of the State of Rio de Janeiro (23º01'S, 44º19'W), Brazil, were necropsied to study their infracommunities of metazoan parasites. Nine species of metazoan parasites were collected: 1 digenean, 1 monogenean, 1 acantocephalan, 1 nematode, 4 copepods, and 1 isopod, and 96.2% of the fishes were parasitized by one or more metazoan, with mean of 85.3 ± 122.9 parasite/fish. The digenean Acanthocollaritrema umbilicatum Travassos, Freitas & Bührnheim represented the majority of the parasites specimens collected, totaling, 94.7%. This species was the most abundant, prevalent, and dominant, showing positive correlation with the host's total body length and parasite abundance. The copepod species Acantholochus unisagittatus Tavares & Luque presented differences in abundance in relation to sex of host. The mean diversity in the infracommunities of C. undecimalis was H = 0.095 ± 0.116, with no correlation with the host's total body length but correlated with the host's sex. No pair of parasite species showed positive or negative association or covariation. The dominance of digenean A. umbilicatum in the later juvenile common snook parasite community could be related with the predatory food habits of common snook and an apparent feeding transition period which might occasion great exposure to infective forms.

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6

Tringali, M. D., and T. M. Bert. "The genetic stock structure of common snook (Centropomus undecimalis)." Canadian Journal of Fisheries and Aquatic Sciences 53, no. 5 (May 1, 1996): 974–84. http://dx.doi.org/10.1139/f96-027.

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7

Álvarez-González, Carlos Alfonso. "Partial characterization of digestive proteases of fat snook (Centropomus paralellus)." Hidrobiológica 27, no. 3 (December 15, 2017): 419–27. http://dx.doi.org/10.24275/uam/izt/dcbs/hidro/2017v27n3/alvarez.

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8

Álvarez-González, Carlos Alfonso. "Partial characterization of digestive proteases of fat snook (Centropomus paralellus)." Hidrobiológica 27, no. 3 (December 15, 2017): 419–27. http://dx.doi.org/10.24275/uam/izt/dcbi/hidro/2017v27n3/alvarez.

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9

Soto-Rodriguez, SA, R. Lozano-Olvera, SM Abad-Rosales, JM Martínez-Brown, and L. Ibarra-Castro. "Susceptibility of Pacific white snook Centropomus viridis to Vibrio species." Diseases of Aquatic Organisms 134, no. 3 (May 23, 2019): 189–95. http://dx.doi.org/10.3354/dao03370.

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10

Brame, AB, CC McIvor, EB Peebles, and DJ Hollander. "Site fidelity and condition metrics suggest sequential habitat use by juvenile common snook." Marine Ecology Progress Series 509 (August 27, 2014): 255–69. http://dx.doi.org/10.3354/meps10902.

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11

Roberts, Steven B., Leslie F. Jackson, William King, Ronald G. Taylor, Harry J. Grier, and Craig V. Sullivan. "Annual Reproductive Cycle of the Common Snook: Endocrine Correlates of Maturation." Transactions of the American Fisheries Society 128, no. 3 (May 1999): 436–45. http://dx.doi.org/10.1577/1548-8659(1999)128<0436:arcotc>2.0.co;2.

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12

Alvarez‐Lajonchère, Luis, and Ronald G. Taylor. "Economies of scale for juvenile production of common snook (Centropomus undecimalisBloch)." Aquaculture Economics & Management 7, no. 5-6 (January 2003): 273–92. http://dx.doi.org/10.1080/13657300309380345.

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13

Brennan, Nathan P., Meaghan C. Darcy, and Kenneth M. Leber. "Predator-free enclosures improve post-release survival of stocked common snook." Journal of Experimental Marine Biology and Ecology 335, no. 2 (August 2006): 302–11. http://dx.doi.org/10.1016/j.jembe.2006.04.001.

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14

Wakida-Kusunoki, Armando Toyokazu. "Mexican snook (Centropomus poeyi ), a new predator of devil fish (Pterygoplichthys pardalis)." Hidrobiológica 26, no. 1 (April 15, 2016): 147–49. http://dx.doi.org/10.24275/uam/izt/dcbs/hidro/2016v26n1/wakida.

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15

Young, JM, BG Yeiser, and JA Whittington. "Spatiotemporal dynamics of spawning aggregations of common snook on the east coast of Florida." Marine Ecology Progress Series 505 (May 28, 2014): 227–40. http://dx.doi.org/10.3354/meps10774.

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16

Young, Joy M., Beau G. Yeiser, James A. Whittington, and Jynessa Dutka‐Gianelli. "Maturation of female common snook Centropomus undecimalis : implications for managing protandrous fishes." Journal of Fish Biology 97, no. 5 (September 28, 2020): 1317–31. http://dx.doi.org/10.1111/jfb.14475.

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17

Terán-Martínez, Jazmín, Rocío Rodiles-Hernández, Marco A. A. Garduño-Sánchez, and Claudia Patricia Ornelas-García. "Molecular Characterization of the Common Snook, Centropomus undecimalis (Bloch, 1792) in the Usumacinta Basin." Diversity 13, no. 8 (July 29, 2021): 347. http://dx.doi.org/10.3390/d13080347.

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The common snook is one of the most abundant and economically important species in the Usumacinta basin in the Gulf of Mexico, which has led to overfishing, threatening their populations. The main goal of the present study was to assess the genetic diversity and structure of the common snook along the Usumacinta River in order to understand the population dynamics and conservation status of the species. We characterized two mitochondrial markers (mtCox1 and mtCytb) and 11 microsatellites in the Usumacinta basin, which was divided into three zones: rainforest, floodplain and river delta. The mitochondrial data showed very low diversity, showing some haplotypic diversity differences between the rainforest and delta zones. In contrast, we consistently recovered two genetic clusters in the Usumacinta River basin with the nuclear data in both the DAPC and STRUCTURE analyses. These results were consistent with the AMOVA analyses, which showed significant differences among the genetic clusters previously recovered by DAPC and STRUCTURE. In terms of diversity distribution, the floodplain zone corresponded to the most diverse zone according to the mitochondrial and nuclear data, suggesting that this is a transition zone in the basin. Our results support the relevance of the molecular characterization and monitoring of the fishery resources at the Usumacinta River to better understand their connectivity, which could help in their conservation and management.

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18

Díaz-Jaimes, Píndaro, Edson Sandoval-Castellanos, and Manuel Uribe-Alcocer. "Comparative population structure of three snook species (Teleostei: Centropomidae) from the eastern central Pacific." Ichthyological Research 54, no. 4 (November 26, 2007): 380–87. http://dx.doi.org/10.1007/s10228-007-0413-3.

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19

Winner, Brent L., David A. Blewett, Robert H. McMichael, and Cameron B. Guenther. "Relative Abundance and Distribution of Common Snook along Shoreline Habitats of Florida Estuaries." Transactions of the American Fisheries Society 139, no. 1 (January 2010): 62–79. http://dx.doi.org/10.1577/t08-215.1.

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20

Adams, Aaron J., R. Kirby Wolfe, and Craig A. Layman. "Preliminary Examination of How Human-driven Freshwater Flow Alteration Affects Trophic Ecology of Juvenile Snook (Centropomus undecimalis) in Estuarine Creeks." Estuaries and Coasts 32, no. 4 (May 8, 2009): 819–28. http://dx.doi.org/10.1007/s12237-009-9156-x.

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21

Santos, A. A., R. C. Gutierre, M. M. Antoniazzi, M. J. T. Ranzani-Paiva, M. R. R. Silva, C. T. F. Oshima, and M. I. Egami. "Morphocytochemical, immunohistochemical and ultrastructural characterization of the head kidney of fat snook Centropomus parallelus." Journal of Fish Biology 79, no. 7 (November 2, 2011): 1685–707. http://dx.doi.org/10.1111/j.1095-8649.2011.02718.x.

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22

Massie, Jordan A., Bradley A. Strickland, Rolando O. Santos, Javiera Hernandez, Natasha Viadero, Ross E. Boucek, Hugh Willoughby, Michael R. Heithaus, and Jennifer S. Rehage. "Going Downriver: Patterns and Cues in Hurricane-Driven Movements of Common Snook in a Subtropical Coastal River." Estuaries and Coasts 43, no. 5 (August 5, 2019): 1158–73. http://dx.doi.org/10.1007/s12237-019-00617-y.

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23

Stevens, Philip W., Jynessa Dutka-Gianelli, Eric J. Nagid, Alexis A. Trotter, Kevin G. Johnson, Travis Tuten, and James A. Whittington. "Niche Partitioning Among Snook (Pisces: Centropomidae) in Rivers of Southeastern Florida and Implications for Species Range Limits." Estuaries and Coasts 43, no. 2 (December 1, 2019): 396–408. http://dx.doi.org/10.1007/s12237-019-00650-x.

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24

SEYOUM, SEIFU, MICHAEL D. TRINGALI, and JAMIE G. SULLIVAN. "Isolation and characterization of 27 polymorphic microsatellite loci for the common snook, Centropomus undecimalis." Molecular Ecology Notes 5, no. 4 (December 2005): 924–27. http://dx.doi.org/10.1111/j.1471-8286.2005.01118.x.

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25

Ross, C., R. W. Tilghman, J. X. Hartmann, and F. Mari. "Distribution of parvalbumin isotypes in adult snook and their potential applications as species‐specific biomarkers." Journal of Fish Biology 51, no. 3 (September 1997): 561–72. http://dx.doi.org/10.1111/j.1095-8649.1997.tb01512.x.

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26

Borges, João Carlos Shimada, Leandro Nogueira Pressinotti, Vicente Gomes, and José Roberto Machado Cunha da Silva. "Lipidic and proteic absorption in digestive tract of tropical fat snook (Centropomus parallelus, POEY 1860)." Journal of Experimental Marine Biology and Ecology 386, no. 1-2 (April 2010): 39–44. http://dx.doi.org/10.1016/j.jembe.2010.02.013.

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27

Stevens, Philip W., Jynessa Dutka-Gianelli, Eric J. Nagid, Alexis A. Trotter, Kevin G. Johnson, Travis Tuten, and James A. Whittington. "Correction to: Niche Partitioning among Snook (Pisces: Centropomidae) in Rivers of Southeastern Florida and Implications for Species Range Limits." Estuaries and Coasts 43, no. 2 (December 18, 2019): 438–39. http://dx.doi.org/10.1007/s12237-019-00674-3.

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28

Wilson, Raymond R., Kim A. Donaldson, Marc E. Frischer, and Thomas B. Young. "Mitochondrial DNA Control Region of Common Snook and Its Prospect for Use as a Genetic Tag." Transactions of the American Fisheries Society 126, no. 4 (July 1997): 594–606. http://dx.doi.org/10.1577/1548-8659(1997)126<0594:mdcroc>2.3.co;2.

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29

Lowerre-Barbieri, Susan K., Frederic E. Vose, and James A. Whittington. "Catch-and-Release Fishing on a Spawning Aggregation of Common Snook: Does it Affect Reproductive Output?" Transactions of the American Fisheries Society 132, no. 5 (September 2003): 940–52. http://dx.doi.org/10.1577/t02-001.

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30

ITAGAKI, MICHAEL KENGO, MARIO KATSURAGAWA, CELINA MARIA MARCONDES PIMENTEL, IDILI DA ROCHA OLIVEIRA, and MARCIO HIDEKAZU OHKAWARA. "Early development of fat snook, Centropomus parallelus (Poey 1860) (Teleostei, Centropomidae) from Southeastern Brazil." Zootaxa 3669, no. 1 (June 5, 2013): 65. http://dx.doi.org/10.11646/zootaxa.3669.1.7.

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31

Brennan, Nathan P., Kenneth M. Leber, H. Lee Blankenship, John M. Ransier, and Roger DeBruler. "An Evaluation of Coded Wire and Elastomer Tag Performance in Juvenile Common Snook under Field and Laboratory Conditions." North American Journal of Fisheries Management 25, no. 2 (May 2005): 437–45. http://dx.doi.org/10.1577/m04-003.1.

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32

Taylor, Ronald G., James A. Whittington, William E. Pine, and Kenneth H. Pollock. "Effect of Different Reward Levels on Tag Reporting Rates and Behavior of Common Snook Anglers in Southeast Florida." North American Journal of Fisheries Management 26, no. 3 (August 2006): 645–51. http://dx.doi.org/10.1577/m04-185.1.

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33

MARTÍNEZ-BROWN, JUAN MANUEL, JAIME NAVARRO-FLORES, FRANCISCO JAVIER GARCÍA-RODRÍGUEZ, LEONARDO IBARRA-CASTRO, CARMEN ELVIRA VARGAS-PERALTA, MIGUEL ÁNGEL DEL RÍO-PORTILLA, and RODRIGO MARTÍNEZ-MORENO. "Revision of the diagnostic characters of two morphologically similar snook species, Centropomus viridis and C. nigrescens (Carangiformes: Centropomidae)." Zootaxa 4915, no. 3 (January 22, 2021): 326–38. http://dx.doi.org/10.11646/zootaxa.4915.3.2.

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Historically, the taxonomic identification of the two snook species, Centropomus viridis and C. nigrescens, has been challenging due to their morphological similarity and the inconsistency of the characters used for diagnosis. Therefore, this study aimed to evaluate the usefulness of the morphologic, meristic, and morphometric characters currently being used to identify C. viridis and C. nigrescens, based on molecular data. The results showed that the gas-bladder shape (i.e., C. viridis with diverticula and C. nigrescens without diverticula) was the only morphological character univocally related to genetic identification. Likewise, geometric morphometrics separated two groups; each corresponds to only one of two genetically (and gas bladder shape) identified species. Of all the meristic characters examined, only the second dorsal fin ray count (nine for C. viridis and ten for C. nigrescens) was related to the gas bladder shape and genetic identity; therefore, it is the only external character with a diagnostic utility to separate each species.

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34

Li, Chenhong, Betancur-R. Ricardo, Wm Leo Smith, and Guillermo Ortí. "Monophyly and interrelationships of Snook and Barramundi (Centropomidae sensu Greenwood) and five new markers for fish phylogenetics." Molecular Phylogenetics and Evolution 60, no. 3 (September 2011): 463–71. http://dx.doi.org/10.1016/j.ympev.2011.05.004.

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35

Malinowski, Christopher, Julie Cavin, Jeffrey Chanton, Lia Chasar, Felicia Coleman, and Christopher Koenig. "Trophic Relationships and Niche Partitioning of Red Drum Sciaenops ocellatus and Common Snook Centropomus undecimalis in Coastal Estuaries of South Florida." Estuaries and Coasts 42, no. 3 (January 10, 2019): 842–56. http://dx.doi.org/10.1007/s12237-018-00512-y.

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36

Stevens, Philip W., Matthew E. Kimball, Garrett M. Elmo, Kyle L. Williams, Jared L. Ritch, and Derek P. Crane. "Investigation into the Occurrence of Juvenile Common Snook Centropomus undecimalis, a Subtropical Estuarine Sport Fish, in Saltmarshes Beyond Their Established Range." Estuaries and Coasts 44, no. 5 (January 15, 2021): 1477–83. http://dx.doi.org/10.1007/s12237-020-00884-0.

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37

Brennan, Nathan P., Carl J. Walters, and Kenneth M. Leber. "Manipulations of Stocking Magnitude: Addressing Density-Dependence in a Juvenile Cohort of Common Snook (Centropomus undecimalis)." Reviews in Fisheries Science 16, no. 1-3 (February 20, 2008): 215–27. http://dx.doi.org/10.1080/10641260701689022.

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38

Violante-González, Juan, Scott Monks, Agustín Rojas-Herrera, and Salvador Gil Guerrero. "Richness and Species Composition of Helminth Communities in Yellowfin Snook (Centropomus robalito) (Centropomidae) from Coastal Lagoons in Guerrero, Mexico." Comparative Parasitology 78, no. 1 (January 2011): 84–94. http://dx.doi.org/10.1654/4450.1.

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39

Assis, Daniel Alvares Silveira de, Danieli Marinho Nobre, Marcelo Carneiro de Freitas, Leonardo Evangelista Moraes, and Alexandre Clistenes de Alcântara Santos. "Reproductive biology of the protandric hermaphrodite fat snook Centropomus parallelus Poey 1860 in a tropical estuary, northeastern Brazil." Studies on Neotropical Fauna and Environment 54, no. 3 (September 2, 2019): 225–35. http://dx.doi.org/10.1080/01650521.2019.1663594.

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40

Costa Filho, João, Mônica Yumi Tsuzuki, Giovanni Lemos de Mello, Luiz Cláudio Miletti, Karim Hahn Lüchmann, and Carlos André da Veiga Lima-Rosa. "Growth of juvenile common snook (Centropomus undecimalis Bloch, 1792) reared at different temperatures and salinities: Morphometric parameters, RNA/DNA, and protein/DNA ratios." Journal of Applied Aquaculture 29, no. 3-4 (June 29, 2017): 199–206. http://dx.doi.org/10.1080/10454438.2017.1334615.

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41

Rhody, N. R., C. L. Neidig, H. J. Grier, K. L. Main, and H. Migaud. "Assessing Reproductive Condition in Captive and Wild Common Snook Stocks: A Comparison between the Wet Mount Technique and Histological Preparations." Transactions of the American Fisheries Society 142, no. 4 (July 2013): 979–88. http://dx.doi.org/10.1080/00028487.2013.788564.

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42

Cianciotto, Anthony C., Jonathan M. Shenker, Aaron J. Adams, Jacob J. Rennert, and David Heuberger. "Modifying mosquito impoundment management to enhance nursery habitat value for juvenile common Snook (Centropomus undecimalis) and Atlantic tarpon (Megalops atlanticus)." Environmental Biology of Fishes 102, no. 2 (January 8, 2019): 403–16. http://dx.doi.org/10.1007/s10641-018-0838-8.

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43

Andrade, H., J. Santos, and R. Taylor. "Life-history traits of the common snook Centropomus undecimalis in a Caribbean estuary and large-scale biogeographic patterns relevant to management." Journal of Fish Biology 82, no. 6 (April 26, 2013): 1951–74. http://dx.doi.org/10.1111/jfb.12123.

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44

Pülmanns, Nathalie, Gustavo Adolfo Castellanos‐Galindo, and Uwe Krumme. "Tidal‐diel patterns in feeding and abundance of armed snook Centropomus armatus from macrotidal mangrove creeks of the tropical eastern Pacific Ocean." Journal of Fish Biology 93, no. 5 (October 29, 2018): 850–59. http://dx.doi.org/10.1111/jfb.13788.

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45

Costa e Silva, Gisleine Hoffmann, Matheus Oliveira Freitas, and Vinícius Abilhoa. "Reproductive biology of the fat snook Centropomus parallelus Poey , 1860 ( Teleostei, Centropomidae ) and implications for its management in the southern Atlantic Ocean." Journal of Fish Biology 99, no. 2 (March 21, 2021): 669–72. http://dx.doi.org/10.1111/jfb.14718.

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46

Donaldson, Kim A., and Raymond R. Wilson. "Amphi-Panamic Geminates of Snook (Percoidei: Centropomidae) Provide a Calibration of the Divergence Rate in the Mitochondrial DNA Control Region of Fishes." Molecular Phylogenetics and Evolution 13, no. 1 (October 1999): 208–13. http://dx.doi.org/10.1006/mpev.1999.0625.

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47

Mendoza-Franco, Edgar F., Juan Violante-González, and Víctor M. Vidal-Martínez. "A NEW DIPLECTANID (MONOGENEA) GENUS AND SPECIES FROM THE GILLS OF THE BLACK SNOOK, CENTROPOMUS NIGRESCENS (PERCIFORMES: CENTROPOMIDAE) OF THE PACIFIC COAST OF MEXICO." Journal of Parasitology 92, no. 3 (June 2006): 481–85. http://dx.doi.org/10.1645/ge-3538.1.

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48

Anderson, Joel, Damon Williford, Alin González, Chris Chapa, Fernando Martinez‐Andrade, and R. Deborah Overath. "Demographic, Taxonomic, and Genetic Characterization of the Snook Species Complex ( Centropomus spp.) along the Leading Edge of Its Range in the Northwestern Gulf of Mexico." North American Journal of Fisheries Management 40, no. 1 (February 2020): 190–208. http://dx.doi.org/10.1002/nafm.10394.

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49

MENDOZA-GARFIAS, BERENIT, and GERARDO PÉREZ-PONCE DE LEÓN. "Phyllodistomum centropomi sp. n. (Digenea: Gorgoderidae), a parasite of the fat snook, Centropomus parallelus (Osteichthyes: Centropomidae), in the Papaloapan River at Tlacotalpan, Veracruz State, Mexico." Zootaxa 1056, no. 1 (September 30, 2005): 43. http://dx.doi.org/10.11646/zootaxa.1056.1.3.

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Phyllodistomum centropomi n. sp. (Digenea: Gorgoderidae) is described from the urinary bladder of Centropomus parallelus (Osteichthyes: Centropomidae) from the Papaloapan River in Veracruz State, Mexico. This species is distinguished from its congeners in North America, either marine or freshwater, in having the vitelline glands located in a posterolateral position to the ovary and the margin of the hindbody possessing slight undulations with muscular indentations from the level of testes to the posterior end of the body. The new species most closely resembles P. mayesi Brooks & MacDonald, 1986, a parasite of Trachycorystes insignis in the Río Atrato, in the vicinity of Quibdo, Choco, Colombia, since both possesses postovarian paired vitelline glands, but P. centropomi differs by having muscular undulations on the margin of hindbody and an oral sucker/acetabulum ratio close to unity.

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CARVALHO-FILHO, ALFREDO, JOICIANE DE OLIVEIRA, CAMILA SOARES, and JULIANA ARARIPE. "A new species of snook, Centropomus (Teleostei: Centropomidae), from northern South America, with notes on the geographic distribution of other species of the genus." Zootaxa 4671, no. 1 (September 16, 2019): 81–92. http://dx.doi.org/10.11646/zootaxa.4671.1.6.

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Abstract:

Centropomus irae sp. nov. (Centropomidae) is described from two localities in the state of Amapá, northern Brazil. The new species differs from all its congeners by the typically brown-colored lateral line, the relatively smaller mean interorbital width (4.1% of SL vs. 5.2–6.9%), mean snout length (8.9% of SL vs. 9.8–11.1%), mean diameter of the orbit (4.5% of SL vs. 5.4–7.3%), and mean mandible length (15.7% of SL vs.19.9–21.6%). The new species can also be distinguished from the similar Centropomus undecimalis by the number of scales around the caudal peduncle (18–23, usually 19–21, vs. 22–28, usually 24–27). With Centropomus irae sp. nov., seven species of the genus are now known to occur in the western Atlantic. The distribution of Centropomus in Brazilian waters is updated and a key to the species of this genus is presented. [Zoobank URL: urn:lsid:zoobank.org:act:3D497B38-48A5-4A6E-B377-6D57E82D4DE4[

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