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Journal articles on the topic 'Marine fishes'

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1

Barrett, Luke T., Arthur de Lima, and Jordan S. Goetze. "Evidence of a biomass hotspot for targeted fish species within Namena Marine Reserve, Fiji." Pacific Conservation Biology 25, no. 2 (2019): 204. http://dx.doi.org/10.1071/pc18034.

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Namena is Fiji’s oldest and second largest no-take marine reserve, and has relatively high abundance and biomass of targeted fishes within its boundaries due to a high level of protection since its creation in 1997 (formalised in 2005). Following anecdotal reports of exceptionally high fish abundance at the Grand Central Station dive site within Namena, we conducted a 500-m meandering diver-operated video transect along the main reef formation, to obtain abundance, length and biomass estimates for fish species targeted by local fishers. Our census revealed extremely high diversity, abundance and biomass (11436kgha−1) of targeted fishes. While demersal reef fishes were present at higher densities than on typical fished reefs in the region, they were dwarfed by aggregations of reef-associated pelagics, namely the barracuda Sphyraena forsteri (5540kgha−1) and the trevally Caranx sexfasciatus (4448kgha−1). These estimates are comparable to those of historically unfished or ‘pristine’ locations, an unexpected finding given the historical fishing pressure within the reserve before its establishment and ongoing pressure in surrounding fished areas. This finding presents Grand Central Station as a useful reference site for ecologists and managers, and highlights the ability of protected coral reefs to support or attract very high densities of fish.
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2

D'Alessandro, Evan K. "Marine Fishes of Florida." Bulletin of Marine Science 92, no. 3 (July 1, 2016): 381. http://dx.doi.org/10.5343/bms.br.2016.0003.

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3

Winfield, Ian J. "MARINE FISHES OF FLORIDA." Journal of Fish Biology 91, no. 5 (November 2017): 1528–29. http://dx.doi.org/10.1111/jfb.13465.

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4

Metzger, David C. H., and Patricia M. Schulte. "Epigenomics in marine fishes." Marine Genomics 30 (December 2016): 43–54. http://dx.doi.org/10.1016/j.margen.2016.01.004.

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5

Robinson, Mary. "Marine Fishes of Florida." Reference Reviews 31, no. 6 (August 21, 2017): 30–31. http://dx.doi.org/10.1108/rr-04-2017-0087.

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6

Whiteman, E. A., and I. M. Côté. "Monogamy in marine fishes." Biological Reviews 79, no. 2 (May 2004): 351–75. http://dx.doi.org/10.1017/s1464793103006304.

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7

Kovačić, Marcelo, Vasilis Gerovasileiou, and Robert A. Patzner. "Fishes in Marine Caves." Fishes 9, no. 6 (June 20, 2024): 243. http://dx.doi.org/10.3390/fishes9060243.

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Fishes in marine caves have attracted limited attention by the scientific community in comparison to subterranean fishes which have lost eyes and pigmentation. They constitute a largely unexplored component of marine fish diversity, except for the relatively well-studied marine caves of the Mediterranean Sea. These habitats are characterized by steep environmental gradients of decreasing light and decreasing water exchange. The fishes recorded so far in marine caves are not exclusive residents of this habitat and they are also present at least in the other mesolithial habitats. In the Mediterranean marine caves, 132 fishes have been recorded to date, representing about 17% of the total Mediterranean fish species richness. Most of these species are reported from the anterior cave zones where some light still exists, while a smaller number of species are known from the totally dark zones. Among them, 27.3% are accidental visitors, 53.8% are the regular mesolithial visitors and switchers between mesolithion and open water, 5.3% are permanent residents of the mesolithion, but also occur in other habitats, and 13.6% are exclusive permanent residents of mesolithion. Some mesolithial exclusive permanent residents recorded in marine caves share similar morphology, probably as adaptations to these habitats.
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8

Tupper, Mark, and Murray A. Rudd. "Species-specific impacts of a small marine reserve on reef fish production and fishing productivity in the Turks and Caicos Islands." Environmental Conservation 29, no. 4 (December 2002): 484–92. http://dx.doi.org/10.1017/s0376892902000346.

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Marine reserves are widely considered to potentially benefit reef fisheries through emigration, yet the empirical basis for predicting the extent of this for small reserves is weak. The effects of fishing pressure and habitat on biomass and catch per unit effort (CPUE) of three species of exploited reef fish were studied at South Caicos, Turks and Caicos Islands. Distribution and abundance of hogfish (Lachnolaimus maximus) and white margate (Haemulon album) were inversely correlated with cover of fleshy macroalgae. Nassau grouper (Epinephelus striatus) were positively associated with vertical relief, but were unaffected by algal cover. Mean size, density, and biomass of hogfish were higher in a small (4 km2) marine reserve than on fished reefs, as was biomass of white margate. CPUE of hogfish was inversely related to distance from the centre of the reserve, suggesting that spillover of this species from the reserve to adjacent reefs may enhance local yields, possibly providing economic incentives for fishers to comply with reserve regulations. Fishing pressure, however, had no apparent effect on Nassau grouper. Larger fishes and those that migrate to spawn, such as economically valuable Nassau grouper, may move over too large a range to be effectively protected by small marine reserves. Small reserves may not protect all fish, but they can increase the biomass of smaller or more sedentary reef fishes and may be a useful tool for the conservation or management of species such as hogfish. Other policy options, such as seasonal spawning closures or total allowable catches, need to be considered for larger, more mobile fishes in the Turks and Caicos Islands.
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9

McAlpine, Donald F. "The Ocean Pout, Zoarces americanus, and the Ocean Sunfish, Mola mola: Additions to the Marine Ichthyofauna of the Lower Saint John River System, New Brunswick, with a Summary of Marine Fish Reported from the Estuary." Canadian Field-Naturalist 127, no. 1 (July 14, 2013): 38. http://dx.doi.org/10.22621/cfn.v127i1.1405.

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Recent records for the Ocean Pout, Zoarces americanus (collected 11 February 2011), and the Ocean Sunfish, Mola mola (photograph taken 24 June 2012), in the lower Saint John River system, New Brunswick, add to the list of marine fishes reported from this oceanographically unique estuary system. A total of 62 species of strictly freshwater, anadromous, catadromous, and marine fishes have now been recorded in the Saint John River system, with 49 of these in the Saint John River sensu stricto. The Acadian Redfish, Sebastes faciatus, a species assessed as threatened by the Committee on the Status of Endangered Wildlife in Canada, appears to be among these. While strictly marine fishes may contribute relatively little to the overall biomass of fishes in the Saint John River system, marine species account for 30.6% of the biodiversity of fishes in the river to date. This suggests that marine fishes may be a more significant component of the ichthyofauna of the lower Saint John River system than is generally recognized.
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10

P., Arturo Acero, Juan José Orellana Amador, and Juan Jose Orellana Amador. "Marine Fishes of Los Cobanos: Fishes of El Salvador." Copeia 1988, no. 2 (May 18, 1988): 505. http://dx.doi.org/10.2307/1445900.

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11

Saldanha, Luiz. "Marine Fishes, Habitats and Conservation." Netherlands Journal of Zoology 42, no. 2-3 (1991): 190–99. http://dx.doi.org/10.1163/156854291x00270.

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12

Montgomery, John. "Migration ecology of marine fishes." New Zealand Journal of Marine and Freshwater Research 49, no. 4 (October 2, 2015): 503. http://dx.doi.org/10.1080/00288330.2015.1096800.

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13

LAKRA, W. S., M. S. VERMA, M. GOSWAMI, K. K. LAL, V. MOHINDRA, P. PUNIA, A. GOPALAKRISHNAN, K. V. SINGH, R. D. WARD, and P. HEBERT. "DNA barcoding Indian marine fishes." Molecular Ecology Resources 11, no. 1 (December 13, 2010): 60–71. http://dx.doi.org/10.1111/j.1755-0998.2010.02894.x.

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14

Morris, Corey. "MIGRATION ECOLOGY OF MARINE FISHES." Journal of Fish Biology 88, no. 4 (April 2016): 1669–70. http://dx.doi.org/10.1111/jfb.12913.

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15

Risto, Melissa. "MARINE FISHES OF ARCTIC CANADA." Journal of Fish Biology 94, no. 5 (May 2019): 828. http://dx.doi.org/10.1111/jfb.13962.

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16

McIntyre, A. D. "Forage Fishes in Marine Ecosystems." Fisheries Research 51, no. 1 (April 2001): 94–95. http://dx.doi.org/10.1016/s0165-7836(00)00311-8.

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17

Bohlmeyer, D. A., and J. R. Gold. "Genetic studies in marine fishes." Marine Biology 108, no. 2 (June 1991): 197–206. http://dx.doi.org/10.1007/bf01344334.

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18

McDevitt-Irwin, Jamie Marie, Susanna Drake Fuller, Catharine Grant, and Julia Kathleen Baum. "Missing the safety net: evidence for inconsistent and insufficient management of at-risk marine fishes in Canada." Canadian Journal of Fisheries and Aquatic Sciences 72, no. 10 (October 2015): 1596–608. http://dx.doi.org/10.1139/cjfas-2015-0030.

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Marine conservation is often perceived as being in conflict with fisheries management. In Canada, at-risk marine fishes denied listing under the Species at Risk Act (SARA) are meant to receive comparable measures under the Fisheries Act. We assess the effectiveness of these Acts by examining (i) how long it takes a marine fish assessed as being at risk to move through the process and receive conservation measures, (ii) whether there are biases against marine fishes in the SARA process additional to the known listing bias, and (iii) when denied listing, to what extent these species are protected by the Fisheries Act. Overall, at-risk marine fishes typically spend 3.25 years under consideration for SARA, during which time they receive no additional protection. Endangered and Threatened marine fishes (i.e., those most at risk) face the greatest bias and receive the least protection; their SARA decisions are typically delayed, with almost 5 years usually passing between their COSEWIC (Committee on the Status of Endangered Wildlife in Canada) assessment and listing decision; most (70.6%) are then denied listing, after which the Fisheries Act provides few of the SARA-required measures. For SARA-listed marine fishes, recovery strategies are usually late and to date no action plans have been produced. Marine fish conservation is hindered by SARA’s slow pace, incomplete recovery measures, and inadequate implementation of the Fisheries Act. We provide recommendations for improving conservation of at-risk marine fishes in Canada.
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19

Clark, Colin W. "Modelling the behaviour of fishers and fishes." ICES Journal of Marine Science 75, no. 3 (December 9, 2017): 932–40. http://dx.doi.org/10.1093/icesjms/fsx212.

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Abstract I describe my personal evolution as a modeller of behaviour, both human and (non-human) animal behaviour, using dynamic state-variable models. At first I worked in renewable resource Economics, especially the economics of marine fisheries where I collaborated extensively with Gordon R. Munro. Subsequently, in collaboration with Marc Mangel (and many field biologists) I worked in Behavioural Ecology. Mathematical models have played a major role in both of these subjects, but until recently mostly static models were used, on the grounds that dynamic (not to mention stochastic) models were too difficult to work with. I express the hope that our use of relatively simple (but not too simple) dynamic models has established the fact that such models can be extremely helpful, perhaps essential, in understanding many aspects of behaviour.
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20

Kamal, Sadia Afrin, Md Nur Alam Chad, Jakir Hossain, Afshana Ferdous, and Roksana Jahan. "Availability of Marine Fishes in Cox’s Bazar, Bangladesh: A Case Study on the BFDC Landing Center." Croatian Journal of Fisheries 80, no. 3 (September 1, 2022): 133–40. http://dx.doi.org/10.2478/cjf-2022-0014.

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Abstract Fish availability in the coastal landing center highlights the assumption of stocks in the marine fishing zone of the ocean. This study, therefore, aimed to analyze the availability of marine fishes in the Bangladesh Fisheries Development Corporation (BFDC) landing center, Cox’s Bazar, Bangladesh between January 2021 and May 2021. A total of 54 species were recorded, of which 42 were marine fishes, 7 were shellfishes and 5 were large fishes. The dominant orders were Perciformes (56%), Scombriformes (17%) and Clupeiformes (10%). More than 56% of the total marine fishes were classified as Least Concern, nearly 10% were categorized as Near Threatened and 2% were marked Vulnerable. The dominant orders of shellfish were Portunidae (43%), followed by Penaidae (29%), Loligonidae (14%) and Octopopidae (14%). Shrimp Penaeous monodon had the highest consumer demand, whereas consumer demand for non-conventional shellfish was comparatively low. Most of the shellfish were categorized as Least Concern. Among large fishes, the wider availability of sharks (five species) and rays (two species) was observed in the winter and monsoon season, although the consumer demand for those large fishes was low. The Vulnerable sharks and rays were Sphyma zygaena and Mobula birostris. This study elucidates the present scenario of marine fishes in the BFDC fish landing center, Cox’s Bazar, Bangladesh.
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21

Gao, Yu-Miao, Ke-Shu Zou, Lei Zhou, Xian-De Huang, Yi-Yang Li, Xiang-Yang Gao, Xiao Chen, and Xiao-Yong Zhang. "Deep Insights into Gut Microbiota in Four Carnivorous Coral Reef Fishes from the South China Sea." Microorganisms 8, no. 3 (March 18, 2020): 426. http://dx.doi.org/10.3390/microorganisms8030426.

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Investigations of gut microbial diversity among fish to provide baseline data for wild marine fish, especially the carnivorous coral reef fishes of the South China Sea, are lacking. The present study investigated the gut microbiota of four carnivorous coral reef fishes, including Oxycheilinus unifasciatus, Cephalopholis urodeta, Lutjanus kasmira, and Gnathodentex aurolineatus, from the South China Sea for the first time using high-throughput Illumina sequencing. Proteobacteria, Firmicutes, and Bacteroidetes constituted 98% of the gut microbiota of the four fishes, and 20 of the gut microbial genera recovered in this study represent new reports from marine fishes. Comparative analysis indicated that the four fishes shared a similar microbial community, suggesting that diet type (carnivorous) might play a more important role in shaping the gut microbiota of coral reef fishes than the species of fish. Furthermore, the genera Psychrobacter, Escherichia-Shigella, and Vibrio constituted the core microbial community of the four fishes, accounting for 61–91% of the total sequences in each fish. The lack of the genus Epulopiscium in the four fishes was in sharp contrast to what has been found in coral reef fishes from the Red Sea, in which Epulopiscium was shown to be the most dominant gut microbial genus in seven herbivorous coral reef fishes. In addition, while unique gut microbial genera accounted for a small proportion (8–13%) of the total sequences, many such genera were distributed in each coral reef fish species, including several genera (Endozoicomonas, Clostridium, and Staphylococcus) that are frequently found in marine fishes and 11 new reports of gut microbes in marine fishes. The present study expands our knowledge of the diversity and specificity of gut microbes associated with coral reef fishes.
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22

Willis, Trevor J., and Russell C. Babcock. "A baited underwater video system for the determination of relative density of carnivorous reef fish." Marine and Freshwater Research 51, no. 8 (2000): 755. http://dx.doi.org/10.1071/mf00010.

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Estimates of the relative density of fishes form the basis of many marine ecological studies as well as the assessment of effects of fishing or pollution. Plasticity in the behavioural response of large reef fishes to SCUBA divers means that commonly used underwater visual census (UVC) techniques do not always provide reliable estimates of relative density. The paper describes the system configuration, deployment methods, testing and use of a remotely deployed baited underwater video (BUV) system for the survey of carnivorous reef fishes (snapper, Pagrus auratus and blue cod,Parapercis colias) in marine reserves of northern New Zealand. Concurrent UVC and BUV surveys inside and outside a marine reserve showed that, whereas UVC detected few snapper in either area (resulting in little confidence in statistically significant results), BUV demonstrated significant differences in relative density. Conversely, blue cod were found to occur at significantly higher densities within the reserve by UVC, but not by BUV. The provision of accurate estimates of fish size (<20 mm error) from video footage also illustrated differences in size structure between protected and fished populations. The data suggest that a combination of survey techniques is likely to be necessary where multispecies assemblages are being assessed.
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23

Popper, Arthur N., Jane Fewtrell, Michael E. Smith, and Robert D. McCauley. "Anthropogenic Sound: Effects on the Behavior and Physiology of Fishes." Marine Technology Society Journal 37, no. 4 (December 1, 2003): 35–40. http://dx.doi.org/10.4031/002533203787537050.

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Anthropogenic sound in the marine environment continues to increase. Sound sources range from increased vessel traffic to transient but intense sounds such as those produced by seismic air guns, pile driving, or some sonars. While most interest in anthropogenic sounds has focused on marine mammals, there is an increasing concern regarding the impact of such sounds on fishes and marine invertebrates. Since the inner ear hearing receptors of fishes are similar to those of marine mammals, any effects seen on the hearing receptors of marine mammals may also be found in fishes and vice versa. Despite increasing interest in the effects of sounds on fishes, this issue has only been addressed on the most limited scale. Here we review the current literature in this area. It has been reported that high sound levels can damage the inner ear sensory cells, produce hearing loss (threshold shifts), elicit stress responses, and alter the behavior of fishes. At least in terms of hearing loss, these effects are modulated by exposure sound level and duration. The effects of various types of sound (e.g., impulsive vs. continuous) and long-term impacts of how anthropogenic sounds affect the behavior and ecology of fishes need exploration in the future.
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HABIB, KAZI AHSAN, and MD JAYEDUL ISLAM. "An updated checklist of Marine Fishes of Bangladesh." Bangladesh Journal of Fisheries 32, no. 2 (January 15, 2021): 357–67. http://dx.doi.org/10.52168/bjf.2020.32.40.

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A checklist of the marine fishes of Bangladesh is presented with their scientific, common andBangla or local names. The global IUCN Red List catagories of these species are also provided. Thisinventory of the marine fish species is compiled from different major and valid published scientific papers,reports and books published within last 50 years from 1970 to 2020. The directory covers a total of 740species belonging to 389 Genera of 145 Families and 30 Orders. Among the fish species, 53.38% areexclusively marine and 46.62% are found in both brackish and marine water. Besides, 296 species of fishesare reef associated and 204 of these are recorded from the Saint Martin’s Island. Further, 271 species ofbrakishwater and/or marine fishes are commonly observed in the Sundarbans mangrove ecosystem and itsadjacent sea area. About 7% of the total marine fishes of Bangladesh are identified as threatened as per globalIUCN Red List. However, the conservation status of the marine fish species of Bangladesh has not yet beenassessed locally by IUCN which is essential. The updated checklist will constitute the reference inventory ofmarine fishes of the coastal and maritime area of the country.
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25

HUNTER, JANET A., and THOMAS H. CRIBB. "Transversotrematidae (Platyhelminthes: Trematoda) are rich and abundant on Indo-Pacific fishes." Zootaxa 2442, no. 1 (May 3, 2010): 25. http://dx.doi.org/10.11646/zootaxa.2442.1.2.

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The Transversotrematidae, perhaps because of their unique and obscure habitat under the scales of fishes, have been little reported in surveys and studies of trematodes of marine fishes. At present there are just three fully marine species recognized. We have surveyed 2604 individuals, from 359 species and 71 families, of marine fishes from a range of sites mainly from coral reefs in the Indo-Pacific. We found infections on 87 species and 15 families of fishes; one family, Monodactylidae, is new for transversotrematids. Morphological and molecular analyses suggest that, in addition to Crusziella formosa which parasitizes only mugilids, there are three complexes of species of Transversotrema; one associated with mullids only, one with haemulids, labrids, lethrinids and scarids, and one associated with at least 13 families of fishes. Molecular evidence suggests that these complexes comprise at least 22 species. Overall we conclude that the richness of this family has been significantly underestimated and that it is rich and abundant on fishes of the Indo-Pacific.
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26

MARCENIUK, Alexandre Pires, Bruno Eleres SOARES, Matheus Marcos ROTUNDO, Rodrigo Antunes CAIRES, Ricardo de Souza ROSA, Wagner César Rosa dos SANTOS, Ana Patrícia Barros CORDEIRO, et al. "The bycatch of piramutaba, Brachyplatystoma vaillantii industrial fishing in a salinity and depth gradient in the Amazon estuary, Brazil." Acta Amazonica 53, no. 2 (June 2023): 93–106. http://dx.doi.org/10.1590/1809-4392202200342.

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ABSTRACT The piramutaba, Brachyplatystoma vaillantii is a freshwater catfish that is the most abundant fishery resource in the Amazon estuary. Piramutaba trawling is done on industrial fishing scale and is characterized by the presence of many freshwater and marine bycatch species, with and without commercial value. Here we describe the bycatch of the industrial fishery of piramutaba in the Amazon estuary and evaluate the relationship of two important environmental factors, depth and salinity, with the accidental capture of freshwater and marine fishes in the Amazon estuary in the rainy and dry seasons. We identified 21 cartilaginous fish species (19.1% freshwater and 80.9% marine) and 125 bony fish species (25.6% freshwater and 74.4% marine). The bycatch included 64 species without commercial value (43% of all bycatch species), which are always discarded. Freshwater and estuarine fishes exhibited significantly higher abundances in shallower environments, while marine fishes were similarly abundant along the entire depth gradient. On the contrary, the abundance of freshwater fishes significantly decreased, and that of estuarine and marine fishes significantly increased with increasing salinity. Regarding the conservation status of the bycatch species, one is classified as vulnerable (VU), and seven as critically endangered (CR). The information on the bycatch of piramutaba fishery in the Amazon estuary is important to subsidize regional fisheries policies and the management of protected areas.
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27

Soldo, Alen, and Rigers Bakiu. "Checklist of marine fishes of Albania." Acta Adriatica 62, no. 1 (July 26, 2021): 63–73. http://dx.doi.org/10.32582/aa.62.1.4.

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This paper presents an updated checklist of marine fishes of Albania and the first one published in the English language. The checklist contains 262 species compiled from published literature and personal surveys.
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28

Fricke, Ronald. "European Red List of Marine Fishes." Marine Biology Research 11, no. 9 (August 20, 2015): 1004–7. http://dx.doi.org/10.1080/17451000.2015.1064535.

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29

Couch, John A., H. Moller, and K. Anders. "Diseases and Parasites of Marine Fishes." Estuaries 9, no. 3 (September 1986): 229. http://dx.doi.org/10.2307/1352135.

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30

Ravichandr, S., K. Kumaravel, G. Rameshkuma, and T. T. AjithKumar. "Antimicrobial Peptides from the Marine Fishes." Research Journal of Immunology 3, no. 2 (February 1, 2010): 146–56. http://dx.doi.org/10.3923/rji.2010.146.156.

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31

ZEMLAK, TYLER S., ROBERT D. WARD, ALLAN D. CONNELL, BRONWYN H. HOLMES, and PAUL D. N. HEBERT. "DNA barcoding reveals overlooked marine fishes." Molecular Ecology Resources 9 (May 2009): 237–42. http://dx.doi.org/10.1111/j.1755-0998.2009.02649.x.

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32

Rüber, Lukas, and Rafael Zardoya. "RAPID CLADOGENESIS IN MARINE FISHES REVISITED." Evolution 59, no. 5 (May 2005): 1119–27. http://dx.doi.org/10.1111/j.0014-3820.2005.tb01048.x.

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33

Clements, K. D., and J. H. Choat. "Fermentation in Tropical Marine Herbivorous Fishes." Physiological Zoology 68, no. 3 (May 1995): 355–78. http://dx.doi.org/10.1086/physzool.68.3.30163774.

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34

Sommerville, Christina. "Diseases and parasites of marine fishes." Marine Pollution Bulletin 18, no. 4 (April 1987): 195. http://dx.doi.org/10.1016/0025-326x(87)90247-5.

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35

Tsikliras, Athanassios C., Efthimia Antonopoulou, and Konstantinos I. Stergiou. "Spawning period of Mediterranean marine fishes." Reviews in Fish Biology and Fisheries 20, no. 4 (February 19, 2010): 499–538. http://dx.doi.org/10.1007/s11160-010-9158-6.

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36

HOBBS, J. P. A., G. P. JONES, and P. L. MUNDAY. "Extinction Risk in Endemic Marine Fishes." Conservation Biology 25, no. 5 (June 15, 2011): 1053–55. http://dx.doi.org/10.1111/j.1523-1739.2011.01698.x.

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37

Velansky, P. V., and E. Ya Kostetsky. "Lipids of marine cold-water fishes." Russian Journal of Marine Biology 34, no. 1 (January 2008): 51–56. http://dx.doi.org/10.1134/s1063074008010070.

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38

Moore, Glenn I., Susan M. Morrison, J. Barry Hutchins, Gerald R. Allen, and Alison Sampey. "Kimberley marine biota. Historical data: fishes." Records of the Western Australian Museum, Supplement 84, no. 1 (2014): 161. http://dx.doi.org/10.18195/issn.0313-122x.84.2014.161-206.

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39

Rüber, Lukas, and Rafael Zardoya. "RAPID CLADOGENESIS IN MARINE FISHES REVISITED." Evolution 59, no. 5 (2005): 1119. http://dx.doi.org/10.1554/04-394.

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40

Hutchings, Jeffrey A. "Collapse and recovery of marine fishes." Nature 406, no. 6798 (August 2000): 882–85. http://dx.doi.org/10.1038/35022565.

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41

Evelyn, Trevor P. T. "Diseases and parasites of marine fishes." Aquaculture 67, no. 3-4 (December 1987): 385–86. http://dx.doi.org/10.1016/0044-8486(87)90221-3.

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42

Vincent, Amanda C. J., and Heather J. Hall. "The threatened status of marine fishes." Trends in Ecology & Evolution 11, no. 9 (September 1996): 360–61. http://dx.doi.org/10.1016/0169-5347(96)30041-4.

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43

Sanchez-Quintana, Damian, and Juan M. Hurle. "Ventricular myocardial architecture in marine fishes." Anatomical Record 217, no. 3 (March 1987): 263–73. http://dx.doi.org/10.1002/ar.1092170307.

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44

Purohit, Ritu, and Shouriehebal Soni. "Isolation and Identification of Vibrio sp. from Marine Fishes of Mumbai, Maharashtra, India." UTTAR PRADESH JOURNAL OF ZOOLOGY 45, no. 15 (July 9, 2024): 179–87. http://dx.doi.org/10.56557/upjoz/2024/v45i154233.

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Vibrio is a common bacterium found in marine fishes. Vibrio species are pathogenic to humans and cause various gastrointestinal diseases. Fish markets, fish harvesting areas, vectors like flies, seawater and sometimes fresh water bodies are the source of spread of this bacterium. Improper handling or pathogen contamination during transit has an impact not only on human health but also on the population of marine fish. Vibrio is known to be a human pathogen, the onset and spread of this bacterium causes severe diarrhoea. In this study, the presence of Vibrio species in marine water fishes was determined from fishes collected from various fish markets in Mumbai, Maharashtra. Various biochemical tests were performed to isolate and identify the Vibrio species. In the family Vibrionaceae three species such as Vibrio cholera, Vibrio parahaemolyticus and Vibrio vulnificus were identified. Additionally, a survey was conducted using google forms to understand the consumption rate of fish by people and also to gauge the awareness among public about the bacterial disease caused by consumption of fishes. It was observed that a large number of individuals consumed various types of fishes including marine and freshwater fishes on a regular basis. People also consume raw fish delicacies. However, very few individuals were aware of the bacteria and its related diseases, most of the participants were unaware of the presence of bacteria like Vibrio cholera and its associated diseases.
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45

Hutchings, Jeffrey A. "Conservation biology of marine fishes: perceptions and caveats regarding assignment of extinction risk." Canadian Journal of Fisheries and Aquatic Sciences 58, no. 1 (January 1, 2001): 108–21. http://dx.doi.org/10.1139/f00-228.

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Quantitative criteria used to assign species to categories of extinction risk may seriously overestimate these risks for marine fishes. Contemporary perception is that marine fishes may be less vulnerable to extinction than other taxa, because of great natural variability in abundance, high fecundity, rapid population growth, and an intrinsically high capability of recovering from low population size. Contrary to perception, however, there appears to be generally little theoretical or empirical support for the hypotheses that marine fish are more likely to experience large reductions in population size, to produce unusually high levels of recruitment, to have higher reproductive rates, or to recover more rapidly from prolonged population declines than nonmarine fishes. Although existing population-decline criteria may not accurately reflect probabilities of biological extinction, they do appear to reflect the converse-population recovery. Insufficient support for contemporary perceptions of their susceptibility to extinction, coupled with caveats associated with the assignment of extinction risk, suggest that significant increases in the population-decline thresholds used to assign marine fishes to at-risk categories would be inconsistent with a precautionary approach to fisheries management and the conservation of marine biodiversity.
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46

C.S., Vidhya, Susmi Biswas, Sourav Gangopadhyay, Jayeeta Majumder, G. Vidyasagar Reddy, Abhijit Debnath, Ashiq Hussain Magrey, K. K. Sivakumar, Aparna Srivastava, and Nadiya Afreen. "Exploring Human Health Benefits from Marine Biomedical Research with Fishes." UTTAR PRADESH JOURNAL OF ZOOLOGY 45, no. 11 (May 6, 2024): 59–68. http://dx.doi.org/10.56557/upjoz/2024/v45i114070.

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Marine organisms, particularly fishes, harbor a treasure trove of bioactive compounds with immense potential for human health applications. In this review, we delve into the diverse array of bioactive molecules derived from marine fishes and their implications for biomedical research. We explore the therapeutic properties of fish-derived compounds, including antimicrobial peptides, omega-3 fatty acids, collagen, and bioactive peptides, among others andthe mechanisms of action and preclinical studies supporting the use of these compounds in various human health conditions, such as cardiovascular disease, cancer, inflammatory disorders, and neurodegenerative diseases. Additionally, we highlight the importance of sustainable sourcing and ethical considerations in marine biomedical research. Overall, this review underscores the significance of marine fishes as a source of novel therapeutic agents and the promising avenues they offer for advancing human health.
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47

Lekshmi, P. S. Swathi, R. Narayanakumar, and Shyam S. Salim. "Market Efficiency Indicators in Marine Fish Marketing in Goa, India." Journal of Agricultural Science 12, no. 7 (June 15, 2020): 112. http://dx.doi.org/10.5539/jas.v12n7p112.

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The Indian State of Goa has a coastal length of 104 Kms and the State contributes 1.85% to the marine fish production of the country. A study was conducted to assess the market efficiency indicators such as Gross Marketing Margin, Percentage Share of Fisherman in the Consumers Rupee (PSFCR) and the Coefficient of variation. The study revealed that high value fishes such as cobia, silver Whiting, seer fishes, prawns and milk shark recorded a comparatively higher price spread. Varieties which recorded higher PSFCR were speckled prawn (72.86%), cobia (70.31%), seerfish (69.98%), Brown shrimps or ginga prawns (69.43%), pony fish (67.58%) and milk shark (65.61%). At the point of first sales, high value fishes such as cobia, seerfishes, prawns and silver biddy had a co-efficient of variation of less than 10% indicating a higher price stability. High value fishes such as ribbon fishes, seerfishes, cobia, indian white prawn, barracudas, brown prawns, speckled prawns, kadal shrimps and half beaks were among the list of fishes which recorded a low co-efficient of variation of less than 10% at the point of last sales.
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48

Bawazir, Gamal Mohammed, and Zaher Ali Al-Agwan. "Marine ornamental Fishes in the Red Sea: Statusand trade." University of Aden Journal of Natural and Applied Sciences 24, no. 2 (March 22, 2022): 441–48. http://dx.doi.org/10.47372/uajnas.2020.n2.a11.

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The ornamental fish trade is rapidly expanding and there is a growing recreational demand for aquarium fishes in international markets. This paper aims to initially assess the status of the marine ornamental fishes and their trade in the Yemeni Red Sea. For this purpose, a field survey was conducted in May-June (2006) in 42 sites in this coast, and information regarding the trade was collected. These sites were located in 40 islands where coral reefs are the most dominant habitats. There were statistically differences in the number of ornamental fishes between and within the sites. Many species of such fishes were targeted for trade in unsustainable manners. This could affect the marine ecosystem in Yemen if such trade continues without unsustainable management.
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Yates, DC, SI Lonhart, and SL Hamilton. "Effects of marine reserves on predator-prey interactions in central California kelp forests." Marine Ecology Progress Series 655 (November 26, 2020): 139–55. http://dx.doi.org/10.3354/meps13526.

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Marine reserves are often designed to increase density, biomass, size structure, and biodiversity by prohibiting extractive activities. However, the recovery of predators following the establishment of marine reserves and the consequent cessation of fishing may have indirect negative effects on prey populations by increasing prey mortality. We coupled field surveys with empirical predation assays (i.e. tethering experiments) inside and outside of 3 no-take marine reserves in kelp forests along the central California coast to quantify the strength of interactions between predatory fishes and their crustacean prey. Results indicated elevated densities and biomass of invertebrate predators inside marine reserves compared to nearby fished sites, but no significant differences in prey densities. The increased abundance of predators inside marine reserves translated to a significant increase in mortality of 2 species of decapod crustaceans, the dock shrimp Pandalus danae and the cryptic kelp crab Pugettia richii, in tethering experiments. Shrimp mortality rates were 4.6 times greater, while crab mortality rates were 7 times greater inside reserves. For both prey species, the time to 50% mortality was negatively associated with the density and biomass of invertebrate predators (i.e. higher mortality rates where predators were more abundant). Video analyses indicated that macro-invertivore fishes arrived 2 times faster to tethering arrays at sites inside marine reserves and began attacking tethered prey more rapidly. The results indicate that marine reserves can have direct and indirect effects on predators and their prey, respectively, and highlight the importance of considering species interactions in making management decisions.
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Miller, Elizabeth Christina, Kenji T. Hayashi, Dongyuan Song, and John J. Wiens. "Explaining the ocean's richest biodiversity hotspot and global patterns of fish diversity." Proceedings of the Royal Society B: Biological Sciences 285, no. 1888 (October 10, 2018): 20181314. http://dx.doi.org/10.1098/rspb.2018.1314.

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For most marine organisms, species richness peaks in the Central Indo-Pacific region and declines longitudinally, a striking pattern that remains poorly understood. Here, we used phylogenetic approaches to address the causes of richness patterns among global marine regions, comparing the relative importance of colonization time, number of colonization events, and diversification rates (speciation minus extinction). We estimated regional richness using distributional data for almost all percomorph fishes (17 435 species total, including approximately 72% of all marine fishes and approximately 33% of all freshwater fishes). The high diversity of the Central Indo-Pacific was explained by its colonization by many lineages 5.3–34 million years ago. These relatively old colonizations allowed more time for richness to build up through in situ diversification compared to other warm-marine regions. Surprisingly, diversification rates were decoupled from marine richness patterns, with clades in low-richness cold-marine habitats having the highest rates. Unlike marine richness, freshwater diversity was largely derived from a few ancient colonizations, coupled with high diversification rates. Our results are congruent with the geological history of the marine tropics, and thus may apply to many other organisms. Beyond marine biogeography, we add to the growing number of cases where colonization and time-for-speciation explain large-scale richness patterns instead of diversification rates.
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