Movement patterns of large bigeye tuna (Thunnus obesus) in the open ocean, determined using ultrasonic telemetry

By L. Dagorn, P. Bach, E. Josse. 2000

237 citations recorded by the source corpus.

Subfields: Ecology, Global and Planetary Change, Nature and Landscape Conservation

View Paper: https://www.semanticscholar.org/paper/d979507f43b9bc57d2eb5efb2b177f26999600f6

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Ecology

1. Daniel W. Fuller
2. K. Schaefer
3. B. Popp
4. K. Holland
5. Frederic Menard
6. N. Nasby-Lucas
7. M. Domeier
8. H. Dewar

In Global and Planetary Change

1. B. Block
2. M. Domeier
3. N. Nasby-Lucas
4. Daniel W. Fuller
5. K. Schaefer
6. H. Dewar
7. Frederic Menard
8. B. Popp

In Nature and Landscape Conservation

1. B. Block
2. M. Domeier
3. N. Nasby-Lucas
4. H. Dewar
5. D. W. Sims
6. Daniel W. Fuller
7. G. Hays
8. K. Weng

Citations in the corpus

• Does habitat or depth influence catch rates of pelagic species (2007, background): “Alternatively, other factors such as the deep scattering layer may be paramount in explaining bigeye tuna catch rates as several studies have demonstrated an overlap between the vertical distribution of bigeye tuna and micronekton biomass during the day and night (Josse et al. 1998; Dagorn et al. 20”
• Satellite tracking of the World's largest bony fish, the ocean sunfish (Mola mola L.) in the North East Atlantic (2009, background): “For some fish, marked verticalmovementsaresometimeslinkedtore-warmingatthesurface or to fish only beingable tospend limited time in deep sub-oxic waters (Carey and Robison, 1981; Holland et al., 1992; Dagorn et al., 2000 ).”
• Tuna food habits related to the micronekton distribution in French Polynesia (2002, background): “The vertical behaviour of this species, as observed by sonic tracking in the study area (Bach et al. 1998; Dagorn et al. 2000), as well as the taxa observed in its stomach contents show that bigeye forage during the day on the deep scattering layers or on myctophid aggregations when they are present”
• Movements, behavior and habitat preferences of juvenile white sharks Carcharodon carcharias in the eastern Pacific (2007, background): “Twilight activity has been noted in a wide range of pelagic fishes including tunas (Thunnini) (Dagorn et al. 2000, Kitagawa et al. 2000, Schaefer & Fuller 2002), billfishes (Xiphidae, Istiophoridae) (Carey & Robison 1981, Holland et al. 1990a) and mako sharks Isurus oxyrinchus (Sepulveda et al.…”
• Inferring the depth distribution of catchability for pelagic fishes and correcting for variations in the depth of longline fishing gear (2005, background): “The efficacy of those thresholds will vary seasonally, spatially, among species, and with body size (Dagorn et al. 2000).”
• An overview of historical changes in the fishing gear and practices of pelagic longliners, with particular reference to Japan’s Pacific fleet (2007, background): “, ambient temperature, oxygen concentration, light levels, prey and predators (Dagorn et al. 2000).”
• Movements of bluefin tuna (Thunnus thynnus) in the northwestern Atlantic Ocean recorded by pop-up satellite archival tags (2005, background): “Holland et al. (1992) and Dagorn et al. (2000) suggested that small bigeye tuna make frequent daytime excursions into surface waters in order to increase their body temperatures and repay oxygen debt.”
• Insights into Young of the Year White Shark, Carcharodon carcharias, Behavior in the Southern California Bight (2004, methodology): “The punctuated vertical excursions observed in Figure 3b are similar to patterns that have been observed in a number of species employing both behavioral (blue sharks, Carey & Scharold 1990) and physiological (bigeye tuna, Holland et al. 1992, Dagorn et al. 2000) thermoregulation.”
• Opportunistic predation in tuna: a size-based approach (2006, background): “Results of electronic tagging have shown that adult bigeye tuna are able to reach very deep layers, and that they usually make successive vertical, U-shape dives (e.g. Dagorn et al. 2000, Musyl et al. 2003).”
• A review of the adaptive significance and ecosystem consequences of zooplankton diel vertical migrations (2003, background): “For example, tracked bigeye tuna and swordfish have been shown sometimes to move up into shallow water during the day, possibly to re-warm (Carey & Robison, 1981; Dagorn et al., 2000).”
• Hydrological and trophic characteristics of tuna habitat: consequences on tuna distribution and longline catchability (2002, background): “Using simultaneous acoustic data (on both tunas and their prey), experimental longline data, and hydrological data collected during the ECOTAP Program (a joint scientific project between IRD, Institut de Recherche pour le Développement; IFREMER, Institut Français de Recherche pour l’Exploitation de ”
• The biology and ecology of the ocean sunfish Mola mola: a review of current knowledge and future research perspectives (2009, result): “Similar behaviour has been observed in a variety of fish species such as swordfish Xiphias gladius (Carey and Robison 1981), blue shark Prionace glauca (Carey and Scharold 1990) and bluefin ((Thunnus thynnus) and bigeye (T. obesus) tuna ( Dagorn et al. 2000; Kitagawa et al. 2007).”
• Periodic behavior and residence time of yellowfin and bigeye tuna associated with fish aggregating devices around Okinawa Islands, as identified with automated listening stations (2005, methodology): “The horizontal and vertical movements of yellowfin and bigeye tuna around FADs and in the open ocean have been well documented by ultrasonic tracking and archival tagging (Yonemori 1984; Holland et al. 1990; Cayre´ 1991; Brill et al. 1999; Block et al. 1997; Dagorn et al. 2000a, 2000b; Schaefer an”
• Vertical movements, behavior, and habitat of bigeye tuna (Thunnus obesus) in the equatorial eastern Pacific Ocean, ascertained from archival tag data (2010, background): “Historical studies using ultrasonic telemetry of fine-scale movements and short-term behavior of bigeye equipped with acoustic tags, while associated with anchored FADs off Hawaii (Holland et al. 1990) and while non-associated in pelagic waters off French Polynesia ( Dagorn et al. 2000 ), described ”
• A rapid ontogenetic shift in the diet of juvenile yellowfin tuna from Hawaii (2006, background): “Tunas have evolved the ability to physiologically thermoregulate their body temperature, and are thereby able to pursue prey from the surface mixed layer into deeper, colder water, and to return to the surface mixed layer (Holland et al. 1992; Holland and Sibert 1994; Block et al. 1997; Dagorn et a”
• Use of Pop-up Satellite Archival Tags to Demonstrate Survival of Blue Marlin (Makaira nigricans) Released from Pelagic Longline Gear (2003, background): “This pattern is similar to diurnal vertical migrations observed in bigeye tuna (Thunnus obesus) (Holland et al., 1990; Dagorn et al., 2000), and swordfi sh (Sedberry and Loefer, 2001) and may relate to feeding within the deep scattering layer.”
• Movement patterns, depth preferences, and stomach temperatures of free-swimming juvenile mako sharks, Isurus oxyrinchus, in the Southern California Bight (2004, unknown): “Although these trends are consistent with those described for other pelagic species known to follow and prey on the vertically migrating deep scattering layer (DSL) (Carey and Robinson 1981; Holland et al. 1990; Dagorn et al. 2000; Schaefer and Fuller 2002), all but one of the suspected mako feedi”
• Bigeye Tuna (Thunnus obesus) behaviour and phisiology and their relevance to stock assessments and fishery biology (2005, background): “…and correlated with environmental conditions, (e.g., Dizon et al. 1978, Carey and Robison 1981, Carey and Olson 1982, Holland et al. 1990a, 1990b, Carey 1990, Brill et al. 1993, 1999, Dagorn et al. 2000a, 2000b, Arnold and Dewar 2001, Gunn and Block 2001, Graves et al. 2002, Musyl et al. 2003).”