Global habitat preferences of commercially valuable tuna
Open accessAI snapshot
Written from the paper’s full text.
TL;DR
This study uses longline CPUE from 1958–2007 for six tuna species across the Atlantic, Indian, and Pacific Oceans to compare global habitat preferences with quotient analysis and Generalized Additive Models. It finds tropical tunas prefer warm, low-oxygen, stratified waters, while Atlantic and southern bluefin tunas prefer higher chlorophyll and tolerate the most extreme sea surface height anomalies and mixed layer depths.
Key findings
- Full GAMs explained 45% (bigeye) to 64% (skipjack) of null deviance; all final models retained TEMP5, salinity, SSH, MLD, and DCHL.
- Quotient analysis showed tropical tunas prefer warmer surface waters than temperate tunas: yellowfin preferred >25°C, while bigeye and skipjack preferred 20–28°C; albacore avoided waters below 14°C, and southern bluefin preference and Atlantic bluefin tolerance extended down to 4°C.
- Atlantic bluefin tolerated the widest range of environmental conditions, including the widest temperature tolerance range (approximately 1–20°C), high salinity above 37 PSU, and negative SSH anomalies; southern bluefin preferred mixed layer depths beyond approximately 300 m.
- Tropical tunas generally preferred lower oxygen environments than temperate tunas; yellowfin preferred relatively low oxygen waters (<0.2 mmol/l), bigeye tolerated them, and skipjack avoided waters below 0.1 mmol/l.
Methods
- Longline catch and effort data were obtained from the five TRFMOs for 1958–2007, except southern bluefin from 1965 and eastern Pacific stocks only until 2004; no skipjack longline data were available from WCPFC. Data were aggregated by quarter and 5°×5° resolution, and nominal CPUE was computed as catch per number of hooks, using only positive CPUE records.
- Environmental variables came from the PISCES biogeochemical model: surface temperature (TEMP5), temperature at 100 m (TEMP100), sea surface salinity, dissolved oxygen at 100 m, sea surface height, mixed layer depth, chlorophyll, and mesozooplankton averaged over 0–100 m.
- Habitat preferences were assessed with quotient analysis using 400 re-sampling iterations to test preference/tolerance/avoidance, and with GAMs assuming lognormal positive CPUE, spline functions with smoothness restricted to 4, fixed factors for year, season, and stock, and stepwise backward selection by AIC; TEMP100, oxygen, and zooplankton were excluded from full GAMs due to collinearity.
Limitations
- The paper states that CPUE may not accurately reflect population abundance due to changes in fishing practice, fleet efficiency, or environmental effects on catchability, although fixed factors were included and interpreting abundance trends was out of scope.
- The paper states that collinearity prevented inclusion of oxygen and other correlated variables in the final GAMs, and that predictions outside the observed range were unrealistic for some species, such as skipjack in the Mediterranean and at extreme latitudes.
- The paper states that longline data mostly catch adult tunas, so results mainly reflect adult habitat preferences; it also notes that spatio-temporally averaged chlorophyll may not capture frontal effects, prey field observations are generally lacking, and tagging studies are often local and short-term.
Model-written summary. Check it against the paper before relying on it.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
22 of 79 cited sources checked · 13 supported · 0 flagged · accuracy not yet measured
- Premisecitation
Temperature and oxygen affect important biological processes and thus determine the spatial distribution of tunas.
“Temperature and oxygen affect important biological processes and thus determine the spatial distribution of tunas (Barkley et al., 1978;Boyce et al., 2008;Brill, 1994;Strama et al., 2012).”
Quote in the paperSubstantial claim1 of 3 sources checked- cites Barkley et al., 1978
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites Boyce et al., 2008 source
The Introduction links physiological temperature tolerance to tuna range boundaries and identifies temperature as a strong predictor of distribution. It mentions oxygen content only as a factor hypothesized to correlate with abundance and distribution; it does not establish that oxygen affects biological processes and thereby determines tuna distribution. The cited claim states that relationship more definitively than this paper does. (LLM, conf=0.86)
Experimental — accuracy not yet measured - cites Brill, 1994 source
- Premisecitation
Salinity can influence large-scale spatial distribution of tunas.
“Salinity can influence large scale spatial distribution (e.g.Fromentin et al., 2014;Maury et al., 2001;Reygondeau et al., 2012).”
Quote in the paperNot a substantial claim2 of 3 sources checked - Premisecitation
Habitat studies using fishery or survey data are often spatially limited and focused on single species.
“Habitat studies using fishery or survey data are often spatially limited and focused on single species (e.g.Chen et al., 2005;Sagarminaga and Arrizabalaga, 2010).”
Quote in the paperSubstantial claim1 of 2 sources checked- cites Chen et al., 2005 source
The Introduction describes limitations in the spatial coverage of past fishery-oceanography studies, and this paper’s own habitat analysis focuses on one species, albacore. But it uses fishery and environmental data across the whole Indian Ocean, so Chen et al. is not itself an example of a spatially limited study. (LLM, conf=0.85)
Experimental — accuracy not yet measured - cites Sagarminaga and Arrizabalaga, 2010 source
- Premisereasoning
There are few studies where the habitat preferences of a group of species are analysed using similar datasets and methods at broad spatial scales.
“In fact, there are few studies where the habitat preferences of a group of species are analysed using similar datasets and methods at broad spatial scales (but see Reygondeau et al. 2012).”
Quote in the paperSubstantial claim1 of 1 sources checked- cites Reygondeau et al. 2012 source
- Premisecitation
The distribution of prey is one of the main drivers of the spatial distribution and behaviour of tunas.
“In addition to the physical environment, the distribution of prey is also one of the main drivers of the spatial distribution and behaviour of tunas (Bertignac et al., 1998;Schick and Lutcavage, 2009, tunas, but data on tuna prey distribution and abundance is scarce and is mostly available from models (Lehodey et al., 1998).”
Quote in the paperNot a substantial claim1 of 3 sources checked- cites Bertignac et al., 1998 source
- cites Schick and Lutcavage, 2009 source
The Results report a significant association between herring density and bluefin tuna presence, and the Discussion says prey distribution predicted bluefin presence better than SST fronts. The study covers a one-week snapshot in the Gulf of Maine; it does not establish prey distribution as a main driver of behaviour or of tuna distribution generally. (LLM, conf=0.88)
Experimental — accuracy not yet measured - cites Lehodey et al., 1998 source
- Interpretationown data
Atlantic bluefin tuna can also tolerate a wide range of biotic environments in terms of plankton concentrations.
“our findings tend to confirm that Atlantic bluefin can also tolerate a wide range of biotic environments (in terms of plankton concentrations).”
Quote in the paperSubstantial claim1 of 1 sources checked- cites Fromentin et al., 2014 source
The Results and Discussion describe a wide *abiotic* niche for Atlantic bluefin tuna, based on temperature, salinity and depth. The Data section says chlorophyll concentration could not be included in the niche model, so our copy does not establish tolerance across a wide range of plankton concentrations. (LLM, conf=0.78)
Experimental — accuracy not yet measured
- Interpretationnone given
Temperature preferences provided in Boyce et al. (2008) are comparable to those provided in this study.
“For example, temperature preferences provided in Boyce et al. (2008) are comparable to those provided in this study.”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites Boyce et al. (2008) source
- Rests on an assumption: The response curves of the final GAMs can be interpreted as habitat suitability for the tuna species.
- Premisecitation
There have been several studies using alternative techniques, datasets and models, providing comprehensive descriptions of the habitat preferences of tunas in the past.
“There have been several studies using alternative techniques, datasets and models, providing comprehensive descriptions of the habitat preferences of tunas in the past (see Boyce et al., 2008;Brill, 1994;Brill and Lutcavage, 2001;Sund et al., 1981).”
Quote in the paperNot a substantial claim1 of 3 sources checked- cites Boyce et al., 2008 source
The Abstract and Database sections describe a study that compiled temperature preferences and tolerances for tuna and billfish species from 190 publications and used an empirical model to predict global richness patterns. This supports citing Boyce et al. as an example of a study using datasets and modelling to examine tuna preferences, but its focus is thermal preferences, not comprehensive habitat preferences more broadly. The supplied copy gives no page numbers for these passages. (LLM, conf=0.82)
Experimental — accuracy not yet measured - cites Brill, 1994 source
- cites Brill and Lutcavage, 2001
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Interpretationcitation
Trophic resources play a major role in the spatial distribution of tunas.
“trophic resources must play a major role in the spatial distribution of tunas, as suggested by several relatively small scale studies (Bestley et al., 2009;Lezama et al., 2010;Schick and Lutcavage, 2009) and the fact that tunas conduct, as part of their life cycles, extensive trophic migrations to exploit seasonally productive areas (e.g.Dufour et al. 2010, Fonteneau et al., 2008).”
Quote in the paperNot a substantial claim1 of 3 sources checked - Interpretationcitation
Atlantic bluefin tuna prefer negative SSH characteristic of mesoscale cyclonic eddies.
“Results with respect to SSH were consistent with other finer scale studies suggesting Atlantic bluefin preference for negative SSH characteristic of mesoscale cyclonic eddies (Teo and Block, 2010)”
Quote in the paperSubstantial claim1 of 1 sources checked- cites Teo and Block, 2010 source
- Interpretationcitation
Spatio-temporally averaged DCHL values might not best determine the distribution of these visual predators by themselves, compared with DCHL fronts to which tunas might be attracted.
“spatio-temporally averaged DCHL values might not best determine, by themselves, the distribution of these visual predators, compared with DCHL fronts to which tunas might be attracted (Brill and Lutcavage, 2001;Royer et al., 2004;Sagarminaga and Arrizabalaga, 2014).”
Quote in the paperNot a substantial claim1 of 3 sources checked- cites Brill and Lutcavage, 2001
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites Royer et al., 2004 source
In “Spatial distribution of bluefin tuna schools” (page unavailable), the paper reports that pooled chlorophyll-concentration values did not distinguish school locations, whereas schools tended to be near ocean-colour fronts. It concludes that fronts may describe relationships over entire seasons better than ocean-colour values. The paper does not identify its chlorophyll measure as DCHL, so it does not establish the claim specifically for DCHL values or DCHL fronts. (LLM, conf=0.83)
Experimental — accuracy not yet measured - cites Sagarminaga and Arrizabalaga, 2014 source
- Findingown data
Atlantic and southern bluefin tuna tolerate the most extreme sea surface height anomalies.
“The two species also tolerate most extreme sea surface height anomalies and highest mixed layer depths.”
Quote in the paperSubstantial claim- The authors state this as an assumption: CPUE is a proxy for fish abundance.
- Findingown data
Atlantic bluefin tuna tolerates the widest range of environmental conditions.
“In general, Atlantic bluefin tuna tolerates the widest range of environmental conditions.”
Quote in the paperSubstantial claim- The authors state this as an assumption: CPUE is a proxy for fish abundance.
- Findingown data
Similar patterns between species are observed for subsurface temperature (TEMP100).
“Similar patterns between species are observed for the subsurface temperature (TEMP100).”
Quote in the paperNot a substantial claim - Findingown data
Compared to temperate tunas, tropical tunas prefer stratified waters.
“Results confirmed that, compared to temperate tunas, tropical tunas prefer warm, anoxic, stratified waters.”
Quote in the paperSubstantial claim- The authors state this as an assumption: CPUE is a proxy for fish abundance.
- Findingown data
Compared to temperate tunas, tropical tunas prefer anoxic waters.
“Results confirmed that, compared to temperate tunas, tropical tunas prefer warm, anoxic, stratified waters.”
Quote in the paperSubstantial claim- The authors state this as an assumption: CPUE is a proxy for fish abundance.
- Findingnone given
Albacore and skipjack showed clearly defined preferred salinity ranges at around 36-37 PSU.
“Albacore and skipjack showed clearly defined preferred salinity ranges, at around 36-37 PSU.”
Quote in the paperNot a substantial claim - Findingown data
For all species, the full GAMs selected with the AIC criteria included all five environmental variables TEMP5, SAL, SSH, MLD and DCHL.
“For all species, the full GAMs selected with the AIC criteria included all the 5 environmental variables TEMP5, SAL, SSH, MLD and DCHL.”
Quote in the paperNot a substantial claim- The authors state this as an assumption: Positive CPUE observations follow a lognormal error distribution.
- The authors state this as an assumption: The niche model is unimodal.
- Rests on an assumption: Changes in abundance and catchability are likely to occur at the stock level.
- Findingnone given
Tropical tunas, as well as albacore, prefer slightly negative or positive values of SSH.
“Tropical tunas, as well as albacore, prefer slightly negative or positive values of SSH.”
Quote in the paperSubstantial claim - Findingown data
Model predicted distributional ranges and relative densities matched well the observations.
“In general, model predicted distributional ranges and relative densities matched well the observations (Figure 2).”
Quote in the paperSubstantial claim - Findingown data
In the case of MLD, the percentage of null deviance explained was moderate, ranging between 10% (yellowfin) and 2% (skipjack).
“In the case of MLD, the percentage explained was moderate, ranging between 10% (in the case of yellowfin) and 2% (in the case of skipjack).”
Quote in the paperNot a substantial claim- The authors state this as an assumption: Positive CPUE observations follow a lognormal error distribution.
- The authors state this as an assumption: The niche model is unimodal.
- Rests on an assumption: Changes in abundance and catchability are likely to occur at the stock level.
- Findingown data
Bigeye, yellowfin and southern bluefin tuna showed less clearly defined preference windows that included lower salinity waters, as low as 33 PSU in the case of yellowfin.
“Bigeye, yellowfin and southern bluefin tuna showed less clearly defined preference windows that included lower salinity waters, as low as 33 PSU in the case of yellowfin.”
Quote in the paperNot a substantial claim - Findingown data
The percentage of null deviance explained by DCHL and ZOO was generally moderate, between 8% and 1%.
“The percentage of null deviance explained by DCHL and ZOO was also generally moderate, between 8% and 1%.”
Quote in the paperNot a substantial claim- The authors state this as an assumption: Positive CPUE observations follow a lognormal error distribution.
- The authors state this as an assumption: The niche model is unimodal.
- Rests on an assumption: Changes in abundance and catchability are likely to occur at the stock level.
- Findingreasoning
Atlantic bluefin showed a marked preference and tolerance for high salinity waters (above 37 PSU).
“Atlantic bluefin showed a marked preference and tolerance for high salinity waters (above 37 PSU), probably linked to the role of Mediterranean waters in their life cycle.”
Quote in the paperSubstantial claim - Findingnone given
Yellowfin and albacore can tolerate higher SSH than bigeye and skipjack.
“Yellowfin and albacore can tolerate higher SSH than bigeye and skipjack.”
Quote in the paperNot a substantial claim - Findingnone given
Atlantic bluefin tuna can tolerate a similar range of oxygen values.
“Atlantic bluefin tuna can also tolerate a similar range of oxygen values.”
Quote in the paperNot a substantial claim - Findingown data
Relatively low DCHL and ZOO waters are preferred by tropical tunas and albacore compared to both bluefin tunas.
“In general, relatively low DCHL and ZOO waters are preferred by tropical tunas and albacore, compared to both bluefin tunas, for which the preference and tolerance ranges are not very well defined, but results suggest that they can tolerate a wide range of DCHL and ZOO values.”
Quote in the paperSubstantial claim - Findingown data
For temperate tunas, the ranges of preference and tolerance are shifted to colder waters.
“In the case of temperate tunas, the ranges of preference and tolerance are shifted to colder waters.”
Quote in the paperSubstantial claim - Findingnone given
All tropical tunas avoided oxygen rich environments that temperate tunas preferred/tolerated.
“All tropical tunas avoided oxygen rich environments that temperate tunas preferred/tolerated.”
Quote in the paperNot a substantial claim - Findingown data
The full GAMs explained between 45% (bigeye) and 64% (skipjack) of the null deviance.
“The full GAMs explained between 45% (for bigeye) and 64% (for skipjack) of the null deviance (table 2).”
Quote in the paperNot a substantial claim- The authors state this as an assumption: Positive CPUE observations follow a lognormal error distribution.
- The authors state this as an assumption: The niche model is unimodal.
- Rests on an assumption: Changes in abundance and catchability are likely to occur at the stock level.
- Findingown data
Atlantic and southern bluefin tuna prefer higher concentrations of chlorophyll than the rest.
“Atlantic and southern bluefin tuna prefer higher concentrations of chlorophyll than the rest.”
Quote in the paperSubstantial claim- The authors state this as an assumption: CPUE is a proxy for fish abundance.
- Findingown data
Salinity explained between 17% and 4% of the null deviance for southern bluefin, skipjack, albacore and Atlantic bluefin, with less than 2% for yellowfin and bigeye.
“Salinity explained between 17% and 4% of the null deviance for southern bluefin, skipjack, albacore and Atlantic bluefin, with less than 2% for yellowfin and bigeye.”
Quote in the paperNot a substantial claim- The authors state this as an assumption: Positive CPUE observations follow a lognormal error distribution.
- The authors state this as an assumption: The niche model is unimodal.
- Rests on an assumption: Changes in abundance and catchability are likely to occur at the stock level.
- Findingnone given
Relatively stratified waters (mixed layer depth < 80 m) are preferred by tropical tunas compared to temperate tunas.
“Relatively stratified waters (mixed layer depth < 80 m) are preferred by tropical tunas compared to temperate tunas.”
Quote in the paperSubstantial claim - Findingown data
Among tropical tunas, yellowfin tuna prefers a higher surface temperature range (beyond 25°C) than bigeye and skipjack tuna (between 20°C and 28°C).
“Among the tropical tunas, yellowfin prefers a higher (beyond 25ºC) surface temperature range than bigeye and skipjack (between 20ºC and 28ºC).”
Quote in the paperSubstantial claim - Findingown data
Compared to temperate tunas, tropical tunas prefer warm waters.
“Results confirmed that, compared to temperate tunas, tropical tunas prefer warm, anoxic, stratified waters.”
Quote in the paperSubstantial claim- The authors state this as an assumption: CPUE is a proxy for fish abundance.
- Findingnone given
In general, tropical tunas preferred lower oxygen environments than temperate tunas.
“In general, tropical tunas preferred lower oxygen environments than temperate tunas.”
Quote in the paperSubstantial claim - Findingown data
Atlantic and southern bluefin tuna tolerate the highest mixed layer depths.
“The two species also tolerate most extreme sea surface height anomalies and highest mixed layer depths.”
Quote in the paperSubstantial claim- The authors state this as an assumption: CPUE is a proxy for fish abundance.
- Findingown data
The proportion of null deviance explained by the two temperature-related variables ranged between 38% (southern bluefin) and 2% (skipjack) of total deviance.
“The proportion of null deviance explained by these two temperature related variables ranged between 38% (for southern bluefin) and 2% (skipjack) of total deviance.”
Quote in the paperNot a substantial claim- The authors state this as an assumption: Positive CPUE observations follow a lognormal error distribution.
- The authors state this as an assumption: The niche model is unimodal.
- Rests on an assumption: Changes in abundance and catchability are likely to occur at the stock level.
- Findingown data
Temperature and oxygen both explained a relatively high percentage of deviance in univariate GAMs.
“They both explained a relatively high percentage of deviance in univariate GAMs”
Quote in the paperNot a substantial claim- Rests on an assumption: Longline catch per unit effort (CPUE) is a valid proxy for tuna habitat preferences.
- Findingreasoning
Southern bluefin tuna showed wide tolerance ranges to environmental conditions.
“To a lesser degree, southern bluefin tuna also showed wide tolerance ranges to environmental conditions”
Quote in the paperNot a substantial claim- Rests on an assumption: The quotient analysis's preference, tolerance and avoidance ranges validly indicate species-specific habitat preferences.
- Findingown data
Atlantic bluefin tuna is the only species where TEMP5 is relatively non-important.
“In fact, it is the only species where TEMP5 is relatively non important.”
Quote in the paperSubstantial claim- Rests on an assumption: The quotient analysis's preference, tolerance and avoidance ranges validly indicate species-specific habitat preferences.
- Findingown data
Similar environmental preferences were estimated with GAMs and quotient analyses, especially for variables showing most contrasting response curves in the final GAMs (TEMP5, SAL and SSH).
“Although GAMs are statistically more rigorous than quotient analyses, similar environmental preferences were estimated with both approaches, especially for the variables showing most contrasting response curves in the final GAMs (TEMP5, SAL and SSH).”
Quote in the paperNot a substantial claim- Rests on an assumption: The response curves of the final GAMs can be interpreted as habitat suitability for the tuna species.
- Findingown data
Preferred mixed layer depths were between 50 and 400 m for albacore, bigeye and yellowfin tunas.
“Preferred mixed layer depths were between 50 and 400m for albacore, bigeye and yellowfin tunas.”
Quote in the paperSubstantial claim- Rests on an assumption: The response curves of the final GAMs can be interpreted as habitat suitability for the tuna species.
- Findingown data
For skipjack, suitable habitat was predicted in areas with no observations, e.g., the Mediterranean, and at extreme latitudes around 60oS and 60oN.
“In the case of skipjack (for which data were not available over the whole globe and is a bycatch species in longline fisheries), suitable habitat was predicted in areas with no observations, e.g. the Mediterranean, and at extreme latitudes around 60ºS in the southern ocean and at around 60ºN in the north Atlantic.”
Quote in the paperNot a substantial claim - Findingown data
Some response curves were relatively flat during most of the observed range (e.g., DCHL for bigeye and skipjack, or MLD for yellowfin and skipjack).
“In spite of being selected in the final model, some response curves were relatively flat during most of the observed range (e.g.DCHL for bigeye and skipjack, or MLD for yellowfin and skipjack), suggesting a relatively low influence of these environmental variables compared to the others.”
Quote in the paperNot a substantial claim- Rests on an assumption: The response curves of the final GAMs can be interpreted as habitat suitability for the tuna species.
- Findingnone given
Skipjack model predictions within the observational range were reasonable.
“However, skipjack model predictions within the observational range were reasonable.”
Quote in the paperNot a substantial claim - Findingown data
The quotient analysis showed the widest tolerance ranges (for TEMP5, TEMP100, SAL, SSH, MLD, and ZOO) for Atlantic bluefin tuna.
“The quotient analysis showed the widest tolerance ranges (i.e. for TEMP5, TEMP100, SAL, SSH, MLD, and ZOO) for Atlantic bluefin tuna.”
Quote in the paperSubstantial claim- Rests on an assumption: The quotient analysis's preference, tolerance and avoidance ranges validly indicate species-specific habitat preferences.
- Findingown data
The correlation between temperature and oxygen impeded inclusion of oxygen in the final model.
“but the correlation between them impeded inclusion of oxygen in the final”
Quote in the paperNot a substantial claim - Findingown data
Relatively high CPUE for bigeye tuna is observed between 40oS and 40oN.
“Relatively high CPUE for bigeye tuna is also observed between 40ºS and 40ºN”
Quote in the paperNot a substantial claim- Rests on an assumption: Longline catch per unit effort (CPUE) is a valid proxy for tuna habitat preferences.
- Findingnone given
TEMP5 and SSH generally showed more contrast in comparison to MLD and DCHL.
“TEMP5 and SSH generally showed more contrast in comparison to those of MLD and DCHL.”
Quote in the paperNot a substantial claim- Rests on an assumption: Longline catch per unit effort (CPUE) is a valid proxy for tuna habitat preferences.
- Findingown data
In yellowfin tuna, MLD appeared slightly more important than SSH.
“In the case of yellowfin, MLD appeared slightly more important than SSH.”
Quote in the paperNot a substantial claim- Rests on an assumption: Longline catch per unit effort (CPUE) is a valid proxy for tuna habitat preferences.
- Findingown data
Highest yellowfin CPUE are found around the equator.
“while highest yellowfin CPUE are found around the equator.”
Quote in the paperNot a substantial claim- Rests on an assumption: Longline catch per unit effort (CPUE) is a valid proxy for tuna habitat preferences.
- Findingown data
Atlantic bluefin tuna shows the northernmost distribution, up to around 60°N, including the Mediterranean Sea.
“Atlantic bluefin tuna shows the northernmost distribution, up to around 60°N, including the Mediterranean Sea.”
Quote in the paperNot a substantial claim- Rests on an assumption: Longline catch per unit effort (CPUE) is a valid proxy for tuna habitat preferences.
- Findingown data
DCHL response curves showed relatively higher influences in yellowfin and albacore compared to bigeye or skipjack, where response curves were rather flat.
“response curves for this variable showed relatively higher influences in these two species compared to bigeye or skipjack where the response curves were rather flat.”
Quote in the paperSubstantial claim- Rests on an assumption: Longline catch per unit effort (CPUE) is a valid proxy for tuna habitat preferences.
- Findingown data
Southern bluefin tuna CPUE shows the southernmost distribution, mainly between 30°S to 50°S in the Indian and Western Pacific Ocean.
“Southern bluefin tuna CPUE shows the southernmost distribution, and was caught mainly between 30°S to 50°S in the Indian and Western Pacific Ocean.”
Quote in the paperNot a substantial claim- Rests on an assumption: Longline catch per unit effort (CPUE) is a valid proxy for tuna habitat preferences.
- Premisecitation
Current knowledge about tuna habitat preferences remains fragmented and heterogeneous because it relies mainly on regional or local studies using a variety of approaches that are difficult to combine.
“current knowledge about tuna habitat preferences remains fragmented and heterogeneous, because it relies mainly on regional or local studies that have used a variety of approaches making them difficult to combine.”
- Also stated in: § 1. Introduction · plain
“In spite of its pivotal role in future implementations of the EAFM within TRFMOs, current knowledge about tuna habitat preferences remains fragmented and heterogeneous.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Hobday and Evans, 2013 source
- Also stated in: § 1. Introduction · plain
- Premisecitation
Biotic and abiotic environmental variables affect tuna distribution and abundance.
“Biotic and abiotic environmental variables affect tuna distribution and abundance (Lehodey et al., 1997, Ravier and Fromentin, 2004and Sund et al., 1981).”
Quote in the paperSubstantial claim0 of 3 sources checked - Interpretationnone given
The Atlantic bluefin preference and tolerance for high salinity waters is probably linked to the role of Mediterranean waters in their life cycle.
“Atlantic bluefin showed a marked preference and tolerance for high salinity waters (above 37 PSU), probably linked to the role of Mediterranean waters in their life cycle.”
Quote in the paperNot a substantial claim - Premisecitation
Mixed layer depth can limit the vertical distribution of tuna and tuna-like species.
“The mixed layer depth can limit the vertical distribution of tuna and tuna like species (Bernal et al., 2009;Prince et al., 2010), while the sea surface height anomaly (SSH) provides information on the open-ocean physical habitat of pelagic species.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites Bernal et al., 2009
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites Prince et al., 2010 source
- Premisereasoning
Comparison between different habitat preferences is difficult due to differences in datasets, methods, and studied areas, affecting the ability to determine which environmental variables are the most important drivers of tuna distribution.
“In this context, comparison between different habitat preferences is difficult due to differences in the datasets, methods, and studied areas, and this affects our ability to determine which environmental variables are the most important drivers of tuna distribution.”
Quote in the paperSubstantial claim - Study design and conductreasoning
Due to collinearity issues, not all environmental variables were included in the GAMs.
“However, due to collinearity issues, not all environmental variables were included in the GAMs.”
Quote in the paperSubstantial claim - Premisecitation
When available, previous studies on tuna habitat are limited to a single species and/or small areas.
“When available, these studies are limited to a single species and/or small areas (e.g.Dell et al., 2011).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Dell et al., 2011 source
- Premisecitation
Temperature and oxygen are important variables determining tuna habitat.
“temperature and oxygen are considered to be important variables determining tuna habitat (Brill, 1994;Li et al., 2012).”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites Brill, 1994 source
- cites Li et al., 2012
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Premisecitation
Biophysical models integrate, in addition to data on physical habitat, biological dynamics (e.g., movement) that can concentrate the distribution of the population with respect to that of suitable habitat.
“However, another important difference is that biophysical models integrate, in addition to data on the physical habitat, biological dynamics (e.g.movement) that can concentrate the distribution of the population with respect to that of the suitable habitat (Dueri et al 2014).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Dueri et al 2014 source
- Interpretationown data
Atlantic bluefin tuna is the species able to tolerate the widest ranges of environmental conditions.
“suggests that bluefin tuna is the species able to tolerate the widest ranges of environmental conditions, as supported by its physiological capabilities (Block et al., 2001;Block and Stevens, 2001).”
Quote in the paperSubstantial claim0 of 2 sources checked - Interpretationcitation
Southern bluefin tuna's wide tolerance ranges are probably due to the diversity of habitats encountered in the southern ocean and plastic behaviours in response to their changing ocean environment.
“probably due to the diversity of habitats encountered in the southern ocean and the plastic behaviours in response to their changing ocean environment (Bestley et al., 2009).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Bestley et al., 2009 source
- Interpretationnone given
For southern bluefin tuna, the predicted distribution in Eastern Australia was consistent with Hobday and Hartmann (2006) and Hartog et al. (2011).
“In the case of southern bluefin tuna, the predicted distribution in Eastern Australia was consistent with Hobday and Hartmann (2006) and Hartog et al. (2011).”
Quote in the paperNot a substantial claim0 of 2 sources checked- Rests on an assumption: The response curves of the final GAMs can be interpreted as habitat suitability for the tuna species.
- Interpretationreasoning
The environmental variables with relatively flat response curves (DCHL for bigeye and skipjack, MLD for yellowfin and skipjack) have relatively low influence compared to other variables.
“suggesting a relatively low influence of these environmental variables compared to the others.”
Quote in the paperNot a substantial claim- Rests on an assumption: The response curves of the final GAMs can be interpreted as habitat suitability for the tuna species.
- Premisecitation
Tagging data are often biased to areas closest to deployments because of short temporal periods at liberty and an associated lack of dispersal across the full extent of the species range.
“Tagging data are often biased to those areas closest to deployments because of short temporal periods at liberty and an associated lack of dispersal across the full extent of the species range (Hobday and Evans, 2013).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Hobday and Evans, 2013 source
- Study design and conductnone given
The general lack of prey field observations at both small and larger spatial scales prevents the study of their impact on tuna distribution.
“The general lack of prey field observations at both small and larger spatial scales prevents the study of their impact on tuna distribution.”
Quote in the paperNot a substantial claim - Premisecitation
Dell et al. (2011) found MLD to be more important than SSH for yellowfin in the Tasman Sea.
“Dell et al. (2011) who, using a detailed fishery database, found MLD to be more important than SSH for yellowfin in the Tasman Sea.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Dell et al., 2011 source
- Study design and conductreasoning
The effects of DCHL fronts on tuna distribution might not be detectable with the spatio-temporal resolution used in this study.
“the effects of such fronts on tuna distribution might not be detectable with the spatio-temporal resolution used in this study.”
Quote in the paperNot a substantial claim - Interpretationcitation
Skipjack tuna prefer zero to positive SSH anomalies.
“skipjack preference for zero to positive anomalies (Mugo et al., 2010).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Mugo et al., 2010 source
- Premisecitation
Dell et al. (2011) also identified DCHL as one of the important variables for yellowfin.
“However, they also identified DCHL as one of the important variables for yellowfin.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Dell et al., 2011 source
- Interpretationown data
These three variables are among the most important drivers of tuna spatial distribution.
“This, together with the univariate GAM results, suggests that these three variables are among the most important drivers of tuna spatial distribution.”
Quote in the paperSubstantial claim
- May combine two claims. 41
- Classified as probably not a substantial claim. 16
May combine two claims.
PremisecitationPISCES has been extensively validated and can realistically simulate seasonal, interannual and decadal physical and biogeochemical ocean variability.
“PISCES has been extensively validated and has demonstrated the ability to realistically simulate seasonal, interannual and decadal physical and biogeochemical ocean variability.”
Quote in the paperSubstantial claim1 of 1 sources checked- cites Aumont and Bopp, 2006 source
Section 3.2 (Chlorophyll; page unavailable) reports that PISCES qualitatively reproduces observed chlorophyll patterns for May and November, supporting a limited claim about seasonal biogeochemical simulation. Section 3 (Model Mean State; page unavailable) explicitly says its comparisons are not an exhaustive validation. The paper does not establish realistic interannual or decadal physical and biogeochemical variability, so the broader claim overstates its evidence. (LLM, conf=0.88)
Experimental — accuracy not yet measured
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationGAMs have been previously used to study habitat preferences of many tuna species using fishery data, larval survey data, and electronic tagging data.
“GAMs have been previously used to study habitat preferences of many tuna species using fishery data (Lan et al., 2013;Maury et al., 2001;Mugo et al., 2010;Sagarminaga and Arrizabalaga 2010), larval survey data (Rooker et al., 2013) as well as electronic tagging data (Hazen et al., 2013).”
Quote in the paperNot a substantial claim1 of 3 sources checkedMay combine two claims.
PremisecitationLonglines resemble long baited transects and catch a wide range of species in a consistent way over a vast spatial scale.
“Longlines resemble long baited transects and catch a wide range of species in a consistent way over a vast spatial scale and longline catch data have been previously used to analyse changes in abundance (Myers and Worm, 2003), diversity (Worm et al., 2005), range contraction (Worm and Tittensor, 2011) and biogeography (Reygondeau et al., 2012).”
Quote in the paperSubstantial claim1 of 3 sources checkedProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationExtensive longline datasets with broad spatio-temporal coverage have supported a number of studies on tuna distribution and habitat preferences.
“In fact, extensive longline datasets with broad spatio-temporal coverage have supported a number of studies in relation to tuna distribution and habitat preferences (e.g.Fromentin et al., 2014;Reygondeau et al., 2012;Worm and Tittensor, 2011).”
Quote in the paperNot a substantial claim3 of 3 sources checkedProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationReygondeau et al. (2012) proposed a conceptual scheme where yellowfin, bigeye, albacore and bluefin species dominated different ecoregions as latitude increased.
“Reygondeau et al. (2012) proposed a conceptual scheme where yellowfin, bigeye, albacore and bluefin species dominated different ecoregions as latitude increased.”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites Reygondeau et al. (2012) source
May combine two claims.
FindingcitationFor Atlantic bluefin, the model identifies the Mediterranean and northern Atlantic (>40oN) as most suitable, with habitat suitability increasing further north beyond the northern range of observations and decreasing towards the equator and southern hemisphere.
“In the case of Atlantic bluefin, the model identifies the Mediterranean and the northern Atlantic (>40ºN) as most suitable, habitat suitability increasing further north beyond the northern range of the observations and decreasing towards the equator and southern hemisphere in spite of important catches that occurred in the past (Fromentin et al., 2014).”
Quote in the paperSubstantial claim1 of 1 sources checked- cites Fromentin et al., 2014 source
Split into 2 atoms — 0 confirmed, 2 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
Experimental — accuracy not yet measured
May combine two claims.
Findingown dataIn the case of albacore, our quotient analysis results for temperature preference (up to and beyond 20oC) are comparable to those of Hazen et al. (2013), while our GAM results suggest somewhat lower preferred values (around 15oC), more in line with Boyce et al. (2008) and Lan et al. (2012).
“In the case of albacore, our quotient analysis results for temperature preference (up to and beyond 20ºC) are comparable to those of Hazen et al. (2013), while our GAM results suggest somewhat lower preferred values (around 15ºC), more in line with Boyce et al. (2008) and Lan et al. (2012).”
Quote in the paperNot a substantial claim1 of 3 sources checked- cites Hazen et al. (2013) source
- cites Boyce et al. (2008) source
Split into 2 atoms — 0 confirmed, 2 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
Experimental — accuracy not yet measured - cites Lan et al. (2012) source
- Rests on an assumption: The response curves of the final GAMs can be interpreted as habitat suitability for the tuna species.
May combine two claims.
InterpretationreasoningOur predicted distributional ranges for albacore, bigeye and yellowfin were comparable to those in Worm and Tittensor (2011), but were more extensive for both bluefin species and skipjack.
“Our predicted distributional ranges for albacore, bigeye and yellowfin were also comparable to those in Worm and Tittensor (2011), but were more extensive for both bluefin species and skipjack.”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites Worm and Tittensor (2011) source
- Rests on an assumption: The response curves of the final GAMs can be interpreted as habitat suitability for the tuna species.
May combine two claims.
Findingown dataIn the univariate GAMs, the stock factor explained a relatively high proportion of the null deviance for skipjack (23%), bigeye (20%) and albacore (12%), but less than 1% for other species.
“In the univariate GAMs, the”
Quote in the paperNot a substantial claim- The authors state this as an assumption: Positive CPUE observations follow a lognormal error distribution.
- The authors state this as an assumption: The niche model is unimodal.
- Rests on an assumption: Changes in abundance and catchability are likely to occur at the stock level.
May combine two claims.
Findingown dataScatterplots between environmental variables suggested high collinearity (R2 > abs(0.6)) between TEMP5 and TEMP100, TEMP5 and O2, and DCHL and ZOO.
“Scatterplots between environmental variables suggested high collinearity (R 2 >abs(0.6))between TEMP5 and TEMP100, TEMP5 and O2, and DCHL and ZOO (Figure 1).”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Findingown dataThe full GAMs generally included the three-way stock:year:season interaction for fixed factors, except for albacore (stock:year and stock:season) and southern bluefin (year:season).
“They also generally included the three way stock:year:season interaction for fixed factors, except in the case of albacore where the interactions stock:year and stock:season were kept in the final model, and in the case of southern bluefin, with a single stock, where the year:season interaction was included.”
Quote in the paperNot a substantial claim- The authors state this as an assumption: Positive CPUE observations follow a lognormal error distribution.
- The authors state this as an assumption: The niche model is unimodal.
- Rests on an assumption: Changes in abundance and catchability are likely to occur at the stock level.
May combine two claims.
Findingown dataBluefin tunas can tolerate a wide range of DCHL and ZOO values, although their preference and tolerance ranges are not very well defined.
“In general, relatively low DCHL and ZOO waters are preferred by tropical tunas and albacore, compared to both bluefin tunas, for which the preference and tolerance ranges are not very well defined, but results suggest that they can tolerate a wide range of DCHL and ZOO values.”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataAlbacore avoids waters below 14°C, which are preferred or tolerated by both Atlantic bluefin and southern bluefin.
“Albacore avoids waters below 14ºC, which are preferred or tolerated by both Atlantic bluefin and southern bluefin.”
Quote in the paperSubstantial claimMay combine two claims.
Findingnone givenAlbacore preference and tolerance ranges extend to about 200 m, while southern bluefin tuna preference range extends to highly mixed waters with mixed layer depths of several hundred meters that Atlantic bluefin tuna tolerates.
“Albacore preference and tolerance ranges extend to about 200 m, while southern bluefin tuna preference range extends to highly mixed waters with mixed layer depths of several hundred meters that Atlantic bluefin tuna tolerates.”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataSSH was the environmental variable that explained the highest percentage of deviance (22%) for Atlantic bluefin, and between 28% and 5% for the rest of the species, except for albacore (<1%).
“SSH was the environmental variable that explained the highest percentage of deviance (22%) in the case of Atlantic bluefin, and between 28% and 5% for the rest of the species, except for albacore (<1%).”
Quote in the paperNot a substantial claim- The authors state this as an assumption: Positive CPUE observations follow a lognormal error distribution.
- The authors state this as an assumption: The niche model is unimodal.
- Rests on an assumption: Changes in abundance and catchability are likely to occur at the stock level.
May combine two claims.
Findingown dataOxygen, highly correlated with temperature, explained similar proportions of null deviance.
“Oxygen, highly correlated with temperature, explained similar proportions.”
Quote in the paperNot a substantial claim- The authors state this as an assumption: Positive CPUE observations follow a lognormal error distribution.
- The authors state this as an assumption: The niche model is unimodal.
- Rests on an assumption: Changes in abundance and catchability are likely to occur at the stock level.
May combine two claims.
Findingown dataTEMP5 was the most important variable for yellowfin tuna, as TEMP100 was for southern bluefin.
“TEMP5 was the most important variable for yellowfin tuna, as TEMP100 was for southern bluefin.”
Quote in the paperNot a substantial claim- The authors state this as an assumption: Positive CPUE observations follow a lognormal error distribution.
- The authors state this as an assumption: The niche model is unimodal.
- Rests on an assumption: Changes in abundance and catchability are likely to occur at the stock level.
May combine two claims.
Findingnone givenAmong temperate tunas, albacore showed a relatively narrow preference-tolerance range compared to southern bluefin, which showed the largest oxygen preference values.
“Among the temperate tunas, albacore showed a relatively narrow preference-tolerance range compared to southern bluefin that showed the largest oxygen preference values.”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataThe percent deviance explained by the year factor varied between 2% (bigeye) and 21% (skipjack), while the season factor explained minor deviance (<2% in all cases except for bluefin).
“The percent deviance explained by the”
Quote in the paperNot a substantial claim- The authors state this as an assumption: Positive CPUE observations follow a lognormal error distribution.
- The authors state this as an assumption: The niche model is unimodal.
- Rests on an assumption: Changes in abundance and catchability are likely to occur at the stock level.
May combine two claims.
Findingnone givenYellowfin tuna preferred a wide range of relatively low oxygen waters (<0.2 mmol/l) while bigeye tolerated them.
“Yellowfin tuna preferred a wide range of relatively low oxygen waters (<0.2mmol/l) while bigeye tolerated them.”
Quote in the paperSubstantial claimMay combine two claims.
Findingnone givenSkipjack tolerance range was more restricted and avoided waters below 0.1 mmol/l.
“Skipjack tolerance range was more restricted and avoided waters below 0.1 mmol/l.”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataThe quotient analysis suggests that Atlantic bluefin tuna has no well-established temperature preference but the widest temperature tolerance range (approximately between 1°C and 20°C).
“It is remarkable that this analysis suggests that there is no well-established temperature preference, but the widest temperature tolerance range (approximately between 1ºC and 20ºC) for Atlantic bluefin tuna.”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataThe preference range for southern bluefin and the tolerance range for Atlantic bluefin extend down to 4°C.
“The preference range for southern bluefin and the tolerance range for Atlantic bluefin extend down to 4ºC (Figure 3, Figure S1).”
Quote in the paperNot a substantial claimMay combine two claims.
Findingnone givenBluefin tunas showed preference and tolerance for negative SSH values, with Atlantic bluefin preferring the most negative values.
“On the contrary, bluefin tunas showed preference and tolerance for negative SSH values, Atlantic bluefin preferring most negative values.”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataBigeye and yellowfin showed decreasing salinity trends beyond 34 and 35 PSU respectively, while skipjack showed increasing trends.
“Bigeye and yellowfin showed decreasing trends beyond 34 and 35 PSU respectively, but increasing trends were seen for skipjack.”
Quote in the paperNot a substantial claim- Rests on an assumption: The response curves of the final GAMs can be interpreted as habitat suitability for the tuna species.
May combine two claims.
Findingown dataSSH response curves suggested positive SSH anomalies were preferred by southern bluefin, albacore and skipjack, and negative SSH anomalies were preferred by Atlantic bluefin, bigeye, yellowfin and also by skipjack.
“Response curves for SSH suggested that positive SSH anomalies were preferred by southern bluefin, albacore and skipjack, and negative SSH anomalies were preferred by Atlantic bluefin, bigeye, yellowfin and also by skipjack.”
Quote in the paperSubstantial claim- Rests on an assumption: The response curves of the final GAMs can be interpreted as habitat suitability for the tuna species.
May combine two claims.
Findingown dataSouthern bluefin tuna preferred mixed layer depths beyond approximately 300 m, while Atlantic bluefin showed a clear preference for increasing mixed layer depths.
“Southern bluefin tuna preferred mixed layer depths beyond approximately 300 m, while Atlantic bluefin showed a clear preference for increasing mixed layer depths.”
Quote in the paperSubstantial claim- Rests on an assumption: The response curves of the final GAMs can be interpreted as habitat suitability for the tuna species.
May combine two claims.
Findingown dataFor southern bluefin, models predicted suitable habitat in the northern fringe (>40oN) where there are no observations, but middle latitudes would act as a barrier to potential expansion from south to north.
“In the case of southern bluefin, the models predicted suitable habitat also in the northern fringe (>40ºN) of the planet (where there are no observations of southern bluefin), but middle latitudes would act as a barrier to potential expansion from south to north.”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataFitted smooth curves show preference for warm waters (20-30oC) for tropical tunas, temperate waters (around 15oC) for albacore and Atlantic bluefin tuna, and colder waters (<10oC) for southern bluefin.
“The fitted smooth curves show the preference for warm waters (between 20ºC and 30ºC) in the case of tropical tunas, for temperate waters (around 15ºC) in the case of albacore and Atlantic bluefin tuna, and for colder waters (< 10ºC) in the case of southern bluefin.”
Quote in the paperSubstantial claim- Rests on an assumption: The response curves of the final GAMs can be interpreted as habitat suitability for the tuna species.
May combine two claims.
Findingown dataPredictions for albacore, yellowfin, and bigeye were reasonable, with poor habitat predictions out of the observed range (e.g., north of 50oN and south of 50oS).
“The predictions for the species with most extensive data coverage (albacore, yellowfin, bigeye) were reasonable, with poor habitat predictions out of the observed range (e.g.north of 50ºN and south of 50ºS).”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataAlbacore preferred low DCHL waters, while southern bluefin, Atlantic bluefin and yellowfin showed an optimum at relatively high DCHL concentrations.
“Albacore preferred low DCHL waters, while southern bluefin, Atlantic bluefin and yellowfin showed an optimum at relatively high concentrations.”
Quote in the paperSubstantial claim- Rests on an assumption: The response curves of the final GAMs can be interpreted as habitat suitability for the tuna species.
May combine two claims.
Findingown dataSalinity response curves showed a peak slightly above 35 PSU for southern bluefin, remained high above 36 PSU for Atlantic bluefin, and showed an increasing trend beyond 36 PSU for albacore.
“Salinity response curves showed a peak slightly above 35 PSU for southern bluefin, remained high above 36 PSU for Atlantic bluefin and showed an increasing trend beyond 36 PSU for albacore.”
Quote in the paperSubstantial claim- Rests on an assumption: The response curves of the final GAMs can be interpreted as habitat suitability for the tuna species.
May combine two claims.
Findingown dataAlbacore is a temperate to subtropical species with highest CPUEs between 20o-40o of each hemisphere.
“Albacore is a temperate to subtropical species with highest CPUEs between 20º-40º of each hemisphere.”
Quote in the paperNot a substantial claim- Rests on an assumption: Longline catch per unit effort (CPUE) is a valid proxy for tuna habitat preferences.
May combine two claims.
Findingown dataSkipjack's northernmost distribution is limited to around 40oN, and highest CPUEs are observed around 20o latitude in each hemisphere.
“In the case of skipjack, whose northernmost distribution is limited to around 40ºN, highest CPUEs are observed around 20º latitude in each hemisphere.”
Quote in the paperNot a substantial claim- Rests on an assumption: Longline catch per unit effort (CPUE) is a valid proxy for tuna habitat preferences.
May combine two claims.
PremisecitationMost tagging studies are local with short deployment periods and provide information about habitat characteristics only around deployment areas.
“most tagging studies are local with short deployment periods (e.g.Cosgrove et al., 2014), and provide information about habitat characteristics only around deployment areas (Hobday and Evans, 2013).”
Quote in the paperSubstantial claim0 of 2 sources checkedProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductnone givenMissing values were omitted before the stepwise selection, so that model comparisons were based on the same dataset.
“Missing values were omitted before the stepwise selection, so that model comparisons were based on the same dataset.”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim.
PremisecitationA GAM enables fitting non-linear models for a wide family of statistical distributions.
“A GAM enables fitting non-linear models for a wide family of statistical distributions, and thus is preferred to some other habitat modelling approaches (Guisan and Zimmermann, 2000).”
Quote in the paperSubstantial claim0 of 2 sources checked- cites Hastie and Tibshirani, 1990
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites Guisan and Zimmermann, 2000 source
May combine two claims.
PremisereasoningPelagic longlines show the largest spatio-temporal coverage among fishing methods, having operated for several decades across all oceans and targeting all main commercial tuna species except skipjack.
“Among the fishing methods, pelagic longlines show the largest spatio-temporal coverage, since they have operated for several decades across all oceans, targeting all main commercial tuna species except skipjack.”
Quote in the paperSubstantial claimMay combine two claims.
PremisecitationSome environmental variables (e.g., temperature, DCHL) have been used in previous studies, but description of habitat preferences based on other variables (e.g., MLD, ZOO) is rarely found in the literature.
“Some of these variables (e.g.temperature, DCHL) have been used in previous studies (e.g.Sagarminaga and Arrizabalaga 2010;Mugo et al., 2010), but description of the habitat preferences based on other variables (e.g.MLD, ZOO) is rarely found in the literature.”
Quote in the paperSubstantial claim0 of 2 sources checkedMay combine two claims.
Interpretationown dataOur habitat predictions are generally consistent with Reygondeau et al.'s conceptual scheme, although latitudinal ranges of suitable habitat for bigeye tuna were comparable to those of albacore.
“Our habitat predictions are generally consistent with that view, although latitudinal ranges of suitable habitat for bigeye tuna were comparable to those of albacore.”
Quote in the paperNot a substantial claim- Rests on an assumption: The response curves of the final GAMs can be interpreted as habitat suitability for the tuna species.
May combine two claims.
Interpretationown dataHazen et al. (2013) estimated an optimum of around 20oC for yellowfin, while our results of both quotient analysis and GAM suggest a preference for waters of up to 30oC.
“However, Hazen et al. (2013), using an extensive and detailed tagging dataset, estimated an optimum of around 20ºC for yellowfin, while our results of both the quotient analysis and the GAM suggest a preference for waters of up to 30ºC.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Hazen et al. (2013) source
- Rests on an assumption: The response curves of the final GAMs can be interpreted as habitat suitability for the tuna species.
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationFishery data have been criticised for inducing biased conclusions about stock abundance trends because CPUE series may not accurately reflect trends of population abundance due to changes in fishing practice, efficiency of fleets or environmental effects on catchability.
“Fishery data have been criticised for inducing biased conclusions about stock abundance trends because CPUE series may not accurately reflect trends of population abundance due to changes in fishing practice, efficiency of the fleets or environmental effects on catchability, among others (see Maunder and Punt, 2004;Maunder et al., 2006;Polacheck, 2006).”
Quote in the paperNot a substantial claim0 of 3 sources checkedProbably not a substantial claim: may not pass S2 (checkable), S3 (load-bearing).
InterpretationreasoningConsidering differences in the nature of the data and the approach used, our results are generally consistent with several other studies.
“Considering the differences in the nature of the data and the approach used, our results are generally consistent with several other studies.”
Quote in the paperNot a substantial claim- Rests on an assumption: The response curves of the final GAMs can be interpreted as habitat suitability for the tuna species.
Probably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductreasoningIn the GAMs, fixed factors were included to accommodate changes in abundance and catchability.
“In our case, we included fixed factors in the GAMs to accommodate changes in abundance and catchability.”
Quote in the paperNot a substantial claimMay combine two claims.
InterpretationreasoningThe environmental variables in areas where skipjack suitable habitat was predicted outside observations are out of the ranges used in the skipjack model, and thus the GAM predictions there are unrealistic.
“The environmental variables in these areas are out of the ranges used in the skipjack model and thus the GAM predictions are unrealistic.”
Quote in the paperNot a substantial claimMay combine two claims.
Interpretationown dataThe 25%-75% interquartile range of the temperature preference profile in Cheung et al. (2013) is consistent with our estimates, but for temperate tunas the tolerance we estimated extended to colder waters.
“The 25%-75% interquartile range of the temperature preference profile in Cheung et al. (2013) is also consistent with our estimates, but in the case of temperate tunas the tolerance we estimated extended to colder waters.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Cheung et al. (2013) source
- Rests on an assumption: The response curves of the final GAMs can be interpreted as habitat suitability for the tuna species.
May combine two claims.
InterpretationreasoningOur habitat predictions showed a slightly higher latitudinal range compared to those predicted by coupled biophysical models for skipjack in the Pacific, Indian, and worldwide, and for Pacific bigeye tuna.
“However, our habitat predictions showed a slightly higher latitudinal range compared to those predicted by coupled biophysical models in the case of skipjack in the Pacific Ocean (Bell et al., 2013;Lehodey et al., 2013), Indian Ocean (Dueri, 2012), and worldwide (Dueri, 2014), as well as in the case of Pacific bigeye tuna (Lehodey et al., 2010).”
Quote in the paperNot a substantial claim0 of 3 sources checked- Rests on an assumption: The response curves of the final GAMs can be interpreted as habitat suitability for the tuna species.
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationBriand et al. (2011) suggested DCHL is important for Pacific albacore.
“The importance of DCHL was also suggested by Briand et al. (2011), using a detailed fishery dataset, for Pacific albacore.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Briand et al., 2011 source
Probably not a substantial claim: may not pass S2 (checkable).
InterpretationreasoningFishery data remain a valuable source of information to analyse global habitat of tunas at broad spatial and temporal scales.
“In the meantime, fishery data remain a valuable source of information to analyse global habitat of tunas at broad spatial and temporal scales.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S2 (checkable), S3 (load-bearing).
PremisecitationTrophodynamics of tunas are complex and dynamic.
“trophodynamics of tunas are complex and dynamic (Young et al., 2014).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Young et al., 2014
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
Probably not a substantial claim: may not pass S2 (checkable), S3 (load-bearing). May combine two claims.
Interpretationnone givenThe mechanisms through which salinity could affect tuna distribution remain unclear and could be a proxy of other underlying processes.
“However, the mechanisms through which salinity could affect tuna distribution remain unclear and could be a proxy of other underlying processes.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationMaury et al. (2001) suggested that low salinities could indicate favourable trophic areas induced by fluvial water supplies.
“Maury et al. (2001) suggested that low salinities could indicate favourable trophic areas induced by fluvial water supplies.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Maury et al., 2001 source
Probably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductnone givenNo data on skipjack caught by longline was available from the Western and Central Pacific.
“No data on skipjack caught by longline was available from the Western and Central Pacific.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationThe importance of salinity for tuna distribution remains controversial in the literature.
“The importance of salinity for tuna distribution remains controversial in the literature, with some suggesting it is not important in influencing oceanic distribution (Sund et al., 1981), while others have found it to be influential (e.g.Bernal et al., 2009;Maury et al., 2001;Reygondeau et al., 2012).”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites Sund et al., 1981
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites Bernal et al., 2009
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites Maury et al., 2001 source
May combine two claims.
Interpretationown dataSalinity is important for tuna distribution, as supported by GAM results showing variable response curves for all species.
“Our GAM results tend to support the importance of salinity since this variable showed variable response curves for all the species.”
Quote in the paperSubstantial claim
The authors state this as an assumption.
CPUE is a proxy for fish abundance.
“the CPUE was assumed to be a proxy for fish abundance.”
The paper relies on this without support.
Tunas show a wide vertical distribution.
“For this study, and because tunas show a wide vertical distribution, we selected the following variables to characterise the surface and subsurface environment:”
The authors state this as an assumption.
Positive CPUE observations follow a lognormal error distribution.
“Positive CPUE observations were assumed to follow a lognormal error distribution and they were modelled as a function of the environmental variables, as well as fixed factors for”
The authors state this as an assumption.
The niche model is unimodal.
“The degree of smoothness of model terms was restricted to 4 in order to assume a unimodal niche model (sensu Hutchinson, 1957).”
The paper relies on this without support.
Changes in abundance and catchability are likely to occur at the stock level.
“Changes in abundance and catchability are likely to occur at the stock level and so three way interactions among fixed factors were considered in the full GAMs.”
The paper relies on this without support.
The response curves of the final GAMs can be interpreted as habitat suitability for the tuna species.
“The final GAMs were kept as those describing the habitat of the tuna species, and their response curves for environmental variables were interpreted in terms of habitat suitability (Figure 4).”
The paper relies on this without support.
Longline catch per unit effort (CPUE) is a valid proxy for tuna habitat preferences.
“our study reflects mostly habitat preferences for adult tunas (since it is based on longline data that mostly catches adult fish)”
The paper relies on this without support.
The quotient analysis's preference, tolerance and avoidance ranges validly indicate species-specific habitat preferences.
“Summary of quotient analyses, with species specific preference (green), tolerance (yellow) and avoidance (red) ranges for each environmental variable.”
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Skipjack performs migratory movements conditioned by SST and prey availability.
“It typically preys on small (2-5 cms) pelagic fishes, crustaceans and cephalopods (Magnuson, 1969;Roger, 1994;Druon et al., 2017), and performs migratory movements conditioned by SST and preys availability (Arrizabalaga et al., 2015;Druon et al., 2017).”
From African desert dust influences migrations and fisheries of the Atlantic skipjack-tuna (2023) · cites this paper as Arrizabalaga et al., 2015
Section 2.1 (page unavailable) includes skipjack among highly migratory tunas, and the Discussion (page unavailable) says tunas make trophic migrations to exploit productive areas. The paper also models skipjack habitat in relation to surface temperature, but it does not establish that skipjack’s migratory movements specifically are conditioned by both SST and prey availability. (LLM, conf=0.84)
Experimental — accuracy not yet measuredSkipjack tuna inhabits warm waters, preferably those with a sea surface temperature (SST) between 20 and 28°C.
“Skipjack tuna inhabits warm waters, preferably those with a sea surface temperature (SST) between 20 and 28 • C (Arrizabalaga et al., 2015).”
From African desert dust influences migrations and fisheries of the Atlantic skipjack-tuna (2023) · cites this paper as Arrizabalaga et al., 2015
Cites
R: A Language and Environment for Statistical Computing
R Core Team (2000) · doi:10.32614/r.manuals · Cited by 355,706 · see citing works
Generalized Additive Models: An Introduction with R
Wood, S. N. (2017) · doi:10.1201/9781315370279 · Cited by 13,852 · see citing works
Brown, R. A., Hastie, T. J., & Tibshirani, R. J. (1991) · Biometrics · doi:10.2307/2532174 · Cited by 8,262 · see citing works
Koyak, R. A., Hastie, T. J., & Tibshirani, R. J. (1991) · Journal of the American Statistical Association · doi:10.2307/2290538 · Cited by 7,717 · see citing works
Predictive habitat distribution models in ecology
Guisan, A., & Zimmermann, N. E. (2000) · Ecological Modelling · doi:10.1016/s0304-3800(00)00354-9 · Cited by 7,359 · see citing works
Hutchinson, G. E. (1957) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.1957.022.01.039 · Cited by 6,228 · see citing works
Orr, J. C., Fabry, V. J., Aumont, O., Bopp, L., Doney, S. C., Feely, R. A., Gnanadesikan, A., Gruber, N., Ishida, A., Joos, F., et al. (2005) · Nature · doi:10.1038/nature04095 · Cited by 4,590 · see citing works
Self-citationHastie, T. J., & Tibshirani, R. J. (2014) · Wiley StatsRef: Statistics Reference Online · doi:10.1002/9781118445112.stat03141 · Cited by 3,156 · see citing works
Rapid worldwide depletion of predatory fish communities
Myers, R. A., & Worm, B. (2003) · Nature · doi:10.1038/nature01610 · Cited by 2,969 · see citing works
Chambers, J., & Hastie, T. (1991) · doi:10.2307/1269676 · Cited by 2,597
Chambers, J. M., Hastie, T., & Pregibon, D. (1990) · Physica-Verlag eBooks · doi:10.1007/978-3-642-50096-1_48 · Cited by 1,763 · see citing works
Tracking apex marine predator movements in a dynamic ocean
Block, B., Jonsen, I., Jorgensen, S., Winship, A., Shaffer, S. A., Bograd, S., Hazen, E., Foley, D., Breed, G., Harrison, A.-L., et al. (2011) · Nature · doi:10.1038/nature10082 · Cited by 1,339 · see citing works
Standardizing catch and effort data: a review of recent approaches
Maunder, M. N., & Punt, A. E. (2004) · Fisheries Research · doi:10.1016/j.fishres.2004.08.002 · Cited by 1,336 · see citing works
Signature of ocean warming in global fisheries catch
Cheung, W. W. L., Watson, R., & Pauly, D. (2013) · Nature · doi:10.1038/nature12156 · Cited by 913 · see citing works
Electronic tagging and population structure of Atlantic bluefin tuna
Block, B. A., Teo, S. L. H., Walli, A., Boustany, A., Stokesbury, M. J. W., Farwell, C. J., Weng, K. C., Dewar, H., & Williams, T. D. (2005) · Nature · doi:10.1038/nature03463 · Cited by 781 · cited 1× · see citing works
“Although some large deployment efforts have characterised habitat preference and movement patterns at relevant scales for management (e.g. Block et al., 2005; Block et al., 2011; Hartog et al., 2011; Hazen et al., 2013; Hobday and Hartmann, 2006), most tagging studies are local with short…”
BackgroundGlobalizing results from ocean in situ iron fertilization studies
Aumont, O., & Bopp, L. (2006) · Global Biogeochemical Cycles · doi:10.1029/2005gb002591 · Cited by 709 · see citing works
Migratory Movements, Depth Preferences, and Thermal Biology of Atlantic Bluefin Tuna
Block, B. A., Dewar, H., Blackwell, S. B., Williams, T. D., Prince, E. D., Farwell, C. J., Boustany, A., Teo, S. L. H., Seitz, A., Walli, A., et al. (2001) · Science · doi:10.1126/science.1061197 · Cited by 697 · see citing works
CONCLUDING REMARKS OF THE CHAIRMANPreprint
Stern, C. (1950) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.1950.015.01.039 · Cited by 676 · see citing works
Interpreting catch per unit effort data to assess the status of individual stocks and communities
Maunder, M. N., Sibert, J. R., Fonteneau, A., Hampton, J., Kleiber, P., & Harley, S. J. (2006) · ICES Journal of Marine Science · doi:10.1016/j.icesjms.2006.05.008 · Cited by 582 · see citing works
Expansion of oxygen minimum zones may reduce available habitat for tropical pelagic fishes
Stramma, L., Prince, E. D., Schmidtko, S., Luo, J., Hoolihan, J. P., Visbeck, M. H., Wallace, D. W. R., Brandt, P. N., & Körtzinger, A. (2011) · Nature Climate Change · doi:10.1038/nclimate1304 · Cited by 556 · see citing works
Predicted habitat shifts of Pacific top predators in a changing climate
Hazen, E. L., Jorgensen, S., Rykaczewski, R. R., Bograd, S. J., Foley, D. G., Jonsen, I. D., Shaffer, S. A., Dunne, J. P., Costa, D. P., Crowder, L. B., et al. (2013) · Nature Climate Change · doi:10.1038/nclimate1686 · Cited by 499 · see citing works
El Niño Southern Oscillation and tuna in the western Pacific
Lehodey, P., Bertignac, M., Hampton, J., Lewis, A., & Picaut, J. (1997) · Nature · doi:10.1038/39575 · Cited by 494 · cited 1× · see citing works
“Biotic and abiotic environmental variables affect tuna distribution and abundance (Lehodey et al., 1997, Ravier and Fromentin, 2004 and Sund et al., 1981).”
BackgroundResponse of diatoms distribution to global warming and potential implications: A global model study
Bopp, L., Aumont, O., Cadule, P., Alvain, S., & Gehlen, M. (2005) · Geophysical Research Letters · doi:10.1029/2005gl023653 · Cited by 455 · see citing works
Global Patterns of Predator Diversity in the Open Oceans
Worm, B., Sandow, M., Oschlies, A., Lotze, H. K., & Myers, R. A. (2005) · Science · doi:10.1126/science.1113399 · Cited by 419 · see citing works
Mixed responses of tropical Pacific fisheries and aquaculture to climate change
Bell, J. D., Ganachaud, A., Gehrke, P. C., Griffiths, S. P., Hobday, A. J., Hoegh-Guldberg, O., Johnson, J. E., Le Borgne, R., Lehodey, P., Lough, J. M., et al. (2013) · Nature Climate Change · doi:10.1038/nclimate1838 · Cited by 321 · see citing works
Life on the Edge: Marine Life and Fronts
Olson, D. B., Hitchcock, G. L., Mariano, A. J., Ashjian, C. J., Peng, G., Nero, R. W., & Podestá, G. (1994) · Oceanography · doi:10.5670/oceanog.1994.03 · Cited by 281 · see citing works
Lehodey, P., Senina, I., & Murtugudde, R. (2008) · Progress in Oceanography · doi:10.1016/j.pocean.2008.06.004 · Cited by 272 · see citing works
BRILL, R. W. (1994) · Fisheries Oceanography · doi:10.1111/j.1365-2419.1994.tb00098.x · Cited by 252 · see citing works
(1981) · Cited by 234 · see citing works
Spatial Processes and Management of Marine Populations
Kruse, G. H. (2001) · Alaska Sea Grant, University of Alaska Fairbanks eBooks · doi:10.4027/spmmp.2001 · Cited by 231 · see citing works
Zainuddin, M., Kiyofuji, H., Saitoh, K., & Saitoh, S. (2006) · Deep Sea Research Part II Topical Studies in Oceanography · doi:10.1016/j.dsr2.2006.01.007 · Cited by 228 · see citing works
Teo, S. L. H., Boustany, A., Dewar, H., Stokesbury, M. J. W., Weng, K. C., Beemer, S., Seitz, A. C., Farwell, C. J., Prince, E. D., & Block, B. A. (2007) · Marine Biology · doi:10.1007/s00227-006-0447-5 · Cited by 226 · see citing works
Near real-time spatial management based on habitat predictions for a longline bycatch species
HOBDAY, A. J., & HARTMANN, K. (2006) · Fisheries Management and Ecology · doi:10.1111/j.1365-2400.2006.00515.x · Cited by 208 · see citing works
The trophodynamics of marine top predators: Current knowledge, recent advances and challenges
Young, J. W., Hunt, B. P. V., Cook, T. R., Llopiz, J. K., Hazen, E. L., Pethybridge, H. R., Ceccarelli, D., Lorrain, A., Olson, R. J., Allain, V., et al. (2015) · Deep Sea Research Part II: Topical Studies in Oceanography · doi:10.1016/j.dsr2.2014.05.015 · Cited by 195 · see citing works
Self-citationSchaefer, K. M., Fuller, D. W., & Block, B. A. (2007) · Marine Biology · doi:10.1007/s00227-007-0689-x · Cited by 191 · see citing works
Range contraction in large pelagic predators
Worm, B., & Tittensor, D. P. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1102353108 · Cited by 173 · see citing works
Walli, A., Teo, S. L. H., Boustany, A., Farwell, C. J., Williams, T., Dewar, H., Prince, E., & Block, B. A. (2009) · PLoS ONE · doi:10.1371/journal.pone.0006151 · Cited by 170 · see citing works
Modelling the impact of climate change on Pacific skipjack tuna population and fisheries
Lehodey, P., Senina, I., Calmettes, B., Hampton, J., & Nicol, S. (2013) · Climatic Change · doi:10.1007/s10584-012-0595-1 · Cited by 167 · see citing works
Performance of pop-up satellite archival tags
Musyl, M. K., Domeier, M., Nasby-Lucas, N., Brill, R., McNaughton, L. M., Swimmer, J., Lutcavage, M., Wilson, S. G., Galuardi, B., & Liddle, J. (2011) · Marine Ecology Progress Series · doi:10.3354/meps09202 · Cited by 162 · see citing works
Galuardi, B., Royer, F., Golet, W., Logan, J., Neilson, J., & Lutcavage, M. (2010) · Canadian Journal of Fisheries and Aquatic Sciences · doi:10.1139/f10-033 · Cited by 159 · see citing works
Rill, R. W. B., & Lutcavage, M. E. (2001) · Cited by 157 · see citing works
MUGO, R., SAITOH, S., NIHIRA, A., & KUROYAMA, T. (2010) · Fisheries Oceanography · doi:10.1111/j.1365-2419.2010.00552.x · Cited by 149 · cited 9× · see citing works
“Some of these variables (e.g. temperature, DCHL) have been used in previous studies (e.g. Sagarminaga and Arrizabalaga 2010; Mugo et al., 2010), but description of the habitat preferences based on other variables (e.g. MLD, ZOO) is rarely found in the literature.”
BackgroundMethodResultInfluentialSeasonal forecasting of tuna habitat for dynamic spatial management
Hobday, A. J., Hartog, J. R., Spillman, C. M., & Alves, O. (2011) · Canadian Journal of Fisheries and Aquatic Sciences · doi:10.1139/f2011-031 · Cited by 144 · see citing works
Ocean scale hypoxia-based habitat compression of Atlantic istiophorid billfishes
PRINCE, E. D., LUO, J., PHILLIP GOODYEAR, C., HOOLIHAN, J. P., SNODGRASS, D., ORBESEN, E. S., SERAFY, J. E., ORTIZ, M., & SCHIRRIPA, M. J. (2010) · Fisheries Oceanography · doi:10.1111/j.1365-2419.2010.00556.x · Cited by 140 · see citing works
Effects of temperature on global patterns of tuna and billfish richness
Boyce, D., Tittensor, D., & Worm, B. (2008) · Marine Ecology Progress Series · doi:10.3354/meps07237 · Cited by 139 · cited 6× · see citing works
“Temperature and oxygen affect important biological processes and thus determine the spatial distribution of tunas (Barkley et al., 1978; Boyce et al., 2008; Brill, 1994; Strama et al., 2012).”
BackgroundMethodResultInfluentialPodestá, G., Browder, J. A., & Hoey, J. J. (1993) · Continental Shelf Research · doi:10.1016/0278-4343(93)90109-b · Cited by 138 · see citing works
Olivier, M. (2009) · Progress In Oceanography · doi:10.1016/j.pocean.2009.09.013 · Cited by 137 · see citing works
LEHODEY, P., ANDRE, J., BERTIGNAC, M., HAMPTON, J., STOENS, A., MENKES, C., MEMERY, L., & GRIMA, N. (1998) · Fisheries Oceanography · doi:10.1046/j.1365-2419.1998.00063.x · Cited by 135 · see citing works
Projecting the impacts of climate change on skipjack tuna abundance and spatial distribution
Dueri, S., Bopp, L., & Maury, O. (2014) · Global Change Biology · doi:10.1111/gcb.12460 · Cited by 131 · see citing works
Lutcavage, M. E., Brill, R. W., Skomal, G. B., Chase, B. C., Goldstein, J. L., & Tutein, J. (2000) · Marine Biology · doi:10.1007/s002270000302 · Cited by 126 · see citing works
Preliminary forecasts of Pacific bigeye tuna population trends under the A2 IPCC scenario
Lehodey, P., Senina, I., Sibert, J., Bopp, L., Calmettes, B., Hampton, J., & Murtugudde, R. (2010) · Progress In Oceanography · doi:10.1016/j.pocean.2010.04.021 · Cited by 124 · see citing works
Schaefer, K. M., & Fuller, D. W. (2010) · Marine Biology · doi:10.1007/s00227-010-1524-3 · Cited by 122 · see citing works
Rooker, J. R., Kitchens, L. L., Dance, M. A., Wells, R. J. D., Falterman, B. J., & Cornic, M. (2013) · PLoS ONE · doi:10.1371/journal.pone.0076080 · Cited by 122 · see citing works
Association between bluefin tuna schools and oceanic features in the western Mediterranean
Royer, F., Fromentin, J., & Gaspar, P. (2004) · Marine Ecology Progress Series · doi:10.3354/meps269249 · Cited by 107 · see citing works
Self-citationLan, K.-W., Evans, K., & Lee, M.-A. (2013) · Climatic Change · doi:10.1007/s10584-012-0637-8 · Cited by 106 · see citing works
Polacheck, T. (2006) · Marine Policy · doi:10.1016/j.marpol.2005.06.016 · Cited by 106 · see citing works
Ravier, C., & Fromentin, J. (2004) · Fisheries Oceanography · doi:10.1111/j.1365-2419.2004.00284.x · Cited by 105 · see citing works
Aranda, G., Abascal, F. J., Varela, J. L., & Medina, A. (2013) · PLoS ONE · doi:10.1371/journal.pone.0076445 · Cited by 105 · see citing works
Feeding ecology of wild migratory tunas revealed by archival tag records of visceral warming
Bestley, S., Patterson, T. A., Hindell, M. A., & Gunn, J. (2008) · Journal of Animal Ecology · doi:10.1111/j.1365-2656.2008.01437.x · Cited by 105 · see citing works
Bernal, M., Stratoudakis, Y., Coombs, S., Angelico, M. M., de Lanzós, A. L., Porteiro, C., Sagarminaga, Y., Santos, M., Uriarte, A., Cunha, E., et al. (2007) · Progress in Oceanography · doi:10.1016/j.pocean.2007.04.018 · Cited by 104 · see citing works
Galuardi, B., & Lutcavage, M. (2012) · PLoS ONE · doi:10.1371/journal.pone.0037829 · Cited by 101 · see citing works
Biogeography of tuna and billfish communities
Reygondeau, G., Maury, O., Beaugrand, G., Fromentin, J. M., Fonteneau, A., & Cury, P. (2012) · Journal of Biogeography · doi:10.1111/j.1365-2699.2011.02582.x · Cited by 100 · see citing works
Climate impacts on albacore and bluefin tunas migrations phenology and spatial distribution
Dufour, F., Arrizabalaga, H., Irigoien, X., & Santiago, J. (2010) · Progress In Oceanography · doi:10.1016/j.pocean.2010.04.007 · Cited by 97 · see citing works
Self-citationSkipjack tuna, Katsuwonus pelamis, habitat based on temperature and oxygen requirements
Barkley, R. A. (1978) · Fishery Bulletin · Cited by 93 · see citing works
Ensemble analysis of the future distribution of large pelagic fishes off Australia
Hobday, A. J. (2010) · Progress In Oceanography · doi:10.1016/j.pocean.2010.04.023 · Cited by 92 · see citing works
Teo, S. L. H., & Block, B. A. (2010) · PLoS ONE · doi:10.1371/journal.pone.0010756 · Cited by 91 · see citing works
CHEN, I., LEE, P., & TZENG, W. (2005) · Fisheries Oceanography · doi:10.1111/j.1365-2419.2004.00322.x · Cited by 88 · cited 4× · see citing works
“This is in agreement with Dell et al. (2011) who, using a detailed fishery database, found MLD to be more important than SSH for yellowfin in the Tasman Sea.”
BackgroundMethodResultInfluentialHartog, J. R., Hobday, A. J., Matear, R., & Feng, M. (2011) · Deep Sea Research Part II: Topical Studies in Oceanography · doi:10.1016/j.dsr2.2010.06.005 · Cited by 87 · see citing works
Handegard, N. O., du Buisson, L., Brehmer, P., Chalmers, S. J., Robertis, A. D., Huse, G., Kloser, R. J., Macaulay, G. J., Olivier, M., Ressler, P. H., et al. (2012) · Fish and Fisheries · doi:10.1111/j.1467-2979.2012.00480.x · Cited by 86 · see citing works
Bertignac, M., Lehodey, P., & Hampton, J. (1998) · Fisheries Oceanography · doi:10.1046/j.1365-2419.1998.00065.x · Cited by 85 · see citing works
Fromentin, J., Reygondeau, G., Bonhommeau, S., & Beaugrand, G. (2014) · Fisheries Oceanography · doi:10.1111/fog.12050 · Cited by 76 · see citing works
der Lingen, V. (2001) · Medical Entomology and Zoology · Cited by 75 · see citing works
A new model to assess the probability of occurrence of a species, based on presence-only data
Beaugrand, G., Lenoir, S., Ibáñez, F., & Manté, C. (2010) · Marine Ecology Progress Series · doi:10.3354/meps08939 · Cited by 74 · see citing works
Mesoscale exploitation of a major tuna concentration in the Indian Ocean
Fonteneau, A., Lucas, V., Tew-Kai, E., et al. (2008) · Aquatic Living Resources · doi:10.1051/alr:2008028 · Cited by 61 · see citing works
Potential feeding and spawning habitats of Atlantic bluefin tuna in the Mediterranean Sea
Druon, J., Fromentin, J., Aulanier, F., & Heikkonen, J. (2011) · Marine Ecology Progress Series · doi:10.3354/meps09321 · Cited by 61 · see citing works
Maury, O., Gascuel, D., Marsac, F., Fonteneau, A., & Rosa, A.-L. D. (2001) · Canadian Journal of Fisheries and Aquatic Sciences · doi:10.1139/f00-261 · Cited by 61 · see citing works
The Eco-physiology of Swimming and Movement Patterns of Tunas, Billfishes, and Large Pelagic Sharks
Bernal, D., Sepulveda, C., Musyl, M., & Brill, R. (2010) · Fish Locomotion · doi:10.1201/b10190-14 · Cited by 61 · see citing works
Biogeochemical impact of tropical instability waves in the equatorial Pacific
Gorgues, T., Menkes, C., Aumont, O., Vialard, J., Dandonneau, Y., & Bopp, L. (2005) · Geophysical Research Letters · doi:10.1029/2005gl024110 · Cited by 52 · see citing works
Self-citationDetecting climate impacts with oceanic fish and fisheries data
Hobday, A. J., & Evans, K. (2013) · Climatic Change · doi:10.1007/s10584-013-0716-5 · Cited by 50 · see citing works
Giant Marine Reserves Pose Vast Challenges
Pala, C. (2013) · Science · doi:10.1126/science.339.6120.640 · Cited by 50 · see citing works
Goñi, N., & Arrizabalaga, H. (2010) · Progress In Oceanography · doi:10.1016/j.pocean.2010.04.016 · Cited by 49 · see citing works
Self-citationArrizabalaga, H., Pereira, J., Royer, F., Galuardi, B., Goñi, N., Artetxe, I., Arregi, I., & Lutcavage, M. (2008) · Fisheries Oceanography · doi:10.1111/j.1365-2419.2008.00464.x · Cited by 48 · see citing works
Self-citationBRIAND, K., MOLONY, B., & LEHODEY, P. (2011) · Fisheries Oceanography · doi:10.1111/j.1365-2419.2011.00599.x · Cited by 47 · see citing works
Albaina, A., Iriondo, M., Velado, I., Laconcha, U., Zarraonaindia, I., Arrizabalaga, H., Pardo, M. Á., Lutcavage, M. E., Grant, W. S., & Estonba, A. (2013) · Animal Genetics · doi:10.1111/age.12051 · Cited by 47 · see citing works
Self-citationDELL, J., WILCOX, C., & HOBDAY, A. J. (2011) · Fisheries Oceanography · doi:10.1111/j.1365-2419.2011.00591.x · Cited by 46 · see citing works
BESTLEY, S., GUNN, J. S., & HINDELL, M. A. (2009) · Fisheries Oceanography · doi:10.1111/j.1365-2419.2009.00509.x · Cited by 45 · see citing works
Inclusion of prey data improves prediction of bluefin tuna (<i>Thunnus thynnus</i>) distribution
SCHICK, R. S., & LUTCAVAGE, M. E. (2009) · Fisheries Oceanography · doi:10.1111/j.1365-2419.2008.00499.x · Cited by 42 · see citing works
Climate impacts and oceanic top predators: moving from impacts to adaptation in oceanic systems
Hobday, A. J., Young, J. W., Abe, O., da Costa, D. P., Cowen, R. K., Evans, K., Gasalla, M. A., Kloser, R. J., Olivier, M., & Weng, K. C. (2013) · Reviews in Fish Biology and Fisheries · doi:10.1007/s11160-013-9311-0 · Cited by 41 · see citing works
Lan, K.-W., Kawamura, H., Lee, M.-A., Lu, H.-J., Shimada, T., Hosoda, K., & Sakaida, F. (2012) · Fisheries Research · doi:10.1016/j.fishres.2011.08.017 · Cited by 39 · see citing works
Schaefer, K. M., Fuller, D. W., & Flores, G. A. (2013) · Fisheries Oceanography · doi:10.1111/fog.12047 · Cited by 38 · see citing works
Cosgrove, R., Arregui, I., Arrizabalaga, H., Goni, N., & Sheridan, M. (2014) · Fisheries Research · doi:10.1016/j.fishres.2013.10.013 · Cited by 38 · see citing works
Self-citationModelling the skipjack tuna dynamics in the Indian Ocean with APECOSM-E: Part 1. Model formulation
Dueri, S., Faugeras, B., & Maury, O. (2012) · Ecological Modelling · doi:10.1016/j.ecolmodel.2012.02.007 · Cited by 36 · see citing works
SAGARMINAGA, Y., & ARRIZABALAGA, H. (2010) · Fisheries Oceanography · doi:10.1111/j.1365-2419.2010.00532.x · Cited by 31 · see citing works
Self-citationLezama-Ochoa, A., Boyra, G., Goñi, N., Arrizabalaga, H., & Bertrand, A. (2010) · Progress in Oceanography · doi:10.1016/j.pocean.2010.04.006 · Cited by 30 · see citing works
Self-citationRelationship of Northeast Atlantic albacore juveniles with surface thermal and chlorophyll-a fronts
Sagarminaga, Y., & Arrizabalaga, H. (2014) · Deep Sea Research Part II: Topical Studies in Oceanography · doi:10.1016/j.dsr2.2013.11.006 · Cited by 24 · see citing works
Self-citationMaury, O., Miller, K. A., Campling, L., Arrizabalaga, H., Aumont, O., Bodin, Ö., Guillotreau, P., Hobday, A. J., Marsac, F., Suzuki, Z., et al. (2013) · Current Opinion in Environmental Sustainability · doi:10.1016/j.cosust.2013.05.008 · Cited by 22 · see citing works
Self-citationThe True Challenge of Giant Marine Reserves
Kaplan, D. M., Pascal Bach, A., Bonhommeau, S., et al. (2013) · Science · doi:10.1126/science.340.6134.810-b · Cited by 20 · see citing works
Climate and oceanic fisheries: recent observations and projections and future needs
Salinger, M. J., Bell, J. D., Evans, K., Hobday, A. J., Allain, V., Brander, K., Dexter, P., Harrison, D. E., Hollowed, A. B., Lee, B., et al. (2012) · Climatic Change · doi:10.1007/s10584-012-0652-9 · Cited by 18 · see citing works
Development of integrated habitat indices for bigeye tuna, Thunnus obesus, in waters near Palau
Li, Y., Song, L., Nishida, T., et al. (2012) · Marine and Freshwater Research · doi:10.1071/mf12072 · Cited by 6 · see citing works
Flagged first, then by citations
Research works printed but not linked: 2
- Block, 2001, vol. 19
- FAO, 2011. Tuna and tuna-like species. In: Review of the State of World Marine Fishery Resources. FAO Fisheries and Aquaculture Technical Paper No. 569. Rome, pp. 227–243.
Cited by
Sorted by citations
Climate change, tropical fisheries and prospects for sustainable development
Lam, V. W. Y., Allison, E. H., Bell, J. D., Blythe, J. L., Cheung, W. W. L., Frölicher, T. L., Gasalla, M. A., & Sumaila, U. R. (2020) · Nature Reviews Earth & Environment · doi:10.1038/s43017-020-0071-9 · Cited by 323 · see citing works
Large-scale distribution of tuna species in a warming ocean
Erauskin‐Extramiana, M., Arrizabalaga, H., Hobday, A. J., Cabré, A., Ibaibarriaga, L., Arregui, I., Murua, H., & Chust, G. (2019) · Global Change Biology · doi:10.1111/gcb.14630 · Cited by 176 · see citing works
“In general, regional and local studies have used a variety of approaches, with knowledge gaps for most of the large pelagic species, such as critical environmental conditions (Trenkel et al., 2014) making them difficult to compare in the absence of a common baseline (Arrizabalaga et al., 2015).”
BackgroundMethodInfluentialSelf-citationScales, K. L., Hazen, E. L., Jacox, M. G., Edwards, C. A., Boustany, A. M., Oliver, M. J., & Bograd, S. J. (2016) · Ecography · doi:10.1111/ecog.02272 · Cited by 130 · see citing works
“Temporally-averaged environmental data fields of coarse spatial resolution are often used to contextualise movement or sightings datasets for wide-ranging marine predators (e.g. Kaschner et al. 2006; Louzao et al. 2011; Mannocci et al. 2014; Arrizabalaga et al. 2015; Mannocci et al. 2015).”
BackgroundAtlantic Multidecadal Oscillations drive the basin-scale distribution of Atlantic bluefin tuna
Faillettaz, R., Beaugrand, G., Goberville, E., & Kirby, R. (2019) · Science Advances · doi:10.1126/sciadv.aar6993 · Cited by 87 · see citing works
Habitat suitability of the Atlantic bluefin tuna by size class: An ecological niche approach
Druon, J., Fromentin, J., Hanke, A. R., Arrizabalaga, H., Damalas, D., Tičina, V., Quílez-Badia, G., Ramirez, K., Arregui, I., Tserpes, G., et al. (2016) · Progress In Oceanography · doi:10.1016/j.pocean.2016.01.002 · Cited by 89 · see citing works
“Positive and near null SSHa levels, which are mostly driven by high SSTs and linked with relatively low productive environments, effectively segregate worldwide the habitat of tropical from temperate tuna species (Arrizabalaga et al., 2015; Teo and Block, 2010).”
BackgroundSelf-citationModelling the oceanic habitats of two pelagic species using recreational fisheries data
Brodie, S. J., Hobday, A. J., Smith, J. A., Everett, J. D., Taylor, M. D., Gray, C. A., & Suthers, I. M. (2015) · Fisheries Oceanography · doi:10.1111/fog.12122 · Cited by 79 · see citing works
“The physiological limits of species are an important driver in their pelagic distributions, and thermal preferences have been identified using SDMs for tunas (Arrizabalaga et al., 2015), whale sharks © 2015 John Wiley & Sons Ltd, Fish.”
BackgroundThe environmental niche of the global high seas pelagic longline fleet
Crespo, G. O., Dunn, D. C., Reygondeau, G., Boerder, K., Worm, B., Cheung, W. W. L., Tittensor, D. P., & Halpin, P. N. (2018) · Science Advances · doi:10.1126/sciadv.aat3681 · Cited by 77 · see citing works
Review of albacore tuna, Thunnus alalunga, biology, fisheries and management
Nikolic, N., Morandeau, G., Hoarau, L., West, W. M., Arrizabalaga, H., Hoyle, S., Nicol, S., Bourjea, J., Puech, A., Farley, J. H., et al. (2016) · Reviews in Fish Biology and Fisheries · doi:10.1007/s11160-016-9453-y · Cited by 70 · see citing works
“This is in agreement with Arrizabalaga et al. (2015) who found that albacore prefer larger oxygen values than tropical tunas (bigeye, yellowfin, skipjack (Katsuwonus pelamis)).”
BackgroundResultInfluentialSelf-citationChampion, C., Hobday, A., Tracey, S., & Pecl, G. (2018) · Global Change Biology · doi:10.1111/gcb.14398 · Cited by 51 · see citing works
Hsu, T.-Y., Chang, Y., Lee, M.-A., Wu, R.-F., & Hsiao, S.-C. (2021) · Remote Sensing · doi:10.3390/rs13050861 · Cited by 55 · see citing works
“2 PSU for the world oceans [16]; 5th and 95th percentile values ranged from 34.”
BackgroundDruon, J.-N., Chassot, E., Murua, H., & Lopez, J. (2017) · Frontiers in Marine Science · doi:10.3389/fmars.2017.00315 · Cited by 55 · see citing works
“SKJ habitat is associated with a sea surface temperature (SST) range between 18 and 30◦C (Barkley et al., 1978), with a preferred range between 23 and 28◦C (e.g., Arrizabalaga et al., 2015).”
BackgroundMethodResultInfluentialEcological bridges and barriers in pelagic ecosystems
Briscoe, D. K., Hobday, A. J., Carlisle, A. B., Scales, K. L., Eveson, J. P., Arrizabalaga, H., Druon, J. N., & Fromentin, J. (2016) · Deep Sea Research Part II Topical Studies in Oceanography · doi:10.1016/j.dsr2.2016.11.004 · Cited by 51 · see citing works
Self-citationLaconcha, U., Iriondo, M., Arrizabalaga, H., Manzano, C., Markaide, P., Montes, I., Zarraonaindia, I., Velado, I., Bilbao, E., Goñi, N., et al. (2015) · PLoS ONE · doi:10.1371/journal.pone.0128247 · Cited by 51 · see citing works
Self-citationFrédou, F. L., Kell, L., Frédou, T., Gaertner, D., Potier, M., Bach, P., Travassos, P., Hazin, F., & Ménard, F. (2017) · Deep Sea Research Part II Topical Studies in Oceanography · doi:10.1016/j.dsr2.2016.10.008 · Cited by 43 · see citing works
Self-citationErauskin-Extramiana, M., Chust, G., Arrizabalaga, H., Cheung, W. W. L., Santiago, J., Merino, G., & Fernandes-Salvador, J. A. (2023) · Global and Planetary Change · doi:10.1016/j.gloplacha.2023.104055 · Cited by 45 · see citing works
Self-citationImpacts of climate change on marine top predators: Advances and future challenges
Hobday, A. J., Arrizabalaga, H., Evans, K., Nicol, S., Young, J. W., & Weng, K. C. (2015) · Deep Sea Research Part II Topical Studies in Oceanography · doi:10.1016/j.dsr2.2015.01.013 · Cited by 44 · see citing works
Self-citationLezama‐Ochoa, N., Murua, H., Chust, G., van Loon, E. E., Ruiz, J., Hall, M. A., Chavance, P., Molina, A., & Villarino, E. (2016) · Frontiers in Marine Science · doi:10.3389/fmars.2016.00034 · Cited by 45 · see citing works
“These environmental variables were selected by their general relevance for (epi) pelagic species and their relation to the specific oceanographic conditions in each Ocean (Sund et al., 1981; Martínez Rincón, 2012; Arrizabalaga et al., 2015).”
Self-citationGlobal patterns and inferences of tuna movements and trophodynamics from stable isotope analysis
Logan, J. M., Pethybridge, H., Lorrain, A., et al. (2020) · Deep Sea Research Part II Topical Studies in Oceanography · doi:10.1016/j.dsr2.2020.104775 · Cited by 37 · see citing works
Salazar, J. E., Benavides, I. F., Portilla-Cabrera, C. V., et al. (2021) · Regional Studies in Marine Science · doi:10.1016/j.rsma.2021.101829 · Cited by 35 · see citing works
Liu, S., Tian, Y., Liu, Y., et al. (2022) · Deep Sea Research Part II Topical Studies in Oceanography · doi:10.1016/j.dsr2.2022.105227 · Cited by 34 · see citing works
Arregui, I., Galuardi, B., Goñi, N., Lam, C. H., Fraile, I., Santiago, J., Lutcavage, M. E., & Arrizabalaga, H. (2018) · ICES Journal of Marine Science · doi:10.1093/icesjms/fsy056 · Cited by 34 · see citing works
“However, warm-bodied bluefin tuna tolerate a wide range of environmental conditions (Arrizabalaga et al., 2015), which may explain this LOC pattern, despite lower ambient temperatures.”
BackgroundSelf-citationGuerranti, C., Cau, A., Renzi, M., et al. (2016) · Journal of Environmental Science and Health Part B · doi:10.1080/03601234.2016.1191886 · Cited by 34 · see citing works
Evidence and patterns of tuna spawning inside a large no-take Marine Protected Area
Hernández, C., Witting, J. H., Willis, C., Thorrold, S., Llopiz, J., & Rotjan, R. (2019) · Scientific Reports · doi:10.1038/s41598-019-47161-0 · Cited by 32 · see citing works
Zhang, T., Song, L., Yuan, H., Song, B., & Ngando, N. E. (2021) · Fisheries Oceanography · doi:10.1111/fog.12539 · Cited by 33 · see citing works
Mondal, S., Vayghan, A. H., Lee, M.-A., Wang, Y.-C., & Semedi, B. (2021) · Remote Sensing · doi:10.3390/rs13142669 · Cited by 25 · see citing works
“[63] reported that albacore favors relatively low chlorophyll levels (0.”
BackgroundXue, Y., Tanaka, K. R., Yu, H., et al. (2018) · Marine Biology Research · doi:10.1080/17451000.2018.1447673 · Cited by 29 · see citing works
“mation for predicting the effects of climate changes and support effective spatial and/or temporal based management strategies (Hsieh et al. 2010; Manderson et al. 2011; Arrizabalaga et al. 2015).”
BackgroundInfluentialPhylotranscriptomic Insights into the Diversification of Endothermic Thunnus Tunas
Ciezarek, A., Osborne, O., Shipley, O. N., Brooks, E., Tracey, S., McAllister, J., Gardner, L., Sternberg, M., Block, B., & Savolainen, V. (2018) · Molecular biology and evolution · doi:10.1093/molbev/msy198 · Cited by 29 · see citing works
“Electronic tagging has shown that the three bluefin tuna species are especiallycold-tolerant,feedingaslargeadultsinhighlatitudes insubpolarwaterswhereseatemperaturescanbeaslowas9 Catthesurfaceand0–2 (cid:2) Catdepth(Bestleyetal.2009;Block et al. 2011; Arrizabalaga et al. 2015; Wilson et al. 2015).”
BackgroundLiu, X., Wang, J., Zhang, Y., Yu, H., Xu, B., Zhang, C., Ren, Y., & Xue, Y. (2019) · Fisheries Research · doi:10.1016/j.fishres.2019.05.019 · Cited by 28 · see citing works
Vayghan, A. H., Lee, M., Weng, J., Mondal, S., Ching-Te, L., & Wang, Y. (2020) · Remote Sensing · doi:10.3390/rs12162515 · Cited by 29 · see citing works
“Moreover, migration is triggered by food availability, which is mainly indicated by SSC and optimal SST [17,28,58,61].”
BackgroundAn ecosystem-driven model for spatial dynamics and stock assessment of North Atlantic albacore
Dragon, A., Senina, I. N., Titaud, O., Calmettes, B., Conchon, A., Arrizabalaga, H., & Lehodey, P. (2015) · Canadian Journal of Fisheries and Aquatic Sciences · doi:10.1139/cjfas-2014-0338 · Cited by 27 · see citing works
Self-citationENSO drives near-surface oxygen and vertical habitat variability in the tropical Pacific
Leung, S. W., Thompson, L., McPhaden, M. J., & Mislan, K. A. S. (2019) · Environmental Research Letters · doi:10.1088/1748-9326/ab1c13 · Cited by 30 · see citing works
“…and yellowfin tuna (Ingham et al 1977, Barkley et al 1978, Evans et al 1981, Gooding et al 1981, Bushnell et al 1990, Prince and Goodyear 2006, Arrizabalaga et al 2015), which make up the vast majority of tuna caught in the western and central tropical Pacific (Pons et al 2017) (see…”
BackgroundOrue, B., Pennino, M., López, J., Moreno, G., Santiago, J., Ramos, L., & Murua, H. (2020) · Frontiers in Marine Science · doi:10.3389/fmars.2020.00441 · Cited by 27 · see citing works
“, 1978) and a preferred range from 23 to 28C (Arrizabalaga et al., 2015).”
BackgroundResultMunschy, C., Bodin, N., Potier, M., Héas-Moisan, K., Pollono, C., Degroote, M., West, W. M., Hollanda, S. J., Puech, A., Bourjea, J., et al. (2016) · Environmental Research · doi:10.1016/j.envres.2016.03.042 · Cited by 24 · see citing works
A fishing route optimization decision support system: The case of the tuna purse seiner
Granado, I., Hernando, L., Uriondo, Z., et al. (2023) · European Journal of Operational Research · doi:10.1016/j.ejor.2023.07.009 · Cited by 26 · see citing works
Trueman, C., Artetxe-Arrate, I., Kerr, L. A., Meijers, A., Rooker, J., Sivankutty, R., Arrizabalaga, H., Belmonte, A., Deguara, S., Goñi, N., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-41930-2 · Cited by 18 · see citing works
Self-citationEarlier migration and distribution changes of albacore in the Northeast Atlantic
Chust, G., Goikoetxea, N., Ibaibarriaga, L., Sagarmínaga, Y., Arregui, I., Fontán, A., Irigoien, X., & Arrizabalaga, H. (2019) · Fisheries Oceanography · doi:10.1111/fog.12427 · Cited by 26 · see citing works
Self-citationTidd, A. N., Brouwer, S. L., & Pilling, G. M. (2017) · Fish and Fisheries · doi:10.1111/faf.12207 · Cited by 25 · see citing works
Are shifts in species distribution triggered by climate change? A swordfish case study
Erauskin‐Extramiana, M., Arrizabalaga, H., Cabré, A., et al. (2019) · Deep Sea Research Part II Topical Studies in Oceanography · doi:10.1016/j.dsr2.2019.104666 · Cited by 25 · see citing works
Self-citationAfrican desert dust influences migrations and fisheries of the Atlantic skipjack-tuna
Rodríguez, S., Riera, R., Fonteneau, A., Alonso-Pérez, S., & López-Darias, J. (2023) · Atmospheric Environment · doi:10.1016/j.atmosenv.2023.120022 · Cited by 23 · see citing works
“It typically preys on small (2 – 5 cms) pelagic fishes, crustaceans and cephalopods (Magnuson, 1969; Roger, 1994; Druon et al., 2017), and performs migratory movements conditioned by SST and preys availability (Arrizabalaga et al., 2015; Druon et al., 2017).”
Yang, S., Zhang, H., Fan, W., et al. (2022) · Frontiers in Marine Science · doi:10.3389/fmars.2022.881036 · Cited by 22 · see citing works
“The salinity, SSH, chlorophyll-a, and primary production also have important effects on the spatial distribution of tuna (Briand et al., 2011; Arrizabalaga et al., 2015; Nataniel et al., 2021).”
BackgroundMachine-learning aiding sustainable Indian Ocean tuna purse seine fishery
Goikoetxea, N., Goienetxea, I., Fernandes, J. A., Goñi, N., Granado, I., Quincoces, I., Ibaibarriaga, L., Ruiz, J., Murua, H., & Caballero, A. (2024) · Ecological Informatics · doi:10.1016/j.ecoinf.2024.102577 · Cited by 22 · see citing works
Self-citationWu, Y., Lan, K., Evans, K., et al. (2022) · Scientific Reports · doi:10.1038/s41598-022-17882-w · Cited by 21 · see citing works
When 1+1 can be >2: Uncertainties compound when simulating climate, fisheries and marine ecosystems
Evans, K., Brown, J. N., Gupta, A. S., Nicol, S., Hoyle, S., Matear, R. J., & Arrizabalaga, H. (2014) · Deep Sea Research Part II Topical Studies in Oceanography · doi:10.1016/j.dsr2.2014.04.006 · Cited by 20 · see citing works
Self-citationTórres-Irineo, E., Salas, S., Euán-Ávila, J. I., et al. (2021) · Frontiers in Marine Science · doi:10.3389/fmars.2021.643318 · Cited by 20 · see citing works
“The SST has been considered as a key variable regarding species distribution in marine ecosystems, while NPP refers to available carbon for consumption by the heterotrophic community and is estimated from a chlorophyll-based model (e.g., Arrizabalaga et al., 2015; Lezama-Ochoa et al., 2016).”
MethodZainuddin, M., Safruddin, S., Farhum, A., Budimawan, B., Hidayat, R., Selamat, M. B., Wiyono, E., Ridwan, M., Syamsuddin, M. L., & Ihsan, Y. N. (2023) · Remote Sensing · doi:10.3390/rs15051268 · Cited by 22 · see citing works
Song, L., Li, T., Zhang, T., Sui, H., Li, B., & Zhang, M. (2023) · Fisheries Oceanography · doi:10.1111/fog.12643 · Cited by 20 · see citing works
Uranga, J., Arrizabalaga, H., Boyra, G., et al. (2017) · PLoS ONE · doi:10.1371/journal.pone.0171382 · Cited by 20 · see citing works
Self-citationIdentifying optimal variables for machine-learning-based fish distribution modeling
Xu, S., Wang, J., Chen, X., & Zhu, J. (2024) · Canadian Journal of Fisheries and Aquatic Sciences · doi:10.1139/cjfas-2023-0197 · Cited by 19 · see citing works
Global hotspots of shark interactions with industrial longline fisheries
Burns, E. S., Bradley, D., & Thomas, L. R. (2023) · Frontiers in Marine Science · doi:10.3389/fmars.2022.1062447 · Cited by 19 · see citing works
“Bigeye and yellowfin tuna catch is highest in the central oceans whereas albacore tuna catch is distributed across the southern oceans, consistent with each species' habitat preferences (Arrizabalaga et al., 2015).”
BackgroundYang, S., Yu, L., Wang, F., Chen, T., Fei, Y., Zhang, S., & Fan, W. (2023) · Fishes · doi:10.3390/fishes8020078 · Cited by 20 · see citing works
Nataniel, A. N., López, J., & Soto, M. (2021) · Fisheries Research · doi:10.1016/j.fishres.2021.106073 · Cited by 19 · see citing works
Mammel, M., Naimullah, M., Vayghan, A. H., Hsu, J., Lee, M.-A., Wu, J.-H., Wang, Y.-C., & Lan, K.-W. (2022) · Remote Sensing · doi:10.3390/rs14122932 · Cited by 17 · see citing works
Chang, Y.-J., Hsu, J., Lai, P.-W., Lan, K.-W., & Tsai, W.-P. (2021) · Frontiers in Marine Science · doi:10.3389/fmars.2021.731950 · Cited by 18 · see citing works
Mondal, S., Lee, M.-A., Weng, J.-S., Osuka, K. E., Chen, Y.-K., & Ray, A. (2023) · Marine Pollution Bulletin · doi:10.1016/j.marpolbul.2023.115733 · Cited by 16 · see citing works
“The SST is a key predictor of the relative frequency of any species in surface waters (Chen et al., 2005; Phillips et al., 2014; Arrizabalaga et al., 2015).”
BackgroundLin, H.-L., Wang, J., Zhu, J., & Chen, X. (2023) · ICES Journal of Marine Science · doi:10.1093/icesjms/fsad163 · Cited by 17 · see citing works
Duncan, R., Brophy, D., & Arrizabalaga, H. (2018) · Fisheries Research · doi:10.1016/j.fishres.2017.12.011 · Cited by 19 · see citing works
Self-citationTidd, A., Blanchard, J., Kell, L., & Watson, R. (2018) · Scientific Reports · doi:10.1038/s41598-018-28805-z · Cited by 14 · see citing works
Self-citationHabitat analysis of the commercial tuna of the Eastern Tropical Pacific Ocean
Hu, C., Harrison, D. P., Hinton, M. G., Siegrist, Z., & Kiefer, D. A. (2018) · Fisheries Oceanography · doi:10.1111/fog.12263 · Cited by 18 · see citing works
Environmental Factors Determine Tuna Fishing Vessels’ Behavior in Tonga
Vaihola, S., & Kininmonth, S. (2023) · Fishes · doi:10.3390/fishes8120602 · Cited by 15 · see citing works
Yati, E., Sadiyah, L., Satria, F., et al. (2024) · Marine Environmental Research · doi:10.1016/j.marenvres.2024.106540 · Cited by 16 · see citing works
Global knowledge domain and prospects in tuna research: A bibliometric analysis
Xie, J., Bian, Z.-Q., Wu, Q., Tao, L., Wu, F., & Lin, T. (2021) · Aquaculture & Fisheries · doi:10.1016/j.aaf.2021.09.005 · Cited by 17 · see citing works
Zhou, C., Wan, R., Cao, J., Xu, L., Wang, X., & Zhu, J. (2020) · Fisheries Oceanography · doi:10.1111/fog.12500 · Cited by 15 · see citing works
Continental‐scale hotspots of pelagic fish abundance inferred from commercial catch records
Bouchet, P. J., Meeuwig, J. J., Huang, Z. X., Letessier, T. B., Nichol, S., Caley, M. J., & Watson, R. A. (2017) · Global Ecology and Biogeography · doi:10.1111/geb.12619 · Cited by 15 · see citing works
“The trophodynamics and habitat usage of tunas, billfishes and their relatives are complex, dynamic and niche-dependent such that species occupying temperate or tropical eco-regions may exhibit contrasting tolerance for, and responses to, similar environmental signals (Arrizabalaga et al., 2015).”
BackgroundDell’Apa, A., Boenish, R., Fujita, R. M., & Kleisner, K. M. (2023) · Frontiers in Marine Science · doi:10.3389/fmars.2023.1206911 · Cited by 16 · see citing works
Relano, V., & Pauly, D. F. (2022) · Sustainability · doi:10.3390/su14095577 · Cited by 14 · see citing works
“Skipjack (Katsuwonus pelamis) Skipjack tuna (Katsuwonus pelamis) can be found between 40◦ N and 40◦ S [31,32], being more abundant in tropical and subtropical waters of the Pacific [32], within 20◦ N of the equator [33].”
BackgroundEffect of oceanographic parameters on daily albacore catches in the Northeast Atlantic
Goñi, N., Didouan, C., Arrizabalaga, H., Chifflet, M., Arregui, I., Goikoetxea, N., & Santiago, J. (2015) · Deep Sea Research Part II Topical Studies in Oceanography · doi:10.1016/j.dsr2.2015.01.012 · Cited by 14 · see citing works
Self-citationMichael, P. E., Wilcox, C., Tuck, G. N., Hobday, A. J., & Strutton, P. G. (2016) · Deep Sea Research Part II Topical Studies in Oceanography · doi:10.1016/j.dsr2.2016.12.003 · Cited by 14 · see citing works
Marine megafauna niche coexistence and hotspot areas in a temperate ecosystem
Louzao, M., Valeiras, J., García‐Barcelona, S., et al. (2019) · Continental Shelf Research · doi:10.1016/j.csr.2019.07.013 · Cited by 14 · see citing works
Lopetegui-Eguren, L., Poos, J., Arrizabalaga, H., Guirhem, G. L., Murua, H., Lezama-Ochoa, N., Griffiths, S., Gondra, J. R., Sabarros, P., Báez, J., et al. (2022) · Frontiers in Marine Science · doi:10.3389/fmars.2022.863602 · Cited by 10 · see citing works
Self-citationHabitat modeling of mature albacore (Thunnus alalunga) tuna in the Indian Ocean
Mondal, S., & Lee, M. (2023) · Frontiers in Marine Science · doi:10.3389/fmars.2023.1258535 · Cited by 14 · see citing works
Dunn, N., & Curnick, D. J. (2019) · Aquatic Conservation Marine and Freshwater Ecosystems · doi:10.1002/aqc.3204 · Cited by 13 · see citing works
“The importance of temperature as a determinant of tuna distribution has been shown in numerous studies (Arrizabalaga et al., 2015; Barkley, Neill, & Gooding, 1978; Brill & Lutcavage, 2001; Mugo et al., 2010; Zagaglia et al., 2004) and the range of water temperatures in this study is within the…”
BackgroundResultInfluentialOrue, B., López, J., Pennino, M., Moreno, G., Santiago, J., & Murua, H. (2020) · Deep Sea Research Part II Topical Studies in Oceanography · doi:10.1016/j.dsr2.2020.104747 · Cited by 13 · see citing works
Zhang, T., Hu, G., Song, L., et al. (2024) · Fisheries Oceanography · doi:10.1111/fog.12701 · Cited by 12 · see citing works
Zhou, X., Chen, Z., Xiong, P., et al. (2022) · Fishes · doi:10.3390/fishes7050218 · Cited by 12 · see citing works
“For example, some studies showed that MLD had an important effect on tuna habitat distribution [57].”
ResultClimate Change Potential Impacts on the Tuna Fisheries in the Exclusive Economic Zones of Tonga
Vaihola, S., & Kininmonth, S. (2023) · Diversity · doi:10.3390/d15070844 · Cited by 12 · see citing works
Modelling fish physico-thermal habitat selection using functional regression
Boudreault, J., St‐Hilaire, A., Chebana, F., et al. (2021) · Journal of Ecohydraulics · doi:10.1080/24705357.2020.1840313 · Cited by 12 · see citing works
“…2003; Scheuerell et al. 2006; de Kerckhove et al. 2015; Neuswanger et al. 2015; Johnston et al. 2017; Montgomery et al. 2018) or to inform the regulation of commercial and recreational exploitation of fauna (e.g. Arrizabalaga et al. 2015; Li et al. 2015; Pennino et al. 2016; Wheaton et al. 2018).”
BackgroundPower, C., Carabott, M., Widdicombe, M., et al. (2023) · PeerJ · doi:10.7717/peerj.15763 · Cited by 11 · see citing works
“thynnus, before returning to Australian waters (Arrizabalaga et al., 2015).”
Vaihola, S., Yemane, D., & Kininmonth, S. (2023) · Diversity · doi:10.3390/d15101091 · Cited by 10 · see citing works
“Alba-core, which is known to be temperate species, is also caught in Tongan waters and is known to have temperature preference range between 20 ◦ C and 30 ◦ C in each hemisphere [20].”
BackgroundInfluentialSeasonal productivity of the equatorial Atlantic shaped by distinct wind-driven processes
Brandt, P., Körner, M., Moum, J., Roch, M., Subramaniam, A., Czeschel, R., Krahmann, G., Dengler, M., & Kiko, R. (2025) · Nature Geoscience · doi:10.1038/s41561-024-01609-9 · Cited by 8 · see citing works
“Phytoplankton photosynthesis and organic matter production fuel productive marine ecosystems in the eastern equatorial Atlantic and Pacific 2,3 , supporting top predators such as economically important tropical tuna species 4,5 .”
Valls, M., Saber, S., Gómez, M. J., Reglero, P., & Mele, S. (2021) · Journal of Fish Biology · doi:10.1111/jfb.14935 · Cited by 10 · see citing works
The pelagic habitat analysis module for ecosystem‐based fisheries science and management
Harrison, D. P., Hinton, M. G., Kohin, S., et al. (2017) · Fisheries Oceanography · doi:10.1111/fog.12194 · Cited by 10 · see citing works
Martínez-Rincón, R., & Acosta-Pachón, T. A. (2022) · Progress in Oceanography · doi:10.1016/j.pocean.2022.102786 · Cited by 7 · see citing works
Michael, P. E., Tuck, G., Strutton, P., & Hobday, A. (2015) · Fisheries Oceanography · doi:10.1111/fog.12123 · Cited by 11 · see citing works
Todorović, S., Juan-Jordá, M. J., Arrizabalaga, H., & Murua, H. (2019) · Marine Policy · doi:10.1016/j.marpol.2019.103700 · Cited by 9 · see citing works
Self-citationLiu, L., Wan, R., Wu, F., Wang, Y.-C., Zhu, Y., & Zhou, C. (2025) · ICES Journal of Marine Science · doi:10.1093/icesjms/fsaf003 · Cited by 9 · see citing works
Mylona, D. (2021) · Anthropozoologica · doi:10.5252/anthropozoologica2021v56a2 · Cited by 11 · see citing works
Nataniel, A. N., Pennino, M. G., López, J., & Soto, M. (2021) · Fisheries Oceanography · doi:10.1111/fog.12568 · Cited by 11 · see citing works
Dumont, A., Sabarros, P. S., Sabarros, P. S., et al. (2024) · ICES Journal of Marine Science · doi:10.1093/icesjms/fsae043 · Cited by 9 · see citing works
Dhurmeea, Z., Pethybridge, H., Langlais, C., Somes, C., Nikolic, N., Bourjea, J., Appadoo, C., & Bodin, N. (2020) · Deep Sea Research Part I: Oceanographic Research Papers · doi:10.1016/j.dsr.2020.103286 · Cited by 7 · see citing works
Lopes, P. F. M., Andrade, L. C. A., Pennino, M. G., & Leite, T. (2021) · Fisheries Oceanography · doi:10.1111/fog.12534 · Cited by 9 · see citing works
Dupaix, A., Dagorn, L., Deneubourg, J., et al. (2024) · Ecological Applications · doi:10.1002/eap.3018 · Cited by 8 · see citing works
Yang, S., Wang, L., Fei, Y., et al. (2024) · Regional Studies in Marine Science · doi:10.1016/j.rsma.2023.103366 · Cited by 8 · see citing works
Li, M., Yang, X.-M., Wang, Y., Wang, Y.-H., & Zhu, J.-F. (2024) · Journal of Marine Science and Engineering · doi:10.3390/jmse12061002 · Cited by 7 · see citing works
ROLE OF SUB SURFACE TEMPERATURE, SALINITY AND CHLOROPHYLL TO ALBACORE TUNA ABUNDANCE IN INDIAN OCEAN
Novianto, D., & Susilo, E. (2016) · Indonesian Fisheries Research Journal · doi:10.15578/ifrj.22.1.2016.17-26 · Cited by 8 · see citing works
International collaboration and comparative research on ocean top predators under CLIOTOP
Hobday, A. J., Arrizabalaga, H., Evans, K., Scales, K. L., Senina, I. N., & Weng, K. C. (2017) · Deep Sea Research Part II Topical Studies in Oceanography · doi:10.1016/j.dsr2.2017.03.008 · Cited by 8 · see citing works
Self-citationMondal, S., Ray, A., Lee, M., & Boas, M. (2023) · Journal of Marine Science and Engineering · doi:10.3390/jmse11081565 · Cited by 7 · see citing works
Matsubara, N., Aoki, Y., Aoki, A., et al. (2024) · Frontiers in Marine Science · doi:10.3389/fmars.2024.1353918 · Cited by 7 · see citing works
Castrejón, M., Pittman, J. B., Ramírez-González, J., et al. (2024) · Ocean & Coastal Management · doi:10.1016/j.ocecoaman.2024.107436 · Cited by 7 · see citing works
Rumpa, A., Najamuddin, N., Safruddin, S., et al. (2022) · Biodiversitas Journal of Biological Diversity · doi:10.13057/biodiv/d230421 · Cited by 7 · see citing works
“…such as surface temperature, currents, salinity, and chlorophyll-a concentration based on remote sensing and geographic Information systems (Arrizabalaga et al. 2015; Ghufron et al. 2019; Seloi et al. 2019) and information based on local knowledge of fishermen (Moreno et al. 2007; Macusi…”
Background
- Authors
- Arrizabalaga, H., Dufour, F., Kell, L., Merino, G., Ibaibarriaga, L., Chust, G., Irigoien, X., Santiago, J., Murua, H., Fraile, I., Chifflet, M., Goikoetxea, N., Sagarminaga, Y., Aumont, O., Bopp, L., Herrera, M., Marc Fromentin, J., & Bonhomeau, S.
- Affiliations
- AZTI (ES)
- International Commission for the Conservation of Atlantic Tunas (ES)
- Venue
- Deep Sea Research Part II: Topical Studies in Oceanography
- Publisher
- Elsevier BV
- Published
- 2015-03
- Volume
- 113
- Pages
- 102-112
- ISSN
- 0967-0645 (ISSN-L)
- OpenAlex
- W2037723922
- Semantic Scholar
- 8593a7cd0965d2a821fa75e8bbd894edf02396e7
- Cited by
- 194
- References
- 98
- Citations by year
- 2026: 26 · 2025: 17 · 2024: 25 · 2023: 24 · 2022: 16 · 2021: 18 · 2020: 12 · 2019: 15 · 2018: 11 · 2017: 8 · 2016: 12 · 2015: 8 · 2014: 1
- FWCI
- 7.87
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Deep Sea Research Part II Topical Studies in Oceanography (publishedVersion)
- HAL (Le Centre pour la Communication Scientifique Directe) (submittedVersion)
- Institutional Archive of Ifremer (French Research Institute for Exploitation of the Sea) (submittedVersion)
- AZTI Institutional Repository (submittedVersion, cc-by-nc-sa)
- King Abdullah University of Science and Technology Repository (King Abdullah University of Science and Technology) (submittedVersion, cc-by-nc-nd)
- INFM-OAR (INFN Catania) (submittedVersion, other-oa)
- Funders
- EU Marie Curie EST
- METAOCEANS (MEST-CT-2005–019678)
- European Commission (264933)
- EURO-BASIN: European Union Basin-scale Analysis, Synthesis and Integration
- Topics
- Physical Sciences › Environmental Science › Global and Planetary Change › Marine and fisheries research
- Physical Sciences › Environmental Science › Nature and Landscape Conservation › Fish Ecology and Management Studies
- Life Sciences › Agricultural and Biological Sciences › Aquatic Science › Fish Biology and Ecology Studies
- Keywords
- tuna, habitat preference, ecosystem approach to fisheries, Thunnus thynnus, southern bluefin tuna, albacore tuna, bigeye tuna, yellowfin tuna, skipjack tuna, chlorophyll, sea level anomalies, mixed layer depth, water column stratification, anoxic waters
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Claims read by deepseek-v4.1-flash under definition version 3 (extract-v3) on 2026-10-16.
Classified by jev-1.13-20260917 (gold-guideline-v0.2) on 2026-10-16.
Cited sources are checked by gpt-6-sol.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review