Effects of temperature on global patterns of tuna and billfish richness
Open accessAbstract
Although tunas and billfishes are of substantial economic importance and conservation concern, global patterns of diversity and distribution remain poorly understood.Many species are highly migratory and able to tolerate a wide thermal range.In the present study, ambient water temperature data for 18 species of tuna and billfish from 190 literature sources were combined according to geographical location.An empirical modelling approach was used to relate temperature tolerances of tunas and billfishes to their global diversity patterns.Mean preferred and tolerated temperature ranges were calculated for each species in the adult and juvenile life stages.Mean tolerance data were then overlaid in order to fit models relating the species richness of tunas and billfishes to ambient water temperature.The best-fit model was used in conjunction with gridded water temperature data to predict global species richness patterns.Cumulative species richness predictions from water temperature data were positively correlated with observed longline-derived richness data (r = 0.577, p < 0.0001).Diversity consistently peaked at intermediate latitudes (10 to 35° N and S) in a manner similar to other pelagic taxa.This analysis provides evidence that the ambient water temperature tolerances of tunas and billfishes can be used to predict broad species richness patterns on a global scale.
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Written from the paper’s full text.
TL;DR
Temperature tolerances compiled for 18 tuna and billfish species predicted global richness patterns that correlated with longline-derived richness, peaking at intermediate latitudes. The best-fit third-order polynomial predicted peak richness at ~22.5°C and at 100 m depth gave the strongest correlation with observed data.
Key findings
- Cumulative temperature-predicted species richness was positively correlated with rarefied longline-derived richness at 100 m (r = 0.577, p < 0.0001), stronger than at 0 m (r = 0.282) or 50 m (r = 0.420).
- The best-fit third-order polynomial predicted peak species richness at T_optimum ≈ 22.5°C (r² = 0.978); separately, peak richness was ~21°C for Thunnus (r² = 0.976) and ~24°C for Istiophoridae and Xiphidae (r² = 0.919).
- Predicted richness peaked at intermediate latitudes (10 to 35° N and S) and declined toward polar and equatorial regions; maximum predicted richness was higher in the Indo-Pacific (11 species, T_optimum ≈ 22°C, r² = 0.978) than the Atlantic (9 species, T_optimum ≈ 21°C, r² = 0.979).
- Among tunas, body length was positively related to maximum temperature range (r = 0.881, p = 0.0004), but not among billfishes (r = 0.456, p = 0.297); spawning occurred in waters about 5°C warmer than those typically inhabited by juveniles or adults.
Methods
- Compiled ambient water temperature tolerances and preferences for 18 tuna and billfish species from 190 publications published January 1950 to April 2006, separated by adult, juvenile, and larval life stages where data allowed.
- Calculated mean temperature tolerances and species richness at 1°C increments, fitted second-, third-, and fourth-order polynomial regressions plus inverse polynomial and Poisson GLMs, and selected the best-fit third-order polynomial using AIC.
- Predicted global richness from NOAA World Ocean Atlas 2001 mean water temperature at 0, 50, and 100 m on a 5° grid, then compared predictions with rarefied species richness from Japanese pelagic longline logbook data (1952–1999) across 5° × 5° cells (n = 1983 cells), including percentile binning for spatial comparison.
Limitations
- The paper states that temperature data were unavailable for any spearfish, 2 tuna species, and sparse for 8 of the studied species, and that detailed effects of water temperature on spawning behavior remain poorly resolved.
- The paper states that other regionally important factors—such as ocean fronts, reefs, shelf breaks, seamounts, eddies, and productivity—were not taken into account, and that depth mismatches between database temperature records and the 100 m prediction depth, plus variation in vertical distribution and possible tracking-vessel effects, are sources of error.
- The paper notes that longlining data exclude some coastal areas within Exclusive Economic Zones and that longlining included spearfishes but excluded many smaller tunas included in the present data set; it also reports overprediction in the Atlantic and southern Indian Oceans, which it suggests may relate to exploitation.
Model-written summary. Check it against the paper before relying on it.
Integrity signals
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Cites
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Claims the paper makes
1 of 57 cited sources checked · 1 supported · 0 flagged
- Findingown data
Marlins, sailfishes, and many small tropical tunas (kawakawa, little tunny, and skipjack) were less tolerant of low water temperatures than the larger species of tuna and billfish (bluefin, bigeye, yellowfin, and swordfish).
“Furthermore, marlins, sailfishes, and many small tropical tunas (kawakawa, little tunny, and skipjack) were less tolerant of low water temperatures than the larger species of tuna and billfish (bluefin, bigeye, yellowfin, and swordfish) (Table 1, Fig. 1A).”
Quote in the paperSubstantial claim - Findingown data
Total species richness against water temperature was best approximated by a third-order polynomial regression model yielding a predicted peak in species richness at Topt ≈ 22.5°C (r2 = 0.978).
“Total species richness against water temperature was best approximated by a third-order polynomial regression model yielding a predicted peak in species richness at a water temperature of T optimum ≈ 22.5°C (r 2 = 0.978) (Fig. 2C).”
Quote in the paperSubstantial claim - Findingown data
The model under-predicted relative species richness in the northwest Atlantic and Pacific Oceans.
“The model under-predicted relative species richness in the northwest Atlantic and Pacific Oceans (Fig. 4C).”
Quote in the paperNot a substantial claim- The authors state this as an assumption: Rarefaction correctly orders cells in terms of relative species richness.
- Rests on an assumption: The difference between rarefied and actual (asymptotic) species richness values varies between cells.
- Rests on an assumption: The Japanese longline data set encompasses the estimated global range of all tuna and billfish species, excluding some coastal areas within individual countries' Exclusive Economic Zones.
- Findingown data
Mean temperature preferences for marlins and sailfishes were skewed towards the warmer end of their mean tolerance range.
“While mean temperature preferences for these species were approximately centred on the mean tolerance range, mean preferences for marlins (5 species) and sailfishes (2 species) were skewed towards the warmer end of their mean tolerance range.”
Quote in the paperNot a substantial claim - Findingown data
The largest discrepancies between predicted and rarefied percentiles were in mid-latitudinal regions of the Atlantic and Indian Oceans, where the model over-predicted relative species richness.
“The largest discrepancies were noted for mid-latitudinal regions of the Atlantic and Indian Oceans, where the model appeared to over-predict relative species richness (Fig. 4C).”
Quote in the paperNot a substantial claim- The authors state this as an assumption: Rarefaction correctly orders cells in terms of relative species richness.
- Rests on an assumption: The difference between rarefied and actual (asymptotic) species richness values varies between cells.
- Rests on an assumption: The Japanese longline data set encompasses the estimated global range of all tuna and billfish species, excluding some coastal areas within individual countries' Exclusive Economic Zones.
- Findingown data
Polynomial regression fits predicted peak richness at a lower Topt for Thunnus (~21°C, r2 = 0.976) than for Istiophoridae and Xiphidae (~24°C, r2 = 0.919).
“Polynomial regression fits of tuna and billfish species richness against water temperature (Fig. 2A), predicted peak richness at a lower temperature (T optimum ) for Thunnus (~21°C, r 2 = 0.976) than for Istiophoridae and Xiphidae (~24°C, r 2 = 0.919).”
Quote in the paperSubstantial claim - Findingown data
Mean temperature preferences for bluefin tunas, swordfish, bigeye, albacore, and yellowfin were approximately centred on their mean tolerance range.
“While mean temperature preferences for these species were approximately centred on the mean tolerance range, mean preferences for marlins (5 species) and sailfishes (2 species) were skewed towards the warmer end of their mean tolerance range.”
Quote in the paperNot a substantial claim - Findingown data
Temperature-predicted species richness at 100 m was positively correlated with normalized rarefied species richness from the 1990s (r = 0.577, p < 0.0001).
“Cumulative species richness predictions from water temperature data were positively correlated with observed longline-derived richness data (r = 0.577, p < 0.0001).”
- Also stated in: § RESULTS · plain
“When plotted against normalized rarefied species richness from the 1990s, there was a higher degree of correlation at 100 m (r = 0.577, p < 0.0001) (Fig. 3A) than at 0 m (r = 0.282, p < 0.0001) or 50 m (r = 0.420, p < 0.0001) (Table 2).”
Quote in the paperSubstantial claim- The authors state this as an assumption: Rarefaction correctly orders cells in terms of relative species richness.
- Rests on an assumption: The difference between rarefied and actual (asymptotic) species richness values varies between cells.
- Rests on an assumption: The Japanese longline data set encompasses the estimated global range of all tuna and billfish species, excluding some coastal areas within individual countries' Exclusive Economic Zones.
- Also stated in: § RESULTS · plain
- Findingown data
Bluefin tunas Thunnus thynnus, T. orientalis and T. maccoyi, swordfish Xiphias gladius, and bigeye tuna T. obesus had the largest ranges of mean temperature tolerance, followed by albacore T. alalunga and yellowfin T. albacares.
“Of the 18 species for which we compiled data, bluefin tunas Thunnus thynnus, T. orientalis and T. maccoyi, swordfish Xiphias gladius, and bigeye tuna T. obesus had the largest ranges of mean temperature tolerance, followed by albacore T. alalunga and yellowfin T. albacares (Table 1, Fig. 1A).”
Quote in the paperSubstantial claim - Findingown data
Correlation between temperature-predicted and rarefied species richness was higher at 100 m than at 0 m or 50 m.
“When plotted against normalized rarefied species richness from the 1990s, there was a higher degree of correlation at 100 m (r = 0.577, p < 0.0001) (Fig. 3A) than at 0 m (r = 0.282, p < 0.0001) or 50 m (r = 0.420, p < 0.0001) (Table 2).”
Quote in the paperSubstantial claim- The authors state this as an assumption: Rarefaction correctly orders cells in terms of relative species richness.
- Rests on an assumption: The difference between rarefied and actual (asymptotic) species richness values varies between cells.
- Rests on an assumption: The Japanese longline data set encompasses the estimated global range of all tuna and billfish species, excluding some coastal areas within individual countries' Exclusive Economic Zones.
- Findingown data
Comparisons across ocean basins predicted higher maximum species richness in the Indo-Pacific (11 species, Topt ≈ 22°C, r2 = 0.978) than the Atlantic (9 species, Topt ≈ 21°C, r2 = 0.979).
“Comparisons across ocean basins (Fig. 2B) predicted higher maximum species richness in the Indo-Pacific (11 species, T optimum ≈ 22°C, r 2 = 0.978) than the Atlantic (9 species, T optimum ≈ 21°C, r 2 = 0.979).”
Quote in the paperSubstantial claim - Findingown data
The latitudinal pattern was strongest for the Pacific Ocean, where 2 well-defined bands of peak species richness were observed (20 to 35° N and S).
“This latitudinal pattern was strongest for the Pacific Ocean, where 2 well-defined bands of peak species richness were observed (20 to 35° N and S).”
Quote in the paperNot a substantial claim - Findingown data
Our billfish model was strongly driven by the inclusion of swordfishes (Xiphidae), which possessed a mean minimum temperature tolerance 10°C colder than the most cold-tolerant species of marlin or sailfish (Istiophoridae).
“Our billfish model was strongly driven by the inclusion of swordfishes (Xiphidae), which possessed a mean minimum temperature tolerance 10°C colder than the most cold-tolerant species of marlin or sailfish (Istiophoridae).”
Quote in the paperSubstantial claim - Findingown data
Spatial patterns of temperature-predicted species richness at 100 m appeared to coincide reasonably well with longline derived estimates.
“Spatial patterns of temperature-predicted species richness at 100 m (Fig. 3B) appeared to coincide reasonably well with longline derived estimates (Fig. 3C).”
Quote in the paperSubstantial claim- The authors state this as an assumption: Rarefaction correctly orders cells in terms of relative species richness.
- Rests on an assumption: The difference between rarefied and actual (asymptotic) species richness values varies between cells.
- Rests on an assumption: The Japanese longline data set encompasses the estimated global range of all tuna and billfish species, excluding some coastal areas within individual countries' Exclusive Economic Zones.
- Findingown data
Predicted species richness for tunas and billfishes was a nonlinear function of water temperature best approximated by a third-order polynomial.
“When multiple species' temperature tolerance ranges were superimposed, predicted species richness for tunas and billfishes was a nonlinear function of water temperature (Fig. 2) best approximated by a thirdorder polynomial.”
Quote in the paperSubstantial claim - Findingown data
Peak species richness was predicted to occur at ~24°C for billfishes.
“Peak species richness was predicted to occur at ~21°C for tunas and 24°C for billfishes (Fig. 2A).”
Quote in the paperSubstantial claim - Findingreasoning
Predicted species richness was better fit against estimated longlining diversity with increasing depth.
“Predicted species richness was better fit against estimated longlining diversity with both increasing depth and (generally) through time (Table 2).”
Quote in the paperNot a substantial claim - Findingown data
Comparing ocean basins, highest species richness was predicted in the Indian and Pacific Oceans, followed by the Atlantic.
“Comparing ocean basins, highest species richness was predicted in the Indian and Pacific Oceans, followed by the Atlantic (Fig. 2B).”
Quote in the paperSubstantial claim - Findingnone given
Our predicted global species diversity peaks at around 2°C lower than that derived from longlining data.
“Taken as a whole, our predicted global species diversity peaks at around 2°C lower than that derived from longlining data.”
Quote in the paperSubstantial claim - Findingown data
In all oceans, predicted species richness peaked at intermediate latitudes (10 to 35°N and S), with declining richness towards the poles and equator.
“In all oceans, predicted species richness peaked at intermediate latitudes (10 to 35°N and S), with declining richness towards the poles and equator (Figs.3A & 4A).”
Quote in the paperSubstantial claim - Findingown data
Among tunas, the positive relationship between species body length and maximum temperature range was significant (r = 0.881, p = 0.0004).
“A positive relationship between species body length and maximum temperature range was significant among tunas (r = 0.881, p = 0.0004) but not for billfishes (r = 0.456, p = 0.297)”
Quote in the paperSubstantial claim - Findingreasoning
The species with the widest temperature ranges were swordfish, bigeye, albacore and bluefin tunas.
“The species with the widest temperature ranges were swordfish, bigeye, albacore and bluefin tunas (Fig. 1A).”
Quote in the paperSubstantial claim - Findingown data
Peak species richness was predicted to occur at ~21°C for tunas.
“Peak species richness was predicted to occur at ~21°C for tunas and 24°C for billfishes (Fig. 2A).”
Quote in the paperSubstantial claim - Findingown data
Temperature preferences for most marlins and sailfishes (Istiophoridae) were skewed towards the warm end of the mean tolerance distribution.
“While temperature preferences for these species were centred around the mean tolerance, those for most marlins and sailfishes (Istiophoridae) were skewed towards the warm end of the mean tolerance distribution (Fig. 1A).”
Quote in the paperNot a substantial claim - Findingreasoning
Predicted species richness was better fit against estimated longlining diversity through time (generally).
“Predicted species richness was better fit against estimated longlining diversity with both increasing depth and (generally) through time (Table 2).”
Quote in the paperNot a substantial claim - Findingown data
Spatial differences between predicted and rarefied models based on binned percentiles revealed overpredictions of relative species richness in the north and south Atlantic and southern Indian Oceans.
“Spatial differences between predicted and rarefied models based on binned percentiles revealed overpredictions of relative species richness in the north and south Atlantic and southern Indian Oceans (Fig. 4C).”
Quote in the paperSubstantial claim - Findingown data
Among billfishes, the relationship between species body length and maximum temperature range was not significant (r = 0.456, p = 0.297).
“A positive relationship between species body length and maximum temperature range was significant among tunas (r = 0.881, p = 0.0004) but not for billfishes (r = 0.456, p = 0.297)”
Quote in the paperSubstantial claim - Findingown data
There was a positive correlation between temperature-predicted species richness and richness obtained from longlining data.
“Despite this variation, there was a positive correlation between temperature-predicted species richness and richness obtained from longlining data (Fig 3A).”
Quote in the paperSubstantial claim - Findingcitation
The vast majority of information within the database was collected from subsurface tracking experiments such as satellite-tracking, ultrasonic telemetry, and acoustic tracking.
“The vast majority of information within the database was collected from subsurface tracking experiments such as satellite-tracking (Block et al. 2001), ultrasonic telemetry (Brill et al. 2002), and acoustic tracking (Bach et al. 2003).”
Quote in the paperSubstantial claim - Findingown data
Our spatial analyses demonstrated high congruence between observed and temperature-predicted species richness.
“Nonetheless, our spatial analyses demonstrated high congruence between observed and temperature-predicted species richness.”
Quote in the paperSubstantial claim- Rests on an assumption: The rarefied species richness derived from Japanese longlining data (1990-1999) accurately reflects true tuna and billfish species richness.
- Rests on an assumption: Temperature at 100 m depth is an adequate predictor of tuna and billfish species richness despite vertical variation.
- Findingown data
There are still information gaps for particular species.
“While the development of satellite and other tagging technologies has greatly increased our understanding of the distribution patterns of tunas and billfishes (Sedberry & Loefer 2001, Boustany et al. 2002, Graves et al. 2002, Block et al. 2005), there are still information gaps for particular species.”
Quote in the paperSubstantial claim - Premisecitation
Community-wide patterns of abundance and richness of tunas and billfishes remain poorly understood.
“While tagging studies have added to our knowledge of the current ranges and distribution patterns for individual species of tuna and billfish (Block et al. 2001), community-wide patterns of abundance and richness remain poorly understood (Worm et al. 2005).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Worm et al. 2005 source
- Interpretationown data
This analysis provides evidence that ambient water temperature tolerances of tunas and billfishes can be used to predict broad species richness patterns on a global scale.
“This analysis provides evidence that the ambient water temperature tolerances of tunas and billfishes can be used to predict broad species richness patterns on a global scale.”
Quote in the paperSubstantial claim- The authors state this as an assumption: Rarefaction correctly orders cells in terms of relative species richness.
- Rests on an assumption: The difference between rarefied and actual (asymptotic) species richness values varies between cells.
- Rests on an assumption: The Japanese longline data set encompasses the estimated global range of all tuna and billfish species, excluding some coastal areas within individual countries' Exclusive Economic Zones.
- Premisecitation
Japanese logbook data are the only globally consistent data on species composition, catch, and effort for all tunas and billfishes.
“Japanese logbook data are compiled from the world's largest longline fleet and are the only globally consistent data on species composition, catch, and effort for all tunas and billfishes (Worm et al. 2005).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Worm et al. 2005 source
- Premisecitation
The selected tuna and billfish species are fished with like gear.
“These species were selected as they are all regionally heterothermic predators that share common ecological niches, are fished with like gear, and exhibit comparable oceanographic preferences (reviewed by Sund et al. 1981, Brill & Lutcavage 2001, reviewed by Worm et al. 2005).”
Quote in the paperSubstantial claim0 of 3 sources checked- cites Sund et al. 1981
- cites Brill & Lutcavage 2001
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites Worm et al. 2005 source
- Premisecitation
The selected tuna and billfish species share common ecological niches.
“These species were selected as they are all regionally heterothermic predators that share common ecological niches, are fished with like gear, and exhibit comparable oceanographic preferences (reviewed by Sund et al. 1981, Brill & Lutcavage 2001, reviewed by Worm et al. 2005).”
Quote in the paperSubstantial claim0 of 3 sources checked- cites Sund et al. 1981
- cites Brill & Lutcavage 2001
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites Worm et al. 2005 source
- Premisecitation
The upper and lower bounds of individual species geographic ranges appear to relate to their physiological temperature tolerances.
“Despite these adaptations, the upper and lower bounds of individual species geographic ranges appear to relate to their physiological temperature tolerances (Brill 1994, Brill & Lutcavage 2001).”
Quote in the paperSubstantial claim0 of 2 sources checked- cites Brill 1994 source
- cites Brill & Lutcavage 2001
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Premisecitation
The selected tuna and billfish species are all regionally heterothermic predators.
“These species were selected as they are all regionally heterothermic predators that share common ecological niches, are fished with like gear, and exhibit comparable oceanographic preferences (reviewed by Sund et al. 1981, Brill & Lutcavage 2001, reviewed by Worm et al. 2005).”
Quote in the paperSubstantial claim0 of 3 sources checked- cites Sund et al. 1981
- cites Brill & Lutcavage 2001
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites Worm et al. 2005 source
- Premisecitation
The selected tuna and billfish species exhibit comparable oceanographic preferences.
“These species were selected as they are all regionally heterothermic predators that share common ecological niches, are fished with like gear, and exhibit comparable oceanographic preferences (reviewed by Sund et al. 1981, Brill & Lutcavage 2001, reviewed by Worm et al. 2005).”
Quote in the paperSubstantial claim0 of 3 sources checked- cites Sund et al. 1981
- cites Brill & Lutcavage 2001
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites Worm et al. 2005 source
- Premisecitation
Water temperature has repeatedly emerged as the best single predictor of species density and distribution.
“Of these, water temperature has repeatedly emerged as the best single predictor of species density and distribution (Lee et al. 2005, Worm et al. 2005).”
Quote in the paperSubstantial claim0 of 2 sources checked- cites Lee et al. 2005
- cites Worm et al. 2005 source
- Interpretationcitation
Ambient water temperature may be used to predict species richness patterns of tunas and billfishes on a global scale.
“This suggests that ambient water temperature may be used to predict the species richness patterns of tunas and billfishes on a global scale.”
Quote in the paperSubstantial claim - Interpretationown data
The theory that tunas were originally tropical species is further supported by the need of their larvae for extremely warm waters.
“The theory that tunas were originally tropical species is further supported by the need of their larvae for extremely warm waters (Fig. 1B).”
Quote in the paperNot a substantial claim - Premisecitation
Swordfish, bigeye, albacore and bluefin tunas display longer migrations and deeper dives than other species of tuna and billfish.
“They also display longer migrations and deeper dives than other species of tuna and billfish (reviewed by Sund et al. 1981, Fromentin & Fonteneau 2001).”
Quote in the paperSubstantial claim0 of 2 sources checked- cites Sund et al. 1981
- cites Fromentin & Fonteneau 2001 source
- Interpretationreasoning
Variation in heterothermy among tuna species of different sizes may partially explain why body size limits thermal range.
“This variation in heterothermy among tuna species of different sizes may partially explain why body size limits thermal range.”
Quote in the paperNot a substantial claim - Premisecitation
Billfishes are unable to tolerate extremely cold temperatures for extended periods, except swordfish.
“As visual predators, billfishes maintain their brains (and eyes) at elevated temperatures in order to hunt in colder waters, and are unable to tolerate extremely cold temperatures for extended periods (except swordfish: Fritsches et al. 2005).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Fritsches et al. 2005 source
- Interpretationreasoning
Extended 'cooling' dives by Atlantic bluefin tuna in the Gulf of Mexico may be a mechanism employed by adult fish to tolerate the high temperatures favourable for rapid larval development.
“This may be a mechanism employed by adult fish to tolerate the high tempera-tures favourable for rapid larval development.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Teo et al. 2007 source
- Premisecitation
Atlantic bluefin tuna spawning in the similarly warm Gulf of Mexico were observed to undertake extended 'cooling' dives to deeper waters in between short spawning events at the surface.
“For example, Atlantic bluefin tuna spawning in the similarly warm Gulf of Mexico were observed to undertake extended 'cooling' dives to deeper waters in between short spawning events at the surface (Teo et al. 2007).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Teo et al. 2007 source
- Interpretationreasoning
Above-optimal temperatures appear to have a negative effect on richness.
“Above-optimal temperatures appear to have a negative effect on richness.”
Quote in the paperSubstantial claim - Interpretationreasoning
Temperatures above optimal are likely unsuitable for large tunas, which generate significant metabolic heat.
“These temperatures are likely unsuitable for large tunas, which generate significant metabolic heat.”
Quote in the paperSubstantial claim - Premisecitation
As visual predators, billfishes maintain their brains (and eyes) at elevated temperatures in order to hunt in colder waters.
“As visual predators, billfishes maintain their brains (and eyes) at elevated temperatures in order to hunt in colder waters, and are unable to tolerate extremely cold temperatures for extended periods (except swordfish: Fritsches et al. 2005).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Fritsches et al. 2005 source
- Premisecitation
Tunas generally possess greater heterothermic capacities relative to billfishes.
“Given that tunas generally possess greater heterothermic capacities relative to billfishes (Dickson 1995), these results are consistent with previous studies.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Dickson 1995 source
- Premisecitation
A decrease in species richness was documented in the western Pacific 'warm pool', where the highest mean annual ocean temperatures at 100 m (> 28°C) are found.
“A decrease in species richness was documented in the western Pacific 'warm pool' (Worm et al. 2005), where the highest mean annual ocean temperatures at 100 m (> 28°C) are found (Conkright et al. 2002).”
Quote in the paperSubstantial claim0 of 2 sources checked- cites Worm et al. 2005 source
- cites Conkright et al. 2002
- Study design and conductown data
The best-fit third-order polynomial model had the lowest AIC value of the models tested.
“Using the best-fit third-order polynomial model (lowest AIC value of those tested) we predicted species richness from water temperature using published global mean water temperature data at 0, 50, and 100 m depth on a 5° grid, derived from the NOAA World Ocean Atlas 2001 (Conkright et al. 2002).”
Quote in the paperSubstantial claim - Interpretationcitation
Overpredictions of relative species richness in the Atlantic Ocean are possibly the result of prolonged and well-documented exploitation in this region relative to the Pacific Ocean, where exploitation has been substantial but with a potentially lesser effect.
“Overpredictions of relative species richness in the Atlantic Ocean are possibly the result of prolonged and well-documented exploitation in this region (Myers & Worm 2003) relative to the Pacific Ocean, where exploitation has been substantial but with a potentially lesser effect (Sibert et al. 2006).”
Quote in the paperSubstantial claim0 of 2 sources checked - Interpretationreasoning
The widest temperature ranges of swordfish, bigeye, albacore and bluefin tunas are likely due to greater physiological tolerance of colder temperatures, opening a wider range of potential habitats from temperate to sub-tropical waters.
“This is likely due to the fact that these species are more physiologically tolerant of colder temperatures, opening up a wider range of potential habitats, from temperate to sub-tropical waters.”
Quote in the paperSubstantial claim - Interpretationreasoning
The improvement in fit with increasing water depth is best explained by the fact that 100 m is the most common depth at which longline hooks are set, resulting in the best fit against empirical longline data.
“The improvement in fit with increasing water depth is best explained by the fact that 100 m is the most common depth at which longline hooks are set, resulting in the best fit against empirical longline data.”
Quote in the paperSubstantial claim- Rests on an assumption: 100 m is the most common depth at which longline hooks are set.
- Interpretationcitation
The increase in temperature tolerance range with increasing body size among tunas is consistent with the theory that tunas were originally inshore tropical fishes which, through endothermic adaptations, became less vulnerable to environmental variability and reduced their competition with other species.
“Taken as a whole, the increase in temperature tolerance range with increasing body size among tunas is consistent with the theory that tunas were originally inshore tropical fishes which, through endothermic adaptations, became less vulnerable to environmental variability and reduced their competition with other species (Sharp 1978).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Sharp 1978 source
- Interpretationreasoning
Given the evidence for overexploitation, overpredictions in both the Atlantic and southern Indian Oceans are consistent with the hypothesis that exploitation of these species has caused shifts in species distributions.
“Given the evidence for overexploitation, overpredictions in both the Atlantic and southern Indian Oceans are consistent with the hypothesis that exploitation of these species has caused shifts in species distributions.”
Quote in the paperNot a substantial claim - Premisecitation
Variation in size, complexity, number, and positioning of heat-exchanging organs (retia) among different species of tuna results in varying degrees of heterothermy.
“Additionally, the variation in size, complexity, number, and positioning of heat-exchanging organs (retia) among different species of tuna results in varying degrees of heterothermy (Block & Stevens 2001).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Block & Stevens 2001 source
- Study design and conductreasoning
Using temperature at 100 m to predict patterns of richness when temperature information was gathered at a range of depths will likely not completely capture distribution patterns.
“Using temperature at 100 m to predict patterns of richness when temperature information was gathered at a range of depths will likely not completely capture distribution patterns.”
Quote in the paperNot a substantial claim - Premisecitation
Variation in vertical distribution occurs within species.
“Variation in vertical distribution also occurs within species.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Hanamoto 1974
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Premisecitation
Topographic features such as ocean fronts, reefs, shelf breaks and seamounts have been shown to be areas of high tuna and billfish abundance and diversity.
“Topographic features such as ocean fronts, reefs, shelf breaks and seamounts have been shown to be areas of high tuna and billfish abundance and diversity (reviewed by Worm et al. 2003).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Worm et al. 2003 source
- Premisecitation
Regions identified in the report as the most severely exploited included high seas tuna fishing grounds in the Atlantic and Indian Oceans, where the proportion of stocks classified as overexploited, depleted or recovering were between 46 and 66 % of the total.
“Regions identified in the report as the most severely exploited included high seas tuna fishing grounds in the Atlantic and Indian Oceans, where the proportion of stocks classified as overexploited, depleted or recovering were between 46 and 66 % of the total.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Maguire et al. 2006
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Study design and conductreasoning
The variation between the depth at which pelagic longline gear is set and the actual vertical distribution of each species may be an additional source of error.
“This variation between the depth at which pelagic longline gear is set and the actual vertical distribution of each species may be an additional source of error.”
Quote in the paperNot a substantial claim
- Classified as probably not a substantial claim. 16
- The quote only partly states this claim. 1
- May combine two claims. 18
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationThe development of satellite and other tagging technologies has greatly increased our understanding of the distribution patterns of tunas and billfishes.
“While the development of satellite and other tagging technologies has greatly increased our understanding of the distribution patterns of tunas and billfishes (Sedberry & Loefer 2001, Boustany et al. 2002, Graves et al. 2002, Block et al. 2005), there are still information gaps for particular species.”
Quote in the paperNot a substantial claim1 of 3 sources checkedProbably not a substantial claim: may not pass S3 (load-bearing). The quote only partly states this claim.
Findingnone givenCorrelations between predicted and rarefied species richness tended to strengthen marginally over time.
“Correlations tended to strengthen marginally over time.”
Quote in the paperNot a substantial claim- The authors state this as an assumption: Rarefaction correctly orders cells in terms of relative species richness.
- Rests on an assumption: The difference between rarefied and actual (asymptotic) species richness values varies between cells.
- Rests on an assumption: The Japanese longline data set encompasses the estimated global range of all tuna and billfish species, excluding some coastal areas within individual countries' Exclusive Economic Zones.
May combine two claims.
Findingown dataSpawning occurs in waters much warmer (ΔT ≈ 5°C) than those typically inhabited by juveniles or adults, often on the upper fringes of the reported mean adult temperature tolerance range.
“Results indicated that spawning occurs in waters that are much warmer (ΔT ≈ 5°C) than those typically inhabited by juveniles or adults, and which have temperatures that are often on the upper fringes of the reported mean adult temperature tolerance range; this was the case, for example, in southern and pacific bluefin tunas and albacore tuna (Table 1, Fig. 1).”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataMaximum predicted and observed global species richness both occurred at intermediate latitudes (10 to 35° N and S), and decreased towards polar and equatorial regions.
“Diversity consistently peaked at intermediate latitudes (10 to 35° N and S) in a manner similar to other pelagic taxa.”
- Also stated in: § RESULTS · plain
“Maximum predicted and observed global species richness both occurred at intermediate latitudes (10 to 35° N and S), and decreased towards polar and equatorial regions.”
Quote in the paperSubstantial claim- The authors state this as an assumption: Rarefaction correctly orders cells in terms of relative species richness.
- Rests on an assumption: The difference between rarefied and actual (asymptotic) species richness values varies between cells.
- Rests on an assumption: The Japanese longline data set encompasses the estimated global range of all tuna and billfish species, excluding some coastal areas within individual countries' Exclusive Economic Zones.
- Also stated in: § RESULTS · plain
May combine two claims.
Findingown dataTemperature studies were sparse for kawakawa and little tunny and lacking for longtail tuna, blackfin tuna, shortbill spearfish, longbill spearfish, and Mediterranean spearfish.
“Temperature studies were sparse for kawakawa and little tunny and lacking for longtail tuna Thunnus tonggol, blackfin tuna Thunnus atlanticus, shortbill spearfish Tetrapturus angustirostris, longbill spearfish Tetrapturus pfluegeri and Mediterranean spearfish Tetrapturus pelone.”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataTotal global predicted species richness was strongly related to water temperature, with peak species richness predicted at ~22.5°C (r2 = 0.978, p < 0.0001).
“Total global predicted species richness was strongly related to water temperature, with peak species richness predicted at ~22.5°C (r 2 = 0.978, p < 0.0001) (Fig. 2C).”
Quote in the paperSubstantial claimMay combine two claims.
Findingnone givenMarlins, sailfishes, and most small tropical tuna species (kawakawa, little tunny, and skipjack tuna) appeared to possess a higher tolerance for warmer waters and a lower tolerance for colder waters.
“Unsurprisingly, marlins, sailfishes, and most small tropical tuna species (kawakawa, little tunny, and skipjack tuna) appeared to possess a higher tolerance for warmer waters and a lower tolerance for colder waters.”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataIn the Atlantic and Indian Oceans, predicted species richness peaks were more widely distributed, although still occurring at intermediate latitudes (10 to 35° N and S).
“In the Atlantic and Indian Oceans, predicted species richness peaks were more widely distributed, although still occurring at intermediate latitudes (10 to 35° N and S) (Fig. 4A).”
Quote in the paperSubstantial claimMay combine two claims.
Findingnone givenData regarding water temperature tolerances and preferences were unavailable for any species of spearfish, 2 species of tunas, and sparse for 8 of the species of tuna and billfish studied here.
“Data regarding water temperature tolerances and preferences were unavailable for any species of spearfish, 2 species of tunas, and sparse for 8 of the species of tuna and billfish studied here.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationThis latitudinal pattern is similar to that previously found for the diversity of tunas and billfishes, as well as foraminifera and other zooplankton groups.
“This latitudinal pattern is similar to that previously found for the diversity of tunas and billfishes (Worm et al. 2003(Worm et al. , 2005)), as well as foraminifera and other zooplankton groups (Rutherford et al. 1999).”
Quote in the paperNot a substantial claim0 of 3 sources checkedProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationBigeye tuna are capable of diving to depths of 600 m.
“For example, bigeye tuna are capable of diving to depths of 600 m (Hanamoto 1987, Brill & Lutcavage 2001)”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites Hanamoto 1987
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites Brill & Lutcavage 2001
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
May combine two claims.
PremisecitationSeveral species maintain warm brains, and many larger species of tuna (albacore, bigeye, yellowfin, and bluefins) conserve heat in their viscera.
“For instance, several species maintain warm brains, and many larger species of tuna (albacore, bigeye, yellowfin, and bluefins) conserve heat in their viscera.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Block & Stevens 2001 source
May combine two claims.
InterpretationreasoningTunas generally are found in more temperate waters, migrate further and dive deeper than billfishes (except swordfish).
“Accordingly, tunas generally are found in more temperate waters, migrate further and dive deeper than billfishes (except swordfish).”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
InterpretationreasoningThe improvement in fit in more recent decades is potentially the result of more accurate empirical richness estimates due to the greater geographic distribution and magnitude of fishing effort by the Japanese longlining fleet in these decades.
“The improvement in fit in more recent decades is potentially the result of more accurate empirical richness estimates due to the greater geographic distribution and magnitude of fishing effort by the Japanese longlining fleet in these decades.”
Quote in the paperNot a substantial claim- Rests on an assumption: More recent decades have more accurate empirical richness estimates due to greater geographic distribution and magnitude of fishing effort by the Japanese longlining fleet.
Classified as probably not a substantial claim.
Study design and conductown dataSecond-, third-, and fourth-order polynomial linear regression models were checked for fit using AIC values after testing assumptions of normality and homogeneity of variance.
“Second-, third-, and fourth-order polynomial linear regression models were fitted to these data and checked for fit using Akaike Information Criterion (AIC) values, after testing assumptions of normality and homogeneity of variance.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationNorthern bluefin are known to undertake trans-Atlantic migrations spanning a wide range of thermal habitats.
“and northern bluefin are known to undertake trans-Atlantic migrations spanning a wide range of thermal habitats (Block et al. 2005).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Block et al. 2005 source
Probably not a substantial claim: may not pass S3 (load-bearing).
InterpretationreasoningThe difference between predicted and longlining-derived global species diversity peaks may be related to variation in sampling methods, sampling depth, or other unmeasured covariates.
“This difference may be related to variation in sampling methods, sampling depth, or other unmeasured covariates.”
Quote in the paperNot a substantial claimMay combine two claims.
InterpretationcitationWhile temperature may be among the best global predictors for the distribution of these species, other factors are regionally important.
“While temperature may be among the best global predictors for the distribution of these species, other factors are regionally important (Worm et al. 2005).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Worm et al. 2005 source
May combine two claims.
PremisecitationMarlins and sailfishes are predominantly epipelagic, remaining largely within the upper mixed layer, with occasional dives as deep as 200 m.
“Marlins and sailfishes are predominantly epipelagic, remaining largely within the upper mixed layer (Brill et al. 1993), with occasional dives as deep as 200 m (Block et al. 1992).”
Quote in the paperNot a substantial claim0 of 2 sources checkedProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
InterpretationcitationGiven that tunas generally possess greater heterothermic capacities relative to billfishes, these results are consistent with previous studies.
“Given that tunas generally possess greater heterothermic capacities relative to billfishes (Dickson 1995), these results are consistent with previous studies.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Dickson 1995 source
Probably not a substantial claim: may not pass S3 (load-bearing).
InterpretationreasoningSpawning behaviour of tunas and billfishes that prefer very warm waters may also account for the fact that optimal water temperature was lower in this study compared with longlining records, which may target spawning aggregations.
“Spawning behaviour of tunas and billfishes that prefer very warm waters may also account for the fact that optimal water temperature was lower in this study compared with longlining records, which may target spawning aggregations.”
Quote in the paperNot a substantial claimMay combine two claims.
Interpretationown dataBody size may limit the thermal range for tunas but not billfishes.
“suggesting that body size may limit the thermal range for tunas but not billfishes.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationPrevious work on freshwater ectothermic fish species and other tunas found increased physiological temperature tolerance with increased body size.
“This finding is consistent with previous work on freshwater ectothermic fish species (Magnuson et al. 1979) and other tunas (Barkley et al. 1978, Sharp 1978), which found increased physiological temperature tolerance with increased body size.”
Quote in the paperNot a substantial claim0 of 3 sources checkedProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationNorthern bluefin tuna can dive to depths in excess of 1000 m, encountering an exceptionally wide thermal range.
“Northern bluefin tuna, for example, can dive to depths in excess of 1000 m, encountering an exceptionally wide thermal range (Block et al. 2005).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Block et al. 2005 source
May combine two claims.
PremisecitationA recent assessment from the United Nations Food and Agriculture Organization indicated that 4 major tuna species (albacore, Atlantic and southern bluefin, and bigeye tunas) are overexploited or depleted in the Atlantic Ocean, whereas in the Indian and Pacific Oceans only 2 species are listed as fully exploited or depleted.
“This is supported by a recent assessment from the United Nations Food and Agriculture Organization (Maguire et al. 2006), which indicated that 4 major tuna species (albacore, Atlantic and southern bluefin, and bigeye tunas) are overexploited or depleted in the Atlantic Ocean, whereas in the Indian and Pacific Oceans only 2 species are listed as fully exploited or depleted.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Maguire et al. 2006
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
Probably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductreasoningVariation between the depth at which database temperature information was recorded and that used to predict ranges (100 m) is another possible source of error.
“Variation between the depth at which database temperature information was recorded and that used to predict ranges (100 m) is another possible source of error.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S2 (checkable).
Interpretationown dataThe ability to accurately identify key oceanographic variables, such as temperature, that underlie large-scale tuna and billfish range distributions may have implications for conservation and management.
“The ability to accurately identify key oceanographic variables, such as temperature, that underlie large-scale tuna and billfish range distributions may have implications for conservation and management.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationOceanic fronts and eddies frequently attract tunas and billfishes, likely because they can enhance and concentrate local productivity.
“Similarly, oceanic fronts and eddies frequently attract tunas and billfishes (Sund et al. 1981, Laurs et al. 1984, Fiedler & Bernard 1987, Santos 1994), likely because they can enhance and concentrate local productivity (Wolanski & Hamner 1988, Oschlies & Garçon 1998).”
Quote in the paperNot a substantial claim0 of 3 sources checkedProbably not a substantial claim: may not pass S4 (based). May combine two claims.
Study design and conductnone givenAs mean water temperature is not related to the occurrence of these habitat features, their effects on tuna and billfish abundance and richness have not been taken into account in this analysis.
“As mean water temperature is not related to the occurrence of these habitat features, their effects on tuna and billfish abundance and richness have not been taken into account in this analysis.”
Quote in the paperNot a substantial claim- Rests on an assumption: Mean water temperature is not related to the occurrence of ocean fronts, reefs, shelf breaks and seamounts.
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationBigeye tuna catch rates as a function of depth vary with latitude in the eastern tropical Pacific, possibly relating to zonal currents.
“For example, bigeye tuna catch rates as a function of depth have been shown to vary with latitude in the eastern tropical Pacific, possibly relating to zonal currents (Hanamoto 1974).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Hanamoto 1974
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
May combine two claims.
Interpretationown dataThe analysis allows prediction of the occurrence of tuna and billfish diversity hotspots and the effects of variation in temperature on those features, e.g. through the El Niño Southern Oscillation or gradual ocean warming.
“It allows prediction of the occurrence of tuna and billfish diversity hotspots and the effects of variation in temperature on those features, e.g. through the El Niño Southern Oscillation or gradual ocean warming.”
Quote in the paperSubstantial claim- Rests on an assumption: The rarefied species richness derived from Japanese longlining data (1990-1999) accurately reflects true tuna and billfish species richness.
- Rests on an assumption: Temperature at 100 m depth is an adequate predictor of tuna and billfish species richness despite vertical variation.
The authors state this as an assumption.
Rarefaction correctly orders cells in terms of relative species richness.
“Although we assumed that rarefaction correctly orders cells in terms of relative species richness, the difference between rarefied and actual (asymptotic) species richness values varies between cells.”
The paper relies on this without support.
The difference between rarefied and actual (asymptotic) species richness values varies between cells.
“Although we assumed that rarefaction correctly orders cells in terms of relative species richness, the difference between rarefied and actual (asymptotic) species richness values varies between cells.”
The paper relies on this without support.
The Japanese longline data set encompasses the estimated global range of all tuna and billfish species, excluding some coastal areas within individual countries' Exclusive Economic Zones.
“The longlining data set encompasses the estimated global range of all tuna and billfish species, excluding some coastal areas within individual countries' Exclusive Economic Zones.”
The paper relies on this without support.
More cold-tolerant Thunnus spp. and swordfish are capable of diving to depths well below 200 m, where temperatures are much lower.
“In contrast, the more coldtolerant Thunnus spp.and swordfish are capable of diving to depths well below 200 m, where temperatures are much lower.”
The paper relies on this without support.
These species maintain elevated deep muscle temperatures which enable them to remain active in colder waters.
“These species maintain elevated deep muscle temperatures which enable them to remain active in colder waters.”
The paper relies on this without support.
100 m is the most common depth at which longline hooks are set.
“The improvement in fit with increasing water depth is best explained by the fact that 100 m is the most common depth at which longline hooks are set, resulting in the best fit against empirical longline data.”
The paper relies on this without support.
More recent decades have more accurate empirical richness estimates due to greater geographic distribution and magnitude of fishing effort by the Japanese longlining fleet.
“The improvement in fit in more recent decades is potentially the result of more accurate empirical richness estimates due to the greater geographic distribution and magnitude of fishing effort by the Japanese longlining fleet in these decades.”
The paper relies on this without support.
Longlining data included spearfishes Tetrapturus spp. but excluded many smaller tunas (kawakawa, little tunny, and slender tuna), all of which are included in the present data set.
“Furthermore, longlining data included spearfishes Tetrapturus spp.but excluded many smaller tunas (kawakawa, little tunny, and slender tuna), all of which are included in the present data set; such variation may also be partly responsible for discrepancies.”
The paper relies on this without support.
Mean water temperature is not related to the occurrence of ocean fronts, reefs, shelf breaks and seamounts.
“As mean water temperature is not related to the occurrence of these habitat features, their effects on tuna and billfish abundance and richness have not been taken into account in this analysis.”
The paper relies on this without support.
Subsurface tracking methods accurately record ambient water temperature regardless of depth.
“Such methods accurately record ambient water temperature regardless of depth.”
The paper relies on this without support.
The rarefied species richness derived from Japanese longlining data (1990-1999) accurately reflects true tuna and billfish species richness.
“Linear regression fit of predicted species richness at 100 m depth against rarefied species richness from longlining data (1990-1999).”
The paper relies on this without support.
The temperature tolerances and preferences compiled from various sources are accurate and representative for each species.
“Data regarding water temperature tolerances and preferences were unavailable for any species of spearfish, 2 species of tunas, and sparse for 8 of the species of tuna and billfish studied here.”
The paper relies on this without support.
Temperature at 100 m depth is an adequate predictor of tuna and billfish species richness despite vertical variation.
“Using temperature at 100 m to predict patterns of richness when temperature information was gathered at a range of depths will likely not completely capture distribution patterns.”
The paper relies on this without support.
The 18 species studied represent global tuna and billfish richness.
“cumulative (all 18 species, all oceans)”
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?
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).”
From Global habitat preferences of commercially valuable tuna (2015) · cites this paper as Boyce et al., 2008
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 measuredIn 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).”
From Global habitat preferences of commercially valuable tuna (2015) · cites this paper as Boyce et al. (2008)
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 measuredThere 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).”
From Global habitat preferences of commercially valuable tuna (2015) · cites this paper as Boyce et al., 2008
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 measuredTemperature is a key factor in determining the distributions of adult tuna.
“Temperature is a key factor in determining the distributions of adult tuna (Worm et al. 2005, Boyce et al. 2008, Tittensor et al. 2010), as well as of larvae (present study).”
From Worldwide distributions of tuna larvae: revisiting hypotheses on environmental requirements for spawning habitats (2014) · cites this paper as Boyce et al. 2008
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.”
From Global habitat preferences of commercially valuable tuna (2015) · cites this paper as Boyce et al. (2008)
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
Each contradiction between two passages listed here was confirmed by an independent check.
Cumulative model peaks below its reported optimum
MajorThe stated cumulative polynomial reaches its maximum at approximately 21.6°C, not the reported ~22.5°C.
“Total species richness against water temperature was best approximated by a third-order polynomial regression model yielding a predicted peak in species richness at a water temperature of T optimum ≈ 22.5°C (r 2 = 0.978) (Fig. 2C).”
“(C) cumulative (all 18 species, all oceans): y = -0.0047x 3 + 0.1705x 2 -0.796x.”
Billfish model peaks below its reported optimum
MajorThe stated billfish polynomial reaches its maximum at approximately 22.6°C, not the reported ~24°C.
“predicted peak richness at a lower temperature (T optimum ) for Thunnus (~21°C, r 2 = 0.976) than for Istiophoridae and Xiphidae (~24°C, r 2 = 0.919).”
“Istiophoridae and Xiphidae: y = -0.0028x 3 + 0.114x 2 -0.8676x (blue)”
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Sharp, G. D. (1978) · The Physiological Ecology of Tunas · doi:10.1016/b978-0-12-639180-0.50032-x · Cited by 92 · see citing works
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Maguire, J.-J. (2006) · Medical Entomology and Zoology · Cited by 86 · see citing works
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Activity Patterns of Striped Marlin in the Southern California Bight
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Predator Diversity Hotspots in the Blue Ocean
Worm, B. (2005) · Helmholtz Centre for Ocean Research Kiel (GEOMAR) · Cited by 13 · see citing works
Self-citationCollins, A. G. (2000) · doi:10.1666/0094-8373(2000)026
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Seamounts are hotspots of pelagic biodiversity in the open ocean
Morato, T., Hoyle, S., Allain, V., & Nicol, S. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0910290107 · Cited by 410 · see citing works
“This methodology has been extensively used to compare the species richness obtained from longline fishing fleets (11, 14, 42).”
MethodGlobal habitat preferences of commercially valuable tuna
Arrizabalaga, H., Dufour, F., Kell, L., Merino, G., Ibaibarriaga, L., Chust, G., Irigoien, X., Santiago, J., Murua, H., Fraile, I., et al. (2015) · Deep Sea Research Part II: Topical Studies in Oceanography · doi:10.1016/j.dsr2.2014.07.001 · Cited by 194 · 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).”
BackgroundMethodResultInfluentialGlobal Diversity Hotspots and Conservation Priorities for Sharks
Lucifora, L. O., García, V. B., & Worm, B. (2011) · PLoS ONE · doi:10.1371/journal.pone.0019356 · Cited by 177 · see citing works
“In the Western Central Pacific, an equatorial center of diversity has been reported in the Philippines, although two secondary peaks of diversity off Taiwan and Eastern Australia, on the edges of the study area, were also detected [28], coinciding with the patterns found for tunas and billfishes [24–26].”
BackgroundSelf-citationRange 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
“This resulted in warmer average ocean conditions and changes in prey fields (29), which may have contributed to the observed range changes, particularly in warm-adapted species like skipjack tuna and sailfish (30).”
BackgroundSelf-citationGlobal latitudinal variations in marine copepod diversity and environmental factors
Rombouts, I., Beaugrand, G., Ibáñez, F., Gasparini, S., Chiba, S., & Legendre, L. (2009) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2009.0742 · Cited by 147 · see citing works
Marine Fisheries Management in a Changing Climate: A Review of Vulnerability and Future Options
Johnson, J. E., & Welch, D. (2009) · Reviews in Fisheries Science · doi:10.1080/10641260903434557 · Cited by 141 · see citing works
“Importantly, mobile species can shift their distributions and ranges in response to changes in temperature gradients and spatial patterns of plankton productivity (Soto, 2002; Sabates et al., 2006; Boyce et al., 2008; Munday et al., 2008).”
BackgroundPast and future decline of tropical pelagic biodiversity
Yasuhara, M., Wei, C., Kučera, M., et al. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1916923117 · Cited by 128 · see citing works
Self-citationMarine biodiversity and climate change
Worm, B., & Lotze, H. K. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-821575-3.00021-9 · Cited by 113 · see citing works
Self-citationReglero, P., Tittensor, D., Álvarez-Berastegui, D., Aparicio-González, A., & Worm, B. (2014) · Marine Ecology Progress Series · doi:10.3354/meps10666 · Cited by 106 · see citing works
Self-citationA cascade of warming impacts brings bluefin tuna to Greenland waters
MacKenzie, B. R., Payne, M., Boje, J., Høyer, J. L., & Siegstad, H. (2014) · Global Change Biology · doi:10.1111/gcb.12597 · Cited by 100 · see citing works
“…temperature for bluefin tuna habitat in the region, we are aware that the species does occasionally experience much colder temperatures (0–5 °C; Boyce et al., 2008; Fromentin et al., 2013) and can therefore tolerate such cold temperatures for at least short periods of time (e.g.…”
BackgroundMethodDiversity of deep‐water cetaceans in relation to temperature: implications for ocean warming
Whitehead, H., McGill, B. J., & Worm, B. (2008) · Ecology Letters · doi:10.1111/j.1461-0248.2008.01234.x · Cited by 93 · see citing works
“Individual species responses to temperature yield a pattern of biodiversity that changes dynamically with climatic fluctuations (Worm et al. 2005; Boyce et al. 2008 ).”
BackgroundSelf-citationEnsemble 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
Global Connectivity of Southern Ocean Ecosystems
Murphy, E. J., Johnston, N. M., Hofmann, E. E., Phillips, R. A., Jackson, J. A., Constable, A. J., Henley, S. F., Melbourne-Thomas, J., Trebilco, R., Cavanagh, R. D., et al. (2021) · Frontiers in Ecology and Evolution · doi:10.3389/fevo.2021.624451 · Cited by 93 · see citing works
Murua, H., Rodriguez-Marin, E., Neilson, J. D., Farley, J. H., & Juan-Jordá, M. J. (2017) · Reviews in Fish Biology and Fisheries · doi:10.1007/s11160-017-9474-1 · Cited by 89 · see citing works
“And why do the growth performance of yellowfin and skipjack tunas differ so much given they share similar habitats with similar water temperature preferences (between 18 and 26 C) (Boyce et al. 2008)?”
BackgroundReglero, P., Ciannelli, L., Alvarez-Berastegui, D., Balbín, R., López-Jurado, J., & Alemany, F. (2012) · Marine Ecology Progress Series · doi:10.3354/meps09800 · Cited by 89 · see citing works
“In general, tuna larvae have a narrower and warmer range of temperature preferences than the adults (Boyce et al. 2008), in turn suggesting that spawning habitats are more re stric ted than adult foraging grounds.”
BackgroundBottom-up drivers of global patterns of demersal, forage, and pelagic fishes
Petrik, C. M., Stock, C. A. A., Andersen, K. H., van Denderen, P. D., & Watson, J. R. (2019) · Progress In Oceanography · doi:10.1016/j.pocean.2019.102124 · Cited by 86 · see citing works
Woodworth‐Jefcoats, P. A., Polovina, J. J., & Drazen, J. C. (2016) · Global Change Biology · doi:10.1111/gcb.13471 · Cited by 80 · see citing works
Jiang, F., Zhang, J., Gao, H., Cai, Z., Zhou, X., Li, S., & Zhang, T. (2019) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2019.135335 · Cited by 74 · see citing works
Hill, N. J., Tobin, A. J., Reside, A. E., Pepperell, J. G., & Bridge, T. C. L. (2016) · Global Change Biology · doi:10.1111/gcb.13129 · Cited by 74 · see citing works
“Habitat suitability of mobile species is determined by a range of environmental (e.g. temperature; Boyce et al., 2008) and ecological parameters (e.”
BackgroundReview 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
“The available catch data indicates that a water temperature range of 14–21 C is preferred by albacore (Clemens 1961; Talbot and Penrith 1962; Flittner 1963; Laurs and Lynn 1977; Johnsson 1961 quoted by Penney et al. 1998; Santiago 2004; Boyce et al. 2008; Childers et al. 2011; Hu et al. 2011; IATTC 2013).”
BackgroundGlobal patterns in marine predatory fish
van Denderen, P. D., Lindegren, M., MacKenzie, B. R., Watson, R. A., & Andersen, K. H. (2017) · Nature Ecology & Evolution · doi:10.1038/s41559-017-0388-z · Cited by 67 · see citing works
Bioenergetics, Trophic Ecology, and Niche Separation of Tunas
(2016) · Advances in Marine Biology · doi:10.1016/bs.amb.2016.06.002 · Cited by 69 · see citing works
Sliding baselines and shuffling species: implications of climate change for marine conservation
Hobday, A. J. (2011) · Marine Ecology · doi:10.1111/j.1439-0485.2011.00459.x · Cited by 67 · see citing works
Dambacher, J. M., Young, J. W., Olson, R. J., Allain, V., Galván‐Magaña, F., Lansdell, M. J., Bocanegra-Castillo, N., Alatorre-Ramírez, V., Cooper, S. P., & Duffy, L. M. (2010) · Progress In Oceanography · doi:10.1016/j.pocean.2010.04.011 · Cited by 65 · see citing works
“One is through direct physiological responses of predators to increasing water temperature (Sharp and Dizon, 1978; Boyce et al., 2008).”
BackgroundLife in 3-D: life history strategies in tunas, mackerels and bonitos
Juan-Jordá, M. J., Mosqueira, I., Freire, J., & Dulvy, N. K. (2013) · Reviews in Fish Biology and Fisheries · doi:10.1007/s11160-012-9284-4 · Cited by 64 · see citing works
“maccoyii) which can tolerate a wide thermal range from feeding grounds in cold temperate waters to spawning grounds in warmer waters (Boyce et al. 2008).”
BackgroundAtlantic bluefin tuna spawn at suboptimal temperatures for their offspring
Reglero, P., Ortega, A., Balbín, R., Abascal, F. J., Medina, A., Blanco, E., de-la-Gándara, F., Álvarez‐Berastegui, D., Hidalgo, M., Rasmuson, L. K., et al. (2018) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2017.1405 · Cited by 67 · see citing works
Lucifora, L. O., García, V. B., Menni, R. C., & Worm, B. (2011) · Biodiversity and Conservation · doi:10.1007/s10531-011-0189-7 · Cited by 59 · see citing works
Self-citationBycatch mitigation of protected and threatened species in tuna purse seine and longline fisheries
Swimmer, Y., Zollett, E. A., & Gutierrez, A. (2020) · Endangered Species Research · doi:10.3354/esr01069 · Cited by 59 · see citing works
Muhling, B., Liu, Y.-Y., Lee, S.-K., Lamkin, J., Roffer, M., Muller-Karger, F., & Walter, J. F. (2015) · Journal of Marine Systems · doi:10.1016/j.jmarsys.2015.01.010 · Cited by 57 · see citing works
“Lastly, the body size of many tunas and billfishes determines their thermal tolerances, with smaller fish generally more tolerant of warm waters, and less tolerant of cold (Barkley et al., 1978; Boyce et al., 2008; Brill, 1994).”
BackgroundTrebilco, R., Halpern, B. S., Flemming, J. M., Field, C., Blanchard, W., & Worm, B. (2011) · Biological Conservation · doi:10.1016/j.biocon.2011.02.024 · Cited by 56 · see citing works
“Both fishing and SST have well-known impacts on pelagic biodiversity, and are considered the two major drivers (Boyce et al., 2008; Lehodey et al., 2003; Sund et al., 1981).”
BackgroundSelf-citationArmel, B. Y. D., Dagorn, L., Amandè, M. J., et al. (2020) · Fisheries Research · doi:10.1016/j.fishres.2020.105613 · Cited by 52 · see citing works
“Water temperature, for example, is known to have an effect on both the acoustic signal (Bamber and Hill, 1979; Straube and Arthur, 1994) and the abundance of tuna (Boyce et al., 2008).”
BackgroundSu, N.-J., Sun, C.-L., Punt, A., Yeh, S.-Z., & Dinardo, G. (2011) · ICES Journal of Marine Science · doi:10.1093/icesjms/fsr028 · Cited by 53 · see citing works
“variables have been hypothesized to affect the density and distribution of blue marlin, such as water temperature, ocean fronts, current speed, oxygen content, prey availability, and zooplankton abundance (Boyce et al., 2008).”
BackgroundInfluentialRelative Impacts of Simultaneous Stressors on a Pelagic Marine Ecosystem
Woodworth‐Jefcoats, P. A., Blanchard, J. L., & Drazen, J. C. (2019) · Frontiers in Marine Science · doi:10.3389/fmars.2019.00383 · Cited by 48 · see citing works
Cannibalism among size classes of larvae may be a substantial mortality component in tuna
Reglero, P., Urtizberea, A., Torres, A., Alemany, F., & Fiksen, Ÿ. (2011) · Marine Ecology Progress Series · doi:10.3354/meps09187 · Cited by 47 · see citing works
“The spawning strategy of tuna includes long distance migration to spawn in warm waters of low productivity (Graham & Dickson 2004, Boyce et al. 2008) but high larval abundances of several species of tuna.”
BackgroundDELL, J., WILCOX, C., & HOBDAY, A. J. (2011) · Fisheries Oceanography · doi:10.1111/j.1365-2419.2011.00591.x · Cited by 46 · see citing works
Marine Biodiversity and Climate Change
Worm, B., & Lotze, H. K. (2015) · Elsevier eBooks · doi:10.1016/b978-0-444-63524-2.00013-0 · Cited by 45 · see citing works
Self-citationTowards a Fishing Pressure Prediction System for a Western Pacific EEZ
Cimino, M. A., Anderson, M., Schramek, T., Merrifield, S. T., & Terrill, E. (2019) · Scientific Reports · doi:10.1038/s41598-018-36915-x · Cited by 41 · see citing works
Habitat and food partitioning of billfishes (Xiphioidei)
Shimose, T., Yokawa, K., & Saito, H. (2010) · Journal of Fish Biology · doi:10.1111/j.1095-8649.2010.02628.x · Cited by 38 · see citing works
“And temperature recorded in the present study (24·9–30·1◦ C) is higher than the known mean temperature tolerance of K. audax 16·82–25·49◦ C (Boyce et al., 2008).”
BackgroundInfluentialPhillips, A. J., Ciannelli, L., Brodeur, R. D., Pearcy, W. G., & Childers, J. (2014) · ICES Journal of Marine Science · doi:10.1093/icesjms/fst238 · Cited by 36 · see citing works
“28C (Boyce et al., 2008), juveniles are known to have specific sea surface temperature (SST) preferences ranging from 15–19.”
BackgroundDiversity and distribution of hyperiid amphipods along a latitudinal transect in the Atlantic Ocean
Burridge, A. K., Tump, M., Vonk, R., et al. (2016) · Progress In Oceanography · doi:10.1016/j.pocean.2016.08.003 · Cited by 34 · see citing works
Key climate change stressors of marine ecosystems along the path of the East African coastal current
Jacobs, Z., Yool, A., Jebri, F., Srokosz, M. A., van Gennip, S. J., Kelly, S., Roberts, M. J., Sauer, W., Queirós, A. M., Osuka, K. E., et al. (2021) · Ocean & Coastal Management · doi:10.1016/j.ocecoaman.2021.105627 · Cited by 36 · see citing works
“The upper estimated thermal tolerances of skipjack tuna and kawakawa (Euthynnus affinis) are 30 ◦C and 30.5 ◦C, respectively (Lehodey et al., 2011; Boyce et al., 2008).”
BackgroundInfluentialA shallow scattering layer structures the energy seascape of an open ocean predator
Arostegui, M. C., Muhling, B. A., Culhane, E., et al. (2023) · Science Advances · doi:10.1126/sciadv.adi8200 · Cited by 30 · see citing works
Bio-telemetry as an Essential Tool in Movement Ecology and Marine Conservation
Heylen, B. C., & Nachtsheim, D. A. (2018) · Springer eBooks · doi:10.1007/978-3-319-93284-2_7 · Cited by 29 · see citing works
Lan, K., Chang, Y., & Wu, Y. (2019) · Deep Sea Research Part II Topical Studies in Oceanography · doi:10.1016/j.dsr2.2019.104681 · Cited by 28 · see citing works
Khan, A. M. A., Nasution, A. M., Purba, N. P., Rizal, A., Zahidah, Hamdani, H., Dewanti, L. P., Junianto, Nurruhwati, I., Sahidin, A., et al. (2020) · Fisheries Research · doi:10.1016/j.fishres.2019.105471 · Cited by 21 · see citing works
Interactions Between a Large Marine Protected Area, Pelagic Tuna and Associated Fisheries
Curnick, D. J., Collen, B., Koldewey, H. J., Jones, K. E., Kemp, K. M., & Ferretti, F. (2020) · Frontiers in Marine Science · doi:10.3389/fmars.2020.00318 · Cited by 30 · see citing works
Jansen, T., Nielsen, E., Rodríguez-Ezpeleta, N., Arrizabalaga, H., Post, S., & MacKenzie, B. (2020) · Canadian Journal of Fisheries and Aquatic Sciences · doi:10.1139/cjfas-2020-0156 · Cited by 22 · see citing works
“The map was created in R using the package ‘lattice’ v.0.20-41 (Deepayan, 2008) and ‘maps’ 487 v.3.3.0 (Brownrigg et al., 2018).”
MethodInfluentialWatai, M., Hiraoka, Y., Ishihara, T., et al. (2018) · Marine Ecology Progress Series · doi:10.3354/meps12807 · Cited by 26 · see citing works
Shimose, T., Yokawa, K., Saito, H., & Tachihara, K. (2012) · Bulletin of Marine Science · doi:10.5343/bms.2011.1025 · Cited by 29 · see citing works
Impacts of Climate Change on Pelagic Fish and Fisheries
Muhling, B. A., Lindegren, M., Clausen, L. W., Hobday, A. J., & Lehodey, P. (2017) · Wiley eBooks · doi:10.1002/9781119154051.ch23 · Cited by 25 · see citing works
Reglero, P., Blanco, E., Alemany, F., Ferrà, C., Álvarez‐Berastegui, D., Ortega, A., de-la-Gándara, F., Aparicio‐González, A., & Folkvord, A. (2018) · Marine Ecology Progress Series · doi:10.3354/meps12516 · Cited by 24 · see citing works
Machine-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
Marine copepod diversity patterns and the metabolic theory of ecology
Rombouts, I., Beaugrand, G., Ibáñez, F., et al. (2010) · Oecologia · doi:10.1007/s00442-010-1866-z · Cited by 21 · see citing works
“In the marine environment, the influence of temperature on broad-scale distributions of foraminifers (Rutherford et al. 1999), copepods (Rombouts et al. 2009; Beaugrand et al. 2010) and fish (Boyce et al. 2008; Hiddink and ter Hofstede 2008) is well documented.”
Kim, Y., Delgado, D., Cano, I. A., & Sawada, Y. (2015) · Fisheries Science · doi:10.1007/s12562-015-0901-8 · Cited by 19 · see citing works
Operationalizing climate risk in a global warming hotspot
Boyce, D., Tittensor, D., Fuller, S., Henson, S., Kaschner, K., Reygondeau, G., Schleit, K., Saba, V., Shackell, N., Stanley, R., et al. (2022) · bioRxiv · doi:10.1038/s44183-024-00067-5 · Cited by 17 · see citing works
“However, mammals and endo-thermic fi shes (e.g. tunas, bill fi shes) that can sometimes inhabit depths over 1000 m were not excluded; despite their ability to range into deeper waters, their distribution is often well explained by surface temperatures 111,112 .”
Self-citationThoya, P. Z., Kadagi, N. I., Wambiji, N., Williams, S. M., Pepperell, J. G., Möllmann, C., Schiele, K. S., & Maina, J. M. (2022) · Diversity and Distributions · doi:10.1111/ddi.13525 · Cited by 21 · see citing works
Lin, C., Wei, C., Ho, S. L., & Lo, L. (2023) · Science Advances · doi:10.1126/sciadv.adf0656 · Cited by 20 · see citing works
Nikolic, N., Montes, I., Lalire, M., Puech, A., Bodin, N., Arnaud‐Haond, S., Kerwath, S., Corse, E., Gaspar, P., Hollanda, S. J., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-72369-w · Cited by 20 · see citing works
Vanderlaan, A. S. M., Hanke, A. R., Chassé, J., & Neilson, J. D. (2013) · Fisheries Oceanography · doi:10.1111/fog.12049 · Cited by 19 · see citing works
Seasonal changes in fish assemblage structure at a shallow seamount in the Gulf of California
Jorgensen, S. J., Klimley, A. P., Muhlia‐Melo, A., & Morgan, S. G. (2016) · PeerJ · doi:10.7717/peerj.2357 · Cited by 19 · see citing works
Diversity of deep-water cetaceans and primary productivity
Whitehead, H., O’Brien, K., & Worm, B. (2010) · Marine Ecology Progress Series · doi:10.3354/meps08619 · Cited by 19 · see citing works
“…this physiologically based relationship between cetacean diversity and SST may be reinforced by similarly structured diversity patterns in prey species, including zooplankton (Rutherford et al. 1999, Beaugrand et al. 2002) and fish (Worm et al. 2005, Boyce et al. 2008, Hiddink & ter Hofstede 2008).”
BackgroundSelf-citationOrtega‐García, S., Camacho-Bareño, E., & Martínez‐Rincón, R. O. (2014) · Fisheries Research · doi:10.1016/j.fishres.2014.09.007 · Cited by 18 · see citing works
Changes in Marine Biodiversity as an Indicator of Climate Change
Worm, B., & Lotze, H. (2009) · Elsevier eBooks · doi:10.1016/b978-0-444-53301-2.00014-2 · Cited by 18 · see citing works
Self-citationThe universal evolutionary and ecological significance of 20 oC
Costello, M. J., Corkrey, R., Bates, A. E., Burrows, M. T., Chaudhary, C., Edgar, G. J., Stuart‐Smith, R. D., Yasuhara, M., & Wei, C. (2023) · Frontiers of Biogeography · doi:10.21425/f5fbg61673 · Cited by 17 · see citing works
Farchadi, N., Hinton, M., Thompson, A., & Yin, Z. (2019) · Marine Ecology Progress Series · doi:10.3354/meps12996 · Cited by 14 · see citing works
“…species primarily inhabit oceanic waters of the Pacific Ocean, where sea surface temperatures (SSTs) are between 24 and 30°C (Graves et al. 2002, Boyce et al. 2008, Su et al. 2008, Chiang et al. 2015, Carlisle et al. 2017), chlorophyll a (chl a) concentrations are <1 mg m−3 (Su et al. 2008),…”
BackgroundNeogene Bony Fishes from the Bahía Inglesa Formation, Northern Chile
Oyanadel-Urbina, P., Gracia, C. D., Carrillo-Briceño, J. D., et al. (2021) · Ameghiniana · doi:10.5710/amgh.26.05.2021.3375 · Cited by 16 · see citing works
Martínez-Rincón, R., Ortega-García, S., Vaca-Rodríguez, J. G., & Griffiths, S. (2015) · Marine and Freshwater Research · doi:10.1071/mf14062 · Cited by 16 · see citing works
A hypothesis of a redistribution of North Atlantic swordfish based on changing ocean conditions
Schirripa, M. J., Abascal, F. J., Andrushchenko, I., et al. (2016) · Deep Sea Research Part II Topical Studies in Oceanography · doi:10.1016/j.dsr2.2016.08.002 · Cited by 15 · see citing works
“If the areas of the CPUE analysis are colored according to the sign of the β parameter they follow very closely the stock boundaries suggested by genetic mapping (Bremer et al., 2005), as well as those from tagging (Neilson et al., 2014).”
MethodLong-term monitoring dataset of fish assemblages impinged at nuclear power plants in northern Taiwan
Chen, H., Liao, Y.-C., Chen, C., et al. (2015) · Scientific Data · doi:10.1038/sdata.2015.71 · Cited by 15 · see citing works
Dell’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
Arostegui, M. C., Braun, C. D., & Gaube, P. (2018) · Fisheries Oceanography · doi:10.1111/fog.12413 · Cited by 14 · see citing works
Reglero, P., Balbín, R., Ortega, A., Álvarez‐Berastegui, D., Gordoa, A., Torres, A. P., Moltó, V., Pascual, A., de-la-Gándara, F., & Alemany, F. (2013) · Scientia Marina · doi:10.3989/scimar.03759.28a · Cited by 13 · see citing works
“Salinity, temperature and dynamic height distributions were interpolated onto a uniform grid of 4 nmi x 4 nmi by using minimum error variance methods (Bretherton et al. 1976) with a correlation length of 18 nmi and a maximum allowed rms error for the interpolated field of 20%.”
MethodArostegui, M. C., Gaube, P., & Braun, C. D. (2019) · Fisheries Research · doi:10.1016/j.fishres.2019.03.005 · 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
García, C. B., & Posada, C. (2017) · Latin American Journal of Aquatic Research · doi:10.3856/vol41-issue3-fulltext-21 · Cited by 12 · see citing works
Gracia, C. D., Villalobos‐Segura, E., Ballen, G. A., Carnevale, G., & Kriwet, J. (2024) · Papers in Palaeontology · doi:10.1002/spp2.1559 · Cited by 10 · see citing works
Su, N., Sun, C., Punt, A. E., Yeh, S., DiNardo, G. T., & Chang, Y. (2013) · ICES Journal of Marine Science · doi:10.1093/icesjms/fss191 · Cited by 11 · see citing works
“In previous research, preferred thermal ranges for fish species were mostly chosen subjectively using published data because there were no clear guidelines to define them (e.g. Boyce et al., 2008).”
MethodHobday, A. J., Griffiths, S. P., & Ward, T. (2012) · Cited by 10 · see citing works
Putri, A. R. S., Zainuddin, M., Musbir, M., Hidayat, R., & Mustapha, M. A. (2021) · Biodiversitas Journal of Biological Diversity · doi:10.13057/biodiv/d220758 · Cited by 9 · see citing works
“Indeed, several studies in tropical waters have also found that skipjack tuna is caught in the same range as this study, such as a study conducted in Indonesian waters with an SST range of 29.5-31.5 °C (Zainuddin et al. 2017) and 30-32 °C (Boyce et al. 2008).”
BackgroundInfluentialHatzonikolakis, Y., Tsiaras, K. P., Tserpes, G., Somarakis, S., John, M. S., Peristeraki, P. N., Raitsos, D. Ε., & Triantafyllou, G. (2021) · Marine Ecology Progress Series · doi:10.3354/meps13861 · Cited by 10 · see citing works
Life history of marine fishes and their implications for the future oceans
Petrik, C. M. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-817945-1.00016-2 · Cited by 9 · see citing works
Species diversity of pelagic chaetognaths in the Indo-Pacific region
Miyamoto, H., Kotori, M., Itoh, H., et al. (2014) · Journal of Plankton Research · doi:10.1093/plankt/fbu001 · Cited by 9 · see citing works
Global pattern of phylogenetic species composition of shark and its conservation priority
Chen, H., & Kishino, H. (2015) · Ecology and Evolution · doi:10.1002/ece3.1724 · Cited by 9 · see citing works
“The diversity of tuna and billfish consistently peaked at intermediate latitudes (10 – 35 ° ), which is similar to other pelagic taxa (Boyce et al. 2008).”
Varela, J., Santos, C. P., Nunes, E., Pissarra, V., Pires, S., Ribeiro, B. P., Vieira, E. M. A., Repolho, T., Queiroz, N. C., Freitas, R., et al. (2025) · Frontiers in Marine Science · doi:10.3389/fmars.2025.1490317 · Cited by 8 · see citing works
Alemany, D., Rico, M. R., Lagos, Á. N., Martos, P., Mendiolar, M., & Carozza, C. (2021) · Marine and Fishery Sciences (MAFIS) · doi:10.47193/mafis.3422021010602 · Cited by 9 · see citing works
“…la biodiversidad marina ha sido correlacionada positivamente con sistemas de alta productividad como los frentes (Worm et al. 2005; Rosa et al. 2008), así como también con la producción primaria (Boyce et al. 2010) y con la temperatura superficial del mar (Worm et al. 2005; Boyce et al. 2008).”
BackgroundVieira, J. M. S., Costa, P. A. S., Braga, A. C., Clemente, S. C. D. S., Ferreira, C. E. L., & da Silva, J. P. (2021) · Latin American Journal of Aquatic Research · doi:10.3856/vol49-issue5-fulltext-2689 · Cited by 8 · see citing works
“bigeye and the yellowfin tuna can be found in water temperatures ranging between 3 and 31°C (Boyce et al. 2008).”
BackgroundInfluentialIndustrial fisheries have reversed the carbon sequestration by tuna carcasses into emissions
Mouillot, D., Derminon, S., Mariani, G., Senina, I. N., Fromentin, J., Lehodey, P., & Troussellier, M. (2023) · Global Change Biology · doi:10.1111/gcb.16823 · Cited by 8 · see citing works
Vaske‐Júnior, T., Travassos, P., Pinheiro, P. B., et al. (2011) · Brazilian Journal of Aquatic Science and Technology · doi:10.14210/bjast.v15n1.p65-70 · Cited by 8 · see citing works
Florida’s Oceans and Marine Habitats in a Changing Climate
Morey, S. L., Koch, M. S., Liu, Y., & Lee, S. (2017) · Florida Climate Institute eBooks · doi:10.17125/fci2017.ch13 · Cited by 8 · see citing works
“2015) into the Gulf of Mexico as temperate waters warm to 30-32 oC (>16 oC), temperature ranges where they are currently found (Boyce et al. 2008).”
BackgroundMatsubara, N., Aoki, Y., Aoki, A., et al. (2024) · Frontiers in Marine Science · doi:10.3389/fmars.2024.1353918 · Cited by 7 · see citing works
Setiawati, M. D., Rachman, H. A., As-syakur, A. R., Setiawan, R., Syahailatua, A., & Wouthuyzen, S. (2024) · Deep-sea research. Part II, Topical studies in oceanography · doi:10.1016/j.dsr2.2024.105400 · Cited by 7 · see citing works
An Exploratory Analysis to Identify Reproductive Strategies of Billfishes
Salcedo-Bo, S., & Arreguı́n-Sánchez, F. (2011) · Journal of Fisheries and Aquatic Science · doi:10.3923/jfas.2011.578.591 · Cited by 7 · see citing works
Impacts of central-Pacific El Niño and physical drivers on eastern Pacific bigeye tuna
Lian, P., & Gao, L. (2024) · Journal of Oceanology and Limnology · doi:10.1007/s00343-023-3051-3 · Cited by 5 · see citing works
“However, with the development of fishing technologies, many stocks, e.g., BET and other important tuna species, face overfishing status, particularly tuna fisheries (Block et al., 1998; Boyce et al., 2008; Harrison et al., 2017; Xu et al., 2019; Kim et al., 2020).”
Farchadi, N., Hinton, M., Thompson, A., & Yin, Z. (2018) · doi:10.22371/02.2018.016 · Cited by 4 · see citing works
“…factors, studies have suggested that sea surface temperature has the most influence on the spatial distribution of both species in the Pacific Ocean (Holland et al. 1990, Graves et al. 2002, Prince and Goodyear 2006, Boyce et al. 2008, Su et al. 2008, Chiang et al. 2015, Carlisle et al. 2017).”
BackgroundResultThe Future of Marine Animal Populations
Worm, B., Lotze, H. K., Jonsen, I. D., et al. (2010) · doi:10.1002/9781444325508.ch16 · Cited by 5 · see citing works
Self-citationWilliams, C. T., Arostegui, M. C., Braun, C. D., et al. (2022) · Journal of the Marine Biological Association of the United Kingdom · doi:10.1017/s0025315422000820 · Cited by 4 · see citing works
“audax (21–24°C; Boyce et al., 2008); in the central and southern portions of the basin, the mean sea surface temperature does not decrease below 28 and 29°C, respectively, except in winter (Shaltout, 2019).”
BackgroundMalara, D., Battaglia, P., Arostegui, M. C., et al. (2024) · Frontiers in Marine Science · doi:10.3389/fmars.2024.1362169 · Cited by 4 · see citing works
Marine Climate Change in Australia
Chambers, L. E., Dann, P., Devney, C. A., Dunlop, N., & Woehler, E. J. (2012) · Cited by 4 · see citing works
Marín‐Enríquez, E., & Muhlia‐Melo, A. (2018) · Ciencias Marinas · doi:10.7773/cm.v44i1.2727 · Cited by 4 · see citing works
- Authors
- Boyce, D., Tittensor, D., & Worm, B.
- Venue
- Marine Ecology Progress Series
- Publisher
- Inter-Research Science Center
- Published
- 2008-02-26
- Volume
- 355
- Pages
- 267-276
- ISSN
- 0171-8630 (ISSN-L)
- 1616-1599
- OpenAlex
- W2139585483
- Semantic Scholar
- 4c1b29b2614cfd624d64adbf059bc75f329e09bb
- Cited by
- 139
- References
- 39
- Citations by year
- 2026: 8 · 2025: 8 · 2024: 10 · 2023: 7 · 2022: 4 · 2021: 10 · 2020: 9 · 2019: 11 · 2018: 9 · 2017: 7 · 2016: 8 · 2015: 7 · 2014: 6 · 2013: 4 · 2012: 8
- FWCI
- 6.78
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Marine Ecology Progress Series (publishedVersion)
- Funders
- Alfred P. Sloan Foundation
- National Oceanic and Atmospheric Administration
- 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, billfish, species richness, water temperature, heat tolerance, thermal preference, latitudinal diversity gradient, species distribution, pelagic fish, longline survey, global biodiversity patterns
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.
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