Worldwide distributions of tuna larvae: revisiting hypotheses on environmental requirements for spawning habitats
Open accessAbstract
Tuna are among the most ubiquitous oceanic predators, and range globally from the equator to temperate regions (0 to 55° latitude).While the distribution of adult fish has been mapped from fishing records, the extent of tuna spawning and larval habitats is less well understood.We compiled and analyzed data on the global distributions of larval occurrence for 7 major oceanic tuna species to investigate environmental predictors of larval habitat.Our results showed that tuna larvae occur within the adults' distributional range, but were restricted to lower latitudes and higher water temperatures than adults, largely consistent with Schaefer's 'temperature hypothesis'.Temperature requirements explained much of the variation in larval occurrence, though temperature by itself tended to over-predict the extent of larval habitats.We also demonstrate that tuna larvae have an elevated probability of occurrence at intermediate values of eddy kinetic energy, generally supporting Bakun's 'ocean triad hypothesis', which relates tuna larval habitats to mesoscale oceanographic activity.However, some deviations in this pattern were also observed, such as for albacore.Regions of suitable larval habitats were most commonly found in western boundary currents, where warm water masses coincide with intermediate eddy kinetic energy.Bluefin tuna species are exceptional though, in that their spawning habitats tended to be much more confined than predicted from oceanographic conditions.Our results provide support for a combination of the 2 hypotheses to explain global environmental requirements for tuna larvae.We have identified oceanographic parameters that can easily be measured by remote sensing and features that should be considered when determining areas of critical habitat for tuna larvae.
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Written from the paper’s full text.
TL;DR
This study compiled global larval occurrence records for 7 tuna species and modeled presence/absence against sea-surface temperature (SST) and eddy kinetic energy (EKE). It found support for a combination of the temperature and ocean triad hypotheses, with larvae restricted to warmer, lower-latitude waters than adults and generally peaking at intermediate EKE, except for bluefin tunas and albacore.
Key findings
- Tuna larvae occupied a much narrower range than adults: generally 30°S–30°N, except Mediterranean larvae above 35°N, whereas adults ranged from 60°S to 60°N. Larvae preferred warmer waters, with maximum temperature tolerances ≥28.5°C for all species; minima were <22°C for skipjack, yellowfin, albacore, bigeye and Pacific bluefin, but >24°C for Atlantic and southern bluefin. Maximum larval occurrence probabilities were mostly at SSTs of 27.4–27.8°C, except Atlantic bluefin (26.5°C) and Pacific bluefin (25.3°C).
- Temperature was positively related to larval occurrence in all species analyzed, with a lower tolerance around 20°C, lower than Schaefer’s 24°C spawning boundary; however, temperature alone over-predicted plausible larval habitats for all species, especially bluefin tunas.
- EKE effects varied: skipjack, yellowfin and bigeye larvae had highest occurrence at intermediate EKE of 0.01–0.06 m² s⁻²; Atlantic bluefin showed a linear positive relationship; albacore showed a negative linear relationship; southern bluefin EKE was not significant. Model deviance explained was 39.6% for skipjack, 38.9% for yellowfin, 32% for bigeye and 29.3% for albacore.
- Suitable larval habitats were most common in western boundary currents where warm water masses coincide with intermediate EKE; bluefin tuna spawning habitats were much more spatially confined than predicted from oceanographic conditions.
Methods
- The authors reviewed scientific and grey literature on tuna larval surveys, retaining 150 articles, of which 92 reported georeferenced tuna larval catches. They mapped presence/absence for 7 oceanic tuna species in 1678 5° × 5° grid cells between 70°S and 70°N, excluding land; absence data came from geo-referenced absences in targeted cruises and historical ichthyoplankton surveys.
- Seasonal SST from satellite remote sensing and EKE calculated from satellite-altimetry-derived geostrophic velocity components were averaged to 5° cells. Larval presence/absence was modeled with binomial generalized additive models (GAMs) using smoothing splines for SST and EKE, with an area term added for wide-ranging species; stepwise backwards selection chose best models.
- Larval temperature tolerances were estimated from probability density histograms of observed occurrences by SST; adult temperature tolerances were taken from Boyce et al. (2008). Adult ranges for comparison came from Worm & Tittensor (2011).
Limitations
- Stated in the paper: the combined database had good spatial coverage but individual surveys were spatially and temporally fragmented, not internationally coordinated, and often covered only restricted areas within main spawning grounds; presence-absence data provide occurrence but not relative abundance or density; larval species identification from morphology can be problematic, especially in the Gulf of Mexico; sampling years ranged from the 1920s to the 2000s; EKE values were missing for the Mediterranean, so no predictions were obtained there; bigeye tuna data are few and interpretations should be cautious.
- Evident from the text: the GAMs are correlative and cannot establish the mechanisms linking SST/EKE to larval survival; EKE is used as a proxy for mesoscale activity and frontal density; the 5° grid may miss smaller-scale or topographically induced mesoscale structures in confined seas; adult range comparisons rely on contemporary ranges from Worm & Tittensor (2011), which may not match the temporal coverage of larval surveys.
Model-written summary. Check it against the paper before relying on it.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
13 of 56 cited sources checked · 6 supported · 0 flagged · accuracy not yet measured
- Interpretationown data
The results support the ocean triad hypothesis.
“This supports the ocean triad hypothesis (Bakun 2006).”
Quote in the paperSubstantial claim1 of 1 sources checked- cites Bakun 2006 source
- Rests on an assumption: Seasonal SST and EKE averaged over 5° × 5° grid cells represent the environmental conditions relevant to tuna larval occurrence.
- Rests on an assumption: Larval presence/absence records compiled from different years and sources are comparable enough to model global environmental relationships.
- Rests on an assumption: Species-level morphological identifications in the source articles are accurate enough for the analyses.
- Premisecitation
Growth rates of tuna increase with temperature.
“Regarding favorable temperatures for growth, the compilation of data from different tuna species suggests increasing growth rates with temperature (Reglero et al. 2011), but further studies are needed at the species level.”
Quote in the paperSubstantial claim1 of 1 sources checked- cites Reglero et al. 2011 source
The “Maximum specific growth rate” section reports that specific growth rates of Pacific bluefin tuna larvae increased with temperature, and the “Mortality effect of size-surfing cannibalism” section likewise describes faster larval growth in warmer water. The cited paper supports the temperature–growth relationship for larvae, but the cited passage does not establish it from a compilation of growth data across different tuna species. (LLM, conf=0.82)
Experimental — accuracy not yet measured
- Study design and conductcitation
Surveys often covered restricted areas within the limits of the main spawning areas, a common issue in icthyoplankton surveys.
“Surveys often covered restricted areas within the limits of the main spawning areas, a common issue in icthyoplankton surveys (Bernal et al. 2007).”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites Bernal et al. 2007 source
- Findingcitation
Physiological temperature limits for gonad development and egg development obtained from experiments matched the spatially observed larval temperature tolerance limits well.
“Physiological temperature limits for biological processes such as gonad development and egg development obtained from experiments (Sawada et al. 2005, Margulies et al. 2007, Masuma et al. 2008) matched the spatially observed larval temperature tolerance limits well.”
Quote in the paperSubstantial claim1 of 3 sources checked- cites Sawada et al. 2005 source
The spawning and rearing sections report temperatures at which Pacific bluefin tuna spawned and larvae were raised in captivity. They do not establish physiological temperature limits for gonad or egg development, or compare those temperatures with spatially observed larval tolerance limits. The indexed passages provide section labels but no specific page numbers. (LLM, conf=0.82)
Experimental — accuracy not yet measured - cites Margulies et al. 2007
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites Masuma et al. 2008 source
- Premisecitation
Temperature 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).”
Quote in the paperSubstantial claim1 of 3 sources checked
- Premisecitation
The loophole hypothesis has been partially tested for bluefin tuna in the Balearic Sea.
“The loophole hypothesis has been partially tested for bluefin tuna in the Balearic Sea (Reglero et al. 2011), but needs to be tested for other species and locations in the future.”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites Reglero et al. 2011 source
- Findingown data
Southern bluefin tuna larvae were found only in the tropical East Indian Ocean.
“Southern bluefin tuna larvae were found only in the tropical East Indian Ocean (Fig. 2c).”
Quote in the paperNot a substantial claim - Findingown data
There was a significant positive effect of temperature in all of the species analyzed.
“We found a significant positive effect of temperature in all of the species analyzed.”
Quote in the paperSubstantial claim- Rests on an assumption: Seasonal SST and EKE averaged over 5° × 5° grid cells represent the environmental conditions relevant to tuna larval occurrence.
- Rests on an assumption: Larval presence/absence records compiled from different years and sources are comparable enough to model global environmental relationships.
- Rests on an assumption: Species-level morphological identifications in the source articles are accurate enough for the analyses.
- Findingnone given
Atlantic bluefin tuna, skipjack tuna and yellowfin tuna had slightly higher upper tolerance limits for adults than for larvae.
“Atlantic bluefin tuna, skipjack tuna and yellow fin tuna had slightly higher upper tolerance limits for adults than for larvae.”
Quote in the paperNot a substantial claim- Rests on an assumption: Species-level morphological identifications in the source articles are accurate enough for the analyses.
- Findingown data
Atlantic bluefin tuna larvae were found only in semi-enclosed seas: the Mediterranean Sea and the Gulf of Mexico.
“The Atlantic bluefin tuna larvae were found only in semi-enclosed seas: the Mediterranean Sea and the Gulf of Mexico (Fig. 2a).”
Quote in the paperSubstantial claim - Findingown data
The predictive power of the model was insufficient to separate the observed spatial patterns for each bluefin tuna species.
“Therefore, the predictive power of the model was insufficient to separate the observed spatial patterns for each bluefin tuna species (Table 1), but suggested that specific areas of predominance for the 3 species share common characteristics in terms of SST and EKE (Fig. 6a-c).”
Quote in the paperSubstantial claim- Rests on an assumption: Seasonal SST and EKE averaged over 5° × 5° grid cells represent the environmental conditions relevant to tuna larval occurrence.
- Rests on an assumption: Larval presence/absence records compiled from different years and sources are comparable enough to model global environmental relationships.
- Rests on an assumption: Species-level morphological identifications in the source articles are accurate enough for the analyses.
- Findingown data
The probability of larval occurrence was positively related to temperature, with larvae having a higher probability of occurrence when temperatures were >20°C in skipjack, yellowfin, albacore and bigeye tuna.
“The probability of larval occurrence was positively related to temperature, with larvae having a higher probability of occurrence when temperatures were > 20°C in the 4 species (Fig. 5a-d).”
Quote in the paperSubstantial claim- Rests on an assumption: Seasonal SST and EKE averaged over 5° × 5° grid cells represent the environmental conditions relevant to tuna larval occurrence.
- Rests on an assumption: Larval presence/absence records compiled from different years and sources are comparable enough to model global environmental relationships.
- Rests on an assumption: Species-level morphological identifications in the source articles are accurate enough for the analyses.
- Findingown data
The model fit including both variables, SST and EKE, was significant for skipjack, yellowfin, albacore and bigeye tuna.
“The model fit including both variables, SST and EKE, was significant for skipjack, yellowfin, albacore and bigeye tuna (Table 2).”
Quote in the paperSubstantial claim- Rests on an assumption: Seasonal SST and EKE averaged over 5° × 5° grid cells represent the environmental conditions relevant to tuna larval occurrence.
- Rests on an assumption: Larval presence/absence records compiled from different years and sources are comparable enough to model global environmental relationships.
- Rests on an assumption: Species-level morphological identifications in the source articles are accurate enough for the analyses.
- Findingreasoning
Plausible larval habitats for Pacific and southern bluefin tuna were over-predicted in the eastern Indian Sea and some equatorial areas.
“Plausible larval habitats for Pacific and southern bluefin tuna were over-predicted in the eastern Indian Sea and some equatorial areas which probably show similar characteristics to the more confined regions.”
Quote in the paperSubstantial claim- Rests on an assumption: Seasonal SST and EKE averaged over 5° × 5° grid cells represent the environmental conditions relevant to tuna larval occurrence.
- Rests on an assumption: Larval presence/absence records compiled from different years and sources are comparable enough to model global environmental relationships.
- Rests on an assumption: Species-level morphological identifications in the source articles are accurate enough for the analyses.
- Findingown data
Larval occurrences increased with EKE, plateauing around intermediate values of 0.01 to 0.06 m2 s-2, then decreasing slightly for skipjack, yellowfin and bigeye tuna.
“Larval occurrences increased with EKE, plateauing around intermediate values of 0.01 to 0.06 m 2 s -2 , then decreasing slightly for skipjack (Fig. 5e), yellowfin (Fig. 5f) and bigeye (Fig. 5g).”
Quote in the paperSubstantial claim- Rests on an assumption: Seasonal SST and EKE averaged over 5° × 5° grid cells represent the environmental conditions relevant to tuna larval occurrence.
- Rests on an assumption: Larval presence/absence records compiled from different years and sources are comparable enough to model global environmental relationships.
- Rests on an assumption: Species-level morphological identifications in the source articles are accurate enough for the analyses.
- Findingown data
The model predicted very low larval occurrences for the 3 bluefin tunas in all areas.
“The model predicted very low larval occurrences for the 3 bluefin tunas in all areas (Fig. 6a-c).”
Quote in the paperNot a substantial claim- Rests on an assumption: Seasonal SST and EKE averaged over 5° × 5° grid cells represent the environmental conditions relevant to tuna larval occurrence.
- Rests on an assumption: Larval presence/absence records compiled from different years and sources are comparable enough to model global environmental relationships.
- Rests on an assumption: Species-level morphological identifications in the source articles are accurate enough for the analyses.
- Findingown data
Pacific bluefin tuna larvae were confined to the area between Japan and the Philippines.
“The Pacific bluefin tuna larvae were confined to the area between Japan and the Philippines (Fig. 2b).”
Quote in the paperNot a substantial claim - Findingown data
Tuna larvae are generally confined to a much narrower spatial range than adult tuna.
“Tuna larvae were generally confined to a much narrower spatial range than adults (Figs. 2 & 3).”
- Also stated in: § DISCUSSION · plain
“Our results show that tuna larvae are confined to a much narrower range of habitat than adult fish.”
Quote in the paperSubstantial claim - Also stated in: § DISCUSSION · plain
- Findingown data
Observed cells with positive occurrences of tuna larvae were usually in the upper range of the tolerance of temperatures for all species.
“Observed cells with positive occurrences of tuna larvae were usually in the upper range of the tolerance of temperatures for all species (Fig. 10).”
Quote in the paperSubstantial claim- Rests on an assumption: Species-level morphological identifications in the source articles are accurate enough for the analyses.
- Findingown data
The probability of albacore larvae occurring in a cell was negatively and linearly related to EKE.
“In contrast, the probability of albacore larvae occurring in a cell was negatively and linearly related to EKE (Fig. 5h).”
Quote in the paperSubstantial claim- Rests on an assumption: Seasonal SST and EKE averaged over 5° × 5° grid cells represent the environmental conditions relevant to tuna larval occurrence.
- Rests on an assumption: Larval presence/absence records compiled from different years and sources are comparable enough to model global environmental relationships.
- Rests on an assumption: Species-level morphological identifications in the source articles are accurate enough for the analyses.
- Findingcitation
Eggs and larvae can also be caught at 20 to 21°C in the Balearic Sea.
“though eggs and larvae can also be caught at 20 to 21°C in the Balearic Sea (Reglero et al. 2013).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Reglero et al. 2013
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Findingown data
Atlantic bluefin tuna and southern bluefin tuna had higher minimum thermal tolerances than the other tuna species.
“Though both Atlantic bluefin tuna and southern bluefin tuna had higher minimum tolerances than the other species, all tuna species were shown to have narrower thermal tolerances during spawning than foraging.”
Quote in the paperSubstantial claim - Findingown data
Maximum temperature thresholds for tuna larvae are > 30°C according to our analyses.
“Maximum temperature thresholds are > 30°C according to our analyses.”
Quote in the paperSubstantial claim - Findingcitation
Larval temperature preferences in the Gulf of Mexico, the Japanese Sea and the Mediterranean Sea support our results.
“Larval temperature preferences in the Gulf of Mexico, the Japanese Sea and the Mediterranean Sea support our results (Alemany et al. 2010, Muhling et al. 2010), though eggs and larvae can also be caught at 20 to 21°C in the Balearic Sea (Reglero et al. 2013).”
Quote in the paperSubstantial claim0 of 2 sources checked - Findingnone given
Temperature alone resulted in an over-prediction of plausible larval habitats for all species, especially the bluefin tuna species.
“However, temperature alone resulted in an over-prediction of plausible larval habitats for all species, especially the bluefin tuna species.”
Quote in the paperSubstantial claim- Rests on an assumption: Seasonal SST and EKE averaged over 5° × 5° grid cells represent the environmental conditions relevant to tuna larval occurrence.
- Rests on an assumption: Larval presence/absence records compiled from different years and sources are comparable enough to model global environmental relationships.
- Rests on an assumption: Species-level morphological identifications in the source articles are accurate enough for the analyses.
- Findingown data
All tuna species have narrower thermal tolerances during spawning than foraging.
“Though both Atlantic bluefin tuna and southern bluefin tuna had higher minimum tolerances than the other species, all tuna species were shown to have narrower thermal tolerances during spawning than foraging.”
Quote in the paperSubstantial claim - Findingown data
Temperature is a key factor in determining the distributions of tuna larvae.
“The distributional range in tunas during the larval phase was related to temperature (temperature hypothesis), though with a lower limit (20°C) than the 24°C traditionally used to delineate tuna spawning-ground boundaries (Schaefer 2001).”
Quote in the paperSubstantial claim - Findingnone given
Atlantic bluefin tuna larvae are present in enclosed seas such as the Gulf of Mexico and the Mediterranean Sea.
“Atlantic bluefin tuna larvae are present in enclosed seas such as the Gulf of Mexico and the Mediterranean Sea.”
Quote in the paperNot a substantial claim- Rests on an assumption: Sampled cells where no tuna larvae were caught represent true absence of tuna larvae.
- Rests on an assumption: The compiled larval data from different sources and time periods are comparable and can be combined into a single global analysis.
- Findingown data
Temperature alone resulted in an overestimation of plausible spawning grounds.
“We also showed that temperature alone resulted in an overestimation of plausible spawning grounds.”
Quote in the paperSubstantial claim- Rests on an assumption: Sampled cells where no tuna larvae were caught represent true absence of tuna larvae.
- Rests on an assumption: The compiled larval data from different sources and time periods are comparable and can be combined into a single global analysis.
- Rests on an assumption: The generalized additive models with SST and EKE capture the main environmental drivers of larval occurrence.
- Findingown data
Our results provide support for a combination of the 2 hypotheses in most tuna species.
“We tested 2 hypotheses regarding environmental spawning requirements for tuna, and our results provide support for a combination of the 2 hypotheses in most tuna species.”
Quote in the paperSubstantial claim- Rests on an assumption: Sampled cells where no tuna larvae were caught represent true absence of tuna larvae.
- Rests on an assumption: The compiled larval data from different sources and time periods are comparable and can be combined into a single global analysis.
- Rests on an assumption: The generalized additive models with SST and EKE capture the main environmental drivers of larval occurrence.
- Findingown data
Tuna larvae also preferred intermediate EKE values that were associated with the south and north equatorial currents.
“Tuna larvae also preferred intermediate EKE values that were associated with the south and north equatorial currents, respectively.”
Quote in the paperSubstantial claim- Rests on an assumption: Sampled cells where no tuna larvae were caught represent true absence of tuna larvae.
- Rests on an assumption: The compiled larval data from different sources and time periods are comparable and can be combined into a single global analysis.
- Rests on an assumption: The generalized additive models with SST and EKE capture the main environmental drivers of larval occurrence.
- Findingown data
The EKE values with the highest probability of occurrence for tuna larvae, combined with optimal temperatures, were associated with warm western boundary currents: the Gulf Stream, Brazil Current, Kuroshio Current, East Australia Current and Agulhas Current.
“The EKE values with the highest probability of occurrence for tuna larvae, combined with optimal temperatures, were associated with warm western boundary currents: the Gulf Stream and the Brazil Current in the North and South Atlantic, respectively, the Kuroshio Current in the North Pacific, the East Australia Current in the South Pacific and the Agulhas Current in the Indian Ocean.”
Quote in the paperSubstantial claim- Rests on an assumption: Sampled cells where no tuna larvae were caught represent true absence of tuna larvae.
- Rests on an assumption: The compiled larval data from different sources and time periods are comparable and can be combined into a single global analysis.
- Rests on an assumption: The generalized additive models with SST and EKE capture the main environmental drivers of larval occurrence.
- Findingown data
Intermediate intensity mesoscale processes were an important factor in global larval distribution patterns.
“Intermediate intensity mesoscale processes (ocean triad hypothesis) were also found to be an important factor in global larval distribution patterns.”
Quote in the paperSubstantial claim- Rests on an assumption: Sampled cells where no tuna larvae were caught represent true absence of tuna larvae.
- Rests on an assumption: The compiled larval data from different sources and time periods are comparable and can be combined into a single global analysis.
- Rests on an assumption: The generalized additive models with SST and EKE capture the main environmental drivers of larval occurrence.
- Findingown data
Tuna larvae were more likely to occur in areas with intermediate EKE values of > 0.02 m2 s-2.
“We found tuna larvae were more likely to occur in areas with intermediate EKE values of > 0.02 m 2 s -2 , supporting the hypothesis that larvae are more likely to occur in areas where mesoscale activity is observed.”
Quote in the paperSubstantial claim- Rests on an assumption: Sampled cells where no tuna larvae were caught represent true absence of tuna larvae.
- Rests on an assumption: The compiled larval data from different sources and time periods are comparable and can be combined into a single global analysis.
- Rests on an assumption: The generalized additive models with SST and EKE capture the main environmental drivers of larval occurrence.
- Interpretationreasoning
Specific areas of predominance for the 3 bluefin tuna species share common characteristics in terms of SST and EKE.
“Therefore, the predictive power of the model was insufficient to separate the observed spatial patterns for each bluefin tuna species (Table 1), but suggested that specific areas of predominance for the 3 species share common characteristics in terms of SST and EKE (Fig. 6a-c).”
Quote in the paperSubstantial claim- Rests on an assumption: Seasonal SST and EKE averaged over 5° × 5° grid cells represent the environmental conditions relevant to tuna larval occurrence.
- Rests on an assumption: Larval presence/absence records compiled from different years and sources are comparable enough to model global environmental relationships.
- Rests on an assumption: Species-level morphological identifications in the source articles are accurate enough for the analyses.
- Interpretationown data
The conjecture that the boundaries of tuna spawning grounds are located between the 24°C isotherms may need to be revisited.
“Therefore, the conjecture that the boundaries of tuna spawning grounds are located between the 24°C isotherms (Schaefer 2001) may 213 Variable df Prob Deviance UBRE explained (%) score Atlantic bluefin tuna SST 1 0.005 EKE 1 0.03 Total model 14 -0.98Pacific bluefin tuna SST 1.8 0.12 EKE 1.8 0.001 Total model 20 -0.98 Southern bluefin tuna SST 1 < 0.001 EKE 1.4 0.003 Total model 21 -0.93 Table 1.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Schaefer 2001 source
- Rests on an assumption: Seasonal SST and EKE averaged over 5° × 5° grid cells represent the environmental conditions relevant to tuna larval occurrence.
- Rests on an assumption: Larval presence/absence records compiled from different years and sources are comparable enough to model global environmental relationships.
- Rests on an assumption: Species-level morphological identifications in the source articles are accurate enough for the analyses.
- Study design and conductcitation
Albacore can be confounded with yellowfin tuna in smaller larval size categories.
“Albacore can be confounded with yellowfin tuna in smaller larval size categories (Matsumoto et al. 1972).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Matsumoto et al. 1972
- Study design and conductcitation
The morphological description by Matsumoto (1958), confirmed by subsequent authors, is used in most oceans to identify skipjack tuna.
“The morphological description by Matsumoto (1958), confirmed by Matsumoto et al. (1972), Collette et al. (1984), Olivar & Fortuño (1991), Alema ny (1997) and Richards (2006), is used in most oceans to identify skipjack tuna.”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites Matsumoto (1958)
- cites Matsumoto et al. (1972)
- cites Richards (2006)
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Interpretationreasoning
Spawning temperature preferences for tuna species could be linked to the physiological thresholds for adult spawning and larval development.
“Spawning temperature preferences for tuna species could be linked to the physiological thresholds for adult spawning and larval development.”
Quote in the paperSubstantial claim - Study design and conductcitation
Molecular identification has confirmed occurrences of yellowfin tuna in the Strait of Florida, the Panama Bight and the Pacific Ocean.
“Molecular identification has confirmed occurrences in the Strait of Florida (Richardson et al. 2006, Llopiz et al. 2010), the Panama Bight (Wexler et al. 2007) and the Pacific Ocean (Paine et al. 2008).”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites Richardson et al. 2006
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites Wexler et al. 2007
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites Paine et al. 2008 source
- Interpretationreasoning
The observed correlations with warm water masses and intermediate EKE suggest a general predominance of suitable larval habitats in the western boundary currents compared to eastern.
“The observed correlations with warm water masses and intermediate EKE suggest a general predominance of suitable larval habitats in the western boundary currents compared to eastern.”
Quote in the paperSubstantial claim- Rests on an assumption: Seasonal SST and EKE averaged over 5° × 5° grid cells represent the environmental conditions relevant to tuna larval occurrence.
- Rests on an assumption: Larval presence/absence records compiled from different years and sources are comparable enough to model global environmental relationships.
- Rests on an assumption: Species-level morphological identifications in the source articles are accurate enough for the analyses.
- Interpretationown data
The species could separate their habitats based on their different preferences for areas characterized by different EKE values, especially albacore compared to skipjack, yellowfin and bigeye tuna.
“Despite the 4 species being distributed in the Pacific, Indian and Atlantic Oceans, the species could separate their habitats based on their different preferences for areas characterized by different EKE values, especially albacore compared to skipjack, yellowfin and bigeye tuna.”
Quote in the paperSubstantial claim- Rests on an assumption: Seasonal SST and EKE averaged over 5° × 5° grid cells represent the environmental conditions relevant to tuna larval occurrence.
- Rests on an assumption: Larval presence/absence records compiled from different years and sources are comparable enough to model global environmental relationships.
- Rests on an assumption: Species-level morphological identifications in the source articles are accurate enough for the analyses.
- Interpretationown data
Tuna larval habitat is related to the occurrence of mesoscale oceanographic activity.
“Tuna larval habitat is related to the occurrence of mesoscale oceanographic activity.”
Quote in the paperSubstantial claim- Rests on an assumption: Seasonal SST and EKE averaged over 5° × 5° grid cells represent the environmental conditions relevant to tuna larval occurrence.
- Rests on an assumption: Larval presence/absence records compiled from different years and sources are comparable enough to model global environmental relationships.
- Rests on an assumption: Species-level morphological identifications in the source articles are accurate enough for the analyses.
- Interpretationreasoning
Local food enrichment driven by eddies or frontal structures may help larvae to survive.
“Therefore, local food enrichment driven by eddies or frontal structures may help larvae to survive.”
Quote in the paperSubstantial claim - Interpretationown data
The spatial patterns for the larval occurrences of the 3 bluefin tuna species suggest these species share similar characteristics in their habitats.
“The spatial patterns for the larval occurrences of the 3 bluefin tuna species in this study suggest these species share similar characteristics in their habitats.”
Quote in the paperSubstantial claim- Rests on an assumption: Sampled cells where no tuna larvae were caught represent true absence of tuna larvae.
- Rests on an assumption: The compiled larval data from different sources and time periods are comparable and can be combined into a single global analysis.
- Rests on an assumption: The generalized additive models with SST and EKE capture the main environmental drivers of larval occurrence.
- Premisenone given
At broad scales, tuna deposit eggs and, therefore, larvae into oligotrophic, low-productivity areas.
“At broad scales, tuna deposit eggs and, therefore, larvae into oligotrophic, low-productivity areas (e.g.Mediterranean Sea).”
Quote in the paperNot a substantial claim - Premisecitation
EKE has not been used to estimate larval habitats.
“Though EKE has been used in several studies to model the spatial distribution of adult tuna (e.g.Worm et al. 2005, Zainuddin et al. 2008), it has not been used to estimate larval habitats.”
Quote in the paperSubstantial claim0 of 2 sources checked - Premisecitation
Pacific bluefin tuna larvae entering anticyclonic eddies after hatching increase their chances of successfully arriving in nursery regions.
“It has been shown that Pacific bluefin tuna larvae entering anticyclonic eddies after hatching in crease their chances of successfully arriving in nursery regions (Kitagawa et al. 2010).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Kitagawa et al. 2010 source
- Classified as probably not a substantial claim. 27
- May combine two claims. 37
Probably not a substantial claim: may not pass S3 (load-bearing).
InterpretationcitationHigher temperatures are expected to increase metabolic costs in tuna larvae, as observed in scombrid larvae.
“The temperature effects on meta bolism have not been specifically studied in tuna larvae; however, higher temperatures are ex pected to increase metabolic costs, as has been observed in scombrid larvae (Giguère et al. 1988).”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites Giguère et al. 1988 source
Classified as probably not a substantial claim.
PremisecitationThe ocean triad hypothesis suggests tuna spawning generally occurs in areas with mesoscale oceanographic features such as fronts and eddies.
“The ocean triad hypothesis suggests tuna spawning generally occurs in areas with mesoscale oceanographic features such as fronts and eddies (Bakun 2006).”
Quote in the paperSubstantial claim1 of 1 sources checked- cites Bakun 2006 source
The “Illustration: North Atlantic bluefin tuna” section links bluefin spawning areas to fronts and mesoscale eddies, and the “Illustration: North Pacific albacore tuna” section describes another favourable eddy-associated larval habitat. The paper presents these as examples of ocean-triad processes, but does not establish that tuna generally spawn in such areas across species. (LLM, conf=0.83)
Experimental — accuracy not yet measured
Probably not a substantial claim: may not pass S1 (asserted). May combine two claims.
PremisecitationEddies are associated with high productivity, increasing the chances of larval survival.
“Bakun (2006) proposed that eddies are associated with high productivity, increasing the chances of larval survival.”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites Bakun 2006 source
The MESOSCALE EDDIES section says eddy processes can produce high biological productivity and reproductive success. But OPPORTUNITY AND ADVANTAGE (p. 117) cautions that food-rich conditions can also attract predators: improved larval survival depends on adequate food coinciding with sufficiently low predation, not productivity alone. (LLM, conf=0.84)
Experimental — accuracy not yet measured
Classified as probably not a substantial claim.
PremisecitationPeaks of food abundance during both the planktivorous and the piscivorous stages of larval development may be a determinant of survival in these oligotrophic areas.
“Peaks of food abundance during both the planktivorous and the piscivorous stages of larval development may be a determinant of survival in these oligotrophic areas (Reglero et al. 2011).”
Quote in the paperSubstantial claim1 of 1 sources checked- cites Reglero et al. 2011 source
The Model simulations section links zooplankton density to food limitation during planktivory, and Summary and broader potential implications links prey density to mortality during piscivory. The paper therefore supports a role for food availability, but the passages do not identify peaks of food abundance at both stages as a determinant of survival. Page numbers were not provided in our copy. (LLM, conf=0.78)
Experimental — accuracy not yet measured
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationA preference for similar ranges of EKE has been reported for adult breeding Atlantic bluefin tuna distributions in the Gulf of Mexico, and mesoscale activity is commonly found in areas with larvae.
“A preference for similar ranges of EKE has been re ported for adult breeding Atlantic bluefin tuna distributions in the Gulf of Mexico (Teo et al. 2007), and mesoscale activity is commonly found in areas with larvae (Muhling et al. 2013).”
Quote in the paperNot a substantial claim1 of 2 sources checkedMay combine two claims.
PremisecitationTuna species show a preference for mesoscale structures with moderate activity to spawn, but avoid high EKE.
“In general, tuna species show a preference for mesoscale structures, with moderate activity to spawn, but avoid high EKE (Teo et al. 2007, Reglero et al. 2012, Muhling et al. 2013); one factor involved could be the opportunity to disperse during the larval stage.”
Quote in the paperSubstantial claim2 of 3 sources checked- cites Teo et al. 2007 source
- cites Reglero et al. 2012 source
The Spatial portioning section says western-stock bluefin tuna breed close to mesoscale structures, and the Results report the best albacore model fit at slow to intermediate geostrophic velocities. But the Results also report a preference for high frontal activity in bluefin tuna and a positive relationship with high geostrophic velocities in bullet tuna. The paper does not establish that tuna species generally avoid high eddy kinetic energy (EKE). (LLM, conf=0.84)
Experimental — accuracy not yet measured - cites Muhling et al. 2013 source
The Discussion (page unavailable) reports that Atlantic bluefin tuna larvae in both study areas were most likely to occur in regions of moderate mesoscale activity, not strong directional flow; it also infers that adults concentrated spawning in moderate currents away from large energetic eddies. The paper does not establish this preference for tuna species generally or specifically measure avoidance of high eddy kinetic energy (EKE). (LLM, conf=0.86)
Experimental — accuracy not yet measured
May combine two claims.
Findingown dataSkipjack, yellowfin and bigeye tuna were distributed throughout the tropics in every ocean, both as adults and larvae.
“Skipjack, yellowfin and bigeye tuna were, in contrast, distributed throughout the tropics in every ocean, both as adults and larvae (Fig. 3a-c), while albacore larvae were also found at higher latitudes in the Mediterranean Sea with low occurrences in the equatorial zone (Fig. 3d).”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataMaximum probabilities of occurrence of larvae for most species were predominantly in SSTs between 27.4 and 27.8°C, whereas Atlantic and Pacific bluefin tuna were, on average, found at slightly colder temperatures (26.5 and 25.3°C, respectively).
“Maximum probabilities of occurrence of larvae for most of the species were pre dominantly in SSTs between 27.4 and 27.8°C, whereas Atlantic and Pacific bluefin tuna were, on average, found at slightly colder temperatures (26.5 and 25.3°C, respectively).”
Quote in the paperSubstantial claim- Rests on an assumption: Species-level morphological identifications in the source articles are accurate enough for the analyses.
May combine two claims.
Findingown dataBigeye tuna were predicted to occur in every ocean, being distributed in the equatorial area, but predicted probabilities of occurrence were lower than those for skipjack and yellowfin tuna.
“Bigeye tuna were predicted to occur in every ocean, being distributed in the equatorial area, but predicted probabilities of occurrence were lower than those for skipjack and yellowfin tuna (Fig. 7c).”
Quote in the paperNot a substantial claim- Rests on an assumption: Seasonal SST and EKE averaged over 5° × 5° grid cells represent the environmental conditions relevant to tuna larval occurrence.
- Rests on an assumption: Larval presence/absence records compiled from different years and sources are comparable enough to model global environmental relationships.
- Rests on an assumption: Species-level morphological identifications in the source articles are accurate enough for the analyses.
May combine two claims.
Findingown dataTuna larvae occur within the adults' distributional range, but are restricted to lower latitudes and higher water temperatures than adults.
“Our results showed that tuna larvae occur within the adults' distributional range, but were restricted to lower latitudes and higher water temperatures than adults, largely consistent with Schaefer's 'temperature hypothesis'.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Schaefer 2001 source
May combine two claims.
Findingown dataThe prediction for albacore matched well with the absence of larvae in the equatorial zone, predominantly in areas with lower EKE and higher temperature, which was also found at northern latitudes.
“The prediction for albacore matched well with the absence of larvae in the equatorial zone, predominantly in areas with lower EKE and higher temperature, which, in addition, was also found at northern latitudes (Figs.7d, 8 & 9).”
Quote in the paperSubstantial claim- Rests on an assumption: Seasonal SST and EKE averaged over 5° × 5° grid cells represent the environmental conditions relevant to tuna larval occurrence.
- Rests on an assumption: Larval presence/absence records compiled from different years and sources are comparable enough to model global environmental relationships.
- Rests on an assumption: Species-level morphological identifications in the source articles are accurate enough for the analyses.
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Findingown dataAtlantic bluefin tuna larvae were present in the Mediterranean Sea, but no predictions were obtained for this area because EKE values were not available.
“Atlantic bluefin tuna larvae were also present in the Mediterranean Sea, but no predictions were ob tained for this area, since EKE values were not available.”
Quote in the paperNot a substantial claim- Rests on an assumption: Seasonal SST and EKE averaged over 5° × 5° grid cells represent the environmental conditions relevant to tuna larval occurrence.
- Rests on an assumption: Larval presence/absence records compiled from different years and sources are comparable enough to model global environmental relationships.
- Rests on an assumption: Species-level morphological identifications in the source articles are accurate enough for the analyses.
May combine two claims.
Findingown dataTuna larvae preferred warmer waters and tended to have narrower temperature tolerances, on average, than adults.
“Tuna larvae preferred warmer waters and tended to have narrower temperature tolerances, on average, than adults (Table 3).”
Quote in the paperSubstantial claim- Rests on an assumption: Species-level morphological identifications in the source articles are accurate enough for the analyses.
May combine two claims.
Findingnone givenFor albacore and southern bluefin tuna, the larval thermal range was found to extend above the upper thermal range of adults (25.2°C compared to 30°C in albacore, 28.4°C compared to 30.2°C in southern bluefin tuna).
“For albacore and southern bluefin tuna, the larval thermal range was found to extend above the upper thermal range of adults (25.2°C compared to 30°C in albacore, 28.4°C compared to 30.2°C in southern bluefin tuna).”
Quote in the paperNot a substantial claim- Rests on an assumption: Species-level morphological identifications in the source articles are accurate enough for the analyses.
May combine two claims.
Findingown dataSpatial patterns of skipjack and yellowfin tuna were predicted well by the model, with larvae distributed broadly throughout the tropics.
“Spatial patterns of skipjack and yellowfin tuna were predicted well by the model, with larvae distributed broadly throughout the tropics (Fig. 7a,b).”
Quote in the paperSubstantial claim- Rests on an assumption: Seasonal SST and EKE averaged over 5° × 5° grid cells represent the environmental conditions relevant to tuna larval occurrence.
- Rests on an assumption: Larval presence/absence records compiled from different years and sources are comparable enough to model global environmental relationships.
- Rests on an assumption: Species-level morphological identifications in the source articles are accurate enough for the analyses.
May combine two claims.
Findingown dataTuna larvae generally occupy latitudes between 30°S and 30°N, except in the Mediterranean Sea where larvae are found upwards of 35°N, whereas adults range from 60°S to 60°N.
“In general, tuna larvae were found to occupy latitudes between 30°S and 30°N (with the exception of the Mediterranean Sea where larvae are found upwards of 35°N), whereas adults were found to have a much larger range, from 60°S to 60°N (Figs. 2 & 3).”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataThe probability of larvae occurring in a cell increased with EKE, linearly in Atlantic bluefin tuna, and plateauing around intermediate values of 0.01 to 0.06 m2 s-2 in Pacific bluefin tuna, but EKE was not significant in explaining the occurrence of southern bluefin tuna.
“The probability of larvae occurring in a cell increased with EKE, linearly in Atlantic bluefin tuna (Fig. 4c), and plateauing around intermediate values of 0.01 to 0.06 m 2 s -2 in Pacific bluefin tuna (Fig. 4d), but were not significant in explaining the occurrence of southern bluefin tuna (Table 1).”
Quote in the paperSubstantial claim- Rests on an assumption: Seasonal SST and EKE averaged over 5° × 5° grid cells represent the environmental conditions relevant to tuna larval occurrence.
- Rests on an assumption: Larval presence/absence records compiled from different years and sources are comparable enough to model global environmental relationships.
- Rests on an assumption: Species-level morphological identifications in the source articles are accurate enough for the analyses.
May combine two claims.
Findingown dataAll tuna species showed similar maximum temperature tolerances of ≥28.5°C, but different minima: <22°C in skipjack tuna, yellowfin tuna, albacore, bigeye tuna and Pacific bluefin tuna and >24°C in Atlantic bluefin tuna and southern bluefin tuna.
“All species showed similar maximum temperature tolerances of ≥28.5°C, but different minima: < 22°C in skipjack tuna, yellowfin tuna, albacore, bigeye tuna and Pacific bluefin tuna and > 24°C in Atlantic bluefin tuna and southern bluefin tuna (Fig 10, Table 3).”
Quote in the paperSubstantial claim- Rests on an assumption: Species-level morphological identifications in the source articles are accurate enough for the analyses.
May combine two claims.
Findingown dataThe probability of larval occurrence was positively and linearly related to temperature in Atlantic bluefin tuna and southern bluefin tuna, but temperature did not significantly explain the occurrence of Pacific bluefin tuna.
“The probability of larval occurrence was positively and linearly related to temperature in Atlantic bluefin tuna (Fig. 4a) and southern bluefin tuna (Fig. 4b) larvae, but did not significantly explain the occurrence of Pacific bluefin tuna (Table 1).”
Quote in the paperSubstantial claim- Rests on an assumption: Seasonal SST and EKE averaged over 5° × 5° grid cells represent the environmental conditions relevant to tuna larval occurrence.
- Rests on an assumption: Larval presence/absence records compiled from different years and sources are comparable enough to model global environmental relationships.
- Rests on an assumption: Species-level morphological identifications in the source articles are accurate enough for the analyses.
May combine two claims.
Findingown dataAlbacore larvae were also found at higher latitudes in the Mediterranean Sea with low occurrences in the equatorial zone.
“Skipjack, yellowfin and bigeye tuna were, in contrast, distributed throughout the tropics in every ocean, both as adults and larvae (Fig. 3a-c), while albacore larvae were also found at higher latitudes in the Mediterranean Sea with low occurrences in the equatorial zone (Fig. 3d).”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataTuna larvae are not typically found in areas of low EKE, and have the highest probability of occurrence at intermediate values of EKE.
“According to our results, tuna larvae are not typically found in areas of low EKE, and have the highest probability of occurrence at intermediate values of EKE.”
Quote in the paperSubstantial claim- Rests on an assumption: Seasonal SST and EKE averaged over 5° × 5° grid cells represent the environmental conditions relevant to tuna larval occurrence.
- Rests on an assumption: Larval presence/absence records compiled from different years and sources are comparable enough to model global environmental relationships.
- Rests on an assumption: Species-level morphological identifications in the source articles are accurate enough for the analyses.
May combine two claims.
Findingown dataAlbacore showed the completely opposite pattern: their larvae are distributed above and below 10°N and 10°S, avoiding the equatorial waters, a spatial pattern that is well modeled when the negative influence of EKE in the occurrence of albacore larvae is taken into account.
“However, albacore showed the completely opposite pattern.Their larvae are distributed above and below 10°N and 10°S, avoiding the equatorial waters, a spatial pattern that is well modeled when the negative influence of EKE in the occurrence of albacore larvae is taken into account.”
Quote in the paperSubstantial claim- Rests on an assumption: Seasonal SST and EKE averaged over 5° × 5° grid cells represent the environmental conditions relevant to tuna larval occurrence.
- Rests on an assumption: Larval presence/absence records compiled from different years and sources are comparable enough to model global environmental relationships.
- Rests on an assumption: Species-level morphological identifications in the source articles are accurate enough for the analyses.
May combine two claims.
FindingreasoningHere we have identified oceanographic parameters (mesoscale eddies and SST) that can easily be measured by remote sensing and features (eastern boundary currents, semi-enclosed seas) that should be considered when determining areas of critical habitat for tuna larvae.
“Here we have identified oceanographic parameters (mesoscale eddies and SST) that can easily be measured by remote sensing and features (eastern boundary currents, semi-enclosed seas) that should be considered when determining areas of critical habitat for tuna larvae.”
Quote in the paperSubstantial claim- Rests on an assumption: Sampled cells where no tuna larvae were caught represent true absence of tuna larvae.
- Rests on an assumption: The compiled larval data from different sources and time periods are comparable and can be combined into a single global analysis.
- Rests on an assumption: The generalized additive models with SST and EKE capture the main environmental drivers of larval occurrence.
May combine two claims.
Findingnone givenEastern boundary currents have EKE values < 0.01 to 0.02 m2 s-2 and are associated with colder temperatures.
“In contrast, eastern boundary currents have EKE values < 0.01 to 0.02 m 2 s -2 and are associated with colder temperatures.”
Quote in the paperSubstantial claim- Rests on an assumption: Sampled cells where no tuna larvae were caught represent true absence of tuna larvae.
- Rests on an assumption: The compiled larval data from different sources and time periods are comparable and can be combined into a single global analysis.
- Rests on an assumption: The generalized additive models with SST and EKE capture the main environmental drivers of larval occurrence.
May combine two claims.
Findingown dataA combination of temperature > 20°C and intermediate EKE provided the greatest explanatory power for most larval distributions, except for the 3 bluefin tuna species and albacore.
“A combination of the 2 hypotheses (areas delineated both by temperature > 20°C and with an intermediate EKE) provided the greatest explanatory power for most larval distributions, except for in the 3 bluefin tuna species, which had more restricted spawning locations, and albacore, which preferred low EKE values.”
Quote in the paperSubstantial claim- Rests on an assumption: Sampled cells where no tuna larvae were caught represent true absence of tuna larvae.
- Rests on an assumption: The compiled larval data from different sources and time periods are comparable and can be combined into a single global analysis.
- Rests on an assumption: The generalized additive models with SST and EKE capture the main environmental drivers of larval occurrence.
May combine two claims.
Findingown dataThe probability of larval occurrence was linear and positively related to EKE in Atlantic bluefin tuna, but linear and negatively related in albacore.
“The probability of larval occurrence was linear and positively related to EKE in Atlantic bluefin tuna, but linear and negatively related in albacore.”
Quote in the paperSubstantial claim- Rests on an assumption: Sampled cells where no tuna larvae were caught represent true absence of tuna larvae.
- Rests on an assumption: The compiled larval data from different sources and time periods are comparable and can be combined into a single global analysis.
- Rests on an assumption: The generalized additive models with SST and EKE capture the main environmental drivers of larval occurrence.
May combine two claims.
Findingown dataThe distributional range in tunas during the larval phase was related to temperature, with a lower limit of 20°C.
“The distributional range in tunas during the larval phase was related to temperature (temperature hypothesis), though with a lower limit (20°C) than the 24°C traditionally used to delineate tuna spawning-ground boundaries (Schaefer 2001).”
Quote in the paperSubstantial claim- Rests on an assumption: Sampled cells where no tuna larvae were caught represent true absence of tuna larvae.
- Rests on an assumption: The compiled larval data from different sources and time periods are comparable and can be combined into a single global analysis.
- Rests on an assumption: The generalized additive models with SST and EKE capture the main environmental drivers of larval occurrence.
May combine two claims.
Interpretationown dataBoth SST and EKE were major predictors for the spatial distribution of tuna larvae, but the trends of the 2 environmental predictors differed among species.
“Both SST and EKE were found to be major predictors for the spatial distribution of tuna larvae, but the trends of the 2 environmental predictors differed among species.”
Quote in the paperSubstantial claim- Rests on an assumption: Seasonal SST and EKE averaged over 5° × 5° grid cells represent the environmental conditions relevant to tuna larval occurrence.
- Rests on an assumption: Larval presence/absence records compiled from different years and sources are comparable enough to model global environmental relationships.
- Rests on an assumption: Species-level morphological identifications in the source articles are accurate enough for the analyses.
May combine two claims.
Interpretationown dataThe lower temperature tolerance for tuna larvae appears to be 20°C, at least for some species, though most positive occurrences were observed in warmer temperatures.
“According to our results, the lower temperature tolerance for tuna larvae appears to be 20°C, at least for some species, though most positive occurrences were observed in warmer temperatures.”
Quote in the paperSubstantial claim- Rests on an assumption: Seasonal SST and EKE averaged over 5° × 5° grid cells represent the environmental conditions relevant to tuna larval occurrence.
- Rests on an assumption: Larval presence/absence records compiled from different years and sources are comparable enough to model global environmental relationships.
- Rests on an assumption: Species-level morphological identifications in the source articles are accurate enough for the analyses.
May combine two claims.
InterpretationcitationBroader larval distributions were found for species that mature early in life and do not attain a large size, in contrast to the larger tuna species, which mature at an older age and have a narrower distribution as larvae, a pattern that correlates with tropical versus temperate tuna.
“Broader larval distributions were found for species that mature early in life and do not attain a large size, in contrast to the larger tuna species, which mature at an older age and have a narrower distribution as larvae (Fromentin & Fonteneau 2001), a pattern that correlates with tropical versus temperate tuna.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Fromentin & Fonteneau 2001 source
- Rests on an assumption: Seasonal SST and EKE averaged over 5° × 5° grid cells represent the environmental conditions relevant to tuna larval occurrence.
- Rests on an assumption: Larval presence/absence records compiled from different years and sources are comparable enough to model global environmental relationships.
- Rests on an assumption: Species-level morphological identifications in the source articles are accurate enough for the analyses.
Probably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductnone givenSkipjack tuna benefits from the most extensive sampling at large and regional scales.
“This species benefits from the most extensive sampling at large and regional scales.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductcitationYellowfin tuna can usually be identified using the works by Matsumoto (1958) and Matsumoto et al. (1972).
“This species can usually be identified using the works by Matsumoto (1958) and Matsumoto et al. (1972).”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites Matsumoto (1958)
- cites Matsumoto et al. (1972)
Probably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductreasoningIn some areas, albacore is usually included in the group Thunnus sp.
“Therefore, in some areas, it is usually in clud ed in the group Thunnus sp.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationSkipjack tuna larvae have a forebrain pigment that helps separate them from Thunnus species.
“This species has a forebrain pigment that helps to separate them from Thunnus species (Richards 2006).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Richards 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 conductcitationAlbacore larvae have been described by Matsumoto et al. (1972), Alemany (1997) and Richards (2006).
“Albacore larvae have been de scribed by Matsumoto et al. (1972), Alemany (1997) and Richards (2006).”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites Matsumoto et al. (1972)
- cites Alemany (1997)
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites Richards (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).
PremisecitationAn increase of water temperatures before and during spawning is needed for adult tunas to release eggs.
“An increase of water temperatures before and during spawning is needed for the adult tunas to release eggs (Margulies et al. 2007).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Margulies et al. 2007
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
May combine two claims.
Study design and conductcitationBigeye tuna larvae have been reported in the Gulf of Mexico, but further molecular analyses did not identify bigeye tuna in the Strait of Florida.
“Bigeye tuna larvae have been reported in the Gulf of Mexico (Nishikawa et al. 1985, Estévez et al. 1993), but further molecular analyses did not identify bigeye tuna in the Strait of Florida (Richardson et al. 2006).”
Quote in the paperSubstantial claim0 of 3 sources checked- cites Nishikawa et al. 1985
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites Estévez et al. 1993
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites Richardson et al. 2006
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
May combine two claims.
Interpretationown dataGlobal patterns in larval distribution were easier to predict in skipjack and yellowfin tuna than in bluefin tuna species, where spawning areas and larval habitats appear much more spatially constrained.
“However, the global patterns in larval distribution were easier to predict in skipjack and yellowfin tuna than in bluefin tuna species, where spawning areas and larval habitats appear much more spatially constrained.”
Quote in the paperSubstantial claim- Rests on an assumption: Seasonal SST and EKE averaged over 5° × 5° grid cells represent the environmental conditions relevant to tuna larval occurrence.
- Rests on an assumption: Larval presence/absence records compiled from different years and sources are comparable enough to model global environmental relationships.
- Rests on an assumption: Species-level morphological identifications in the source articles are accurate enough for the analyses.
Probably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductcitationMolecular markers have confirmed skipjack tuna identifications based on morphological traits in the Pacific Sea and the Gulf of Mexico.
“The use of molecular markers is rare but has confirmed skipjack identifications based on morphological traits in the Pacific Sea (Paine et al. 2008) and the Gulf of Mexico (Richardson et al. 2010).”
Quote in the paperNot a substantial claim0 of 2 sources checkedMay combine two claims.
Study design and conductnone givenThe combined database shows good spatial coverage, though individual surveys were very fragmented spatially and temporally and were not coordinated internationally.
“The combined database shows good spatial coverage, though individual surveys were very fragmented spatially and temporally and were not coordinated internationally.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationTemperature has a consistent and dominant role in structuring broad-scale marine diversity patterns.
“In general, temperature has a consistent and dominant role in structuring broad-scale marine diversity patterns (Tittensor et al. 2010).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Tittensor et al. 2010 source
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductcitationAlbacore may be a problem where both species co-occur, but not in the Mediterranean where only albacore is present and readily identified.
“This may be a problem where both species co-occur, but not in the Mediterranean where only albacore is present and readily identified (Alemany 1997).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Alemany 1997
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). May combine two claims.
PremisecitationOceanographic discontinuities have been suggested to limit the range distribution of marine species by acting as a boundary, but also through their influence on larval dispersal and recruitment.
“In addition, oceanographic discontinuities have been suggested to limit the range distribution of marine species by acting as a boundary, but also through their influence on larval dispersal and recruitment (Gaylord & Gaines 2000).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Gaylord & Gaines 2000 source
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductnone givenMatsumoto et al. (1972) is usually used for species identification of bigeye tuna and to determine its distribution in regional studies in the Pacific and Indian Oceans.
“Matsumoto et al. (1972) is usually used for species identification of bigeye tuna and to determine its distribution in regional studies in the Pacific and Indian Oceans.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Matsumoto et al. (1972)
Probably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductcitationIdentifications of yellowfin tuna benefit from descriptions of individuals cultured in the laboratory.
“Identifications of yellowfin tuna also benefit from the descriptions of individuals cultured in the laboratory (e.g.Margulies et al. 2007).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Margulies et al. 2007
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).
InterpretationreasoningThe preference of albacore for regions with low EKE values may be an adaptation to separate their larval habitat from that of the other species.
“The preference of albacore for regions with low EKE values may be an adaptation to separate their larval habitat from that of the other species.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
InterpretationreasoningA trade-off between predation and food availability may be the reason why larvae prefer mesoscale structures within broad-scale oligotrophic areas.
“A trade-off between predation and food availablity may be the reason why larvae prefer mesoscale structures within broad-scale oligotrophic areas.”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim.
Premisenone givenThis study provides the first compilation of published data for tuna larvae on a broad spatial scale.
“This study provides the first compilation of published data for tuna larvae on a broad spatial scale.”
Quote in the paperSubstantial claimClassified as probably not a substantial claim.
InterpretationreasoningRegions of high EKE could be less suitable for spawning if larvae end up in less optimal areas for later growth and survival as a result of the influence of strong currents on transport.
“Regions of high EKE could be less suitable for spawning if larvae end up in less optimal areas for later growth and survival as a result of the influence of strong currents on transport.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S4 (based). May combine two claims.
InterpretationreasoningIf intermediate EKE values associated with mesoscale structures influence the spatial distribution of feeding resources, this may increase larval survival.
“If intermediate EKE values associated with mesoscale structures influence the spatial distribution of feeding resources, this may increase larval survival.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationThere is very limited scientific information on the spatio-temporal spawning patterns of tuna species and strong uncertainties in knowledge of many biological parameters, including reproduction, of tuna species.
“There is very limited scientific information on the spatio-temporal spawning patterns of tuna species (Schaefer 2001) and strong uncertainties in our knowledge of many biological parameters, including reproduction, of tuna species.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Schaefer 2001 source
Classified as probably not a substantial claim. May combine two claims.
InterpretationcitationThere would be low food availability and, consequently, low predator abundances, as suggested by the loophole hypothesis.
“Thus, there would be low food availability and, consequently, low predator abundances, as suggested by the socalled 'loophole hypothesis ' (Bakun & Broad 2003, Irigoien et al. 2007).”
Quote in the paperSubstantial claim0 of 2 sources checkedProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationOne constraint on the implementation of HSMPAs is limited knowledge regarding the biodiversity of oceanic species and the identification of the parameters that should be measured.
“One constraint on the implementation of HSMPAs is limited knowledge regarding the biodiversity of oceanic species and the identification of the parameters that should be measured (UNEP-WCMC 2008).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites UNEP-WCMC 2008
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). May combine two claims.
InterpretationreasoningEKE obtained from sea-surface height anomalies may be a good indicator of mesoscale activity in most of the oceans, but in confined areas mesoscale structures can be induced by topography or occur at a smaller scale than the grid size used in this study.
“EKE obtained from sea-surface height anomalies may be a good indicator of mesoscale activity in most of the oceans.But in such confined areas mesoscale structures can be induced by topography or occur at a smaller scale than the grid size used in this study.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
InterpretationreasoningOne factor involved in the preference for mesoscale structures could be the opportunity to disperse during the larval stage.
“In general, tuna species show a preference for mesoscale structures, with moderate activity to spawn, but avoid high EKE (Teo et al. 2007, Reglero et al. 2012, Muhling et al. 2013); one factor involved could be the opportunity to disperse during the larval stage.”
Quote in the paperNot a substantial claim
The paper relies on this without support.
Seasonal SST and EKE averaged over 5° × 5° grid cells represent the environmental conditions relevant to tuna larval occurrence.
“Both monthly EKE and SST values were averaged at each 5° × 5° cell of the analysis grid to obtain seasonal (3 mo) data.”
The paper relies on this without support.
Larval presence/absence records compiled from different years and sources are comparable enough to model global environmental relationships.
“Standardized data on larval densities were not available for comparison across studies and oceans; hence, we were forced to focus on larval presence records only.”
“Furthermore, larval sampling cruises were not routinely recorded over the years in different areas, so we have combined different sampling years, with the earliest cruises dating from the 1920s and the latest from the 2000s.”
The paper relies on this without support.
Species-level morphological identifications in the source articles are accurate enough for the analyses.
“Larval tuna identification at species level can be problematic when based on morphological descriptions, especially in the Gulf of Mexico (Richards et al. 1990).”
“We have carefully reviewed the basis for taxonomical descriptions in the articles used as data sources for our analyses.”
The paper relies on this without support.
Sampled cells where no tuna larvae were caught represent true absence of tuna larvae.
“Sampled cells where no tuna larvae were obtained from geo-referenced icthyoplankton surveys are shown in dark orange.Areas with missing data are shown in white”
The paper relies on this without support.
The compiled larval data from different sources and time periods are comparable and can be combined into a single global analysis.
“A total of 1678 grid cells, excluding land cells, between 70°S and 70°N were mapped according to the available information on the presence or absence of tuna larvae for every species.”
The paper relies on this without support.
The generalized additive models with SST and EKE capture the main environmental drivers of larval occurrence.
“predicted values were derived from a generalized additive model including SST and EKE as predictor variables when significant.”
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?
The eastern Indian Ocean (R2) serves as the principal spawning area, and the temperate region (R3) functions as the feeding grounds for bigeye tuna.
“It is generally believed that the eastern Indian Ocean (R2) serves as the principal spawning area, and the temperate region (R3) functions as the feeding grounds for bigeye tuna (Reglero et al., 2014; Muhling et al., 2017; Fu, 2019).”
From Impacts of phytoplankton availability on bigeye tuna (Thunnus obesus) recruitment in the Indian Ocean (2024) · cites this paper as Reglero et al., 2014
The Results (page unavailable) place bigeye tuna larvae throughout the tropics in every ocean, which supports spawning in the Indian Ocean but not the eastern Indian Ocean as its principal spawning area. The paper does not identify a temperate region as bigeye tuna feeding grounds; its statement about larvae in the tropical East Indian Ocean concerns southern bluefin tuna. (LLM, conf=0.84)
Experimental — accuracy not yet measuredFor bigeye tuna, which primarily spawn in tropical regions, prey availability is more relevant than temperature to larvae.
“In particular, for species such as bigeye tuna, which primarily spawn in tropical regions, prey availability is more relevant than temperature to larvae (Reglero et al., 2014; Shropshire et al., 2022).”
From Impacts of phytoplankton availability on bigeye tuna (Thunnus obesus) recruitment in the Indian Ocean (2024) · cites this paper as Reglero et al., 2014
The Results place predicted bigeye larval occurrence in equatorial waters and find that both temperature and eddy kinetic energy significantly predict its occurrence (page not available in our copy). The ocean triad hypothesis section suggests that local food enrichment may help tuna larvae survive, but does not establish that prey availability matters more than temperature for bigeye larvae. (LLM, conf=0.84)
Experimental — accuracy not yet measuredTo spawn, all tuna species return to tropical or subtropical locations, which are typically oligotrophic and warm.
“However, to spawn, all tuna species return to tropical or subtropical locations, which are typically oligotrophic and warm (Sund et al., 1981;Reglero et al., 2014).”
From Evolutionary and ecological constraints of fish spawning habitats (2015) · cites this paper as Reglero et al., 2014
Bigeye tuna eggs hatch into larvae about 3 mm in length in a few days, develop foraging and swimming organs quickly, and grow into juveniles within the first month of life.
“Eggs laid typically hatch into larvae (about 3 mm in length) in a few days, develop foraging and swimming organs quickly, and then grow into juveniles within the first month of life (Miyashita et al., 2001; Reglero et al., 2014).”
From Impacts of phytoplankton availability on bigeye tuna (Thunnus obesus) recruitment in the Indian Ocean (2024) · cites this paper as Reglero et al., 2014
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.
Temperature is called significant for every species despite the Pacific bluefin result
MajorThe discussion claims a significant temperature effect in all species, whereas the results explicitly say temperature did not significantly explain Pacific bluefin larval occurrence.
“We found a significant positive effect of temperature in all of the species analyzed.”
“but did not significantly explain the occurrence of Pacific bluefin tuna (Table 1).”
Southern bluefin EKE is called nonsignificant despite its reported p-value
MajorThe results say EKE was not significant for southern bluefin tuna, but Table 1 reports an EKE probability of 0.003.
“but were not significant in explaining the occurrence of southern bluefin tuna (Table 1).”
“Southern bluefin tuna SST 1 < 0.001 EKE 1.4 0.003 Total model 21 -0.93”
Skipjack model table lists SST twice
MinorTable 2 gives two different SST rows for skipjack tuna, although the stated model contains one SST term alongside area and EKE. The table does not explain which SST result applies.
“| Skipjack tuna | | | | | | SST | 1 | 0.005 | | | | Area | 1.9 | < 0.001 | | | | SST | 2 | < 0.001 | | | | EKE | 2 | < 0.001 | | |”
“P species,s,i,j = a + s 0 (area i,j ) + s 1 (SST s,i,j ) + s 2 (EKE s,i,j ) + ε(2)”
The final sampling season has two different end months
MinorThe methods define the last sampling season as October to November, while the seasonal environmental-data figure defines it as October to December.
“sampling season of the year (January to March, April to June, July to September, October to November).”
“Figure: 8 Fig. 8 . Fig. 8. Spatial distribution of SST as obtained from the NOAA/ NASA AVHRR Oceans Pathfinder project for (a) January to March, (b) April to June, (c) July to September and (d) October to December, used as predictors in the model”
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“For example, most species of tuna spawn in oligotrophic subtropical environments (Reglero et al. 2014).”
Evolutionary and ecological constraints of fish spawning habitats
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“However, to spawn, all tuna species return to tropical or subtropical locations, which are typically oligotrophic and warm (Sund et al., 1981; Reglero et al., 2014).”
BackgroundHabitat suitability of the Atlantic bluefin tuna by size class: An ecological niche approach
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“Intermediate levels of Eddy Kinetic Energy (EKE), which is derived from SSHa, were shown to strongly favour pelagic fish spawning (ABFT – Bakun, 2013; Teo et al., 2007; Teo and Block, 2010; Tuna species – Reglero et al., 2014; Small pelagic species – Asch and Checkley, 2013).”
BackgroundSelf-citationBottom-up drivers of global patterns of demersal, forage, and pelagic fishes
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Muhling, B. A., Lamkin, J. T., Alemany, F., García, A., Farley, J., Ingram, G. W., Berastegui, D. A., Reglero, P., & Carrion, R. L. (2017) · Reviews in Fish Biology and Fisheries · doi:10.1007/s11160-017-9471-4 · Cited by 82 · see citing works
Self-citationModelling the oceanic habitats of two pelagic species using recreational fisheries data
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“In comparison to the widely used logistic regression approaches (Maxwell et al., 2009; Reglero et al., 2014; Sequeira et al., 2014), PPMs change the response variable to a metric of abundance rather than probability, and can thus improve the biological interpretation of results.”
MethodPecoraro, C., Zudaire, I., Bodin, N., Murua, H., Taconet, P., Díaz‐Jáimes, P., Cariani, A., Tinti, F., & Chassot, E. (2016) · Reviews in Fish Biology and Fisheries · doi:10.1007/s11160-016-9460-z · Cited by 72 · see citing works
“Endothermic capabilities are acquired during the juvenile stage and consequently, YFT larvae are confined to a much narrower range of habitats than adults (Reglero et al. 2014).”
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
Self-citationMoore, B. R., Bell, J. D., Evans, K., Farley, J. H., Grewe, P. M., Hampton, J., Marie, A. D., Minte‐Vera, C. V., Nicol, S., Pilling, G. M., et al. (2020) · Fisheries Research · doi:10.1016/j.fishres.2020.105525 · Cited by 62 · see citing works
“bitats and support extensive fisheries worldwide (FAO, 2018; Reglero et al., 2014).”
BackgroundInteractions of tuna fisheries with the Galápagos marine reserve
Boerder, K., Bryndum‐Buchholz, A., & Worm, B. (2017) · Marine Ecology Progress Series · doi:10.3354/meps12399 · Cited by 57 · see citing works
“The hotspot lies downstream from predominant east-west currents, which may transport adult tuna as well as larvae and juveniles into the hotspot area (Reglero et al. 2014).”
BackgroundSelf-citationLarge Pelagic Fish Are Most Sensitive to Climate Change Despite Pelagification of Ocean Food Webs
Petrik, C. M., Stock, C. A. A., Andersen, K. H., van Denderen, P. D., & Watson, J. R. (2020) · Frontiers in Marine Science · doi:10.3389/fmars.2020.588482 · Cited by 55 · see citing works
“Third, basin-wide migrations of large pelagics across oligotrophic regions are often in search of favorable larval environments (e.g., Bakun, 2013; Reglero et al., 2014) during which adults feed advantageously at mesoscale features (e.”
BackgroundNot all who wander are lost: Improving spatial protection for large pelagic fishes
Boerder, K., Schiller, L., & Worm, B. (2019) · Marine Policy · doi:10.1016/j.marpol.2019.04.013 · Cited by 53 · see citing works
“This strategy, however, may not be as suitable for opportunistic spawners, such as yellowfin tuna (Thunnus albacares), which are less bound to particular locations [78].”
BackgroundSelf-citationDomingues, R. M., Goni, G. J., Bringas, F. G., Muhling, B. A., Lindo‐Atichati, D., & Walter, J. F. (2016) · Fisheries Oceanography · doi:10.1111/fog.12152 · Cited by 48 · see citing works
“adults target specific habitats or oceanographic features as spawning grounds (Reglero et al., 2014), as they can detect and respond to oceanographic gradients (Humston et al.”
BackgroundLaiz-Carrión, R., Gerard, T., Uriarte, A., Malca, E., Quintanilla, J., Muhling, B., Alemany, F., Privoznik, S., Shiroza, A., Lamkin, J., et al. (2015) · PLoS ONE · doi:10.1371/journal.pone.0133406 · Cited by 44 · see citing works
Laiz-Carrión, R., Gerard, T., Suca, J., Malca, E., Uriarte, A., Quintanilla, J., Privoznik, S., Llopiz, J., Lamkin, J., & García, A. (2019) · Marine Ecology Progress Series · doi:10.3354/meps12958 · Cited by 37 · see citing works
Álvarez-Berastegui, D., Ciannelli, L., Aparicio-González, A., Reglero, P., Hidalgo, M., López-Jurado, J., Tintoré, J., & Alemany, F. (2014) · PLoS ONE · doi:10.1371/journal.pone.0109338 · Cited by 45 · see citing works
“Thus, the work presented here sheds new light to modeling spatial distribution and investigating key ecological processes of species highly dependent on the variability of the pelagic environment, like spawning ecology of many of the big tuna species are [41].”
BackgroundSelf-citationAbundance and habitat associations of tuna larvae in the surface water of the Gulf of Mexico
Cornic, M., Smith, B. L., Kitchens, L. L., Bremer, J. R. A., & Rooker, J. R. (2017) · Hydrobiologia · doi:10.1007/s10750-017-3330-0 · Cited by 39 · see citing works
“atlanticus, and the optimal temperature range is 28–29 C (Wexler et al., 2011; Reglero et al., 2014).”
BackgroundInfluentialOhshimo, S., Sato, T., Okochi, Y., Tanaka, S., Ishihara, T., Ashida, H., & Suzuki, N. (2018) · Aquatic Living Resources · doi:10.1051/alr/2018022 · Cited by 37 · see citing works
“In addition, habitats of tuna and tuna-like species could be shifted by climate change (Reglero et al., 2014).”
BackgroundMuhling, B. A., Brill, R., Lamkin, J. T., Roffer, M. A., Lee, S.-K., Liu, Y., & Muller-Karger, F. (2017) · ICES Journal of Marine Science · doi:10.1093/icesjms/fsw215 · Cited by 36 · see citing works
Artetxe-Arrate, I., Fraile, I., Crook, D. A., Zudaire, I., Arrizabalaga, H., Greig, A., & Murua, H. (2019) · Marine and Freshwater Research · doi:10.1071/mf19067 · Cited by 36 · see citing works
“In particular, the equatorial area (0– 108S) and the Mozambique Channel have been identified as primary and secondary spawning areas (Reglero et al. 2014; Indian Ocean Tuna Commission 2017b).”
BackgroundÁlvarez‐Berastegui, D., Hidalgo, M., Tugores, M. P., Reglero, P., Aparicio‐González, A., Ciannelli, L., Juza, M., Mourre, B., Pascual, A., López‐Jurado, J. L., et al. (2016) · ICES Journal of Marine Science · doi:10.1093/icesjms/fsw041 · Cited by 36 · see citing works
Self-citationCornic, M., & Rooker, J. R. (2018) · Fisheries Research · doi:10.1016/j.fishres.2017.12.015 · Cited by 35 · see citing works
“It has been observed that potential environmental changes can impact the spatial and temporal dynamics of spawning areas, which influence the distribution and abundance of tuna larvae (Lindo-Atichati et al., 2012; Reglero et al., 2014).”
BackgroundEvidence and patterns of tuna spawning inside a large no-take Marine Protected Area
Hernández, C., Witting, J. H., Willis, C., Thorrold, S., Llopiz, J., & Rotjan, R. (2019) · Scientific Reports · doi:10.1038/s41598-019-47161-0 · Cited by 32 · see citing works
Shropshire, T. A., Morey, S. L., Chassignet, E. P., Karnauskas, M., Coles, V. J., Malca, E., Laiz-Carrión, R., Fiksen, Ø., Reglero, P., Shiroza, A., et al. (2022) · Journal of Plankton Research · doi:10.1093/plankt/fbab041 · Cited by 30 · see citing works
“Mesoscale variability and the resulting spatiotemporal extent of favorable larval habitat has been estimated for larval ABT by previous studies (Domingues et al., 2016; Muhling et al., 2013; Reglero et al., 2014).”
Self-citationRichardson, A. J., Downes, K. J., Nolan, E. T., Brickle, P., Brown, J., Weber, N. L., & Weber, S. B. (2018) · Aquatic Conservation Marine and Freshwater Ecosystems · doi:10.1002/aqc.2936 · Cited by 30 · see citing works
Dell’Apa, A., Carney, K. J., Davenport, T. M., & Carle, M. V. (2018) · Marine Environmental Research · doi:10.1016/j.marenvres.2018.07.017 · Cited by 29 · see citing works
“These results are in accordance with an observed larval temperature preference threshold of 30 °C for tuna species, generally (Reglero et al., 2014), and an observed larval temperature preference threshold of about 28 – 30 °C for blue fi n and yellow fi n tuna (Muhling et al., 2010, 2011; Wexler et…”
Burrows, M., Browning, J. S., Breitbart, M., Murawski, S. A., & Peebles, E. B. (2018) · Fisheries Oceanography · doi:10.1111/fog.12404 · 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
Self-citationLandry, M. R., Beckley, L. E., & Muhling, B. A. (2019) · ICES Journal of Marine Science · doi:10.1093/icesjms/fsy184 · Cited by 24 · see citing works
“Further, though the spawning regions are characterized by mesoscale eddies and fronts, the waters selected for spawning generally have retention characteristics, often with less kinetic energy than at other times of the year (Reglero et al., 2014).”
BackgroundSmith, J. A., Buil, M. P., Muhling, B. A., Tommasi, D., Brodie, S. J., Frawley, T. H., Fiechter, J., Koenigstein, S., Himes‐Cornell, A., Alexander, M. A., et al. (2023) · Progress In Oceanography · doi:10.1016/j.pocean.2023.102973 · Cited by 24 · see citing works
“Swordfish in the CCS are managed internationally by the Western and Central Pacific Fishery Commission (WCPFC) and the Inter-American Tropical Tuna Commission (IATTC), and in U.S. waters of the CCS by the PFMC which includes swordfish in its highly migratory species (HMS) Fisheries Management Plan (Appendix A).”
BackgroundFine-scale horizontal distributions of multiple species of larval tuna off the Nansei Islands, Japan
Tawa, A., Kodama, T., Sakuma, K., Ishihara, T., & Ohshimo, S. (2019) · Marine Ecology Progress Series · doi:10.3354/meps13216 · Cited by 24 · see citing works
Atlantic bluefin tuna spawn early to avoid metabolic meltdown in larvae
Fiksen, Ø., & Reglero, P. (2022) · Ecology · doi:10.1002/ecy.3568 · Cited by 22 · see citing works
Self-citationÁlvarez-Ellacuria, I., Rasmuson, L. K., Gerard, T., Laiz‐Carrión, R., Hidalgo, M., Lamkin, J. T., Malca, E., Ferrà, C., Torres, A. P., Álvarez‐Berastegui, D., et al. (2021) · Oceans · doi:10.3390/oceans2010004 · Cited by 22 · see citing works
“Water temperatures above 20 ◦C are related to suitable larval habitats for tuna species [18,19].”
BackgroundSelf-citationRathnasuriya, M. I. G., Mateos‐Rivera, A., Skern‐Mauritzen, R., Wimalasiri, H. B. U. G. M., Jayasinghe, R. P. P. K., Krakstad, J., & Dalpadado, P. (2021) · Marine Biodiversity · doi:10.1007/s12526-021-01169-w · Cited by 22 · see citing works
Reglero, P., Santos, M., Balbín, R., Laiz‐Carrión, R., Álvarez‐Berastegui, D., Ciannelli, L., Jiménez, E., & Alemany, F. (2017) · Deep Sea Research Part II Topical Studies in Oceanography · doi:10.1016/j.dsr2.2017.03.013 · Cited by 20 · see citing works
Self-citationThe key role of the Northern Mozambique Channel for Indian Ocean tropical tuna fisheries
Chassot, E., Bodin, N., Sardenne, F., & Obura, D. O. (2019) · Reviews in Fish Biology and Fisheries · doi:10.1007/s11160-019-09569-9 · Cited by 19 · see citing works
Reproduction of Atlantic bluefin tuna
Medina, A. (2020) · Fish and Fisheries · doi:10.1111/faf.12489 · Cited by 18 · see citing works
Habitat analysis of the commercial tuna of the Eastern Tropical Pacific Ocean
Hu, C., Harrison, D. P., Hinton, M. G., Siegrist, Z., & Kiefer, D. A. (2018) · Fisheries Oceanography · doi:10.1111/fog.12263 · Cited by 18 · see citing works
Moore, B. R., Adams, T., Allain, V., Bell, J. D., Bigler, M., Bromhead, D., Clark, S., Davies, C. R., Evans, K., Faasili, U., et al. (2020) · Fisheries Research · doi:10.1016/j.fishres.2020.105524 · Cited by 17 · see citing works
“Several authors, however, posit that actual spawning areas for tunas may be more spatially and temporally restricted than this (Reglero et al., 2014; Muhling et al., 2017), and several temporally-consistent spawning ‘hot spots’ have been identified for yellowfin and bigeye tunas (e.g., McPherson,…”
The Seychelles Tuna Fishery and Climate Change
Marsac, F. (2017) · Wiley eBooks · doi:10.1002/9781119154051.ch16 · Cited by 18 · see citing works
Seasonal distribution of fish larvae in mangrove-seagrass seascapes of Zanzibar (Tanzania)
Tarimo, B., Winder, M., Mtolera, M. S. P., et al. (2022) · Scientific Reports · doi:10.1038/s41598-022-07931-9 · Cited by 15 · see citing works
Gleiber, M. R., Sponaugle, S., & Cowen, R. K. (2020) · ICES Journal of Marine Science · doi:10.1093/icesjms/fsaa201 · 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
Lan, K., Wu, Y., Chen, L., Naimullah, M., & Lin, T. S. (2021) · Frontiers in Marine Science · doi:10.3389/fmars.2021.614594 · Cited by 14 · see citing works
Pratt, C. J., Denley, D., & Meta×as, A. (2022) · Oecologia · doi:10.1007/s00442-022-05110-1 · Cited by 14 · see citing works
Frawley, T. H., Muhling, B. A., Brodie, S. J., Blondin, H. E., Welch, H., Arostegui, M. C., Bograd, S. J., Braun, C. D., Cimino, M. A., Farchadi, N., et al. (2023) · Fish and Fisheries · doi:10.1111/faf.12791 · Cited by 14 · see citing works
“In the North Pacific, alba - core spawning has been reported in subtropical waters between the Philippines and Hawai'i where sea surface temperatures exceed 22– 24°C (Ashida et al., 2020 ; Reglero et al., 2014 ).”
BackgroundArtetxe-Arrate, I., Fraile, I., Clear, N., Darnaude, A. M., Dettman, D., Pécheyran, C., Farley, J. H., & Murua, H. (2021) · Marine Ecology Progress Series · doi:10.3354/meps13769 · Cited by 13 · see citing works
Quintanilla-Hervás, J. M., Borrego‐Santos, R., Malca, E., Swalethorp, R., Landry, M. R., Gerard, T., Lamkin, J. T., Garcı́a, A., & Laiz‐Carrión, R. (2024) · Animals · doi:10.3390/ani14091319 · Cited by 13 · see citing works
“The two main environmental influences on the early life stages of tunas are temperature and food availability [31–35].”
BackgroundOntogeny of regional endothermy in Pacific bluefin tuna (Thunnus orientalis)
Malik, A., Dickson, K. A., Kitagawa, T., et al. (2020) · Marine Biology · doi:10.1007/s00227-020-03753-3 · Cited by 13 · see citing works
Vertical distribution of larval Pacific bluefin tuna, Thunnus orientalis, in the Japan Sea
Kodama, T., Ohshimo, S., Tawa, A., Furukawa, S., Nohara, K., Takeshima, H., Chiba, S. N., Ishihara, T., Sawai, E., Kawazu, M., et al. (2020) · Deep Sea Research Part II Topical Studies in Oceanography · doi:10.1016/j.dsr2.2020.104785 · Cited by 11 · see citing works
Varela, J. L., Sorell, J. M., Macías, D., et al. (2018) · Fisheries Research · doi:10.1016/j.fishres.2018.08.004 · Cited by 12 · see citing works
Artetxe-Arrate, I., Fraile, I., Farley, J. H., Darnaude, A. M., Clear, N., Dettman, D. L., Davies, C. R., Marsac, F., & Murua, H. (2021) · Oceans · doi:10.3390/oceans2030026 · Cited by 13 · see citing works
Russo, S., Torri, M., Patti, B., Reglero, P., Álvarez-Berastegui, D., Cuttitta, A., & Sarà, G. (2021) · Frontiers in Marine Science · doi:10.3389/fmars.2021.708775 · Cited by 10 · see citing works
“The results reinforce the idea that tuna eggs and larvae are mainly found in oceanic waters and are constrained by temperatures above 20C, at which they can develop and survive (Reglero et al., 2014).”
ResultSelf-citationMuñoz‐Abril, L., Torres, M., Valle, C. A., Rubianes-Landázuri, F., Galván-Magaña, F., Canty, S. W. J., Terán, M., Brandt, M., Chaves, J., & Grewe, P. (2022) · PLoS ONE · doi:10.1371/journal.pone.0272713 · Cited by 8 · see citing works
“Recent observations reported within the past ten years also support these findings and have demonstrated high occurrences of yellowfin tuna larvae within this regional area of the EPO [56, 57].”
ResultChanto-García, D. A., Saber, S., Macías, D., et al. (2021) · Environmental Science and Pollution Research · doi:10.1007/s11356-021-15700-w · Cited by 10 · see citing works
“But, in the last decades, this pelagic species seems to expand its niche reaching the Mediterranean waters (Reglero et al. 2014; Saber et al. 2020), cohabiting with resident T. alalunga populations (Arrizabalaga et al. 2004).”
BackgroundA global, historical database of tuna, billfish, and saury larval distributions
Buenafe, K. C., Everett, J., Dunn, D., Mercer, J., Suthers, I., Schilling, H., Hinchliffe, C., Dabalà, A., & Richardson, A. (2022) · Scientific Data · doi:10.1038/s41597-022-01528-7 · Cited by 9 · see citing works
Cornic, M., & Rooker, J. (2021) · Journal of Marine Systems · doi:10.1016/j.jmarsys.2021.103524 · Cited by 8 · see citing works
“thynnus (Muhling et al., 2010, 2012; Reglero et al., 2014) and it has been demonstrated that mean abundance during daytime of T.”
BackgroundMethodResultInfluentialArtetxe-Arrate, I., Fraile, I., Farley, J. H., Darnaude, A. M., Clear, N., Rodríguez‐Ezpeleta, N., Dettman, D. L., Pécheyran, C., Krug, I., Médieu, A., et al. (2021) · PLoS ONE · doi:10.1371/journal.pone.0249327 · Cited by 9 · see citing works
“Besides, the submesoscale activity present in the nursery areas can minimize long-distance dispersal, by retaining the larvae near their spawning area [46, 47].”
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
“For some smaller warm-water tunas, adult feeding and spawning grounds greatly overlap (Collette & Nauen 1983, Reglero et al. 2014), and the highest productivity in the Cabo Frio region during the summer favors zooplankton as well as clupeids, an important food group for adults of E. alletteratus…”
BackgroundKumar, K. V. A., Deepa, K. P., Rafeeq, M. M. M., Renjima, G. S., Manjebrayakath, H., Smitha, B., Saravanane, N., Prabhakaran, M., Sanjeevan, V. N., & Sudhakar, M. (2020) · Marine Biology Research · doi:10.1080/17451000.2019.1704018 · Cited by 7 · see citing works
“pelamis are generally considered as archetypal oceanic species (Sund et al. 1981; Reglero et al. 2014) and studies on the larval”
BackgroundInfluentialFujioka, K., Aoki, Y., Tsuda, Y., Okamoto, K., Tsuchida, H., Sasaki, A., & Kiyofuji, H. (2024) · Journal of Fish Biology · doi:10.1111/jfb.15767 · Cited by 8 · see citing works
Rypina, I., Dotzel, M. M., Pratt, L., Hernández, C., & Llopiz, J. (2021) · Progress in Oceanography · doi:10.1016/j.pocean.2021.102514 · Cited by 5 · see citing works
“Selective spawning by bluefin has been inferred from larval presence and adult tagging in the Gulf of Mexico and Mediterranean Sea (Richards et al., 1989; Reglero et al., 2014; Lindo-Atichati et al., 2012; Domingues et al., 2016, Garcia et al., 2005, Teo et al., 2007).”
Evidence of isotopic maternal transmission influence on bluefin tuna (Thunnus thynnus) larval growth
Quintanilla-Hervás, J. M., Malca, E., Lamkin, J. T., Garcı́a, A., & Laiz‐Carrión, R. (2023) · Marine Environmental Research · doi:10.1016/j.marenvres.2023.106112 · Cited by 7 · see citing works
Toward an environmental predictor of tuna recruitment
Woodworth‐Jefcoats, P. A., & Wren, J. L. K. (2020) · Fisheries Oceanography · doi:10.1111/fog.12487 · Cited by 7 · see citing works
Near-global spawning strategies of large pelagic fish
Buenafe, K. C. V., Neubert, S., Scales, K. L., Dunn, D. C., Everett, J. D., Flower, J., Suthers, I. M., Granados-Dieseldorff, P., Dabalà, A., Esturas, K. J., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-63106-w · Cited by 8 · see citing works
“Reglero et al. 13 also found that most tuna spawned in waters of intermediate values of mesoscale activity from eddies, supporting the triad hypothesisofBakun(2006) 15 thatlinksfavorablespawningareastothe physical environment, and suggests that co-location might be a valuable strategy.”
InfluentialVieira, J. M. S., Costa, P. A. S., Braga, A. C., Clemente, S. C. D. S., Ferreira, C. E. L., & da Silva, J. P. (2022) · Aquatic Living Resources · doi:10.1051/alr/2022010 · Cited by 6 · see citing works
“…some smaller tunas, adult feeding and spawning grounds considerably overlap, and sardines and anchovies, which are important food items for frigate tuna, are commonly found associated to upwelled waters in Brazil (Collette and Nauen, 1983; Valentin, 2001; Reglero et al., 2014; Herath et al., 2019).”
BackgroundReglero, P., Tugores, M. P., Titelman, J., Santandreu, M. M., Martin, M., Balbín, R., Álvarez‐Berastegui, D., Torres, A. P., Calcina, N. L., Leyva, L., et al. (2025) · Journal of Plankton Research · doi:10.1093/plankt/fbaf006 · Cited by 6 · see citing works
“…for species inhabiting tropical warm waters (e.g. yellowfin tuna, Thunnus albacares , bigeye tuna, Thunnus obesus ) and for species, such as the Atlantic bluefin tuna ( Thunnus thynnus ), that are well-adapted to cold waters with seasonally warmer periods (Schaefer, 2001; Reglero et al. ,2014).”
Self-citationDewar, H., Snodgrass, O. E., Muhling, B. A., & Schaefer, K. M. (2022) · PLoS ONE · doi:10.1371/journal.pone.0269069 · Cited by 4 · see citing works
Andrews, A. H., Eveson, J. P., Welte, C., Okamoto, K., Satoh, K., Krusic‐Golub, K., Lougheed, B. C., Macdonald, J. I., Roupsard, F., & Farley, J. H. (2024) · ICES Journal of Marine Science · doi:10.1093/icesjms/fsae074 · Cited by 4 · see citing works
Taboada, F. G., Park, J., Muhling, B. A., Tommasi, D., Tanaka, K. R., Rykaczewski, R. R., Stock, C. A. A., & Sarmiento, J. L. (2022) · Journal of Applied Ecology · doi:10.1111/1365-2664.14346 · Cited by 4 · see citing works
Critical thermal limits of Atlantic bluefin tuna (Thunnus thynnus) larvae
Moyano, M., Blanco, E., Ortega, A., et al. (2026) · Journal of Thermal Biology · doi:10.1016/j.jtherbio.2026.104410 · Cited by 3 · see citing works
Self-citationAnderson, G., Macdonald, J. I., Lal, M. M., Hampton, J., Smith, N., & Rico, C. (2023) · Frontiers in Marine Science · doi:10.3389/fmars.2023.1204884 · Cited by 3 · see citing works
Nyuji, M., Soma, S., Higuchi, K., et al. (2024) · Aquaculture · doi:10.1016/j.aquaculture.2024.741359 · Cited by 3 · see citing works
Puerto, M. Á., Saber, S., de Urbina, J. M. O., Gómez-Vives, M. J., García‐Barcelona, S., & Macías, D. (2022) · Scientia Marina · doi:10.3989/scimar.05292.051 · Cited by 4 · see citing works
“Temperature is a very important factor determining the distribution of both adult top predators and larvae (Worm et al. 2005, Reglero et al. 2014).”
BackgroundOrtega, A., Reglero, P., de-la-Gándara, F., et al. (2024) · Fisheries Research · doi:10.1016/j.fishres.2024.107066 · Cited by 3 · see citing works
Self-citationHidalgo, M., Reglero, P., Álvarez‐Berastegui, D., Torres, A. P., Álvarez-Ellacuria, I., Rodríguez, J. M., Carbonell, A., Balbín, R., & Alemany, F. (2015) · Marine Environmental Research · doi:10.1016/j.marenvres.2015.01.001 · Cited by 3 · see citing works
“Recent studies show that the global pattern of marine fish larvae follows large scale gradients (Reglero et al., 2014).”
BackgroundSelf-citationLaiz‐Carrión, R., Gerard, T., Uriarte, A., Malca, E., Muhling, B. A., Alemany, F., Privoznik, S. L., & Shiroza, A. (2014) · DIGITAL.CSIC (Spanish National Research Council (CSIC)) · Cited by 3 · see citing works
Wang, Y., Zhang, Y., Geng, Z., & Zhu, J. (2024) · Frontiers in Marine Science · doi:10.3389/fmars.2024.1392273 · Cited by 2 · see citing works
“The eastern Indian Ocean (R2 in our study) is believed as the main spawning area of bigeye tuna (Reglero et al., 2014; Muhling et al., 2017).”
Navigating large scale ocean science in a Pacific small island developing state
Claassens, L., Hernández, C. M., Biondi, P., Jaskiel, J. E., Karanassos, C. M., Mesengei, M., Nestor, V., Otto, E. I., Renguul, H., Rotjan, R., et al. (2024) · Pacific Conservation Biology · doi:10.1071/pc24062 · Cited by 2 · see citing works
Borrego‐Santos, R., Quintanilla-Hervás, J. M., Laiz‐Carrión, R., García, A., Malca, E., Abascal, F. J., Die, D. J., Riveiro, I., Swalethorp, R., & Landry, M. R. (2025) · Deep Sea Research Part II Topical Studies in Oceanography · doi:10.1016/j.dsr2.2025.105572 · Cited by 2 · see citing works
Changes in spawning patterns of mature and immature female largehead hairtail (Trichiurus japonicus)
Namgung, J., Moon, H.-N., Kim, S., et al. (2025) · Fisheries and aquatic sciences · doi:10.47853/fas.2025.e63 · Cited by 2 · see citing works
Laiz‐Carrión, R., Borrego‐Santos, R., Quintanilla-Hervás, J. M., Quezada‐Romegialli, C., Malca, E., Swalethorp, R., Abascal, F. J., Pennino, M. G., Vargas‐Yáñez, M., Johnstone, C., et al. (2025) · Deep Sea Research Part II Topical Studies in Oceanography · doi:10.1016/j.dsr2.2025.105585 · Cited by 2 · see citing works
Labonne, M., Darnaude, A. M., Fily, T., Petit, C., Nikolic, N., Parker, D., Norman, S., Clear, N., Farley, J., Eveson, J., et al. (2024) · Fishes · doi:10.3390/fishes9010038 · Cited by 1 · see citing works
“These could be located either off South Africa in the southeastern Atlantic or along the Brazilian coast in the southwestern Atlantic, where catches of immature albacore tuna are frequent [15,18].”
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Ottmann, D., Reglero, P., Alemany, F., Álvarez‐Berastegui, D., Martín, M., & Fiksen, Ø. (2022) · Limnology and Oceanography Letters · doi:10.1002/lol2.10241 · Cited by 2 · see citing works
“Furthermore, adults are highly fecund fishes that target spawning grounds shared with other tunas, facilitating encounters among larvae (Reglero et al. 2014).”
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Self-citationDistribution, growth, and transport of larval fishes and implications for population dynamics
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Unveiling population structure in South Pacific albacore: insights from genetics and growth
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“Several larval albacore were collected from tows in the eastern region 55 , and predictions of larval distribution also suggest potential occurrences in the eastern subtropical regions 56 .”
Climate-induced shifts in swordfish spawning habitat in the Western Mediterranean
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Self-citationRichardson, D. E., Marancik, K. E., Adamus, M., Broughton, E. A., Cowen, R. K., Gerard, T., Hernández, C. M., Hoey, J., Llopiz, J., Lutcavage, M., et al. (2026) · Progress in Oceanography · doi:10.1016/j.pocean.2026.103687
Lunar cycle drives family-specific larval fish assemblages in the tropical nearshore ecosystemPreprint
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Pennino, M., Muhling, B., Malca, E., Laiz-Carrión, R., Quintanilla, J., Borrego-Santos, R., Vargas-Yáñez, M., Abascal, F., Beckley, L., & Landry, M. R. (2026) · Deep-sea research. Part II, Topical studies in oceanography · doi:10.1016/j.dsr2.2026.105605 · Cited by 1 · see citing works
Casaucao-Aguilar, A., Mourre, B., Tugores, M. P., Balbín, R., Díaz‐Barroso, L., Hernández‐Carrasco, I., Reglero, P., & Álvarez‐Berastegui, D. (2026) · Frontiers in Marine Science · doi:10.3389/fmars.2026.1705858 · Cited by 1 · see citing works
“For these species, spawning areas are typically characterized by warm oligotrophic waters with low kinetic energy and complex mesoscale oceanography (Muhling et al., 2017; Reglero et al., 2014).”
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“Barriers to dispersal like sub-optimal conditions for adults (e.g., lack of preferred habitat or forage) and lower tolerance for environmental fluctuations in larvae (Reglero et al. 2014) may therefore contribute to the maintenance of structure in yellowfin if present.”
Mnich, A., Zavell, M. D., Muhling, B. A., Hernández, C. M., & Cadrin, S. X. (2026) · Integrative and Comparative Biology · doi:10.1093/icb/icag041
- Authors
- Reglero, P., Tittensor, D., Álvarez-Berastegui, D., Aparicio-González, A., & Worm, B.
- Venue
- Marine Ecology Progress Series
- Publisher
- Inter-Research Science Center
- Published
- 2014-03-31
- Volume
- 501
- Pages
- 207-224
- ISSN
- 0171-8630 (ISSN-L)
- 1616-1599
- OpenAlex
- W2312411547
- Semantic Scholar
- 93d5321db6e8f91ce9daddbb68801a21955350a2
- Cited by
- 106
- References
- 87
- Citations by year
- 2026: 12 · 2025: 9 · 2024: 9 · 2023: 6 · 2022: 9 · 2021: 14 · 2020: 11 · 2019: 7 · 2018: 11 · 2017: 6 · 2016: 6 · 2015: 3 · 2014: 3
- FWCI
- 3.02
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Marine Ecology Progress Series (publishedVersion)
- DIGITAL.CSIC (Spanish National Research Council (CSIC)) (submittedVersion, cc-by-nc-nd)
- Funders
- California Institute of Technology
- National Oceanic and Atmospheric Administration
- Jet Propulsion Laboratory
- 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
- Physical Sciences › Earth and Planetary Sciences › Oceanography › Oceanographic and Atmospheric Processes
- Keywords
- tuna larvae, spawning grounds, larval distribution, eddy kinetic energy, western boundary currents, bluefin tuna, albacore tuna, critical habitat, water temperature, remote sensing
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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