Correction: Local versus Generalized Phenotypes in Two Sympatric Aurelia Species: Understanding Jellyfish Ecology Using Genetics and Morphometrics
Open accessAbstract
For individuals living in environmentally heterogeneous environments, a key component for adaptation and persistence is the extent of phenotypic differentiation in response to local environmental conditions.In order to determine the extent of environmentally induced morphological variation in a natural population distributed along environmental gradients, it is necessary to account for potential genetic differences contributing to morphological differentiation.In this study, we set out to quantify geographic morphological variation in the moon jellyfish Aurelia exposed at the extremes of a latitudinal environmental gradient in the Gulf of Mexico (GoM).We used morphological data based on 28 characters, and genetic data taken from mitochondrial cytochrome oxidase I (COI) and nuclear internal transcribed spacer 1 (ITS-1).Molecular analyses revealed the presence of two genetically distinct species of Aurelia co-occurring in the GoM: Aurelia sp. 9 and Aurelia c.f. sp. 2, named for its divergence from (for COI) and similarity to (for ITS-1) Aurelia sp. 2 (Brazil).Neither species exhibited significant population genetic structure between the Northern and the Southeastern Gulf of Mexico; however, they differed greatly in the degree of geographic morphological variation.The morphology of Aurelia sp. 9 exhibited ecophenotypic plasticity and varied significantly between locations, while morphology of Aurelia c.f. sp. 2 was geographically invariant (i.e., canalized).The plastic, generalist medusae of Aurelia sp. 9 are likely able to produce environmentally-induced, "optimal" phenotypes that confer high relative fitness in different environments.In contrast, the non-plastic generalist individuals of Aurelia c.f. sp. 2 likely produce environmentally-independent phenotypes that provide the highest fitness across environments.These findings suggest the two Aurelia lineages co-occurring in the GoM were likely exposed to different past environmental conditions (i.e., different selective pressures) and evolved different strategies to cope with environmental variation.This study highlights the importance of using genetics and morphometric data to understand jellyfish ecology, evolution and systematics.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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?
A. sp. 9 is synonymized under A. marginalis.
“we decided to synonymize A. sp. 9 under A. marginalis, as in this species’ description, Agassiz (1862) mentions the distinct rose color of the gonads, which is also presented by Chiaverano, Bayha & Graham (2016) for A. sp. 9 when compared to A. cf. sp. 2 (A. montyi sp. nov.)”
From The importance of molecular characters when morphological variability hinders diagnosability: systematics of the moon jellyfish genus <i>Aurelia</i> (Cnidaria: Scyphozoa) (2021) · cites this paper as Chiaverano, Bayha & Graham, 2016
The Categorical features section (page unavailable) reports that gonad color differs between Aurelia sp. 9 and Aurelia c.f. sp. 2, supporting the comparison for which Chiaverano et al. are cited. It does not identify the color as rose or synonymize A. sp. 9 under A. marginalis; the citing sentence presents synonymization as its authors’ own decision. (LLM, conf=0.83)
Experimental — accuracy not yet measuredAgassiz (1862) mentions the distinct rose color of the gonads in A. marginalis, which is also presented by Chiaverano, Bayha & Graham (2016) for A. sp. 9 when compared to A. cf. sp. 2.
“we decided to synonymize A. sp. 9 under A. marginalis, as in this species’ description, Agassiz (1862) mentions the distinct rose color of the gonads, which is also presented by Chiaverano, Bayha & Graham (2016) for A. sp. 9 when compared to A. cf. sp. 2 (A. montyi sp. nov.)”
From The importance of molecular characters when morphological variability hinders diagnosability: systematics of the moon jellyfish genus <i>Aurelia</i> (Cnidaria: Scyphozoa) (2021) · cites this paper as Chiaverano, Bayha & Graham, 2016
The Categorical features section reports that gonad tissue color differed between Aurelia sp. 9 and Aurelia c.f. sp. 2 independently of location. It does not specify that the gonads of Aurelia sp. 9 were rose-colored, so that detail is not supported by our copy. (LLM, conf=0.86)
Experimental — accuracy not yet measuredChiaverano, Bayha & Graham (2016) sequenced one specimen from Dauphin Island (DI'03-4), which in their COI phylogeny did not group with any other species, while in the ITS1 phylogeny fell within A. marginalis.
“Chiaverano, Bayha & Graham (2016) sequenced one specimen from Dauphin Island (DI’03-4), which in their COI phylogeny did not group with any other species, while in the ITS1 phylogeny fell within A. marginalis (previously recognized as Aurelia sp. 9; also see Table S4 and Figs. S5–S6).”
From The importance of molecular characters when morphological variability hinders diagnosability: systematics of the moon jellyfish genus <i>Aurelia</i> (Cnidaria: Scyphozoa) (2021) · cites this paper as Chiaverano, Bayha & Graham, 2016
The Molecular analysis section reports that specimen DI'03-4 did not group with any species in the COI phylogeny, and the Fig. 4 caption identifies DI as Dauphin Island. The ITS-1 results describe clades but do not place DI'03-4 specifically within one; our copy also calls the relevant lineage Aurelia sp. 9, without identifying it as A. marginalis. No page numbers are available in our copy. (LLM, conf=0.87)
Experimental — accuracy not yet measuredControlled conditions that reflect a certain morphological pattern corroborate the hypothesis for environmentally determined morphological plasticity.
“Controlled conditions that reflect a certain morphological pattern corroborates the hypothesis for environmentally determined morphological plasticity, which has already been demonstrated for medusae of an Aurelia species in the field (Chiaverano, Bayha & Graham, 2016).”
From The importance of molecular characters when morphological variability hinders diagnosability: systematics of the moon jellyfish genus <i>Aurelia</i> (Cnidaria: Scyphozoa) (2021) · cites this paper as Chiaverano, Bayha & Graham, 2016
The Discussion (page not provided) reports geographic morphological variation in field-sampled Aurelia sp. 9 without significant genetic structure and interprets it as likely environmentally induced plasticity. That supports the cited field example, but the paper presents plasticity as a likely explanation, not as conclusively demonstrated. The citing authors’ statement about their controlled conditions is not attributed to this source. (LLM, conf=0.86)
Experimental — accuracy not yet measuredSize correction was applied to all individuals by adapting the method of Lleonart, Salat & Torres (2000) to account for allometric differences.
“we scaled all individuals to the same f1 by adapting the method of Lleonart, Salat & Torres, (2000), which has been previously used for various animals including jellyfish (Chiaverano, Bayha & Graham, 2016).”
From The importance of molecular characters when morphological variability hinders diagnosability: systematics of the moon jellyfish genus <i>Aurelia</i> (Cnidaria: Scyphozoa) (2021) · cites this paper as Chiaverano, Bayha & Graham, 2016
These two taxa considered as separate species should not come as a surprise, as previous studies also demonstrated the occurrence of another sympatric species in the area, A. montyi sp. nov.
“These two taxa considered as separate species should not come as a surprise, as previous studies also demonstrated the occurrence of another sympatric species in the area, A. montyi sp. nov. (recognized as Aurelia cf. sp. 2 in Chiaverano, Bayha & Graham, 2016; described herein).”
From The importance of molecular characters when morphological variability hinders diagnosability: systematics of the moon jellyfish genus <i>Aurelia</i> (Cnidaria: Scyphozoa) (2021) · cites this paper as Chiaverano, Bayha & Graham, 2016
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
No references could be resolved yet.
Research works printed but not linked: 90
- Moran NA. The evolutionary maintenance of alternative phenotypes. Am Nat. 1992; 1: 971-989.
- Donaldson-Matasci M, Lachmann M, Bergstrom C. Phenotypic diversity as an adaptation to environ- mental uncertainty. Evol Ecol Res. 2008; 10: 493-515.
- Stearns S. The evolutionary significance of phenotypic plasticity. Bioscience. 1989; 39: 436-445.
- Sultan SE, Spencer HG. Metapopulation structure favors plasticity over local adaptation. Am Nat. 2002; 160: 271-283. doi: 10.1086/341015 PMID: 18707492 · DOI
- Torres-Dowdall J, Handelsman CA, Reznick DN, Ghalambor CK. Local adaptation and the evolution of phenotypic plasticity in Trinidadian guppies (Poecilia reticulata). Evolution. 2012; 66: 3432-43. doi: 10. 1111/j.1558-5646.2012.01694.x PMID: 23106708 · DOI
- Pigliucci M. Phenotypic Plasticity: Beyond Nature and Nurture. JHU Press; 2001.
- Kawecki T, Ebert D. Conceptual issues in local adaptation. Ecol Lett. 2004; 7: 1225-1241.
- Crispo E. Modifying effects of phenotypic plasticity on interactions among natural selection, adaptation and gene flow. J Evol Biol. 2008; 21: 1460-1469. doi: 10.1111/j.1420-9101.2008.01592.x PMID: 18681916 · DOI
- Murren C, Auld J, Callahan H. Constraints on the evolution of phenotypic plasticity: limits and costs of phenotype and plasticity. Heredity. 2015; 115: 293-301. doi: 10.1038/hdy.2015.8 PMID: 25690179 · DOI
- Siegal M, Bergman A. Waddington's canalization revisited: developmental stability and evolution. Proc Natl Acad Sci. 2002; 16: 10528-10532.
- Flatt T. The evolutionary genetics of canalization. Q Rev Biol. 2005; 80: 287-316. PMID: 16250465
- Alvarado-Serrano D. Localized versus generalist phenotypes in a broadly distributed tropical mammal: how is intraspecific variation distributed across disparate environments? BMC Evol Biol. 2013; 13:1- 16.
- Dawson MN, Hamner WM. A character-based analysis of the evolution of jellyfish blooms: adaptation and exaptation. Hydrobiologia. 2009; 616: 193-215.
- Purcell J, Arai M. Interactions of pelagic cnidarians and ctenophores with fish: a review. Hydrobiologia. 2001; 451: 27-44.
- Stibor H, Tokle N. Feeding and asexual reproduction of the jellyfish Sarsia gemmifera in response to resource enrichment. Oecologia. 2003; 135: 202-208. PMID: 12698341
- Richardson JA, Bakun A, Hays GC, Gibbons MJ. The jellyfish joyride: causes, consequences and man- agement responses to a more gelatinous future. Trends Ecol Evol. 2009; 24: 312-322. doi: 10.1016/j. tree.2009.01.010 PMID: 19324452 · DOI
- Robinson KL, Ruzicka JJ, Hernandez FJ, Graham WM, Decker MB, Brodeur RD, et al. Evaluating energy flows through jellyfish and gulf menhaden (Brevoortia patronus) and the effects of fishing on the northern Gulf of Mexico ecosystem. ICES J Mar Sci. 2015; doi: 10.1093/icesjms/fsv088 · DOI
- Doyle T, Haas H De. Widespread occurrence of the jellyfish Pelagia noctiluca in Irish coastal and shelf waters. J Plankton Res. 2008; 30: 963-968.
- Dong Z, Liu D, Keesing JK. Jellyfish blooms in China: Dominant species, causes and consequences. Mar Pollut Bull. 2010; 60: 954-963. doi: 10.1016/j.marpolbul.2010.04.022 PMID: 20553695 · DOI
- Delannoy CMJ, Houghton JDR, Fleming NEC, Ferguson HW. Mauve Stingers (Pelagia noctiluca) as carriers of the bacterial fish pathogen Tenacibaculum maritimum. Aquaculture. 2011; 311: 255-257.
- Purcell J, Uye S, Lo W. Anthropogenic causes of jellyfish blooms and their direct consequences for humans: a review. Mar Ecol Prog Ser. 2007; 350: 153-174.
- Daryanabard R, Dawson MN. Jellyfish blooms: Crambionella orsini (Scyphozoa: Rhizostomeae) in the Gulf of Oman, Iran, 2002-2003. J Mar Biol Assoc UK. 2008; 88: 477-483.
- Fenner PJ, Williamson JA, Burnett JW. Clinical aspects of envenomation by marine animals. Toxicon. 1996; 34: 41-101.
- Chiaverano LM, Holland BS, Crow GL, Blair L, Yanagihara AA. Long-term fluctuations in circalunar beach aggregations of the box jellyfish Alatina moseri in Hawaii, with links to environmental variability. PLOS ONE 8(10): e77039. doi: 10.1371/journal.pone.0077039 PMID: 24194856 · DOI
- Robinson KL, Graham WM. Long-term change in the abundances of northern Gulf of Mexico scypho- medusae Chrysaora sp. and Aurelia spp. with links to climate variability. Limnol Ocean. 2013; 58: 235- 253.
- Purcell JE. Jellyfish and ctenophore blooms coincide with human proliferations and environmental per- turbations. Ann Rev Mar Sci. 2012; 4: 209-235. PMID: 22457974
- Lucas CH. Reproduction and life history statregies of the common jellyfish, Aurelia aurita, in relation to its ambient environment. Hydrobiologia. 2001; 451: 229-246.
- Condon RH, Duarte CM, Pitt KA, Robinson KL, Lucas CH, Sutherland KR, et al. Recurrent jellyfish blooms are a consequence of global oscillations. Proc Natl Acad Sci. 2013; 110: 1000-1005. doi: 10. 1073/pnas.1210920110 PMID: 23277544 · DOI
- Arnold S. Morphology, performance and fitness. Am Zool. 1983; 23: 347-361.
- Dawson MN. Macro-morphological variation among cryptic species of the moon jellyfish, Aurelia (Cni- daria: Scyphozoa). Mar Biol. 2003; 143: 369-379.
- Holland BS, Dawson MN, Crow GL, Hofmann DK. Global phylogeography of Cassiopea (Scyphozoa: Rhizostomeae): molecular evidence for cryptic species and multiple invasions in the Hawaiian Islands. Mar Biol. 2004; 145: 1119-1128.
- Bayha KM, Dawson MN. New Family of Allomorphic Jellyfishes, Drymonematidae (Scyphozoa, Disco- medusae), Emphasizes Evolution in the Functional Morphology and Trophic Ecology of Gelatinous Zooplankton. Biol Bull. 2010; 219: 249-267. PMID: 21183445
- Dawson MN. Cyanea capillata is not a cosmopolitan jellyfish: morphological and molecular evidence for C. annaskala and C. rosea (Scyphozoa: Semaeostomeae: Cyaneidae) in south-eastern Australia. Invertebr Syst. 2005; 19: 361-370.
- Dawson MN. Morphological variation and systematics in the Scyphozoa: Mastigias (Rhizostomeae, Mastigiidae)-a golden unstandard? Hydrobiologia. 2005; 537: 185-206.
- Lohrenz S, Fahnenstiel G, Redalje D. Variations in primary production of northern Gulf of Mexico conti- nental shelf waters linked to nutrient inputs from the Mississippi river. Mar Ecol. 1997; 155:45-54.
- Holt R, Gomulkiewicz R. How does immigration influence local adaptation? A reexamination of a famil- iar paradigm. Am Nat. 1997; 149: 563-572.
- Tienderen P Van. Generalists, specialists, and the evolution of phenotypic plasticity in sympatric popu- lations of distinct species. Evolution. 1997; 1: 1372-1380.
- Ausubel F, Brent R, Kingston R, Moore D, Seidman J, Smith J SK. Current Protocols in Molecular Biol- ogy. Wiley and Sons, New York. Wiley and Sons, New York; 1989.
- Dawson MN, Jacobs DK. Molecular evidence for cryptic species of Aurelia aurita (Cnidaria: Scypho- zoa). Biol Bull. 2001; 200: 92-96. PMID: 11249217
- Dawson MN. Five new subespecies of Mastigias (Scyphozoa: Rhizostomeae: Mastigiidae) from marine lakes, Palau, Micronesia. J Mar Biol Assoc United Kingdom. 2005; 85: 679-694.
- Dawson MN, Gupta AS, England MH. Coupled biophysical global ocean mode and molecular genetic analyses identify multiple introductions of crytogenic species. Proc Natl Acad Sci. 2005; 102: 11968- 11973. PMID: 16103373
- Vrijenhoek R. DNA primers for amplification of mitochondrial cytochrome c oxidase subunit I from diverse metazoan invertebrates. Mol Mar Biol Biotechnol. 1994; 3: 294-9. PMID: 7881515
- Bayha K. The molecular systematics and population genetics of four coastal ctenophores and scypho- zoan jellyfish of the US Atlantic and Gulf of Mexico. PhD Dissertation, The University of Delaware. 2005.
- Larkin M, Blackshields G, Brown N. Clustal W and Clustal X version 2.0. Bioinformatics. 2007; 23: 2947-2948. PMID: 17846036
- Katoh K, Standley D. MAFFT multiple sequence alignment software version 7: improvements in perfor- mance and usability. Mol Biol Evol. 2013; 30:772-80. doi: 10.1093/molbev/mst010 PMID: 23329690 · DOI · Paper page
- Katoh K, Toh H. Recent developments in the MAFFT multiple sequence alignment program. Briefings Bioinformatics. 2008; 9:286-98.
- Schroth W, Jarms G, Streit B, Schierwater B. Speciation and phylogeography in the cosmopolitan marine moon jelly, Aurelia sp. BMC Evol Biol. 2002; 2: 1-10. PMID: 11801181
- Castresana J. Selection of conserved blocks from multiple alignments for their use in phylogenetic anal- ysis. Mol Biol Evol. 2000; 17: 540-52. PMID: 10742046
- Guindon S, Dufayard J-F, Lefort V, Anisimova M, Hordijk W, Gascuel O. New algorithms and methods to estimate maximum-likelihood phylogenies: assessing the performance of PhyML 3.0. Syst Biol. 59: 307-21. doi: 10.1093/sysbio/syq010 PMID: 20525638 · DOI · Paper page
- Darriba D, Taboada G, Doallo R, Posada D. jModelTest 2: more models, new heuristics and parallel computing. Nat Methods. 2012; 9: 772.
- Ronquist F, Teslenko M, van der Mark P, Ayres DL, Darling A, Höhna S, et al. MrBayes 3.2: efficient Bayesian phylogenetic inference and model choice across a large model space. Syst Biol. 2012; 61: 539-42. doi: 10.1093/sysbio/sys029 PMID: 22357727 · DOI
- Bayha KM, Dawson MN, Collins AG, Barbeitos MS, Haddock SHD. Evolutionary relationships among scyphozoan jellyfish families based on complete taxon aampling and phylogenetic analyses of 18S and 28S ribosomal DNA. Integr Comp Biol. 2010; 50: 436-455. doi: 10.1093/icb/icq074 PMID: 21558214 · DOI · Paper page
- Tamura K, Dudley J, Nei M, Kumar S. MEGA4: molecular evolutionary genetics analysis (MEGA) soft- ware version 4.0. Mol Biol Evol. 2007; 24: 1596-1599. PMID: 17488738
- Gouy M, Guindon S, Gascuel O. SeaView version 4: A multiplatform graphical user interface for sequence alignment and phylogenetic tree building. Mol Biol Evol. 2010; 27: 221-224. doi: 10.1093/ molbev/msp259 PMID: 19854763 · DOI
- Excoffier L, Lischer H. Arlequin suite ver 3.5: a new series of programs to perform population genetics analyses under Linux and Windows. Mol Ecol Resour. 2010; 10: 564-567. doi: 10.1111/j.1755-0998. 2010.02847.x PMID: 21565059 · DOI
- Clement M, Posada D, Crandall K. TCS: a computer program to estimate gene genealogies. Mol Ecol. 2000; 9: 1657-1659. PMID: 11050560
- Greenberg N, Garthwaite RL, Potts DC. Allozyme and morphological evidence for a newly introduced species of Aurelia in San Francisco Bay, California. Mar Biol. 1996; 125: 401-410.
- Miyake H, Iwao K, Kakinuma Y. Life history and environment of Aurelia aurita. South Pacific Study. 1997; 17: 273-285.
- Bolton TZ, Graham WM. Morphological variation among populations of an invasive jellyfish. Mar Ecol Prog Ser. 2004; 278: 125-139.
- Lleonart J, Salat J, Torres GJ. Removing allometric effects of body size in morphological analysis. J Theor Biol. 2000; 205: 85-93. PMID: 10860702
- Dawson MN. Cyanea capillata is not a cosmopolitan jellyfish: morphological and molecular evidence for C. annaskala and C. rosea (Scyphozoa: Semaeostomeae: Cyaneidae) in south-eastern Australia. Invertebr Syst. 2005; 19: 361-370.
- Kolbasova GD, Zalevsky AO, Gafurov AR, Gusev PO, Ezhova MA, Zheludkevich AA, et al. A new spe- cies of Cyanea jellyfish sympatric to C. capillata in the White Sea. Polar Biol. 2015; 38: 1439-1451.
- Huang D, Meier R, Todd PA, Chou LM. Slow mitochondrial COI sequence evolution at the base of the metazoan tree and its implications for DNA barcoding. J Mol Evol. 2008; 66: 167-74. doi: 10.1007/ s00239-008-9069-5 PMID: 18259800 · DOI
- He J, Zheng L, Zhang W, Lin Y. Life cycle reversal in Aurelia sp.1 (Cnidaria, Scyphozoa). PLOS One. 2015; 10: e0145314. doi: 10.1371/journal.pone.0145314 PMID: 26690755 · DOI
- Knowlton N, Weigt L. New dates and new rates for divergence across the Isthmus of Panama. Royal Soc Lon B: Biol Sci. 1998; 265: 2257-2263.
- Peterson KJ, Lyons JB, Nowak KS, Takacs CM, Wargo MJ, McPeek MA. Estimating metazoan diver- gence times with a molecular clock. Proc Natl Acad Sci. 2004 101: 6536-6541. PMID: 15084738
- Marko P. Fossil calibration of molecular clocks and the divergence times of geminate species pairs sep- arated by the Isthmus of Panama. Mol Biol Evol. 2002; 19: 2005-2021. PMID: 12411609
- Govindarajan A, Halanych K, Cunningham C. Mitochondrial evolution and phylogeography in the hydrozoan Obelia geniculata (Cnidaria). Mar Biol. 2005; 146: 213-22.
- Stopar K, Ramšak A, Trontelj P, Malej A. Lack of genetic structure in the jellyfish Pelagia noctiluca (Cni- daria: Scyphozoa: Semaeostomeae) across European seas. Mol Phylogenetics Evol 2010; 57: 417- 28.
- Crispo E, Chapman L. Geographic variation in phenotypic plasticity in response to dissolved oxygen in an African cichlid fish. J Evol Biol. 2010; 23: 2091-103. doi: 10.1111/j.1420-9101.2010.02069.x PMID: 20722894 · DOI
- Saint-Laurent R, Legault M, Bernatchez L. Divergent selection maintains adaptive differentiation despite high gene flow between sympatric rainbow smelt ecotypes (Osmerus mordax Mitchill). Mol Ecol. 2003; 12: 315-30. PMID: 12535084
- Lind M, Ingvarsson P, Johansson H. Gene flow and selection on phenotypic plasticity in an island sys- tem of Rana temporaria. Evolution. 2011; 65: 684-697. doi: 10.1111/j.1558-5646.2010.01122.x PMID: 20825480 · DOI
- Price T. The role of phenotypic plasticity in driving genetic evolution. Proc Royal Soc London B: Biol Sci. 2003; 270: 1433-1440.
- Scheiner SM, Holt RD. The genetics of phenotypic plasticity. X. Variation versus uncertainty. Ecol Evol. 2012; 2: 751-767. doi: 10.1002/ece3.217 PMID: 22837824 · DOI
- Roden C, Lohoefner RR, Rogers CM, Mullin K, Hoggard BW. Aspects of the ecology of the moon jelly- fish, Aurelia aurita, in the northern Gulf of Mexico. Northeast Gulf Sci. 1990; 11: 63-67.
- Lucas CH, Lawes S. Sexual reproduction of the scyphomedusa Aurelia aurita in relation to temperature and variable food supply. Mar Biol. 1998; 131: 629-638.
- Ishii H, Båmstedt U. Food regulation of growth and maturation in a natural population of Aurelia aurita. J Plankton Res. 1998; 20: 805-816.
- Atkinson D. Temperature and organism size-a biological law for ectotherms? Adv Ecol Res. 1994; 25: 1-58.
- Kingsolver JG, Huey RB. Size, temperature, and fitness: three rules. Evol Ecol Res. 2008; 10: 251- 268.
- Stearns SC. The Evolution of Life Histories. Oxford Univ Press Oxford. 1992;
- Lucas CH. Population dynamics of Aurelia aurita (Scyphozoa) from an isolated brackish lake, with par- ticular reference to sexual reproduction. J Plankton Res. 1996; 18: 987-1007.
- Saucedo L. Fecundidad de la medusa Stomolophus meleagris (Rhizostomeae: Stomolophidae) en el Golfo de California. Revista de Biología Tropical. 2012; 60: 1721-1729.
- Ishii H, Takagi A. Development time of planulae larvae on the oral arms of the scyphomedusa Aurelia aurita. J Plankton Res. 2003; 25: 1447-1450.
- Le Rouzic A, Álvarez-Castro JM, Hansen TF. The Evolution of canalization and evolvability in stable and fluctuating environments. Evol Biol. 2013; 40: 317-340.
- Crispo E. The Baldwin effect and genetic assimilation: revisiting two mechanisms of evolutionary change mediated by phenotypic plasticity. Evolution 2007; 61: 2469-2479. PMID: 17714500
- Gibson G, Wagner G. Canalization in evolutionary genetics: a stabilizing theory? BioEssays. 2000; 22: 372-380. PMID: 10723034
- Debat V, David P. Mapping phenotypes: canalization, plasticity and developmental stability. Trends Ecol Evol. 2001; 16: 555-561.
- Conover DO, Schultz ET. Phenotypic similarity and the evolutionary significance of countergradient variation. Trends Ecol Evol. 1995; 10: 248-252. doi: 10.1016/S0169-5347(00)89081-3 PMID: 21237029 · DOI
- Dawson MN, Martin DL. Geographic variation and ecological adaptation in Aurelia aurita (Scyphozoa, Semaestomeae): some implications from molecular phylogenetics. Hydrobiologia. 2001; 451: 259- 273.
- Lessios H. The great American schism: divergence of marine organisms after the rise of the Central American Isthmus. Annu Rev Ecol Evol Syst. 2008; 1:63-91.
Cited by
Sorted by citations
Lawley, J. W., Gamero-Mora, E., Maronna, M. M., Chiaverano, L. M., Stampar, S. N., Hopcroft, R. R., Collins, A. G., & Morandini, A. C. (2021) · PeerJ · doi:10.7717/peerj.11954 · Cited by 71 · see citing works
Self-citation
- Authors
- Chiaverano, L. M., Bayha, K. M., & Graham, W. M.
- Affiliations
- Australian Museum (AU)
- American Association For The Advancement of Science (US)
- Stennis Space Center (US)
- Venue
- PLOS ONE
- Publisher
- Public Library of Science (PLoS)
- Published
- 2016-08-25
- Volume
- 11
- Issue
- 8
- Pages
- e0162118
- ISSN
- 1932-6203 (ISSN-L)
- OpenAlex
- W4244416466
- Cited by
- 5
- References
- 0
- Citations by year
- 2021: 4 · 2019: 1
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- cc-by
- Locations
- PLoS ONE (publishedVersion, cc-by)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- NOAA Institutional Repository (submittedVersion, cc-by)
- Funders
- National Science Foundation (9733441)
- Mississippi-Alabama Sea Grant Consortium
- Topics
- Physical Sciences › Earth and Planetary Sciences › Paleontology › Marine Invertebrate Physiology and Ecology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic diversity and population structure
- Physical Sciences › Environmental Science › Ecology › Coral and Marine Ecosystems Studies
- Keywords
- Aurelia, Aurelia aurita, phenotypic plasticity, morphological variation, canalization, sympatric species, population structure, COI, ITS1, Gulf of Mexico
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.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review