Intraspecific Morphometric Variation in a New Species of Ceratomyxa Thélohan 1892 (Cnidaria) from the South Atlantic Ocean: An Ecomorphological Study Using Geometric Morphometrics

. 2025 Jan 16 ; 14 (1) : . [epub] 20250116

Status PubMed-not-MEDLINE Jazyk angličtina Země Švýcarsko Médium electronic

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid39857309

A new species of Ceratomyxa (Ceratomyxidae, Myxosporea) was found infecting the gall bladder of the Argentine croaker Umbrina canosai Berg 1895 (Sciaenidae, Perciformes) from the Argentine sea. Using an integrative taxonomic approach that combines morphological, bioecological, and molecular analyses, we provide evidence that clearly differentiates this species from known taxa and formally describe Ceratomyxa fialai as a new species. This study is the first to apply landmark-based geometric morphometrics (GM) in myxozoan research, providing a detailed analysis of conspecific morphometric variation of ceratomyxid myxospores, examining their natural variation within and among different ceratomyxids infecting the gall bladder of U. canosai. Using GM analyses, we successfully capture and quantify phenotypic variation at the organismal level. Our results suggest that myxospore shape variation may be driven by both developmental noise and phenotypic plasticity. The work highlights the utility of GM in advancing the understanding of myxozoan morphology and its evolutionary implications and emphasizes the need for further research on myxospore shape evolution and its ecological and adaptive significance in natural populations.

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Kent M.L., Andree K.B., Bartholomew J.L., El-Matbouli M., Desser S.S., Devlin R.H., Feist S.W., Hedrick R.P., Hoffmann R.W., Khattra J., et al. Recent Advances in Our Knowledge of the Myxozoa. J. Eukaryot. Microbiol. 2001;48:395–413. doi: 10.1111/j.1550-7408.2001.tb00173.x. PubMed DOI

Lom J., Dyková I. Myxozoan genera: Definition and notes on taxonomy, life-cycle terminology and pathogenic species. Folia Parasitol. 2006;53:1–36. doi: 10.14411/fp.2006.001. PubMed DOI

Eszterbauer E., Atkinson S., Diamant A., Morris D., El-Matbouli M., Hartikainen H. Myxozoan Life Cycles: Practical Approaches and Insights. In: Okamura B., Gruhl A., Bartholomew J., editors. Myxozoan Evolution, Ecology and Development. Springer; Cham, Switzerland: 2015. pp. 175–198. DOI

Okamura B., Hartigan A., Naldoni J. Extensive uncharted biodiversity: The parasite dimension. Integr. Comp. Biol. 2018;58:1132–1145. doi: 10.1093/icb/icy039. PubMed DOI

Eiras J.C. Synopsis of the species of Ceratomyxa Thélohan, 1892 (Myxozoa: Myxosporea: Ceratomyxidae) Syst. Parasitol. 2006;65:49–71. doi: 10.1007/s11230-006-9039-5. PubMed DOI

Gunter N.L., Whipps C.M., Adlard R.D. Ceratomyxa (Myxozoa: Bivalvulida): Robust taxon or genus of convenience? Int. J. Parasitol. 2009;39:1395–1405. doi: 10.1016/j.ijpara.2009.04.008. PubMed DOI

Gunter N.L., Adlard R.D. The demise of Leptotheca Thélohan, 1895 (Myxozoa: Myxosporea: Ceratomyxidae) and assignment of its species to Ceratomyxa Thélohan, 1892 (Myxosporea: Ceratomyxidae), Ellipsomyxa Køie, 2003 (Myxosporea: Ceratomyxidae), Myxobolus Bütschli, 1882 and Sphaerospora Thélohan, 1892 (Myxosporea: Sphaerosporidae) Syst. Parasitol. 2010;75:81–104. doi: 10.1007/s11230-009-9227-1. PubMed DOI

Özer A., Yurakhno V., Öztürk T., Kornyychuk Y.M. Myxosporean parasites of Ceratomyxa merlangi and Myxidium gadi in whiting Merlangius merlangus: A comparative epizootiological analysis based on samples from two localities off southern and northern coasts of the Black Sea. Parasitol. Res. 2017;116:2463–2469. doi: 10.1007/s00436-017-5550-7. PubMed DOI

Abdel-Baki A.-A.S., Al-Qahtani H.A., Almalki E., Al-Quraishy S., Ghamdi A.A., Mansour L. Morphometric criteria and partial sequence of the 18S rRNA gene of Ceratomyxa sultani n. sp. from the gallbladder of Upeneus margarethae in the Arabian Gulf, with a note on its seasonal prevalence. Saudi J. Biol. Sci. 2018;25:597–603. doi: 10.1016/j.sjbs.2017.12.001. PubMed DOI PMC

Eiras J.C., Cruz C., Saravia A. Synopsis of the species of Ceratomyxa Thélohan, 1892 (Cnidaria, Myxosporea, Ceratomyxidae) described between 2007 and 2017. Syst. Parasitol. 2018;95:427–446. doi: 10.1007/s11230-018-9791-3. PubMed DOI

Garbouj M., Rangel L.F., Santos M.J., Bahri S. Ceratomyxa gouletti n. sp. (Myxosporea: Ceratomyxidae), a parasite of the red scorpionfish Scorpaena scrofa (L.) from Tunisian waters. Parasitol. Res. 2018;117:1933–1939. doi: 10.1007/s00436-018-5888-5. PubMed DOI

Zatti S.A., Atkinson S.A., Maia A.A.M., Bartholomew J.L., Adriano E.A. Ceratomyxa gracillima n. sp. (Cnidaria: Myxosporea) provides evidence of panmixia and ceratomyxid radiation in the Amazon basin. Parasitology. 2018;145:1137–1146. doi: 10.1017/S0031182017002323. PubMed DOI

Qiao Y., Shao Y., Pengsakul T., Chen C., Shuli S., Zheng S., Wu W., Hardjo T.B. Morphological and molecular characterization of Ceratomyxa batam n. sp. (Myxozoa: Ceratomyxidae) infecting the gallbladder of the cultured Trachinotus ovatus (Perciformes: Carangidae) in Batam Island, Indonesia. Parasitol. Res. 2019;118:1647–1651. doi: 10.1007/s00436-019-06217-w. PubMed DOI

Thabet A., Abdel-Baki A.-A.S., Harrath A.H., Mansour L. Morphological and molecular aspects of Ceratomyxa ghannouchensis n. sp. and C. pallida Thélohan 1894 infecting the bogue, Boops boops (L.) J. Nat. Hist. 2019;53:541–556. doi: 10.1080/00222933.2019.1597202. DOI

Zhang D., Zhao Y., Yang S., Yang C. Morphological and Molecular Identification of a Novel Species, Ceratomyxa siganicola n. sp. (Myxozoa: Ceratomyxidae) from Siganus fuscescens, in East China Sea. Acta Parasitol. 2019;64:596–602. doi: 10.2478/s11686-019-00077-1. PubMed DOI

Azizi R., Yemmen C., Rangel L.F., Santos M.J., Bahri S. Morphology, seasonality and molecular characterization of Ceratomyxa draconis n. sp. parasite of Trachinus draco (L.) from the Bay of Bizerte, Tunisia. Parasitol. Res. 2020;119:2431–2438. doi: 10.1007/s00436-020-06664-w. PubMed DOI

Bouderbala K., Rangel L.F., Santos M.J., Bahri S. Ceratomyxa mennani n. sp. (Myxosporea: Bivalvulida) parasitizing the gallbladder of the dusky grouper Epinephelus marginatus (Serranidae) from Tunisian waters. Parasitol. Res. 2020;119:1515–1522. doi: 10.1007/s00436-020-06649-9. PubMed DOI

da Silva M.F., Ferreira Barroso de Carvalho A.E., Hamoy I., Matos E.R. Coelozoic parasite of the family Ceratomyxidae (Myxozoa, Bivalvulida) described from motile vermiform plasmodia found in Hemiodus unimaculatus Bloch, 1794. Parasitol. Res. 2021;119:871–878. doi: 10.1007/s00436-019-06505-5. PubMed DOI

Surendran S., Chandran A., Vijayagopal P., Sanil N.K. Morphological and molecular characterization of Ceratomyxa xanthopteri n. sp. (Myxosporea: Ceratomyxidae) from the marine ornamental fish Acanthurus xanthopterus Valenciennes 1835 (Acanthuridae) off Vizhinjam coast, Kerala. Parasitol. Res. 2021;120:2445–2453. doi: 10.1007/s00436-021-07168-x. PubMed DOI

Alama-Bermejo G., Hernández-Orts J.S., Huchon D., Atkinson S.D. Two novel myxosporean parasite species of Ceratomyxa Thélohan, 1892 from the banded cusk-eel Raneya brasiliensis (Kaup) (Ophidiiformes: Ophidiidae) off Patagonia, Argentina. Parasitol. Res. 2021;85:102433. doi: 10.1016/j.parint.2021.102433. PubMed DOI

Lom J., Arthur J.R. A guideline for the preparation of species descriptions in Myxosporea. J. Fish Dis. 1989;12:151–156. doi: 10.1111/j.1365-2761.1989.tb00287.x. DOI

Heiniger H., Gunter N.L., Adlard R.D. Relationships between four novel ceratomyxid parasites from the gall bladders of labrid fishes from Heron Island, Australia. Parasitol. Int. 2008;57:158–165. doi: 10.1016/j.parint.2007.11.006. PubMed DOI

Bookstein F.L. Combining the tools of Geometric Morphometrics. In: Marcus L.F., Corti M., Loy A., Naylor G.J.P., Slice D.E., editors. Advances in Morphometrics. Springer; Boston, MA, USA: 1996. pp. 131–151. DOI

Adams D.C., Rohlf F.J., Slice D.E. Geometric morphometrics: Ten years of progress following the ‘revolution’. Ital. J. Zool. 2004;71:5–16. doi: 10.1080/11250000409356545. DOI

Zelditch M., Swiderski D.L., Sheets H.D. Geometric Morphometrics for Biologists: A Primer. 2nd ed. Elsevier Science; Amsterdam, The Netherlands: 2012. 488p. DOI

Marcotegui P., Islas-Ortega A., Cantatore D., Reshaid Y., Montes M., Barneche J., Martorelli S. Two methods for geometric morphometric analysis of trichodinids from killifishes. Parasitol. Res. 2024;123:332. doi: 10.1007/s00436-024-08354-3. PubMed DOI

Zhai Y., Whipps C.M., Gu Z., Guo Q., Wu Z., Wang H., Liu Y. Intraspecific morphometric variation in myxosporeans. Folia Parasitol. 2016;63:011. doi: 10.14411/fp.2016.011. PubMed DOI

Sitjá-Bobadilla A., Alvarez-Pellitero P. Light and electron-microscopic description of Ceratomyxa labracis n. sp. and a redescription of C. diplodae (Myxosporea, Bivalvulida) from wild and cultured Mediterranean Sea Bass Dicentrarchus labrax (L.) (Teleostei, Serranidae) Syst. Parasitol. 1993;26:215–223. doi: 10.1007/BF00009729. DOI

Bartošová-Sojkovaá P., Lövy A., Reed C.C., Lisnerová M., Tomková T., Holzer A.S., Fiala I. Life in a rock pool: Radiation and population genetics of myxozoan parasites in hosts inhabiting restricted spaces. PLoS ONE. 2018;13:e0194042. doi: 10.1371/journal.pone.0194042. PubMed DOI PMC

Morrison C.M., Martelli D.J., Leggiadro C., O’Neil D. Ceratomyxa drapanopsettae in the gallbladder of Atlantic halibut Hippoglossus hippoglossus, from the northwest Atlantic Ocean. Folia Parasitol. 1996;43:20–36. PubMed

Fiala I., Bartošová P. History of myxozoan character evolution on the basis of rDNA and EF-2 data. BMC Evol. Biol. 2010;10:228. doi: 10.1186/1471-2148-10-228. PubMed DOI PMC

Liu Y., Lövy A., Gu Z., Fiala I. Phylogeny of Myxobolidae (Myxozoa) and the evolution of myxospore appendages in the Myxobolus clade. Int. J. Parasit. 2019;49:523–530. doi: 10.1016/j.ijpara.2019.02.009. PubMed DOI

Lisnerová M., Lisner A., Cantatore D.M.P., Schaeffner B.C., Pecková H., Tyml T., Fiala I., Bartošová-Sojková P., Holzer A.S. Correlated evolution of fish host length and parasite spore size: A tale from myxosporeans inhabiting elasmobranchs. Int. J. Parasitol. 2022;52:97–110. doi: 10.1016/j.ijpara.2021.05.008. PubMed DOI

Hallgrimsson B., Hall B.K. Variation: A Central Concept in Biology. Elsevier Academic Press; Burlington, MA, USA: 2005. 592p

Willmore K.E., Young N.M., Richtsmeier J.T. Phenotypic Variability: Its Components, Measurement and Underlying Developmental Processes. Evol. Biol. 2007;34:99–120. doi: 10.1007/s11692-007-9008-1. DOI

Schneider C.A., Rasband W.S., Eliceiri K.W. “NIH Image to ImageJ: 25 years of image analysis”. Nat. Methods. 2012;9:671–675. doi: 10.1038/nmeth.2089. PubMed DOI PMC

Stoffel M.A., Nakagawa S., Schielzeth H. rptR: Repeatability estimation and variance decomposition by generalized linear mixed-effects models. Methods Ecol. Evol. 2017;8:1639–1644. doi: 10.1111/2041-210X.12797. DOI

Rohlf F.J. The tps series of software. Hystrix Ital. J. Mammal. 2015;26:9–12. doi: 10.4404/hystrix-26.1-11264. DOI

Kassambara A., Mundt F. factoextra: Extract and Visualize the Results of Multivariate Data Analyses; R Package Version 1.0.7. 2020. [(accessed on 1 May 2024)]. Available online: https://CRAN.R-project.org/package=factoextra.

Adams D.C., Collyer M.L., Kaliontzopoulou A. Geomorph: Software for Geometric Morphometric Analyses; R Package Version 3.2.1; 2020. [(accessed on 1 May 2024)]. Available online: https://cran.r-project.org/web/packages/geomorph/index.html.

Schlager S. Morpho and Rvcg–Shape Analysis in R. In: Zheng G., Li S., Szekely G., editors. Statistical Shape and Deformation Analysis. Academic Press; London, UK: 2017. pp. 217–256.

Collyer M.L., Adams D.C. RRPP: RRPP: An R package for fitting linear models to high-dimensional data using residual randomization. Methods Ecol. Evol. 2018;9:1772–1779. doi: 10.1111/2041-210X.13029. DOI

Collyer M.L., Adams D.C. RRPP: Linear Model Evaluation with Randomized Residuals in a Permutation Procedure. 2020. [(accessed on 1 May 2024)]. Available online: https://cran.r-project.org/web/packages/RRPP/index.html.

Gower J.C. Generalized Procrustes analysis. Psychometrika. 1975;40:33–51. doi: 10.1007/BF02291478. DOI

Rohlf F.J., Slice D.E. Extensions of the Procrustes method for the optimal superimposition of landmarks. Syst. Zool. 1990;39:40–59. doi: 10.2307/2992207. DOI

Yezerinac S.M., Loogheed S.C., Handford P. Measurement error and morphometric studies: Statistical power and observer experience. Syst. Biol. 1992;41:471–482. doi: 10.1093/sysbio/41.4.471. DOI

Claude J. Morphometrics with R. Springer; New York, NY, USA: 2008. 317p

Bookstein F.L. Measuring and Reasoning. Numerical Inference in the Sciences. Cambridge University Press; Cambridge, UK: 2014. 519p

Mardia K.V., Bookstein F.L., Moreton I. Statistical assessment of bilateral symmetry of shapes. Biometrika. 2000;87:285–300. doi: 10.1093/biomet/87.2.285. DOI

Klingenberg C.P., Burluenga M., Meyer A. Shape analysis of symmetric structures: Quantifying variation among individuals and asymmetry. Evolution. 2002;56:1909–1920. doi: 10.1111/j.0014-3820.2002.tb00117.x. PubMed DOI

Bookstein F.L. Morphometric Tools for Landmark Data: Geometry and Biology. Cambridge University Press; Cambridge, UK: 1991. 435p

Goodall C.R. Procrustes methods in the statistical analysis of shape (with discussion) J. Roy. Stat. Soc. Ser. B. 1991;53:285–339. doi: 10.1111/j.2517-6161.1991.tb01825.x. DOI

Collyer M.L., Adams D.C. A method for analysis of phenotypic change described by high-dimensional data. Heredity. 2015;115:357–365. doi: 10.1038/hdy.2014.75. PubMed DOI PMC

Anderson M.J. Distance-based tests for homogeneity of multivariate dispersions. Biometrics. 2006;62:245–253. doi: 10.1111/j.1541-0420.2005.00440.x. PubMed DOI

Barta J.R., Martin D.S., Liberator P.A., Dashkevicz M., Anderson J.W., Feighner S.D., Elbrecht A., Perkins-Barrow A., Jenkins M.C., Danforth H.D., et al. Phylogenetic relationship among eight Eimeria species infecting domestic fowl inferred using complete small subunit ribosomal DNA sequences. J. Parasit. 1997;83:262–271. doi: 10.2307/3284453. PubMed DOI

Fiala I., Hlavničková M., Kodádková A., Freeman M.A., Bartošová-Sojková P., Atkinson S.D. Evolutionary origin of Ceratonova shasta and phylogeny of the marine myxosporean lineage. Mol. Phyl. Evol. 2015;86:75–89. doi: 10.1016/j.ympev.2015.03.004. PubMed DOI

Altschul S.F., Madden T.L., Schäffer A.A., Zhang J., Zhang Z., Miller W., Lipman D.J. Gapped BLASTn and PSI-BLAST: A new generation of protein database search programs. Nucleic Acids Res. 1997;25:3389–33902. doi: 10.1093/nar/25.17.3389. PubMed DOI PMC

Katoh K., Standley D.M. MAFFT multiple sequence alignment software Version 7: Improvements in performance and usability. Mol. Biol. Evol. 2013;30:772–780. doi: 10.1093/molbev/mst010. PubMed DOI PMC

Kearse M., Moir R., Wilson A., Stones-Havas S., Cheung M., Sturrock S., Buxton S., Cooper A., Markowitz S., Duran C., et al. Geneious Basic: An integrated and extendable desktop software platform for the organization and analysis of sequence data. Bioinformatics. 2012;28:1647–1649. doi: 10.1093/bioinformatics/bts199. PubMed DOI PMC

Stamatakis A. RAxML-VI-HPC: Maximum likelihood-based phylogenetic analyses with thousands of taxa and mixed models. Bioinformatics. 2006;22:2688–2690. doi: 10.1093/bioinformatics/btl446. PubMed DOI

Posada D. jModelTest: Phylogenetic model averaging. Mol. Biol. Evol. 2008;25:1253–1256. doi: 10.1093/molbev/msn083. PubMed DOI

Ronquist F., Huelsenbeck J.P. MrBayes 3: Bayesian phylogenetic inference under mixed models. Bioinformatics. 2003;19:1572–1574. doi: 10.1093/bioinformatics/btg180. PubMed DOI

Davis H.S. The Myxosporidia of the Beaufort region, a systematic and biological study. Bull. US. Bur. Fish. 1917;35:199–252.

Rocha S., Casal G., Rangel L., Castro R., Severino R., Azevedo C., João Santos M. Ultrastructure and phylogeny of Ceratomyxa auratae n. sp. (Myxosporea: Ceratomyxidae), a parasite infecting the gilthead seabream Sparus aurata (Teleostei: Sparidae) Parasitol. Int. 2015;64:305–313. doi: 10.1016/j.parint.2015.04.002. PubMed DOI

Heiniger H., Adlard R.D. Molecular identification of cryptic species of Ceratomyxa Thélohan, 1892 (Myxosporea: Bivalvulida) including the description of eight novel species from apogonid fishes (Perciformes: Apogonidae) from Australian waters. Acta Parasitol. 2013;58:342–360. doi: 10.2478/s11686-013-0149-3. PubMed DOI

Sarkar N.K., Pramanik A.K. Ceratomyxa dayscinaenae sp. n. (Myxozoa: Ceratomyxidae) a myxosporean parasite in the teleost from the Hooghly estuary, West Bengal, India. Acta Protozool. 1994;33:121–124.

Brickle P., Kalavati C., MacKenzie K. Two new species of myxozoan parasites (Myxosporea, Bivalvulida) from toothfish Dissostichus eleginoides Smitt, 1898 (Pisces, Nototheniidae) Acta Parasitol. 2001;46:250–253. doi: 10.21504/10962/365599. DOI

Tanzola D., Guagliardo S., Galeano N., Schwerdt C., González R. Ceratomyxa elegans Jameson, 1929 (Myxozoa: Ceratomyxidae) parásito de peces batracoididos en el Mar Argentino. Nat. Neotrolpicalis. 2006;37:61–66. doi: 10.14409/natura.v1i37.3838. DOI

Evdokimova E.B. Myxosporidians of teleost fishes from the Patagonian Shelf (The Atlantic Coast of Argentina) Parazitologiya. 1977;11:166–178. (In Russian) PubMed

Gunter N.L., Adlard R.D. Seven new species of Ceratomyxa Thélohan, 1892 (Myxozoa) from the gall-bladders of serranid fishes from the Great Barrier Reef, Australia. Syst. Parasitol. 2009;73:1–11. doi: 10.1007/s11230-008-9162-6. PubMed DOI

Sobecka E., Szostakowska B., Ziętara M.S., Więcaszek B. Morphological and molecular characterization of Ceratomyxa gurnardi sp. n. (Myxozoa: Ceratomyxidae) infecting the gallbladder of the grey gurnard Eutrigla gurnardus (L.) (Scorpaeniformes, Triglidae) Parasitol. Res. 2013;112:731–735. doi: 10.1007/s00436-012-3193-2. PubMed DOI

Cousseau M.B., Perrotta R.G. Peces Marinos de Argentina: Biología, Distribución, Pesca. 4th ed. INIDEP; Mar del Plata, Argentina: 2013. 193p

Canel D., Levy E., Soares I.A., Braicovich P., Haimovici M., Luque J.L., Timi S. Stocks and migrations of the demersal fish Umbrina canosai (Sciaenidae) endemic from the subtropical and temperate Southwestern Atlantic revealed by its parasites. Fish. Res. 2019;214:10–18. doi: 10.1016/j.fishres.2019.02.001. DOI

Canel D., Levy E., Braicovich P.E., Haimovici M., Timi S. Ontogenetic asynchrony in fish migrations may lead to disparate parasite assemblages: Implications for its use as biological tags. Fish. Res. 2021;239:105941. doi: 10.1016/j.fishres.2021.105941. DOI

Cantatore D.M.P., Irigoitia M.M., Holzer A.S., Bartošová-Sojková P., Pecková H., Fiala I., Timi S. The description of two new species of Chloromyxum from skates in the Argentine Sea reveals that a limited geographic host distribution causes phylogenetic lineage separation of myxozoans in Chondrichthyes. Parasites. 2018;25:47. doi: 10.1051/parasite/2018051. PubMed DOI PMC

Sardella N.H., Avendaño M.F.J., Timi S. Parasite communities of Genypterus blacodes and G. brasiliensis (Pisces: Ophidiidae) from Argentina. Helminthologia. 1998;35:209–218.

Meglitsch P.A. Some coelozoic myxosporidia from New Zealand fishes. I. General and family Ceratomyxidae. Trans. R. Soc. N. Z. 1960;88:265–365.

Alama-Bermejo G., Raga J.A., Holzer A.S. Host-parasite relationship of Ceratomyxa puntazzi n. sp. (Myxozoa: Myxosporea) and sharpsnout seabream Diplodus puntazzo (Walbaum, 1792) from the Mediterranean with first data on ceratomyxid host specificity in sparids. Vet. Parasitol. 2011;182:181–192. doi: 10.1016/j.vetpar.2011.05.012. PubMed DOI

Azevedo C., Rocha S., Casal C., Saõ Clemente S.C., Matos P., Al-Quraishy S., Matos E. Ultrastructural description of Ceratomyxa microlepis sp. nov. (Phylum Myxozoa): A parasite infecting the gall bladder of Hemiodus microlepis, a freshwater teleost from the Amazon River. Mem. Inst. Osw. Cruz. 2013;108:150–154. doi: 10.1590/0074-0276108022013004. PubMed DOI PMC

Palmer A.R., Strobeck C. Fluctuating asymmetry and developmental stability: Heritability of observable variation vs. heritability of inferred cause. J. Evol. Biol. 1997;10:39–49. doi: 10.1046/j.1420-9101.1997.10010039.x. DOI

Leamy L.J., Klingenberg C.P. The genetics and evolution of fluctuating asymmetry. Annu. Rev. Ecol. Evol. Syst. 2005;36:1–21. doi: 10.1146/annurev.ecolsys.36.102003.152640. DOI

Lewontin R.C. The Triple Helix: Gene, Organism, and Environment. Harvard University Press; Cambridge, MA, USA: 2000. 160p

Ryabov A., Kerimoglu O., Litchman E., Olenina I., Roselli L., Basset A., Stanca E., Blasius B. Shape matters: The relationship between cell geometry and diversity in phytoplankton. Ecol. Lett. 2021;24:847–861. doi: 10.1111/ele.13680. PubMed DOI

Des Roches S., Post D.M., Turley N.E., Bailey J.K., Hendry A.P., Kinnison M.T., Schweitzer J.A., Palkovacs E.P. The ecological importance of intraspecific variation. Nat. Ecol. Evol. 2018;2:57–64. doi: 10.1038/s41559-017-0402-5. PubMed DOI

Fontes I., Hallett S.L., Mo T.A. Comparative Epidemiology of Myxozoan Diseases. In: Okamura B., Gruhl A., Bartholomew J., editors. Myxozoan Evolution, Ecology and Development. Springer; Cham, Switzerland: 2015. pp. 317–341. DOI

Hallett S.L., Hartigan A., Atkinson S.D. Myxozoans on the Move: Dispersal Modes, Exotic Species, and Emerging Diseases. In: Okamura B., Gruhl A., Bartholomew J., editors. Myxozoan Evolution, Ecology and Development. Springer; Cham, Switzerland: 2015. pp. 343–362. DOI

Feist S.W., Morris D.J., Alama-Bermejo G., Holzer A.S. Cellular Processes in Myxozoans. In: Okamura B., Gruhl A., Bartholomew J., editors. Myxozoan Evolution, Ecology and Development. Springer; Cham, Switzerland: 2015. pp. 139–154. DOI

Okamura B., Gruhl A., Bartholomew J.L. An Introduction to Myxozoan Evolution, Ecology and Development. Springer International Publishing; Berlin/Heidelberg, Germany: 2015. 441p

Rossin M.A., Cantatore D.M.P., Lisnerová M., Taglioretti V., Holzer A.S. Henneguya (Cnidaria: Myxobolidae) species infecting Oligosarcus jenynsii (Characiformes: Characidae) in a Neotropical shallow lake from Argentina: Morphological and molecular characterisation. Folia Parasitol. 2024;71:005. doi: 10.14411/fp.2024.005. PubMed DOI

Kovaleva O., Shulman S. Special Features of the Myxosporidian Fauna from Sea and Ocean Fishes. In: Hargis W., editor. Parasitology and Pathology of Marine Organisms of the World Ocean. NOAA; Washington, DC, USA: 1984. pp. 55–58. NOAA Technical Report NMFS 25.

Xiao C., Desser S.S. Actinosporean stages of myxosporean parasites of oligochaetes from Lake Sasajewun, Algonquin Park, Ontario: New forms of triactinomyxon and raabeia. J. Parasitol. 1998;84:998–1009. doi: 10.2307/3284634. PubMed DOI

Yokoyama H., Grabner D., Shirakashi S. Transmission biology of the Myxozoa. Health Environ. Aquac. 2012;10:29571. doi: 10.5772/29571. DOI

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