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Spreadsheet Template for Trophic Guild Data for Fungi

Spreadsheet template for <a href="https://doi.org/10.5281/zenodo.14646717">Trophic guild data for fungi</a>

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Trophic guild data for fungi

Data on trophic guilds of fungi derived from the following sources: Alker AP, Smith GW, Kim K. 2001. Characterization of Aspergillus sydowii (Thom et Church), a fungal pathogen of Caribbean sea fan corals. Hydrobiologia 460:105–11. Bauer, R., Begerow, D., Sampaio, J.P., Weiβ, M., Oberwinkler, F., 2006. The simple-septate basidiomycetes: a synopsis. Mycol Progress 5, 41–66. Blackwell, W.H., Letcher, P.M. and Powell, M.J., 2019. Review of Nucleophaga (a primitive,__cryptomycotan__genus): Summary of named and unnamed species, with discussion of contemporary and historical observations. Phytologia, 101, pp.1-18. Cali A., Becnel J.J., Takvorian P.M. (2016) Microsporidia. In: Archibald J. et al. (eds) Handbook of the Protists. Springer, Cham. Canter, H. M., G. H. M. Jaworski. 1982. Some Observation on the Alga Fragilaria crotonensis Kitton and its Parasitism by Two Chytridiaceous Fungi. Annals of Botany 49(4):429–446. Cavalier-Smith, T., Chao, E.E., Lewis, R., 2018. Multigene phylogeny and cell evolution of chromist infrakingdom Rhizaria: contrasting cell organisation of sister phyla Cercozoa and Retaria. Protoplasma 255, 1517–1574. Chen, X., Lili, L., Zhang, Y., Zhang, J., Ouyang, S., Zhang, Q., Tong, Y., Xu, J. and Zuo, S., 2017. Functional analysis of polygalacturonase gene RsPG2 from Rhizoctonia solani, the pathogen of rice sheath blight. European Journal of Plant Pathology, 149(2), pp.491-502. Dewel, R. A., J. D. Joines, and J. J. Bond. 1985. A new chytridiomycete parasitizing the tardigrade Milnesium tardigradum. Canad. J. Bot. 63:1525- 1534. Dwyer, J., Burwell, B., Humber, R.A., Mcleod, C., Fleetwood, M., Johnson, T. 2006. Schizangiella serpentis infection in a Virginia ratsnake (Elaphe obsoleta). Veterinary Pathology. 43(5):819-819.  Embree, R.W. and Indoh, H., 1967. Aquamortierella, a new genus in the Mucorales. Bulletin of the Torrey Botanical Club, pp. 464-467.  Gryganskyi, A.P., Humber, R.A., Smith, M.E., Miadlikovska, J., Wu, S., Voigt, K., Walther, G., Anishchenko, I.M. and Vilgalys, R., 2012. Molecular phylogeny of the Entomophthoromycota. Molecular Phylogenetics and Evolution, 65(2), pp.682-694. Guo, Y., Jud, W., Weikl, F. et al. 2021. Volatile organic compound patterns predict fungal trophic mode and lifestyle. Commun Biol 4:673. He, M.-Q., Zhao, R.-L., Hyde, K.D., Begerow, D., Kemler, M., Yurkov, A., McKenzie, E.H.C., Raspé, O., Kakishima, M., Sánchez-Ramírez, S., Vellinga, E.C., Halling, R., Papp, V., Zmitrovich, I.V., Buyck, B., Ertz, D., Wijayawardene, N.N., Cui, B.-K., Schoutteten, N., Liu, X.-Z., Li, T.-H., Yao, Y.-J., Zhu, X.-Y., Liu, A.-Q., Li, G.-J., Zhang, M.-Z., Ling, Z.-L., Cao, B., Antonín, V., Boekhout, T., da Silva, B.D.B., De Crop, E., Decock, C., Dima, B., Dutta, A.K., Fell, J.W., Geml, J., Ghobad-Nejhad, M., Giachini, A.J., Gibertoni, T.B., Gorjón, S.P., Haelewaters, D., He, S.-H., Hodkinson, B.P., Horak, E., Hoshino, T., Justo, A., Lim, Y.W., Menolli, N., Me&scaron;ić, A., Moncalvo, J.-M., Mueller, G.M., Nagy, L.G., Nilsson, R.H., Noordeloos, M., Nuytinck, J., Orihara, T., Ratchadawan, C., Rajchenberg, M., Silva-Filho, A.G.S., Sulzbacher, M.A., Tkalčec, Z., Valenzuela, R., Verbeken, A., Vizzini, A., Wartchow, F., Wei, T.-Z., Weiß, M., Zhao, C.-L., Kirk, P.M., 2019. Notes, outline and divergence times of Basidiomycota. Fungal Diversity 99, 105–367. Karpov, S.A., Mamkaeva, M.A., Aleoshin, V.V., Nassonova, E., Lilje, O. and Gleason, F.H., 2014. Morphology, phylogeny, and ecology of the aphelids (Aphelidea, Opisthokonta) and proposal for the new superphylum Opisthosporidia. Frontiers in Microbiology, 5, p.112. Kramer, C. L. (1958). A new genus in the Protomycetaceae. Mycologia, 50(6), 916-926. Kubanek J, Jensen PR, Keifer PA, Sullards MC, Collins DO, Fenical W. 2003. Seaweed resistance to microbial attack: a targeted chemical defence against marine fungi. Proc. Natl. Acad. Sci. USA 100: 6916–21.  Küpper FC, Maier I, Müller DG, Loiseaux-de Goer S, Guillou L. 2006. Phylogenetic affinities of two eukaryotic pathogens of marine macroalgae, Eurychasma dicksonii (Wright) Magnus and Chytridium polysiphoniae Cohn. Cryptogam. Algol. 27:165–84. Martel, A., Spitzen-van der Sluijs, A., Blooi, M., Bert, W., Ducatelle, R., Fisher, M.C., Woeltjes, A., Bosman, W., Chiers, K., Bossuyt, F. and Pasmans, F., 2013. Batrachochytrium salamandrivorans sp. nov. causes lethal chytridiomycosis in amphibians. Proceedings of the National Academy of Sciences, 110(38), pp.15325-15329. Möckel, L., Meusemann, K., Misof, B., Schwartze, V.U., De Fine Licht, H.H., Voigt, K., Stielow, B., de Hoog, S., Beutel, R.G., Buellesbach, J., 2022. Phylogenetic Revision and Patterns of Host Specificity in the Fungal Subphylum Entomophthoromycotina. Microorganisms 10, 256. Naranjo-Ortiz, M.A., Gabaldón, T., 2019. Fungal evolution: diversity, taxonomy and phylogeny of the Fungi. Biol Rev Camb Philos Soc 94, 2101–2137. Olive, L. S. 1980. Caulochytrium protostelioides sp. nov., a New Chytrid with Aerial Sporangia. American Journal of Botany 67(4):568-574. Patterson, D., 1999. The Diversity of Eukaryotes. The American Naturalist 154(supplement):S96-S124. Powell, M.J. 1984. Fine structure of the unwalled thallus of Rozella polyphagi in its host Polyphagus euglenae. Mycologia 76:1039-1048. Powell M.J. 1993. Looking at Mycology with a Janus Face: A Glimpse at Chytridiomycetes Active in the Environment. Mycologia 85:1-20. Powell M.J. 2016. Blastocladiomycota. In: Archibald J. et al. (eds) Handbook of the Protists. Springer, Cham. Powell M.J. 2016. Chytridiomycota. In: Archibald J. et al. (eds) Handbook of the Protists. Springer, Cham. Riccioni C, Belfiori B, Rubini A, Bucci G, Ianigro M (2024). Dataset of endophytic and forest fungi (IBBR-CNR-FABI-01). Consiglio Nazionale delle Ricerche, Istituto di Bioscienze e BioRisorse (CNR-IBBR). Occurrence dataset https://doi.org/10.15468/arjsuy accessed via GBIF.org on 2025-01-14. Schüßler, A., 2012. The Geosiphon–Nostoc endosymbiosis and its role as a model for arbuscular mycorrhiza research. In Fungal associations (pp. 77-91). Springer, Berlin, Heidelberg. Sekimoto, S., Rochon, D., Long, J.E. et al. 2011. A multigene phylogeny of Olpidium and its implications for early fungal evolution. BMC Evol Biol 11:331. Strassert, J.F.H., Wurzbacher, C., Hervé, V. et al. Long rDNA amplicon sequencing of insect-infecting nephridiophagids reveals their affiliation to the Chytridiomycota and a potential to switch between hosts. Sci Rep 11, 396 (2021). Toome, M., Roberson, R.W., Aime, M.C., 2013. Meredithblackwellia eburnea gen. et sp. nov., Kriegeriaceae fam. nov. and Kriegeriales ord. nov.—toward resolving higher-level classification in Microbotryomycetes. Mycologia 105, 486–495. Vilela, L.A.F. and Damásio, M.M., 2021. Molecular and cellular changes of arbuscular mycorrhizal fungi-plant interaction in pesticide contamination. Chapter 41 in Handbook of Bioremediation (pp. 649-656). Academic Press. Walker, G., Dorrell, R., Schlacht, A., Dacks, J., 2011. Eukaryotic systematics: A user__s guide for cell biologists and parasitologists. Parasitology 138, 1638–63. Wijayawardene, N.N., Hyde, K.D., Rajeshkumar, K.C., Hawksworth, D.L., Madrid, H., Kirk, P.M., Braun, U., Singh, R.V., Crous, P.W., Kukwa, M., Lücking, R., Kurtzman, C.P., Yurkov, A., Haelewaters, D., Aptroot, A., Lumbsch, H.T., Timdal, E., Ertz, D., Etayo, J., Phillips, A.J.L., Groenewald, J.Z., Papizadeh, M., Selbmann, L., Dayarathne, M.C., Weerakoon, G., Jones, E.B.G., Suetrong, S., Tian, Q., Castañeda-Ruiz, R.F., Bahkali, A.H., Pang, K.-L., Tanaka, K., Dai, D.Q., Sakayaroj, J., Hujslová, M., Lombard, L., Shenoy, B.D., Suija, A., Maharachchikumbura, S.S.N., Thambugala, K.M., Wanasinghe, D.N., Sharma, B.O., Gaikwad, S., Pandit, G., Zucconi, L., Onofri, S., Egidi, E., Raja, H.A., Kodsueb, R., Cáceres, M.E.S., Pérez-Ortega, S., Fiuza, P.O., Monteiro, J.S., Vasilyeva, L.N., Shivas, R.G., Prieto, M., Wedin, M., Olariaga, I., Lateef, A.A., Agrawal, Y., Fazeli, S.A.S., Amoozegar, M.A., Zhao, G.Z., Pfliegler, W.P., Sharma, G., Oset, M., Abdel-Wahab, M.A., Takamatsu, S., Bensch, K., de Silva, N.I., De Kesel, A., Karunarathna, A., Boonmee, S., Pfister, D.H., Lu, Y.-Z., Luo, Z.-L., Boonyuen, N., Daranagama, D.A., Senanayake, I.C., Jayasiri, S.C., Samarakoon, M.C., Zeng, X.-Y., Doilom, M., Quijada, L., Rampadarath, S., Heredia, G., Dissanayake, A.J., Jayawardana, R.S., Perera, R.H., Tang, L.Z., Phukhamsakda, C., Hernández-Restrepo, M., Ma, X., Tibpromma, S., Gusmao, L.F.P., Weerahewa, D., Karunarathna, S.C., 2017. Notes for genera: Ascomycota. Fungal Diversity 86, 1–594. World Health Organization, 2022. WHO fungal priority pathogens list to guide research, development and public health action. Geneva: World Health Organization.

Fig. 7 in Longitudinal use of feeding resources and distribution of fish trophic guilds in a coastal Atlantic stream, southern Brazil

Fig. 7. Spearman correlations between the distribution (percentage frequency) of guilds and scores of the first axis of the principal components analysis (PCA1) applied to the correlation matrix of abiotic variables. White circle = headwaters; gray circle = middle stretch; and black circle = mouth of the Vermelho River, East Atlantic basin, Antonina, Paraná State, Brazil.

Fig. 5 in Longitudinal use of feeding resources and distribution of fish trophic guilds in a coastal Atlantic stream, southern Brazil

Fig. 5. Longitudinal niche breadth (B values) of each fish trophic guild in the Vermelho River, East Atlantic basin, Antonina, Paraná State, Brazil. Aq = aquatic; ter = terrestrial.

Fig. 4 in Longitudinal use of feeding resources and distribution of fish trophic guilds in a coastal Atlantic stream, southern Brazil

Fig. 4. Mean ± standard error of diet breadth (B) of fish trophic guilds in the Vermelho River, East Atlantic basin, Antonina, Paraná State, Brazil. Aq = aquatic; ter = terrestrial. Piscivores and omnivores are not included in the ANOVA.

Fig. 6 in Longitudinal use of feeding resources and distribution of fish trophic guilds in a coastal Atlantic stream, southern Brazil

Fig. 6. Density (a) and biomass (b) of trophic guilds along the longitudinal gradient of the Vermelho River, East Atlantic basin, Antonina, Paraná State, Brazil. Aq = aquatic; ter = terrestrial.

Fig. 3 in Longitudinal use of feeding resources and distribution of fish trophic guilds in a coastal Atlantic stream, southern Brazil

Fig. 3. Ordination of fish species in the respective trophic guilds (a, b, c) and food items (d, e, f) along the longitudinal gradient of the Vermelho River, East Atlantic basin, Antonina, Paraná State, Brazil. Circles represent species belonging to the same trophic guild. Codes according to Table 3.

Fig. 2 in Longitudinal use of feeding resources and distribution of fish trophic guilds in a coastal Atlantic stream, southern Brazil

Fig. 2. Ordination of sampling sections along the environmental gradient defined by the first two axes of the principal components analysis (PCA1 and PCA2) applied to the correlation matrix of abiotic variables of the Vermelho River, East Atlantic basin, Antonina, Paraná State, Brazil.

Fig. 1 in Longitudinal use of feeding resources and distribution of fish trophic guilds in a coastal Atlantic stream, southern Brazil

Fig. 1. Location of the Vermelho River, East Atlantic basin, Antonina, Paraná State, Brazil. Black circles indicate the sampling sections; arrow indicates the direction of flow.

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Figure 2 in Diet composition, guild structure and trophic relationships of wintering birds of prey in an estuarine wetland (The Evros Delta National Park, Greece)

Figure 2. Cluster analysis (dendrogram) based on the biomass proportions of the diets of the seven species of birds of prey studied in Evros Delta.

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Figure 1 in Diet composition, guild structure and trophic relationships of wintering birds of prey in an estuarine wetland (The Evros Delta National Park, Greece)

Figure 1. Diet compiled for the most important prey taxa of the seven species of birds of prey studied in the Evros Delta, a) by biomass (upper graph) and b) by numbers (lower graph) (Shannon index/Evenness are shown below each species name).

Fig. 3 in Effects of latitude, host body size, and host trophic guild on patterns of diversity of helminths associated with humans, wild and domestic mammals of Mexico

Fig. 3. Phylogenetic generalized least squares (PGLS) regression of host body mass (values were log-transformed) with richness of helminths associated to wildlife hosts (values were corrected for sampling effort).

Fig. 2 in Effects of latitude, host body size, and host trophic guild on patterns of diversity of helminths associated with humans, wild and domestic mammals of Mexico

Fig. 2. Relationships between latitude and the average taxonomic distinctness of overall helminths (A) and nematodes (B).

Fig. 4 in Effects of latitude, host body size, and host trophic guild on patterns of diversity of helminths associated with humans, wild and domestic mammals of Mexico

Fig. 4. Parasite richness and average taxonomic distinctness by host trophic guild (the size of circle represents the number of hosts belonging to each trophic guild).

Fig. 1 in Effects of latitude, host body size, and host trophic guild on patterns of diversity of helminths associated with humans, wild and domestic mammals of Mexico

Fig. 1. Maps showing the geographic locations of the records, classified by phylum of the subsetted database.

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Trophic guild data for microbial eukaryotes

Data on trophic guilds of microbial eukaryotes derived from the following sources: Adl, S.M., Bass, D., Lane, C.E., Luke&scaron;, J., Schoch, C.L., Smirnov, A., Agatha, S., Berney, C., Brown, M.W., Burki, F., Cárdenas, P., Čepička, I., Chistyakova, L., Campo, J. del, Dunthorn, M., Edvardsen, B., Eglit, Y., Guillou, L., Hampl, V., Heiss, A.A., Hoppenrath, M., James, T.Y., Karnkowska, A., Karpov, S., Kim, E., Kolisko, M., Kudryavtsev, A., Lahr, D.J.G., Lara, E., Gall, L.L., Lynn, D.H., Mann, D.G., Massana, R., Mitchell, E.A.D., Morrow, C., Park, J.S., Pawlowski, J.W., Powell, M.J., Richter, D.J., Rueckert, S., Shadwick, L., Shimano, S., Spiegel, F.W., Torruella, G., Youssef, N., Zlatogursky, V., Zhang, Q., 2019. Revisions to the Classification, Nomenclature, and Diversity of Eukaryotes. Journal of Eukaryotic Microbiology 66, 4–119. <a href="https://doi.org/10.1111/jeu.12691">https://doi.org/10.1111/jeu.12691</a> Aleoshin, V.V., Mylnikov, A.P., Mirzaeva, G.S., Mikhailov, K.V. and Karpov, S.A., 2016. Heterokont Predator Develorapax marinus gen. et sp. nov.–A Model of the Ochrophyte Ancestor. Frontiers in microbiology, 7, p.1194. <a href="https://doi.org/10.3389/fmicb.2016.01194">https://doi.org/10.3389/fmicb.2016.01194</a> Ann PJ, Huang JH, Wang IT, Ko WH, 2006. Pythiogeton zizaniae, a new species causing basal stalk rot of water bamboo in Taiwan. Mycologia 98: 116e120. <a title="https://doi.org/10.1080/15572536.2006.11832717" href="https://doi.org/10.1080/15572536.2006.11832717">https://doi.org/10.1080/15572536.2006.11832717</a> Azevedo C., Hine P.M. (2016) Haplosporidia. In: Archibald J. et al. (eds) Handbook of the Protists. Springer, Cham. <a href="https://doi.org/10.1007/978-3-319-32669-6_16-1">https://doi.org/10.1007/978-3-319-32669-6_16-1</a> Baldauf S.L., Strassmann J.E. (2017) Dictyostelia. In: Archibald J. et al. (eds) Handbook of the Protists. Springer, Cham. <a href="https://doi.org/10.1007/978-3-319-32669-6_14-1">https://doi.org/10.1007/978-3-319-32669-6_14-1</a>  Beakes G.W., Thines M. (2016) Hyphochytriomycota and Oomycota. In: Archibald J. et al. (eds) Handbook of the Protists. Springer, Cham. <a href="https://doi.org/10.1007/978-3-319-32669-6_26-1">https://doi.org/10.1007/978-3-319-32669-6_26-1 </a> Bell, E.M. and Laybourn‐Parry, J., 2003. Mixotrophy in the antarctic phytoflagellate Pyramimonas gelidicola (Chlorophyta: Prasinophyceae). Journal of Phycology, 39(4), pp.644-649. <a href="https://doi.org/10.1046/j.1529-8817.2003.02152.x">https://doi.org/10.1046/j.1529-8817.2003.02152.x</a> Bennett R.M., Honda D., Beakes G.W., Thines M. (2017) Labyrinthulomycota. In: Archibald J. et al. (eds) Handbook of the Protists. Springer, Cham. <a href="https://doi.org/10.1007/978-3-319-32669-6_25-1">https://doi.org/10.1007/978-3-319-32669-6_25-1</a> Bernard, Catherine, Alastair G. B. Simpson & David J. Patterson (2000) Some free-living flagellates (protista) from anoxic habitats Ophelia 52(2):113-142. <a href="https://doi.org/10.1080/00785236.1999.10409422">https://doi.org/10.1080/00785236.1999.10409422</a> Bigelow, D. M., Olsen, M. W., & Gilbertson, R. L. (2005). Labyrinthula terrestris sp. nov., a new pathogen of turf grass. Mycologia 97:185–190. <a href="https://doi.org/10.1080/15572536.2006.11832852">https://doi.org/10.1080/15572536.2006.11832852</a> Boltovskoy D., Anderson O.R., Correa N.M. (2017) Radiolaria and Phaeodaria. In: Archibald J. et al. (eds) Handbook of the Protists. Springer, Cham. <a href="https://doi.org/10.1007/978-3-319-32669-6_19-2">https://doi.org/10.1007/978-3-319-32669-6_19-2</a> Bourland, W. A. & Struder-Kypke, M. C. 2010. Agolohymena aspidocauda nov. gen., nov. spec., a histophagous freshwater tetrahymenid ciliate in the family Deltopylidae (Ciliophora, Hymenostomatia), from Idaho (northwest USA): morphology, ontogenesis and molecular phylogeny. Eur. J. Protistol. 46:221–242. <a href="https://doi.org/10.1016/j.ejop.2010.04.003">https://doi.org/10.1016/j.ejop.2010.04.003</a> Bower, S. M., McLean, N., & Whitaker, D. J. (1989). Mechanism of infection by Labyrinthuloides haliotidis (Protozoa, Labyrinthomorpha), a parasite of abalone (Haliotis kamtschatka) (Mollusca, Gastropoda). Journal of Invertebrate Pathology, 53, 401–409. Buaya, A. T., Ploch, S., Inaba, S., & Thines, M. (2019). Holocarpic oomycete parasitoids of red algae are not Olpidiopsis. Fungal systematics and evolution 4:21–31. <a href="https://doi.org/10.3114/fuse.2019.04.03">https://doi.org/10.3114/fuse.2019.04.03</a> Bulman S., Neuhauser S. (2016) Phytomyxea. In: Archibald J. et al. (eds) Handbook of the Protists. Springer, Cham. <a href="https://doi.org/10.1007/978-3-319-32669-6_24-1">https://doi.org/10.1007/978-3-319-32669-6_24-1</a> Burki, F., Roger, A.J., Brown, M.W., Simpson, A.G.B., 2020. The New Tree of Eukaryotes. Trends in Ecology & Evolution 35, 43–55. <a href="https://doi.org/10.1016/j.tree.2019.08.008">https://doi.org/10.1016/j.tree.2019.08.008</a> Carr, M., Leadbeater, B. S., Hassan, R., Nelson, M., & Baldauf, S. L. (2008). Molecular phylogeny of choanoflagellates, the sister group to Metazoa. Proceedings of the National Academy of Sciences of the United States of America, 105(43):16641–16646. <a href="https://doi.org/10.1073/pnas.0801667105">https://doi.org/10.1073/pnas.0801667105</a> Cavalier-Smith, T., & Chao, E. E. (2004). Protalveolate phylogeny and systematics and the origins of Sporozoa and dinoflagellates (phylum Myzozoa nom. nov.). European Journal of Protistology 40(3):185-212. <a href="https://doi.org/10.1016/j.ejop.2004.01.002">https://doi.org/10.1016/j.ejop.2004.01.002</a> Cavalier-Smith, T., 2018. Kingdom Chromista and its eight phyla: a new synthesis emphasising periplastid protein targeting, cytoskeletal and periplastid evolution, and ancient divergences. Protoplasma 255, 297–357. <a href="https://doi.org/10.1007/s00709-017-1147-3">https://doi.org/10.1007/s00709-017-1147-3</a> Cavalier-Smith, T., Chao, E.E.-Y., 2006. Phylogeny and megasystematics of phagotrophic heterokonts (kingdom Chromista). J. Mol. Evol. 62, 388–420. <a href="https://doi.org/10.1007/s00239-004-0353-8">https://doi.org/10.1007/s00239-004-0353-8</a> Cavalier-Smith, T., Chao, E.E., Lewis, R., 2018. Multigene phylogeny and cell evolution of chromist infrakingdom Rhizaria: contrasting cell organisation of sister phyla Cercozoa and Retaria. Protoplasma 255, 1517–1574. <a href="https://doi.org/10.1007/s00709-018-1241-1">https://doi.org/10.1007/s00709-018-1241-1</a> Čepička I., Dolan M.F., Gile G.H. (2016) Parabasalia. In: Archibald J. et al. (eds) Handbook of the Protists. Springer, Cham. <a href="https://doi.org/10.1007/978-3-319-32669-6_9-1">https://doi.org/10.1007/978-3-319-32669-6_9-1</a> Cho, Anna, Denis V. Tikhonenkov, Elisabeth Hehenberger, Anna Karnkowska, Alexander P. Mylnikov, and Patrick J. Keeling. 2022. Monophyly of Diverse Bigyromonadea and their Impact on Phylogenomic Relationships Within Stramenopiles. Molecular Phylogenetics and Evolution 171: 107468. <a href="https://doi.org/10.1016/j.ympev.2022.107468">https://doi.org/10.1016/j.ympev.2022.107468</a> Cook, M.E., Graham, L.E., 2016. Chlorokybophyceae, Klebsormidiophyceae, Coleochaetophyceae, in: Archibald, J.M., Simpson, A.G.B., Slamovits, C.H., Margulis, L., Melkonian, M., Chapman, D.J., Corliss, J.O. (Eds.), Handbook of the Protists. 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Fig. 1 in Trophic guilds of fishes in sandbank habitats of a Neotropical river

Fig. 1. Scores for the fish species (a) and their food items (b) along Axes 1 and 2, derived from detrended correspondence analysis (DCA). The circles in (a) indicate the groups determined by the k-means analysis.

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Fig. 2 in Trophic guilds of fishes in sandbank habitats of a Neotropical river

Fig. 2. Proportions of terrestrial, aquatic, and undetermined resources used by the fish trophic groups.