Díez B, Ininbergs K. Ecological importance of cyanobacteria. In Cyanobacteria (pp. 41–63). John Wiley & Sons, Ltd. (2013) https://doi.org/10.1002/9781118402238.ch3
Fristachi A, Sinclair JL, Hall S, Berkman JAH, Boyer G, Burkholder J, et al. Occurrence of cyanobacterial harmful algal blooms workgroup report. Adv Experimental Med Biol. 2008;619:45–103. https://doi.org/10.1007/978-0-387-75865-7_3
Google Scholar
Huisman J, Codd GA, Paerl HW, Ibelings BW, Verspagen JMH, Visser PM. Cyanobacterial blooms. Nat Rev Microbiol. 2018;16:471–83. https://doi.org/10.1038/s41579-018-0040-1
Google Scholar
Plaas HE, Paerl HW. Toxic Cyanobacteria: A Growing Threat to Water and Air Quality. In Environmental Science and Technology (Vol. 55, Issue 1, pp. 44–64). American Chem Soc. 2021. https://doi.org/10.1021/acs.est.0c06653
Kurmayer R, Deng L, Entfellner E. Role of toxic and bioactive secondary metabolites in colonization and bloom formation by filamentous cyanobacteria Planktothrix. Harmful Algae. 2016;54:69–86. https://doi.org/10.1016/j.hal.2016.01.004
Google Scholar
Rohrlack T, Christiansen G, Kurmayer R. Putative antiparasite defensive system involving ribosomal and nonribosomal oligopeptides in cyanobacteria of the genus planktothrix. Appl Environ Microbiol. 2013;79:2642–7. https://doi.org/10.1128/AEM.03499-12
Google Scholar
Legnani E, Copetti D, Oggioni A, Tartari G, Palumbo MT, Morabito G. Planktothrix rubescens’ seasonal dynamics and vertical distribution. J Limnol. 2005;64:61–73.
Google Scholar
Walsby A, Ng G, Dunn C, Davis PA. Comparison of the depth where Planktothrix rubescens stratifies and the depth where the daily insolation supports its neutral buoyancy. New Phytologist. 2004;162:133–45. https://doi.org/10.1111/j.1469-8137.2004.01020.x
Google Scholar
Bruning K. Effects of temperature and light on the population dynamics of the Asterionella-Rhizophydium association. J Plankton Res. 1991a;13:707–19. https://doi.org/10.1093/plankt/13.4.707
Google Scholar
Rohrlack T, Haande S, Molversmyr Å, Kyle M. Environmental Conditions Determine the Course and Outcome of Phytoplankton Chytridiomycosis. 2015;1–17. https://doi.org/10.1371/journal.pone.0145559
Tao Y, Wolinska J, Hölker F, Agha R. Light intensity and spectral distribution affect chytrid infection of cyanobacteria via modulation of host fitness. Parasitology. 2020;147:1206–15. https://doi.org/10.1017/S0031182020000931
Google Scholar
Davis PA, Walsby A. Comparison of measured growth rates with those calculated from rates of photosynthesis in Planktothrix spp. isolated from Blelham Tarn, English Lake District. New Phytologist. 2002;156:225–39. https://doi.org/10.1046/j.1469-8137.2002.00495.x
Google Scholar
Oberhaus L, Briand JF, Leboulanger C, Jacquet S, Humbert JF. Comparative effects of the quality and quantity of light and temperature on the growth of Planktothrix agardhii and P. rubescens 1. J Phycol. 2007;43:1191–9. https://doi.org/10.1111/j.1529-8817.2007.00414.x
Google Scholar
Reynolds CS Growth and replication of phytoplankton. In The Ecology of Phytoplankton (pp. 145–77). Cambridge University Press (2009). https://doi.org/10.1017/CBO9780511542145.005
Litchman E, Klausmeier CA . Trait-based community ecology of phytoplankton. Ann Rev Ecol, Evol, Syst. 2008;39:615–39.
Edwards KF, Thomas MK, Klausmeier CA, Litchman E. Phytoplankton growth and the interaction of light and temperature: A synthesis at the species and community level. Limnol Oceanography. 2016;61:1232–44.
Google Scholar
Thomas MK, Kremer CT, Litchman E. Environment and evolutionary history determine the global biogeography of phytoplankton temperature traits. Global Ecol Biogeog. 2016;25:75–86. https://doi.org/10.1111/geb.12387
Google Scholar
Bright DI, Walsby A. The daily integral of growth by Planktothrix rubescens calculated from growth rate in culture and irradiance in Lake Zürich. New Phytologist. 2000;146:301–16. https://doi.org/10.1046/j.1469-8137.2000.00640.x
Google Scholar
Jann-Para G, Schwob I, Feuillade M. Occurrence of toxic Planktothrix rubescens blooms in lake Nantua, France. Toxicon. 2004;43:279–85.
Google Scholar
Jacquet S, Briand JF, Leboulanger C, Avois-Jacquet C, Oberhaus L, Tassin B, et al. The proliferation of the toxic cyanobacterium Planktothrix rubescens following restoration of the largest natural French lake (Lac du Bourget). Harmful Algae. 2005;4:651–72.
Google Scholar
Lenard T. Metalimnetic bloom of Planktothrix rubescens in relation to environmental conditions. Oceanological Hydrobiological Studies. 2009;38:45–53.
Van den Wyngaert S, Salcher MM, Pernthaler J, Zeder M, Posch T. Quantitative dominance of seasonally persistent filamentous cyanobacteria (Planktothrix rubescens) in the microbial assemblages of a temperate lake. Limnol Oceanogr. 2011;56:97–109.
Google Scholar
Walsby A. Stratification by cyanobacteria in lakes: A dynamic buoyancy model indicates size limitations met by Planktothrix rubescens filaments. New Phytologist. 2005;168:365–76. https://doi.org/10.1111/j.1469-8137.2005.01508.x
Google Scholar
Conroy JD, Kane DD, Quinlan EL, Edwards WJ, Culver DA. Abiotic and biotic controls of phytoplankton biomass dynamics in a freshwater tributary, estuary, and large lake ecosystem: Sandusky bay (lake erie) chemostat. Inland Waters. 2017;7:473–92. https://doi.org/10.1080/20442041.2017.1395142
Google Scholar
Sommer U, Maciej Gliwics Z, Lampert W, Duncan A. The PEG-model of seasonal succession of planktonic events in fresh waters. Archiv Für Hydrobiologie. 1986;106:433–71.
Sommer U, Adrian R, De Senerpont Domis L, Elser JJ, Gaedke U, Ibelings B, et al. Beyond the plankton ecology group (PEG) model: Mechanisms driving plankton succession. Ann Rev Ecol, Evol, Syst. 2012;43:429–48. https://doi.org/10.1146/annurev-ecolsys-110411-160251
Google Scholar
Hatcher MJ, Dunn AM Parasites in ecological communities: from interactions to ecosystems. Cambridge University Press (2011).
Marcogliese DJ. Parasites: Small Players with Crucial Roles in the Ecological Theater. EcoHealth. 2004;1:151–64. https://doi.org/10.1007/s10393-004-0028-3
Google Scholar
Sime-Ngando T, Lafferty KD, Biron DG. Roles and Mechanisms of Parasitism in Aquatic Microbial Communities. 2007. https://doi.org/10.3389/978-2-88919-588-6
Frenken T, Alacid E, Berger SA, Bourne EC, Gerphagnon M, Grossart HP, et al. Integrating chytrid fungal parasites into plankton ecology: research gaps and needs. Environmental Microbiology. 2017;19:3802–22. https://doi.org/10.1111/1462-2920.13827
Google Scholar
Brussaard CPD, Kuipers B, Veldhuis MJW. A mesocosm study of Phaeocystis globosa population dynamics: I. Regulatory role of viruses in bloom control. Harmful Algae. 2005;4:859–74. https://doi.org/10.1016/j.hal.2004.12.015
Google Scholar
Gerphagnon M, Macarthur DJ, Gachon C, Van Ogtrop F, Latour D, et al. The biological factors affecting the dynamics of cyanobacterial blooms. 2009.
Gleason FH, Jephcott TG, Küpper FC, Gerphagnon M, Sime-Ngando T, Karpov SA, et al. Potential roles for recently discovered chytrid parasites in the dynamics of harmful algal blooms. Fungal Biol Rev. 2015;29:20–33. https://doi.org/10.1016/j.fbr.2015.03.002
Google Scholar
Ibelings BW, Gsell AS, Mooij WM, Van Donk E, Van Den Wyngaert S, De Senerpont Domis LN. Chytrid infections and diatom spring blooms: Paradoxical effects of climate warming on fungal epidemics in lakes. Freshwater Biol. 2011;56:754–66. https://doi.org/10.1111/j.1365-2427.2010.02565.x
Google Scholar
Kagami M, De Bruin A, Ibelings BW, Van Donk E. Parasitic chytrids: Their effects on phytoplankton communities and food-web dynamics. Hydrobiologia. 2007;578:113–29. https://doi.org/10.1007/s10750-006-0438-z
Google Scholar
Lips KR, Brem F, Brenes R, Reeve JD, Alford RA, Voyles J, et al. Emerging infectious disease and the loss of biodiversity in a Neotropical amphibian community. PNAS. 2005;103:3165–70.
Google Scholar
McKenzie VJ, Peterson AC. Pathogen pollution and the emergence of a deadly amphibian pathogen. Molecular Ecol. 2012;21:5151–4. https://doi.org/10.1111/mec.12013
Google Scholar
Skerratt LF, Berger L, Speare R, Cashins S, McDonald KR, Phillott AD, et al. Spread of chytridiomycosis has caused the rapid global decline and extinction of frogs. EcoHealth. 2007;4:125–34. https://doi.org/10.1007/s10393-007-0093-5
Google Scholar
Ibelings BW, De Bruin A, Kagami M, Rijkeboer M, Brehm M, Van Donk E. Host parasite interactions between freshwater phytoplankton and chytrid fungi (Chytridiomycota). J Phycol. 2004;40:437–53.
Google Scholar
Bosch J, Martínez-Solano I, García-París. Evidence of a chytrid fungus infection involved in the decline of the common midwife toad (Alytes obstetricans) in protected areas of central Spain. Biological Conserv. 2001;97:331–7. https://doi.org/10.1016/S0006-3207(00)00132-4
Google Scholar
Bruning K, Lingeman R, Ringelberg J. Estimating the impact of fungal parasites on phytoplankton populations. Limnol Oceanogr. 1992;37:252–60. https://doi.org/10.4319/lo.1992.37.2.0252
Google Scholar
Paterson RA. Infestation of Chytridiaceous Fungi on Phytoplankton in Relation to Certain Environmental Factors. Ecology. 1960;41:416–24. https://doi.org/10.2307/1933316
Google Scholar
Ṣen B. Fungal parasitism of planktonic algae in Shearwater. IV: Parasitic occurrence of a new chytrid species on the blue-green alga Microcystis aeruginosa Kuetz. emend. Elenkin. 1998.
van Donk E, Ringelberg J. The effect of fungal parasitism on the succession of diatoms in Lake Maarsseveen I. Netherlands Freshwater Biol. 1983;13:241–51. https://doi.org/10.1111/j.1365-2427.1983.tb00674.x
Google Scholar
Agha R, Saebelfeld M, Manthey C, Rohrlack T, Wolinska J. Chytrid parasitism facilitates trophic transfer between bloom-forming cyanobacteria and zooplankton (Daphnia). Scientific Rep. 2016;6. https://doi.org/10.1038/srep35039
Frenken T, Wierenga J, van Donk E, Declerck SAJ, de Senerpont Domis LN, Rohrlack T, et al. Fungal parasites of a toxic inedible cyanobacterium provide food to zooplankton. Limnol Oceanogr. 2018;63:2384–93. https://doi.org/10.1002/lno.10945
Google Scholar
Kagami M, von Elert E, Ibelings BW, de Bruin A, van Donk E. The parasitic chytrid, Zygorhizidium, facilitates the growth of the cladoceran zooplankter, Daphnia, in cultures of the inedible alga, Asterionella. Proc Biological Sci/ Royal Soc. 2007;274:1561–6. https://doi.org/10.1098/rspb.2007.0425
Google Scholar
Gsell AS, de Senerpont Domis LN, van Donk E, Ibelings BW. Temperature alters host genotype-specific susceptibility to chytrid infection. PLoS One. 2013;8:e71737. https://doi.org/10.1371/journal.pone.0071737
Google Scholar
McKindles KM, Manes MA, McKay RM, Davis TW, Bullerjahn GS. Environmental factors affecting chytrid (Chytridiomycota) infection rates on Planktothrix agardhii. J Plankton Res. 2021a;43:658–72.
Google Scholar
Fallowfield HJ, Daft MJ. The extracellular release of dissolved organic carbon by freshwater cyanobacteria and algae and the interaction with Lysobacter CP-1. Br Phycol J. 1988;1617:317–26. https://doi.org/10.1080/00071618800650351
Google Scholar
Mueller B, den Haan J, Visser PM, Vermeij MJA, van Duyl FC. Effect of light and nutrient availability on the release of dissolved organic carbon (DOC) by Caribbean turf algae. Scientific Rep. 2016;6:1–9. https://doi.org/10.1038/srep23248
Google Scholar
Bruning K. Infection of the diatom Asterionella by a chytrid. II. Effects of light on survival and epidemic development of the parasite. J Plankton Res. 1991c;13:119–29. https://doi.org/10.1093/plankt/13.1.119
Google Scholar
Van den Wyngaert S, Gsell AS, Spaak P, Ibelings BW. Herbicides in the environment alter infection dynamics in a microbial host-parasite system. Environ Microbiol. 2013;15:837–47. https://doi.org/10.1111/j.1462-2920.2012.02874.x
Google Scholar
Almocera AES, Hsu SB, Sy PW. Extinction and uniform persistence in a microbial food web with mycoloop: Limiting behavior of a population model with parasitic fungi. Mathematical Biosci Eng. 2019;16:516–37.
Google Scholar
Frenken T, Miki T, Kagami M, Van de Waal DB, Van Donk E, Rohrlack T, et al. The potential of zooplankton in constraining chytrid epidemics in phytoplankton hosts. Ecology. 2020;101. https://doi.org/10.1002/ecy.2900
Gerla DJ, Gsell AS, Kooi BW, Ibelings BW, Van Donk E, Mooij WM. Alternative states and population crashes in a resource-susceptible-infected model for planktonic parasites and hosts. FMeier, M. H. et al. (2015) Neuropsychological Decline in Schizophrenia from the Premorbid to Post-Onset Period: Evidence from a Population-Representative Longitudinal Study. American J Psychiatry. 2013;58:538–51. https://doi.org/10.1111/fwb.12010
Google Scholar
Miki T, Takimoto G, Kagami M. Roles of parasitic fungi in aquatic food webs: A theoretical approach. Freshwater Biol. 2011;56:1173–83. https://doi.org/10.1111/j.1365-2427.2010.02562.x
Google Scholar
Guillard RRL, Lorenzen CJ. Yellow-green algae with chlorophyllid C. In Phycology. 1972;8:10–14.
Google Scholar
McKindles KM, Jorge AN, McKay RM, Davis TW, Bullerjahn GS. Isolation and characterization of Rhizophydiales (Chytridiomycota), obligate parasites of Planktothrix agardhii in a Laurentian Great Lakes embayment. Appl Environ Microbiol. 2021b;87:e02308–20.
Google Scholar
R Core Team. (2021). R: A Language and Environment for Statistical Computing.
RStudio Team. (2021). RStudio: Integrated Development Environment for R (1.4.1106).
Wickham, H (2016). ggplot2: Elegant Graphics for Data Analysis. Springer-Verlag New York.
Wickham H, Averick M, Bryan J, Chang W, McGowan LD, François R, et al. Welcome to the {tidyverse}. J Open Source Software. 2019;4:1686. https://doi.org/10.21105/joss.01686
Google Scholar
Champely, S (2018). PairedData (1.1.1).
Soetaert K, Petzoldt T, Setzer RW. Solving Differential Equations in {R}: Package deSolve. J Statistical Software. 2010;33:1–25. https://doi.org/10.18637/jss.v033.i09
Google Scholar
Frenken T, Velthuis M, de Senerpont Domis LN, Stephan S, Aben R, Kosten S, et al. Warming accelerates termination of a phytoplankton spring bloom by fungal parasites. Global Change Biol. 2016;22:299–309. https://doi.org/10.1111/gcb.13095
Google Scholar
Scholz B, Vyverman W, Küpper FC, Ólafsson HG, Karsten U. Effects of environmental parameters on chytrid infection prevalence of four marine diatoms: A laboratory case study. Botanica Marina. 2017;60:419–31. https://doi.org/10.1515/bot-2016-0105
Google Scholar
Sønstebø JH, Rohrlack T. Possible implications of Chytrid parasitism for population subdivision in freshwater cyanobacteria of the genus Planktothrix. Appl Environ Microbiol. 2011;77:1344–51. https://doi.org/10.1128/AEM.02153-10
Google Scholar
Bruning K. Infection of the diatom Asterionella by a chytrid. I. Effects of light on reproduction and infectivity of the parasite. J Plankton Res. 1991b;13:103–17. https://doi.org/10.1093/plankt/13.1.103
Google Scholar
Muehlstein LK, Amon JP, Leffler DL. Chemotaxis in the Marine Fungus Rhizophydium littoreum. Appl Environ Microbiol. 1988;54:1668–72. https://doi.org/10.1128/aem.54.7.1668-1672.1988
Google Scholar
Esch GW, Fernández JC. Introduction. In A Functional Biology of Parasitism (pp. 1–25). Springer Netherlands (1993). https://doi.org/10.1007/978-94-011-2352-5_1
Gerphagnon M, Colombet J, Latour D, Sime-Ngando T. Spatial and temporal changes of parasitic chytrids of cyanobacteria. Scientific Rep. 2017;7:6056. https://doi.org/10.1038/s41598-017-06273-1
Google Scholar
Maier MA, Peterson TD. Prevalence of chytrid parasitism among diatom populations in the lower Columbia River (2009–2013). Freshwater Biol. 2017;62:414–28. https://doi.org/10.1111/fwb.12876
Google Scholar
Sime-Ngando T. Phytoplankton chytridiomycosis: Fungal parasites of phytoplankton and their imprints on the food web dynamics. Front Microbiol. 2012;3:361. https://doi.org/10.3389/fmicb.2012.00361
Google Scholar
Kagami M, Urabe J. Mortality of the planktonic desmid, Staurastrum dorsidentiferum, due to interplay of fungal parasitism and low light conditions. SIL Proceed. 2002;28:1001–5. https://doi.org/10.1080/03680770.2001.11901868
Google Scholar
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