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A discrete, stochastic model of colonial phytoplankton population size structure: Development and application to in situ imaging‐in‐flow cytometer observations of Dinobryon
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/lno.11468openalex-snapshot
Environmental drivers of population variability in colony‐forming marine diatoms
inferredcites →https://doi.org/10.1007/bf00182132openalex-snapshot
Light-dependent phagotrophy in the freshwater mixotrophic chrysophyte Dinobryon cylindricum
inferredcites →https://doi.org/10.1007/s00442-020-04677-xopenalex-snapshot
Grazing resistance and poor food quality of a widespread mixotroph impair zooplankton secondary production
inferredcites →https://doi.org/10.1007/s10750-019-04112-0openalex-snapshot
Biogeography and ecology of freshwater chrysophyte cysts in Finland
inferredcites →https://doi.org/10.1016/0025-5564(74)90013-3openalex-snapshot
Cutting down recursive trees
inferredcites →https://doi.org/10.1016/s0022-5320(79)90115-1openalex-snapshot
The lorica of Dinobryon
inferredcites →https://doi.org/10.1038/s41598-020-65997-9openalex-snapshot
Assessing morphological congruence in Dinobryon species and their stomatocysts, including a newly established Dinobryon pediforme–stomatocyst connection
inferredcites →https://doi.org/10.1093/plankt/10.2.219openalex-snapshot
Ecological investigations of blooms of colonial Phaeocystis pouchetti—I. Abundance, biochemical composition, and metabolic rates
inferredcites →https://doi.org/10.1093/plankt/fbl054openalex-snapshot
Phosphorus gain by bacterivory promotes the mixotrophic flagellate Dinobryon spp. during re-oligotrophication
inferredcites →https://doi.org/10.1093/plankt/fbp098openalex-snapshot
Phytoplankton in a changing world: cell size and elemental stoichiometry
inferredcites →https://doi.org/10.1111/j.0022-3646.1995.00019.xopenalex-snapshot
THE MARINE MIXOTROPH DINOBRYON BALTICUM (CHRYSOPHYCEAE): PHAGOTROPHY AND SURVIVAL IN A COLD OCEAN1
inferredcites →https://doi.org/10.1111/j.0022-3646.1995.00070.xopenalex-snapshot
CHRYSOPHYTE POPULATION AND ENCYSTMENT PATTERNS IN TWO CANADIAN LAKES1
inferredcites →https://doi.org/10.1111/j.1469-8137.1967.tb06020.xopenalex-snapshot
MICROFIBRILS IN THE LORICA OF THE FRESHWATER ALGA DINOBRYON
inferredcites →https://doi.org/10.1111/j.1529-8817.1981.tb00840.xopenalex-snapshot
CHARACTERISTICS OF SEXUAL AND ASEXUAL RESTING CYST (STATOSPORE) FORMATION IN DINOBRYON CYLINDRICUM IMHOF (CHRYSOPHYTA)1
inferredcites →https://doi.org/10.1111/j.1529-8817.1986.tb04165.xopenalex-snapshot
HETEROTHALLIC SEXUALITY AND DENSITY DEPENDENT ENCYSTMENT IN THE CHRYSOPHYCEAN ALGA SYNURA PETERSENII KORSH.1
inferredcites →https://doi.org/10.1126/science.192.4242.885openalex-snapshot
Surface/Volume Ratio: Implications for Phytoplankton Morphology
inferredcites →https://doi.org/10.1126/science.231.4737.493openalex-snapshot
Bacterial Grazing by Planktonic Lake Algae
inferredcites →https://doi.org/10.1146/annurev.fluid.35.101101.161220openalex-snapshot
S MALL -S CALE H YDRODYNAMICS IN L AKES
inferredcites →https://doi.org/10.13140/rg.2.2.25965.87527openalex-snapshot
How do algae form multicellular groups?
inferredcites →https://doi.org/10.1371/journal.pone.0008679openalex-snapshot
Growth Rate Consequences of Coloniality in a Harmful Phytoplankter
inferredcites →https://doi.org/10.14288/1.0095969openalex-snapshot
Colonies as defence in the freshwater phytoplankton genus Dinobryon (Chrysophyceae)
inferredcites →https://doi.org/10.2216/i0031-8884-42-4-393.1openalex-snapshot
Chrysophyte odour production: resource-mediated changes at the cell and population levels
inferredcites →https://doi.org/10.2307/3222943openalex-snapshot
Studies on Variability in the Genus Dinobryon (Mastigophora)
inferredcites →https://doi.org/10.3354/ame01673openalex-snapshot
Role of temperature in growth, feeding, and vertical distribution of the mixotrophic chrysophyte Dinobryon
inferredcites →https://doi.org/10.3354/meps273043openalex-snapshot
Encystment probability and encystment rate: new terms to quantitatively describe formation of resting cysts in planktonic microbial populations
inferredcites →https://doi.org/10.4319/lo.1989.34.4.0673openalex-snapshot
Seasonal patterns of bacterivory by flagellates, ciliates, rotifers, and cladocerans in a freshwater planktonic community
inferredcites →https://doi.org/10.4319/lom.2007.5.195openalex-snapshot
A submersible imaging‐in‐flow instrument to analyze nano‐and microplankton: Imaging FlowCytobot
inferredcites →https://doi.org/10.4319/lom.2007.5.204openalex-snapshot
Automated taxonomic classification of phytoplankton sampled with imaging‐in‐flow cytometry
inferredcites →https://doi.org/10.7872/crya.v32.iss2.2011.157openalex-snapshot
Invited Review - Fight on Plankton! or, Phytoplankton Shape and Size as Adaptive Tools to Get Ahead in the Struggle for Life
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/lom3.70009openalex-snapshot
What is “accuracy”? Rethinking machine learning classifier performance metrics for highly imbalanced, high variance, zero‐inflated species count data
inferred← citeshttps://doi.org/10.1007/s11071-025-11936-0openalex-snapshot
A stochastic phytoplankton-zooplankton model for the impact of climate change and environmental disturbance on the growth of phytoplankton
inferred← citeshttps://doi.org/10.1016/j.optlastec.2024.111000openalex-snapshot
Flow stokes microscopy for high throughput classification of marine particles
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