All Stories

  1. Feeding in mixoplankton enhances phototrophy increasing bloom-induced pH changes with ocean acidification
  2. Mucus-Trap-Assisted Feeding Is a Common Strategy of the Small Mixoplanktonic Prorocentrum pervagatum and P. cordatum (Prorocentrales, Dinophyceae)
  3. Errata and re-visitation of “What is the limit for photoautotrophic plankton growth rates?” (Flynn and Raven, 2017)
  4. Trait trade-offs in phagotrophic microalgae: the mixoplankton conundrum
  5. The Mixoplankton Database (MDB): Diversity of photo‐phago‐trophic plankton in form, function, and distribution across the global ocean
  6. Plankton digital twins—a new research tool
  7. ‘Boom‐and‐busted’ dynamics of phytoplankton‐virus interactions explain the paradox of the plankton
  8. Deuterium in marine organic biomarkers: toward a new tool for quantifying aquatic mixotrophy
  9. Niche separation between different functional types of mixoplankton: results from NPZ-style N-based model simulations
  10. Mixotrophic protists and a new paradigm for marine ecology: where does plankton research go now?
  11. Sampling bias misrepresents the biogeographical significance of constitutive mixotrophs across global oceans
  12. Toward a mechanistic understanding of trophic structure: inferences from simulating stable isotope ratios
  13. Effects of growth rate, cell size, motion, and elemental stoichiometry on nutrient transport kinetics
  14. Dynamic changes in carbonate chemistry in the microenvironment around single marine phytoplankton cells
  15. Oceanic protists with different forms of acquired phototrophy display contrasting biogeographies and abundance
  16. Physiology limits commercially viable photoautotrophic production of microalgal biofuels
  17. The role of coccolithophore calcification in bioengineering their environment
  18. Coupling a simple irradiance description to a mechanistic growth model to predict algal production in industrial-scale solar-powered photobioreactors
  19. Metabolic and physiological changes in Prymnesium parvum when grown under, and grazing on prey of, variable nitrogen:phosphorus stoichiometry
  20. Ocean Acidification Affects the Phyto-Zoo Plankton Trophic Transfer Efficiency
  21. Defining Planktonic Protist Functional Groups on Mechanisms for Energy and Nutrient Acquisition: Incorporation of Diverse Mixotrophic Strategies
  22. Modelling alkaline phosphatase activity in microalgae under orthophosphate limitation: the case of Phaeocystis globosa
  23. Acclimation, adaptation, traits and trade-offs in plankton functional type models: reconciling terminology for biology and modelling
  24. climate change affects the base of the marine food chain
  25. Modeling DOM Biogeochemistry
  26. understanding what feeds the fish
  27. Introduction to the BASIN Special Issue: State of art, past present a view to the future
  28. Influence of the N:P supply ratio on biomass productivity and time-resolved changes in elemental and bulk biochemical composition of Nannochloropsis sp.
  29. Climate change changes the nutritional value of oceanic primary producers
  30. Parental exposure to elevated pCO2 influences the reproductive success of copepods
  31. is the potential for algal biofuels really as good as the hype?
  32. European sea bass, Dicentrarchus labrax, in a changing ocean
  33. Have we been underestimating the effects of ocean acidification in zooplankton?
  34. for decades we have misrepresented how the marine food web functions - this explains why
  35. Rapid determination of bulk microalgal biochemical composition by Fourier-Transform Infrared spectroscopy
  36. Cutting the Canopy to Defeat the “Selfish Gene”; Conflicting Selection Pressures for the Integration of Phototrophy in Mixotrophic Protists
  37. The role of mixotrophic protists in the biological carbon pump
  38. Acquired phototrophy in Mesodinium and Dinophysis – A review of cellular organization, prey selectivity, nutrient uptake and bioenergetics
  39. Monster potential meets potential monster: pros and cons of deploying genetically modified microalgae for biofuels production
  40. Erratum: Changes in pH at the exterior surface of plankton with ocean acidification
  41. Misuse of the phytoplankton-zooplankton dichotomy: the need to assign organisms as mixotrophs within plankton functional types
  42. Review of climate change impacts on marine aquaculture in the UK and Ireland
  43. Changes in pH at the exterior surface of plankton with ocean acidification
  44. Modelling mixotrophy in harmful algal blooms: More or less the sum of the parts?
  45. Modeling of HABs and eutrophication: Status, advances, challenges
  46. Do external resource ratios matter?
  47. Selection for fitness at the individual or population levels: Modelling effects of genetic modifications in microalgae on productivity and environmental safety
  48. IS THE GROWTH RATE HYPOTHESIS APPLICABLE TO MICROALGAE?1
  49. End-To-End Models for the Analysis of Marine Ecosystems: Challenges, Issues, and Next Steps
  50. Ecological modelling in a sea of variable stoichiometry: Dysfunctionality and the legacy of Redfield and Monod
  51. Placing microalgae on the biofuels priority list: a review of the technological challenges
  52. Going for the slow burn: why should possession of a low maximum growth rate be advantageous for microalgae?
  53. AFestschriftin honour of Professor John A. Raven
  54. Phytoplankton in a changing world: cell size and elemental stoichiometry
  55. Phagotrophy in the origins of photosynthesis in eukaryotes and as a complementary mode of nutrition in phototrophs: relation to Darwin's insectivorous plants
  56. Building the "perfect beast": modelling mixotrophic plankton
  57. Food-density-dependent inefficiency in animals with a gut as a stabilizing mechanism in trophic dynamics
  58. Aldehyde-induced insidious effects cannot be considered as a diatom defence mechanism against copepods
  59. Attack is not the best form of defense: Lessons from harmful algal bloom dynamics
  60. Allometry and stoichiometry of unicellular, colonial and multicellular phytoplankton
  61. MODELING THE RELEASE OF DISSOLVED ORGANIC MATTER BY PHYTOPLANKTON1
  62. USE, ABUSE, MISCONCEPTIONS AND INSIGHTS FRoM QUOTA MODELS — THE DROOP CELL QUOTA MODEL 40 YEARS ON
  63. The importance of the form of the quota curve and control of non-limiting nutrient transport in phytoplankton models
  64. Morphological Controls on Cannibalism in a Planktonic Marine Phagotroph
  65. ... and goodbye for now!
  66. Importance of Interactions between Food Quality, Quantity, and Gut Transit Time on Consumer Feeding, Growth, and Trophic Dynamics
  67. Accounting for grazing dynamics in nitrogen-phytoplankton-zooplankton (NPZ) models
  68. Accounting for variation in prey selectivity by zooplankton
  69. Promotion of harmful algal blooms by zooplankton predatory activity
  70. Reply to Horizons Article 'Plankton functional type modelling: running before we can walk' Anderson (2005): II. Putting trophic functionality into plankton functional types
  71. Corrigendum
  72. Development of a robust marine ecosystem model to predict the role of iron in biogeochemical cycles: A comparison of results for iron-replete and iron-limited areas, and the SOIREE iron-enrichment experiment
  73. Chlorophyll content and fluorescence responses cannot be used to gauge reliably phytoplankton biomass, nutrient status or growth rate
  74. Castles built on sand: dysfunctionality in plankton models and the inadequacy of dialogue between biologists and modellers
  75. Modelling marine phytoplankton growth under eutrophic conditions
  76. Predator-prey interactions: is 'ecological stoichiometry' sufficient when good food goes bad?
  77. Phytoplankton blooms: a 'loophole' in microzooplankton grazing impact?
  78. Nutritional Status and Diet Composition Affect the Value of Diatoms as Copepod Prey
  79. Incorporating plankton respiration in models of aquatic ecosystem function
  80. Interrelationships between the pathways of inorganic nitrogen assimilation in the cyanobacterium Gloeothece can be described using a mechanistic mathematical model
  81. Do we need complex mechanistic photoacclimation models for phytoplankton?
  82. Application of a two-compartment one-toxin model to predict the toxin accumulation in Pacific oysters in Hiroshima Bay, Japan
  83. The influence of changes in predation rates on marine microbial predator/prey interactions: a modelling study
  84. Modelling multi-nutrient interactions in phytoplankton; balancing simplicity and realism
  85. Operation of light-dark cycles within simple ecosystem models of primary production and the consequences of using phytoplankton models with different abilities to assimilate N in darkness
  86. A Modelling Exploration of Vertical Migration by Phytoplankton
  87. HOW CRITICAL IS THE CRITICAL N:P RATIO?1
  88. A Modelling Exploration of Vertical Migration by Phytoplankton
  89. The large capacity for dark nitrate-assimilation in diatoms may overcome nitrate limitation of growth
  90. Modelling suggests that optimization of dark nitrogen-assimilation need not be a critical selective feature in phytoplankton
  91. Toxin production in migrating dinoflagellates: a modelling study of PSP producing Alexandrium
  92. N-ASSIMILATION IN THE NOXIOUS FLAGELLATE HETEROSIGMA CARTERAE (RAPHIDOPHYCEAE): DEPENDENCE ON LIGHT, N-SOURCE, AND PHYSIOLOGICAL STATE1
  93. N‐ASSIMILATION IN THE NOXIOUS FLAGELLATE HETEROSIGMA CARTERAE (RAPHIDOPHYCEAE): DEPENDENCE ON LIGHT, N‐SOURCE, AND PHYSIOLOGICAL STATE 1
  94. A comparison of two N-irradiance interaction models of phytoplankton growth
  95. Growth dynamics and toxicity of Alexandrium fundyense (Dinophyceae): the effect of changing N∶P supply ratios on internal toxin and nutrient levels
  96. A mechanistic model of photoinhibition
  97. Modelling phosphate transport and assimilation in microalgae; how much complexity is warranted?
  98. Utilization of dissolved inorganic carbon (DIC) and the response of the marine flagellateIsochrysis galbanato carbon or nitrogen stress
  99. INTERACTIONS BETWEEN IRON, LIGHT, AMMONIUM, AND NITRATE: INSIGHTS FROM THE CONSTRUCTION OF A DYNAMIC MODEL OF ALGAL PHYSIOLOGY
  100. Interactions between nitrate and ammonium in Emiliania huxleyi
  101. Amino acid uptake by the toxic dinoflagellate Alexandrium fundyense
  102. Release of nitrite by marine dinoflagellates: development of a mathematical simulation
  103. BOOK REVIEWS
  104. Modelling the interactions between ammonium and nitrate uptake in marine phytoplankton
  105. A short version of the ammonium-nitrate interaction model
  106. An automated HPLC method for the rapid analysis of paralytic shellfish toxins from dinoflagellates and bacteria using precolumn oxidation at low temperature
  107. Prey selection and rejection by a microflagellate; implications for the study and operation of microbial food webs
  108. Changes in toxins, intracellular and dissolved free amino acids of the toxic dinoflagellate Gymnodinium catenatum in response to changes in inorganic nutrients and salinity
  109. GROWTH OF HETEROSIGMA CARTERAE (RAPHIDOPHYCEAE) ON NITRATE AND AMMONIUM AT THREE PHOTON FLUX DENSITIES: EVIDENCE FOR N STRESS IN NITRATE-GROWING CELLS1
  110. Modelling interactions between phytoplankton and bacteria under nutrient-regenerating conditions
  111. Predator-prey interactions between Isochrysis galbana and Oxyrrhis marina . III. Mathematical modelling of predation and nutrient regeneration
  112. Carbon-nitrogen relations during batch growth ofNannochloropsis oculata (Eustigmatophyceae) under alternating light and dark
  113. Predator-prey interactions between Isochrysis galbana and Oxyrrhis marina . II. Release of non-protein amines and faeces during predation of Isochrysis
  114. Predator-prey interactions between Isochrysis galbana and Oxyrrhis marina . I. Changes in particulate δ 13 C
  115. Modelling temporal decoupling between biomass and numbers during the transient nitrogen-limited growth of a marine phytoflagellate
  116. Changes in fatty acids, amino acids and carbon/nitrogen biomass during nitrogen starvation of ammonium- and nitrate-grownIsochrysis galbana
  117. Relationships between photopigments, cell carbon, cell nitrogen and growth rate for a marine nanoflagellate
  118. Algal carbon–nitrogen metabolism: a biochemical basis for modelling the interactions between nitrate and ammonium uptake
  119. Composition of intracellular and extracellular pools of amino acids, and amino acid utilization of microalgae of different sizes
  120. Changes in intracellular and extracellular ?-amino acids in Gloeothece during N2-fixation and following addition of ammonium
  121. Fluctuations in the intracellular amino acids ofGloeotheceduring nitrogen fixation and following addition of ammonium
  122. The ratio of glutamine:glutamate in microalgae: a biomarker for N-status suitable for use at natural cell densities
  123. The concept of “primary production” in aquatic ecology
  124. Effects of N deprivation and darkness on composition of free amino acid pool in and on amino acid release from diatom Phaeodactylum tricornutum Bohlin
  125. The simultaneous assimilation of ammonium and l-arginine by the marine diatom Phaeodactylum tricornutum Bohlin