All Stories

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