On the public citation graph

Assessment of Microzooplankton Grazing on Heterosigma akashiwo Using a Species- Specific Approach Combining Quantitative Real-Time PCR (QPCR) and Dilution Methods

https://doi.org/10.1007/s00248-007-9263-9

0 signed · 118 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.

Claim with ORCID

Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.

See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/nt.2620030202openalex-snapshot

Interactions between bacteria and harmful algae: A review

inferredcites →https://doi.org/10.1006/meth.2001.1262openalex-snapshot

Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

inferredcites →https://doi.org/10.1007/978-1-4615-8714-9openalex-snapshot

Culture of Marine Invertebrate Animals

inferredcites →https://doi.org/10.1007/978-1-4615-8714-9_3openalex-snapshot

Culture of Phytoplankton for Feeding Marine Invertebrates

inferredcites →https://doi.org/10.1007/978-1-4684-3890-1openalex-snapshot

Primary Productivity in the Sea

inferredcites →https://doi.org/10.1007/978-1-4684-3890-1_24openalex-snapshot

Nutrient Regeneration and Primary Production in the Sea

inferredcites →https://doi.org/10.1007/978-94-011-4976-1_22openalex-snapshot

A Framework for a Delaware Inland Bays Environmental Classification

inferredcites →https://doi.org/10.1007/bf00349570openalex-snapshot

Virus-like particles in Heterosigma akashiwo (Raphidophyceae): a possible red tide disintegration mechanism

inferredcites →https://doi.org/10.1007/bf00392743openalex-snapshot

Impact of copepod grazing on the red-tide flagellate Chattonella antiqua

inferredcites →https://doi.org/10.1007/bf00397668openalex-snapshot

Estimating the grazing impact of marine micro-zooplankton

inferredcites →https://doi.org/10.1007/bf02696046openalex-snapshot

Linkage between microzooplankton grazing and phytoplankton growth in a Gulf of Mexico estuary

inferredcites →https://doi.org/10.1007/s00248-006-9030-3openalex-snapshot

Use of Quantitative Real-Time PCR to Investigate the Dynamics of the Red Tide Dinoflagellate Lingulodinium polyedrum

inferredcites →https://doi.org/10.1016/b978-0-12-693010-8.50008-6openalex-snapshot

The Planktonic Marine Flagellates

inferredcites →https://doi.org/10.1016/b978-012693018-4/50007-0openalex-snapshot

The Planktonic Marine Flagellates

inferredcites →https://doi.org/10.1016/j.hal.2004.03.001openalex-snapshot

A bacterium that inhibits the growth of Pfiesteria piscicida and other dinoflagellates

inferredcites →https://doi.org/10.1016/j.hal.2004.03.003openalex-snapshot

Predator–prey interactions between a planktonic ciliate Strombidium sp. (Ciliophora, Oligotrichida) and the dinoflagellate Pfiesteria piscicida (Dinamoebiales, Pyrrophyta)

inferredcites →https://doi.org/10.1016/j.hal.2004.06.011openalex-snapshot

Microbial herbivory on the brown tide alga, Aureococcus anophagefferens: results from natural ecosystems, mesocosms and laboratory experiments

inferredcites →https://doi.org/10.1016/j.hal.2004.06.012openalex-snapshot

Pico- and nanoplankton dynamics during bloom initiation of Aureococcus in a Long Island, NY bay

inferredcites →https://doi.org/10.1016/j.hal.2004.06.013openalex-snapshot

Ecology of phytoplankton communities dominated by Aureococcus anophagefferens: the role of viruses, nutrients, and microzooplankton grazing

inferredcites →https://doi.org/10.1016/j.hal.2005.09.001openalex-snapshot

Bottom-up controls on a mixed-species HAB assemblage: A comparison of sympatric Chattonella subsalsa and Heterosigma akashiwo (Raphidophyceae) isolates from the Delaware Inland Bays, USA

inferredcites →https://doi.org/10.1016/s0924-7963(01)00061-6openalex-snapshot

Taxon-specific growth and selective microzooplankton grazing of phytoplankton in the Northeast Atlantic

inferredcites →https://doi.org/10.1016/s1568-9883(03)00019-2openalex-snapshot

Feeding by ciliates on two harmful algal bloom species, Prymnesium parvum and Prorocentrum minimum

inferredcites →https://doi.org/10.1016/s1568-9883(04)00025-3openalex-snapshot

A bacterium that inhibits the growth of Pfiesteria piscicida and other dinoflagellates

inferredcites →https://doi.org/10.1023/a:1005951706152openalex-snapshot

A Framework for a Delaware Inland Bays Environmental Classification

inferredcites →https://doi.org/10.1038/36285openalex-snapshot

Mutation of the mouse klotho gene leads to a syndrome resembling ageing.

inferredcites →https://doi.org/10.1046/j.1529-8817.2003.01162.xopenalex-snapshot

CHARACTERIZATION OF HaRNAV, A SINGLE‐STRANDED RNA VIRUS CAUSING LYSIS OF HETEROSIGMA AKASHIWO (RAPHIDOPHYCEAE)1

inferredcites →https://doi.org/10.1093/plankt/19.5.603openalex-snapshot

Predation by a photosynthetic dinoflagellate Gyrodinium instriatum on loricated ciliates

inferredcites →https://doi.org/10.1093/plankt/20.9.1711openalex-snapshot

Growth and grazing of a large heterotrophic dinoflagellate, Noctiluca scintillans, in laboratory cultures

inferredcites →https://doi.org/10.1093/plankt/6.1.195openalex-snapshot

Abundance and productivity of heterotrophic nanoplankton in Georgia coastal waters

inferredcites →https://doi.org/10.1101/gr.6.10.986openalex-snapshot

Real time quantitative PCR.

inferredcites →https://doi.org/10.1111/j.1439-0485.1981.tb00096.xopenalex-snapshot

The Influence of Grazing by two Acartia Species on Olisthodiscus luteus CARTER

inferredcites →https://doi.org/10.1111/j.1529-8817.2006.00285.xopenalex-snapshot

RAPHIDOPHYCEAE [CHADEFAUD EX SILVA] SYSTEMATICS AND RAPID IDENTIFICATION: SEQUENCE ANALYSES AND REAL‐TIME PCR ASSAYS1

inferredcites →https://doi.org/10.1111/j.1529-8817.2012.01212.xopenalex-snapshot

DESCRIPTION OF VIRIDILOBUS MARINUS (GEN. ET SP. NOV.), A NEW RAPHIDOPHYTE FROM DELAWARE'S INLAND BAYS

inferredcites →https://doi.org/10.1111/j.1550-7408.2003.tb00134.xopenalex-snapshot

Feeding by the Heterotrophic Dinoflagellate Oxyrrhis marina on the Red‐Tide Raphidophyte Heterosigma akashiwo: a Potential Biological Method to Control Red Tides Using Mass‐Cultured Grazers

inferredcites →https://doi.org/10.1111/j.1550-7408.2004.tb00292.xopenalex-snapshot

Mixotrophy in the Phototrophic Harmful Alga Cochlodinium polykrikoides (Dinophycean): Prey Species, the Effects of Prey Concentration, and Grazing Impact

inferredcites →https://doi.org/10.1128/aem.66.11.4641-4648.2000openalex-snapshot

Development of Real-Time PCR Assays for Rapid Detection of Pfiesteria piscicida and Related Dinoflagellates

inferredcites →https://doi.org/10.1128/aem.70.2.1199-1206.2004openalex-snapshot

Development of a Real-Time PCR Assay for Rapid Detection and Quantification ofAlexandrium minutum(a Dinoflagellate)

inferredcites →https://doi.org/10.1289/ehp.02110465openalex-snapshot

New fish-killing alga in coastal Delaware produces neurotoxins.

inferredcites →https://doi.org/10.2144/99271bm13openalex-snapshot

Rapid DNA Extraction from Ferns for PCR–Based Analyses

inferredcites →https://doi.org/10.2307/1352932openalex-snapshot

Microzooplankton Grazing and Nitrogen Excretion across a Surface Estuarine-Coastal Interface

inferredcites →https://doi.org/10.2331/suisan.57.1409openalex-snapshot

Isolation of a Marine Gliding Bacterium That Kills Chattonella antiqua (Raphidophyceae)

inferredcites →https://doi.org/10.3354/ame01292openalex-snapshot

Quantitative real-time PCR for detecting germination of Heterosigma akashiwo and Chattonella subsalsa cysts from Delaware’s Inland Bays, USA

inferredcites →https://doi.org/10.3354/ame022261openalex-snapshot

Grazing on Pfiesteria piscicida by microzooplankton

inferredcites →https://doi.org/10.3354/ame024153openalex-snapshot

New biocompatible tracer particles: use for estimation of microzooplankton grazing, digestion, and growth rates

inferredcites →https://doi.org/10.3354/ame024275openalex-snapshot

Assessing temporal and spatial variability in Pfiesteria piscicida distributions using molecular probing techniques

inferredcites →https://doi.org/10.3354/ame026247openalex-snapshot

Dinoflagellate grazing on the raphidophyte Fibrocapsa japonica

inferredcites →https://doi.org/10.3354/ame028079openalex-snapshot

Grazing by microzooplankton on Pfiesteria piscicida cultures with different histories of toxicity

inferredcites →https://doi.org/10.3354/ame028289openalex-snapshot

Growth and grazing rates of the prostomatid ciliate Tiarina fusus on red-tide and toxic algae

inferredcites →https://doi.org/10.3354/ame030207openalex-snapshot

Direct estimates of the contribution of viral lysis and microzooplankton grazing to the decline of a Micromonas spp. population

inferredcites →https://doi.org/10.3354/ame036181openalex-snapshot

Feeding by the marine planktonic ciliate Strombidinopsis jeokjo on common heterotrophic dinoflagellates

inferredcites →https://doi.org/10.3354/ame038249openalex-snapshot

Feeding by the mixotrophic red-tide dinoflagellate Gonyaulax polygramma: mechanisms, prey species, effects of prey concentration, and grazing impact

inferredcites →https://doi.org/10.3354/ame039121openalex-snapshot

Effects of Heterosigma akashiwo (Raphidophyceae) on protist grazers: laboratory experiments with ciliates and heterotrophic dinoflagellates

inferredcites →https://doi.org/10.3354/ame040121openalex-snapshot

Evaluating vertical migration behavior of harmful raphidophytes in the Delaware Inland Bays utilizing quantitative real-time PCR

inferredcites →https://doi.org/10.3354/ame040133openalex-snapshot

Feeding by phototrophic red-tide dinoflagellates: five species newly revealed and six species previously known to be mixotrophic

inferredcites →https://doi.org/10.3354/ame041145openalex-snapshot

Growth rates and starvation survival of three species of the pallium-feeding, thecate dinoflagellate genus Protoperidinium

inferredcites →https://doi.org/10.3354/ame044263openalex-snapshot

Distribution of the heterotrophic dinoflagellate Pfiesteria piscicida in Korean waters and its consumption of mixotrophic dinoflagellates, raphidophytes and fish blood cells

inferredcites →https://doi.org/10.3354/meps042199openalex-snapshot

Clearance of bacteria-sized particles by natural populations of nanoplankton in the Chesapeake Bay outflow plume

inferredcites →https://doi.org/10.3354/meps120053openalex-snapshot

A refined dilution technique for measuring the community grazing impact of microzooplankton, with experimental tests in the central equatorial Pacific

inferredcites →https://doi.org/10.3354/meps259303openalex-snapshot

Relative grazing impact of microzooplankton and mesozooplankton on a bloom of the toxic dinoflagellate Alexandrium minutum

inferredcites →https://doi.org/10.3354/meps260033openalex-snapshot

Effects of high pH on the growth and survival of six marine heterotrophic protists

inferredcites →https://doi.org/10.3354/meps270199openalex-snapshot

Moderate increase in the biomass of omnivorous copepods may ease grazing control of planktonic algae

inferredcites →https://doi.org/10.3354/meps280085openalex-snapshot

Feeding by the heterotrophic dinoflagellates Gyrodinium dominans and G. spirale on the red-tide dinoflagellate Prorocentrum minimum

inferredcites →https://doi.org/10.3354/meps295069openalex-snapshot

Feeding and grazing impact of the newly described heterotrophic dinoflagellate Stoeckeria algicida on the harmful alga Heterosigma akashiwo

inferredcites →https://doi.org/10.3354/meps322085openalex-snapshot

Bacterivory by co-occurring red-tide algae, heterotrophic nanoflagellates, and ciliates

inferredcites →https://doi.org/10.4319/lo.1991.36.1.0050openalex-snapshot

Pigment‐specific rates of phytoplankton growth and microzooplankton grazing in the open subarctic Pacific Ocean

inferredcites →https://doi.org/10.4319/lo.1994.39.8.1985openalex-snapshot

Fluorometric analysis of chlorophyll a in the presence of chlorophyll b and pheopigments

inferredcites →https://doi.org/10.4319/lo.1995.40.4.0827openalex-snapshot

Taxon-specific analysis of microzooplankton grazing rates and phytoplankton growth rates

inferredcites →https://doi.org/10.4319/lo.1998.43.1.0117openalex-snapshot

Conditions necessary for Chattonella antiqua red tide outbreaks

inferredcites →https://doi.org/10.4319/lo.2002.47.1.0129openalex-snapshot

Impacts of nutrients and grazing mortality on the abundance of Aureococcus anophagefferens during a New York brown tide bloom

inferredcites →https://doi.org/10.4319/lo.2002.47.2.0545openalex-snapshot

Viruses causing lysis of the toxic bloom‐forming alga Heterosigma akashiwo(Raphidophyceae) are widespread in coastal sediments of British Columbia, Canada

inferredcites →https://doi.org/10.4319/lo.2002.47.5.1346openalex-snapshot

Iron‐sulfur‐phosphorus cycling in the sediments of a shallow coastal bay: Implications for sediment nutrient release and benthic macroalgal blooms

inferredcites →https://doi.org/10.4319/lom.2003.1.92openalex-snapshot

The use of quantitative polymerase chain reaction for the detection and enumeration of the harmful alga Aureococcus anophagefferens in environmental samples along the United States East Coast

inferredcites →https://doi.org/10.4319/lom.2005.3.381openalex-snapshot

Improved quantitative real‐time PCR assays for enumeration of harmful algal species in field samples using an exogenous DNA reference standard

inferredcites →https://doi.org/10.4319/lom.2006.4.193openalex-snapshot

Simultaneous enumeration of multiple raphidophyte species by quantitative real-time PCR: capabilities and limitations

inferredcites →https://doi.org/10.4319/lom.2011.1.92openalex-snapshot

The use of quantitative polymerase chain reaction for the detection and enumeration of the harmful alga Aureococcus anophagefferens in environmental samples along the United States East Coast

inferredcites →https://doi.org/10.5194/os-1-1-2005openalex-snapshot

The reliability of grazing rate estimates from dilution experiments: Have we over-estimated rates of organic carbon consumption by microzooplankton?

inferredcites →https://doi.org/10.5194/os-1-39-2005openalex-snapshot

Reality checks on microbial food web interactions in dilution experiments: responses to the comments of Dolan and McKeon

inferredcites →https://doi.org/10.5860/choice.35-3284openalex-snapshot

Identifying marine phytoplankton

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.11646/phytotaxa.127.1.19zenodo-depositor-declared

MIDTAL (Microarrays for the Detection of Toxic Algae)

inferred← citeshttps://doi.org/10.1002/9781118994672.ch7openalex-snapshot

Food Web and Ecosystem Impacts of Harmful Algae

inferred← citeshttps://doi.org/10.1002/lno.12297openalex-snapshot

Environmental and ecological drivers of harmful algal blooms revealed by automated underwater microscopy

inferred← citeshttps://doi.org/10.1007/s00248-012-0019-9openalex-snapshot

Contrasting Community versus Population-Based Estimates of Grazing and Virus-Induced Mortality of Phytoplankton

inferred← citeshttps://doi.org/10.1007/s00267-025-02156-8openalex-snapshot

Comparison of Two Molecular Methods, Quantitative Polymerase Chain Reaction and Sandwich Hybridization Assay, for Monitoring the Harmful Algal Bloom Species, Heterosigma akashiwo

inferred← citeshttps://doi.org/10.1007/s10811-018-1444-zopenalex-snapshot

Critical comparison of molecular methods for detection and enumeration of the harmful algal species, Heterosigma akashiwo, in environmental water samples

inferred← citeshttps://doi.org/10.1007/s10811-021-02538-5openalex-snapshot

Development of a recombinase polymerase amplification combined with lateral flow dipstick assay for rapid and sensitive detection of Heterosigma akashiwo

inferred← citeshttps://doi.org/10.1007/s10811-025-03635-5openalex-snapshot

Development of a novel quantitative PCR assay for the toxic dinoflagellate Karenia brevis and its application for measuring in situ microzooplankton grazing impact

inferred← citeshttps://doi.org/10.1007/s12237-025-01629-7openalex-snapshot

Assessing Environmental Drivers and Protist Community Dynamics that Shaped the Historic August 2022 Heterosigma akashiwo Bloom in San Francisco Bay, California

inferred← citeshttps://doi.org/10.1016/b978-0-12-822861-6.00019-4openalex-snapshot

Current applications and technological advances in quantitative real-time PCR (qPCR): a versatile tool for the study of phytoplankton ecology

inferred← citeshttps://doi.org/10.1016/j.ecss.2012.10.004openalex-snapshot

Effects of climatic variability on phytoplankton community structure and bloom development in the eutrophic, microtidal, New River Estuary, North Carolina, USA

inferred← citeshttps://doi.org/10.1016/j.hal.2007.05.006openalex-snapshot

A comparison of future increased CO2 and temperature effects on sympatric Heterosigma akashiwo and Prorocentrum minimum

inferred← citeshttps://doi.org/10.1016/j.hal.2007.12.018openalex-snapshot

Using quantitative real-time PCR to study competition and community dynamics among Delaware Inland Bays harmful algae in field and laboratory studies

inferred← citeshttps://doi.org/10.1016/j.hal.2009.08.009openalex-snapshot

Expansion of potentially harmful algal taxa in a Georgia Estuary (USA)

inferred← citeshttps://doi.org/10.1016/j.hal.2010.07.005openalex-snapshot

Fraser river sockeye salmon marine survival decline and harmful blooms of Heterosigma akashiwo

inferred← citeshttps://doi.org/10.1016/j.hal.2013.10.005openalex-snapshot

Raphidophyte red tides in Korean waters

inferred← citeshttps://doi.org/10.1016/j.hal.2013.10.009openalex-snapshot

Red tides in Masan Bay, Korea in 2004–2005: II. Daily variations in the abundance of heterotrophic protists and their grazing impact on red-tide organisms

inferred← citeshttps://doi.org/10.1016/j.hal.2014.05.014openalex-snapshot

Effects of growth phase, diel cycle and macronutrient stress on the quantification of Heterosigma akashiwo using qPCR and SHA

inferred← citeshttps://doi.org/10.1016/j.hal.2016.10.005openalex-snapshot

Development of real-time RT-PCR for detecting viable Cochlodinium polykrikoides (Dinophyceae) cysts in sediment

inferred← citeshttps://doi.org/10.1016/j.hal.2016.11.009openalex-snapshot

Selective growth promotion of bloom-forming raphidophyte Heterosigma akashiwo by a marine bacterial strain

inferred← citeshttps://doi.org/10.1016/j.hal.2020.101804openalex-snapshot

Functional trait thermal acclimation differs across three species of mid-Atlantic harmful algae

inferred← citeshttps://doi.org/10.1016/j.hal.2024.102789openalex-snapshot

Zooplankton grazing can facilitate and control the proliferation of harmful algal blooms caused by Dinophysis acuminata in NY, USA, estuaries

inferred← citeshttps://doi.org/10.1016/j.watres.2009.06.051openalex-snapshot

Harmful algae and their potential impacts on desalination operations off southern California

inferred← citeshttps://doi.org/10.1038/ismej.2008.101openalex-snapshot

Protists are microbes too: a perspective

inferred← citeshttps://doi.org/10.1093/plankt/fbq151openalex-snapshot

Detecting copepod grazing on low-concentration populations of Alexandrium fundyense using PCR identification of ingested prey

inferred← citeshttps://doi.org/10.1093/plankt/fbx039openalex-snapshot

Effects of zooplankton grazing on the bloom-forming Cyanothece sp. in a subtropical estuarine lake

inferred← citeshttps://doi.org/10.1111/1462-2920.14049openalex-snapshot

Eukaryotic phytoplankton community spatiotemporal dynamics as identified through gene expression within a eutrophic estuary

inferred← citeshttps://doi.org/10.1111/j.1529-8817.2009.00781.xopenalex-snapshot

NITRATE REDUCTASE (NR1) SEQUENCE AND EXPRESSION IN THE HARMFUL ALGA HETEROSIGMA AKASHIWO (RAPHIDOPHYCEAE)1

inferred← citeshttps://doi.org/10.1111/j.1529-8817.2012.01212.xopenalex-snapshot

DESCRIPTION OF VIRIDILOBUS MARINUS (GEN. ET SP. NOV.), A NEW RAPHIDOPHYTE FROM DELAWARE'S INLAND BAYS

inferred← citeshttps://doi.org/10.1111/j.1550-7408.2011.00550.xopenalex-snapshot

Mixotrophy in Red Tide Algae Raphidophytes1

inferred← citeshttps://doi.org/10.1128/aem.00580-15openalex-snapshot

Community-Level and Species-Specific Associations between Phytoplankton and Particle-Associated Vibrio Species in Delaware's Inland Bays

inferred← citeshttps://doi.org/10.1146/annurev-marine-120709-142802openalex-snapshot

Marine Protistan Diversity

inferred← citeshttps://doi.org/10.3354/ame01292openalex-snapshot

Quantitative real-time PCR for detecting germination of Heterosigma akashiwo and Chattonella subsalsa cysts from Delaware’s Inland Bays, USA

inferred← citeshttps://doi.org/10.3354/ame01354openalex-snapshot

Feeding by raphidophytes on the cyanobacterium Synechococcus sp.

inferred← citeshttps://doi.org/10.3354/ame01391openalex-snapshot

Growth and grazing of microzooplankton in response to the harmful alga Heterosigma akashiwo in prey mixtures

inferred← citeshttps://doi.org/10.3354/ame01514openalex-snapshot

Microzooplankton grazing before, during and after a cyanobacterial bloom in Vancouver Lake, Washington, USA

inferred← citeshttps://doi.org/10.3354/ame01679openalex-snapshot

Potential viral stimulation of primary production observed during experimental determinations of phytoplankton mortality

inferred← citeshttps://doi.org/10.3389/fmars.2025.1687609openalex-snapshot

Validation of a modified Landry-Hassett dilution technique to quantify the growth and mortality rates of subpopulations of planktonic microbes

inferred← citeshttps://doi.org/10.5697/oc.54-2.287openalex-snapshot

The link between shrimp farm runoff and blooms of toxic Heterosigma akashiwo in Red Sea coastal waters

inferred← citeshttps://doi.org/10.5772/25265openalex-snapshot

Molecular Techniques to Estimate Biodiversity with Case Studies from the Marine Phytoplankton

Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.