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Morphological variation in a small Thalassiosira species (Bacillariophyta) under different culture regimes

https://doi.org/10.1515/bot.2011.063

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What this work says

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

inferredcites →https://doi.org/10.1006/ecss.2000.0590openalex-snapshot

Spatial and Temporal Dynamics of Phytoplankton Communities in a Freshwater Tidal Estuary (Schelde, Belgium)

inferredcites →https://doi.org/10.1007/bf00448966openalex-snapshot

Temperature effects on the valve structure of the bipolar diatoms Thalassiosira antarctica and Porosira glacialis

inferredcites →https://doi.org/10.1007/bf01274072openalex-snapshot

Influence of environmental factors on the development of the valve in diatoms

inferredcites →https://doi.org/10.1007/bf01611916openalex-snapshot

Der Formwechsel der pennaten Diatomeen (Kieselalgen)

inferredcites →https://doi.org/10.1016/j.ecss.2009.01.024openalex-snapshot

Changes in phytoplankton diversity and community composition along the salinity gradient of the Schelde estuary (Belgium/The Netherlands)

inferredcites →https://doi.org/10.1016/j.ejop.2007.04.003openalex-snapshot

Classification of the peritrich ciliate Opisthonecta matiensis (Martín-Cereceda et al. 1999) as Telotrochidium matiense nov. comb., based on new observations and SSU rDNA phylogeny

inferredcites →https://doi.org/10.1029/ar017p0313openalex-snapshot

Morphologic Variability in Fasciculated Diatoms as Exemplified by Thalassiosira Tumida (Janisch) Hasle, Comb. Nov.

inferredcites →https://doi.org/10.1038/209217a0openalex-snapshot

Short-term Temperature and Light Conditions associated with Auxospore Formation in the Marine Centric Diatom Coscinodiscus concinnus W. Smith

inferredcites →https://doi.org/10.1046/j.1365-2672.2002.01576.xopenalex-snapshot

Stimulation of Alexandrium fundyense growth by bacterial assemblages from the Bay of Fundy

inferredcites →https://doi.org/10.1080/00071617400650021openalex-snapshot

The auxospore wall of the marine diatomMelosira nummuloides(Dillw.) C. Ag. and related species

inferredcites →https://doi.org/10.1080/00071618600650161openalex-snapshot

Notes on some smallThalassiosiraspecies (Bacillariophyceae) from the plankton of the lower thames and other British Estuaries (identified by transmission electron microscopy)

inferredcites →https://doi.org/10.1080/00071618800650341openalex-snapshot

Changes in valve morphology ofThalassiosira decipiens(Bacillariophyceae) cultured in media of four different salinities

inferredcites →https://doi.org/10.1080/00222936908695866openalex-snapshot

I.—On the structure of the Diatomaceous frustule, and its genetic cycle

inferredcites →https://doi.org/10.1080/0269249x.2006.9705667openalex-snapshot

CELL WALL MORPHOLOGY AND SYSTEMATIC IMPORTANCE OFTHALASSIOSIRA RITSCHERI(HUSTEDT) HASLE, WITH A DESCRIPTION OFSHIONODISCUSGEN. NOV.

inferredcites →https://doi.org/10.1080/09670260701352288openalex-snapshot

Thalassiosiraspecies (Bacillariophyceae, Thalassiosirales) in the North Sea at Helgoland (German Bight) and Sylt (North Frisian Wadden Sea) – a first approach to assessing diversity

inferredcites →https://doi.org/10.1093/oxfordjournals.aob.a086269openalex-snapshot

Auxospore Structure, Initial Valves and the Development of Populations of Stephanodiscus in Farmoor Reservoir

inferredcites →https://doi.org/10.1111/j.0022-3646.1992.00856.xopenalex-snapshot

LIFE CYCLE OF A STEPHANODISCUS SP. (BACILLARIOPHYTA)1

inferredcites →https://doi.org/10.1111/j.1529-8817.1972.tb04044.xopenalex-snapshot

THALASSIOSIRA ECCENTRICA (EHRENB.) CLEVE, T. SYMMETRICA SP. NOV., AND SOME RELATED CENTRIC DIATOMS1

inferredcites →https://doi.org/10.1111/j.1529-8817.1980.tb03052.xopenalex-snapshot

VALVE AND BAND MORPHOLOGY OF SOME FRESHWATER DIATOMS. III. PRE‐ AND POST‐AUXOSPORE FRUSTULES AND THE INITIAL CELL OFMELOSIRA ROESEANA1

inferredcites →https://doi.org/10.1111/j.1529-8817.2006.00244.xopenalex-snapshot

OOGAMOUS REPRODUCTION, WITH TWO‐STEP AUXOSPORULATION, IN THE CENTRIC DIATOM THALASSIOSIRA PUNCTIGERA (BACILLARIOPHYTA)1

inferredcites →https://doi.org/10.1127/0029-5035/2002/0074-0373openalex-snapshot

The diatom genus Thalassiosira: species from the northern San Matias Gulf (Rio Negro, Argentina)

inferredcites →https://doi.org/10.1127/archiv-hydrobiol/145/1999/479openalex-snapshot

Population dynamics of Cyclotella ocellata (Bacillariophyceae): endogenous and exogenous factors

inferredcites →https://doi.org/10.1139/b70-133openalex-snapshot

Production of male gametes and auxospores in a polymorphic clone of the centric diatom Cyclotella

inferredcites →https://doi.org/10.1139/b71-182openalex-snapshot

Salinity-related polymorphism in the brackish-water diatom Cyclotella cryptica

inferredcites →https://doi.org/10.1515/bot.2006.053openalex-snapshot

Autogamic reproductive behavior and sex cell structure in Thalassiosira angulata (Bacillariophyta)

inferredcites →https://doi.org/10.1515/botm.1996.39.1-6.103openalex-snapshot

The Diatom Genus Thalassiosira (Bacillariophyta) in the Estuaries of the Schelde (Belgium/The Netherlands) and the Elbe (Germany)

inferredcites →https://doi.org/10.2216/i0031-8884-14-4-205.1openalex-snapshot

An effect of osmotic pressure on the valve morphology of the diatom Skeletonema subsalsum (A. Cleve) Bethge

inferredcites →https://doi.org/10.2216/i0031-8884-34-6-533.1openalex-snapshot

Restoration of cell size by vegetative cell enlargement in Coscinodiscus wailesii (Bacillariophyceae)

inferredcites →https://doi.org/10.2216/i0031-8884-38-6-437.1openalex-snapshot

The species concept in diatoms

inferredcites →https://doi.org/10.3989/scimar.2002.66n3233openalex-snapshot

Nanoplankton protists from the western Mediterranean Sea. I. Occurrence, ultrastructure, taxonomy and ecological role of the mixotrophic flagellate Ollicola vangoorii (Chrysomonadidae = Chrysophyceae p.p.)

inferredcites →https://doi.org/10.4319/lo.1981.26.6.1057openalex-snapshot

Spines on diatoms: Do copepods care?1

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.375.2.4zenodo-depositor-declared

Tiny diatoms Minidiscus vodyanitskiyi sp. nov. (Bacillariophyta) from the Sea of Azov and consideration of polygonal areolae pattern

inferred← citeshttps://doi.org/10.1080/09670262.2013.843204openalex-snapshot

Morphology, taxonomy and distribution of Stephanodiscus triporus (Bacillariophyceae) and related taxa

inferred← citeshttps://doi.org/10.1111/1462-2920.13398openalex-snapshot

Physiological adjustments and transcriptome reprogramming are involved in the acclimation to salinity gradients in diatoms

inferred← citeshttps://doi.org/10.1111/jpy.13308openalex-snapshot

Distinct glycoconjugate cell surface structures make the pelagic diatom Thalassiosira rotula an attractive habitat for bacteria

inferred← citeshttps://doi.org/10.1111/pre.12084openalex-snapshot

T halassiosira sundarbana sp. nov. ( B acillariophyta), an estuarine diatom from S undarbans mangrove ecoregion based on morphology and molecular phylogeny

inferred← citeshttps://doi.org/10.1134/s1063074014050083openalex-snapshot

The variability of the morphological and structural elements of the frustule in genetically homogeneous and heterogeneous groups of the diatom Nitzschia rectilonga Takano, 1983 (Bacillariophyta)

inferred← citeshttps://doi.org/10.1371/journal.pone.0181980openalex-snapshot

Transfer of the small diatoms Thalassiosira proschkinae and T. spinulata to the genus Minidiscus and their taxonomic re-description

inferred← citeshttps://doi.org/10.2216/15-66.1openalex-snapshot

Species diversity of the genus Thalassiosira (Thalassiosirales, Bacillariophyta) in South Korea and its biogeographical distribution in the world

inferred← citeshttps://doi.org/10.26428/1606-9919-2016-185-132-145openalex-snapshot

Intrapopulation heterogeneity of cell volume for the alga Attheya ussurensis under stress conditions

inferred← citeshttps://doi.org/10.3989/scimar.04331.06copenalex-snapshot

Morphological adaptations to small size in the marine diatom Minidiscus comicus

inferred← citeshttps://doi.org/10.5091/plecevo.2019.1632openalex-snapshot

Eileen J. Cox: her journey with diatoms

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