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Exploring strategies for nanoflagellates living in a wet desert
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/9780470999271.ch13openalex-snapshot
Pelagic Microbes - Protozoa and the Microbial Food Web
inferredcites →https://doi.org/10.1002/jcp.1030470307openalex-snapshot
The role of photosynthesis in the physiology of ochromonas
inferredcites →https://doi.org/10.1007/978-94-017-0809-8openalex-snapshot
Atlas of Chrysophycean Cysts
inferredcites →https://doi.org/10.1007/bf02015056openalex-snapshot
Relationship between phototrophy and phagotrophy in the mixotrophic chrysophytePoterioochromonas malhamensis
inferredcites →https://doi.org/10.1016/0022-0981(94)90238-0openalex-snapshot
The effect of long-term low bacterial density on the growth kinetics of three marine heterotrophic nanoflagellates
inferredcites →https://doi.org/10.1016/s0932-4739(98)80055-2openalex-snapshot
Conceptual models of mixotrophy in planktonic protists and some ecological and evolutionary implications
inferredcites →https://doi.org/10.1017/cbo9780511752292.006openalex-snapshot
Comparative aspects of chrysophyte nutrition with emphasis on carbon, phosphorus and nitrogen
inferredcites →https://doi.org/10.1017/cbo9780511752292.007openalex-snapshot
Mixotrophy in chrysophytes
inferredcites →https://doi.org/10.1023/a:1020591307260openalex-snapshot
Significance of predation by protists in aquatic microbial food webs
inferredcites →https://doi.org/10.1046/j.1365-2427.1999.00476.xopenalex-snapshot
Effects of prey abundance and light intensity on the mixotrophic chrysophyte Poterioochromonas malhamensis from a mesotrophic lake
inferredcites →https://doi.org/10.1046/j.1529-8817.2001.00127.xopenalex-snapshot
GRAZING AND GROWTH OF THE MIXOTROPHIC CHRYSOMONAD POTERIOOCHROMONAS MALHAMENSIS (CHRYSOPHYCEAE) FEEDING ON ALGAE
inferredcites →https://doi.org/10.1080/00071617600650411openalex-snapshot
Vertical migration patterns in phytoplankton of mixed species composition
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a078130openalex-snapshot
Physiological Responses of Phytoflagellates to Dissolved Organic Substrate Additions. 1. Dominant Role of Heterotrophic Nutrition in Poterioochromonas malhamensis (Chrysophyceae)
inferredcites →https://doi.org/10.1093/plankt/13.1.167openalex-snapshot
The annual cycle of heterotrophic freshwater nanoflagellates: role of bottom-up versus top-down control
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/10.1093/plankt/fbh139openalex-snapshot
Potential toxicity of chrysophytes affiliated with Poterioochromonas and related 'Spumella-like' flagellates
inferredcites →https://doi.org/10.1111/j.0022-3646.1972.00010.xopenalex-snapshot
YELLOW-GREEN ALGAE WITH CHLOROPHYLLIDE C1,2
inferredcites →https://doi.org/10.1111/j.0022-3646.1996.00037.xopenalex-snapshot
LIGHT AND ELECTRON MICROSCOPY OF GRAZING BY POTERIOOCHROMONAS MALHAMENSIS (CHRYSOPHYCEAE) ON A RANGE OF PHYTOPLANKTON TAXA1
inferredcites →https://doi.org/10.1111/j.1462-2920.2005.00743.xopenalex-snapshot
High diversity of the ‘ Spumella ‐like’ flagellates: an investigation based on the SSU rRNA gene sequences of isolates from habitats located in six different geographic regions
inferredcites →https://doi.org/10.1111/j.1529-8817.1972.tb03995.xopenalex-snapshot
YELLOW‐GREEN ALGAE WITH CHLOROPHYLLIDE C1,2
inferredcites →https://doi.org/10.1128/aem.64.5.1910-1918.1998openalex-snapshot
Grazing Pressure by a Bacterivorous Flagellate Reverses the Relative Abundance ofComamonas acidovoransPX54 andVibrioStrain CB5 in Chemostat Cocultures
inferredcites →https://doi.org/10.1128/aem.69.3.1442-1451.2003openalex-snapshot
Isolation of Novel Ultramicrobacteria Classified as Actinobacteria from Five Freshwater Habitats in Europe and Asia
inferredcites →https://doi.org/10.1128/aem.69.9.5248-5254.2003openalex-snapshot
Isolation of Strains Belonging to the Cosmopolitan Polynucleobacter necessarius Cluster from Freshwater Habitats Located in Three Climatic Zones
inferredcites →https://doi.org/10.1128/aem.70.10.5787-5793.2004openalex-snapshot
Strain-Specific Differences in the Grazing Sensitivities of Closely Related Ultramicrobacteria Affiliated with the Polynucleobacter Cluster
inferredcites →https://doi.org/10.1128/aem.71.8.4539-4547.2005openalex-snapshot
Low Intraspecific Diversity in a Polynucleobacter Subcluster Population Numerically Dominating Bacterioplankton of a Freshwater Pond
inferredcites →https://doi.org/10.1242/jcs.s3-93.21.71openalex-snapshot
On the Nutrition of Ochromonas
inferredcites →https://doi.org/10.2307/2265495openalex-snapshot
Utilization of Substitutable Carbon and Phosphorus Sources by the Mixotrophic Chrysophyte Ochromonas Sp
inferredcites →https://doi.org/10.2307/2265496openalex-snapshot
Laboratorary Experiments with a Mixotrophic Chrysophyte and Obligately Phagotrophic and Photographic Competitors
inferredcites →https://doi.org/10.3354/ame022243openalex-snapshot
Comparative studies on the feeding behavior of two heterotrophic nanoflagellates: the filter-feeding choanoflagellate Monosiga ovata and the raptorial-feeding kinetoplastid Rhynchomonas nasuta
inferredcites →https://doi.org/10.3354/ame027195openalex-snapshot
Food concentration-dependent regulation of food selectivity of interception-feeding bacterivorous nanoflagellates
inferredcites →https://doi.org/10.3354/ame034139openalex-snapshot
Single-cell analysis of bacterial growth, cell size, and community structure in the Delaware estuary
inferredcites →https://doi.org/10.3354/ame036247openalex-snapshot
Effects of prey abundance and light intensity on nutrition of a mixotrophic flagellate and its competitive relationship with an obligate heterotroph
inferredcites →https://doi.org/10.3354/meps009025openalex-snapshot
Ecology of Heterotrophic Microflagellates. III. Adaptations to Heterogeneous Environments
inferredcites →https://doi.org/10.3354/meps010257openalex-snapshot
The Ecological Role of Water-Column Microbes in the Sea
inferredcites →https://doi.org/10.3354/meps105167openalex-snapshot
A comparison of the growth kinetics of six marine heterotrophic nanoflagellates fed with one bacterial species
inferredcites →https://doi.org/10.3354/meps201137openalex-snapshot
Physiology of the mixotrophic dinoflagellate Fragilidium subglobosum. II. Effects of time scale and prey concentration on photosyntheticperformance
inferredcites →https://doi.org/10.4319/lo.1988.33.4.0504openalex-snapshot
The microflagellate‐picoplankton food linkage in the water column of Lake Biwa
inferredcites →https://doi.org/10.4319/lo.1989.34.1.0155openalex-snapshot
Phagotrophic sustenance of a metalimnetic phytoplankton peak
inferredcites →https://doi.org/10.4319/lo.1990.35.2.0433openalex-snapshot
Carbon, nitrogen, and phosphorus budgets for the mixotrophic phytoflagellate Poterioochromonas malhamensis (Chrysophyceae) during bacterial ingestion
inferredcites →https://doi.org/10.4319/lo.1990.35.8.1821openalex-snapshot
Heterotrophic, autotrophic, and mixotrophic nanoflagellates: Seasonal abundances and bacterivory in a eutrophic lake
inferredcites →https://doi.org/10.4319/lo.1997.42.4.0687openalex-snapshot
Zooplankton grazing and growth: Scaling within the 2‐2,‐μm body size range
inferredcites →https://doi.org/10.4319/lo.2000.45.3.0569openalex-snapshot
Carbon to volume relationships for dinoflagellates, diatoms, and other protist plankton
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1007/s13127-018-0365-7zenodo-depositor-declared
Genome size of chrysophytes varies with cell size and nutritional mode
inferred← citeshttps://doi.org/10.1007/s13127-022-00554-yzenodo-depositor-declared
Phylogenetic and functional diversity of Chrysophyceae in inland waters
inferred← citeshttps://doi.org/10.1002/9780470281840.ch11openalex-snapshot
Protistan Grazing on Marine Bacterioplankton
inferred← citeshttps://doi.org/10.1002/lno.10759openalex-snapshot
Bacterial prey food characteristics modulate community growth response of freshwater bacterivorous flagellates
inferred← citeshttps://doi.org/10.1016/j.cub.2023.11.046openalex-snapshot
Rapid diversification of a free-living protist is driven by adaptation to climate and habitat
inferred← citeshttps://doi.org/10.1038/s41396-018-0057-5openalex-snapshot
Cryptophyta as major bacterivores in freshwater summer plankton
inferred← citeshttps://doi.org/10.1080/09670262.2024.2442041openalex-snapshot
Exploring the factors shaping microscopic morphological traits: insights from the chrysophycean genus Synura (Stramenopiles)
inferred← citeshttps://doi.org/10.1093/ismeco/ycag218openalex-snapshot
Beyond protist generalizations: different evolutionary trajectories in closely related microbial species
inferred← citeshttps://doi.org/10.1093/plankt/fbn112openalex-snapshot
The algal osmolyte DMSP as a microzooplankton grazing deterrent in laboratory and field studies
inferred← citeshttps://doi.org/10.1111/1462-2920.15911openalex-snapshot
Dominant marine heterotrophic flagellates are adapted to natural planktonic bacterial abundances
inferred← citeshttps://doi.org/10.1111/j.1462-2920.2006.01175.xopenalex-snapshot
Differential thermal adaptation of clonal strains of a protist morphospecies originating from different climatic zones
inferred← citeshttps://doi.org/10.1111/j.1462-2920.2010.02222.xopenalex-snapshot
Aggregate formation in a freshwater bacterial strain induced by growth state and conspecific chemical cues
inferred← citeshttps://doi.org/10.1111/j.1529-8817.2010.00871.xopenalex-snapshot
CULTIVATION-INDEPENDENT SPECIES IDENTIFICATION OF DINOBRYON SPECIES (CHRYSOPHYCEAE) BY MEANS OF MULTIPLEX SINGLE-CELL PCR1
inferred← citeshttps://doi.org/10.1111/j.1574-6941.2009.00800.xopenalex-snapshot
Antibiotic effects of three strains of chrysophytes (Ochromonas, Poterioochromonas) on freshwater bacterial isolates
inferred← citeshttps://doi.org/10.1111/jpy.13093openalex-snapshot
Morphological evolution of silica scales in the freshwater genus Synura (Stramenopiles)
inferred← citeshttps://doi.org/10.1111/jpy.13496openalex-snapshot
Nanopatterns on silica scales of Mallomonas (Chrysophyceae, Stramenopiles): Unraveling UV resistance potential and diverse response to UVA and UVB radiation
inferred← citeshttps://doi.org/10.1128/aem.01455-10openalex-snapshot
Scent of Danger: Floc Formation by a Freshwater Bacterium Is Induced by Supernatants from a Predator-Prey Coculture
inferred← citeshttps://doi.org/10.1371/journal.pone.0008465openalex-snapshot
Reverse Evolution: Driving Forces Behind the Loss of Acquired Photosynthetic Traits
inferred← citeshttps://doi.org/10.1371/journal.pone.0168183openalex-snapshot
Quantitative Proteomics Reveals Ecophysiological Effects of Light and Silver Stress on the Mixotrophic Protist Poterioochromonas malhamensis
inferred← citeshttps://doi.org/10.3354/ame01518openalex-snapshot
Species-specific patterns in the vulnerability of carbon-starved bacteria to protist grazing
inferred← citeshttps://doi.org/10.3354/ame01662openalex-snapshot
Influence of nutrients and light on autotrophic, mixotrophic and heterotrophic freshwater chrysophytes
inferred← citeshttps://doi.org/10.3354/ame01853openalex-snapshot
Effects of short-term flooding on aquatic and terrestrial microeukaryotic communities: a mesocosm approach
inferred← citeshttps://doi.org/10.3354/ame045089openalex-snapshot
Stuck in the mud: suspended sediments as a key issue for survival of chrysomonad flagellates
inferred← citeshttps://doi.org/10.3389/fmicb.2019.01498openalex-snapshot
Interaction-Specific Changes in the Transcriptome of Polynucleobacter asymbioticus Caused by Varying Protistan Communities
inferred← citeshttps://doi.org/10.4067/s0716-078x2011000300010openalex-snapshot
Ecomicrobiology and microbial assimilative capacity of the oligotrophic Andean Lake Laja, Chile
inferred← citeshttps://doi.org/10.4319/lo.2009.54.1.0171openalex-snapshot
SSU rRNA gene variation resolves population heterogeneity and ecophysiological differentiation within a morphospecies (Stramenopiles , Chrysophyceae )
inferred← citeshttps://doi.org/10.4319/lo.2014.59.5.1477openalex-snapshot
A finely tuned symphony of factors modulates the microbial food web of a freshwater reservoir in spring
inferred← citeshttps://doi.org/10.5507/fot.2023.003openalex-snapshot
Effects of stressors on growth and competition between different cryptic taxa affiliated with Ochromonadales (Chrysophyceae)
inferred← citeshttps://doi.org/10.7287/peerj.2832v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Comprehensive transcriptome analysis provides new insights into nutritional strategies and phylogenetic relationships of chrysophytes (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.2832v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Comprehensive transcriptome analysis provides new insights into nutritional strategies and phylogenetic relationships of chrysophytes (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.2832v0.1/reviews/3openalex-snapshot
Peer Review #3 of "Comprehensive transcriptome analysis provides new insights into nutritional strategies and phylogenetic relationships of chrysophytes (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.2832v0.2/reviews/1openalex-snapshot
Peer Review #1 of "Comprehensive transcriptome analysis provides new insights into nutritional strategies and phylogenetic relationships of chrysophytes (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.2832v0.2/reviews/2openalex-snapshot
Peer Review #2 of "Comprehensive transcriptome analysis provides new insights into nutritional strategies and phylogenetic relationships of chrysophytes (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.2832v0.2/reviews/3openalex-snapshot
Peer Review #3 of "Comprehensive transcriptome analysis provides new insights into nutritional strategies and phylogenetic relationships of chrysophytes (v0.2)"
inferred← citeshttps://doi.org/10.7717/peerj.2832openalex-snapshot
Comprehensive transcriptome analysis provides new insights into nutritional strategies and phylogenetic relationships of chrysophytes
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