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Comparative ultrastructure of pyrenoids inTrebouxia (Microthamniales, Chlorophyta)
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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/fedr.4910940605openalex-snapshot
Ettl, H., Grundriß der allgemeinen Algologie. 549 S., 260 Abb. VEB Gustav Fischer Verlag. Jena, 1980. Preis 59,– M
inferredcites →https://doi.org/10.1007/bf00386966openalex-snapshot
Elektronenoptische Untersuchungen an Flechten
inferredcites →https://doi.org/10.1007/bf00387655openalex-snapshot
Das Vorkommen von St�rke in Chlorophyceen-Phycobionten
inferredcites →https://doi.org/10.1007/bf00936344openalex-snapshot
Zoospore ultrastructure in species ofTrebouxia andPseudotrebouxia (Chlorophyta)
inferredcites →https://doi.org/10.1007/bf00936348openalex-snapshot
The lichen algaTrebouxia: does it occur free-living?
inferredcites →https://doi.org/10.1007/bf00936349openalex-snapshot
Seasonal variations in the fine structure ofHypogymnia physodes (lichenizedAscomycetes) and itsTrebouxia photobiont
inferredcites →https://doi.org/10.1007/bf00984574openalex-snapshot
�ber die Bedeutung der Cytologie f�r die Algentaxonomie, dargestellt anTrebouxia (Chlorellales, Chlorophyceae)
inferredcites →https://doi.org/10.1007/bf00990760openalex-snapshot
�ber die Phycobionten der SektionCystophora vonChaenotheca, insbesondereDictyochloropsis splendida undTrebouxia simplex, spec. nova
inferredcites →https://doi.org/10.1007/bf01276362openalex-snapshot
Ultrastructural changes in the pyrenoid of the lichenParmelia sulcata stored under controlled conditions
inferredcites →https://doi.org/10.1007/bf01276653openalex-snapshot
Structural modifications of the phycobiont in the lichen thallus
inferredcites →https://doi.org/10.1007/bf01279870openalex-snapshot
Zoospore ultrastructure in the green algaFriedmannia israelensis: An absolute configuration analysis
inferredcites →https://doi.org/10.1007/bf01282285openalex-snapshot
Studies on the ultrastructure of some cyanolichen haustoria
inferredcites →https://doi.org/10.1007/bf01637248openalex-snapshot
The ultrastructure of cellular division (autosporogenesis) in the coccoid green alga,Trebouxia aggregata, revealed by rapid freeze fixation and freeze substitution
inferredcites →https://doi.org/10.1016/s0003-9365(88)80057-5openalex-snapshot
Zellteilung und Sporulation als wichtige Unterscheidungsmerkmale bei Grünalgen (Chlorophyta)
inferredcites →https://doi.org/10.1016/s0003-9365(88)80061-7openalex-snapshot
Trebouxia (Pleurastrales, Chlorophyta) as a Phycobiont in the Lichen Genus Diploschistes
inferredcites →https://doi.org/10.1016/s0022-5320(69)90033-1openalex-snapshot
A low-viscosity epoxy resin embedding medium for electron microscopy
inferredcites →https://doi.org/10.1017/s002428298700015xopenalex-snapshot
Thallus Development and Phycobionts of the Parasitic Lichen Diploschistes Muscorum
inferredcites →https://doi.org/10.1017/s0024282988000076openalex-snapshot
The Effect of Desiccation on Pyrenoid Structure in the Oceanic Lichen Parmelia Laevigata
inferredcites →https://doi.org/10.1080/00071618100650261openalex-snapshot
Fate of eyespot lipid globules after zoospore settlement in the green algaPleurastrum terrestreFritsch et John
inferredcites →https://doi.org/10.1080/00071618200650081openalex-snapshot
Virus-like particles in the scaly green flagellateMesostigma viride
inferredcites →https://doi.org/10.1083/jcb.17.1.208openalex-snapshot
THE USE OF LEAD CITRATE AT HIGH pH AS AN ELECTRON-OPAQUE STAIN IN ELECTRON MICROSCOPY
inferredcites →https://doi.org/10.1083/jcb.4.4.475openalex-snapshot
Staining of Tissue Sections for Electron Microscopy with Heavy Metals
inferredcites →https://doi.org/10.1111/j.1529-8817.1968.tb04720.xopenalex-snapshot
ELECTRON MICROSCOPY OF THE LICHEN PHYSCZA AZPOLIA (EHRH.) NYL.1,2
inferredcites →https://doi.org/10.1111/j.1529-8817.1969.tb02608.xopenalex-snapshot
THE ULTRASTRUCTURE OF LICHENS. I. A GENERAL SURVEY
inferredcites →https://doi.org/10.1111/j.1529-8817.1971.tb01475.xopenalex-snapshot
ULTRASTRUCTURE OF THE PYRENOID OFTREBOUXIAINRAMALINA MENZIESIITUCK.1,2
inferredcites →https://doi.org/10.1111/j.1529-8817.1971.tb01482.xopenalex-snapshot
THE ULTRASTRUCTURE OF LICHENS. II.CLADONIA CRISTATELLA: THE LICHEN AND ITS ISOLATED SYMBIONTS1,2,3
inferredcites →https://doi.org/10.1111/j.1529-8817.1971.tb01495.xopenalex-snapshot
COMPARATIVE ULTRASTRUCTURE OF CULTURED SPECIES OF TREBOUXIA1,2
inferredcites →https://doi.org/10.1111/j.1529-8817.1975.tb02781.xopenalex-snapshot
CELL DIVISION IN THE FILAMENTOUS PLEURASTRUM AND ITS COMPARISON WITH THE UNICELLULARPLATYMONAS(CHLOROPHYCEAE)1
inferredcites →https://doi.org/10.1201/9780849379901.ch7openalex-snapshot
Systematics of the green algae
inferredcites →https://doi.org/10.2216/i0031-8884-14-3-125.1openalex-snapshot
Trebouxia de Pulmaly (Chlorophyceae, Chlorococcales) and Pseudotrebouxia gen. nov. (Chlorophyceae, Chlorosarcinales)
inferredcites →https://doi.org/10.2216/i0031-8884-21-3-355.1openalex-snapshot
Etude ultrastructurale comparée du pyrénoïde et des parois dans les genres Ulothrix, Chlorothrix et Urospora
inferredcites →https://doi.org/10.2216/i0031-8884-25-4-551.1openalex-snapshot
Use of Hepes buffer for microalgal culture media and fixation for electron microscopy
inferredcites →https://doi.org/10.2216/i0031-8884-6-2-127.1openalex-snapshot
A Guide to the Algae Occurring as Lichen Symbionts: Isolation, Culture, Cultural Physiology, and Identification
inferredcites →https://doi.org/10.2307/3627105openalex-snapshot
Ultrastructure of the Lichen Xanthoria fallax
inferredcites →https://doi.org/10.2307/3627337openalex-snapshot
Some Ultrastructural Aspects of the Pyrenoid of the Chaetophoracean Alga Pleurastrum
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.219.2.2zenodo-depositor-declared
Vulcanochloris (Trebouxiales, Trebouxiophyceae), a new genus of lichen photobiont from La Palma, Canary Islands, Spain
inferred← citeshttps://doi.org/10.11646/phytotaxa.295.1.5zenodo-depositor-declared
Asterochloris sejongensis sp. nov. (Trebouxiophyceae, Chlorophyta) from King George Island, Antarctica
inferred← citeshttps://doi.org/10.5252/cryptogamie-algologie2022v43a9zenodo-depositor-declared
Trebouxia maresiae sp. nov. (Trebouxiophyceae, Chlorophyta), a New Lichenized Species of Microalga Found in Coastal Environments
inferred← citeshttps://doi.org/10.1006/lich.1999.0232openalex-snapshot
Photobiont Inventory of a Lichen Community Growing on Heavy-Metal-Rich Rock
inferred← citeshttps://doi.org/10.1006/mpev.1999.0711openalex-snapshot
The Distribution of Group I Introns in Lichen Algae Suggests That Lichenization Facilitates Intron Lateral Transfer
inferred← citeshttps://doi.org/10.1007/978-3-031-41648-4_7openalex-snapshot
Umbilicaria muhlenbergii: A Model for Studying Molecular Mechanisms Regulating Initial Fungal Symbiotic Interactions with Algal Cells
inferred← citeshttps://doi.org/10.1007/978-3-642-74061-9_16openalex-snapshot
Systematics, Morphology and Ecology of Lichenized Fungi
inferred← citeshttps://doi.org/10.1007/978-3-642-76293-2_16openalex-snapshot
Systematics and Evolution of the Algae
inferred← citeshttps://doi.org/10.1007/978-3-642-77047-0_18openalex-snapshot
Systematics, Morphology, and Ecology of Lichenized Fungi
inferred← citeshttps://doi.org/10.1007/bf01545966openalex-snapshot
Quantitative approach to the fine structure of both symbionts of nine Umbilicaria species
inferred← citeshttps://doi.org/10.1007/s00239-006-0115-xopenalex-snapshot
Evolution of ITS Ribosomal RNA Secondary Structures in Fungal and Algal Symbionts of Selected Species of Cladonia sect. Cladonia (Cladoniaceae, Ascomycotina)
inferred← citeshttps://doi.org/10.1007/s00248-026-02794-3openalex-snapshot
The Impact of Visible Symptoms of Thallus Damage on the Phycobiota of Mediterranean Epiphytic Lichens
inferred← citeshttps://doi.org/10.1007/s00606-005-0382-xopenalex-snapshot
Observations in Hemichloris antarctica Tschermak-Woess & Friedmann (Chlorophyceae) and the occurrence of a second Hemichloris species, Hemichloris polyspora n. sp
inferred← citeshttps://doi.org/10.1007/s00792-024-01355-1openalex-snapshot
Diversity of lichen mycobionts and photobionts and their relationships in the Ny-Ålesund region (Svalbard, High Arctic)
inferred← citeshttps://doi.org/10.1007/s11103-016-0468-5openalex-snapshot
New features of desiccation tolerance in the lichen photobiont Trebouxia gelatinosa are revealed by a transcriptomic approach
inferred← citeshttps://doi.org/10.1007/s13199-010-0060-8openalex-snapshot
Morphological and phylogenetic study of algal partners associated with the lichen-forming fungus Tephromela atra from the Mediterranean region
inferred← citeshttps://doi.org/10.1007/s13199-020-00709-5openalex-snapshot
Amphitropical variation of the algal partners of Pseudephebe (Parmeliaceae, lichenized fungi)
inferred← citeshttps://doi.org/10.1007/s13199-020-00722-8openalex-snapshot
Multidisciplinary approach to describe Trebouxia diversity within lichenized fungi Buellia zoharyi from the Canary Islands
inferred← citeshttps://doi.org/10.1016/b978-0-443-26534-1.00008-5openalex-snapshot
Lichens and their photobionts: diversity, techniques, and integrative insights
inferred← citeshttps://doi.org/10.1016/j.algal.2021.102561openalex-snapshot
Chloroplast morphology and pyrenoid ultrastructural analyses reappraise the diversity of the lichen phycobiont genus Trebouxia (Chlorophyta)
inferred← citeshttps://doi.org/10.1016/j.algal.2024.103744openalex-snapshot
From spores to gametes: A sexual life cycle in a symbiotic Trebouxia microalga
inferred← citeshttps://doi.org/10.1016/j.cryobiol.2012.02.002openalex-snapshot
Interspecific differences in cryoresistance of lichen symbiotic algae of genus Trebouxia assessed by cell viability and chlorophyll fluorescence
inferred← citeshttps://doi.org/10.1016/j.femsle.2005.01.040openalex-snapshot
A fungus-type β-galactofuranan in the cultivatedTrebouxiaphotobiont of the lichenRamalina gracilis
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2007.02.006openalex-snapshot
First report on polysaccharides of Asterochloris and their potential role in the lichen symbiosis
inferred← citeshttps://doi.org/10.1016/j.plaphy.2018.06.004openalex-snapshot
Relation between water status and desiccation-affected genes in the lichen photobiont Trebouxia gelatinosa
inferred← citeshttps://doi.org/10.1016/j.ympev.2009.09.035openalex-snapshot
Evolutionary inferences based on ITS rDNA and actin sequences reveal extensive diversity of the common lichen alga Asterochloris (Trebouxiophyceae, Chlorophyta)
inferred← citeshttps://doi.org/10.1016/j.ympev.2015.10.021openalex-snapshot
Coordinated ultrastructural and phylogenomic analyses shed light on the hidden phycobiont diversity of Trebouxia microalgae in Ramalina fraxinea
inferred← citeshttps://doi.org/10.1016/j.ympev.2020.106821openalex-snapshot
Formally described species woefully underrepresent phylogenetic diversity in the common lichen photobiont genus Trebouxia (Trebouxiophyceae, Chlorophyta): An impetus for developing an integrated taxonomy
inferred← citeshttps://doi.org/10.1016/s0003-9365(11)80284-8openalex-snapshot
New Aspects of the Reproduction by Autospores in the Lichen Alga Trebouxia (Microthamniales, Chlorophyta)
inferred← citeshttps://doi.org/10.1016/s0378-1097(03)00066-1openalex-snapshot
Linear β-mannose-containing polysaccharide, β-xylan, and amylose from the cultured photobiontTrebouxiasp. of the ascolichenRamalina celastri
inferred← citeshttps://doi.org/10.1016/s0932-4739(98)80023-0openalex-snapshot
Species-specificity of Chlorella for establishment of symbiotic association with Paramecium bursaria — Does infectivity depend upon sugar components of the cell wall?
inferred← citeshttps://doi.org/10.1017/s0024282909008111openalex-snapshot
Genetically divergent algae shape an epiphytic lichen community on Jack Pine in Manitoba
inferred← citeshttps://doi.org/10.1017/s002428291200059xopenalex-snapshot
In vitro culturing and resynthesis of the mycobiont Protoparmeliopsis muralis with algal bionts
inferred← citeshttps://doi.org/10.1017/s0024282917000664openalex-snapshot
A multi-tool approach to assess microalgal diversity in lichens: isolation, Sanger sequencing, HTS and ultrastructural correlations
inferred← citeshttps://doi.org/10.1017/s0024282918000208openalex-snapshot
Untangling the hidden intrathalline microalgal diversity inParmotrema pseudotinctorum:Trebouxia crespoanasp. nov.
inferred← citeshttps://doi.org/10.1017/s0024282921000335openalex-snapshot
Lichen algae: the photosynthetic partners in lichen symbioses
inferred← citeshttps://doi.org/10.1017/s0024282924000069openalex-snapshot
Chloroidium phycobionts (Watanabeales, Trebouxiophyceae) partner with lecanoralean mycobionts in foliicolous lichen communities of Tenerife (Canary Islands) and Navarra (Iberian Peninsula), Spain
inferred← citeshttps://doi.org/10.1017/s0024282926101546openalex-snapshot
From coasts to clades: Trebouxia tabarcae sp. nov. enhances the diversity of known lichen microalgae
inferred← citeshttps://doi.org/10.1017/s0024282990000354openalex-snapshot
Trebouxia Jamesii and the Question of Multinucleate Cells in the Lichen Photobiont Trebouxia
inferred← citeshttps://doi.org/10.1017/s0024282992000380openalex-snapshot
Three-dimensional quantitative description of symbiont ultrastructure within the algal layer oftwo members of the lichen family Umbilicariaceae
inferred← citeshttps://doi.org/10.1017/s0953756202006238openalex-snapshot
An ultrastructural, anatomical and molecular study of the lichenicolous lichen Rimularia insularis
inferred← citeshttps://doi.org/10.1038/s41598-019-44700-7openalex-snapshot
Dynamic evolution of mitochondrial genomes in Trebouxiophyceae, including the first completely assembled mtDNA from a lichen-symbiont microalga (Trebouxia sp. TR9)
inferred← citeshttps://doi.org/10.1038/s41598-020-71046-2openalex-snapshot
Symbiotic microalgal diversity within lichenicolous lichens and crustose hosts on Iberian Peninsula gypsum biocrusts
inferred← citeshttps://doi.org/10.1046/j.0028-646x.2001.00315.xopenalex-snapshot
Myco‐photobiontal selection in a Mediterranean cryptogam community with Fulgensia fulgida
inferred← citeshttps://doi.org/10.1046/j.1469-8137.1998.00231.xopenalex-snapshot
Selectivity of photobiont choice in a defined lichen community: inferences from cultural and molecular studies
inferred← citeshttps://doi.org/10.1046/j.1529-8817.2001.037001160.xopenalex-snapshot
SNOW ALGAE OF THE WINDMILL ISLANDS, CONTINENTAL ANTARCTICA: DESMOTETRA AUREOSPORA, SP. NOV. AND D. ANTARCTICA, COMB. NOV. (CHLOROPHYTA)
inferred← citeshttps://doi.org/10.1046/j.1529-8817.2002.01151.xopenalex-snapshot
PHYLOGENETIC RELATIONSHIPS WITHIN CLADOPHORALES (ULVOPHYCEAE, CHLOROPHYTA) INFERRED FROM 18S rRNA GENE SEQUENCES, WITH SPECIAL REFERENCE TOAEGAGROPILA LINNAEI 1
inferred← citeshttps://doi.org/10.1080/0028825x.2017.1343738openalex-snapshot
The freshwater alga Mucidosphaerium sphagnale (Chlorellaceae: Chlorophyta) in New Zealand: the first record outside Europe
inferred← citeshttps://doi.org/10.1080/09670260500342696openalex-snapshot
Ultrastructural study of the brown algaPetroderma maculiforme(Phaeophyceae) in the free-living state and in lichen symbiosis with the intertidal marine fungusVerrucaria tavaresiae(Ascomycotina)
inferred← citeshttps://doi.org/10.1080/09670262.2024.2441375openalex-snapshot
Revisiting the free-living Trebouxia strains of the Coimbra Collection of Algae (ACOI): Trebouxia valentina sp. nov. (Trebouxiophyceae, Chlorophyta)
inferred← citeshttps://doi.org/10.1080/09670269300650041openalex-snapshot
Three new species and a new record of chaetophoracean (Chlorophyta) algae from terrestrial habitats in Antarctica
inferred← citeshttps://doi.org/10.1080/17435390.2019.1570371openalex-snapshot
Graphene-based materials do not impair physiology, gene expression and growth dynamics of the aeroterrestrial microalga Trebouxia gelatinosa
inferred← citeshttps://doi.org/10.1093/jxb/eraf419openalex-snapshot
Members of the lichen photobiont genus Trebouxia show species-specific photophysiological and transcriptome-level responses to high light
inferred← citeshttps://doi.org/10.1099/ijs.0.000185openalex-snapshot
Molecular phylogeny and ultrastructure of the lichen microalga Asterochloris mediterranea sp. nov. from Mediterranean and Canary Islands ecosystems
inferred← citeshttps://doi.org/10.1111/j.0022-3646.1994.00500.xopenalex-snapshot
ASSESSING THE RELATIONSHIPS OF SOME COCCOID GREEN LICHEN ALGAE AND THE MICROTHAMNIALES (CHLOROPHYTA) WITH 18S RIBOSOMAL RNA GENE SEQUENCE COMPARISONS1
inferred← citeshttps://doi.org/10.1111/j.0022-3646.1995.00114.xopenalex-snapshot
NEW ULTRASTRUCTURAL ASPECTS OF PYRENOIDS OF THE LICHEN PHOTOBIONTTREBOUXZA(MICROTHAMNIALES, CHLOROPHYTA)1
inferred← citeshttps://doi.org/10.1111/j.0022-3646.1995.00813.xopenalex-snapshot
SPECIES‐SPECIFIC DIFFERENCES OF PYRENOIDS IN CHLORELLA (CHLOROPHYTA)1
inferred← citeshttps://doi.org/10.1111/j.1462-2920.2010.02386.xopenalex-snapshot
Two Trebouxia algae with different physiological performances are ever‐present in lichen thalli of Ramalina farinacea . Coexistence versus Competition?
inferred← citeshttps://doi.org/10.1111/j.1472-4669.2010.00256.xopenalex-snapshot
Respiration-induced weathering patterns of two endolithically growing lichens
inferred← citeshttps://doi.org/10.1111/j.1529-8817.1995.tb02559.xopenalex-snapshot
INFERRING TAXONOMIC POSITIONS AND TESTING GENUS LEVEL ASSIGNMENTS IN COCCOID GREEN LICHEN ALGAE: A PHYLOGENETIC ANALYSIS OF 18S RIBOSOMAL RNA SEQUENCES FROM DICTYOCHLOROPSIS RETICULATA AND FROM MEMBERS OF THE GENUS MYRMECIA (CHLOROPHYTA, TREBOUXIOPHYCEAE CL. NOV.) 1
inferred← citeshttps://doi.org/10.1111/j.1529-8817.2007.00345.xopenalex-snapshot
MARINICHLORELLA KAISTIAE GEN. ET SP. NOV. (TREBOUXIOPHYCEAE, CHLOROPHYTA) BASED ON POLYPHASIC TAXONOMY1
inferred← citeshttps://doi.org/10.1111/j.1574-6941.2012.01422.xopenalex-snapshot
Lichen myco- and photobiont diversity and their relationships at the edge of life (McMurdo Dry Valleys, Antarctica)
inferred← citeshttps://doi.org/10.1111/j.1756-1051.2001.tb00824.xopenalex-snapshot
Morphological variation, photobiont association and ITS phylogeny of Chaenotheca phaeocephala and C. subroscida (Coniocybaceae, lichenized ascomycetes)
inferred← citeshttps://doi.org/10.1111/jpy.12381openalex-snapshot
Mixotrophy in the terrestrial green alga Apatococcus lobatus (Trebouxiophyceae, Chlorophyta)
inferred← citeshttps://doi.org/10.1111/jpy.12446openalex-snapshot
Heveochlorella (Trebouxiophyceae): a little‐known genus of unicellular green algae outside the Trebouxiales emerges unexpectedly as a major clade of lichen photobionts in foliicolous communities
inferred← citeshttps://doi.org/10.1111/jpy.12751openalex-snapshot
Molecular and morphological diversity of Trebouxia microalgae in sphaerothallioid Circinaria spp. lichens1
inferred← citeshttps://doi.org/10.1111/plb.70042openalex-snapshot
Zoospore diversity and sexual reproduction in the lichen‐forming genus Trebouxia: From neglected evidence to new facts
inferred← citeshttps://doi.org/10.1186/s12864-025-11933-yopenalex-snapshot
Comparative genomic insights into ecological adaptations and evolutionary dynamics of Trebouxiophyceae algae
inferred← citeshttps://doi.org/10.1639/0007-2745(2000)103[0645:psrmas]2.0.co;2openalex-snapshot
Phylogenetic Species, Reproductive Mode, and Specificity of the Green Alga Trebouxia Forming Lichens with the Fungal Genus Letharia
inferred← citeshttps://doi.org/10.1639/0007-2745(2006)109[0043:gcosia]2.0.co;2openalex-snapshot
Genetic combinations of symbionts in a vegetatively reproducing lichen,Parmotrema tinctorum, based on ITS rDNA sequences
inferred← citeshttps://doi.org/10.2216/04-70.1openalex-snapshot
Taxonomy of Klebsormidium (Klebsormidiales, Charophyceae) in New Zealand streams and the significance of low-pH habitats
inferred← citeshttps://doi.org/10.2216/16-64.1openalex-snapshot
Phylogenetic interpretation of light and electron microscopic features of selected members of the phylogroupMoewusinia(Chlorophyceae), with new generic taxonomy
inferred← citeshttps://doi.org/10.2216/17-134.1openalex-snapshot
The hidden diversity of lichenised Trebouxiophyceae (Chlorophyta)
inferred← citeshttps://doi.org/10.2307/3243858openalex-snapshot
The Lichen Photobiont: What Can It Tell Us about Lichen Systematics?
inferred← citeshttps://doi.org/10.2478/v10182-012-0004-0openalex-snapshot
New Ultrastructural and Physiological Features of the Thallus in Antarctic Lichens
inferred← citeshttps://doi.org/10.3389/fmicb.2022.809804openalex-snapshot
Photobiont Diversity in Lichen Symbioses From Extreme Environments
inferred← citeshttps://doi.org/10.3389/fpls.2017.01144openalex-snapshot
Unraveling the Photoprotective Response of Lichenized and Free-Living Green Algae (Trebouxiophyceae, Chlorophyta) to Photochilling Stress
inferred← citeshttps://doi.org/10.3390/biology11081196openalex-snapshot
Trebouxia lynnae sp. nov. (Former Trebouxia sp. TR9): Biology and Biogeography of an Epitome Lichen Symbiotic Microalga
inferred← citeshttps://doi.org/10.3390/d15020170openalex-snapshot
Low Temperature Scanning Electron Microscopy (LTSEM) Findings on the Ultrastructure of Trebouxia lynnae (Trebouxiophyceae, Lichenized Microalgae)
inferred← citeshttps://doi.org/10.3390/jof10030206openalex-snapshot
Myco–Phycobiont Interactions within the “Ramalina farinacea Group”: A Geographical Survey over Europe and Macaronesia
inferred← citeshttps://doi.org/10.3390/jof9121160openalex-snapshot
Myrmecia, Not Asterochloris, Is the Main Photobiont of Cladonia subturgida (Cladoniaceae, Lecanoromycetes)
inferred← citeshttps://doi.org/10.3390/plants13213008openalex-snapshot
Taxonomic, Physiological, and Biochemical Characterization of Asterarcys quadricellularis AQYS21 as a Promising Sustainable Feedstock for Biofuels and ω-3 Fatty Acids
inferred← citeshttps://doi.org/10.4490/algae.2020.35.2.23openalex-snapshot
Taxonomic study of three new Antarctic Asterochloris (Trebouxio-phyceae) based on morphological and molecular data
inferred← citeshttps://doi.org/10.5507/fot.2009.013openalex-snapshot
The pyrenoid ultrastructure in Oocystis lacustris.
inferred← citeshttps://doi.org/10.5817/cpr2013-1-4openalex-snapshot
Temperature-dependent growth rate and photosynthetic performance of Antarctic symbiotic alga Trebouxia sp. cultivated in a bioreactor
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