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The Strategy of the Red Algal Life History
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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The evolution of sexual reproduction: A model which assumes individual selection
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Translocation of photoassimilated14C in the red algaPolysiphonia lanosa
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Evolution in Sexual and Asexual Populations
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The Life History of Polysiphonia violacea
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LIFE HISTORIES IN THE ALGAE WITH SPECIAL REFERENCE TO THE CHLOROPHYTA, PHAEOPHYTA AND RHODOPHYTA
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An Evolutionary Survey of the Plant Kingdom
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Ancient reproductive modes and criteria of multicellularity
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COLEOCHAETE AND THE ORIGIN OF LAND PLANTS
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Variation of reproductive success in a haplo‐diploid Red Alga, Gracilaria Verrucosa: effects of parental identities and crossing distance
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Reproductive Biology of Eukaryotic Algae
inferred← citeshttps://doi.org/10.1007/978-90-481-3795-4_5openalex-snapshot
Investigations on Reproductive Affinities in Red Algae
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Seasonal occurrence and reproduction of Hypnea charoides (Rhodophyta) in Tung Ping Chau, N.T., Hong Kong SAR, China
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Viability and dissemination of spermatia of Gracilaria verrucosa (Gracilariales, Rhodophyta)
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Long-term and diurnal carpospore discharge patterns in the Ceramiaceae Rhodomelaceae and Delesseriaceae (Rhodophyta)
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Genetic Improvement of Kappaphycus alvarezii (Doty) by Molecular Breeding
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Reproductive ecology of the freshwater red alga Batrachospermum boryanum Sirodot in a temperature headwater stream
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Viability and dissemination of spermatia of Gracilaria verrucosa (Gracilariales, Rhodophyta)
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Size-specific reproductive parameters in red algae: a comparative analysis for two sympatric species from Central Chile
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Intra-clonal variation in the red seaweed Gracilaria chilensis
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Meiospore formation in charophycean algae
inferred← citeshttps://doi.org/10.1016/b978-0-12-409548-9.11265-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-802772-1.00004-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-818305-2.00005-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-323-91803-9.00008-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-443-29827-1.00010-8openalex-snapshot
Macroalgal systematics
inferred← citeshttps://doi.org/10.1016/b978-0-443-33492-4.01002-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.algal.2023.103318openalex-snapshot
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Shifts in foundation species dominance and altered interaction networks after compounding seismic uplift and extreme marine heatwaves
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inferred← citeshttps://doi.org/10.1016/s0022-0981(98)00063-xopenalex-snapshot
Selective mortality on haploid and diploid microscopic stages of Lessonia nigrescens Bory (Phaeophyta, Laminariales)
inferred← citeshttps://doi.org/10.1016/s0022-0981(99)00121-5openalex-snapshot
Spatial and temporal variation in settlement and recruitment of the intertidal barnacle Semibalanus balanoides (L.) (Crustacea: Cirripedia) over a European scale
inferred← citeshttps://doi.org/10.1016/s0065-2296(01)35007-3openalex-snapshot
Intraspecific variation in seaweeds: The application of new tools and approaches
inferred← citeshttps://doi.org/10.1023/a:1017025815001openalex-snapshot
Long-term and diurnal carpospore discharge patterns in the Ceramiaceae, Rhodomelaceae and Delesseriaceae (Rhodophyta)
inferred← citeshttps://doi.org/10.1023/b:hydr.0000020311.42410.84openalex-snapshot
Seasonal occurrence and reproduction of Hypnea charoides (Rhodophyta) in Tung Ping Chau, N.T., Hong Kong SAR, China
inferred← citeshttps://doi.org/10.1038/hdy.2014.82openalex-snapshot
O father where art thou? Paternity analyses in a natural population of the haploid–diploid seaweed Chondrus crispus
inferred← citeshttps://doi.org/10.1038/srep21361openalex-snapshot
Divergence time estimates and the evolution of major lineages in the florideophyte red algae
inferred← citeshttps://doi.org/10.1046/j.1420-9101.1993.6020263.xopenalex-snapshot
Evolution of the alternation of haploid and diploid phases in life cycles. II. Maintenance of the haplo‐diplontic cycle
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Patterns of tetraspore discharge in Caloglossa and Murrayella (Ceramiales, Rhodophyta)
inferred← citeshttps://doi.org/10.1046/j.1529-8817.2002.00193.xopenalex-snapshot
RECENT ADVANCES IN FERTILIZATION ECOLOGY OF MACROALGAE1
inferred← citeshttps://doi.org/10.1073/pnas.2210665119openalex-snapshot
Life cycle and functional genomics of the unicellular red alga Galdieria for elucidating algal and plant evolution and industrial use
inferred← citeshttps://doi.org/10.1080/00071619200650241openalex-snapshot
Gametogenesis, gametes and zygotes: An ecological perspective on sexual reproduction in the algae
inferred← citeshttps://doi.org/10.1080/00318884.2023.2220465openalex-snapshot
New insights into post-fertilization in Dudresnaya (Gigartinales, Rhodophyta) and Acrosymphyton (Acrosymphytales, Rhodophyta)
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Isolation and characterization of phase-specific cDNAs from carposporophytes ofGracilariopsis andersonii(Gracilariales, Rhodophyta)
inferred← citeshttps://doi.org/10.1080/17451000.2018.1510180openalex-snapshot
Unveiling commonalities in understudied habitats of boulder-reefs: life-history traits of the widespread invertebrate and algal inhabitants
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199657148.001.0001openalex-snapshot
The Evolution of Sex Determination
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Copyright Page
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Colour Plates
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199657148.003.0001openalex-snapshot
What are sexes, and why are there sexes?
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199657148.003.0002openalex-snapshot
The diversity of sexual cycles
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199657148.003.0003openalex-snapshot
Molecular mechanisms of sex determination
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199657148.003.0004openalex-snapshot
The quantitative genetics of sex determination
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199657148.003.0005openalex-snapshot
The evolution of sex chromosomes
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199657148.003.0006openalex-snapshot
Evolutionary correlates of sex-determination systems
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199657148.003.0007openalex-snapshot
Transitions among sex-determination systems
inferred← citeshttps://doi.org/10.1093/gbe/evad124openalex-snapshot
The Rhodoexplorer Platform for Red Algal Genomics and Whole-Genome Assemblies for Several Gracilaria Species
inferred← citeshttps://doi.org/10.1093/icb/icl018openalex-snapshot
Functional properties of the isomorphic biphasic algal life cycle
inferred← citeshttps://doi.org/10.1093/icb/icr075openalex-snapshot
Speciation in Red Algae: Members of the Ceramiales as Model Organisms
inferred← citeshttps://doi.org/10.1093/jhered/esaa063openalex-snapshot
Exploring the Genetic Consequences of Clonality in Haplodiplontic Taxa
inferred← citeshttps://doi.org/10.1098/rsbl.2004.0259openalex-snapshot
Paradoxical polyembryony? Embryonic cloning in an ancient order of marine bryozoans
inferred← citeshttps://doi.org/10.1098/rspb.1999.0861openalex-snapshot
Performance of non–motile male gametes in the sea: analysis of paternity and fertilization success in a natural population of a red seaweed,Gracilaria gracilis
inferred← citeshttps://doi.org/10.1098/rspb.2023.1668openalex-snapshot
Sexual selection in seaweed? Testing Bateman's principles in the red alga Gracilaria gracilis
inferred← citeshttps://doi.org/10.1098/rspb.2023.2351openalex-snapshot
Evolution of parental care in haploid–diploid plants
inferred← citeshttps://doi.org/10.1098/rstb.2000.0614openalex-snapshot
The origin of alternation of generations in land plants: a focus on matrotrophy and hexose transport
inferred← citeshttps://doi.org/10.1098/rstb.2005.1794openalex-snapshot
Sexual conflict and the alternation of haploid and diploid generations
inferred← citeshttps://doi.org/10.1098/rstb.2022.0283openalex-snapshot
Hermaphroditic origins of anisogamy
inferred← citeshttps://doi.org/10.1111/1365-2745.14144openalex-snapshot
Towards a trait‐based framework for marine macroalgae: Using categorical data to explore the nature of emergent functional groups
inferred← citeshttps://doi.org/10.1111/eva.12843openalex-snapshot
What’s ploidy got to do with it? Understanding the evolutionary ecology of macroalgal invasions necessitates incorporating life cycle complexity
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HYPNEA MUSCIFORMIS (RHODOPHYTA): ECOLOGICAL INFLUENCE ON GROWTH1
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SIZE HIERARCHY AND THE −3/2 “POWER LAW” RELATIONSHIP IN A COALESCENT SEAWEED1
inferred← citeshttps://doi.org/10.1111/j.0022-3646.1994.00695.xopenalex-snapshot
THE EVOLUTION OF PARASITISM IN RED ALGAE: CELLULAR INTERACTIONS OF ADELPHOPARASITES AND THEIR HOSTS1
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ALTERNATION OF GENERATIONS IN ALGAE: ITS COMPLEXITY, MAINTENANCE AND EVOLUTION
inferred← citeshttps://doi.org/10.1111/j.1529-8817.2005.04024.xopenalex-snapshot
FERTILIZATION SUCCESS CAN DRIVE PATTERNS OF PHASE DOMINANCE IN COMPLEX LIFE HISTORIES1
inferred← citeshttps://doi.org/10.1111/j.1529-8817.2011.00981.xopenalex-snapshot
ABIOTIC REGULATION OF INVESTMENT IN SEXUAL VERSUS VEGETATIVE REPRODUCTION IN THE CLONAL KELP LAMINARIA SINCLAIRII (LAMINARIALES, PHAEOPHYCEAE)1
inferred← citeshttps://doi.org/10.1111/j.1759-6831.2012.00188.xopenalex-snapshot
Evolution of the life cycle in land plants
inferred← citeshttps://doi.org/10.1111/jpy.12294openalex-snapshot
Evidence of ancient genome reduction in red algae (Rhodophyta)
inferred← citeshttps://doi.org/10.1111/jpy.12366openalex-snapshot
The importance of effective sampling for exploring the population dynamics of haploid–diploid seaweeds
inferred← citeshttps://doi.org/10.1111/jpy.12906openalex-snapshot
Incorporating Ploidy Diversity into Ecological and Community Genetics
inferred← citeshttps://doi.org/10.1111/jpy.12930openalex-snapshot
Maintenance of Complex Life Cycles Via Cryptic Differences In The Ecophysiology Of Haploid And Diploid Spores Of An Isomorphic Red Alga1
inferred← citeshttps://doi.org/10.1111/jpy.13088openalex-snapshot
Using RAD‐seq to develop sex‐linked markers in a haplodiplontic alga
inferred← citeshttps://doi.org/10.1111/jpy.13092openalex-snapshot
Revisiting the ‘bank of microscopic forms’ in macroalgal‐dominated ecosystems
inferred← citeshttps://doi.org/10.1111/jpy.13110openalex-snapshot
Differential Frond Growth in the Isomorphic Haploid–diploid Red Seaweed Agarophyton chilense by Long‐term In Situ Monitoring
inferred← citeshttps://doi.org/10.1111/jpy.13339openalex-snapshot
Tetrasporophytic bias coupled with heterozygote deficiency in Antarctic Plocamium sp. (Florideophyceae, Rhodophyta)
inferred← citeshttps://doi.org/10.1111/jpy.13419openalex-snapshot
Identification of reproductive sex‐biased gene expression in Asparagopsis taxiformis (lineage 6) gametophytes
inferred← citeshttps://doi.org/10.1111/jpy.13510openalex-snapshot
Population genetics of the freshwater red alga Batrachospermum gelatinosum (Rhodophyta) I: Frequent intragametophytic selfing in a monoicous, haploid–diploid species
inferred← citeshttps://doi.org/10.1111/jpy.70032openalex-snapshot
Monoicy, dioicy, and genetic structure in three species of Sheathia (Batrachospermales, Rhodophyta)
inferred← citeshttps://doi.org/10.1111/jpy.70143openalex-snapshot
A clonal legacy? Reproductive mode variation in hard‐ and soft‐bottom Gracilaria vermiculophylla populations
inferred← citeshttps://doi.org/10.1111/jpy.70193openalex-snapshot
The evolutionary ecology of reproduction in the red alga Palmaria palmata : Insights from an atypical life cycle
inferred← citeshttps://doi.org/10.1111/mec.12191openalex-snapshot
Intergametophytic selfing and microgeographic genetic structure shape populations of the intertidal red seaweed C hondrus crispus
inferred← citeshttps://doi.org/10.1126/science.abo6661openalex-snapshot
Pollinators of the sea: A discovery of animal-mediated fertilization in seaweed
inferred← citeshttps://doi.org/10.1146/annurev-genet-120215-035227openalex-snapshot
Evolution in the Cycles of Life
inferred← citeshttps://doi.org/10.1146/annurev-micro-020518-120011openalex-snapshot
Algal Sex Determination and the Evolution of Anisogamy
inferred← citeshttps://doi.org/10.1186/s12862-018-1287-xopenalex-snapshot
Differentiation of haploid and diploid fertilities in Gracilaria chilensis affect ploidy ratio
inferred← citeshttps://doi.org/10.1186/s12915-016-0299-5openalex-snapshot
Parallel evolution of highly conserved plastid genome architecture in red seaweeds and seed plants
inferred← citeshttps://doi.org/10.1186/s13059-025-03797-yopenalex-snapshot
Structural and evolutionary features of red algal UV sex chromosomes
inferred← citeshttps://doi.org/10.1242/jeb.242199openalex-snapshot
Effects of food intake and hydration state on behavioral thermoregulation and locomotor activity in the tropidurid lizard Tropidurus catalanensis
inferred← citeshttps://doi.org/10.1371/journal.pone.0170010openalex-snapshot
Phylogenetically Widespread Polyembryony in Cyclostome Bryozoans and the Protracted Asynchronous Release of Clonal Brood-Mates
inferred← citeshttps://doi.org/10.1371/journal.pone.0295409openalex-snapshot
Stable demographic ratios of haploid gametophyte to diploid sporophyte abundance in macroalgal populations
inferred← citeshttps://doi.org/10.1515/bot-2014-0085openalex-snapshot
Life history bias in endophyte infection of the Antarctic rhodophyte, Iridaea cordata
inferred← citeshttps://doi.org/10.1515/bot-2016-0091openalex-snapshot
Seaweed reproductive biology: environmental and genetic controls
inferred← citeshttps://doi.org/10.1890/0012-9615(1999)069[0331:cossia]2.0.co;2openalex-snapshot
COEXISTENCE OF SIMILAR SPECIES IN A SPACE-LIMITED INTERTIDAL ZONE
inferred← citeshttps://doi.org/10.1890/02-4101openalex-snapshot
POPULATION DEMOGRAPHICS IN SPECIES WITH BIPHASIC LIFE CYCLES
inferred← citeshttps://doi.org/10.2216/i0031-8884-20-4-397.1openalex-snapshot
The role of bispores in the life history of the parasitic red alga, Gardneriella tuberifera (Solieriaceae, Gigartinales)
inferred← citeshttps://doi.org/10.2216/i0031-8884-30-2-151.1openalex-snapshot
Schmitzia sanctae-crucis sp. nov. (Calosiphoniaceae, Rhodophyta) and a novel nutritive development to aid in zygote nucleus amplification
inferred← citeshttps://doi.org/10.2216/ph07-84.1openalex-snapshot
Susceptibility of spores of different ploidy levels from AntarcticGigartina skottsbergii(Gigartinales, Rhodophyta) to ultraviolet radiation
inferred← citeshttps://doi.org/10.2307/2398799openalex-snapshot
On the Evolution of Complex Life Cycles in Plants: A Review and an Ecological Perspective
inferred← citeshttps://doi.org/10.2307/2445666openalex-snapshot
Variation of Reproductive Success in a Haplo-Diploid Red Alga, Gracilaria verrucosa: Effects of Parental Identities and Crossing Distance
inferred← citeshttps://doi.org/10.26686/wgtn.17064623openalex-snapshot
A Taxonomic Investigation into the Red Alga Plocamium within New Zealand
inferred← citeshttps://doi.org/10.31390/gradschool_disstheses.6316openalex-snapshot
Molecular Systematics of Red Algae.
inferred← citeshttps://doi.org/10.3158/0015-0746-47.1.17openalex-snapshot
Chapter Four: Life Cycles in Major Lineages of Photosynthetic Eukaryotes, with a Special Reference to the Origin of Land Plants
inferred← citeshttps://doi.org/10.31857/s0042132423060042openalex-snapshot
Reproductive Criteria of Multicellularity and Original Modes of Reproduction
inferred← citeshttps://doi.org/10.3354/meps073083openalex-snapshot
Frond regrowth from basal disc in Iridaea laminarioides (Rhodophyta, Gigartinales) at Mehuin, southern Chile
inferred← citeshttps://doi.org/10.3354/meps09039openalex-snapshot
Does sperm supply limit the number of broods produced by a polyembryonous bryozoan?
inferred← citeshttps://doi.org/10.3390/d11050080openalex-snapshot
Plant Part Age and Size Affect Sessile Macrobenthic Assemblages Associated with a Foliose Red Algae Phycodrys rubens in the White Sea
inferred← citeshttps://doi.org/10.3732/ajb.1300314openalex-snapshot
The evolutionary‐developmental origins of multicellularity
inferred← citeshttps://doi.org/10.3732/ajb.1400526openalex-snapshot
Coleochaete and the origin of sporophytes
inferred← citeshttps://doi.org/10.4067/s0718-19572013000300020openalex-snapshot
Proposal of a fertility index of Hypnea for ecophysiological studies
inferred← citeshttps://doi.org/10.4490/algae.2020.35.12.7openalex-snapshot
Dynamics of spermatial nuclei in trichogyne of the red alga Bostrychia moritziana (Florideophyceae)
inferred← citeshttps://doi.org/10.7717/peerj.19610openalex-snapshot
A predictive framework for identifying source populations of non-native marine macroalgae: Chondria tumulosa in the Pacific Ocean
inferred← citeshttps://doi.org/10.7872/crya.v34.iss1.2013.3openalex-snapshot
A Re-Assessment of Reproductive Anatomy and Postfertilization Development in the Systematics of Grateloupia (Halymeniales, Rhodophyta)
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