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An insect-induced novel plant phenotype for sustaining social life in a closed system
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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/mpev.2000.0887openalex-snapshot
Genetically Distinct Populations in an Asian Soldier-Producing Aphid, Pseudoregma bambucicola (Homoptera: Aphididae), Identified by DNA Fingerprinting and Molecular Phylogenetic Analysis
inferredcites →https://doi.org/10.1007/bf02350208openalex-snapshot
Gall cleaning by the aphidHormaphis betulae
inferredcites →https://doi.org/10.1007/bf02350284openalex-snapshot
Agonistic interactions between ants and gall-living soldier aphids
inferredcites →https://doi.org/10.1007/bf02350874openalex-snapshot
First-instar aphids produced late by the fundatrix ofCeratovacuna nekoashi (Homoptera) defend their closed gall outside
inferredcites →https://doi.org/10.1007/bf02352573openalex-snapshot
Defenders of the aphidNipponaphis distyliicola (Homoptera) in its completely closed gall
inferredcites →https://doi.org/10.1007/s00040-003-0643-yopenalex-snapshot
Altruistic defenders in a gall-forming aphid of the tribe Hormaphidini (Homoptera, Aphididae, Hormaphidinae) on its primary host
inferredcites →https://doi.org/10.1007/s10144-006-0268-xopenalex-snapshot
Herbivory damage does not indirectly influence the composition or excretion of aphid honeydew
inferredcites →https://doi.org/10.1016/s0022-1910(02)00073-2openalex-snapshot
Maintenance of soldier-producing aphids on an artificial diet
inferredcites →https://doi.org/10.1016/s0169-5347(03)00247-7openalex-snapshot
The adaptive significance of insect gall morphology
inferredcites →https://doi.org/10.1073/pnas.0402462101openalex-snapshot
Venomous protease of aphid soldier for colony defense
inferredcites →https://doi.org/10.1080/002229399300227openalex-snapshot
Wax glands, wax production and the functional significance of wax use in three aphid species (Homoptera: Aphididae)
inferredcites →https://doi.org/10.1093/bioinformatics/btg180openalex-snapshot
MrBayes 3: Bayesian phylogenetic inference under mixed models
inferredcites →https://doi.org/10.1093/bioinformatics/btl446openalex-snapshot
RAxML-VI-HPC: maximum likelihood-based phylogenetic analyses with thousands of taxa and mixed models
inferredcites →https://doi.org/10.1093/jxb/44.2.509openalex-snapshot
Uptake and Transport of Calcium and the Possible Causes of Blossom-end Rot in Tomato
inferredcites →https://doi.org/10.1093/jxb/erj067openalex-snapshot
Phloem-sap feeding by animals: problems and solutions
inferredcites →https://doi.org/10.1093/molbev/msn083openalex-snapshot
jModelTest: Phylogenetic Model Averaging
inferredcites →https://doi.org/10.1093/nar/22.22.4673openalex-snapshot
CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice
inferredcites →https://doi.org/10.1098/rsbl.2003.0026openalex-snapshot
Self-sacrificing gall repair by aphid nymphs
inferredcites →https://doi.org/10.1098/rsbl.2003.0089openalex-snapshot
Density triggers soldier production in a social aphid
inferredcites →https://doi.org/10.1098/rspb.1992.0029openalex-snapshot
Altruistic housekeeping in a social aphid
inferredcites →https://doi.org/10.1098/rspb.2008.1628openalex-snapshot
Scab formation and wound healing of plant tissue by soldier aphid
inferredcites →https://doi.org/10.1104/pp.120.3.849openalex-snapshot
Inhibition of Water Channels by HgCl2 in Intact Wheat Root Cells1
inferredcites →https://doi.org/10.1111/j.1469-185x.1981.tb00342.xopenalex-snapshot
CUTICULAR LIPIDS OF TERRESTRIAL PLANTS AND ARTHROPODS: A COMPARISON OF THEIR STRUCTURE, COMPOSITION, AND WATERPROOFING FUNCTION
inferredcites →https://doi.org/10.1111/j.1469-185x.1996.tb00741.xopenalex-snapshot
THE EVOLUTION OF SOLDIERS IN APHIDS
inferredcites →https://doi.org/10.1155/2009/159478openalex-snapshot
Extremely Long-Closed Galls of a Social Aphid
inferredcites →https://doi.org/10.1155/2010/380351openalex-snapshot
A Review of the Biology of Cerataphidini (Hemiptera, Aphididae, Hormaphidinae), Focusing Mainly on Their Life Cycles, Gall Formation, and Soldiers
inferredcites →https://doi.org/10.1303/aez.18.361openalex-snapshot
Relationship between Nola innocua BUTLER (Lepidoptera : Nolidae), a Kleptoparasite, and Aphids which Cause Galls on Distylium racemosum Trees
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.11646/zootaxa.3861.5.6zenodo-depositor-declared
The histo structure of galls induced by aphids as a useful taxonomic character: the case of Rectinasus (Hemiptera, Aphididae, Eriosomatinae)
inferred← citeshttps://doi.org/10.1002/pld3.619openalex-snapshot
Exploring the diversity of galls on Artemisia indica induced by Rhopalomyia species through morphological and transcriptome analyses
inferred← citeshttps://doi.org/10.1007/978-3-031-80064-1_11openalex-snapshot
Structural and Physiological Aspects of Aphid-Induced Galls
inferred← citeshttps://doi.org/10.1007/978-3-031-80064-1_3openalex-snapshot
Epidermis: The First Line of Contact Between Plants and Gall-Inducing Herbivores
inferred← citeshttps://doi.org/10.1007/s00040-018-0604-0openalex-snapshot
Extended lifespan and overlapping of generations in a gall-forming social aphid, Quadrartus yoshinomiyai
inferred← citeshttps://doi.org/10.1007/s00265-023-03315-9openalex-snapshot
Eusocial evolution without a nest: kin structure of social aphids forming open colonies on bamboo
inferred← citeshttps://doi.org/10.1007/s10886-018-0955-zopenalex-snapshot
Chemical Ecology and Sociality in Aphids: Opportunities and Directions
inferred← citeshttps://doi.org/10.1007/s11829-014-9333-0openalex-snapshot
Microscopic study of galls induced by three species of Geopemphigus (Hemiptera: Aphididae: Eriosomatinae) on Pistacia mexicana
inferred← citeshttps://doi.org/10.1007/s11829-016-9470-8openalex-snapshot
Life history of Stenopsylla nigricornis (Hemiptera: Psylloidea: Triozidae) and phytohormones involved in its gall induction
inferred← citeshttps://doi.org/10.1007/s11829-020-09778-1openalex-snapshot
Microscopic study of nine galls induced in Populus nigra by aphids of the Iberian Peninsula
inferred← citeshttps://doi.org/10.1007/s40011-020-01206-xopenalex-snapshot
Histological Study of Leaf Galls Induced by Phylloxera in Vitis (Vitaceae) Leaves
inferred← citeshttps://doi.org/10.1016/bs.aiip.2014.12.005openalex-snapshot
The Physiology and Genomics of Social Transitions in Aphids
inferred← citeshttps://doi.org/10.1016/j.anbehav.2014.08.003openalex-snapshot
Comparative phenotyping across a social transition in aphids
inferred← citeshttps://doi.org/10.1021/acs.langmuir.9b00771openalex-snapshot
Liquid Marbles in Nature: Craft of Aphids for Survival
inferred← citeshttps://doi.org/10.1038/s41598-019-57138-8openalex-snapshot
Microenvironmental analysis of two alternating hosts and their impact on the ecological adaptation of the horned sumac gall aphid Schlechtendalia chinensis (Hemiptera, Pemphiginae)
inferred← citeshttps://doi.org/10.1038/s41598-021-81006-zopenalex-snapshot
Temporal division of labor in an aphid social system
inferred← citeshttps://doi.org/10.1073/pnas.1900917116openalex-snapshot
Exaggeration and cooption of innate immunity for social defense
inferred← citeshttps://doi.org/10.1088/1748-3190/11/5/054001openalex-snapshot
Why is it difficult to wash aphids off from superhydrophobic kale?
inferred← citeshttps://doi.org/10.1093/bioinformatics/btw673openalex-snapshot
PhenoCurve: capturing dynamic phenotype-environment relationships using phenomics data
inferred← citeshttps://doi.org/10.1098/rsbl.2018.0470openalex-snapshot
Water-repellent plant surface structure induced by gall-forming insects for waste management
inferred← citeshttps://doi.org/10.1098/rstb.2024.0383openalex-snapshot
Nutrient flows and trophic interactions in natural microcosms: typologies, boundaries and complexities
inferred← citeshttps://doi.org/10.1101/2022.10.23.513187openalex-snapshot
Eusocial evolution without a nest: kin structure of social aphids forming open colonies on bamboo
inferred← citeshttps://doi.org/10.1109/bibm.2018.8621211openalex-snapshot
OLIVER: A Tool for Visual Data Analysis on Longitudinal Plant Phenomics Data
inferred← citeshttps://doi.org/10.1111/brv.13106openalex-snapshot
Soil–plant–gall relationships: from gall development to ecological patterns
inferred← citeshttps://doi.org/10.1111/een.12867openalex-snapshot
Alteration of free amino acid concentrations in insect galls induced by Andricus mukaigawae (Hymenoptera; Cynipidae)
inferred← citeshttps://doi.org/10.1111/ens.12002openalex-snapshot
The aphid C eratovacuna nekoashi ( H emiptera: A phididae: H ormaphidinae) and its allied species in K orea, J apan and T aiwan
inferred← citeshttps://doi.org/10.1111/ens.12029openalex-snapshot
Formation of long‐lasting galls by overwintered nymphs in the J apanese aphid Q uadrartus yoshinomiyai ( H emiptera: A phididae: H ormaphidinae)
inferred← citeshttps://doi.org/10.1111/ens.12144openalex-snapshot
N ipponaphis species ( A phididae: H ormaphidinae) that form green galls on D istylium racemosum in J apan
inferred← citeshttps://doi.org/10.1111/ens.12290openalex-snapshot
Dermaphis coccidiformis sp. nov. (Hemiptera), an aphid species with asymmetrically sclerotized apterae and “winter alates”
inferred← citeshttps://doi.org/10.1111/ens.12358openalex-snapshot
Two closely related species of Nipponaphis (Hemiptera: Aphididae) that migrate between Distylium racemosum and Machilus trees in Japan
inferred← citeshttps://doi.org/10.1111/ens.12478openalex-snapshot
Revision of the Japanese species of Metanipponaphis (Hemiptera: Aphididae) and its allied genera
inferred← citeshttps://doi.org/10.1111/nph.16340openalex-snapshot
Plants make galls to accommodate foreigners: some are friends, most are foes
inferred← citeshttps://doi.org/10.1139/cjb-2016-0189openalex-snapshot
Revisiting the histological patterns of storage tissues: beyond the limits of gall-inducing taxa
inferred← citeshttps://doi.org/10.1155/2019/1280414openalex-snapshot
Dimorphic Sessile Apterae of the Aphid Neothoracaphis glaucae (Hemiptera) on the Evergreen Oak Quercus glauca
inferred← citeshttps://doi.org/10.1242/jeb.151720openalex-snapshot
Rats concatenate 22 kHz and 50 kHz calls into a single utterance
inferred← citeshttps://doi.org/10.1371/journal.pgen.1008398openalex-snapshot
Genomic dissection of an extended phenotype: Oak galling by a cynipid gall wasp
inferred← citeshttps://doi.org/10.1371/journal.pone.0283464openalex-snapshot
A study on the effect of host plants on Chinese gallnut morphogenesis
inferred← citeshttps://doi.org/10.1523/jneurosci.0262-14.2014openalex-snapshot
Rat Ultrasonic Vocalization Shows Features of a Modular Behavior
inferred← citeshttps://doi.org/10.20944/preprints202106.0494.v1openalex-snapshot
Recent Progress Regarding the Evolution and Molecular Aspect of Insect Gall Formation
inferred← citeshttps://doi.org/10.2354/psj.29.018openalex-snapshot
The World Spread Through Insectivory - Role of Insect-Eating Behavior by Primates in Forest Ecosystem -
inferred← citeshttps://doi.org/10.3389/fpls.2019.00933openalex-snapshot
Plant Manipulation by Gall-Forming Social Aphids for Waste Management
inferred← citeshttps://doi.org/10.3389/fpls.2020.00811openalex-snapshot
A Complex Nutrient Exchange Between a Gall-Forming Aphid and Its Plant Host
inferred← citeshttps://doi.org/10.3390/ani15142036openalex-snapshot
Patrolling and Cleaning: Threat Detection and Response Behaviors of Soldiers in a Social Aphid
inferred← citeshttps://doi.org/10.3390/books978-3-0365-3162-5openalex-snapshot
Molecular Mechanisms of Leaf Morphogenesis
inferred← citeshttps://doi.org/10.3390/ijms22179424openalex-snapshot
Recent Progress Regarding the Molecular Aspects of Insect Gall Formation
inferred← citeshttps://doi.org/10.3410/f.735566356.793559315openalex-snapshot
Faculty Opinions recommendation of Exaggeration and cooption of innate immunity for social defense.
inferred← citeshttps://doi.org/10.70675/ba328d98z1a25z44d8z9c3ez6ac7e9eb6573openalex-snapshot
Evolutionary origin and molecular bases of the gall-inducing life-style in the Gracillariidae
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