On the public citation graph
A Review of the Biology of Cerataphidini (Hemiptera, Aphididae, Hormaphidinae), Focusing Mainly on Their Life Cycles, Gall Formation, and Soldiers
0 signed · 185 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1006/anbe.1996.0069openalex-snapshot
Duelling aphids: intraspecific fighting inAstegopteryx minuta(Homoptera: Hormaphididae)
inferredcites →https://doi.org/10.1006/anbe.2001.1796openalex-snapshot
Behaviour, morphology and the division of labour in two soldier-producing aphids
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/10.1006/mpev.2001.0933openalex-snapshot
Phylogeny and Biogeography of the Flowering Plant Genus Styrax (Styracaceae) Based on Chloroplast DNA Restriction Sites and DNA Sequences of the Internal Transcribed Spacer Region
inferredcites →https://doi.org/10.1007/978-3-540-75957-7_2openalex-snapshot
The Ecology of Altruism in a Clonal Insect
inferredcites →https://doi.org/10.1007/978-94-011-5868-8openalex-snapshot
Aphid Ecology An optimization approach
inferredcites →https://doi.org/10.1007/bf00170595openalex-snapshot
Sex ratio, local mate competition and mating behaviour in the aphid Pemphigus spyrothecae
inferredcites →https://doi.org/10.1007/bf01237835openalex-snapshot
Intergall migration in aphids; a model and a test of ESS dispersal rate
inferredcites →https://doi.org/10.1007/bf01240648openalex-snapshot
A test of geometric hypotheses for soldier investment patterns in the gall producing tropical aphidCerataphis fransseni (Homoptera, Hormaphididae)
inferredcites →https://doi.org/10.1007/bf01242566openalex-snapshot
Caste allometries in the soldier-producing aphidPseudoregma alexanderi (Hormaphididae: Aphidoidea)
inferredcites →https://doi.org/10.1007/bf01314917openalex-snapshot
Life history characteristics and behaviour of the bamboo aphid,Pseudoregma bambucicola (Hemiptera: Pemphigidae), having sterile soldiers
inferredcites →https://doi.org/10.1007/bf02348111openalex-snapshot
Soldiers of a European gall aphid,Pemphigus spyrotecae (Homoptera: Aphidoidea): Why do they molt?
inferredcites →https://doi.org/10.1007/bf02350028openalex-snapshot
Alarm pheromone eliciting attack and escape responses in the sugar cane woolly aphid,Ceratovacuna lanigera (Homoptera, Pemphigidae)
inferredcites →https://doi.org/10.1007/bf02350119openalex-snapshot
Feeding by soldiers of the bamboo aphidPseudoregma koshunensis (Homoptera: Aphididae)
inferredcites →https://doi.org/10.1007/bf02350120openalex-snapshot
Shortened longevity of soldiers of the bamboo aphidPseudoregma koshunensis (Takahashi) (Homoptera: Aphididae) due to attack behaviour
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/bf02350297openalex-snapshot
An aphid species doing a headstand: Butting behavior ofAstegopteryx bambucifoliae (Homoptera: Aphidoidea)
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/bf02763464openalex-snapshot
Social structure and the defensive role of soldiers in a eusocial bamboo aphid, Pseudoregma bambucicola (Homoptera: Aphididae): A test of the defence‐optimization hypothesis
inferredcites →https://doi.org/10.1007/bf02769293openalex-snapshot
Lack of kin discrimination in the eusocial aphid pseudoregmabambucicola (Homoptera: Aphididae)
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/s00040-003-0675-3openalex-snapshot
Logistic model for soldier production in aphids
inferredcites →https://doi.org/10.1007/s00040-005-0839-4openalex-snapshot
Head-plug defense in a gall aphid
inferredcites →https://doi.org/10.1007/s00040-007-0955-4openalex-snapshot
Female production within the gall and male production on leaves by individual alates of a social aphid
inferredcites →https://doi.org/10.1007/s00040-008-0988-3openalex-snapshot
Social parasitism and behavioral interactions between two gall-forming social aphids
inferredcites →https://doi.org/10.1007/s000400050059openalex-snapshot
Behavior and morphology of monomorphic soldiers from the aphid genus Pseudoregma (Cerataphidini, Hormaphididae): implications for the evolution of morphological castes in social aphids
inferredcites →https://doi.org/10.1007/s000400050160openalex-snapshot
Reproductive schedule and factors affecting soldier production in the eusocial bamboo aphid Pseudoregma bambucicola (Homoptera, Aphididae)
inferredcites →https://doi.org/10.1007/s00114-003-0474-8openalex-snapshot
Aphid soldier differentiation: density acts on both embryos and newborn nymphs
inferredcites →https://doi.org/10.1007/s002390010088openalex-snapshot
Evolutionary Studies on Uricases of Fungal Endosymbionts of Aphids and Planthoppers
inferredcites →https://doi.org/10.1007/s10144-005-0218-zopenalex-snapshot
Factors affecting the proportion of sterile soldiers in growing aphid colonies
inferredcites →https://doi.org/10.1016/j.anbehav.2003.08.020openalex-snapshot
Fortress repair in the social aphid species Pemphigus spyrothecae
inferredcites →https://doi.org/10.1016/j.cub.2010.04.057openalex-snapshot
Altruistic Colony Defense by Menopausal Female Insects
inferredcites →https://doi.org/10.1016/j.jinsphys.2003.10.006openalex-snapshot
The proximate cue of density-dependent soldier production in a social aphid
inferredcites →https://doi.org/10.1016/j.jinsphys.2004.08.004openalex-snapshot
Density-dependent induction and suppression of soldier differentiation in an aphid social system
inferredcites →https://doi.org/10.1016/j.jtbi.2004.05.019openalex-snapshot
How many soldiers are optimal for an aphid colony?
inferredcites →https://doi.org/10.1016/j.ympev.2009.12.005openalex-snapshot
Combination of molecular data support the existence of three main lineages in the phylogeny of aphids (Hemiptera: Aphididae) and the basal position of the subfamily Lachninae
inferredcites →https://doi.org/10.1016/s0003-3472(05)80135-6openalex-snapshot
Aphid soldiers discriminate between soldiers and non-soldiers, rather than between kin and non-kin, in Ceratoglyphina bambusae
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/10.1017/cbo9780511721953.008openalex-snapshot
The evolution of sociality in aphids: a clone's-eye view
inferredcites →https://doi.org/10.1017/s1742758400016829openalex-snapshot
Occurrence and Distribution of Cerataphis Palmae (Ghesquierei) (Homoptera: Pemphigidae) on Raphia Palms in Southern Nigeria
inferredcites →https://doi.org/10.1038/241126b0openalex-snapshot
Trans-β-farnesene, Alarm Pheromone of the Green Peach Aphid, Myzus persicae (Sulzer)
inferredcites →https://doi.org/10.1038/318460a0openalex-snapshot
Sex ratios of an aphid subject to local mate competition with variable maternal condition
inferredcites →https://doi.org/10.1038/377495a0openalex-snapshot
A developmental switch sufficient for flower initiation in diverse plants
inferredcites →https://doi.org/10.1038/sj.hdy.6800658openalex-snapshot
Host-associated populations in the lettuce root aphid, Pemphigus bursarius (L.)
inferredcites →https://doi.org/10.1046/j.1343-8786.2003.00012.xopenalex-snapshot
Tuberaphis owadai (Homoptera), a new aphid species forming a large gall on Styrax tonkinensis in northern Vietnam
inferredcites →https://doi.org/10.1046/j.1365-2311.1999.00202.xopenalex-snapshot
Escaping an ecological dead‐end: asexual overwintering and morph determination in the lettuce root aphid Pemphigus bursarius L.
inferredcites →https://doi.org/10.1046/j.1365-294x.2002.01530.xopenalex-snapshot
Clonal mixing in the soldier‐producing aphidPemphigus spyrothecae(Hemiptera: Aphididae)
inferredcites →https://doi.org/10.1046/j.1365-3113.1997.d01-20.xopenalex-snapshot
Determining aphid taxonomic affinities and life cycles with molecular data: a case study of the tribe Cerataphidini (Hormaphididae:Aphidoidea: Hemiptera)
inferredcites →https://doi.org/10.1071/zo9660399openalex-snapshot
A taxonomic study of Australian Aphidoidea (Homoptera)
inferredcites →https://doi.org/10.1073/pnas.0402462101openalex-snapshot
Venomous protease of aphid soldier for colony defense
inferredcites →https://doi.org/10.1073/pnas.201212698openalex-snapshot
Genetic conflict and conditional altruism in social aphid colonies
inferredcites →https://doi.org/10.1080/00222930802610485openalex-snapshot
The biology of carnivorous butterfly larvae (Lepidoptera: Lycaenidae: Miletinae: Miletini) and their ant‐tended hemipteran prey in Thailand and the Philippines
inferredcites →https://doi.org/10.1080/00222939500770101openalex-snapshot
The life cycle and natural history of the tropical aphidCerataphis fransseni(Homoptera: Aphididae: Hormaphidinae), with reference to the evolution of host alternation in aphids
inferredcites →https://doi.org/10.1080/00222939800770911openalex-snapshot
A revision of the Chinese species ofEncarsiaFörster (Hymenoptera: Aphelinidae): parasitoids of whiteflies, scale insects and aphids (Hemiptera: Aleyrodidae, Diaspididae, Aphidoidea)
inferredcites →https://doi.org/10.1080/00305316.1995.10433740openalex-snapshot
The taxonomy of theEncarsia flavoscutellumspecies-group (Hymenoptera: Aphelinidae) parasitoids of Hormaphididae (Homoptera: Aphidoidea)
inferredcites →https://doi.org/10.1080/08927014.1995.9522941openalex-snapshot
Factors affecting the proportion of soldiers in eusocial bamboo aphid,Pseudoregma bambucicola, colonies
inferredcites →https://doi.org/10.1086/284659openalex-snapshot
Why There are So Few Species of Aphids, Especially in the Tropics
inferredcites →https://doi.org/10.1093/aesa/43.4.587openalex-snapshot
List of the Aphididae of the Malay Peninsula, with Descriptions of New Species (Homoptera)
inferredcites →https://doi.org/10.1093/aesa/73.3.327openalex-snapshot
Intergall Migration in the Aphid Genus Pemphigus12
inferredcites →https://doi.org/10.1093/molbev/msn203openalex-snapshot
Evolution of Soldier-Specific Venomous Protease in Social Aphids
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.1994.0071openalex-snapshot
A phylogenetic analysis of soldier evolution in the aphid family Hormaphididae
inferredcites →https://doi.org/10.1098/rspb.1995.0063openalex-snapshot
Phylogenetic evidence that aphids, rather than plants, determine gall morphology
inferredcites →https://doi.org/10.1098/rspb.2000.1222openalex-snapshot
Ant tending influences soldier production 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/10.1111/j.1365-2311.1990.tb00790.xopenalex-snapshot
Plasticity of size and relative fecundity in the aphidophagous lycaenid butterfly, Taraka hamada
inferredcites →https://doi.org/10.1111/j.1365-2311.1995.tb00426.xopenalex-snapshot
Genetic differentiation as a result of adaptation to the phenologies of individual host trees in the galling aphid Kaltenbachiella japonica
inferredcites →https://doi.org/10.1111/j.1365-3113.1993.tb01453.xopenalex-snapshot
THREE INTERESTING APHIDS FROM THE FAR EAST
inferredcites →https://doi.org/10.1111/j.1469-185x.1996.tb00741.xopenalex-snapshot
THE EVOLUTION OF SOLDIERS IN APHIDS
inferredcites →https://doi.org/10.1111/j.1469-7998.1995.tb02746.xopenalex-snapshot
Bite forces used by Japanese macaques (Macaca fuscata yakui) on Yakushima Island, Japan to open aphid‐induced galls on Distylium racemosum (Hamamelidaceae)
inferredcites →https://doi.org/10.1111/j.1479-8298.2004.00061.xopenalex-snapshot
Soldier differentiation during embryogenesis of a social aphid, Pseudoregma bambucicola
inferredcites →https://doi.org/10.1111/j.1479-8298.2006.00165.xopenalex-snapshot
Astegopteryx spinocephala (Hemiptera: Aphididae), a new aphid species producing sterile soldiers that guard eggs laid in their gall
inferredcites →https://doi.org/10.1111/j.1558-5646.1998.tb05148.xopenalex-snapshot
PHYLOGENY OF THE TRIBE CERATAPHIDINI (HOMOPTERA) AND THE EVOLUTION OF THE HORNED SOLDIER APHIDS
inferredcites →https://doi.org/10.1126/science.177.4054.1121openalex-snapshot
Aphid Alarm Pheromone: Isolation, Identification, Synthesis
inferredcites →https://doi.org/10.1127/entom.gen/16/1991/1openalex-snapshot
Enemy Recognition and Defence within Trophobiotic Associations with Ants by the Soldier Caste of Pseudoregma sundanica (Homoptera: Aphidoidea)
inferredcites →https://doi.org/10.1146/annurev.en.04.010159.001035openalex-snapshot
Biology of Aphids
inferredcites →https://doi.org/10.1155/2009/159478openalex-snapshot
Extremely Long-Closed Galls of a Social Aphid
inferredcites →https://doi.org/10.1242/jeb.012120openalex-snapshot
Duelling aphids: electrical penetration graphs reveal the value of fighting for a feeding site
inferredcites →https://doi.org/10.1303/aez.2004.417openalex-snapshot
Biological studies on three Micromus species in Japan (Neuroptera: Hemerobiidae) to evaluate their potential as biological control agents against aphids: 1. Thermal effects on development and reproduction
inferredcites →https://doi.org/10.1303/aez.2005.239openalex-snapshot
Analysis of natural colonies of a social aphid Colophina arma: population dynamics, reproductive schedule, and survey for ecological correlates with soldier production
inferredcites →https://doi.org/10.1303/aez.2006.389openalex-snapshot
Effects of prey species and its density on larval performance of two species of hoverfly larvae, Episyrphus balteatus de Geer and Eupeodes corollae Fabricius (Diptera: Syrphidae)
inferredcites →https://doi.org/10.1303/aez.2007.217openalex-snapshot
Gall surface area is a simple and accurate measure of fitness in Nipponaphidini galling aphids (Homoptera: Aphididae)
inferredcites →https://doi.org/10.1303/aez.26.463openalex-snapshot
Ratio of Sterile Soldiers in the Bamboo Aphid, Pseudoregma bambucicola(Homoptera:Aphididae), Colonies in Relation to Social and Habitat Conditions
inferredcites →https://doi.org/10.1303/aez.27.99openalex-snapshot
Seasonal Occurrence of the Sugar Cane Woolly Aphid, Ceratovacuna lanigera(Homoptera:Aphididae), and Its Predators in Sugar Cane Fields of Okinawa Island
inferredcites →https://doi.org/10.1303/aez.28.246openalex-snapshot
Predators of the Bamboo Aphid Pseudoregma bambucicola(Homoptera:Pemphigidae)in Kagoshima, Southern Japan
inferredcites →https://doi.org/10.1303/aez.33.357openalex-snapshot
Differences in the quality and quantity of honeydew from first instar soldier and ordinary morph nymphs of the bamboo aphid, Pseudoregma koshunensis (Takahashi) (Homoptera : Aphididae)
inferredcites →https://doi.org/10.1673/031.007.3401openalex-snapshot
Physical Contests for Females in the Japanese Beetle,Popillia japonica
inferredcites →https://doi.org/10.1673/031.007.3801openalex-snapshot
A New Soldier-Producing Aphid Species,Pseudoregma baenzigeri,sp. nov., from Northern Thailand
inferredcites →https://doi.org/10.17221/4691-jfsopenalex-snapshot
Bionomics and harmfulness of Tetraneura ulmi (L.) (Aphidinea, Pemphigidae) in elms
inferredcites →https://doi.org/10.18984/lepid.39.3_167openalex-snapshot
Larval Carnivory and Myrmecoxeny, and Imaginal Myrmecophily in Miletine Lycaenids (Lepidoptera, Lycaenidae) on the Malay Peninsula
inferredcites →https://doi.org/10.2307/3298541openalex-snapshot
A Revision of the Imbricate Group of Styrax Series Cyrta (Styracaceae) in Asia
inferredcites →https://doi.org/10.2307/3493507openalex-snapshot
Palm Aphid Control on 'Malayan Dwarf' Coconut Palms
inferredcites →https://doi.org/10.2307/3495277openalex-snapshot
The Aphids and Phylloxera of Bermuda (Homoptera: Aphididae and Phylloxeridae)
inferredcites →https://doi.org/10.2307/3495956openalex-snapshot
Intraspecific Dueling in Palm Aphids, Cerataphis brasiliensis (Homoptera: Hormaphididae)
inferredcites →https://doi.org/10.2307/3496504openalex-snapshot
Colony Defense by Wingpadded Nymphs in Grylloprociphilus imbricator (Hemiptera: Aphididae)
inferredcites →https://doi.org/10.2307/3676435openalex-snapshot
Great Tits Exploit Aphid Galls as a Source of Food
inferredcites →https://doi.org/10.26515/rzsi/v81/i3-4/1984/161216openalex-snapshot
Studies on Ceratovacuna silvestrii (Takahashi) (Homoptera: Aphididae) and its Predator Anisolemnia dilatata (Fab.) on Bambusa Arundinacea
inferredcites →https://doi.org/10.4161/cib.3.1.9694openalex-snapshot
Mechanisms regulating caste differentiation in an aphid social system
inferredcites →https://doi.org/10.5109/22689openalex-snapshot
A revision of the tribe Scymnini from Japan and the Loochoos (Coleoptera: Coccinellidae) : Part II. Genus Scymnus (Subgenus Pullus)
inferredcites →https://doi.org/10.5109/2475openalex-snapshot
OBSERVATIONS ON THE OVIPOSITION BEHAVIOUR OF METASYRPHUS CONFRA TER (DIPTERA, SYRPHIDAE) AND THE DEFENSIVE BEHAVIOUR OF SOLDIERS OF PS’EUDOREGMA BAMBUCICOLA (HOMOPTERA, PEMPHIGIDAE)
inferredcites →https://doi.org/10.5109/2476openalex-snapshot
OBSERVATIONS Op THE PREY-PREDATOR RELATIONSHIP BETWEEN PSEUDOREGMA BAMBUCICOLA (HOMOPTERA, PEMPHIGIDAE) AND METASYRPHUS COiVFRA TER (DIPTERA, SYRPHIDAE), WITH SPECIAL REFERENCE TO THE BEHAVIOUR OF TjHE APHID SOLDIERS
inferredcites →https://doi.org/10.5281/zenodo.16035291openalex-snapshot
Homonymy in the Coccinelidae (Coleoptera), or something fishy about Pseudoscymnus chapin
inferredcites →https://doi.org/10.5281/zenodo.16183887openalex-snapshot
Predatory and parasitic Lepidoptera: Carnivores living on plants
inferredcites →https://doi.org/10.5281/zenodo.16471194openalex-snapshot
Absence of Kin Discrimination Behavior in a Soldier-Producing Aphid, Ceratovacuna japonica (Hemiptera: Pemphigidae; Cerataphidini)
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.4323.2.4zenodo-depositor-declared
A new genus and two new species of galling aphids (Hemiptera: Aphididae) from Distylium (Hamamelidaceae) in Taiwan
inferred← citeshttps://doi.org/10.11646/zootaxa.5507.1.9zenodo-depositor-declared
A new species of Pachyrhabda Meyrick (Lepidoptera: Stathmopodidae) from the Korean Peninsula
inferred← citeshttps://doi.org/10.3897/compcytogen.18.136095zenodo-depositor-declared
Gallophilous theory of cyclical parthenogenesis in aphids (Homoptera, Aphidinea)
inferred← citeshttps://doi.org/10.3897/zookeys.1218.133287zenodo-depositor-declared
Taxonomic notes on the genus Chaitoregma (Hemiptera, Aphididae, Hormaphidinae), with description of a new species from China
inferred← citeshttps://doi.org/10.5281/zenodo.14162389zenodo-depositor-declared
Chaitoregma Hille Ris Lambers & Basu 1966
inferred← citeshttps://doi.org/10.5281/zenodo.14162391zenodo-depositor-declared
Chaitoregma tattakana subsp. tattakana
inferred← citeshttps://doi.org/10.1002/eap.1713openalex-snapshot
Complementary crops and landscape features sustain wild bee communities
inferred← citeshttps://doi.org/10.1002/ecs2.4060openalex-snapshot
First record of antipredator behavior in the gall‐forming aphid Mordwilkoja vagabunda
inferred← citeshttps://doi.org/10.1007/s00040-012-0258-2openalex-snapshot
Buying time for colony mates: the anti-predatory function of soldiers in the eusocial aphid Ceratovacuna japonica (Homoptera, Hormaphidinae)
inferred← citeshttps://doi.org/10.1007/s00040-016-0509-8openalex-snapshot
Soldiers with large weapons behave aggressively against predators: correlated morphological and behavioral defensive traits in a eusocial aphid
inferred← citeshttps://doi.org/10.1007/s00040-024-00979-yopenalex-snapshot
Colony size affects the induction of sterile soldier production in the eusocial aphid Ceratovacuna japonica (Hemiptera: Aphididae)
inferred← citeshttps://doi.org/10.1007/s00248-022-02114-5openalex-snapshot
Strong Linkage Between Symbiotic Bacterial Community and Host Age and Morph in a Hemipteran Social Insect
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/s10682-012-9628-5openalex-snapshot
Soldiers with large weapons in predator-abundant midsummer: phenotypic plasticity in a eusocial aphid
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/s42690-025-01738-7openalex-snapshot
So close and unnoted: a new host plant of Cerataphis brasiliensis (Hempel) (Hemiptera: Aphididae)
inferred← citeshttps://doi.org/10.1016/b978-0-12-818621-3.00006-9openalex-snapshot
Arthropod pests of sugarcane (Saccharum officinarum L.)
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.2017.03.028openalex-snapshot
Lines, loops and spirals: an intraclonal continuum of host location behaviours in walking aphids
inferred← citeshttps://doi.org/10.1016/j.aspen.2021.04.016openalex-snapshot
Ceratovacuna atrovirensa Qiao, a new species from China (Aphididae: Hormaphdinae)
inferred← citeshttps://doi.org/10.1016/j.cois.2023.101142openalex-snapshot
Evolution and molecular mechanisms of wing plasticity in aphids
inferred← citeshttps://doi.org/10.1016/j.cois.2024.101205openalex-snapshot
Social aphids: emerging model for studying insect sociality
inferred← citeshttps://doi.org/10.1016/j.ibmb.2022.103756openalex-snapshot
Reproductive constraint in the social aphid Ceratovacuna japonica: Sterility regulation in the soldier caste of a viviparous insect
inferred← citeshttps://doi.org/10.1016/j.isci.2022.105478openalex-snapshot
Complex host/symbiont integration of a multi-partner symbiotic system in the eusocial aphid Ceratovacuna japonica
inferred← citeshttps://doi.org/10.1016/j.ygcen.2015.09.032openalex-snapshot
Characterization and expression analysis of adipokinetic hormone and its receptor in eusocial aphid Pseudoregma bambucicola
inferred← citeshttps://doi.org/10.1017/9781107338319.007openalex-snapshot
Sociality in Aphids and Thrips
inferred← citeshttps://doi.org/10.1017/s0007485313000321openalex-snapshot
Molecular phylogenetic evidence for paraphyly of Ceratovacuna and Pseudoregma (Hemiptera, Hormaphidinae) reveals late Tertiary radiation
inferred← citeshttps://doi.org/10.1038/ncomms2187openalex-snapshot
An insect-induced novel plant phenotype for sustaining social life in a closed system
inferred← citeshttps://doi.org/10.1038/s41598-018-38475-6openalex-snapshot
A galling insect activates plant reproductive programs during gall development
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/10.1079/cabicompendium.16271openalex-snapshot
Ceratovacuna lanigera (sugarcane woolly aphid)
inferred← citeshttps://doi.org/10.1093/beheco/araf076openalex-snapshot
The kin-selected context of dueling in horned aphids: cooperation or conflict?
inferred← citeshttps://doi.org/10.1093/zoolinnean/zlx048openalex-snapshot
Historical and cospeciating associations between Cerataphidini aphids (Hemiptera: Aphididae: Hormaphidinae) and their primary endosymbiont Buchnera aphidicola
inferred← citeshttps://doi.org/10.1098/rsbl.2012.1053openalex-snapshot
Juveniles and the elderly defend, the middle-aged escape: division of labour in a social aphid
inferred← citeshttps://doi.org/10.1101/2022.08.19.501651openalex-snapshot
Seasonal polyphenism underlies the origin of a sterile caste in aphids
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/10.1101/2025.04.02.646943openalex-snapshot
How The Transition of Aphid Life Cycles Affect Endosymbiotic Bacteria
inferred← citeshttps://doi.org/10.1101/2025.07.09.664008openalex-snapshot
Evolution of multi-partner symbiotic systems in the tribe Cerataphidini: genome reduction of Buchnera and frequent turnover of companion symbionts
inferred← citeshttps://doi.org/10.1111/1744-7917.12070openalex-snapshot
Cannibalism in the pea aphid,Acyrthosiphon pisum
inferred← citeshttps://doi.org/10.1111/1744-7917.12746openalex-snapshot
Diversity of bacteria associated with Hormaphidinae aphids (Hemiptera: Aphididae)
inferred← citeshttps://doi.org/10.1111/1744-7917.13105openalex-snapshot
Mother knows best: reproductive regulation of caste ratio in a social hemipteran
inferred← citeshttps://doi.org/10.1111/azo.12186openalex-snapshot
Buchnera aphidicola of the birch blister aphid, Hamamelistes betulinus (Horváth, 1896) (Insecta, Hemiptera, Aphididae: Hormaphidinae): molecular characterization, transmission between generations and its geographic significance
inferred← citeshttps://doi.org/10.1111/cla.12024openalex-snapshot
A total‐evidence phylogenetic analysis of H ormaphidinae ( H emiptera: A phididae), with comments on the evolution of galls
inferred← citeshttps://doi.org/10.1111/een.13244openalex-snapshot
Body setae of a carnivorous caterpillar are an antagonistic trait against a defensive trait of prey: A case study of the aphidophagous larvae of Taraka hamada (Lepidoptera: Lycaenidae)
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.12174openalex-snapshot
Social aphids use their antennae to perceive density cue for soldier production
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/ens.12492openalex-snapshot
Defensive nymphs and water‐repellency in previously unknown galls of the social aphid Colophina monstrifica ( H emiptera: A phididae: E riosomatinae)
inferred← citeshttps://doi.org/10.1111/evo.13285openalex-snapshot
An alternative pathway to eusociality: Exploring the molecular and functional basis of fortress defense
inferred← citeshttps://doi.org/10.1155/2012/621934openalex-snapshot
Galling Aphids (Hemiptera: Aphidoidea) in China: Diversity and Host Specificity
inferred← citeshttps://doi.org/10.1155/2016/4036571openalex-snapshot
Defensive Nymphs of the Woolly AphidThoracaphis kashifolia(Hemiptera) on the OakQuercus glauca
inferred← citeshttps://doi.org/10.13102/sociobiology.v59i4.518openalex-snapshot
Eggs of a Eusial Aphid’s Predator are Protected Against Attacks by Aphid Soldiers
inferred← citeshttps://doi.org/10.13102/sociobiology.v62i1.116-119openalex-snapshot
Clonal composition of colonies of a eusocial aphid, Ceratovacuna japonica
inferred← citeshttps://doi.org/10.1371/journal.pone.0032706openalex-snapshot
Young Aphids Avoid Erroneous Dropping when Evading Mammalian Herbivores by Combining Input from Two Sensory Modalities
inferred← citeshttps://doi.org/10.2171/jao.43.2openalex-snapshot
Communication tactics of social aphids using their pheromones and plant-gall allelochemicals
inferred← citeshttps://doi.org/10.31610/trudyzin/2024.328.4.595openalex-snapshot
Natural history of cyclical parthenogenesis of aphids (Homoptera: Aphidinea)
inferred← citeshttps://doi.org/10.32473/edis-in924-2012openalex-snapshot
Palm Aphid Cerataphis brasiliensis (Hempel) (Insecta: Hemiptera: Aphidae: Hormaphidinae)
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.2020.00471openalex-snapshot
Reprogramming of the Developmental Program of Rhus javanica During Initial Stage of Gall Induction by Schlechtendalia chinensis
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/insects10060163openalex-snapshot
Functional Morphology and Defensive Behavior in a Social Aphid
inferred← citeshttps://doi.org/10.3390/insects12050416openalex-snapshot
Coexistence of Three Dominant Bacterial Symbionts in a Social Aphid and Implications for Ecological Adaptation
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/10.3897/bdj.8.e58476openalex-snapshot
Brachymna tenuis Stål, 1861 (Hemiptera: Pentatomidae), a new invasive bamboo pest in Korea with notes on insects associated with bamboos
inferred← citeshttps://doi.org/10.3897/zookeys.833.30592openalex-snapshot
Molecular and morphological evidence for the identity of two nominal species of Astegopteryx (Hemiptera, Aphididae, Hormaphidinae)
inferred← citeshttps://doi.org/10.3897/zoologia.38.e60598openalex-snapshot
A new species of aphid of the genus Nipponaphis (Hemiptera: Aphididae: Hormaphidinae) from China, inducing galls on the trunk of a witch-hazel (Hamamelidaceae)
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.