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Studies on the south east Asian ant-plant associationCrematogaster borneensis/Macaranga: Adaptations of the ant partner

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/978-3-642-45501-8_25openalex-snapshot
Venoms and Venom Apparatuses of the Formicidae: Myrmeciinae, Ponerinae, Dorylinae, Pseudomyrmecinae, Myrmicinae, and Formicinae
inferredcites →https://doi.org/10.1007/978-94-009-7994-9openalex-snapshot
Ant-plant interactions in Australia
inferredcites →https://doi.org/10.1007/bf00366526openalex-snapshot
First European record of a queen ant carrying a mealybug during her mating flight
inferredcites →https://doi.org/10.1007/bf00378662openalex-snapshot
Studies of a South East Asian ant-plant association: protection of Macaranga trees by Crematogaster borneensis
inferredcites →https://doi.org/10.1007/bf00379331openalex-snapshot
Passive aggression: An alternative hypothesis for the Piper-Pheidole association
inferredcites →https://doi.org/10.1007/bf01242710openalex-snapshot
Two new myrmecophytic associations from the Malay Peninsula: Ants of the genusCladomyrma (Formicidae, Camponotinae) as partners ofSaraca thaipingensis (Caesalpiniaceae) andCrypteronia griffithii (Crypteroniaceae)
inferredcites →https://doi.org/10.1017/cbo9780511721878openalex-snapshot
The Evolutionary Ecology of Ant–Plant Mutualisms
inferredcites →https://doi.org/10.1038/086277b0openalex-snapshot
The Fauna of British India, including Ceylon and Burma
inferredcites →https://doi.org/10.1111/j.1365-2311.1970.tb00532.xopenalex-snapshot
Insect associations with the swollen thorn acacias
inferredcites →https://doi.org/10.1111/j.1558-5646.1966.tb03364.xopenalex-snapshot
COEVOLUTION OF MUTUALISM BETWEEN ANTS AND ACACIAS IN CENTRAL AMERICA
inferredcites →https://doi.org/10.2307/1934304openalex-snapshot
Protection of Barteria (Passifloraceae) By Pachysima Ants (Pseudomyrmecinae) in a Nigerian Rain Forest
inferredcites →https://doi.org/10.2307/1934677openalex-snapshot
Allelopathy by Myrmecophytes: The Ant Azteca as an Allelopathic Agent of Cecropia
inferredcites →https://doi.org/10.2307/1941029openalex-snapshot
Pruning of Host Plant Neighbors by Ants: An Experimental Approach
inferredcites →https://doi.org/10.2307/2387840openalex-snapshot
Interaction of the Ant-Plant Leonardoxa africana (Caesalpiniaceae) With Its Obligate Inhabitants in a Rainforest in Cameroon
inferredcites →https://doi.org/10.2307/2388703openalex-snapshot
Geographic Variation and Community Structure in an Ant-Plant Mutualism: Azteca and Cecropia in Costa Rica
inferredcites →https://doi.org/10.2307/2424991openalex-snapshot
Mutualism between Three Species of Tropical Piper (Piperaceae) and Their Ant Inhabitants
inferredcites →https://doi.org/10.2307/2989677openalex-snapshot
Dissolution of Mutualism between Cecropia and Its Azteca Ants
inferredcites →https://doi.org/10.3929/ethz-a-000099183openalex-snapshot
Untersuchungen über coccidophile Ameisen aus den Kaffeefeldern von Surinam
inferredcites →https://doi.org/10.5281/zenodo.13395809openalex-snapshot
A comparative morphological study of the proventriculus of ants (Hymenoptera: Formicidae)
inferredcites →https://doi.org/10.5281/zenodo.16033644openalex-snapshot
Interaction of the Bull's-Horn Acacia (Acacia cornigera L.) with an Ant Inhabitant {Pseudomyrmex ferruginea F. Smith) in Eastern Mexico
inferredcites →https://doi.org/10.5281/zenodo.16257641openalex-snapshot
Some nondiaspine Coccidae from the Malay peninsula, with descriptions of apparently new species

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.13102/sociobiology.v63i1.949zenodo-depositor-declared
Taxonomic Revision of the Obligate Plant-Ants of the Genus Crematogaster Lund (Hymenoptera, Formicidae, Myrmicinae), Associated with Macaranga Thouars (Euphorbiaceae) on Borneo and the Malay Peninsula
inferred← citeshttps://doi.org/10.1002/biuz.19910210508openalex-snapshot
Partnerschaften von Pflanzen und Ameisen. Ameisenbäume im malaysischen Regenwald
inferred← citeshttps://doi.org/10.1002/ece3.9760openalex-snapshot
An experimental, behavioral, and chemical analysis of food limitations in mutualistic Crematogaster ant symbionts inhabiting Macaranga host plants
inferred← citeshttps://doi.org/10.1006/bijl.2000.0477openalex-snapshot
Origin of caulinary ant domatia and timing of their onset in plant ontogeny: evolution of a key trait in horizontally transmitted ant-plant symbioses
inferred← citeshttps://doi.org/10.1007/978-3-642-12162-3_9openalex-snapshot
Communication in Ant–Plant Symbioses
inferred← citeshttps://doi.org/10.1007/978-4-431-67008-7_33openalex-snapshot
Ant-Plant Diversity in Peninsular Malaysia, with Special Reference to the Pasoh Forest Reserve
inferred← citeshttps://doi.org/10.1007/bf00318024openalex-snapshot
Pyrrolizidine alkaloid deters ant predators of Utetheisa ornatrix eggs: effects of alkaloid concentration, oxidation state, and prior exposure of ants to alkaloid-laden prey
inferred← citeshttps://doi.org/10.1007/bf00323148openalex-snapshot
Diversity of ant-plant interactions: protective efficacy in Macaranga species with different degrees of ant association
inferred← citeshttps://doi.org/10.1007/bf00940397openalex-snapshot
Domatia as most important adaptations in the evolution of myrmecophytes in the paleotropical tree genusMacaranga (Euphorbiaceae)
inferred← citeshttps://doi.org/10.1007/bf01242710openalex-snapshot
Two new myrmecophytic associations from the Malay Peninsula: Ants of the genusCladomyrma (Formicidae, Camponotinae) as partners ofSaraca thaipingensis (Caesalpiniaceae) andCrypteronia griffithii (Crypteroniaceae)
inferred← citeshttps://doi.org/10.1007/pl00001761openalex-snapshot
Incident daylight as orientation cue for hole-boring ants: prostomata in Macaranga ant-plants
inferred← citeshttps://doi.org/10.1007/s00040-005-0858-1openalex-snapshot
Ant-hemipteran trophobioses in a Bornean rainforest – diversity, specificity and monopolisation
inferred← citeshttps://doi.org/10.1007/s00040-014-0348-4openalex-snapshot
Colony founding by the ant Myrmelachista flavocotea
inferred← citeshttps://doi.org/10.1007/s00040-015-0450-2openalex-snapshot
Establishing an ant-plant mutualism: foundress queen mortality and acquiring the third partner
inferred← citeshttps://doi.org/10.1007/s000400050013openalex-snapshot
Colony foundation and acquisition of coccoid trophobionts by Aphomomyrmex afer (Formicinae): co-dispersal of queens and phoretic mealybugs in an ant-plant-homopteran mutualism?
inferred← citeshttps://doi.org/10.1007/s000400300002openalex-snapshot
Patterns of the Crematogaster-Macaranga association: The ant partner makes the difference
inferred← citeshttps://doi.org/10.1007/s00049-003-0257-xopenalex-snapshot
Main nutrient compounds in food bodies of Mexican Acacia ant-plants
inferred← citeshttps://doi.org/10.1007/s000490050005openalex-snapshot
Chemical composition of the slippery epicuticular wax blooms on Macaranga (Euphorbiaceae) ant-plants
inferred← citeshttps://doi.org/10.1007/s001140050589openalex-snapshot
Reduced Chitinase Activities in Ant Plants of the Genus Macaranga
inferred← citeshttps://doi.org/10.1007/s001140050751openalex-snapshot
Maintaining an ant-plant symbiosis: secondary polygyny in the Macaranga triloba-Crematogaster sp. association
inferred← citeshttps://doi.org/10.1007/s00265-007-0520-1openalex-snapshot
Strategies of a parasite of the ant–Acacia mutualism
inferred← citeshttps://doi.org/10.1007/s002650050538openalex-snapshot
Induced responses to herbivory in the Neotropical ant-plant association between Azteca ants and Cecropia trees: response of ants to potential inducing cues
inferred← citeshttps://doi.org/10.1007/s00442-002-0947-zopenalex-snapshot
Pruning of host plant neighbours as defence against enemy ant invasions: Crematogaster ant partners of Macaranga protected by "wax barriers" prune less than their congeners
inferred← citeshttps://doi.org/10.1007/s00442-002-1110-6openalex-snapshot
Catalpa bignonioides alters extrafloral nectar production after herbivory and attracts ant bodyguards
inferred← citeshttps://doi.org/10.1007/s00442-003-1455-5openalex-snapshot
Interspecific variation in the defensive responses of obligate plant-ants: experimental tests and consequences for herbivory
inferred← citeshttps://doi.org/10.1007/s00442-006-0460-xopenalex-snapshot
The reproductive phenology of an Amazonian ant species reflects the seasonal availability of its nest sites
inferred← citeshttps://doi.org/10.1007/s004420000532openalex-snapshot
On benefits of indirect defence: short- and long-term studies of antiherbivore protection via mutualistic ants
inferred← citeshttps://doi.org/10.1007/s004420000534openalex-snapshot
Nutrient availability and indirect (biotic) defence in a Malaysian ant-plant
inferred← citeshttps://doi.org/10.1007/s004420050303openalex-snapshot
Slippery ant-plants and skilful climbers: selection and protection of specific ant partners by epicuticular wax blooms in Macaranga (Euphorbiaceae)
inferred← citeshttps://doi.org/10.1007/s10144-001-8184-6openalex-snapshot
Non‐ant antiherbivore defenses before plant‐ant colonization in Macaranga myrmecophytes
inferred← citeshttps://doi.org/10.1007/s10144-009-0162-4openalex-snapshot
Phylogeography of the Coccus scale insects inhabiting myrmecophytic Macaranga plants in Southeast Asia
inferred← citeshttps://doi.org/10.1007/s10265-012-0500-zopenalex-snapshot
Change in biomass of symbiotic ants throughout the ontogeny of a myrmecophyte, Macaranga beccariana (Euphorbiaceae)
inferred← citeshttps://doi.org/10.1007/s102650200023openalex-snapshot
Carbon and nitrogen contents of food bodies in three myrmecophytic species of Macaranga: implications for antiherbivore defense mechanisms
inferred← citeshttps://doi.org/10.1007/s10886-007-9369-zopenalex-snapshot
Species-specific Leaf Volatile Compounds of Obligate Macaranga Myrmecophytes and Host-specific Aggressiveness of Symbiotic Crematogaster Ants
inferred← citeshttps://doi.org/10.1007/s10886-007-9404-0openalex-snapshot
The Defensive Role of Volatile Emission and Extrafloral Nectar Secretion for Lima Bean in Nature
inferred← citeshttps://doi.org/10.1007/s10980-013-9917-6openalex-snapshot
Habitat edge effects alter ant-guard protection against herbivory
inferred← citeshttps://doi.org/10.1007/s11258-010-9810-1openalex-snapshot
Correlation between the leaf turnover rate and anti-herbivore defence strategy (balance between ant and non-ant defences) amongst ten species of Macaranga (Euphorbiaceae)
inferred← citeshttps://doi.org/10.1007/s11284-014-1161-2openalex-snapshot
Temporary sterilization behavior of mutualistic partner ants in a Southeast Asian myrmecophyte
inferred← citeshttps://doi.org/10.1007/s11284-016-1374-7openalex-snapshot
Reduced ant defenses in Macaranga myrmecophytes (Euphorbiaceae) infested with a winged phasmid Orthomeria cuprinus
inferred← citeshttps://doi.org/10.1007/s13199-015-0367-6openalex-snapshot
Nematode associates and bacteria in ant-tree symbioses
inferred← citeshttps://doi.org/10.1016/j.anbehav.2006.07.022openalex-snapshot
Protection in an ant–plant mutualism: an adaptation or a sensory trap?
inferred← citeshttps://doi.org/10.1016/j.anbehav.2009.03.010openalex-snapshot
Predatory and trophobiont-tending ants respond differently to fig and fig wasp volatiles
inferred← citeshttps://doi.org/10.1016/j.bse.2005.08.005openalex-snapshot
Chemical composition of leaf volatiles in Macaranga species (Euphorbiaceae) and their potential role as olfactory cues in host-localization of foundress queens of specific ant partners
inferred← citeshttps://doi.org/10.1016/j.fitote.2012.04.020openalex-snapshot
Flavonoids with antiplasmodial and cytotoxic activities of Macaranga triloba
inferred← citeshttps://doi.org/10.1016/j.fitote.2015.04.002openalex-snapshot
Cytotoxic prenylated flavonoids from Macaranga indica
inferred← citeshttps://doi.org/10.1016/j.phytochem.2003.10.026openalex-snapshot
Potential cancer chemopreventive constituents of the leaves of Macaranga triloba
inferred← citeshttps://doi.org/10.1016/j.ympev.2024.108028openalex-snapshot
Exploring the evolutionary dynamics of myrmecophytism: Perspectives from the Southeast Asian Macaranga ant-plant symbiosis
inferred← citeshttps://doi.org/10.1016/s0764-4469(98)80462-9openalex-snapshot
Protection against herbivores of the myrmecophyte Leonardoxa africana (Baill.) Aubrèv. T3 by its principal ant inhabitant Aphomomyrmex afer Emery
inferred← citeshttps://doi.org/10.1016/s1146-609x(00)01091-2openalex-snapshot
Leaf volatile compounds and the distribution of ant patrollingin an ant-plant protection mutualism: Preliminary results onLeonardoxa (Fabaceae: Caesalpinioideae) andPetalomyrmex(Formicidae: Formicinae)
inferred← citeshttps://doi.org/10.1016/s1572-4379(97)80065-6openalex-snapshot
1.3.5 Relationships with ants
inferred← citeshttps://doi.org/10.1017/9781316671825.020openalex-snapshot
The Study of Interspecific Interactions in Habitats under Anthropogenic Disturbance: Importance and Applications
inferred← citeshttps://doi.org/10.1017/s0266467404001567openalex-snapshot
Spatiotemporal patterns in indirect defence of a South-East Asian ant-plant support the optimal defence hypothesis
inferred← citeshttps://doi.org/10.1017/s0266467404001749openalex-snapshot
Leaf damage induces ant recruitment in the Amazonian ant-plant Hirtella myrmecophila
inferred← citeshttps://doi.org/10.1017/s0266467498000327openalex-snapshot
The soft scale (Coccidae) associates of Malaysian ant-plants
inferred← citeshttps://doi.org/10.1017/s0266467499001194openalex-snapshot
Amazonian ant–plant interactions and the nesting space limitation hypothesis
inferred← citeshttps://doi.org/10.1023/a:1012234702403openalex-snapshot
Trade-Off Between Chemical and Biotic Antiherbivore Defense in the South East Asian Plant Genus Macaranga
inferred← citeshttps://doi.org/10.1023/a:1012290820150openalex-snapshot
Chemical Recognition of Partner Plant Species by Foundress Ant Queens in Macaranga–Crematogaster Myrmecophytism
inferred← citeshttps://doi.org/10.1046/j.1440-1703.2000.00318.xopenalex-snapshot
Variations in abiotic defense within myrmecophytic and non‐myrmecophytic species of Macaranga in a Bornean dipterocarp forest
inferred← citeshttps://doi.org/10.1046/j.1440-1703.2001.00442.xopenalex-snapshot
Cospeciation of ants and plants
inferred← citeshttps://doi.org/10.1080/01650521003647647openalex-snapshot
High diversity of ants foraging on extrafloral nectar of bromeliads in the Atlantic rainforest of southern Brazil
inferred← citeshttps://doi.org/10.1080/03946975.1998.10539354openalex-snapshot
Camponotus (Colobopsis)(Mayr 1861) andMacaranga(Thouars 1806): a specific two-partner ant-plant system from Malaysia
inferred← citeshttps://doi.org/10.1086/378682openalex-snapshot
Competition and Coexistence: Exploring Mechanisms That Restrict and Maintain Diversity within Mutualist Guilds
inferred← citeshttps://doi.org/10.1093/aesa/saw047openalex-snapshot
Discovery of a NewCrematogasterSpecies with 10-Segmented Antennae From the Indochina Region, With Description of the Species and Its Phylogenetic Position (Hymenoptera: Formicidae)
inferred← citeshttps://doi.org/10.1093/beheco/arv219openalex-snapshot
Spoils of war and peace: enemy adoption and queen-right colony fusion follow costly intraspecific conflict in acacia ants
inferred← citeshttps://doi.org/10.1093/jexbot/52.363.2057openalex-snapshot
Adaptations to biotic and abiotic stress: Macaranga‐ant plants optimize investment in biotic defence
inferred← citeshttps://doi.org/10.1101/008904openalex-snapshot
SPOILS OF WAR AND PEACE: ENEMY ADOPTION AND QUEEN-RIGHT COLONY FUSION FOLLOW COSTLY INTRASPECIFIC CONFLICT IN ACACIA ANTS
inferred← citeshttps://doi.org/10.1111/een.12665openalex-snapshot
Pseudomyrmex concolor Smith (Formicidae: Pseudomyrmecinae) as induced biotic defence for host plant Tachigali myrmecophila Ducke (Fabaceae: Caesalpinioideae)
inferred← citeshttps://doi.org/10.1111/ens.12093openalex-snapshot
Host‐plant use by two O rthomeria ( P hasmida: A schiphasmatini) species feeding on M acaranga myrmecophytes
inferred← citeshttps://doi.org/10.1111/j.0013-8703.2004.00188.xopenalex-snapshot
Induced biotic responses to herbivory and associated cues in the Amazonian ant‐plant Maieta poeppigii
inferred← citeshttps://doi.org/10.1111/j.0014-3820.2004.tb01678.xopenalex-snapshot
CODIVERSIFICATION IN AN ANT-PLANT MUTUALISM: STEM TEXTURE AND THE EVOLUTION OF HOST USE IN CREMATOGASTER (FORMICIDAE: MYRMICINAE) INHABITANTS OF MACARANGA (EUPHORBIACEAE)
inferred← citeshttps://doi.org/10.1111/j.1095-8312.1991.tb00621.xopenalex-snapshot
Extrafloral nectaries in the genus Macaranga (Euphorbiaceae) in Malaysia: comparative studies of their possible significance as predispositions for myrmecophytism
inferred← citeshttps://doi.org/10.1111/j.1095-8312.1999.tb01893.xopenalex-snapshot
Diversity, evolutionary specialization and geographic distribution of a mutualistic ant-plant complex: Macaranga and Crematogaster in South East Asia
inferred← citeshttps://doi.org/10.1111/j.1095-8312.2005.000423.xopenalex-snapshot
Macaranga ant-plants hide food from intruders: correlation of food presentation and presence of wax barriers analysed using phylogenetically independent contrasts
inferred← citeshttps://doi.org/10.1111/j.1095-8312.2008.00962.xopenalex-snapshot
Interspecific variation in the defensive responses of ant mutualists to plant volatiles
inferred← citeshttps://doi.org/10.1111/j.1095-8339.1992.tb00416.xopenalex-snapshot
Food bodies and their significance for obligate ant-association in the tree genus Macaranga (Euphorbiaceae)
inferred← citeshttps://doi.org/10.1111/j.1365-2435.2010.01818.xopenalex-snapshot
The multiple faces of indirect defences and their agents of natural selection
inferred← citeshttps://doi.org/10.1111/j.1365-2435.2011.01838.xopenalex-snapshot
Evolutionary ecology of plant defences against herbivores
inferred← citeshttps://doi.org/10.1111/j.1365-2745.2008.01390.xopenalex-snapshot
Volatiles of myrmecophytic Piper plants signal stem tissue damage to inhabiting Pheidole ant‐partners
inferred← citeshttps://doi.org/10.1111/j.1420-9101.2010.02200.xopenalex-snapshot
Ant aggression and evolutionary stability in plant-ant and plant-pollinator mutualistic interactions
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2007.02330.xopenalex-snapshot
Indirect defence via tritrophic interactions
inferred← citeshttps://doi.org/10.1111/j.1570-7458.2007.00594.xopenalex-snapshot
Damage to sagebrush attracts predators but this does not reduce herbivory
inferred← citeshttps://doi.org/10.1111/j.1744-7429.1998.tb00050.xopenalex-snapshot
The Contribution of Ant‐Plant Protection Studies to Our Understanding of Mutualism1
inferred← citeshttps://doi.org/10.1111/j.1744-7429.1998.tb00055.xopenalex-snapshot
Spatial and Temporal Variation in the Ant Occupants of a Facultative Ant‐Plant1
inferred← citeshttps://doi.org/10.1111/j.1744-7429.2000.tb00475.xopenalex-snapshot
Difference in Intensity of Ant Defense among Three Species of Macaranga Myrmecophytes in a Southeast Asian Dipterocarp Forest 1
inferred← citeshttps://doi.org/10.1111/j.1744-7429.2003.tb00288.xopenalex-snapshot
Contrasting Responses to Induction Cues by Ants Inhabiting Maieta guianensis (Melastomataceae)
inferred← citeshttps://doi.org/10.1146/annurev.ecolsys.34.011802.132410openalex-snapshot
Protective Ant-Plant Interactions as Model Systems in Ecological and Evolutionary Research
inferred← citeshttps://doi.org/10.1155/2014/396095openalex-snapshot
Inflorescences of the BromeliadVriesea friburgensisas Nest Sites and Food Resources for Ants and Other Arthropods in Brazil
inferred← citeshttps://doi.org/10.1186/s12915-022-01289-0openalex-snapshot
Nitrogen fixation by diverse diazotrophic communities can support population growth of arboreal ants
inferred← citeshttps://doi.org/10.13102/sociobiology.v59i2.607openalex-snapshot
How Do Scale Insects Settle into the Nests of Plant-Ants on Macaranga Myrmecophytes? Dispersal by Wind and Selection by Plant-Ants
inferred← citeshttps://doi.org/10.1371/journal.pone.0116602openalex-snapshot
Congruence of Microsatellite and Mitochondrial DNA Variation in Acrobat Ants (Crematogaster Subgenus Decacrema, Formicidae: Myrmicinae) Inhabiting Macaranga (Euphorbiaceae) Myrmecophytes
inferred← citeshttps://doi.org/10.1371/journal.pone.0192207openalex-snapshot
Transmission of fungal partners to incipient Cecropia-tree ant colonies
inferred← citeshttps://doi.org/10.1646/0006-3606(2000)032[0318:diioad]2.0.co;2openalex-snapshot
Difference in Intensity of Ant Defense among Three Species of Macaranga Myrmecophytes in a Southeast Asian Dipterocarp Forest1
inferred← citeshttps://doi.org/10.1646/03007openalex-snapshot
Contrasting Responses to Induction Cues by Ants Inhabiting Maieta guianensis (Melastomataceae)1
inferred← citeshttps://doi.org/10.18473/lepi.78i4.a3openalex-snapshot
Interspecific Difference in Response to Change in Ant-Defense Intensity during Tree Growth among Three Leaf-Chewing Lepidopteran Species on a Myrmecophyte Species, Macaranga bancana
inferred← citeshttps://doi.org/10.18473/lepi.v68i1.a5openalex-snapshot
Exploitation of Food Bodies onMacarangaMyrmecophytes by Larvae of a Lycaenid Species,Arhopala zylda(Lycaeninae)
inferred← citeshttps://doi.org/10.1890/0012-9658(1998)079[2100:ldaaci]2.0.co;2openalex-snapshot
LEAF DAMAGE AND ASSOCIATED CUES INDUCE AGGRESSIVE ANT RECRUITMENT IN A NEOTROPICAL ANT-PLANT
inferred← citeshttps://doi.org/10.18960/seitai.55.3_431openalex-snapshot
アリ-オオバギ共生系の多様性 : 生物群集への波及効果( 生物間相互作用と群集構造:生態化学量論、間接効果、そして進化)
inferred← citeshttps://doi.org/10.20848/kontyu.20.4_186openalex-snapshot
フィールドでの昆虫研究(5)オオバギ属アリ植物を利用する植食性昆虫の寄主利用-マレーシア・サラワクでの昆虫研究-
inferred← citeshttps://doi.org/10.2307/2960606openalex-snapshot
Food Body Production in Macaranga Triloba (Euphorbiaceae): A Plant Investment in Anti-Herbivore Defence via Symbiotic Ant Partners
inferred← citeshttps://doi.org/10.2307/3546834openalex-snapshot
Dynamic Anti-Herbivore Defense in Ant-Plants: The Role of Induced Responses
inferred← citeshttps://doi.org/10.2307/5880openalex-snapshot
Asymmetries, Compartments and Null Interactions in an Amazonian Ant-Plant Community
inferred← citeshttps://doi.org/10.3233/978-1-60750-972-1-205openalex-snapshot
Signaling and Communication in Plants
inferred← citeshttps://doi.org/10.3759/tropics.19.139openalex-snapshot
Effects of symbiotic coccid on the plant-ant colony growth in the myrmecophyte Macaranga bancana
inferred← citeshttps://doi.org/10.3759/tropics.7.93openalex-snapshot
The Diverse Occupant Fauna in Epiphytic Ant-plants, Hydnophytum moseleyanum (Rubiaceae) in New Guinea.
inferred← citeshttps://doi.org/10.3759/tropics.ms23-07openalex-snapshot
Decrease in the number of symbiotic ant workers on leaves of a myrmecophyte, Macaranga bancana, during its growth
inferred← citeshttps://doi.org/10.3897/jhr.46.5518openalex-snapshot
Protection against herbivory in the mutualism between Pseudomyrmex dendroicus (Formicidae) and Triplaris americana (Polygonaceae)
inferred← citeshttps://doi.org/10.51200/jtbc.v20i.4640openalex-snapshot
Obligate Ant-Associated Macaranga bancana is Better Protected from Herbivory Than Facultative Ant-Associated Macaranga tanarius
inferred← citeshttps://doi.org/10.6084/m9.figshare.20047229openalex-snapshot
Additional file 1 of Nitrogen fixation by diverse diazotrophic communities can support population growth of arboreal ants
inferred← citeshttps://doi.org/10.6084/m9.figshare.20047232openalex-snapshot
Additional file 2 of Nitrogen fixation by diverse diazotrophic communities can support population growth of arboreal ants
inferred← citeshttps://doi.org/10.6084/m9.figshare.20047235openalex-snapshot
Additional file 3 of Nitrogen fixation by diverse diazotrophic communities can support population growth of arboreal ants
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