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Host-parasite relationships in six species ofSphecodes bees and their halictid hosts: Nest intrusion, intranidal behavior, and Dufour's gland volatiles (Hymenoptera: Halictidae)

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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/bf00408464openalex-snapshot
Zum problem des tierischen Parasitismus. I. Teil: Die lebensweise der Schmarotzerbiene Sphecodes monilicornis K. (= Subquadratus SM.) (Hym. Apid.)
inferredcites →https://doi.org/10.1007/bf00606997openalex-snapshot
Social, stimulatory and motivational factors involved in intraspecific nest defense of a primitively eusocial halictine bee
inferredcites →https://doi.org/10.1007/bf00988024openalex-snapshot
Odor correspondence betweenMelitta females and males of their nest parasiteNomada flavopicta K. (Hymenoptera: Apoidea)
inferredcites →https://doi.org/10.1007/bf00995755openalex-snapshot
Macrocyclic lactones and isopentenyl esters in the Dufour's gland secretion of halictine bees (Hymenoptera: Halictidae)
inferredcites →https://doi.org/10.1007/bf01045603openalex-snapshot
Species, individual and kin specific blends in Dufour's gland secretions of halictine bees
inferredcites →https://doi.org/10.1007/bf01338828openalex-snapshot
Production and reproductive function of intercastes inMyrmecina gvaminicola nipponica colonies (Hymenoptera: Formicidae)
inferredcites →https://doi.org/10.1007/bf01338831openalex-snapshot
Ontogenetic patterns of volatiles identified in Dufour's gland extracts from queens and workers of the primitively eusocial halictine bee,Lasioglossum malachmum (Hymenoptera: Halictidae)
inferredcites →https://doi.org/10.1007/bf02222752openalex-snapshot
Usurpation de nids étrangers et parasitisme facultatif chezHalictus scabiosæ (Rossi) (Insecte hyménoptère)
inferredcites →https://doi.org/10.1016/0020-1790(82)90004-xopenalex-snapshot
Systematic relationship of halictinae bees based on the pattern of macrocyclic lactones in the Dufour gland secretion
inferredcites →https://doi.org/10.1016/0169-5347(89)90202-4openalex-snapshot
Cuckoos and parasitic ants: Interspecific brood parasitism as an evolutionary arms race
inferredcites →https://doi.org/10.1016/0305-1978(90)90092-topenalex-snapshot
Kinship in communally nesting Andrena (hymenoptera; andrenidae) bees is indicated by composition of dufour's gland secretions
inferredcites →https://doi.org/10.1016/0305-1978(92)90048-iopenalex-snapshot
Species specificity of Dufour's gland morphology and volatile secretions in kleptoparasitic Sphecodes bees (Hymenoptera: Halictidae)
inferredcites →https://doi.org/10.1016/s0040-4039(01)82988-9openalex-snapshot
Macrocyclic lactones as the defense substances of the termite genus
inferredcites →https://doi.org/10.1093/aesa/81.4.626openalex-snapshot
Comparative Notes on the Biology and Development of Epeolus compactus Cresson, a Cleptoparasite of Colletes kincaidii Cockerell (Hymenoptera: Anthophoridae, Colletidae)
inferredcites →https://doi.org/10.1093/aesa/82.5.616openalex-snapshot
Biology, Immature Development, and Adaptive Behavior of Stelis montana, a Cleptoparasite of Osmia (Hymenoptera: Megachilidae)
inferredcites →https://doi.org/10.1111/j.1365-3032.1984.tb00696.xopenalex-snapshot
Role of labial glands in nesting behaviour of Chalicodoma sicula (Hymenoptera; Megachilidae)
inferredcites →https://doi.org/10.1111/j.1469-185x.1987.tb01640.xopenalex-snapshot
THE ROLES OF SEASONALITY, HOST SYNCHRONY, AND BEHAVIOUR IN THE EVOLUTIONS AND DISTRIBUTIONS OF NEST PARASITES IN HYMENOPTERA (INSECTA). WITH SPECIAL REFERENCE TO BEES (APOIDEA)
inferredcites →https://doi.org/10.1111/j.1469-185x.1992.tb01659.xopenalex-snapshot
INTRASPECIFIC PARASITISM AS AN ALTERNATIVE REPRODUCTIVE TACTIC IN NEST‐BUILDING WASPS AND BEES
inferredcites →https://doi.org/10.1126/science.196.4294.1117openalex-snapshot
Cleptoparasitism and Odor Mimetism in Bees: Do Nomada Males Imitate the Odor of Andrena Females?
inferredcites →https://doi.org/10.1127/entom.gen/18/1993/19openalex-snapshot
Anzahl und Größe der Oozyten im Verhältnis zur Körpergröße und Tageszeit in der Kuckucksbiene Nomada lathburiana (Hymenoptera: Anthophoridae)
inferredcites →https://doi.org/10.1139/z84-238openalex-snapshot
Evolution and host specificity: a study of the invasion success of a specialized bumblebee social parasite
inferredcites →https://doi.org/10.1146/annurev.es.20.110189.001033openalex-snapshot
Behavioral Environments and Evolutionary Change
inferredcites →https://doi.org/10.5281/zenodo.16124564openalex-snapshot
Parasitism of sweat bees in the genus Agapostemon by cuckoo bees in the genus Nomada (Hymenoptera: Halictidae, Anthophoridae)
inferredcites →https://doi.org/10.5281/zenodo.16179271openalex-snapshot
Ovaries, ovarioles, and oocytes in parasitic bees (Hymenoptera: Apoidea)
inferredcites →https://doi.org/10.5281/zenodo.16200549openalex-snapshot
Stones Cement And Guards In Halictine Nest Architecture And Defense
inferredcites →https://doi.org/10.5281/zenodo.16385709openalex-snapshot
The Biology of a Subtropical Population of Halictus ligatus IV: A Cuckoo-Like Caste
inferredcites →https://doi.org/10.5962/bhl.part.24961openalex-snapshot
The parasitic groups of Halictidae (Hymenoptera, Apoidea)

What points at this work

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

inferred← citeshttps://doi.org/10.3897/contrib.entomol.76.e184930zenodo-depositor-declared
A cuckoo slumber party? Rediscovery of Nomada (Pachynomada) asteris Swenk, 1913 (Hymenoptera: Apidae), with notes on unusual male aggregatory behavior
inferred← citeshttps://doi.org/10.1007/bf02040095openalex-snapshot
Sex recognition inDiglyphus isaea walker (Hymenoptera: Eulophidae): Role of an uncommon family of behaviorally active compounds
inferred← citeshttps://doi.org/10.1007/pl00001815openalex-snapshot
Sneak in or repel your enemy: Dufour's gland repellent as a strategy for successful usurpation in the slave-maker Polyergus rufescens
inferred← citeshttps://doi.org/10.1007/s00040-011-0189-3openalex-snapshot
Availability and depletion of fat reserves in halictid foundress queens with a focus on solitary nest founding
inferred← citeshttps://doi.org/10.1007/s00040-024-01000-2openalex-snapshot
Nest protection and foraging behaviour in solitary and social nests of the socially polymorphic orchid bee Euglossa viridissima
inferred← citeshttps://doi.org/10.1007/s00049-009-0009-7openalex-snapshot
Chemical ecology involved in invasion success of the cuckoo bumblebee Psithyrus vestalis and in survival of workers of its host Bombus terrestris
inferred← citeshttps://doi.org/10.1007/s00049-010-0044-4openalex-snapshot
The role of trail pheromones in host nest recognition of the social parasitic bumblebees Bombus bohemicus and Bombus rupestris (Hymenoptera: Apidae)
inferred← citeshttps://doi.org/10.1007/s00265-006-0182-4openalex-snapshot
Generalist cuckoo bees (Hymenoptera: Apoidea: Sphecodes) are species-specialist at the individual level
inferred← citeshttps://doi.org/10.1007/s002650050543openalex-snapshot
Mating expenditures reduced via female sex pheromone modulation in the primitively eusocial halictine bee, Lasioglossum ( Evylaeus ) malachurum (Hymenoptera: Halictidae)
inferred← citeshttps://doi.org/10.1007/s13592-019-00679-8openalex-snapshot
Methods for rearing ground-nesting bees under laboratory conditions
inferred← citeshttps://doi.org/10.1007/s13592-019-00692-xopenalex-snapshot
Do Sphecodes cuckoo bees use chemical insignificance to invade the nests of their social Lasioglossum bee hosts?
inferred← citeshttps://doi.org/10.1007/s13592-024-01121-4openalex-snapshot
Host-parasite interactions between Xenoglossa pruinosa (Apidae: Eucerini) and Triepeolus remigatus (Apidae: Epeolini) are characterized by tolerance and avoidance
inferred← citeshttps://doi.org/10.1016/j.anbehav.2010.05.010openalex-snapshot
Specialist Bombus vestalis and generalist Bombus bohemicus use different odour cues to find their host Bombus terrestris
inferred← citeshttps://doi.org/10.1016/j.thbio.2004.09.001openalex-snapshot
Semetic rings: towards the new concept of mimetic resemblances
inferred← citeshttps://doi.org/10.1039/b712681fopenalex-snapshot
Chemical communication by behaviour-guiding olfactory signals
inferred← citeshttps://doi.org/10.1051/apido:2002035openalex-snapshot
Honeybees Dufour's gland - idiosyncrasy of a new queen signal
inferred← citeshttps://doi.org/10.1051/apido:2008002openalex-snapshot
Phylogeny of Halictidae with an emphasis on endemic African Halictinae
inferred← citeshttps://doi.org/10.1080/00379271.2013.815036openalex-snapshot
Endémisme insulaire et cleptoparasitisme chez lesLasioglossumCurtis 1833 (Hymenoptera : Apoidea : Halictidae) de Nouvelle-Calédonie
inferred← citeshttps://doi.org/10.1111/1748-5967.12723openalex-snapshot
Insight on kleptoparasitic bee, Melecta chinensis (hymenoptera: Apidae), in the Republic of Korea: Morphology, biology and molecular characteristics
inferred← citeshttps://doi.org/10.1111/een.12986openalex-snapshot
Nesting habitat of ground‐nesting bees: a review
inferred← citeshttps://doi.org/10.1111/icad.70004openalex-snapshot
A trait‐based framework to understand and predict the response of wild bee functional groups to anthropogenic landscapes
inferred← citeshttps://doi.org/10.1111/j.1096-0031.2011.00373.xopenalex-snapshot
Dual origins of social parasitism in North American Dialictus (Hymenoptera: Halictidae) confirmed using a phylogenetic approach
inferred← citeshttps://doi.org/10.1111/j.1365-3032.2010.00764.xopenalex-snapshot
How can cleptoparasitic drosophilid flies emerge from the closed brood cells of the red Mason bee?
inferred← citeshttps://doi.org/10.1111/j.1479-8298.2009.00311.xopenalex-snapshot
Segregation of temporal and spatial distribution between kleptoparasites and parasitoids of the eusocial sweat bee, Lasioglossum malachurum (Hymenoptera: Halictidae, Mutillidae)
inferred← citeshttps://doi.org/10.1139/z10-040openalex-snapshot
Cheaters and liars: chemical mimicry at its finestThe present review is one in the special series of reviews on animal-plant interactions.In memory of Jan Tengö (1939–2010), who made exceptional contributions to our understanding of the chemical ecology of solitary bees, including chemical mimicry.
inferred← citeshttps://doi.org/10.1146/annurev.ento.49.061802.123155openalex-snapshot
D EFENSIVE B EHAVIOR OF H ONEY B EES : Organization, Genetics, and Comparisons with Other Bees
inferred← citeshttps://doi.org/10.1186/1471-2148-6-45openalex-snapshot
The evolution of activity breaks in the nest cycle of annual eusocial bees: a model of delayed exponential growth
inferred← citeshttps://doi.org/10.1186/1742-9994-5-2openalex-snapshot
A cuckoo in wolves' clothing? Chemical mimicry in a specialized cuckoo wasp of the European beewolf (Hymenoptera, Chrysididae and Crabronidae)
inferred← citeshttps://doi.org/10.1206/0003-0082(2003)413<0001:eonamo>2.0.co;2openalex-snapshot
Eggs, Ovariole Numbers, and Modes of Parasitism of Cleptoparasitic Bees, with Emphasis on Neotropical Species (Hymenoptera: Apoidea)
inferred← citeshttps://doi.org/10.1371/journal.pone.0064537openalex-snapshot
Flexible Host Choice and Common Host Switches in the Evolution of Generalist and Specialist Cuckoo Bees (Anthophila: Sphecodes)
inferred← citeshttps://doi.org/10.3897/zookeys.127.1670openalex-snapshot
Callosphecodes, a little-known bee (Hymenoptera, Halictidae, Sphecodes)
inferred← citeshttps://doi.org/10.3906/zoo-1501-43openalex-snapshot
A contribution to the kleptoparasitic bees of Turkey: Part I.,the genus Sphecodes Latreille (Hymenoptera: Halictidae)
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