Nesting Biology and Offspring Development of the Cavity-Nesting Solitary Wasp Isodontia elegans (F. Smith) from Trap-Nests in Oregon

2021 ◽  
Vol 81 (4) ◽  
Author(s):  
Ronald C. Spendal ◽  
Kevin M. O'Neill ◽  
Casey M. Delphia
2014 ◽  
Vol 74 (2) ◽  
pp. 493-500
Author(s):  
MLT. Buschini ◽  
CE. Buss

Podium angustifrons Kohl 1902 is a species of solitary wasp which nests in pre-existing cavities, with neotropical distribution in Argentina, Bolivia, Brazil, Colombia, Guyana and French Guyana. The aim of this study was to investigate the nesting biology of P. angustifrons, discussing aspects of their life history. To capture its nests, wooden trap-nests were installed in the Parque Municipal das Araucárias, Guarapuava (PR), Brazil, from January 2003 to April 2009. A total of 29 nests were collected, all during the warmer months. These showed no vestibular and intercalary cells, and their closures were made up of chewed plants and mud mixed with organic materials and resin-coated surfaces, sometimes showing a layer of lichens. The cells were provisioned with various wild species of cockroaches (Chorisoneura sp, Riata sp and Helgaia sp) in the nymph stage and/or adults. The sex ratio was 4.6 females per male, significantly higher that the expected 1:1. Most pre-pupae entered diapause in winter with development time ranging from 187 to 283 days for females and 180 to 283 days for males. Deaths occurred in 41.66% of cells provisioned, 33.33% were attributed to faulty development and 8.33% to Chrysididae.


1961 ◽  
Vol 93 (7) ◽  
pp. 571-573 ◽  
Author(s):  
J. T. Medler

The nesting biology of Hoplitis producta has been reported by several authors, as the species is a common and widely distributed bee in North America east of the Rocky Mountains. Additional records, which have been obtained in connection with trap-nest research on bees and wasps in Wisconsin, are provided to supplement the previous reports.The nests were found in the pith at the butt ends of sumac stick trap-nests. A nest could be recognized readily because the 3 mm. plug that closed the burrow had a more solid texture and a darker color than the surrounding pith at the end of the stick. Rau (1928) found nests in tunnels of elder, sumac or rose stems but could not ascertain whether the bee excavated its own burrows or utilized burrows left by other twig-dwellers. Fischer (1955) stated that the female almost invariably excavated its own burrow. In Wisconsin, freshly cut sumac sticks were placed in the field in the spring; therefore, each of the following records represents a nest in a burrow excavated by the foundress bee.


2019 ◽  
Author(s):  
J Scott MacIvor

AbstractEvaluating resource use and overlap through time and space among and within species having similar habitat requirements informs community-level conservation and coexistence, efforts to monitor species at-risk and biological invasions. Many species share common nesting requirements; one example are cavity-nest bees and wasps, which provision nests in dark and dry holes in wood, plant stems, or other plant-based materials that can be bundled together into ‘trap nests’. In this study, the adult emergence order of 47 species of solitary cavity-nesting bees and wasps, and their parasites (total N>8000 brood cells) were obtained from two hundred identical trap nests set up each year (over three years) to survey these populations across Toronto, Canada and the surrounding region. All brood cells collected were reared in a growth chamber under constant warming temperature and humidity to determine species identity, and adult emergence order. This order ranged from 0 to 38 days, with all mason bees (Osmia spp.) emerging within the first two days, and the invasive resin bee species, Megachile sculpturalis Smith significantly later than all others. Late emerging species i) exhibited significantly greater intraspecific variation in mean emergence day and ii) were significantly larger in body size, compared to early emerging species. Detailing natural history information at the species- and community-level, such as the adult emergence order of coexisting cavity-nesting bees and wasps and their parasites, can inform the timing of deployment of trap nests to support and monitor target species, and refine experimental design to study these easily-surveyed and essential insect communities.


2021 ◽  
Vol 84 ◽  
pp. 75-86
Author(s):  
Alexander V. Fateryga ◽  
Valentina V. Fateryga

Two females of Leptochilus regulus (de Saussure, 1855) were observed nesting in reed stalks of a Fabre’s hive serving as a block of trap nests in Crimea, with the timekeeping of all their nesting behaviours. The building material used by the females to separate the nesting cavity into the cells consisted of pellets of dry soil, gravel particles, and small fragments of tree bark, leaves, and thin stems. Females rapidly carried these items collected in 1.0–1.5 m from the nests. They bonded only the last portions of the building material in each “partition” with a very small amount of mud. An additional amount of unbonded building material items was deposited into the nest after sealing the last nest cell. Females hunted exclusively for small larvae of an anobiid beetle (Coleoptera, Anobiidae); they stored 19–37 prey items per cell. Hunting and provisioning occupied the largest portion of the females’ time budget. Duration of hunting flights was different between the females. The nests of both females contained three brood cells. Cocoons of Chrysis ragusae De Stefani, 1888 (Hymenoptera, Chrysididae) were found in the nests; females of this cuckoo wasp species were also recorded entering the host nests at the stage of provisioning, acting apparently as inquilines. The cocoon ultrastructure of L. regulus is illustrated and discussed.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Michael Mikát ◽  
Eva Matoušková ◽  
Jakub Straka

AbstractBiparental care is very rare in insects, and it was well-documented in only one bee species to this date – Ceratina nigrolabiata. However, biparental care was only recently discovered in this species, and detailed description of natural history of this species is missing. Here, we describe the nesting cycle of C. nigrolabiata. Pairs of C. nigrolabiata are established before female starts offspring provisioning. After provisioning is finished (when youngest offspring reached larval stage), the male abandons the nest. Males which are present in nests where female already finished provisioning brood cells, are probably mainly temporary visitors. The female can perform long-time offspring guarding, but only 22% of completely provisioned nests are guarded by a female. Most nests (54%) are closed and abandoned, when provisioning is completed, and other (24%) are orphaned before provisioning is finished. Guarded nests have statistically higher number of brood cells provisioned than unguarded nests. Generally, C. nigrolabiata is unique among bees due to its biparental behavior, but it has also uncommon traits of nesting biology among Ceratina bees, e.g. fast offspring development in comparison with provisioning rate, and high proportion of nests which are closed and abandoned by mother.


2006 ◽  
Vol 66 (3) ◽  
pp. 919-929 ◽  
Author(s):  
M. L. T. Buschini ◽  
F. Niesing ◽  
L. L. Wolff

This study was carried in the Parque Municipal das Araucárias in the municipality of Guarapuava, state of Paraná, Southern Brazil. Three hundred and sixty five nests of T. lactitarse were obtained using trap-nests of 0.7, 1.0, and 1.3 cm in diameter. All of them had similar architecture, regardless of the diameter of the trap-nest. Completed nests consisted of a linear series of brood cells whose average number per nest was of 3.3, 4.0 and 3.6 for the nests with 0.7 cm, 1.0 cm and 1.3 cm in diameter, respectively. They were constructed more often during the summer. T. lactitarse had two types of life cycles: direct development (without diapause), and delayed development (with diapause during winter). Natural enemies included Chrysididae, Sarcophagidae, Dolichopodidae and Ichneumonidae. Out of 1,353 identified spider prey, 1,313 belonged to the Araneidae family.


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