No abstract

Possible reasons reported in D. melanogaster studies where resistance did not occur after insecticide selection included avoidance and associated microbial complexes. The low level of malathion resistance observed in the selected SWD populations and a field-collected population is useful information in the development of insecticide resistance management programmes. © 2016 Her Majesty the Queen in Right of Canada Pest Management Science © 2016 Society of Chemical Industry.

The effects of pollination treatments on fruit set and five berry characteristics [mass, diameter, number of apparently viable seeds (well-developed, plump with dark seed coat), total seed number (includes apparently viable and partially developed seeds), and harvest date] were examined on three highbush blueberry cultivars. Pollination treatments included unpollinated, open pollinated, emasculated, and three hand pollinations that used pollen from the same flower, from the same cultivar, or from a different cultivar. Berries matured earliest and were smallest with the most apparently viable seeds in `Northland', `Patriot' had the greatest fruit set and smallest seed number, and `Bluecrop' matured the latest. Fruit set was greater, berry size larger, seed number smaller, and maturation later in 1990 than 1991. For all three cultivars, berries were generally smallest, latest maturing, and had the fewest seeds when pollination was prevented and were largest with the most seeds and earliest maturing in open visitation. Emasculation resulted in berries similar to those from unpollinated flowers. For berry characteristics, cross-pollination was of benefit for `Patriot' and possibly `Northland' but not `Bluecrop'. Thus, commercial highbush blueberry planting designs must be based on the pollination requirements of the particular cultivar. `Northland' berries almost always had seeds, while `Patriot' showed high levels and `Bluecrop' low levels of parthenocarpy.

No abstract

No abstract

Can. Ent. 116: 965-974 (1984) Native bee pollinators were collected and observed on cultivated blueberry, raspberry, and cranberry and on natural non-cultivated plants such as blackberry, buttercup, fireweed, thistle, and hairy cat's ear. Higher abundance and diversity of native bees were found on natural vegetation than on berry crops. Native bee populations on berry crops increased from 1981 to 1982, although diversity was similar. Native bees were not abundant enough to ensure adequate pollination of berry crops, and therefore, the use of managed honey bees is advisable. Pesticide impact, competition with managed honey bees, and habitat destruction have probably decreased native bee populations in agricultural areas of the Fraser Valley.The use of a standard measure of native pollinator abundance, bees observed/min/ m2, is recommended for future studies of this kind. ResumeLes abeilles pollinisatrices sauvages ont Ct C prelevCes et observCes sur des cultures de bleuets, de framboisiers et de canneberges, ainsi que sur des plantes non cultivCes dont le d r i e r , le bouton d'or, I'Cpilobe, le chardon et I'oreille de chat. La densit6 et la diversit6 des abeilles sauvages ttaient plus ClevCes sur la vCgCtation naturelle que sur les cultures de petits fruits. Les populations d'abeilles sauvages sur les petits fruits ont augment6 de 1981 a 1982, quoique la diversit6 Ctait similaire. Les abeilles sauvages n'Ctaient pas assez abondantes pour assurer une pollinisation adCquate des cultures de petits fruits de sorte que l'utilisation d'abeilles domestiques est ? i conseiller. Les effets des pesticides, de la concurrence par les abeilles domestiques et de la destruction des habitats ont probablement rCduit les populations naturelles d'abeilles dans les rCgions agricoles de la VallCe du Fraser.L'utilisation d'une mesure standard de I'abondance des pollinisateurs naturels, exprimee en abeilles/min./m2, est recommandCe pour les futures Ctudes de ce genre.

Honey bees, Apis mellifera (L.) (Hymenoptera: Apidae), are parasitized by the microsporidians Nosema apis (Zander) and Nosema ceranae (Fries). Molecular techniques are commonly used to differentiate between these parasites because light microscopy is inadequate. Our objectives were to (i) adapt the previously published duplex polymerase chain reaction (PCR) targeting the 16S rRNA gene of N. apis (321APIS-FOR, 321APIS-REV) and N. ceranae (218MITOC-FOR, 218MITOC-REV) using qualitative real-time PCR assay with SYBR® Green I dye (R-T PCR) and DNA melting-curve analysis, and (ii) determine whether the two Nosema species can be detected simultaneously in honey bees. Total spore counts and purified total genomic DNA were obtained from 37 bee samples (19 individual workers and 18 pooled samples of 15 workers) collected in Nova Scotia, Prince Edward Island, and Newfoundland, Canada. Overall, the prevalence of Nosema species was 86.5% (32/37 samples of bee DNA), based on conventional PCR and the optimized R-T PCR assay. The melting-curve analysis showed three groups of curve profiles that could determine the prevalence of N. apis, N. ceranae, and co-infection (21.9%, 56.2%, and 21.9%, respectively). The duplex R-T PCR assay was efficient, specific, and more sensitive than duplex conventional PCR because co-infection was identified in 5.4% (n = 2) more samples. Sequencing of R-T PCR products confirmed the results of the melting-curve analysis. Duplex R-T PCR with melting-curve analysis is a sensitive and rapid method of detecting N. apis, N. ceranae, and co-infection in honey bees.

No abstract