scholarly journals Suitability of Five Horticulturally Important Armored Scale Insects as Hosts for an Exotic Predaceous Lady Beetle1

1993 ◽  
Vol 11 (1) ◽  
pp. 28-30 ◽  
Author(s):  
Brenda C. Bull ◽  
Michael J. Raupp ◽  
Mark R. Hardin ◽  
Clifford S. Sadof

Abstract Chilocorus kuwanae (Sylvestri) was imported from Korea to the United States for release against the euonymus scale (Unaspis euonymi (Comstock)). Field observations suggest that C. kuwanae feeds on a number of other armored scale insects, including white peach scale (Pseudaulacaspis pentagona (Targionni-Tozzeti)) and obscure scale (Melanaspis obscura (Comstock)). However, such observations have not been rigorously examined under controlled conditions. Our laboratory investigations indicate that C. kuwanae survives and reproduces well on San Jose scale (Quadraspidiotus perniciosus (Comstock)), in addition to euonymus scale. Fecundity was reduced in adults fed white peach scale. Few larvae survived to adulthood when fed oleander scale (Aspidiotus nerii (Bouche)). Adults failed to reproduce on obscure scale; none of the larvae fed this host survived to the pupal stage.

Author(s):  
C. Booth

Abstract A description is provided for Nectria flammea. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOSTS: The fungus occurs on a variety of scale insects, Aspidiotus nerii, Hemiberlesia rapax (53, 1-694), Pseudaulacaspis pentagona (55, 2093) etc. on a wide range of hosts, Acacia, Brachyglottis, Camellia, Citrus, Coffea, Morus, Ribes, Salix, Thea, Weinmannia, etc. GEOGRAPHICAL DISTRIBUTION: Australia, Belize, Fiji, India, Japan, New Zealand, Papua and New Guinea, Tanzania, Tonga, Uganda, South Africa, Sarawak, Zambia. TRANSMISSION: Airborne by ascospores or by moisture droplets as conidia.


ZooKeys ◽  
2019 ◽  
Vol 867 ◽  
pp. 87-96 ◽  
Author(s):  
Scott A. Schneider ◽  
Michael A. Fizdale ◽  
Benjamin B. Normark

Aspidiotini is a species-rich tribe of armored scale insects that includes several polyphagous and specialist pests that are commonly encountered at ports-of-entry to the United States and many other countries. This article describes a newly available online interactive tool that can be used to identify 155 species of Aspidiotini that are recognized as minor to major pests or that are potentially emergent pests. This article lists the species and features included with a description of the development and structure of the key. The interactive key is free to access at https://idtools.org/id/scales/aspidiotini/about_index.php.


2017 ◽  
Vol 27 (5) ◽  
pp. 618-624 ◽  
Author(s):  
Carlos R. Quesada ◽  
Clifford S. Sadof

Insecticidal soap and horticultural oil have the potential to kill individuals within populations of soft-bodied insect pests by suffocation. However, scientific literature is inconsistent about the efficacy of insecticidal soaps and petroleum-based oils against armored scale (Hemiptera: Diaspidae) and soft scale (Hemiptera: Coccidae). We examined the efficacy of horticultural oil and insecticidal soap against armored and soft scales at different developmental life stages. Studies were conducted in the laboratory and field with two species of armored scale [pine needle scale (Chionaspis pinifoliae) and oleander scale (Aspidiotus nerii)] and two species of soft scale [calico scale (Eulecanium cerasorium) and striped pine scale (Toumeylla pini)]. All insecticide applications were made at a rate of 2 gal per 100 gal water. Our laboratory results suggested that horticultural oil and insecticidal soap killed both calico scale (73% and 93%, respectively) and oleander scale (67% and 78%, respectively) when insecticides targeted 1-day-old scales. Scale insects built up tolerance to both materials over time after they settled. However, our field data indicated that horticultural oil had high control of settled armored scale [oleander scale (90%) and pine needle scale (83%)], but failed to control settled soft scale [stripe pine scale (5%)]. Insecticidal soap reduced armored scale [oleander scale (54%)]. Neither horticultural oil nor insecticidal soap significantly reduced populations of adult armored or soft scales compared with a control. Overall, horticultural oil killed a greater percentage of armored scales than soft scales, whereas insecticidal soap gave greater control against soft scales. We suggest that differences were driven by chemical properties of both insect integuments and insecticides. The waxy cover of an armored scale might reduce penetration of polar insecticidal soap whereas polar integument of a soft scale might impede infiltration of the lipophilic horticultural oil. Consequently, timing application to crawler stage is important for effective management of armored or soft scale with horticultural oils and insecticidal soaps.


2019 ◽  
Vol 25 (1/2) ◽  
pp. 85-93
Author(s):  
Gabriela Chesim De Souza ◽  
Luiza Rodrigues Redaelli ◽  
Vera Regina dos Santos Wolff

Olive culture is a recent activity in Rio Grande do Sul, Brazil with little information on its scale insects. Abundance and seasonality of armored scale insects (Hemiptera, Diaspididae) and their parasitism was evaluated in olive orchard, Olea europaea L., cultivar Arbequina, in Caçapava do Sul (30°30′43″ S, 53°29′27″ W), RS, Brazil. Samples were monthly collected from April 2012 to March 2013. At each occasion 20 trees were drawn and, from each quadrant of their canopies (northern, southern, eastern and western) two branches (20 - 30 cm - length and contained at least 20 leaves) were randomly removed, respectively from the inner part and the outer part of the canopy. We found five species of Diaspididae, Aonidiella aurantii (Maskell), Hemiberlesia cyanophylli (Signoret), Acutaspis paulista (Hempel), Aspidiotus nerii Bouché and Melanaspis obscura (Comstock). It was not found an unique pattern of abundance, indicating that these species respond differently to temperature variations between seasons. The armored scale insects were evenly distributed among quadrants. Only H. cyanophylli showed differences in abundance between the inner and outer branches. We registered parasitism in all Diaspididae species; the total parasitism rate was 9.78%.


1968 ◽  
Vol 61 (4) ◽  
pp. 1086-1088 ◽  
Author(s):  
H. L. Maltby ◽  
Eteazar Jimenez-Jimenez ◽  
Paul DeBach

PeerJ ◽  
2017 ◽  
Vol 5 ◽  
pp. e3599 ◽  
Author(s):  
Christian Peeters ◽  
Imre Foldi ◽  
Danièle Matile-Ferrero ◽  
Brian L. Fisher

Mutualisms between ants and sap-sucking insects generally involve clear benefits for both partners: the ants provide protection in exchange for honeydew. However, a single ant genus associates with armoured scale insects (Diaspididae) that do not excrete honeydew. We studied three colonies ofMelissotarsus emeryiants from two localities in Mozambique. Vast numbers of the diaspididMorganella conspicuaoccupied galleries dug by the ants under the bark of living trees. Unlike free-livingM. conspicuaand other diaspidids,M. conspicualiving with ants are known to lack shields, likely because they gain protection against enemies and desiccation. Nevertheless, we documented the occurrence of rare individuals with shields inside ant galleries, indicating that their glands continue to secrete wax and proteins as building material. This is likely to constitute a significant portion of the ants’ diet, in addition to diaspidid exuviae and excretions from the Malpighian tubules. Indeed,Melissotarsusworkers cannot walk outside the galleries due to modified middle legs, forcing them to obtain all nourishment within the tree.Melissotarsusfounding queens, however, must locate a suitable host tree while flying, and acquire diaspidid crawlers. This mutualism involves ants that are highly specialised to chew through living wood, and diaspidids that can also live freely outside the bark. It is extremely widespread in Africa and Madagascar, recorded from 20 tree families, and harmful effects on plant hosts require rapid study.


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