The Sugarcane Scale Insect Aulacaspis tegalensis (Zhnt.) and its Biological Control in Mauritius and East Africa

1973 ◽  
Vol 19 (3) ◽  
pp. 353-367 ◽  
Author(s):  
J. R. Williams ◽  
D. J. Greathead
Insects ◽  
2019 ◽  
Vol 10 (7) ◽  
pp. 195 ◽  
Author(s):  
Birhanu Sisay ◽  
Josephine Simiyu ◽  
Esayas Mendesil ◽  
Paddy Likhayo ◽  
Gashawbeza Ayalew ◽  
...  

The fall armyworm (FAW), Spodoptera frugiperda, threatens maize production in Africa. A survey was conducted to determine the distribution of FAW and its natural enemies and damage severity in Ethiopia, Kenya and Tanzania in 2017 and 2018. A total of 287 smallholder maize farms (holding smaller than 2 hectares of land) were randomly selected and surveyed. FAW is widely distributed in the three countries and the percent of infested maize fields ranged from 33% to 100% in Ethiopia, 93% to 100% in Tanzania and 100% in Kenya in 2017, whereas they ranged from 80% to 100% and 82.2% to 100% in Ethiopia and Kenya, respectively, in 2018. The percent of FAW infestation of plants in the surveyed fields ranged from 5% to 100%. In 2017, the leaf damage score of the average of the fields ranged from 1.8 to 7 (9 = highest level of damage), while 2018, it ranged from 1.9 to 6.8. In 2017, five different species of parasitoids were recovered from FAW eggs and larvae. Cotesia icipe (Hymenoptera: Braconidae) was the main parasitoid recorded in Ethiopia, with a percent parasitism rate of 37.6%. Chelonus curvimaculatus Cameron (Hymenoptera: Braconidae) was the only egg-larval parasitoid recorded in Kenya and had a 4.8% parasitism rate. In 2018, six species of egg and larval parasitoids were recovered with C. icipe being the dominant larval parasitoid, with percentage parasitism ranging from 16% to 42% in the three surveyed countries. In Kenya, Telenomus remus (Hymenoptera: Scelionidae) was the dominant egg parasitoid, causing up to 69.3% egg parasitism as compared to only 4% by C. curvimaculatus. Although FAW has rapidly spread throughout these three countries, we were encouraged to see a reasonable level of biological control in place. Augmentative biological control can be implemented to suppress FAW in East Africa.


1951 ◽  
Vol 42 (1) ◽  
pp. 23-28 ◽  
Author(s):  
J. R. Williams ◽  
L. A. Moutia ◽  
P. R. Hermelin

A brief historical account is given of the spread of the Eucalyptus Snout Beetle, Gonipterus scutellatus Gyll., fron Australia, its country of origin, and of the utilisation of its natural parasite Anaphoidea nitens Gir. for its control on the African mainland.The discovery of G. scutellatus in Mauritius is described. Its entry was effected between 1935–40, and by 1944 it was threatening Eucalyptus plantations over the whole island.A. nitens was introduced in 1946 from East Africa. Establishment was extremely rapid and two years later G. scutellatus was effectively controlled.Notes are given on the bionomics of both host and parasite under Mauritian conditions.Ecological data are briefly discussed.


1981 ◽  
Vol 71 (1) ◽  
pp. 33-46 ◽  
Author(s):  
Aola M. Richards

AbstractLife-cycles and voltinism are described for Rhyzobius ventralis (Erichs.) and R. forestieri (Muls.) living in the region of Sydney, Australia, and also the role each plays in its particular biocoenosis. Colour variation and wax production are described for the larvae, prepupae, pupae and adults of both species, also the defensive and feeding behaviour. New and known host records are listed for both species. Reasons are suggested for the success, partial failure or failure of the species as biological control agents in various parts of the world.


Phytotaxa ◽  
2015 ◽  
Vol 234 (1) ◽  
pp. 63 ◽  
Author(s):  
Juan S Chiriví-Salomón ◽  
Giovanna Danies ◽  
Silvia Restrepo ◽  
Tatiana Sanjuan

A new species of Lecanicillium was found associated with the soft scale insect Pulvinaria caballeroramosae (Coccidae), an important pest of Ficus soatensis (Moraceae) in Bogotá, Colombia. Lecanicillium sabanense sp. nov. differs from similar Lecanicillium spp. mainly in the size of the conidia, in the vertical arrangement of phialides on the host, and in the tomentose mycelium that sparsely covers the cuticle of the host. Phylogenetic analyses using ITS, SSU, LSU, TEF, RPB1, and RPB2 also confirmed the distinctness of this new species. Fungal epizootics were found on female soft scale insects, which may have implications for biological control in the forestry program of the city. The ecology of the fungus as well as its potential use as a biological control agent are further discussed.


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