Potent allelopathy and non-PSTs, non-spirolides toxicity of the dinoflagellate Alexandrium leei to phytoplankton, finfish and zooplankton observed from laboratory bioassays

2021 ◽  
Vol 780 ◽  
pp. 146484
Author(s):  
Lixia Shang ◽  
Yangbing Xu ◽  
Chui Pin Leaw ◽  
Po Teen Lim ◽  
Jiuming Wang ◽  
...  
Keyword(s):  
HortScience ◽  
1998 ◽  
Vol 33 (3) ◽  
pp. 506b-506
Author(s):  
Carol D. Robacker ◽  
S.K. Braman

Azalea lace bug (Stephanitis pyrioides) is the most serious pest on azalea. Results of laboratory bioassays and field evaluations of 17 deciduous azalea taxa have identified three resistant taxa: R. canescens, R. periclymenoides, and R. prunifolium. Highly susceptible taxa are `Buttercup', `My Mary', R. oblongifolium, and the evergreen cultivar `Delaware Valley White'. To determine whether in vitro techniques would have potential value in screening or selecting for resistance, or for the identification of morphological or chemical factors related to resistance, an in-vitro screening assay was developed. In-vitro shoot proliferation was obtained using the medium and procedures of Economou and Read (1984). Shoots used in the bioassays were grown in culture tubes. Two assays were developed: one for nymphs and one for adult lace bugs. To assay for resistance to nymphs, `Delaware Valley White' leaves containing lace bug eggs were disinfested with 70% alcohol and 20% commercial bleach, and incubated in sterile petri plates with moistened filter paper until the nymphs hatched. Five nymphs were placed in each culture tube, and cultures were incubated for about 2 weeks, or until adults were observed. To assay for resistance to adults, five female lace bugs were placed in each culture tube and allowed to feed for 5 days. Data collected on survival and leaf damage was generally supportive of laboratory bioassays and field results. Adult lace bugs had a low rate of survival on resistant taxa. Survival of nymphs was somewhat reduced on resistant taxa.


BioControl ◽  
2017 ◽  
Vol 62 (2) ◽  
pp. 257-268 ◽  
Author(s):  
Chad A. Keyser ◽  
Éverton K. K. Fernandes ◽  
Drauzio E. N. Rangel ◽  
R. Nelson Foster ◽  
Larry E. Jech ◽  
...  

1997 ◽  
pp. 225-276 ◽  
Author(s):  
Niels Nyholm ◽  
Hans Peterson
Keyword(s):  

2010 ◽  
Vol 19 (01) ◽  
pp. 12-17 ◽  
Author(s):  
S. F. Soares ◽  
R. de S. Braga ◽  
L. L. Ferreira ◽  
C. C. B. Louly ◽  
L. A. D. de Sousa ◽  
...  

2021 ◽  
Vol 288 (1965) ◽  
Author(s):  
Michelina Pusceddu ◽  
Desiderato Annoscia ◽  
Ignazio Floris ◽  
Davide Frizzera ◽  
Virginia Zanni ◽  
...  

Honeybees use propolis collected from plants for coating the inner walls of their nest. This substance is also used as a natural antibiotic against microbial pathogens, similarly to many other animals exploiting natural products for self-medication. We carried out chemical analyses and laboratory bioassays to test if honeybees use propolis for social medication against their major ectoparasite: Varroa destructor . We found that propolis is applied to brood cells where it can affect the reproducing parasites, with a positive effect on honeybees and a potential impact on Varroa population. We conclude that propolis can be regarded as a natural pesticide used by the honeybee to limit a dangerous parasite. These findings significantly enlarge our understanding of behavioural immunity in animals and may have important implications for the management of the most important threat to honeybees worldwide.


2021 ◽  
Vol 13 (10) ◽  
pp. 96
Author(s):  
Eduardo Carvalho Faca ◽  
Fabrício Fagundes Pereira ◽  
Winnie Cezario Fernandes ◽  
Ivana Fernandes da Silva ◽  
Valmir Antônio Costa ◽  
...  

The study of the interaction between parasitoid and host, especially the age of these organisms, is an important step towards the implementation of biological control programs. Therefore, we investigated the performance of Ooencyrtus submetallicus (Hymenoptera: Encyrtidae) and Trissolcus sp. aff. urichi (Hymenoptera: Scelionidae) parasitizing eggs of Nezara viridula (Hemiptera: Pentatomidae), considering different ages of the parasitoids and the host. We performed four laboratory bioassays: two using females of O. submetallicus and Trissolcus sp. aff. urichi at 24, 48, 72, 96, 120, or 144 hours of age exposed to parasitism in N. viridula eggs (24 h) and two trials with N. viridula eggs at 24, 48, 72, 96, 120, or 144 hours exposed to the parasitism of O. submetallicus and Trissolcus sp. aff. urichi (24 h). We evaluated the percentage of parasitism and emergence, life cycle length, progeny, sex ratio, and the longevity of the parasitoids. The parasitism of O. submetallicus in N. viridula eggs was influenced by the age of the parasitoid, 120 hours being the minimum to obtain better parasitism. From this age on, there is interference in the longevity of the progeny. Trisolcus sp. aff. urichi, at all ages, parasitized N. viridula eggs relatively well, but with almost no emergence of the parasitized eggs. Females of O. submetallicus parasitized and developed in eggs of N. viridula of all ages. Females of Trissolcus sp. aff. urichi parasitized their host, but there was barely any emergence. These pieces of information regarding the breeding methodology contribute to the implementation of new protocols for the multiplication of these parasitoids in the laboratory, and later, their release in the field.


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