scholarly journals HOST SPECIFICITY ATTRIBUTES OF ZYGOGRAMMA BICOLORATA PALLISTER IN CHITRAKOOT REGION, INDIA

2021 ◽  
Vol 03 (02) ◽  
Author(s):  
Preeti Tripathi ◽  
Ramesh Chandra Tripathi
2021 ◽  
Vol 4 (1) ◽  
pp. 29-41
Author(s):  
Ajaya Shree Ratna Bajracharya ◽  
Resham Bahadur Thapa ◽  
Gopal Bahadur KC ◽  
Shree Baba Pradhan ◽  
Jagat Devi Ranjit

Host-specificity test of Zygogramma bicolorata Pallister (Coleoptra: Chrysomelidae) was conducted in the field and laboratory of National Entomology Research Center, Khumaltar, Lalitpur, Nepal during April to September, 2017. Multiple-choice and no-choice tests were conducted on Agerataum houstoniamum Mill., Bidens pilosa L., Chrysanthemum indicum L., Dahlia pinnata Cav, Guizotia abyssinica L., Helianthus annuus L., Lactuca sativa L., Parthenium hysterophorus L., Perilla frutescence L., Xanthium strumarium L., Zinnia elegans Jacq. and Jasminum officinale L. Among tested plant species, P. hysterophorus was only a preferred host of Z. bicolorata on which both larvae and adults fed. Ovipostion, larval development, pupation and adult emergence of Z. bicolorata occurred successfully on P. hysterophorus completing its life cycle. Larvae consumed H. anuus but could not pupate, and adults fed on it when starved for 5 days in no-choice test.   Both adults and larvae of Z. bicolorata consumed X. strumarium and completed larval and pupal developments, but adults did not oviposit. Adult longevity was significantly reduced after feeding on H. annus (19.00 days) and X. strumarium (29.33 days) compared to P. hysterophorus (83.33 days).


1968 ◽  
Vol 32 (4_Pt_1) ◽  
pp. 297-301 ◽  
Author(s):  
D D Gwinn ◽  
W D Lawton

1968 ◽  
Vol 46 (5) ◽  
pp. 835-843 ◽  
Author(s):  
John E. Bishop

Orconectes propinquus and Cambarus robustus from the Speed River, Sunfish Lake, and Laurel Creek, harbor two branchiobdellids, Cambarincola chirocephala and Pterodrilus distichus. Both adult and cocoon populations of the dominant species (C. chirocephala) are proportional to the size of the host throughout the year, except that first-year crayfish are free of cocoons. The reduction in total number of commensals from autumn to spring can be attributed to severe winter conditions. A subrostral site of preference for adult branchiobdellid attachment, and a dominant abdomen I and II site for cocoon deposition are indicated for O. propinquus. On C. robustus, adults are most commonly found on the antennal bases and among the maxillipeds, and cocoons on the last live abdominal sternites. No host specificity is evident although an unidentified Cambarus sp. from Sunfish Lake is free of commensals. Host incompatibility may explain this, but data from Laurel Creek indicate that silting of the microhabitat is responsible for loss of branchiobdellid population. The crayfish–branchiobdellid relationship is commensal, or at most facultatively parasitic, as adult worms can live without a host for extended periods. Serological testing of rabbit serum containing branchiobdellid antibodies against crayfish serum is negative. The dependence of the egg stage on the host for some undetermined factor or factors is discussed. An Asellus sp. fails to pick up the commensals even when exposed under ideal conditions for colonization.


2021 ◽  
Vol 95 ◽  
Author(s):  
S.A. Kornienko ◽  
L.A. Ishigenova

Abstract Urocystis prolifer Villot, 1880 is an intestinal parasite of Sorex spp. In the Palaearctic. There are significant differences in the descriptions of both adults and stages of ontogenesis of U. prolifer as described by various authors. The experimental infection of intermediate hosts with cestodes has been conducted. An overview of the geographical distribution, infestation of the definitive hosts and the development of the metacestode stages of U. prolifer are presented. The cestode is characterized by an extensive geographic area in the Palaearctic, wide host specificity and very high rates of infection of its definitive host. Urocystis prolifer has been recorded mostly in the taiga and forest zones of Palaearctic. Fourteen species of Sorex were registered as the definitive host. Redescription of U. prolifer and an amended generic diagnosis are provided. A complete description of the ontogeny from oncosphere to fully developed metacestode is given. Features of development of the metacestode are an asexual larval reproduction, the absence of the anterior and posterior obturator valve in the cyst of the fully developed urocyst, as well as excretory bodies.


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