A new genus, Vairimorpha (Protozoa: Microsporida), for Nosema necatrix Kramer 1965: Pathogenicity and life cycle in Spodoptera exempta (Lepidoptera: Noctuidae)

1976 ◽  
Vol 28 (2) ◽  
pp. 177-183 ◽  
Author(s):  
Barbara M. Pilley
2013 ◽  
Vol 30 (4) ◽  
pp. 371-378 ◽  
Author(s):  
Alexandre Specht ◽  
Andrés O. Angulo ◽  
Tania S. Olivares ◽  
Edegar Fronza ◽  
Vânia F. Roque-Specht ◽  
...  

2019 ◽  
Vol 11 (4) ◽  
pp. 126
Author(s):  
Lauren M. Barcelos ◽  
Fabrício O. Fernandes ◽  
Caroline Lopes ◽  
Beatriz M. Emygdio ◽  
Ricardo Valgas ◽  
...  

Saccharine sorghum has been analyzed as a supplementary prime matter for ethanol production, especially during the sugarcane off-season period. However, it has proven to be highly susceptible to insect attacks during the cultivation cycle. The fall armyworm should be emphasized due to its voracity and high damage capacity enhanced by feeding-caused decrease in photosynthetic area. Current analysis studies the biology and determines the nutritional indexes of Spodoptera frugiperda in saccharine sorghum. Cultivars of saccharine sorghum BRS 506, BRS 509 and BRS 511were evaluated. Duration and survival of the egg, caterpillar, pre-pupal and pupal phases were determined, coupled to weight of pupae and caterpillar, life span, fecundity and pre-egg laying period. Although S. frugiperda completed its life cycle on cultivars BRS 506 and BRS 511, egg-laying and egg feasibility rates were low, whereas insects did not lay eggs on cultivar BRS 509. There was no significant difference in feeding intake by S. frugiperda among these three sorghum cultivars. Results suggest that saccharine sorghum is not a suitable host for S. frugiperda. Biological data reveal that the three saccharine sorghum cultivars are recommended for the grain production system since the number of specimens of the next generation is low or null.


2021 ◽  
Vol 13 (1) ◽  
pp. 178-182
Author(s):  
Eknath Shendge ◽  
Bapurao Khaire ◽  
Ramrao Chavan

Among different fruit piercing moths, the genus Othreis are the most harmful, causing widespread damage to pomegranate, citrus and mango fruits causing fruit fall in tropical and subtropical countries. The present communication deals with the study on the biology of  Othreis materna (L) from egg to adult’s death which was carried out  at room temperature of the laboratory  to investigate the delicate and vulnerable stages of its life cycle. The life cycle of the moth was completed within 45-61 days, with an average 55.03 days in case of male and within 47-63 days with an average 57.07±4.92 in case of female. Eggs hatching started at night or early in the morning and duration of hatching was 2.72 days. The eggs measured were about 0.95 to 0.03 mm in diameter. The freshly emerged first instar larvae were light yellowish coloured and translucent. The first instar larvae were very active after hatching and they moved 4 to 6 feet for searching the food. The larvae were fed with the leaves of Tinospora cordifolia (Giloy or Guduchi). The total larval duration in days from first, second, third, fourth and fifth instar varied from 2.12±0.01, 1.81±0.05, 2.87±0.02, 3.90±0.11, 4.74±0.38 in days respectively and total larval period was 15.44±0.57. Pupae were dark brown in colour and total pupation period was of 13.81±0.12 days and total adult duration for male and female was 23.08±0.70 and 25.20±0.66 days respectively. The adult of O. materna was bright orange in colour and of medium size. The male was small than the female. This is first study of this type from Marathwada, which will help to trace the vulnerable and delicate stage of the life cycle of this O. materna.


Zootaxa ◽  
2021 ◽  
Vol 5061 (1) ◽  
pp. 167-176
Author(s):  
BALÁZS BENEDEK ◽  
ANTON V. VOLYNKIN ◽  
JÁNOS BABICS ◽  
AIDAS SALDAITIS

A new genus Burmanyctycia gen. n. is described for the new species Burmanyctycia naumanni sp. n. from Chin State in north-western Myanmar. The new genus is related to the genera Blepharomima Hreblay & L. Ronkay, 1998, Bryotypella Hreblay & L. Ronkay, 1998 and Charanyctycia Hreblay & L. Ronkay, 1998. Two new synonyms are established: Bryotypella = Paranyctycia Hreblay & L. Ronkay, 1998, syn. n. and Bryotypella = Parabole Hreblay & L. Ronkay, 1998, syn. n. Six new combinations are established: Bryotypella minima (Hreblay & L. Ronkay, 1999), comb. n., Bryotypella miraculosa (Hreblay, Peregovits & L. Ronkay, 1999), comb. n., Bryotypella orbiculosa (Hreblay & L. Ronkay, 1998), comb. n., Bryotypella rubiculosa (Hreblay & Ronkay, 1999), comb. n., Bryotypella medionigra (Hreblay & Ronkay, 1998), comb. n. and Bryotypella rectilinea (Hreblay & L. Ronkay, 1998), comb. n. The check-lists of the genera Bryotypella and Charanyctycia are provided. Adults, male and female genitalia of the new and the related taxa are illustrated.  


Zootaxa ◽  
2008 ◽  
Vol 1903 (1) ◽  
pp. 1-95 ◽  
Author(s):  
J. T. TROUBRIDGE

The former genera Oncocnemis Lederer, Apharetra Grote, Hemistilbia Barnes and Benjamin, Adita Grote, Lepipolys Guenée, Homoncocnemis Hampson, and Homohadena Grote are synonymized under Sympistis Hübner. The following are transferred from Oxycnemis Grote to Sympistis: Sympistis franclemonti (Blanchard), comb. n. [Oxycnemis franclemonti Blanchard] and Sympistis subsimplex (Dyar) comb. n. [Oxycnemis subsimplex Dyar]. Two species are transferred to Unciella gen. n. as Unciella primula (Barnes and McDunnough) comb. n. [Oncocnemis primula Barnes and McDunnough] and Unciella flagrantis (Smith) comb. n. [Oncocnemis flagrantis Smith], which along with Leucocnemis Hampson are transferred to tribe Triocnemidini in the Psaphidinae. Supralathosea Barnes and Benjamin is transferred to Psaphidinae: Psaphidini and Catabena pronuba Barnes and McDunnough is transferred to Supralathosea comb. n.. In addition, Cerapoda Smith syn. n. and Prochloridea Barnes and McDunnough syn. n. (Prochloridea is presently in Hodges “unassociated genera”) are synonymized under Rhizagrotis Smith in the Xyleninae. Copanarta sexpunctata Barnes and McDunnough rev. comb. is transferred from Stylopoda to Copanarta. Oncocnemis simplicia Smith syn. n. is synonymized under Homohadena deserta Smith, Oncocnemis mus Troubridge and Crabo syn. n. under Oncocnemis tenuifascia Smith, and Oncocnemis sala Mustelin syn. n. under Oncocnemis aqualis Grote. The following are elevated to species rank: Sympistis deserticola (McDunnough) stat. n., comb. n. [Oncocnemis riparia deserticola McDunnough], Sympistis pallidior (Barnes) stat. n., comb. n. [Oncocnemis figurata pallidior Barnes] and Sympistis pallida (Barnes) stat. n., comb. n. [Oncocnemis homogena pallida Barnes]. The following 50 species are described as new: Sympistis acheron Troubridge, Sympistis amenthes Troubridge, Sympistis amun Troubridge, Sympistis anubis Troubridge, Sympistis anweileri Troubridge and Lafontaine, Sympistis apep Troubridge, Sympistis apis Troubridge, Sympistis babi Troubridge, Sympistis baloghi Troubridge, Sympistis bes Troubridge, Sympistis buchis Troubridge, Sympistis buto Troubridge, Sympistis cherti Troubridge, Sympistis chons Troubridge, Sympistis cleopatra Troubridge, Sympistis cocytus Troubridge, Sympistis collaris Troubridge, Sympistis dischorda Troubridge, Sympistis disfigurata Troubridge, Sympistis doris Dimock and Troubridge, Sympistis hapi Troubridge, Sympistis hathor Troubridge, Sympistis horus Troubridge, Sympistis incubus Troubridge, Sympistis insanina Troubridge, Sympistis isis Troubridge, Sympistis jenniferae Troubridge, Sympistis jocelynae Troubridge, Sympistis khem Troubridge, Sympistis khepri Troubridge, Sympistis knudsoni Troubridge, Sympistis lachrymosa Troubridge, Sympistis min Troubridge, Sympistis mut Troubridge, Sympistis nenun Troubridge, Sympistis opleri Troubridge, Sympistis osiris Troubridge, Sympistis pachet Troubridge, Sympistis ptah Troubridge, Sympistis ra Troubridge, Sympistis richersi Troubridge, Sympistis sakhmet Troubridge, Sympistis septu Troubridge, Sympistis sesmu Troubridge, Sympistis seth Troubridge, Sympistis shait Troubridge, Sympistis shirleyae Troubridge, Sympistis sobek Troubridge, Sympistis sokar Troubridge, and Sympistis serapis Troubridge. Color illustrations are provided for adults of all nearctic Sympistis species. Alphabetical and phylogenetic checklists of North American Oncocnemidinae are also provided, including species formerly placed there, but here transferred to other subfamilies.


Phytotaxa ◽  
2014 ◽  
Vol 164 (2) ◽  
pp. 159
Author(s):  
Giovanni Furnari ◽  
MARIO CORMACI
Keyword(s):  

Feldmann (1970: 249), quoting the results of Hustede (1960), who had shown that Bryopsis halymeniae Berthold (1882: 497) was the gametophyte of a Derbesia sp.[1], pointed out that this species could  not belong to the genus Bryopsis differing from it in chloroplasts with no pyrenoids and gametes without a stigma. On that basis, as well as because of its peculiar life cycle, he stated that Bryopsis halymeniae should  be considered the type of a new genus: Bryopsidella. Even though Feldmann (1970) did not explicitely propose the new combination Bryopsidella halymeniae, such a binomial was reported by Gallardo et al. (1993: 412, note 60) and by Boudouresque & Per-ret-Boudoure-sque (1987: 83).[1]A more complete paper showing that Derbesia neglecta and Bryopsis halymeniae are phases of one species, was later published by Hustede (1964). 


2008 ◽  
pp. 53-59
Author(s):  
George Hangay ◽  
Severiano F. Gayubo ◽  
Marjorie A. Hoy ◽  
Marta Goula ◽  
Allen Sanborn ◽  
...  

1985 ◽  
Vol 6 (2) ◽  
pp. 171-175 ◽  
Author(s):  
Jacob G. Yarro

AbstractThere are five caterpillar instars in the life cycle of Spodoptera exempta (Walk.) when they feed upon star grass, Cynodon dactylon (L.) Pers., maize, Zea mais L. and Kikuyu grass, Pennisetum clandestinum Chiov. at 25–30°C. When the temperature is 18°C, however, there was an additional instar in the cycle. Similarly extra instars are formed on Guinea grass, Panicum maximum Jacq., Setaria plicatilis (Hochst.) Hack, and a sedge, Cyperus maranguensis K. Schm. even when the temperature appears to be sufficiently high for normal development. Occasionally the additional sixth instar is also too small to pupate, in which case a seventh instar is formed. It appears that caterpillars on nutritionally inadequate host plants or those at low temperatures are being partially starved and must continue moulting until the appropriate size is attained or exceeded. Measurements of the head capsule widths or distances between the frontal clypeal setae suggest that only individuals reaching or exceeding a species specific threshold size pupate. Extra moults appear to be an adaptation to environmental fluctuations obtaining within the range of occurrence of S. exempta.


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