The Biology of Cephalonomia waterstoni Gahan (Hym., Bethylidae), a Parasite of Laemophloeus (Col., Cucujidae)

1950 ◽  
Vol 41 (1) ◽  
pp. 79-97 ◽  
Author(s):  
L. H. Finlayson

The paper describes field and laboratory investigations on the bionomics of Cephalonomia waterstoni, a Bethylid parasite of Laemophloeus spp. A table is given in which are listed all the Bethylids attacking insect pests of stored products to which reference could be found in the literature.An infestation of Laemophloeus, associated with two “hot spots” in Manitoba wheat, which supported a large population of Cephalonomia is described.A simple technique for the laboratory culture of Cephalonomia is described.The life-cycle of C. waterstoni with Laemophloeus ferrugineus as host has been worked out.The lengths of egg, larval and cocoon (prepupal and pupal) stages at combinations of 25°C, 30°C. and 60 per cent., 80 per cent. R.H. are given. The egg and larval stages are short, lasting for about six days at 25°C. and four days at 30°C.Within the limits used, the relative humidity appears to have no effect on the duration of development at any stage. On the other hand, temperature exerts a considerable influence; the life-cycle at 30°C. is completed in two weeks but at 25°C. it takes three weeks.Again within the limits used, the mortality appears to increase with decrease in saturation deficit. Mortality ranged from 9 per cent, at S.D. 12·7 mm. to 36·5 per cent, at S.D. 5·0 mm.Without food or water at all combinations of 25–30°C. and 60–80 per cent. R.H. adults live for about four days, with a range of 0·5–9·5 days. There is no difference between the sexes. Unexplained contradictory results were obtained in two experiments.With normal or paralysed host larvae available at 30°C. and 80 per cent. R.H., males live no longer than when no food or water is available but females live for about five weeks at 25°C. and 80 per cent. R.H. and for about four weeks at 30°C. and 80 per cent. R.H.Males fed with sucrose solution at 30°C. and 80 per cent. R.H. live for several days longer than when starved : females live for the same length of time as when fed with host larvae.The pre-oviposition period at 25°C. and 80 per cent. R.H. is about five days; at 30°C. and 80 per cent. R.H. about one and a half days.Fecundity. At 25°C. and 80 per cent. R.H., Cephalonomia lays about 40 eggs on 30 host larvae : at 30°C. and 80 per cent. R.H., about 65 eggs on 40 larvae.Cephalonomia females readily oviposit on larvae that have been paralysed some time previously, and can be induced to oviposit on larvae already bearing eggs.Virgin females produce only male offspring (arrhenotoky).Eggs are laid in groups of one, two or three (rarely four) per larva. Single eggs produce mainly females ; pairs produce mainly one male and one female ; trios produce mainly one male and two females. At 25°C. and 80 per cent. R.H. more single eggs are laid than pairs ; at 30°C. and 80 per cent. R.H. more pairs are laid than singles. This results in the production of a higher proportion of females at 25°C. than at 30°C. The incidence of trios at both temperatures is low.C. waterstoni is equally viable on L. minutus, L. ferrugineus and L. turcicus but shows a marked preference for L. ferrugineus.

2018 ◽  
Vol 14 (1) ◽  
pp. 10-24
Author(s):  
V. N. Fursov ◽  
L. S. Cherney

Darkling beetle Zophobas atratus (Coleoptera, Tenebrionidae) is recorded here for the first time as a new species for the fauna of Ukraine. Detailed study on morphology of preimaginal stages and biology of this species recently introduced to Ukraine, is given here. Zophobas atratus is an important species being easily reared in laboratory cultures and widely distributed in North and South America, Europe, and Asia. Detailed descriptions of all life stages, including egg, young and older larvae, pupa and adult of Z. atratus are required for further taxonomical study of the genus Zophobas, which isn’t yet definitively established. New identification keys for adults and larvae of the genera of tribe Tenebrionini are presented here, based on a comparative analysis of the taxonomic characters of adults and larvae of Z. atratus and species from the genera Tenebrio and Neatus. Comparative analysis of morphology of larva of Z. atratus and larvae of the tribe Cteniopodini of close subfamily Alleculinae was conducted here. The subfamily Alleculinae previously had the rank of family Alleculidae, but our analysis confirmed the reliability of its current taxonomic position as subfamily. The study of morphology of larvae of 1st and 2nd instars of Z. atratus revealed that they are characterized by special taxonomic structures that are not characteristic for oldest instars of larvae of Z. atratus. These characters include absence of spines on caudal segment, presence of a set of 4 setae at posterior margin of tergites of prothorax, metathorax, and 1st to 8th abdominal segments, strongly convex 2nd antennal segment and sensory zone in the form of an open ring on its apex, and etc. Moreover, structure of antenna of larvae of Z. atratus is similar to that of oldest larvae of most species of darkling beetles of the fauna of Ukraine. The most distinctive features of Z. atratus are: sexual dimorphism in structure of clypeus of adults; filiform sclerotized antenna of larva with a continuous sensory zone at apex of 2nd segment, weakly developed 3rd segment; fusion of sclerotized pleurites of 1st–8th abdominal segments with their tergites; sexual dimorphism in structure of 9th abdominal segment of pupa, and presence of two hooks on apex of its appendages. The data of original study of features of life cycle of Z. atratus are given. The pictures and photos of details of morphology of egg, larvae, pupa and adult of Z. atratus are presented. It was recored that life cycle of Z. atratus from laying of egg to the emergence of adult continues from 169 up to 181 days. Adults lived maximum up to 206 days. Maturation of eggs in female after copulation continues 10-11 days. Stage of egg continues 7 days, larva – up to 151 days, including pre-pupal period from 6 to 22 days, pupa – from 8 to 21 days. Twelve larval stages of Z. atratus were recorded in laboratory culture.


2004 ◽  
Vol 64 (2) ◽  
pp. 237-242 ◽  
Author(s):  
M. C. Lacerda ◽  
A. M. R. M. Ferreira ◽  
T. V. Zanuncio ◽  
J. C. Zanuncio ◽  
A. S. Bernardino ◽  
...  

Biological control has been reducing the use of chemical products against insect pests, specially predatory Pentatomidae. Species of this group can present high variations in their life cycle as a result of their diet. Thus, the objective of this research was to study nymph development and reproduction of Podisus distinctus (Stäl, 1860) (Heteroptera: Pentatomidae) fed on Bombyx mori L., 1758 (Lepidoptera: Bombycidae) larvae (T1), compared to those fed on Tenebrio molitor L., 1758 (Coleoptera: Tenebrionidae) (T2) and Musca domestica L., 1758 (Diptera: Muscidae) larvae (T3) at a temperature of 25 ± 0.5ºC, relative humidity of 70 ± 2%, and photophase of 12 h. Predators fed on B. mori showed duration of the nymph phase (18.68 ± 1.02) similar to those fed on T. molitor (18.32 ± 1.49). Pre-oviposition and oviposition periods and number of egg masses, besides eggs and nymphs per female, were higher with B. mori (5.83 ± 2.02; 15.00 ± 7.40; 8.42 ± 1.84; 296.69 ± 154.75; and 228.55 ± 141.04, respectively) while longevity of males and females of P. distinctus was 25.76 ± 16.15 and 35.00 ± 16.15 days with T. molitor, and 20.57 ± 13.60 and 23.46 ± 12.35 days with B. mori, respectively.


2011 ◽  
Vol 8 (4) ◽  
pp. 870-876 ◽  
Author(s):  
Baghdad Science Journal

The study aimes to investigate the effects of leaves & fruits ethanolic extract of Duranta repens L. on biological performance for all stages of life cycle of the mosquito Culex pipiens piepiens L., For this purpose the mosquitoes were reared in the laboratory till the fourth generation .Different concentrations of leaves (800,1000,1200,1400ppm) and fruits (800,1000,1200ppm) were tested on (eggs,larval stages,pupal stages and the adult stages). The results revealed that the extracts gave highest mortality rate for the eggs at(100%) compared with control,fruits extract shown highest mortality rate of the four larval instars (100%)at 1200ppm compared with leave extract at(80,50,33.33,20%).Also the extract caused a high mortality rate for pupal stage compared with fruits extract at(76.66,53.33%)respectively.Also ethanolic extract caused a 83.33,76.66% for male &femail. Developmental deformation was observed.. In conclusion, the findings of the present study indicate that the leaves &fruits extracts of Duranta repens L., , can be widely and effectively used in the control of mosquito.


1987 ◽  
Vol 65 (10) ◽  
pp. 2491-2497 ◽  
Author(s):  
Murray J. Kennedy ◽  
L. M. Killick ◽  
M. Beverley-Burton

Life cycle studies of Paradistomum geckonum (Dicrocoeliidae) were attempted experimentally. The pulmonate gastropod Lamellaxis gracilis served as the first intermediate host; geckonid lizards (Cosymbotus platyurus, Gehyra mutilata, and Hemidactylus frenatus) served as definitive hosts. The life cycle of Mesocoelium sociale (Mesocoeliidae) was studied in naturally infected first intermediate hosts (L. gracilis, Huttonella bicolor) and experimentally in geckonid definitive hosts (C. platyurus, G. mutilata, and H. frenatus). Some naturally infected L. gracilis were infected concurrently with larval stages of both digeneans. Second intermediate hosts, presumed to be arthropods, were experimentally unnecessary. Metacercariae of P. geckonum were not found. Cercariae of M. sociale formed encysted metacercariae in the same individual snails.


Author(s):  
Jan A. Pechenik

I have a Hardin cartoon on my office door. It shows a series of animals thinking about the meaning of life. In sequence, we see a lobe-finned fish, a salamander, a lizard, and a monkey, all thinking, “Eat, survive, reproduce; eat, survive, reproduce.” Then comes man: “What's it all about?” he wonders. Organisms live to reproduce. The ultimate selective pressure on any organism is to survive long enough and well enough to pass genetic material to a next generation that will also be successful in reproducing. In this sense, then, every morphological, physiological, biochemical, or behavioral adaptation contributes to reproductive success, making the field of life cycle evolution a very broad one indeed. Key components include mode of sexuality, age and size at first reproduction (Roff, this volume), number of reproductive episodes in a lifetime, offspring size (Messina and Fox, this volume), fecundity, the extent to which parents protect their offspring and how that protection is achieved, source of nutrition during development, survival to maturity, the consequences of shifts in any of these components, and the underlying mechanisms responsible for such shifts. Many of these issues are dealt with in other chapters. Here I focus exclusively on animals, and on a particularly widespread sort of life cycle that includes at least two ecologically distinct free-living stages. Such “complex life cycles” (Istock 1967) are especially common among amphibians and fishes (Hall and Wake 1999), and within most invertebrate groups, including insects (Gilbert and Frieden 1981), crustaceans, bivalves, gastropods, polychaete worms, echinoderms, bryozoans, and corals and other cnidarians (Thorson 1950). In such life cycles, the juvenile or adult stage is reached by metamorphosing from a preceding, free-living larval stage. In many species, metamorphosis involves a veritable revolution in morphology, ecology, behavior, and physiology, sometimes taking place in as little as a few minutes or a few hours. In addition to the issues already mentioned, key components of such complex life cycles include the timing of metamorphosis (i.e., when it occurs), the size at which larvae metamorphose, and the consequences of metamorphosing at particular times or at particular sizes. The potential advantages of including larval stages in the life history have been much discussed.


2019 ◽  
Vol 94 ◽  
Author(s):  
Y. Kuzmin ◽  
V.V. Tkach ◽  
F.T.V. Melo

Abstract Serpentirhabdias mussuranae n. sp. is described from the lungs of the mussurana, Clelia clelia (Daudin, 1803), from vicinities of Lábrea, Amazonas State, Brazil. The species is characterized by the triangular oral opening, the presence of teeth (onchia) in the oesophastome, the excretory glands longer than the oesophagus and the tail abruptly narrowing in its anterior half and gradually tapering in posterior half. Among the Neotropical representatives of the genus, three species are known to possess the onchia in the oesophastome: S. atroxi, S. moi and S. viperidicus. Serpentirhabdias mussuranae n. sp. differs from S. atroxi and S. viperidicus by its triangular shape of the oral opening and the oesophastome in apical view, vs. round in the latter two congeners. Additionally, S. viperidicus has a larger oesophastome, 13–22 micrometers wide and 13–23 micrometers deep. The new species has relatively longer excretory glands than S. moi. The new species is morphologically and genetically close to S. atroxi, S. moi and S. viperidicus, all parasitic in Brazilian snakes, based on the presence of onchia and the comparison of nucleotide sequences of nuclear ribosomal DNA and mitochondrial cox1 gene (differences varied between 3.8% and 7.1%). Data on the life cycle of S. mussuranae n. sp. is provided, and the life cycle is typical of the genus Serpentirhabdias, with the combination of direct development and heterogony. Free-living larval stages and the adults of amphimictic free-living generation are described. The results of molecular phylogenetic analysis based on nuclear ribosomal internal transcribed spacer (ITS) + partial 28S region and partial mitochondrial cox1 gene are provided.


2005 ◽  
Vol 24 (8) ◽  
pp. 2065 ◽  
Author(s):  
Ross V. Hyne ◽  
Sharyn A. Gale ◽  
Catherine K. King

Zootaxa ◽  
2009 ◽  
Vol 2206 (1) ◽  
pp. 45-61 ◽  
Author(s):  
JOSÉ MARÍA LANDEIRA ◽  
FERNANDO LOZANO-SOLDEVILLA ◽  
JUAN IGNACIO GONZÁLEZ-GORDILLO

The first five zoeal stages of Plesionika narval were obtained from 15 days of laboratory culture. All larval stages are described and illustrated in detail. Zoeal characters are compared with the previous described larvae of Plesionika acanthonotus and Plesionika edwardsii and with undetermined zoeas of Pandalidae from plankton samples.


1955 ◽  
Vol 29 (1-2) ◽  
pp. 27-32 ◽  
Author(s):  
H. M. Gharib

It is well known that the first two larval stages in the life cycle of nematodes belonging to the superfamily Strongloidea, have a freeliving existence. During this time, the larva which hatches from the egg feeds actively, undergoes two moults and grows considerably before reaching the infective stage, when it is ready to invade a definitive host. Under natural conditions this external development takes place in the faeces, which have been deposited by the infected host on ground likely to be contaminated with various bacteria.


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