The life cycle and seasonal variation of Davainea tetraoensis Fuhrmann 1919, a cestode parasite of ruffed grouse, Bonasa umbellus (L.)

1971 ◽  
Vol 49 (1) ◽  
pp. 109-119 ◽  
Author(s):  
Terry A. Dick ◽  
Michael D. B. Burt
Keyword(s):  
Seasonal Variation ◽  
Life Cycle ◽  
Gonad Development ◽  
The Other ◽  
Ruffed Grouse ◽  
Bonasa Umbellus ◽  
Rate Of Development ◽  
Morphological Variations ◽  
Cestode Parasite ◽  
Full Development

Ruffed grouse (Bonasa umbellus) were collected from August 26, 1965, to August 25, 1966, and examined for cestodes. Two morphological variations of Davainea tetraoensis were found, fully developed mature worms being recovered during the summer months and poorly developed winter forms with no mature prolottides being recovered during the winter months. Various causes are considered and investigated experimentally. Changes in diet and changes in photoperiodicity do not seem to effect any change from one form to the other; changes in temperature, however, seem to be closely related to the transition from summer forms to winter forms, this transition occurring at around 0C. The change back to mature forms may be linked to gonad development in the host or to those environmental factors which influence gonad development. Cysticercoids from experimentally infected molluscs are described and compared. The rate of development of cysticercoids in Zonitoides arboreus under different conditions is investigated showing that full development, from oncospheres, can occur within 12 days in small individuals (2 mm) but takes at least 19 days in larger individuals (4.5 mm). Examination of grouse and chickens after experimental infection with up to 450 cysticercoids showed no apparent ill effects, or damage of any kind, to the hosts.

ON THE MORPHOLOGY AND LIFE CYCLE OF THE TREMATODE TANAISIA ZARUDNYI (SKRJABIN, 1924) BYRD AND DENTON, 1950, FROM THE RUFFED GROUSE, BONASA UMBELLUS L.

1965 ◽  
Vol 43 (6) ◽  
pp. 953-969 ◽  
Author(s):  
Newton Kingston
Keyword(s):  
Life Cycle ◽  
Cyst Wall ◽  
Ruffed Grouse ◽  
Kidney Tubules ◽  
Bonasa Umbellus ◽  
Complete Development ◽  
Daughter Sporocyst ◽  
Terrestrial Snails ◽  
Resistance To Infection ◽  
Anguispira Alternata

Tanaisia zarudnyi occurs in the ureters and kidney tubules of ruffed grouse from Ontario and Michigan. The dark brown, operculate eggs are fully developed when oviposited. They remain viable for long periods of time at 2 to −15 °C and can withstand a temperature of −49 °C for 1 to 2 days. They hatch only when ingested by some mollusc. Development occurs in the digestive gland of the terrestrial snails Anguispira alternata and Succinea ovalis. Daughter sporocysts complete development in 6 weeks, by which time they contain undeveloped cercarial bodies. Within the next 2 weeks, most of the distomate. brevicercous cercariae are fully developed. The cercariae encyst within the daughter sporocyst, utilizing the contents of subcuticular glands to form the cyst. Encysted metacercariae are killed in the gizzard when fed to chickens, but excyst when inoculated directly into the duodenum. Excystation apparently results from secretions of the anterior glands of the stimulated metacercaria rather than from digestion of the cyst wall by the host. A 6-week-old ruffed grouse became infected when fed metacercariae, but 9 older ruffed grouse, 17 chickens, 4 white-throated sparrows, and 6 pheasants, fed similarly, were not infected. Apparently there is both host and age resistance to infection with this parasite.

ON THE LIFE CYCLE OF BRACHYLECITHUM ORFI KINGSTON AND FREEMAN, 1959 (TREMATODA: DICROCOELIIDAE), FROM THE LIVER OF THE RUFFED GROUSE, BONASA UMBELLUS L. INFECTIONS IN THE VERTEBRATE AND MOLLUSCAN HOSTS

1965 ◽  
Vol 43 (5) ◽  
pp. 745-764 ◽  
Author(s):  
Newton Kingston
Keyword(s):  
Life Cycle ◽  
Definitive Host ◽  
Ruffed Grouse ◽  
Bonasa Umbellus ◽  
Birth Canal ◽  
Flame Cell ◽  
Larval Stages ◽  
Daughter Sporocyst ◽  
Cercarial Production ◽  
Biliary Ducts

The distribution and life cycle of a dicrocoeliid trematode, Brachylecithum orfi Kingston and Freeman, 1959, from the biliary ducts of the ruffed grouse, Bonasa umbellus, in Ontario and Michigan, have been studied in the definitive host and the intermediate molluscan hosts. Oval, dark brown, operculate eggs contain fully developed miracidia at oviposition. The eggs are coated with a lipid which prevents uptake of water and hatching until they are eaten by a mollusc; they will survive for more than 3 years at 2 °C and will tolerate exposure to −49 °C. The eggs hatch and larval stages develop in Zonitoides arboreus, Z. nitidus, Cionella lubrica, Deroceras laeve, and D. reticulatum, but not in 13 other species of terrestrial molluscs. Small, rounded, daughter sporocysts develop within the saclike mother sporocysts during the first 30 days after ingestion of eggs by suitable molluscs. Daughter sporocyst and cercarial development is completed 89–278 days after infection, depending on the species of mollusc and the temperature. The cercariae escape from the sporocyst endosac through a birth canal into the sinusoidal spaces of the mollusc. They migrate to the lung and out onto the dorsum of the mollusc via the respiratory pore, where they aggregate in numbers in slimeballs that are deposited on the substratum. Cercarial production continues for more than 100 days after onset. The longicercous, mesostomate xiphidiocercariae have a flame cell formula of 2((2 + 2 + 2) + (2 + 2 + 2)); they are provided with 6 preacetabular and 12 postacetabular glands, both groups of which open through pores lateral to the shank of the cercarial stylet. Cercariae in slime masses survive for 48 hours. When exposed to larval Colorado potato beetles, larval willow chrsyomelids, and mound-building ants, the cercariae penetrated the gut wall and encysted in the haemocoel, but died shortly afterwards.

Function of coprophagous beetles (Coleoptera: Scarabaeidae, Geotrupidae, Hydrophilidae) in cattle pastures inferred from pitfall trapping data

2010 ◽  
Vol 27 (2) ◽  
pp. 85-91 ◽  
Author(s):  
Martin Šlachta ◽  
Jan Frelich ◽  
Tomáš Tonka
Keyword(s):  
Seasonal Variation ◽  
Spatial Variation ◽  
Dry Weight ◽  
Seasonal Distribution ◽  
The Other ◽  
Pitfall Trapping ◽  
Other Hand ◽  
Nested Anova ◽  
Species Groups ◽  
Dung Decomposition

Function of coprophagous beetles (Coleoptera: Scarabaeidae, Geotrupidae, Hydrophilidae) in cattle pastures inferred from pitfall trapping dataAn analysis of data on the dry weight biomass of coprophagous beetles in standardized dung (4.5 l) was conducted in order to characterize the spatial and the seasonal distribution of the beetles' biomass in cattle pastures and to elucidate their function in dung decomposition. Nested Anova with factors of farm, site (nested in farm), seasonal period and year was used to evaluate the effect of these factors on the biomass of four functional species groups: the dung dwellers ofScarabaeidae(subfamilyAphodiinae), the dung dwellers ofHydrophilidae, the small tunnellers ofScarabaeidae(subfamilyCoprinae) and the large tunnellers ofGeotrupidae. The spatial variation of biomass (between the sites and the farms) was insignificant (P>0.05) in the two dung-dweller groups and in the large-tunnellers group. On the other hand, a significant (P<0.05) seasonal variation of biomass was found in all but the large tunneller group. In dung dwellers, the spring biomass was formed mainly by two species,Aphodius prodromusandA. sphacelatus. In summer, most of the biomass was accounted for bySphaeridium lunatum, S. scarabaeoidesandA. rufipes. In the two tunneller groups,Onthophagus fracticornis, Geotrupes stercorariusandG. spinigerformed a majority of the biomass in dung.

scholarly journals THE EPIDEMIOLOGY OF PNEUMOCOCCUS INFECTION

1931 ◽  
Vol 53 (4) ◽  
pp. 535-552 ◽  
Author(s):  
Leslie T. Webster ◽  
Thomas P. Hughes
Keyword(s):  
Seasonal Variation ◽  
Host Resistance ◽  
The Other ◽  
Colony Morphology ◽  
Type Transformation ◽  
Wide Ph Range ◽  
Adults And Children ◽  
Nasal Passages ◽  
Ph Range

1. Pneumococci were obtained at one time or another from the nasal passages or throats of 80 per cent of 105 adults and children studied. In adults, they were obtained more frequently from the throat; in children, as often from the nasal passages as from the throat. 2. Of 500 pneumococcus strains studied, 97 per cent proved to be serologically specific. They formed smooth colonies and were for the most part avirulent for mice. Types I and II were obtained from one and two individuals respectively on one occasion only. Type III was obtained from nine individuals; Type XIII from nine individuals; Type XVI and Type XVIII from three individuals, for varying periods in each case. Atypical pneumococci were secured from 13 persons on single and scattered occasions. They varied in colony morphology, did not kill mice, or agglutinate in saline, but flocculated in all types of antipneumococcus sera employed and over a wide pH range in acid buffers. Their occurrence was apparently not associated with any type-transformation or virulence-enhancement process in vivo. 3. Strains of pneumococcus obtained on successive cultures from a given carrier were, with rare exceptions, of the same serological type and were similar in colony morphology, virulence for mice, and other tested biological characteristics. 4. Pneumococci of Types I and II were obtained under conditions suggestive that they lacked a capacity to spread readily; pneumococci of Types III and XIII, on the other hand, were obtained under conditions suggestive that they were spreading from person to person. 5. The persons studied differed consistently with respect to the occurrence of pneumococci. Some were pneumococcus-free, some were transient carriers, some periodic, and some chronic carriers. Data are given which suggest that the differences were due to variations in host resistance. 6. The incidence of pneumococci in all individuals studied underwent a seasonal variation paralleling that of coryza and sore throats in the same persons.

Trypanosoma ontarioensis n.sp. and T. paddae from Corvus brachyrhynchos brachyrhynchos in Ontario, Canada, with notes on the biology of T. ontarioensis n.sp.

1982 ◽  
Vol 60 (9) ◽  
pp. 2107-2115 ◽  
Author(s):  
Patrick T. K. Woo ◽  
Cheryl M. Bartlett
Keyword(s):  
Agar Medium ◽  
Gallus Domesticus ◽  
Blood Agar ◽  
Melopsittacus Undulatus ◽  
Ruffed Grouse ◽  
Bonasa Umbellus ◽  
Southern Ontario ◽  
Corvus Brachyrhynchos ◽  
Domestic Chicks ◽  
Serinus Canarius

Two morphologically distinct trypanosomes (Trypanosoma ontarioensis n.sp. and Trypanosoma paddae) were found by the haematocrit centrifuge technique in the blood of 53% (64 of 121) of Corvus brachyrhynchos brachyrhynchos wintering in southern Ontario. Trypanosoma ontarioensis n.sp. is a small trypanosome with subterminal kinetoplast. It is monomorphic and not host specific. It was readily cultured in diphasic blood-agar medium. Two-week cultures were infective and contained dividing sphaeromastigotes, epimastigotes, and trypomastigotes. Blood trypomastigotes were detected in low numbers in the blood of inoculated birds (Corvus brachyrhynchos brachyrhynchos, Bonasa umbellus, Gallus domesticus, Melopsittacus undulatus, and Serinus canarius) at 28 and 48 days postinfection. The crows, ruffed grouse, and domestic chicks were laboratory raised while the budgerigars and canaries were from pet stores. One canary that was further examined at 180, 360, 540, 730, and 910 days postinfection still had detectable numbers of trypanosomes in its blood.

The butterfly squid Stoloteuthis leucoptera in the Mediterranean

1991 ◽  
Vol 71 (1) ◽  
pp. 47-51 ◽  
Author(s):  
Lidia Orsi Relini ◽  
Daniela Massi
Keyword(s):  
Life Cycle ◽  
Adult Male ◽  
The Other ◽  
Otter Trawl ◽  
Ligurian Sea ◽  
The Mediterranean ◽  
Unique Species ◽  
Recent Immigration

The presence of Stoloteuthis leucoptera in the Mediterranean is recorded on the basis of three specimens, including an adult male, caught by IKMT and by commercial otter-trawl in the Ligurian Sea. The hypothesis of a recent immigration is discussed.The list of Mediterranean cephalopods (Mangold Wirz, 1963; Torchio, 1968; Bello, 1986; Mangold & Boletzsky, 1987) includes the Sepiolidae of the subfamily Heteroteuthinae, whose members are supposed to be pelagic throughout their life cycle. Mangold Wirz (1963) recognizes in the Mediterranean fauna the unique species Heteroteuthis dispar, the other authors include H. atlantis Voss, which Voss himself (1955) reported at Messina. To this group may now be added Stoloteuthis leucoptera (Verrill, 1878) a species until now recorded in limited Atlantic areas. Verrill (1881) wrote “This species is an exceedingly beautiful one, when living, owing to the elegance and brilliancy of its colours and the gracefulness of its movements. In swimming it moves its fins in a manner analogous to the motion of the wings of a butterfly.”

Ruffed Grouse (Bonasa umbellus)

2000 ◽  
Author(s):  
Donald H. Rusch ◽  
Stephen Destefano ◽  
Michael C. Reynolds ◽  
David Lauten
Keyword(s):  
Ruffed Grouse ◽  
Bonasa Umbellus

ENDOGENOUS DEVELOPMENT AND PATHOGENICITY OF EIMERIA ANGUSTA IN THE RUFFED GROUSE, BONASA UMBELLUS

1984 ◽  
Vol 20 (2) ◽  
pp. 100-107
Author(s):  
Ian K. Barker ◽  
Allan Garbutt ◽  
Alex L. Middleton
Keyword(s):  
Endogenous Development ◽  
Ruffed Grouse ◽  
Bonasa Umbellus

scholarly journals Biology of the Wild SilkmothAnaphe panda(Boisduval) in the Kakamega Forest of Western Kenya

2012 ◽  
Vol 2012 ◽  
pp. 1-7 ◽  
Author(s):  
N. Mbahin ◽  
S. K. Raina ◽  
E. N. Kioko ◽  
J. M. Mueke
Keyword(s):  
Life Cycle ◽  
Incubation Period ◽  
Rainy Season ◽  
Dry Season ◽  
Developmental Period ◽  
The Other ◽  
Western Kenya ◽  
Kakamega Forest ◽  
Pupal Period ◽  
Indigenous Forest

A study on the life cycle of the silkmothAnaphe panda(Boisduval) was conducted in two different habitats of the Kakamega Forest in western Kenya: Ikuywa, an indigenous forest, and Isecheno, a mixed indigenous forest. Eggs were laid in clusters, and the incubation period ranged from 40 to 45 days. Larvae fed onBridelia micrantha(Hochst) and passed through seven instars. The developmental period took between 83 to 86 days in the dry season and 112 to118 days in the rainy season. The pupal period ranged between 158 and 178 days in the rainy season and, on the other hand, between 107 and 138 days in the dry season. But the later caught up in development with those that formed earlier. Moths emerged from mid-October until mid-May. Longevity of adultAnaphe pandamoths took between 4 and 6 days, but generally females seemed to live longer than males. The moth also seems to have higher lifespan in the indigenous forest compared to the mixed indigenous forest.

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