Escape of the cercarial body of Gorgoderina vitelliloba from its anterior tail chamber

Mitchell J. B. and Mason A. R. 1978. Escape of the cercarial body of Gorgoderina vitelliloba from its anterior tail chamber. International Journal for Parasitology8: 193–198. Before the cercarial body of Gorgoderina vitelliloba can encyst in the body of its second intermediate host it must escape from the anterior tail chamber where it has been confined throughout the free living cercarial phase. Escape from the tail chamber is influenced by pH, enzymes, bile salts and by the physical nature of its environment. The cercarial body effects its escape after first becoming activated and then breaking its connection with the tail.     

The anterior tail chamber and survival of Gorgoderina vitelliloba

Mitchell J. B., Mason A. R. and Whalley A. J. S. 1980. The anterior tail chamber and survival of Gorgoderina vitelliloba. International Journal for Parasitology10: 181–182. Survival in pond water of intact cystocercous cercariae of Gorgoderina vitelliloba was significantly better than that of isolated cercarial bodies, although the latter were able to survive in Ringer's Solution. Survival of cercarial bodies in water was improved somewhat when sterility was maintained. It is suggested that the wall of the anterior tail chamber protects the body from the osmotic stress imposed by life in fresh water.     

Seasonal influence on the production of Schistosoma haematobium and S. mansoni cercariae in Rhodesia

Batches of Bulinus (Physopsis) globosus and Biomphalaria pfeifferi were exposed to Schistosoma haematobium and S. mansoni respectively each month for a 12-month period. The snails were kept out of doors in Salisbury (highveld) and indoors at Chiredzi (lowveld S. haematobium only) and examined weekly to determine the duration of prepatency, and the number of cercariae produced per infected snail. There was a strong seasonal influence in the highveld experiments which showed sporocyst dormancy in winter and the almost simultaneous maturation of infection in nine batches during early summer. In the lowveld the release of cercariae by infected B. globosus continued throughout the year although numbers fell off in winter. The prepatent period was prolonged in winter, but there was no evidence of sporocyst dormancy.     

Schistosoma mansoni and Schistosoma haematobium: Emergence of schistosome cercariae from snails with darkness and illumination

Biomphalaria glabrata and Bulinus globosus were infected with Schistosoma mansoni and Schistosoma haematobium, respectively, and the effect of different illumination conditions at 25 C on cercarial output was observed for 4 days. In both species, a dark period of 10–14 hr on Day 2 of the observation period resulted in an emergence pattern on Day 3 similar to the regular pattern recorded for Day 1. Total cercarial output on Day 3 was within 30% of the control (Day 1) output. A dark period of between 0 and 8 hr resulted in suppression of cercarial emergence and in abolishment of the regular hourly emergence pattern on Day 3. A dark period of 16–20 hr resulted in an emergence pattern with two peaks, the first occurred at Hour 1, and the other at Hour 5 of the subsequent light period. Interjection of a 1-hr dark period during the light period of Day 3, following short (2–8 hr) exposure to dark on the preceding day, produced an increase in cercarial shedding of S. mansoni immediately after restitution of the light conditions. On the other hand, in S. haematobium, cercarial output was stimulated during the interposed dark period itself.     

Ultrastructural observations on the sensory papillae of juvenile and adult Gorgoderina vitelliloba (Trematoda: Gorgoderidae)

Hoole D. and Mitchell J.B. 1981. Ultrastructural observations on the sensory papillae of juvenile and adult Gorgoderina vitelliloba (Trematoda : Gorgoderidae). International Journal for Parasitology11: 411–417. Ultrastructural observations have been made on the juvenile and adult stages of Gorgoderina vitelliloba from Rana temporaria. Four types of sensory papillae occur; button, rosette, ciliated and domed. Button papillae, which contain a ciliary-rootlet but lack a cilium, occur on the oral sucker, dorsal preacetabular surface and the lateral margins of the fluke. Scanning electron microscopical observations reveal that the tegumental protuberances of the papilla are transformed from a spiked or conical appearance in juvenile flukes to a rounded form in adult flukes. Rosette papillae, which also contain a rootlet, occur on the lip of the ventral sucker of both juvenile and adult flukes. Ciliated papillae only occur on the oral sucker of juvenile flukes. Domed papillae, which contain a large area of electron-dense material, occur on the internal surface of the ventral sucker of both juvenile and adult flukes. The functions of papillae and their possible role in the migration of the parasite are discussed.     

Encapsulation response of the marine prosobranch Cerithidea californica to natural infections of Renicola buchanani sporocysts (Trematoda: Renicolidae)

A hyalinocyte-mediated encapsulation reaction is elicited by sporocysts of Renicola buchanani infecting the anterior mantle region of Cerithidea californica. Three phases of capsule formation are recognized: (1) an initial aggregating of hyalinocytes around each sporocyst in which pseudopodia from encapsulating cells loosely interdigitate with the parasite's tegumental microvilli, (2) the infiltrating of numerous hyalinocytes to form a dense matrix of cells which lies in close contact with the sporocyst's tegument, and (3) the horizontal flattening of hyalinocytes against the sporocyst's surface to form a tightly adhering capsule four to eight cell layers deep. Sporocysts are not harmed as a consequence of encapsulation. Capsule formation in response to R. buchanani sporocysts is considered a type of leucocytic encapsulation, specifically designated hyalinocytic encapsulation.     

Quantification of the age-pigment lipofuscin in known-age octopus (Octopus pallidus): A potential tool for age determination

Stylet increment analysis (SIA) is the key method to age octopus, however, currently it is not reliable for all species. The suitability of the age-pigment lipofuscin as an alternative ageing method for octopus was examined. To determine the relationship between age and lipofuscin known-age octopus (Octopus pallidus) were reared in the laboratory from hatching to eight months old. Twenty-eight individuals at three different ages (3, 6 and 8 months old) were collected for lipofuscin analysis. The first two age groups (n = 5 each) were reared under ambient temperatures, while the oldest group (n = 18) was reared under three different controlled temperature regimes (n = 6 per treatment). For comparison, five wild O. pallidus were also collected for lipofuscin analysis and aged using SIA. Lipofuscin was analysed in the brain tissue and quantified at a commercial ageing centre using standard histological methods. Lipofuscin granules were clearly discernable in the brain tissue, and there was a strong exponential relationship between age and lipofuscin (R² = 0.86). Lipofuscin concentration was not related to sex, temperature or body weight in same-age individuals. Except for one individual, the predicted age of the wild animals, based on the relationship between lipofuscin and age, was close to the age determined using SIA. This study is the first to report lipofuscin in an octopus species and shows that lipofuscin has excellent potential as an alternative ageing method for octopus. This research will have important applications for species which cannot be reliably aged using current ageing methods.     

Transfer and fate of male secretions deposited in the spermatophore of females of Acanthoscelides obtectus Say (Coleoptera Bruchidae)

During mating, males of Acanthoscelides obtectus deposit a spermatophore in the female genital tract. Spermatophore structure subsequently undergoes considerable modification, especially the central portion, which becomes vacuolated. Two methods were used to show that certain male secretions could thus pass into female haemolymph. When young males were injected with [¹⁴C]-arginine or [¹⁴C]-histidine, the accessory glands actively incorporated the isotope and the resulting spermatophores were radioactive. After mating, spermatophore radioactivity declined and then appeared in the haemolymph of females and in the oöcytes after a delay. Immunoelectrophoresis also showed that antigens appeared in the haemolymph of females after mating which reacted against male-gland antiserum. This technique, however, did not enable us to detect the presence of male antigens in the oöcytes formed after mating. The fate of some male secretions in the female and their physiological importance in the control of the female reproductive function were analysed in the present work.     

The role of the accessory reproductive glands and genital ducts in egg pod formation in female Schistocerca gregaria

Removal of the accessory reproductive glands in female Schistocerca gregaria does not prevent the formation of eggplugs as expected. The egg pods formed are incomplete, with froth in the egg plug partially lacking. The extent of collapse is dependent on the time of removal of the glands. These results suggest that the genital ducts (egg calyces and lateral oviducts) play a significant role in the production of egg pod material, and the accessory glands probably participate in the process. Ligation of the glands has the same effect on egg pod structure; secretion accumulates in the glands indicating that, although the contribution made to the egg pod by the glands is small, they are not vestigial and are not acting simply as reservoirs for secretions produced distally. Cautery of the Comstock-Kellogg glands produces no visible change in egg pod structure or in method of formation, and thus their function remains undetermined. In the absence of the ventral median pouch egg masses are laid without the plug. A thin layer of nonvacuolated material is smeared over the walls of the oviposition hole, suggesting that the secretions produced in the upper regions of the genital ducts are added to or modified by an additional secretion from this gland, before being released to the exterior.     

The aerobic metabolism of 14C-sugars and 14CO2 by the daughter sporocysts of Microphallus similis (JÄG) and Macrophallus pygmaeus (Levinsen) (Digenea: Microphallidae)

The sporocysts of Microphallus similis and M. pygmaeus can aerobically utilise radiosugars and ¹⁴ CO₂in vitro. Both have an EMP pathway, TCA cycle, pentose-phosphate shunt, are able to undergo transamination reactions and can synthesise some essential amino acids. Carbon dioxide fixation involves the carboxylation of phosphoenolpyruvate to form oxaloacetate.     

Emergence of Chironomidae from Findley Lake and two ponds in the Cascade Mountains,U.S.A.

From Findley Lake and two ponds in the Cascade Mountains (U.S.A.) Chironomidae started to emerge as soon as the ice thawed in 1972 and 1973. The 1051 Chironomidae that emerged per m² from Findley Lake included 307 individuals ofTanytarsus and 358 ofProcladius. Tanytarsus outnumberedChironomus at all depths from 0 to 19.3 m. The 1506 Chironomidae that emerged per m² from the 4.5 m deep pond included 997 individuals ofTanytarsus. The 1490 Chironomidae that emerged per m² from the 2 m deep pond included 1363 Tanytarsus. The emerging biomass was 216 and 186 mg dry weight per m² in Findley Lake and the 4.5 m deep pond, respectively, and only 78 mg in the 2 m deep pond. Most species had their maximum emergence where there was organic detritus from the surrounding forest.Orthocladius emerged from sand bottom at 2.7 to 5.2 m depth.Stictochironomus emerged from mud and sand at 8.4 m depth.Chironomus emerged from soft mud at 15 to 27.5 m depth.     

Schistosoma mansoni: partial characterization of enzyme(s) secreted from the preacetabular glands of cercariae.

Secretions from the preacetabular glands of cercariae of Schistosoma mansoni were collected over skin surface lipid on a warmed glass surface in a system providing a temperature gradient. Proteolytic activity of these secretions was linear with respect to the numbers of cercariae secreting. The enzyme was relatively storage stable in water or glycine-NaOH buffer. It was highly sensitive to the buffer system, glycine-NaOH buffer providing the highest proteolytic activity against Azocoll and gelatin substrates. In the glycine buffer, the pH optimum for the enzyme was 8.5–8.8; the temperature optimum was 51 C with the Q₁₀ for Azocoll hydrolysis in the range of 30–50 C approximately 2.2. Of the activity 0.4% was lost at 5 C, 1.7% at 35 C, and 100% at 60 C within 10–15 min. Two Sephadex column chromatography fractions showed proteolytic activity against Azocoll. The fraction with greatest activity was not associated with either of the two peaks of high absorbancy at 280 nm, but the lower proteolytic peak coincided with the lower absorbancy peak in the area of peptides below 10,000 MW. Calibration of the Sephadex column with proteins of known molecular weight showed the MW of the main proteolytic fraction of the secretion to be approximately 25,000–27,000.     

Emergence of the damselfly Pyrrhosoma nymphula (Sulzer) (Zygoptera: Coenagrionidae) from two adjacent ponds in northern England

Emergence of the damselfly Pyrrhosoma nymphula was followed closely at two similar and adjacent ponds in northern England. Males emerged earlier than females at both ponds (significantly so at one). The sex ratio was significantly male biased at both ponds. Size of emerging adults declined through the emergence period at both ponds. Adults emerging from one pond did so significantly earlier and were significantly larger than those from the other pond. The density of larvae was approximately twice as high in the pond from which larvae emerged early; this pond was also slightly deeper and usually achieved higher maximum daily water temperatures. These findings are discussed in the light of the conventional view of seasonal regulation in a spring-emerging damselfly.     

Terpenoids from the seed of Thujopsis dolabrata var. Dolabrata

Fourteen mono-, 13 sesqui-, 16 diterpenes, dodecanal, sitosterol and desoxypodophyllotoxin were identified in the seed of T. dolabrata var. dolabrata. Sabinene and α-pinene were found to be the main components of the volatile oil. From the diterpenoid fraction, two new abietane-type compounds (ar-abietatrien-12,16-oxide and 16-hydroxyferruginol) were isolated and their structures were elucidated. Significant differences were observed in the seed diterpenoids when these results were compared with those obtained earlier with T. dolabrata var. hondae.     

In vitro stimulation of cell death in the moulting glands of Oncopeltus fasciatus by 20-hydroxyecdysone

The moulting glands of the milkweed bug, Oncopeltus fasciatus, normally degenerate just before the time of ecdysis to an adult (day 7 of the fifth instar). Morphologically normal cell death can be prematurely stimulated in vitro by 20-hydroxyecdysone. Breakdown is triggered by a 24-hr period of exposure to 20-hydroxyecdysone, but an additional incubation period is required before clear signs of degeneration are manifested. Glands removed after the onset of endogenous ecdysteroid secretion degenerate in vitro in the absence of added hormones. Thus, in the moulting glands of Oncopeltus, ecdysteroids appear to act as an important trigger for metamorphic cell death.     

Morphogenetic and diurnal variation of hypericin in some Hypericum species from Turkey during the course of ontogenesis

The genus Hypericum has received considerable interest from scientists, as it is a source of a variety of biologically active compounds including the hypericins. The present study was conducted to determine ontogenetic, morphogenetic and diurnal variation of the total hypericins content in some species of Hypericum growing in Turkey namely, Hypericum aviculariifolium subsp. depilatum var. depilatum (endemic), Hypericum perforatum and Hypericum pruinatum. The Hypericum plants were harvested from wild populations at vegetative, floral budding, full flowering, fresh fruiting and mature fruiting stages four times a day. Plants were dissected into stem, leaf and reproductive tissues, which were dried separately, and subsequently assayed for total hypericin content. The density of dark glands on leaves at full flowering plants was determined for each species. Floral parts had the highest hypericin content in all species tested. But diurnal fluctuation in the hypericin content of whole plant during the course of ontogenesis varied among the species. It reached the highest level at floral budding and tended to increase at night in H. aviculariifolium subsp. depilatum var. depilatum and H. pruinatum, whereas in H. perforatum hypericin content was the highest at full flowering and no diurnal fluctuation was observed. In general, hypericin content of leaves and whole plant was higher in H. aviculariifolium subsp. depilatum var. depilatum whose leaves had more numerous dark glands than those of the two other species.     

Cloning and expression of the leucine gene from Thermus thermophilus in Escherichia coli

A pBR322-T.leu hybrid plasmid was constructed which contains a 3.75 Md HindIII-fragment derived from Thermus thermophilus HB27 chromosomal DNA. In the Escherichia coli host, this plasmid coded for the β-IPM dehy drogenase (product of leuB) activity, the optimal temperature of which was 80°C, suggesting that information on the thermostability of the enzyme lies in its structural gene. 10-day propagation of E. coli [pBR322-T.leu] at 37°C decreased the temperature optimum from 80°C to 75°C. This change, which was found to depend on the plasmid but not on the host cells, might be due to selection of some mutation at the non-restrictive temperature of 37°C. Our results suggest that the 3.75 Md HindIII-fragment of pBR322-T.leu carries a promoter of the thermophile, which could function in E. coli.     

Molecular cloning of the SUF2 frameshift suppressor gene from Saccharomyces cerevisiae

A genetic approach to the molecular cloning of frameshift suppressor genes from yeast is described. These suppressors act by suppressing +1 G:C base-pair insertion mutations in glycine or proline codons. The cloning regimen involves an indirect screen for yeast transformants which harbor a functional suppressor gene inserted into the autonomously replicating “shuttle” vector YEp13, followed by transfer of the hybrid plasmid from yeast into Escherichia coli. Using this procedure a 10.7-kb DNA fragment carrying the SUF2 frameshift suppressor gene has been isolated. This suppressor acts specifically on +1 G:C insertions in proline codons. When inserted into an integrative vehicle and reintroduced into yeast by transformation, this fragment integrates by homologous recombination in the region of the SUF2 locus on chromosome III. A large proportion of the fragment overlaps with another cloned DNA segment which carries the closely linked CDC10 gene. The SUF2 fragment carries at least two tRNA genes. The SUF2 gene and one of the tRNA genes are located on a 0.85-kb restriction fragment within the 10.7-kb segment. A method is also described for the isolation of DNA fragments carrying alternative alleles of the SUF2 locus. Using this procedure, the wild-type suf2⁺ allele has been cloned.     

Membrane phosphorylation leads to the partial detachment of the chlorophyll a/b protein from Photosystem II

The hypothesis that the chlorophyll fluorescence decline due to membrane phosphorylation is caused principally by the detachment and removal of LHCP from the LHCP-PS II matrix is examined. It is demonstrated that when membranes are phosphorylated in the dark (a) the fluorescence decline is greater when excited by light enriched in wavelengths absorbed mainly by LHCP (475 nm) than when excited by light absorbed to a large extent also by the PS II complex (435 nm), (b) titration with different artificial quenchers of chlorophyll fluorescence is unchanged after the phosphorylation-induced fluorescence decline, and (c) the F_v/F_m ratio does not change after the phosphorylation-induced fluorescence decline. These data indicate that it is indeed principally LHCP that interacts with the quencher (PS I presumably). This interaction involves a small fraction of the total PS II-coupled LHCP, which becomes functionally detached from the LHCP-PS II matrix.