Resource allocation in a social wasp: effects of breeding system and life cycle on reproductive decisions

Organisms must make important decisions on how to allocate resources to reproduction. We investigated allocation decisions in the social wasp Vespula maculifrons to understand how social insects make reproductive choices. We first determined how annual colonies apportioned resources to growth and reproduction by analysing developing brood. In contrast to expectations, colonies invested in both growth (workers) and reproduction (males) simultaneously. In addition, colonies showed evidence of producing males in pulses and reversing their reproductive choices by decreasing investment in males late in the season. This reversal is consistent with theory suggesting that colonies decrease production in males if fitness of late emerging males is low. To further investigate reproductive decisions within colonies, we determined if the male mates of multiply-mated queens varied in their reproductive success over time. Sperm use by queens did vary over time suggesting that male success may depend on sperm clumping within the female reproductive tract. Finally, we tested if colony sex ratio conformed to expectations under kin selection theory that nestmate relatedness would positively correlate with investment in new queens if workers controlled sex allocation. Surprisingly, the proportion of queens produced by colonies was negatively correlated with nestmate relatedness, suggesting that allocation may be shaped by advantages arising from increased genetic diversity resulting from multiple mating by queens. Overall, our study suggests that the reproductive decisions of colonies are flexible and may depend both on environmental cues arising from energetic needs of the colony and genetic cues arising from mating behaviours of queens.     

Extended lifespan traded for diapause in Daphnia

1. Most freshwater crustaceans of the genus Daphnia are cyclically parthenogenetic organisms that are well adapted to unstable habitats due to their short life cycle, wide phenotypic plasticity, and the ability to produce protective diapausing eggs in anticipation of environmental deterioration. Short lifespan and heterogonic reproduction are typical features of Daphnia in a broad spectrum of freshwater habitats, from small temporary pools to large permanent lakes. However, in some locations, departures may be observed from this typical life history pattern to obligate asexuality or extended lifespan. 2. A 3‐year field study in a deep ultraoligotrophic fish‐free alpine‐type lake (Czarny Staw in the Tatra mountains in southern Poland) revealed the coexistence of two closely related asexual lineages of Daphnia of the pulex complex, which differ in body colour (transparent versus orange) and in their strategies for surviving long winters. 3. The ‘transparent’ clone of European origin exhibits an ephemeral lifestyle. It completes its life cycle within a single season, forming two generations of active specimens during the short summer and producing diapausing eggs late in the season. Transparent individuals live no longer than 5–6 months in this cold lake and survive winter exclusively in the form of diapausing eggs. 4. Individuals of the ‘orange’ lineage, which are closely related to eastern Nearctic Daphnia pulicaria, exhibit a biennial lifestyle unique to this genus. They do not form diapausing eggs or produce them only occasionally. Instead, they are active throughout the year and live for up to 13–14 months. Reproduction is postponed until the second year of life when food conditions have improved. Rich lipid reserves accumulated in the first season fuel them during the long winter and permit early reproduction the following spring. 5. Possible reasons for the evolution of obligatory parthenogenesis and long lifespan in Daphnia are discussed.     

Taxonomic status of the Namibian Violet Woodhoopoe Phoeniculus damarensis as determined by mitochondrial DNA

The Violet Woodhoopoe Phoeniculus damarensis damarensis is considered a threatened subspecies and one of ten bird taxa endemic to Namibia and southwestern Angola. This species is distinguished from the more common and widespread Green Woodhoopoe P. purpureus by a variable plumage trait, resulting in uncertainty as to the distribution and degree of overlap between these taxa. Mitochondrial sequences from the cytochrome oxidase I (COI) gene show minimal divergence among Namibian woodhoopoes (0.15%, including P. d. damarensis and P. p. angolensis), and low divergence between Namibian birds and South African (1.06%, P. p. purpureus) or Kenyan (2.30%, P. p. marwitzi) Green Woodhoopoes. Sequences from Namibian woodhoopoes are phylogenetically nested within P. purpureus, rendering this species paraphyletic at mitochondrial DNA. Genetic divergences among Violet and Green Woodhoopoes fall within the range of intraspecific values recorded for avian mitochondrial protein coding genes, and are substantially less than most interspecific values. Comparisons with the related Scimitarbill Rhinopomastus cyanomelas suggest that the low divergences among Green and Violet Woodhoopoes are not an artefact of slow evolutionary rates in Phoeniculidae. We suggest that in the absence of evidence for evolutionary independence or a clear phenotypic diagnosis, the Violet Woodhoopoe should be synonymized with the Green Woodhoopoe. It is the status of this taxon that should be considered in formulating priorities for avian conservation in Namibia.     

Infectivity of Trypanosoma rhodesiense Cultivated at 28°C with Various Tsetse Fly Tissues1

ABSTRACT. Metacyclic trypanosomes developed in populations of procyclic forms of four stocks of Trypanosoma brucei rhodesiense cultivated at 28°C in a liquid medium containing explants of tsetse fly head-salivary glands, alimentary tract, abdominal body wall, or thoracic muscle. The cultures became infective for mice 7–16 days after they were prepared, and infective trypanosomes were present for prolonged periods. In the culture series of stock TRUM 545, infectivity persisted for 138 days when the cultures were terminated. Only one explant of thoracic muscle tissue was required for the production of metacyclic stages in stock TRUM 497 cultures. Infectivity titrations on trypanosome suspensions from cultures of stocks TRUM 497, TRUM 545, and TRUM 567 revealed that only a small proportion of the culture population was infective. Using stock TRUM 530, mice were infected consistently from inoculations of trypanosomes grown in the presence of explants; infectivity of the trypanosomes ceased when the explants were removed from the flasks, but reappeared when they were returned to the cultures. Parasites grown in medium “conditioned” by explants produced sporadic infections in mice. The control cultures of trypanosomes grown in medium alone were generally not infective, but two of the stocks produced occasional parasitemias. Stained samples of infective inocula contained a few epimastigote-like and metacyclic-like trypanosomes.     

Molecular Basis for Fibrillar Aggregation of Tropocollagen

NO model for the three dimensional packing of tropocollagen (TC) molecules into fibrils^1–3 approaches the problem on a molecular level; such analysis requires the assumption of a specific macromolecular structure^4–6 and of a specific aggregation state^7,8 of TC molecules. If the Ramachandran, Rich and Crick structure with the a1 chains in register from the N-terminus and the quarter stagger mode of association are assumed, then corresponding residues in the a chains will be separated by 108° radial angles^4,6. Possible intermolecular associations, producing quarter-staggered⁷ TC aggregation, fall into two general classes: (1) association involving a single chain in one molecule with a single chain in another and (2) complex association loci involving more than one chain in each TC molecule. The former is the more likely possibility and would involve residues on an individual a chain, at intervals governed by the pitch of the super helix, forming a longitudinal edge which associates in a defined plane of contact with a complementary edge in a neighbouring TC molecule^2,4,6.     

Growth of <Emphasis Type="Italic">Theileria parva</Emphasis>-infected Bovine Lymphoid Cells in Irradiated Mice

SEVERAL attempts to establish Theileria parva, the causative organism of East Coast fever of cattle, in laboratory animals^1–4 have failed. The recent successful establishment of T. parva macroschizont-infected bovine lymphoid cells in tissue culture⁵ provided a concentrated source of material which could be used in further attempts to infect laboratory animals.     

Identification of Rhodococcus equi using the polymerase chain reaction

K.S. BELL, J.C. PHILP, N. CHRISTOFI AND D.W.J. AW. 1996. Two regions in the gene coding for 16S rRNA in Rhodococcus equi were selected as species-specific primer sequences for the polymerase chain reaction (PCR). PCR using these primers was tested against 10 strains of R. equi (including the type strain) and gave positive results for all but was negative for all other tested species of Rhodococcus ; representatives of the most closely related genera and a number of other bacterial species. This method could therefore be used to identify this species which can infect the lungs or other organs of horses, pigs, humans and other animals.     

Comparative Leaf Epidermal Anatomy of Mutants of Barley (Hordeum vulgare L. 'Himalaya') which Differ in Leaf Length

We wished to determine the nature of differences in epidermalcell numbers and dimensions between leaves of different lengthin mutants of barley (Hordeum vulgare L. ‘Himalaya’).Three comparisons were made: leaf one (L1)vs. leaf four (L4);wild typevs. nine dwarf mutants and wild typevs. a slender mutant.L1 was shorter than L4, and for most lines this was associatedwith a change in epidermal cell number for the blade, and inboth cell number and length for the sheath. Compared to wildtype, the smaller leaves of dwarf plants generally had shorterand fewer cells in both blade and sheath. The blade of slenderplants was the same length (L1) or longer (L4) than wild type,while the sheath was longer than that of wild type for bothL1 and L4. Slender plants had longer but fewer cells than thewild type along the blade of L1, and shorter but more cellsfor the blade of L4. In the sheath, slender plants had longerand more (L1) or fewer (L4) cells than did the wild type. ForL1, variation in blade width amongst the barley lines was associatedwith a change in file width and file number. For L4, blade widthvaried only with file number, except for slender plants wherenarrow blades were associated with reduced file width. Hencethere was no consistent correlation between changes in cellsize or cell (or file) number with changes in leaf length orwidth. Differences depended on the leaf (L1vs. L4), leaf part(bladevs. sheath), and the nature of the mutation (dwarfvs.slender). Barley (Hordeum vulgare L. ‘Himalaya’); leaf epidermis; dwarf mutant; slender mutant     

Establishment of ectomycorrhizae on the roots of two species of Eucalyptus from fungal spores contained in the faeces of the long-nosed potoroo (Potorous tridactylus)

Abstract The long-nosed potoroo (Potorous tridactylus), a medium-sized, ground-dwelling marsupial, inhabits the foothills and coastal forests of southeastern mainland Australia. Faecal analysis confirmed the mycophagous habit of P. tridactylus at a eucalypt forest site in East Gippsland, Victoria; in one month, the spores of 33 different fungi were identified. The majority of species (27) were hypogeal or subhypogeal gasteromycetes that form ectomycorrhizae with forest trees and shrubs, and included the widespread and common Mesophellia pachytrix. The possible role of mycophagy in establishment of eucalypt-fungal mycorrhizae was investigated in several ways. Fungal spores were viable after passage through the gut of P. tridactylus; application of spore-bearing faeces to seedlings of Eucalyptus sieberi and Eucalyptus globoidea grown in sterile soil produced ectomycorrhizae. Spores of M. pachythrix were among the most common spores in these faeces and some of the resulting ectomycorrhizae were of the type expected from M. pachythrix. In contrast, direct application of M. pachythrix spores from sporocarp tissue to seedlings produced no ectomycorrhizae. Ectomycorrhizae also were established on seedlings grown in unsterilized forest soil, indicating that soil-borne spores had been conditioned, either by passage through the gut of a mammal or some other means, for reaction with the roots of eucalypts. Addition of faeces improved root and shoot growth of seedlings, although we could not determine whether this was primarily due to the formation of ectomycorrhizae, the addition of nutrients in the faeces, or a combination of both. Potorous tridactylus may enhance the re-establishment of mycorrhizal colonies in logged and/or burned forest sites by dispersing in its faeces, the spores of mycorrhizal fungi from sporocarps consumed within the disturbed area, as well as spores from sporocarps eaten in adjacent undisturbed habitat. In performing this function, P. tridactylus may also aid in the recovery of regenerating silvertop ash-stringybark forests.     

The oligomerization of a family of four genetically clustered human gastrointestinal mucins

Mucins are synthesized and secreted by many epithelia. They are complex glycoproteins that offer cytoprotection. In their functional configuration, mucins form oligomers by a biosynthetic process that is poorly understood. A family of four human gastrointestinal mucin genes (MUC2, MUC5AC, MUC5B, and MUC6) is clustered to chromosome 11p15.5. To study oligomerization of these related mucins, we performed metabolic labeling experiments with [35S]amino acids in LS174T cells, and isolated mucin precursors by specific immunoprecipitations that were analyzed on SDS-PAGE. Each of the precursors of MUC2, MUC5AC, MUC5B, and MUC6 formed a single species of disulfide-linked homo-oligomer within 1 h after pulse labeling. Based on apparent molecular masses, these oligomeric precursors were most likely dimers. Inhibition of vesicular RER-to-Golgi transport, with brefeldin A and CCCP, did not affect the dimerization of MUC2 precursors, localizing dimerization to the RER. O-Glycosylation of MUC2 followed dimerization. Inhibition of N- glycosylation by tunicamycin retarded, but did not inhibit, dimerization, indicating that N-glycans play a role in efficient dimerization of MUC2 precursors. Based on sequence homology, the ability of MUC2, MUC5AC, MUC5B and MUC6 to dimerize most likely resides in their C-terminal domains. Thus, the RER-localized dimerization of secretory mucins likely proceeds by similar mechanisms, which is an essential step in the formation of the human gastrointestinal mucus- gels.