Effects of pirimicarb, dimethoate and benomyl on natural enemies of cereal aphids in winter wheat

The insecticides, pirimicarb and dimethoate are commonly applied to cereal crops in the UK and when this study was begun the fungicide benomyl was also regularly used. The effects of these chemicals on natural enemies of cereal aphids were examined in replicated plots of winter wheat. Benomyl did not affect any of the groups examined but it was applied early in the season (April/May) when most natural enemies were few or absent from the crop. Numbers of carabid beetles, staphylinid beetles and spiders, sampled using pitfall traps and a vacuum net sampler, were all reduced by dimethoate but not by pirimicarb, although these effects were only detected by pitfall traps when the small plots were surrounded by polyethylene barriers to prevent inter-plot movements. Parasitic Hymenoptera were decreased by both insecticides, partly due to direct toxicity and partly to host removal. Data on the aphid predators, Coccinellidae, Syrphidae and Chrysopidae were inconclusive because there were very few in the crop due to the scarcity of aphids. Ways in which pesticides can affect natural enemy populations other than by direct mortality and the dangers associated with routine, prophylactic pesticide applications are discussed.     

Comparative floral structure and systematics of Pelagodoxa and Sommieria (Arecaceae)

Floral structure is compared in Pelagodoxa and Sommieria (Arecaceae, Arecoideae). Male flowers have three free, imbricate sepals, three basally congenitally united and apically valvate petals, and six stamens. Anthers are dorsifixed and dehiscence introrse. The sterile gynoecium is tricarpellate. Female flowers have three free, imbricate sepals and three free, imbricate petals, which are slightly fused with the sepals at the base. Four to six staminodes are congenitally united at the base and fused with the ovary for a short distance. The gynoecium is syncarpous. Carpels are almost equal in early development; later the gynoecium becomes pseudomonomerous. The three stigmatic branches are equally developed, apical and sessile. The carpels are (syn-)ascidiate up to the level of the placenta and (sym-)plicate above. Each carpel has one ovule, in the sterile carpels it is aborted at anthesis. The fertile ovule is erect up to anthesis and pendant afterwards because of the bulging out of the ovary. Pollen tube transmitting tracts (PTTT) encompass the secretory epidermis of the ventral slits of each carpel. Floral structure in Pelagodoxa and Sommieria supports the sister group relationship between the two genera suggested in recent molecular phylogenies and reflects their close relationships to a major clade of pseudomonomerous arecoid palms from the Indo-Pacific region.  © 2004 The Linnean Society of London, Botanical Journal of the Linnean Society , 2004, 146 , 27–39.     

Are altitudinal limits of equatorial stream insects reflected in their respiratory performance?

1. We measured respiration of the larvae of aquatic insects from streams in the Ecuadorian Andes in relation to oxygen saturation at 5, 8, 11, 14 and 17 °C. Polycentropus (Polycentropodidae), Lachlania (Oligoneuriidae), Anchytarsus (Ptilodactylidae) and Anacroneuria (Perlidae) represented genera absent from the highest altitudes, reaching 2720, 2930, 3120, 3450 m a.s.l., respectively, while Claudioperla (Gripopterygidae) and Anomalocosmoecus (Limnephilidae) occurred only above 2900 m a.s.l. Our purpose was to determine whether natural altitudinal limits were reflected in physiological critical points on respiration versus oxygen curves and by the effect of temperature on the ability to oxy‐regulate. 2. For all six genera, respiration was affected by oxygen saturation and temperature. Respiration (mg O₂ g⁻¹ AFDM h⁻¹) at 70% oxygen saturation (Michaelis–Menten fitted) varied from 2.6 to 7.6 between genera at 17 °C, and from 1.3 to 2.5 at 5 °C. Q₁₀ values for this temperature interval ranged 1.5–2.9 (mean 2.3). The two “high‐altitude” genera had higher respiration rates at low temperature and oxygen saturation, and their respiration rate saturated at lower temperatures, than three of the four “low‐altitude” genera. 3. The oxy‐regulatory capacity (critical points and initial decrease in respiration versus oxygen regressions) varied among genera and was affected by temperature. Lachlania, Claudioperla and Anomalocosmoecus had a higher ability to oxy‐regulate at low than at high temperatures, Anacroneuria was not clearly affected by temperature, while Polycentropus and Anchytarsus had a greater oxy‐regulatory capacity at high than at low temperature. These results indicate that the ability to oxy‐regulate is related to the temperature (altitude) at which species naturally occur. 4. Upper altitudinal limits of the six genera were not reflected in their respiratory performance, because all genera had critical minima of temperature and oxygen saturation much lower than those occurring at the limits of their natural distribution. So, the altitudinal limit could not be attributed to absolute short‐term physiological tolerance of low temperature and oxygen concentration. 5. Multiple regressions (based on respiration experiments and previously obtained relationships between water temperature, oxygen saturation and altitude) were used to predict how respiration rates should vary with altitude. At the upper limit of the four “low‐altitude” genera, respiration rates were 50–68% of those predicted at the centre of the range. With an arbitrary increase of 400 m above the actual limit, the effect of temperature would be a 13% decrease, and that of oxygen a 2% decrease, in respiration rate of Polycentropus, Lachlania and Anacroneuria, while respiration in Anchytarsus would be reduced by 5% by both factors. 6. It seems that, while the immediate decrease in respiration with increased altitude is caused mainly by a decrease in temperature, the long‐term survival of a species at given altitudes might be more affected by oxygen saturation. Further quantitative and long‐term studies on survival and recruitment in populations and communities are needed to determine the importance of temperature and oxygen for altitudinal limits of aquatic insects.     

Six cryptic species on a single species of host plant: morphometric evidence for possible reproductive character displacement

Abstract 1. Diversification of some highly host‐specific herbivorous insects may occur in allopatry, without shifts in host use. Such allopatric divergence may be accelerated by sexual selection operating on courtship displays. Wing size and shape may affect visual and vibrational courtship displays in tephritid fruit flies. Geometric morphometric methods were used to examine wings of six sympatric cryptic species in the neotropical genus Blepharoneura. All six species feed on flowers of the same species of host (Gurania spinulosa), a neotropical vine in the Cucurbitaceae. Three of the fly species court and mate in close proximity on the host. Thus, courtship behaviours could serve as important reproductive isolating mechanisms. Two sets of hypotheses were tested: (i) species differ in wing shape and wing size; and (ii) species are sexually dimorphic in wing size and wing shape. Wing size differed among a few species, but wing shape differed significantly among all six species. Sexual dimorphism in wing size was found in only one species, but sexual dimorphism in wing shape was found in two of the three species known to court on the same host plant. In the two sexually dimorphic species, wing shape differed among males, but not among females. This suggests that selection for reproductive character displacement might accelerate divergence in wing shape.     

Floral structure in Licuala peltata (Arecaceae: Coryphoideae) with special reference to the architecture of the unusual labyrinthine nectary

The structure and late development of the flowers of the South‐East Asian bee‐pollinated palm Licuala peltata are described with special focus on the architecture of the unusual labyrinthine nectaries. The nectaries are derived from septal nectaries by extensive convolution of the carpel flank surfaces below the ovary throughout the inner floral base, thus also encompassing the inner surface of the corolla–androecium tube. A comparison with septal nectaries elsewhere in Arecaceae and with labyrinthine nectaries in other monocots shows that labyrinthine nectaries situated below the ovary, as described here, are not known from any other palms, but are similar to those of a few Bromeliaceae and, less strongly convoluted, some Haemodoraceae and Xanthorrhoeaceae. In addition, the substantial participation of parts other than the gynoecium in the nectary architecture of Licuala appears unique at the level of monocots. © 2009 The Linnean Society of London, Botanical Journal of the Linnean Society, 2009, 161 , 66–77.