Frugivory and seed dispersal by vertebrates in the Oriental (Indomalayan) Region

Current knowledge of frugivory and seed dispersal by vertebrates in the Oriental Region is summarized. Some degree of frugivory has been reported for many fish and reptile species, almost half the genera of non-marine mammals and more than 40% of bird genera in the region. Highly frugivorous species, for which fruit dominates the diet for at least part of the year, occur in at least two families of reptiles, 12 families of mammals and 17 families of birds. Predation on seeds in fleshy fruits is much less widespread taxonomically: the major seed predators are colobine monkeys and rodents among the mammals, and parrots, some pigeons, and finches among the birds. Most seeds in the Oriental Region, except near its northern margins, are dispersed by vertebrate families which are endemic to the region or to the Old World. Small fruits and large, soft fruits with many small seeds are consumed by a wide range of potential seed dispersal agents, including species which thrive in small forest fragments and degraded landscapes. Larger, bigger-seeded fruits are consumed by progressively fewer dispersers, and the largest depend on a few species of mammals and birds which are highly vulnerable to hunting, fragmentation and habitat loss.     

Host plant effects on the performance of the aphid Aulacorthum solani (Kalt.) (Homoptera: Aphididae) at ambient and elevated CO2

In future elevated CO₂ environments, chewing insects are likely to perform less well than at present because of the effects of increased carbon fixation on their host plants. When the aphid, Aulacorthum solani was reared on bean ( Vicia faba ) and tansy ( Tanacetum vulgare ) plants under ambient and elevated CO_2, performance was enhanced on both hosts at elevated CO₂. The nature of the response was different on each plant species suggesting that feeding strategy may influence an insect's response to elevated CO₂. On bean, the daily rate of production of nymphs was increased by 16% but there was no difference in development time, whereas on tansy, development time was 10% shorter at elevated CO₂ but the rate of production of nymphs was not affected. The same aphid clone therefore responded differently to elevated CO₂ on different host plants. This increase in aphid performance could lead to larger populations of aphids in a future elevated CO₂ environment.     

Euphorine phylogeny: the evolution of diversity in host-utilization by parasitoid wasps (Hymenoptera: Braconidae)

ABSTRACT.

• 1 New data on the phylogeny of the braconid subfamily Euphorinae supports the hypothesis that parasitism of adult insects by Euphorinae originated during parasitism of Chrysomelidae, a group whose larvae are ecologically coincident with adults.
• 2 Evolution of the habit of attacking the adult stage opened a new adaptive zone; subsequently the Euphorinae have diversified on to a phylogenetically greater variety of hosts than any other braconid subfamily.
• 3 Parasitism of eumastacid grasshoppers evolved from beetle parasitism in the tribe Perilitini.
• 4 The tribe Euphorini shows the greatest diversity of hosts utilized. Most attack Heteroptera; however, Chrysopopthorus diversified on to adult Chrysopidae, Euphoriella on to Psocoptera, and Cryptoxilos on to Scolytidae.
• 5 Parasitism of bark beetles (Scolytidae) has evolved independently in three genera: Cosmophorus, Cryptoxilos and Ropalophorus. This is the most specialized form of beetle parasitism by euphorines, since it involves direct parasitism of concealed hosts.
• 6 Parasitism of adult hymenopterans by the tribe Syntretini may be related to attacking hosts while they are foraging at flowers.
• 7 The pattern of diversification in the Euphorinae indicates several adaptive radiations within host orders, as well as a history of major host-shifts between phylogenetically distantly-related host groups: Coleoptera to Orthoptera; Coleoptera to Hymenoptera; Coleoptera to Heteroptera; Heteroptera to Neuroptera, Psocoptera, and back to Coleoptera. Both the‘host taxonomy’and‘host habitat’hypotheses of host-shifting are supported. Host-shifts have involved hosts occurring in the same micro-habitat and usually having similar feeding habits. This is consistent with current theory of host-location by means of host-produced kairomones and visual cues.

     

A Survey of Lectin Binding in Paramecium1

To better understand the general distribution of glycoproteins and the distribution of specific glycoprotein-bound sugar residues in Paramecium, a survey of the binding pattern of selected lectins was carried out in P. tetraurelia, P. caudatum, and P. multimicronucleatum. Lectins studied were concanavalin A (Con A), Griffonia simplicifolia agglutinins I and II (GS I and GS II), wheat germ agglutinin (WGA), Ulex europaeus (UEA I), peanut agglutinin (PNA), Ricinis communis toxin (RCA₆₀) and agglutinin (RCA₁₂₀), soybean agglutinin (SBA), Bauhinia purpurea agglutinin (BPA), Dolichos biflorus agglutinin (DBA), and Maclura pomifera agglutinin (MPA). Those giving the most distinctive patterns were Con A, GS II, WGA, UEA I, and PNA. No significant differences were found between the three species. Concanavalin A, a mannose/glucose-binding lectin, diffusely labeled the cell surface and cytoplasm and, unexpectedly, the nuclear envelopes. Events of nuclear division, and nuclear size and number were thus revealed. Both WGA and GS II, which are N-acetylglucosamine-binding lectins, labeled trichocyst tips, the cell surface, and the oral region, revealing stages of stomatogenesis. The lectin WGA, in addition, labeled the compartments of the phagosome-lysosome system. The lectin PNA, an N-acetyl galactosamine/galactose-binding protein, was very specific for digestive vacuoles. Finally, UEA I, a fucose-binding lectin, brightly labeled trichocysts, both their tips and body outlines. We conclude that a judicious choice of lectins can be used to localize glycoproteins and specific sugar residues as well as to study certain events of nuclear division, cellular morphogenesis, trichocyst discharge, and events in the digestive cycle of Paramecium.     

Effects of fungicide spray regimes on incidence of dicarboximide resistance in grey mould (Botrytis cinerea) on strawberry plants

In tunnel experiments, the efficacy of dicarboximide sprays in controlling grey mould of strawberries was greatly decreased by the presence of dicarboximide-resistant forms of Botrytis cinerea. The use of dichlofluanid, as a tank-mix or in an alternating programme, with a dicarboximide fungicide, procymidone, helped to maintain the efficacy of disease control but failed to prevent an increase in the proportion of dicarboximide-resistant forms of the pathogen. Alternative ‘partner’ fungicides (thiram, chlorothalonil) delayed build-up of resistance to dicarboximides. Build-up of resistance was absent or relatively small in unsprayed plots. Application of dichlofluanid alone was always associated with a substantial increase in dicarboximide resistance, although less than in procymidone-treated plots. Monitoring dicarboximide resistance in the tunnels during the winter, when no further sprays were applied, revealed a gradual decline in the proportion of dicarboximide-resistant forms in all previously treated plots. In laboratory studies on inoculated leaf debris, dichlofluanid treatment induced the build-up of dicarboximide-resistant forms of B. cinerea. Leaf-disc tests revealed cross-resistance of dicarboximide-resistant isolates towards dichlofluanid but not towards thiram or chlorothalonil. Dichlofluanid is widely used for control of B. cinerea and the implications of these results for the practical management of dicarboximide resistance in this pathogen are discussed.     

An outline of a revised classification of Saxifraga L.

GORNALL, R. J., 1987. An outline of a revised classification of Saxifraga. A revised classification of Saxifraga is presented in which 15 sections, 19 subsections and 34 series are recognized. A total of 394 names are accounted for, including the following new taxa, combinations and names: series Hirculoideae (Engler & Irmscher) Gornall, stat. nov.; series Lychnitidae (Engler & Irmscher) Gornall, stat. nov.; series Nulanles (Engler & Irmscher) Gornall, stat. nov.; series Cinctae (H. Sm.) Gornall, stat. nov.; series Gemmiparae (Engler & Irmscher) Gornall, stat. nov.; series Spinulosae (C. B. Clarke) Gornall, stat. nov.; subsection Rosulares Gornall, nom. nov.; subsection Serpyllifoliae Gornall, subscct. nov.; subsection Hemisphaericae (Engler & Irmscher) Gornall, stat. nov.; section Merkianae (Engler & Irmscher) Gornall, stat. nov.; subsection Stellares (Engler & Irmscher) Gornall, stat. nov.; series Birostres Gornall, ser. nov.; series Melanocentrae (Engler & Irmscher) Gornall, stat. nov.; series Astasianlhes (Sternberg) Gornall, stat. nov.; subsection Micranthes (Haworth) Gornall, stat. nov.; series Aulaxis (Haworth) Gornall, stat. nov.; series Dermasea (Haworth) Gornall, stat. nov.; series Micranthes (Haworth) Gornall, stat. nov.; scries Aretioideae (Engler & Irmscher) Gornall, stat. nov.; series Juniperifoliae (Engler & Irmscher) Gornall, stat. nov.; series Lilacinae Gornall, ser. nov.; series Marginatae (Engler & Irmscher) Gornall, stat. nov.; series Squarrosae (Engler & Irmscher) Gornall, stat. nov.; series Rigidae (Engler & Irmscher) Gornall, stat. nov.; subsection Engleria (Siindermann) Gornall, stat. nov; series Subsessiliflorae Gornall, ser. nov.; series Oppositiofoliae (Hayek) Gornall, stat. nov.; series Tetrameridium (Engler) Gornall, stat. nov.; subsection Mutatae (Engler & Irmscher) Gornall, stat. nov.; subsection Florulentae (Engler & Irmscher) Gornall, stat. nov.; section Odontophyllae Gornall, sect, nov.; series Biternatae (Engler & Irmscher) Gornall, stat. nov.; subsection Triplinervium (Gaudin) Gornall, stat. nov.; series Arachnoideae (Engler & Irmscher) Gornall, stat. nov.; subsection Tridactylites (Haworth) Gornall, stat. nov.     

Sexual dimorphism in snake tail length: sexual selection,natural selection,or morphological constraint?

Male snakes typically have longer tails relative to body length than females, but the extent of this dimorphism varies among species. Three hypotheses have been suggested to explain tail dimorphism. The Morphological Constraint Hypothesis proposes that males have relatively longer tails to accommodate hemipenes and retractor muscles. The Female Reproductive Output Hypothesis proposes that females have relatively shorter tails as a secondary result of natural selection for increased reproductive capacity. The Male Mating Ability Hypothesis proposes that sexual selection favours relatively longer tails in males during courtship. These hypotheses make different predictions about the relationships among tail length, body size, male reproductive morphology, female reproductive output, mode of reproduction, and male mating behaviour among and within taxa. Predictions were tested using published data for 56 genera in the family Colubridae and original data for the water snake, Nerodia sipedon. Tail length dimorphism was more male-biased in tam having relatively short tails (r=–0.52, P < 0.001), hemipenes and retractor muscles occupied a greater proportion of the tail in taxa having relatively short tails (r=– 0.71, P < 0.00l and r=– 0.66, P = 0.001, respectively), and tail length dimorphism was more male-biased in taxa in which body size dimorphism was more female-biased (r=– 0.60, P < 0.001). These results support both the Morphological Constraint Hypotheses and the Female Reproductive Output Hypothesis. However, tests of other predictions, including those regarding patterns within N. sipedon , failed to support any of the three hypotheses. Comparisons among taxa suggest several species in which further tests of these hypotheses would be especially appropriate.