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Bruchid Beetles (bruchid + beetle)
Selected AbstractsThe Effect of Dung and Dispersal on Postdispersal Seed Predation of Attalea phalerata (Arecaceae) by Bruchid Beetles,BIOTROPICA, Issue 6 2006Rodrigo S. Rios ABSTRACT Low postdispersal mortality of palm seeds in tapir dung is hypothesized to result from the mechanical barrier provided by dung against bruchid infestation and/or from the distance to adult palms at which seeds are dispersed. We tested these hypotheses by distributing endocarps of Attalea phalerata Mart. ex Spreng. in experimental dung piles in Beni, Bolivia. Predation rates were significantly lower for seeds covered by dung than for exposed or partially covered seeds, but did not differ between seeds placed below and 50 m away from palms. Thus, dung, not short-distance dispersal, protects seeds against bruchid beetles, and may ultimately promote survival of palm seeds. RESÚMEN La baja mortalidad post dispersión de las semillas de la palmera Attalea phalerata Mart. ex Spreng. encontrada en heces de tapir puede ser el resultado de la barrera mecánica que brinda la materia fecal contra la infestación por brúquidos y/o de la distancia a la que son dispersadas las semillas. Pusimos a prueba estas hipótesis distribuyendo endocarpos de A. phalerata en pilas fecales experimentales en el Beni, Bolivia. Las tasas de depredación fueron significativamente menores en semillas completamente cubiertas por materia fecal que en semillas limpias o parcialmente recubiertas, pero no variaron entre semillas debajo y a 50 m de las palmeras madre. Por lo tanto, las heces y no la dispersión de corta distancia protegen a las semillas de brúquidos, promoviendo así la sobrevivencia de semillas. [source] Population Variability and Extinction RiskCONSERVATION BIOLOGY, Issue 6 2000John A. Vucetich We resolve this conflict by attributing negative measured relationships to a statistical artifact that arises because PV tends to be underestimated for populations with short persistence. Such populations do not go extinct quickly as a consequence of low intrinsic variability; instead, the measured variability is low because they go extinct so quickly. Consequently, any underlying positive relationship between PV and ER tends to be obscured. We conducted a series of analyses to evaluate this claim. Simulations showed that negative measured relationships are to be expected, despite an underlying positive relationship. Simulations also identified properties of data, minimizing this bias and thereby permitting meaningful analysis. Experimental data on laboratory populations of a bruchid beetle (Callosobruchus maculatus) supported the simulation results. Likewise, with an appropriate statistical approach (Cox regression on untransformed data), reanalysis of a controversial data set on British island bird populations revealed a significant positive association between PV and ER (p = 0.03). Finally, a similar analysis of time series for naturally regulated animal populations revealed a positive association between PV and quasiextinction risk (p < 0.01). Without exception, our simulation results, experimental findings, reanalysis of published data, and analysis of quasiextinction risk all contradict previous reports of negative or equivocal relationships. Valid analysis of meaningful data provides strong evidence that increased population variability leads to increased extinction risk. Resumen: Los modelos poblacionales generalmente predicen un mayor riesgo de extinción (ER) al aumentar la variabilidad poblacional ( PV ,), a pesar de ello, algunas pruebas empíricas han proporcionado resultados contradictorios. Nosotros hemos resuelto este conflicto mediante la atribución de mediciones de relaciones negativas a un producto estadístico que surge debido a que la PV tiende a ser subestimada para poblaciones de persistencia corta. Estas poblaciones no se extinguen rápidamente como resultado de una variabilidad intrínseca baja; por lo contrario, la variabilidad medida es baja debido a que las poblaciones se extinguen tan rápidamente. Consecuentemente, cualquier relación positiva subyacente entre la PV y el ER tienden a ser opacadas. Llevamos a cabo una serie de análisis para evaluar este argumento. Las simulaciones mostraron que las relaciones negativas medidas son de esperarse, a pesar de una relación positiva subyacente. Las simulaciones también identificaron propiedades de los datos que minimizan este sesgo y por lo tanto permiten un análisis significativo. Los datos experimentales en poblaciones de laboratorio de un coleóptero bruchidae (Callosobruchus maculatus) respaldan los resultados de las simulaciones. De la misma manera, el uso de una técnica estadística adecuada (por ejemplo, la regresión Cox en datos sin transformar), usada en la repetición del análisis de un juego de datos controvertidos de poblaciones de aves de la Isla Británica reveló una asociación positiva significativa entre la PV y el ER (p = 0.03). Finalmente, un análisis similar de series de tiempo para poblaciones de animales reguladas de manera natural revelaron una asociación positiva entre la PV y el riesgo de cuasi-extinción (p < 0.01). Sin excepciones, nuestros resultados de simulaciones, los resultados experimentales, la repetición del análisis de datos publicados, y el análisis de riesgo de cuasi-extinción contradicen informes previos de relaciones negativas o equívocas. Los análisis válidos de datos significativos proveen una evidencia sólida de que los incrementos en la variabilidad poblacional conducen a un incremento en el riego de extinción. [source] Pulp handling by vertebrate seed dispersers increases palm seed predation by bruchid beetles in the northern AmazonJOURNAL OF ECOLOGY, Issue 6 2002Kirsten M. Silvius Abstract 1The simultaneous use of fruits and seeds by invertebrate seed predators and vertebrate seed dispersers produces complex ecological interactions that reduce the predictability of seed fate. 2Cocosoid palm seeds in the Neotropics are subject to high mortality by bruchid beetle infestation and such attack is the major cause of mortality for seeds of the palm Attalea maripa at our study site in the northern Brazilian Amazon. 3The exocarp and mesocarp of 1400 fruits were manipulated in different ways to simulate handling by vertebrates. No eggs of the bruchid beetle, Pachymerus cardo, were laid on intact control fruits, while the highest numbers of eggs were received by fruits whose exocarp and mesocarp had been partially removed, as if by primates and rodents (mean of 15.9 and 18.9 eggs fruit,1, respectively, during the peak fruiting season). Fruits with intact mesocarp but no exocarp, and fruits with all mesocarp and exocarp removed, received low numbers of eggs (mean of 4.6 and 6.6 eggs per fruit, respectively, during the peak fruiting season). Thus both exocarp and mesocarp deter oviposition, and removal of these fruit structures increases fruit susceptibility to infestation. 4Oviposition rates declined as the fruiting season progressed, but oviposition preferences remained the same. Seed mortality was high for any fruit on which eggs were laid. 5Large rodents and primates, which have been considered among the most effective seed dispersers for large-seeded Neotropical trees such as palms, actually increased the susceptibility of seeds to bruchid beetle attack. Removal of (intact) seeds by other dispersers may be necessary to ensure seed survival. 6These results indicate that the reliability of seed dispersers cannot be gauged without a complete understanding of variables that affect seed viability. [source] Effects of maternal age on reproductive traits and fitness components of the offspring in the bruchid beetle, Callosobruchus chinensis (Coleoptera: Bruchidae)PHYSIOLOGICAL ENTOMOLOGY, Issue 4 2002Shin-Ichi Yanagi Abstract. In many insect species, the size and number of eggs decrease with maternal age. Thus, both the size and number of eggs must be considered to know the exact cost of reproduction with maternal age. The resource depletion hypothesis was examined in the bruchid beetle Callosobruchus chinensis. The hypothesis explains why the egg size decreases with maternal age based on the decline of the female's reproductive capacity. A decrease was found in reproductive effort (= egg size × the number of eggs) and the fitness component of offspring with maternal age. The effects of the female's nutritional status on the relationship between maternal age and the reproductive effort of females with and without food and water were also examined. The results indicate that the decrease in size and number of eggs with maternal age can be explained by the resource depletion hypothesis in C. chinensis. [source] Overcompensatory population dynamic responses to environmental stochasticityJOURNAL OF ANIMAL ECOLOGY, Issue 6 2008James C. Bull Summary 1To quantify the interactions between density-dependent, population regulation and density-independent limitation, we studied the time-series dynamics of an experimental laboratory insect microcosm system in which both environmental noise and resource limitation were manipulated. 2A hierarchical Bayesian state-space approach is presented through which it is feasible to capture all sources of uncertainty, including observation error to accurately quantify the density dependence operating on the dynamics. 3The regulatory processes underpinning the dynamics of two different bruchid beetles (Callosobruchus maculatus and Callosobruchus chinensis) are principally determined by environmental conditions, with fluctuations in abundance explained in terms of changes in overcompensatory dynamics and stochastic processes. 4A general, stochastic population model is developed to explore the link between abundance fluctuations and the interaction between density dependence and noise. Taking account of time-lags in population regulation can substantially increase predicted population fluctuations resulting from underlying noise processes. [source] The role of rainfall and predators in determining synchrony in reproduction of savanna trees in Serengeti National Park, TanzaniaJOURNAL OF ECOLOGY, Issue 1 2007SIMON A. R. MDUMA Summary 1We examined the factors determining synchrony in reproduction in nine Acacia and six other tree species in the Serengeti ecosystem. 2We test two hypotheses: (i) an abiotic hypothesis where the primary determinant of synchrony is an adaptation to water availability; and (ii) biotic hypotheses where these adaptations to water can be further refined by additional adaptations to avoid predators, or attract seed and fruit dispersers. 3Flowering and fruiting were recorded monthly for individually marked trees during 1997,2004. Flowering in different species occurs semi-annually, annually or, in the case of one species, once every 2 years. For most species synchrony of flowering was correlated with seasonal rainfall, with lags related to the mean height of the species; small species flowered during the rains while larger species flowered in the dry season. Fruiting seasons occurred at the end of the rains irrespective of the flowering season. 4Most species showed flowering synchrony greater than expected from the distribution of rainfall. This may be related to avoidance of insect seed predators through predator satiation. Two Acacias showed multi-annual fruiting (masting), possibly as a predator avoidance mechanism. Acacia tortilis has two flowering seasons: a dry season flowering with early abortion of pods and a wet season flowering producing successful fruits. 5Two species of Commiphora appeared to be synchronized so as to attract birds that disperse seeds. Acacia tortilis produced indehiscent pods attractive to ungulates, possibly to kill bruchid beetles during digestion and so increase seed viability. 6Our results suggest that synchrony in these trees is caused by a strong interaction between abiotic and biotic factors. Closely related species have different reproductive patterns of synchrony that seem to be adapted to different combinations of rainfall, predators and dispersers. Rainfall is the primary determinant but the activities of predators and dispersers increase the degree of synchrony. [source] Pulp handling by vertebrate seed dispersers increases palm seed predation by bruchid beetles in the northern AmazonJOURNAL OF ECOLOGY, Issue 6 2002Kirsten M. Silvius Abstract 1The simultaneous use of fruits and seeds by invertebrate seed predators and vertebrate seed dispersers produces complex ecological interactions that reduce the predictability of seed fate. 2Cocosoid palm seeds in the Neotropics are subject to high mortality by bruchid beetle infestation and such attack is the major cause of mortality for seeds of the palm Attalea maripa at our study site in the northern Brazilian Amazon. 3The exocarp and mesocarp of 1400 fruits were manipulated in different ways to simulate handling by vertebrates. No eggs of the bruchid beetle, Pachymerus cardo, were laid on intact control fruits, while the highest numbers of eggs were received by fruits whose exocarp and mesocarp had been partially removed, as if by primates and rodents (mean of 15.9 and 18.9 eggs fruit,1, respectively, during the peak fruiting season). Fruits with intact mesocarp but no exocarp, and fruits with all mesocarp and exocarp removed, received low numbers of eggs (mean of 4.6 and 6.6 eggs per fruit, respectively, during the peak fruiting season). Thus both exocarp and mesocarp deter oviposition, and removal of these fruit structures increases fruit susceptibility to infestation. 4Oviposition rates declined as the fruiting season progressed, but oviposition preferences remained the same. Seed mortality was high for any fruit on which eggs were laid. 5Large rodents and primates, which have been considered among the most effective seed dispersers for large-seeded Neotropical trees such as palms, actually increased the susceptibility of seeds to bruchid beetle attack. Removal of (intact) seeds by other dispersers may be necessary to ensure seed survival. 6These results indicate that the reliability of seed dispersers cannot be gauged without a complete understanding of variables that affect seed viability. [source] The Effect of Dung and Dispersal on Postdispersal Seed Predation of Attalea phalerata (Arecaceae) by Bruchid Beetles,BIOTROPICA, Issue 6 2006Rodrigo S. Rios ABSTRACT Low postdispersal mortality of palm seeds in tapir dung is hypothesized to result from the mechanical barrier provided by dung against bruchid infestation and/or from the distance to adult palms at which seeds are dispersed. We tested these hypotheses by distributing endocarps of Attalea phalerata Mart. ex Spreng. in experimental dung piles in Beni, Bolivia. Predation rates were significantly lower for seeds covered by dung than for exposed or partially covered seeds, but did not differ between seeds placed below and 50 m away from palms. Thus, dung, not short-distance dispersal, protects seeds against bruchid beetles, and may ultimately promote survival of palm seeds. RESÚMEN La baja mortalidad post dispersión de las semillas de la palmera Attalea phalerata Mart. ex Spreng. encontrada en heces de tapir puede ser el resultado de la barrera mecánica que brinda la materia fecal contra la infestación por brúquidos y/o de la distancia a la que son dispersadas las semillas. Pusimos a prueba estas hipótesis distribuyendo endocarpos de A. phalerata en pilas fecales experimentales en el Beni, Bolivia. Las tasas de depredación fueron significativamente menores en semillas completamente cubiertas por materia fecal que en semillas limpias o parcialmente recubiertas, pero no variaron entre semillas debajo y a 50 m de las palmeras madre. Por lo tanto, las heces y no la dispersión de corta distancia protegen a las semillas de brúquidos, promoviendo así la sobrevivencia de semillas. [source] | ||||||||||