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1.
Ecology ; 97(6): 1381-7, 2016 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-27459769

RESUMEN

Temporal variability in the distribution of feeding links in a food web can be an important stabilizing factor for these complex systems. Adaptive foraging and prey choice have been hypothesized to cause this link flexibility as organisms adjust their behavior to variation in the prey community. Here, we analyze a 10-yr time series of monthly aphid-parasitoid-secondary-parasitoid networks and show that interaction strengths for polyphagous secondary parasitoids are generally biased toward the larger host species within their fundamental niche; however, in months of higher competition for hosts, size-based biases are reduced. The results corroborate a previous hypothesis stating that host selectivity of parasitoids should be correlated to the relative likelihood of egg limitation vs. time limitation. Our results evince adaptation of foraging behavior to varying conditions affects the distribution of host-parasitoid link strengths, where link-rewiring may be integral to stability in complex communities.


Asunto(s)
Áfidos/parasitología , Ambiente , Conducta Alimentaria , Cadena Alimentaria , Avispas/fisiología , Animales , Tamaño Corporal , Interacciones Huésped-Parásitos , Modelos Biológicos , Factores de Tiempo
2.
Mol Ecol ; 17(17): 3928-38, 2008 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-18662231

RESUMEN

Insect parasitoids play a major role in terrestrial food webs as they are highly diverse, exploit a wide range of niches and are capable of affecting host population dynamics. Formidable difficulties are encountered when attempting to quantify host-parasitoid and parasitoid-parasitoid trophic links in diverse parasitoid communities. Here we present a DNA-based approach to effectively track trophic interactions within an aphid-parasitoid food web, targeting, for the first time, the whole community of parasitoids and hyperparasitods associated with a single host. Using highly specific and sensitive multiplex and singleplex polymerase chain reaction, endoparasitism in the grain aphid Sitobion avenae (F) by 11 parasitoid species was quantified. Out of 1061 aphids collected during 12 weeks in a wheat field, 18.9% were found to be parasitized. Parasitoids responded to the supply of aphids, with the proportion of aphids parasitized increasing monotonically with date, until the aphid population crashed. In addition to eight species of primary parasitoids, DNA from two hyperparasitoid species was detected within 4.1% of the screened aphids, with significant hyperparasitoid pressure on some parasitoid species. In 68.2% of the hyperparasitized aphids, identification of the primary parasitoid host was also possible, allowing us to track species-specific parasitoid-hyperparasitoid links. Nine combinations of primary parasitoids within a single host were found, but only 1.6% of all screened aphids were multiparasitized. The potential of this approach to parasitoid food web research is discussed.


Asunto(s)
Áfidos/parasitología , Grano Comestible , Interacciones Huésped-Parásitos/genética , Himenópteros/genética , Animales , Cartilla de ADN , ADN Mitocondrial/genética , Complejo IV de Transporte de Electrones/genética , Cadena Alimentaria , Genes de Insecto , Genética de Población , Haplotipos , Reacción en Cadena de la Polimerasa/métodos , Dinámica Poblacional , Sensibilidad y Especificidad , Alineación de Secuencia , Análisis de Secuencia de ADN , Especificidad de la Especie
3.
J Anim Ecol ; 77(1): 191-200, 2008 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-17986208

RESUMEN

1. Most communities of insect herbivores are unlikely to be structured by resource competition, but they may be structured by apparent competition mediated by shared natural enemies. 2. The potential of three guilds of natural enemies (parasitoids, fungal entomopathogens and predators) to influence aphid community structure through indirect interactions is assessed. Based on the biology, we predicted that the scope for apparent competition would be greatest for the predator and least for the parasitoid guilds. 3. Separate fully quantitative food webs were constructed for 3 years for the parasitoid guild, 2 years for the pathogen guild and for a single year for the predator guild. The webs were analysed using standard food web statistics designed for binary data, and using information-theory-based metrics that make use of the full quantitative data. 4. A total of 29 aphid, 24 parasitoid, five entomopathogenic fungi and 13 aphid specialist predator species were recorded in the study. Aphid density varied among years, and two species of aphid were particularly common in different years. Omitting these species, aphid diversity was similar among years. 5. The parasitoid web showed the lowest connectance while standard food web statistics suggested the pathogen and predator webs had similar levels of connectance. However, when a measure based on quantitative data was used the pathogen web was intermediate between the other two guilds. 6. There is evidence that a single aphid species had a particularly large effect on the structure of the pathogen food web. 7. The predator and pathogen webs were not compartmentalized, and the vast majority of parasitoids were connected in a single large compartment. 8. It was concluded that indirect effects are most likely to be mediated by predators, a prediction supported by the available experimental evidence.


Asunto(s)
Áfidos/microbiología , Áfidos/parasitología , Cadena Alimentaria , Interacciones Huésped-Parásitos , Interacciones Huésped-Patógeno , Animales , Áfidos/fisiología , Ecosistema , Densidad de Población , Dinámica Poblacional , Crecimiento Demográfico , Conducta Predatoria , Estaciones del Año , Especificidad de la Especie
4.
Appl Environ Microbiol ; 69(12): 7216-23, 2003 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-14660369

RESUMEN

The bacterial communities of aphids were investigated by terminal restriction fragment length polymorphism and denaturing gradient gel electrophoresis analysis of 16S rRNA gene fragments generated by PCR with general eubacterial primers. By both methods, the gamma-proteobacterium Buchnera was detected in laboratory cultures of six parthenogenetic lines of the pea aphid Acyrthosiphon pisum and one line of the black bean aphid Aphis fabae, and one or more of four previously described bacterial taxa were also detected in all aphid lines except one of A. pisum. These latter bacteria, collectively known as secondary symbionts or accessory bacteria, comprised three taxa of gamma-proteobacteria (R-type [PASS], T-type [PABS], and U-type [PAUS]) and a rickettsia (S-type [PAR]). Complementary analysis of aphids from natural populations of four aphid species (A. pisum [n = 74], Amphorophora rubi [n = 109], Aphis sarothamni [n = 42], and Microlophium carnosum [n = 101]) from a single geographical location revealed Buchnera and up to three taxa of accessory bacteria, but no other bacterial taxa, in each aphid. The prevalence of accessory bacterial taxa varied significantly among aphid species but not with the sampling month (between June and August 2000). These results indicate that the accessory bacterial taxa are distributed across multiple aphid species, although with variable prevalence, and that laboratory culture does not generally result in a shift in the bacterial community in aphids. Both the transmission patterns of the accessory bacteria between individual aphids and their impact on aphid fitness are suggested to influence the prevalence of accessory bacterial taxa in natural aphid populations.


Asunto(s)
Áfidos/microbiología , Bacterias/clasificación , Variación Genética , Animales , Bacterias/genética , Bacterias/aislamiento & purificación , Buchnera/clasificación , Buchnera/genética , Buchnera/aislamiento & purificación , ADN Ribosómico/análisis , Ecosistema , Electroforesis en Gel de Poliacrilamida/métodos , Fabaceae/parasitología , Pisum sativum/parasitología , Reacción en Cadena de la Polimerasa/métodos , Polimorfismo de Longitud del Fragmento de Restricción , ARN Ribosómico 16S , Análisis de Secuencia de ADN
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