<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Bonal, Raul</style></author><author><style face="normal" font="default" size="100%">Muñoz, Alberto</style></author><author><style face="normal" font="default" size="100%">MARÍA ESPELTA, JOSEP</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Mismatch between the timing of oviposition and the seasonal optimum. The stochastic phenology of Mediterranean acorn weevils</style></title><secondary-title><style face="normal" font="default" size="100%">Ecological Entomology</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">acorn</style></keyword><keyword><style  face="normal" font="default" size="100%">adult emergence</style></keyword><keyword><style  face="normal" font="default" size="100%">Curculio</style></keyword><keyword><style  face="normal" font="default" size="100%">oviposition</style></keyword><keyword><style  face="normal" font="default" size="100%">Phenology</style></keyword><keyword><style  face="normal" font="default" size="100%">stochastic events</style></keyword><keyword><style  face="normal" font="default" size="100%">Temperature</style></keyword><keyword><style  face="normal" font="default" size="100%">timing of reproduction</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2010</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2010///</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1111/j.1365-2311.2010.01178.x</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">35</style></volume><pages><style face="normal" font="default" size="100%">270 - 278</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">1. The timing of reproduction is predicted to match the period of maximum food availability. In this sense, the case of many phytophagous insects in temperate regions is very illustrative, as their larvae usually depend on a resource only available for a limited period of time each year. 2. For 3 years the interactions between the weevil Curculio elephas and the Mediterranean Holm oak Quercus ilex were studied. Weevil larvae grow within the acorns, feeding on the cotyledons. The timing of oviposition will determine food availability for the larvae, as acorns stop growing once they are attacked. 3. Acorn temporal growing patterns did not change between years and food availability for larvae was at its highest in October, when temperature was still suitable for larval development. However, oviposition phenology did change between years. In 2002 females oviposited later, larvae grew within larger acorns, and their body mass was significantly higher than in 2003 or 2004, when females oviposited into early acorns. 4. Thus, weevils do not always adjust oviposition to the best possible feeding conditions for their offspring. Rather, they seem to maximise their own lifetime fitness, ovipositing as soon as they emerge in late summer. Emergence, in turn, depends strongly on stochastic events such as summer storms in the Mediterranean region. 5. Under a climate change perspective, the trend towards higher August rainfall recorded in our study area may alter oviposition phenology, with the subsequent cascade effects on weevil body size and fitness</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><notes><style face="normal" font="default" size="100%">The following values have no corresponding Zotero field:&lt;br/&gt;publisher: Blackwell Publishing Ltd</style></notes></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">DENUCE, J M</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">OVIPOSITIONAL HOST PLANT PREFERENCE OF SEPIA-OFFICINALIS</style></title><secondary-title><style face="normal" font="default" size="100%">ZEITSCHRIFT FUR NATURFORSCHUNG C-A JOURNAL OF BIOSCIENCES</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">HOST PLANT PREFERENCE</style></keyword><keyword><style  face="normal" font="default" size="100%">oviposition</style></keyword><keyword><style  face="normal" font="default" size="100%">SEPIA-OFFICINA</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">1990</style></year></dates><publisher><style face="normal" font="default" size="100%">VERLAG Z NATURFORSCH</style></publisher><pub-location><style face="normal" font="default" size="100%">POSTFACH 2645, W-7400 TUBINGEN, GERMANY</style></pub-location><volume><style face="normal" font="default" size="100%">45</style></volume><pages><style face="normal" font="default" size="100%">1225-1229</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">The present study was undertaken to verify ancient data in the&lt;br/&gt;literature on ovipositional preference of the cuttlefish Sepia&lt;br/&gt;officinalis for the terrestrial plant Pistacia lentiscus (mastic tree).&lt;br/&gt;- Adult specimens of Sepia were placed in basins together with aerial&lt;br/&gt;parts not only of P. lentiscus, but also of Artemisia arborescens,&lt;br/&gt;Centaurea alba var. deusta, Quercus ilex and Laurus nobilis. The egg&lt;br/&gt;masses deposited on the plants quantified on a daily basis during the 16&lt;br/&gt;day observation period. By far the largest amounts of eggs were found&lt;br/&gt;attached to the stems and petioles of P. lentiscus (51.8%), but Q. ilex&lt;br/&gt;and A. arborescens also scored high as ovipositional host plants (23.1&lt;br/&gt;and 20.2% respectively). L. nobilis and C. alba var. deusta ranked very&lt;br/&gt;low (3.6 and 1.3% respectively). Considering the extremely divergent&lt;br/&gt;shape of the three preferred oviposition substrates, which excludes&lt;br/&gt;affinity for a uniform type of plant, the possibility of chemical&lt;br/&gt;attraction cannot be ruled out.</style></abstract></record></records></xml>