Parasitoids of obscure mealybug,Pseudococcus viburni (Hem.: Pseudococcidae) in California: establishment of Pseudaphycus flavidulus (Hym.: Encyrtidae) and discussion of related parasitoid species

To improve natural suppression of the obscure mealybug, Pseudococcus viburni (Signoret), the parasitoids Pseudaphycus flavidulus (Brèthes) and Leptomastix epona (Walker) (Hymenoptera: Encyrtidae) of Chilean origin were released in California's Central Coast vineyards from 1997 to 1999. A survey for parasitoids of P. viburni was conducted in the Edna Valley appellation wine grape region from 2005 to 2007, 6–8 years after classical biological control releases were discontinued. Two survey methods were used. First, field collections of obscure mealybugs from commercial vineyard blocks (2005–2007) and, second, placement of “sentinel mealybugs” on potted (1 L) grape vines (2006 only). From both survey methods, P. flavidulus was recovered, albeit levels of parasitism were low (less than 0.6%). We also placed longtailed mealybug, Pseudococcus longispinus (Targioni Tozzetti), on potted plants concurrent with placement of sentinel obscure mealybugs in the vineyard in order to measure parasitoid activity on this closely-related mealybug species. No P. flavidulus were recovered from P. longispinus. Other encyrtid parasitoids reared from either P. viburni or P. longispinus were Anagyrus pseudococci (Girault), Leptomastix dactylopii Howard, Leptomastidea abnormis (Girault), Coccidoxenoides perminutus Girault, and Tetracnemoidea peregrina (Compere). A hyperparasitoid, Chaetocerus sp., was also reared. The data are discussed with respect to biological control of vineyard mealybugs and newly developed controls for the Argentine ant, Linepithema humile (Mayr) (Hymenoptera: Formicidae). Because Pseudaphycus species reared from mealybugs are superficially very similar a taxonomic key and discussion of host relationships for selected Pseudaphycus species are provided.     

When is sympatric speciation truly adaptive? An analysis of the joint evolution of resource utilization and assortative mating

The plausibility of sympatric speciation has long been debated among evolutionary ecologists. The process necessarily involves two key elements: the stable coexistence of at least two ecologically distinct types and the emergence of reproductive isolation. Recent theoretical studies within the theoretical framework of adaptive dynamics have shown how both these processes can be driven by natural selection. In the standard scenario, a population first evolves to an evolutionary branching point, next, disruptive selection promotes ecological diversification within the population, and, finally, the fitness disadvantage of intermediate types induces a selection pressure for assortative mating behaviour, which leads to reproductive isolation and full speciation. However, the full speciation process has been mostly studied through computer simulations and only analysed in part. Here I present a complete analysis of the whole speciation process by allowing for the simultaneous evolution of the branching ecological trait as well as a continuous trait controlling mating behaviour. I show how the joint evolution can be understood in terms of a gradient landscape, where the plausibility of different evolutionary paths can be evaluated graphically. I find sympatric speciation unlikely for scenarios with a continuous, unimodal, distribution of resources. Rather, ecological settings where the fitness inferiority of intermediate types is preserved during the ecological branching are more likely to provide opportunity for adaptive, sympatric speciation. Such scenarios include speciation due to predator avoidance or specialization on discrete resources. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Corridor or drift fence? The role of medial moraines for fly dispersal over glacier

Corridors are often considered to promote dispersal between habitat patches. In this paper, we study whether or not corridors induce colonisation of nunataks (ice-free areas in glacier surroundings) by promoting dispersal from lowland to the nunataks. On outlet glaciers, debris originating from nunataks forms the so-called medial moraines that stretch from the nunataks down-glacier to the lowland, forming corridors of debris on the glacier. Aerial dispersal was determined with yellow sticky traps on the moraines, bare glacier and glacier foreland. Dipterans were sampled in pitfall traps on the nunataks. Flying insects that were present on the vegetated glacier foreland belonged to five orders, that is, Diptera, Hemiptera, Hymenoptera, Lepidoptera and Trichoptera. On the glacier and medial moraines, however, mainly dipterans were present, with the majority of individuals found on the moraines. Hoverflies (Syrphidae) were abundant on the moraines and on the edges of nunataks close to the moraines, but were not present on the vegetated foreland. The origin of the hoverflies is thus not the nunataks and not the lowland. Rather, they are brought in by air currents towards the glacier, where they aggregate on a land type where they have a chance of survival, although it is not habitable. Thus, we conclude that the medial moraines do not function as regular corridors but as drift fences that direct the dispersal towards the adjacent land types, that is, the nunataks and the glacier foreland.     

Uncertain biotic and abiotic interactions in benthic communities

We analyze marine benthic communities at different sites in Skagerrak with the purpose of understanding the role of exogenous and endogenous factors in explaining the species' temporal dynamics. The previous finding that the dynamics of these species communities are mainly driven and synchronized by environmental (temperature) forcing was only weakly supported when analyzing single-species dynamics at five sites where four of the species were present every year. There was no consistent pattern in how the temperature affected the realized per capita growth rate, either across species at a given site, or among sites for a given species. Furthermore, there was no net-interaction from the community on a given species strong enough to give rise to second-order dynamics. However, when implementing a Multi Dimensional Scaling (MDS) analysis and incorporating all sampling sites and species -we found that the different communities clustered in relation to depth, hence, communities at the same depth were more "similar" than communities at different depth. Revealing the underlying interactions shaping these marine benthic communities is a challenge that calls for an array of various and complementary approaches.     

Flee or fight uncertainty: plant strategies in relation to anticipated damage

In order to cope with damage, plants have evolved a number of strategies. We incorporate two of those strategies, compensatory regrowth and escaping damage in time, into a mathematical model in an attempt to outline under what circumstances one or the other of these phenotypic traits will evolve. Escaping damage in time is accomplished by flowering and setting seeds at a point of time when the risk of damage is low, whereas a compensatory capacity is made possible by activating a proportion of meristems that are left dormant. Our analysis suggests that damage that is predictable in time will favour phenotypes that flower late in the season and that have a good compensatory capacity. As damage becomes less predictable in time, a strategy that implies flowering as early as possible in the season and with no compensatory capacity at all, becomes advantageous.     

A theory of stochastic harvesting in stochastic environments

We investigate how model populations respond to stochastic harvesting in a stochastic environment. In particular, we show that the effects of variable harvesting on the variance in population density and yield depend critically on the autocorrelation of environmental noise and on whether the endogenous dynamics of the population display over- or undercompensation to density. These factors interact in complicated ways; harvesting shifts the slope of the renewal function, and the net effect of this shift will depend on the sign and magnitude of the other influences. For example, when environmental noise exhibits a positive autocorrelation, the relative importance of a variable harvest to the variance in density increases with overcompensation but decreases with undercompensation. For a fixed harvesting level, an increasing level of autocorrelation in environmental noise will decrease the relative variation in population density when overcompensation would otherwise occur. These and other intricate interactions have important ramifications for the interpretation of time series data when no prior knowledge of demographic or environmental details exists. These effects are important whenever the harvesting rate is sufficiently high or variable, conditions likely to occur in many systems, whether the harvesting is caused by commercial exploitation or by any other strong agent of density-independent mortality.