Éditeur(s) : HAL CCSD Taylor & Francis
Résumé : International audience
ISSN: 1559-2316

hal-01086786
https://hal-agroparistech.archives-ouvertes.fr/hal-01086786
DOI : 10.4161/psb.4.9.9423

Éditeur(s) : HAL CCSD Ecological Society of America
Résumé : International audience
ISSN: 0012-9658

hal-01091094
https://hal-agroparistech.archives-ouvertes.fr/hal-01091094

Éditeur(s) : HAL CCSD Elsevier
Résumé : International audience
We experimentally studied the predatory behavior of Polybia rejecta (Vespidae, Polistinae, Epiponini) towards 2-88 mm-long insects attracted to a UV light trap. Foragers, which began to hunt at 6:30, selected 4-14 mm-long prey insects. Prey detection by sight by hovering wasps was confirmed using decoys. After the wasps landed and walked along a sinuous path, prey were detected by contact or from a distance (1-3cm). This was followed by seizure, stinging (contrarily to most other known cases), prey manipulation and retrieval. Prey that flew off might be caught in flight. The prey load, representing 30.7% of a forager's weight, was optimized by capturing up to six small prey or two medium-sized prey successively (both of which might be consumed in situ). The foragers cut off the wings of larger prey or cut them into two pieces and returned to gather the second piece. The handling time increased exponentially with the weight of the prey. Partial loading (i.e., retrieving a load much inferior to the maximum possible) was likely related to social facilitation, a form of nest-based recruitment that was demonstrated through the experimental elimination of local enhancement by removing foragers (both mechanisms favor the exploitation of favorable patches).
ISSN: 0376-6357

hal-01533217
https://hal-univ-rennes1.archives-ouvertes.fr/hal-01533217
https://hal-univ-rennes1.archives-ouvertes.fr/hal-01533217/document
https://hal-univ-rennes1.archives-ouvertes.fr/hal-01533217/file/Dejean%20et%20al.%20-%20The%20predatory%20behavior%20of%20the%20Neotropical%20social%20w.pdf
DOI : 10.1016/j.beproc.2017.05.011

Éditeur(s) : HAL CCSD
Résumé : One critical challenge for plants is to maintain an adequate nutrient supply under fluctuating environmental conditions. This is particularly true for epiphytic species that have limited or no access to the pedosphere and often live in harsh climates. Bromeliads have evolved key innovations such as epiphytism, water-absorbing leaf trichomes, tank habit and Crassulacean acid metabolism (CAM) photosynthesis that enable them to survive under various environmental conditions. Bromeliads encompass diverse ecological types that live on different substrates (they can be terrestrial, epilithic or epiphytic) and vary in their ability to retain water (they can be tank-forming or tankless) and photosynthetic pathway (i.e. C3 or CAM). In this review, we outline the nutritional modes and specializations that enable bromeliads to thrive in a wide range of nutrient-poor (mostly nitrogen-depleted) environments.Important FindingsBromeliads have evolved a great diversity of morphologies and functional adaptations leading to the existence of numerous nutritional modes. Focusing on species that have absorptive foliar trichomes, we review evidence that bromeliads have evolved multi-faceted nutritional strategies to respond to fluctuations in the supply of natural nitrogen (N). These plants have developed mutualistic associations with many different and functionally diverse terrestrial and aquatic microorganisms and metazoans that contribute substantially to their mineral nutrition and, thus, their fitness and survival. Bacterial and fungal microbiota-assisted N provisioning, protocarnivory, digestive mutualisms and myrmecotrophic pathways are the main strategies used by bromeliads to acquire nitrogen. The combination of different nutritional pathways in bromeliads represents an important adaptation enabling them to exploit nutrient-poor habitats. Nonetheless, as has been shown for several other vascular plants, multiple partners are involved in nutrient acquisition indicating that there have been convergent adaptations to nutrient scarcity. Finally, we point out some gaps in the current knowledge of bromeliad nutrition that offer fascinating research opportunities.
ISSN: 1752-9921

hal-01532637
https://hal.archives-ouvertes.fr/hal-01532637
DOI : 10.1093/jpe/rtv052
PRODINRA : 384521

Éditeur(s) : HAL CCSD Wiley
Résumé : Plant germination and development depend upon a seed's successful dispersal into a suitable habitat and its ability to grow and survive within the surrounding biotic and abiotic environment. The seeds of Aechmea mertensii, a tank-bromeliad species, are dispersed by either Camponotus femoratus or Neoponera goeldii, two ant species that initiate ant gardens (AGs). These two mutualistic ant species influence the vegetative and reproductive traits of the bromeliad through their divergent ecological preferences (i.e. light and substrate). We hypothesised that the seeds dispersed by these two ant species have underlying genetic differences affecting germination, growth and survival of A.mertensii seedlings in different ways. To test this, we used an experimental approach consisting of sowing seeds of A.mertensii: (i) taken from the two AG-ant associations (i.e. seed origin), (ii) in two contrasting light conditions, and (iii) on three different substrates. Light and substrate had significant effects on germination, survival and on eight key leaf traits reflecting plant performance. Seed origin had a significant effect only on germination and on two leaf traits (total dry mass and relative growth rate). Overall, this bromeliad performs better (i.e. high growth and survival rates) when growing both in the shade and in the carton nest developed by C.femoratus ants. These results suggest that the plasticity of the tank bromeliad A.mertensii is mainly due to environment but also to genetic differences related to seed origin, as some traits are heritable. Thus, these two ant species may play contrasting roles in shaping plant evolution and speciation.
ISSN: 1435-8603

hal-01606565
https://hal.archives-ouvertes.fr/hal-01606565
DOI : 10.1111/plb.12452
PRODINRA : 407514

Éditeur(s) : HAL CCSD Wiley
Résumé : International audience
Wasp nests range from simple to complex structures made of paper or mud. Here, we show that a Neotropical wasp of the genus Nitela builds its nest entirely by weaving endophytic fungal hyphae and spider silk harvested from the leaves growing in the understory of the rain forest in French Guiana.
ISSN: 0006-3606

hal-01095857
https://hal-agroparistech.archives-ouvertes.fr/hal-01095857
DOI : 10.1111/j.1744-7429.2010.00645.x

Éditeur(s) : HAL CCSD Wiley
Résumé : International audience
ISSN: 1758-2229

hal-01623623
https://hal.archives-ouvertes.fr/hal-01623623
DOI : 10.1111/1758-2229.12426