Diplochory in western chokecherry: you can��t judge a fruit by its mesocarp

Western chokecherry (Prunus virginiana var. demissa, Rosaceae) is dispersed by frugivorous birds and carnivores, but it has large seeds that are potentially attractive to rodents that could act as seed predators and dispersers. Here, we quantify the benefits of primary dispersal by birds and secondary dispersal by scatter-hoarding rodents. In the fall, avian frugivores (mostly American robins, Turdus migratorius, and cedar waxwings, Bombycilla cedrorum) consumed 87% of the fruit crop and dispersed 67% of the fruit crop away from parent plants. Rodents removed 89% of seeds that simulated bird-dispersed seed rain from transects in riparian zones and 58% from transects in upland habitats. Rodents scatter-hoarded 91.6% of the seeds they removed, burying most in small caches (two to eight seeds) 8?C25?mm deep. About 39% of the seeds in spring caches produced seedlings. Inside rodent-proof exclosures, 52.1% of seeds buried to simulate rodent caches produced seedlings, 29.7% of which were still alive after 1?year. In contrast, only 3.8% of seeds placed on the soil surface, simulating dispersal by avian frugivores, produced seedlings. Seed dispersal by frugivorous birds likely contributes to colonization of unoccupied habitat through long-range dispersal and to escape from distance-dependent seed mortality near the parent plant. Despite seed losses, rodents offer short-range seed dispersal and bury seeds in more favorable sites for germination, improving seedling emergence and establishment. The combined mechanisms of seed dispersal significantly enhanced chokecherry seedling recruitment by providing more dispersal-related benefits than either frugivorous bird or scatter-hoarding rodents could provide alone.     

How to leave or stay on the substratum when you can’t swim? Evidence of the role of mucus thread secretion by postlarvae of Pectinaria koreni (Malmgren) in still water and flume experiments

Through an experimental approach we investigate the role of mucus secretion in postlarvae of Pectinaria koreni (tubicolous polychaete) on their ability to drift within the benthic boundary layer or to stay at the water–substratum interface. Fall velocity measurements were conducted with either living or dead postlarvae which were allowed to sink into a 2 m long Plexiglas cylindrical chamber. Five groups of increasing size-classes were tested ranging from the very first benthic stage (1 mm < Tube_length < 2 mm: membranous tube present accounting for more than 75% of the total tube length) to older stages (6 mm < Tube_length < 10 mm: membranous tube absent). We used these results to propose the first estimates of dispersal distances by several post-larval stages secreting mucus or sinking passively through the water column. Experiments were carried out in the HYCOBENTHOS flume to determine values of critical shear velocity (u _*c) inducing bedload transport and further resuspension of postlarvae of increasing sizes. The influence of mucus secretion by recruits on their ability to stay or quit a ‘suitable’ substratum was investigated by using either living or dead individuals. Results showed that: (a) the ability to secrete mucus rapidly is limited to the younger stages; (b) fall velocity of postlarvae is drastically lowered by mucus secretion (5 orders of magnitude) and is higher for the older stages; (c) dead recruits behave similarly to ‘passive’ recruits; (d) horizontal distances of drift dispersal may be considerable (up to 800 m for a single 22 min trip); (e) mucus secretion may be used by the postlarvae to anchor themselves to the substratum. Cost-benefit of using the mucus secretion as a tool for recruitment and the related spatial scales are discussed.