Secondary substances and their ecological effects on seed dispersal in vertebrate-dispersed fleshy fruit plants

2014 ◽  
Vol 34 (10) ◽  
Author(s):  
潘扬 PAN Yang ◽  
罗芳 LUO Fang ◽  
鲁长虎 LU Changhu
2007 ◽  
Vol 23 (2) ◽  
pp. 471-478 ◽  
Author(s):  
Kazuaki Takahashi ◽  
Tadatoshi Shiota ◽  
Hiroo Tamatani ◽  
Masaru Koyama ◽  
Izumi Washitani

2019 ◽  
Vol 170 ◽  
pp. 103995
Author(s):  
Alejandro Miranda ◽  
Inao A. Vásquez ◽  
Pablo Becerra ◽  
Cecilia Smith-Ramírez ◽  
Cristian A. Delpiano ◽  
...  

Author(s):  
Mikihisa Yamada ◽  
Masaru Hojo ◽  
Akio Imamura

Seed dispersal by ants is an important means of migration for plants. Although many 34 myrmecochorous plants have seeds containing elaiosome, a nutritional reward for ants, some 35 non-myrmecochorous seeds without elaiosomes are also dispersed by ant species. However, the 36 mechanism by which seeds without elaiosomes enable efficient dispersal by ants is scarcely 37 investigated. The seeds of the achlorophyllous and myco-heterotrophic herbaceous plant 38 Monotropastrum humile are very small without elaiosomes and require a fungal host for 39 germination and survival. We performed a bioassay using seeds of M. humile and the ant 40 Nylanderia flavipes to demonstrate ant-mediated seed dispersal. We also analyzed the volatile 41 odors emitted from M. humile seeds and conducted bioassays using dummy seeds coated with 42 seed volatiles. Although elaiosomes were absent from the M. humile seeds, the ants carried the 43 seeds to their nests. They also carried the dummy seeds coated with the seed volatile mixture to 44 the nest, and left some dummy seeds inside the nest and discarded the rest of the dummy seeds 45 outside the nest with a bias toward locations with moisture conditions, which might be 46 conducive to germination. We concluded that seeds of M. humile were dispersed by the ants, 47 and that seed odors were sufficient to induce directed dispersal even without elaiosomes. It is 48 probable that the fleshy fruit producing genus Monotropastrum evolved from the related 49 anemochorous genus Monotropa, which produces capsule fruit. This transformation from 50 anemochory to myrmecochory presents a novel evolutionary pathway toward ant-mediated seed 51 dispersal in an achlorophyllous plant.


Author(s):  
K. Greg Murray ◽  
Sharon Kinsman

The term “plant-animal interactions” includes a diverse array of biologically important relationships. Plant-herbivore relationships (in which an animal feeds on whole plants or parts of them) are examples of exploitation, because one species benefits from the interaction while the other suffers. Plant-pollinator and plant-seed disperser relationships (in which animals disperse pollen or seeds, usually in return for a food reward) are examples of mutualisms because they are beneficial to both parties. Another class of plant-animal mutualisms involves plants that provide nesting sites and/or food rewards to ants, which often protect the plant from herbivores or competing plants. Plantpollinator and plant-seed disperser mutualisms probably originated as cases of exploitation of plants by animals (Thompson 1982, Crepet 1983, Tiffney 1986). Many of the distinctive plant structures associated with animal-mediated pollen and seed dispersal (e.g., flowers, nectaries, attractive odors, fleshy fruit pulp, and thickened seed coats) presumably evolved to attract consumers of floral or seed resources while preventing them from digesting the pollen or seeds. mutualisms in structuring ecological communities. Competition and predator-prey interactions were more common subjects. Botanists had described the characteristics of the plant and animal players in pollination and seed dispersal mutualisms (Knuth 1906, 1908, 1909, Ridley 1930, van der Pijl 1969, Faegri and van der Pijl 1979), but these descriptive works did not fully examine plant-animal mutualisms in the context of communities. The opportunity to work in the neotropics, facilitated by the Organization for Tropical Studies (OTS), the Smithsonian Tropical Research Institute (STRI), and other institutions, attracted the attention of temperate-zone ecologists to the mutualisms that are much more conspicuous components of tropical systems than of temperate ones (Wheelwright 1988b). Plant-pollinator interactions have attracted more attention in Monteverde than plant-frugivore interactions, and plant-herbivore interactions remain conspicuously understudied. This imbalance probably reflects the interests of those who first worked at Monteverde and later returned with their own students, rather than differences in the significance of the interactions at Monteverde or elsewhere. Aside from a few studies of herbivory in particular species (e.g., Peck, “Agroecology of Prosapia,”), even basic surveys remain to be done.


2003 ◽  
Vol 19 (6) ◽  
pp. 619-627 ◽  
Author(s):  
Andrew J. Dennis

Tropical forests around the world contain animals that scatter-hoard fruits and seeds but few are known in Australian tropical forests. This study used both direct observation and spool-and-line tracking of simulated fruits to demonstrate that Australia's smallest kangaroos disperse large numbers of rain-forest fruits and seeds. They did so in two ways, either by scatter-hoarding or by carrying them away from the source to devour the flesh before dropping the seed on to the litter surface. The fruits used included a range of fruit types but particularly species with large fleshy fruit. Caches occurred as a single fruit pressed into the soil and covered with litter a mean distance of 17 m (±2.7 SE) and up to 68 m from the source. Musky rat-kangaroos handled up to 2700 fruits ha-1 mo-1 and they dispersed up to 900 fruits ha-1 mo-1 and cached up to 690 fruits ha-1 mo-1. This behaviour is a significant example of convergent evolution, which reflects similar behaviour found in agoutis, acouchies and squirrels on other continents.


1969 ◽  
Vol 60 (4, Pt.1) ◽  
pp. 284-293 ◽  
Author(s):  
Donald L. Thistlethwaite

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