Traits of perch trees promote seed dispersal of endemic fleshy-fruit species in degraded areas of endangered Mediterranean ecosystems

2019 ◽  
Vol 170 ◽  
pp. 103995
Author(s):  
Alejandro Miranda ◽  
Inao A. Vásquez ◽  
Pablo Becerra ◽  
Cecilia Smith-Ramírez ◽  
Cristian A. Delpiano ◽  
...  
2007 ◽  
Vol 23 (2) ◽  
pp. 471-478 ◽  
Author(s):  
Kazuaki Takahashi ◽  
Tadatoshi Shiota ◽  
Hiroo Tamatani ◽  
Masaru Koyama ◽  
Izumi Washitani

2020 ◽  
Vol 71 (19) ◽  
pp. 5823-5836 ◽  
Author(s):  
Léa Roch ◽  
Sylvain Prigent ◽  
Holger Klose ◽  
Coffi-Belmys Cakpo ◽  
Bertrand Beauvoit ◽  
...  

Abstract Fleshy fruits are very varied, whether in terms of their composition, physiology, or rate and duration of growth. To understand the mechanisms that link metabolism to phenotypes, which would help the targeting of breeding strategies, we compared eight fleshy fruit species during development and ripening. Three herbaceous (eggplant, pepper, and cucumber), three tree (apple, peach, and clementine) and two vine (kiwifruit and grape) species were selected for their diversity. Fruit fresh weight and biomass composition, including the major soluble and insoluble components, were determined throughout fruit development and ripening. Best-fitting models of fruit weight were used to estimate relative growth rate (RGR), which was significantly correlated with several biomass components, especially protein content (R=84), stearate (R=0.72), palmitate (R=0.72), and lignocerate (R=0.68). The strong link between biomass composition and RGR was further evidenced by generalized linear models that predicted RGR with R-values exceeding 0.9. Comparison of the fruit also showed that climacteric fruit (apple, peach, kiwifruit) contained more non-cellulosic cell-wall glucose and fucose, and more starch, than non-climacteric fruit. The rate of starch net accumulation was also higher in climacteric fruit. These results suggest that the way biomass is constructed has a major influence on performance, especially growth rate.


2004 ◽  
Vol 20 (6) ◽  
pp. 599-612 ◽  
Author(s):  
An Bollen ◽  
Linda Van Elsacker ◽  
Jörg U. Ganzhorn

Interactions among fleshy fruits and frugivore assemblages are presented from a 1-y study in the littoral forest of Sainte Luce, south-eastern Madagascar. This community-level approach allowed us to determine food selection by all consumer species and to evaluate the role different frugivores play in seed dispersal and predation. For this, interactions between 136 consumed fruit species and 13 frugivorous species were studied. Fruit and seed size were the most important physical factors determining food selection of all consumer species. Nutritionally birds favoured and mammals avoided lipid-rich fruits. For Cheirogaleus spp., that go into torpor, there was a trend to select sugar-rich fruit pulp. However, for numerous fruit traits the consumer species had no clear feeding preferences and they seemed to be quite flexible, eating whatever was available. This might be related to unpredictable fruit availability and low fruit productivity in the littoral forest, which may also partially explain the low number of frugivores present. Nevertheless frugivores have different impacts on seed dispersal. Eulemur fulvus collaris is particularly important for the dispersal of large-seeded species, while frugivorous birds and flying foxes ensure plant regeneration between and outside forest fragments. In terms of conservation, heterogeneous seed transport is particularly important for this severely degraded littoral forest.


2020 ◽  
Vol 47 (12) ◽  
pp. 1019 ◽  
Author(s):  
Nikolai C. Macnee ◽  
Ria Rebstock ◽  
Ian C. Hallett ◽  
Robert J. Schaffer ◽  
Sean M. Bulley

The outer skin layer in any plant is essential in offering a protective barrier against water loss and pathogen attack. Within fleshy fruit, the skin supports internal cell layers and can provide the initial cues in attracting seed-dispersing animals. The skin of a fruit, termed the exocarp, is a key element of consumer preference and a target for many breeding programs. Across fruiting species there is a huge diversity of exocarp types and these range from a simple single living cell layer (epidermis) often covered with a waxy layer, to complex multicellular suberised and dead cell layers (periderm), with various intermediate russet forms in between. Each exocarp can be interspersed with other structures such as hairs or spines. The epidermis has been well characterised and remains pluripotent with the help of the cells immediately under the epidermis. The periderm, in contrast, is the result of secondary meristematic activity, which replaces the epidermal layers, and is not well characterised in fruits. In this review we explore the structure, composition and mechanisms that control the development of a periderm type fruit exocarp. We draw upon literature from non-fleshy fruit species that form periderm tissue, from which a considerable amount of research has been undertaken.


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.


2007 ◽  
Vol 23 (5) ◽  
pp. 519-528 ◽  
Author(s):  
Elisabet V. Wehncke ◽  
César A. Domínguez

Seed dispersal by frugivorous animals has the potential to affect both the demography and the patterns of gene flow of plant populations. In many tropical and subtropical forests a large number of seeds are efficiently dispersed by ‘non-restricted frugivores’ (NRFs, animals for which fruits do not represent the main bulk of their diet), a group commonly underestimated as seed dispersers. Here, we synthesize data from three different neotropical forests (Argentina, Panama and Costa Rica), evaluating several aspects of seed dispersal by two species of Cebus monkeys. Capuchin monkeys are NRFs broadly distributed throughout Central and South America that are potentially long-distance seed dispersers. In this study we evaluated the influence of the foraging behaviour of Cebus apella and C. capucinus on the patterns of seed dispersal. Even though the distribution of fruit types significantly differed among forests, no evidence of diet selection was found, indicating that the fruits consumed by monkeys represent a random sample of the pool available at each site. Neither seed treatment, nor the evenness with which fruit species were consumed, differed among forests. In contrast, the feeding time per fruiting tree (10–45 min), the diversity of fruits consumed (H = 2–3.3), and seed dispersal distances (100–400 m), differed among the three forests. Thus, capuchin monkeys consume a high diversity of fruits in transit producing a scattered dissemination of seeds in all study forests. This study highlights the ecological and evolutionary significance of seed shadows generated by NRFs, without neglecting the possibility that differences in the distribution of fruit patches, species richness and a range of environmental attributes among the studied forests, exert a strong influence on the outcome of the interaction between NRFs and plants.


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.


1987 ◽  
Vol 65 (11) ◽  
pp. 2291-2296 ◽  
Author(s):  
Elise Jones ◽  
Nathaniel T. Wheelwright

Certain temperate-zone plant species retain their fleshy fruits through the fall and winter. The production of "persistent fruits" has been interpreted as an adaptive reproductive strategy because plants can offer "low-investment" fruits when competition with other plants for seed dispersers is low. In theory fruits are defended chemically against fall pathogens, and palatability improves seasonally with cold-induced chemical changes. We studied the ecology of persistent fruits in Viburnum opulus (Caprifoliaceae), a fleshy-fruited temperate-zone shrub. Viburnum opulus fruits remained uneaten through the fall until most were removed, apparently by avian seed predators. Some shrubs retained fruits through May. Birds in the field and laboratory preferred all other fruit species tested over V. opulus. Palatability of V. opulus fruits to captive American Robins declined rather than improved throughout the winter, contrary to expectation. Tannins and pH remained constant, while sucrose concentration doubled over a 6-month period. Seeds regurgitated by robins in the spring germinated at similar rates as seeds processed the previous fall. Although V. opulus showed some of the theoretically expected adaptations for delayed seed dispersal (chemical defense, germination following spring dispersal), it did not show others (seasonal improvement in palatability). Plants with persistent fruits may depend on years of severe weather and food scarcity for seed dispersal.


2017 ◽  
Author(s):  
Peitao Lü ◽  
Sheng Yu ◽  
Ning Zhu ◽  
Yun-Ru Chen ◽  
Biyan Zhou ◽  
...  

AbstractFleshy fruit evolved independently multiple times during angiosperm history. Many climacteric fruits utilize the hormone ethylene to regulate ripening. The fruitENCODE project shows there are multiple evolutionary origins of the regulatory circuits that govern climacteric fruit ripening. Eudicot climacteric fruits with recent whole-genome duplications (WGDs) evolved their ripening regulatory systems using the duplicated floral identity genes, while others without WGD utilised carpel senescence genes. The monocot banana uses both leaf senescence and duplicated floral-identity genes, forming two interconnected regulatory circuits. H3K27me3 plays a conserved role in restricting the expression of key ripening regulators and their direct orthologs in both the ancestral dry fruit and non-climacteric fleshy fruit species. Our findings suggest that evolution of climacteric ripening was constrained by limited availability of signalling molecules and genetic and epigenetic materials, and WGD provided new resources for plants to circumvent this limit. Understanding these different ripening mechanisms makes it possible to design tailor-made ripening traits to improve quality, yield and minimize postharvest losses.One Sentence SummaryThe fruitENCODE project discovered three evolutionary origins of the regulatory circuits that govern climacteric fruit ripening.


Sign in / Sign up

Export Citation Format

Share Document