The island rule predicts that small animals evolve to become larger on islands, while large animals evolve to become smaller. It has been studied for over half a century, and its validity is fiercely debated. Here, we provide a perspective on the debate by conducting a test of the island rule in plants. Results from an extensive dataset on islands in the southwest Pacific illustrate that plant stature and leaf area obey the island rule, but seed size does not. Our results indicate that the island rule may be more pervasive than previously thought and that support for its predictions varies among functional traits.
Impermeable seed coats, i.e. physical dormancy (PY) influence the germination ecology of plants from 18 angiosperm families. Astragalus adsurgens (Fabaceae; Papilinoidaae) is a perennial plant widespread in temperate regions that is thought to produce both permeable and impermeable seeds. Why seeds vary in the permeability of their coat, in addition to the mechanisms by which impermeable seeds break dormancy, are not completely understood. However, seeds are often consumed by herbivores; a phenomenon that might facilitate the germination of impermeable seeds. Here, we tested whether: (1) moisture content plays a significant role in the onset of seed coat impermeability (and therefore PY) at similar ranges reported for species from tropical ecosystems; and (2) the presence of impermeable coats offer any benefits for seed survival when consumed by animals. We tested these hypotheses using A . adsurgens seeds collected from Inner Mongolia, China. Freshly collected seeds with a moisture content of 9.7% were permeable to water and therefore not physically dormant. However, seeds became impermeable when dried below a threshold of 6.5% moisture content. Treating impermeable seeds with hydrochloric acid effectively broke dormancy. Scanning electron microscope (SEM) revealed that HCl treated seeds had a narrow opening in the hilum and extra-hilar regions, through which water entered. Seeds with impermeable coats survived significantly better than permeable seeds when consumed by cows. Irrespective of coat permeability, most seeds were egested between 12 and 24 h. In seeds that maintained dormancy after gut passage, this was broken by additional acid scarification. Overall results suggest that: (1) seed coat impermeability is induced by reduced moisture content; (2) imbibition primarily occurs at the hilum and extra-hilar region; and (3) impermeable seeds may benefit from endozoochory.
Conceptualizing species interactions as networks has broadened our understanding of ecological communities. However, the factors shaping interaction patterns among species and, therefore, network structure remain unclear. One potentially important factor is the matching of phenotypic traits. Here, we tested for trait matching in a bird-flower visitation network from New Zealand. We first quantified the overall network structure and tested whether flower size could account for differences in the visitation rates of flowering plants. We then explored the relationship between the flower size and bill size. The results showed that the interaction network is nested. Plant species with large flowers received more visits from birds than plant species with small flowers. Moreover, plant species with large flowers were visited more frequently by birds with large bills, while species with smaller flowers were visited more frequently by birds with small bills. Overall, the interaction patterns between birds and flowering plants could be predicted by their morphology, suggesting that phenotypic trait matching is an important predictor of network structure.
The island rule is a putative pattern in island evolution, where small species become larger on islands and large species become smaller. Despite decades of study, a mechanistic explanation for why some taxonomic groups obey the island rule, while others do not, has yet to be identified. Here, we explore whether the island rule might result from evolutionary drift. We derived a simulation model that predicts evolutionary size changes on islands based on random evolutionary trajectories along bounded trait domains. The model consistently predicted the island rule and could account for its occurrence in plants inhabiting islands in the Southwest Pacific. When support for the island rule was not detected, insular gigantism was often observed, suggesting that natural selection was at work. Overall results indicate that evolutionary drift can provide a parsimonious explanation for the island rule, suggesting future work should focus on circumstances where it does not occur.
Dormancy caused by impermeable seed coats, i.e. physical dormancy (PY), regulates the timing of seed germination in species of several genera belonging to 18 angiosperm families. Physical dormancy also occurs in some mimetic species whose seeds mimic brightly coloured, fleshy fruits or arilled seeds. However, the conditions that break dormancy, as well as the location of water gaps in mimetic seeds, remain unclear. Here, we investigated the adaptive role of impermeable coats in the mimetic seeds of Adenanthera pavonina (Fabaceae: Mimosoideae). Specifically, we explored: (i) the conditions that break PY; (ii) the location of the primary water gap that forms during dormancy break; and (iii) the effect of seasonal temperature regimes on seed germination. Seeds were subjected to hot-water treatment, rapid temperature fluctuations and storage at temperatures mimicking summer and autumn conditions. Seed coat anatomy and water-gap regions were characterized using scanning electron microscopy (SEM) and light microscopy. Seeds were artificially buried in the field at 3 and 7 cm depths and exhumed every 6 months for 2 years to monitor germination. Adenanthera pavonina had impermeable seed coats, and thus PY. Seeds treated with hot water and exposed to summer–autumn temperature regimes broke dormancy. Water entered only through the lens (Type-II simple) due to dislodgement of the palisade layer. Seeds buried at 3 cm depth had significantly higher germination than those buried at 7 cm depth, with germination primarily occurring in autumn. Seeds required high summer temperatures followed by moderate autumn temperatures to become permeable to water and germinate in the field during the wet season. We conclude that the impermeable seed coat of A. pavonina is an adaptation that synchronizes germination with the growing season.
The evolution of vascular tissue is a key innovation enabling plants to inhabit terrestrial environments. Here, we demonstrate extra-vascular water transport in a giant, prop-rooted monocot from Lord Howe Island. (Pandanaceae) produces gutter-like leaves that capture rainwater, which is then couriered along a network of channels to the tips of aerial roots, where it is stored by absorptive tissue. This passive mechanism of water acquisition, transport and storage is critical to the growth of aerial prop roots that cannot yet attain water via vascular conduction. This species therefore sheds light on the elaborate means by which plants have evolved to attain water.
Physical dormancy (PY) is typically induced by seed coat impermeability that develops once the moisture content of seeds drops below a species-specific threshold. Considering this, we utilized Albizia julibrissin (Fabaceae) to ask (i) whether seeds that mature on the outer branches of trees (directly exposed to sunlight) are more likely to be impermeable than seeds matured under canopy cover; (ii) whether this difference might be explained by the maternal environment in which the seeds mature; and (iii) which conditions impose secondary dormancy following dispersal? Temperature was tracked in both shaded and sun-exposed seed pods throughout the growing season using data-loggers. Temperatures remained lower in pods under canopy cover than those exposed to direct sunlight. Consequently, the moisture content of seeds collected from sun-exposed branches were significantly lower than seeds matured under canopy cover, thereby producing a higher percentage of impermeable seeds. A dispersal-mimicking experiment revealed that seeds matured in sun-exposed branches and subsequently dispersed to an open site for 4 months were more likely to develop impermeability (i.e. secondary dormancy). The opposite was found to be true for seeds matured in shaded branches and subsequently dispersed to a canopy-covered site. We conclude that the microclimate of both the maternal environment in which seeds mature, and the site to which they disperse, determines the development of primary and secondary dormancy, respectively.
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