"Phoenix in Flight": an unique fruit morphology ensures wind dispersal of seeds of the phoenix tree (Firmiana simplex (L.) W. Wight).

BACKGROUND: Many seed plants produce winged diaspores that use wind to disperse their seeds. The morphology of these diaspores is directly related to the seed dispersal potential. The majority of winged diaspores have flat wings and only seeds; however, some angiosperms, such as Firmiana produce winged fruit with a different morphology, whose seed dispersal mechanisms are not yet fully understood. In this study, we observed the fruit development of F. simplex and determined the morphological characteristics of mature fruit and their effects on the flight performance of the fruit. RESULTS: We found that the pericarp of F. simplex dehisced early and continued to unfold and expand during fruit development until ripening, finally formed a spoon-shaped wing with multiple alternate seeds on each edge. The wing caused mature fruit to spin stably during descent to provide a low terminal velocity, which was correlated with the wing loading and the distribution of seeds on the pericarp. When the curvature distribution of the pericarp surface substantially changed, the aerodynamic characteristics of fruit during descent altered, resulting in the inability of the fruit to spin. CONCLUSIONS: Our results suggest that the curved shape and alternate seed distribution are necessary for the winged diaspore of F. simplex to stabilize spinning during wind dispersal. These unique morphological characteristics are related to the early cracking of fruits during development, which may be an adaptation for the wind dispersal of seeds.

Bubbles help male flowers overcome obstacles during pollination in Hydrilla verticillata.

PREMISE: Pollination in many aquatic plants takes place on the water surface, and the male flowers or stamens often produce gas bubbles underwater; however, the generation mechanism and function of these bubbles are unknown. METHODS: A common submerged plant, Hydrilla verticillata, was used as experimental material to observe the structure of male flowers, analyze the process of bubble generation, and simulate the movement process of the male flower with attached gas bubble in water. RESULTS: The aerenchyma inside the male plants of H. verticillata transported the gas produced by the plant's branches during photosynthesis to the male flower, and the formed gas bubbles became attached to the edge of the perianth. The gas accumulation rate in the attached bubbles increased with light intensity. Once the bubble diameter increased to approximately 3.3 mm, the male flowers with the bubble detached from the plant and floated to the water surface. The removal of the attached bubbles did not affect the male flower detached from the plant; however, the surfacing of male flowers without gas bubbles was easily prevented by the plant's branches in the water, and they could not reach the water surface to complete pollen dispersal. CONCLUSIONS: The gas bubbles produced by male flowers of H. verticillata came from the gas produced by branches under light. These bubbles can help ascending male flowers bypass the obstacles in water and reach the surface to complete pollination.

A water drop-shaped slingshot in plants: geometry and mechanics in the explosive seed dispersal of Orixa japonica (Rutaceae).

BACKGROUND AND AIMS: In angiosperms, many species disperse their seeds autonomously by rapid movement of the pericarp. The fruits of these species often have long rod- or long plate-shaped pericarps, which are suitable for ejecting seeds during fruit dehiscence by bending or coiling. However, here we show that fruit with a completely different shape can also rely on pericarp movement to disperse seeds explosively, as in Orixa japonica. METHODS: Fruit morphology was observed by hard tissue sectioning, scanning electron microscopy and micro-computed tomography, and the seed dispersal process was analysed using a high-speed camera. Comparisons were made of the geometric characteristics of pericarps before and after fruit dehiscence, and the mechanical process of pericarp movement was simulated with the aid of the finite element model. KEY RESULTS: During fruit dehydration, the water drop-shaped endocarp of O. japonica with sandwich structure produced two-way bending deformation and cracking, and its width increased more than three-fold before opening. Meanwhile the same shaped exocarp with uniform structure could only produce small passive deformation under relatively large external forces. The endocarp forced the exocarp to open by hygroscopic movement before seed launching, and the exocarp provided the acceleration for seed launching through a reaction force. CONCLUSIONS: Two layers of water drop-shaped pericarp in O. japonica form a structure similar to a slingshot, which launches the seed at high speed during fruit dehiscence. The results suggest that plants with explosive seed dispersal appear to have a wide variety of fruit morphology, and through a combination of different external shapes and internal structures, they are able to move rapidly using many sophisticated mechanisms.

The structure and development of incompletely closed carpels in an apocarpous species, Sagittaria trifolia (Alismataceae).

• Premise of the study: Carpel closure is commonly considered as a key innovation in angiosperms; however, some families continue to exhibit a variety of forms of incomplete carpel closure. The carpel of Sagittaria species contains an unusual structure. In this study, we confirm the closure type of the carpel of Sagittaria trifolia and discuss its development and evolution.• Methods: Scanning electron microscopy and light microscopy of semithin sections were used to observe the development and the mature structure of the carpel. Pollen tube growth in the carpel and seed germination in the achene was also studied.• Key results: During late carpel development, the middle parts of the carpel margins underwent postgenital fusion. However, at maturity the lowest and uppermost parts of the carpel margins remained open. The mature carpel was incompletely closed and contained a secretion-filled canal, which extended from the stigma to the opening at the carpel base. At that site, pollen tubes could either grow to the ovule or exit the carpel and grow to other carpels. The basal opening also served as an exit point for the seedling to emerge.• Conclusions: Incomplete carpel closure by S. trifolia differs from the closure types recorded in previous studies because two entrances link the ovary in the carpel to the outside environment. This type of carpel closure occurs as a result of the lack of fusion of the carpel margins at the base of the carpel and could improve the seed set and seedling germination of S. trifolia.

Floral development at multiple spatial scales in Polygonum jucundum (Polygonaceae), a distylous species with broadly open flowers.

Distyly, a special polymorph, has evolved in many groups of angiosperms and has attracted attention since Darwin's time. Development studies on distylous taxa have helped us to understand the evolutionary process of this polymorph, but most of these studies focus on species with narrowly tubular corolla. Here, we studied the floral development of Polygonum jucundum, a distylous species with broadly open flowers, at multiple spatial scales. Results showed that the difference in stigma height between flowers of the two morphs was caused by differences in style growth throughout the entire floral development process. The observed difference in anther heights between the two morphs was because the filaments grew faster in short-styled (SS) than in long-styled (LS) flowers in the later stages of floral development. In addition, the longer styles in LS flowers than in SS flowers was because of faster cell division in the early stages of floral development. However, SS flowers had longer filaments than LS flowers primarily because of greater cell elongation. These results indicate that floral development in P. jucundum differs from that of distylous taxa with floral tubes shown in previous studies. Further, we conclude that the presence of distyly in species with open flowers is a result of convergent evolution.