Partly transparent young legume pods: Do they mimic caterpillars for defense and simultaneously enable better photosynthesis?

Being partly or fully transparent as a defense from predation is mostly known in various groups of aquatic animals and various terrestrial arthropods. Plants, being photosynthetic and having cell walls made of various polymers, cannot be wholly transparent. In spite of these inherent limitations, some succulent plant species of arid zones have partially transparent “windows” in order to perform photosynthesis in their below-ground leaves, as defense from herbivores as well as for protection from harsh environmental conditions. Similarly, transparent “windows” or even wholly transparent leaves are found in certain thick or thin, above-ground organs irrespective of aridity. The young pods of various wild annual Mediterranean legume species belonging to the genera Lathyrus, Pisum and Vicia are partly transparent and may therefore look like caterpillars when viewed with back illumination. I propose that this character serves 2 functions: (1) being a type of defensive caterpillar mimicry that may reduce their consumption by various herbivores in that very sensitive stage, and (2) simultaneously allowing better photosynthesis in the rapidly growing seeds and pods. Unlike animals that are transparent for either defensive or aggressive crypsis, in the case of young legume pods it allows them to visually mimic caterpillars for defense.     

Plant fibers: Initiation,growth, model plants,and open questions

Fibers, which are used as a major raw material in the paper industry, as structural components in timber for building, and in the manufacture of wooden items, are among the most important renewable resources. Billions use wood as a major energy source, and fibers are an energy-rich component of wood. They are used for various textiles and as raw material for composites. In this review, I describe the basic characters of fibers, their structure, development, uses, and some of the current major model plants for fiber formation. I discuss open developmental questions and various aspects of further research. Most of the recent progress in the biology of fiber formation, especially in their cell-wall chemistry, emerged from studies of several model plants: Arabidopsis thaliana, Populus sp., Eucalyptus sp., flax, and hemp. I stress the critical need to combine the use of modern methods of research with classical botany. Approaching the issue of fiber formation only by molecular or only by classical methods will not only limit the progress, but may result in critical mistakes. Considering the importance of fibers to humanity, it is surprising how little we know about the biology of fiber formation and how little it is studied as compared, for instance, to the effort to study the genetics and cell biology of flower organ identity.     

Differentiation of the ray system in woody plants

The regulation of vascular ray differentiation has received limited attention, despite the fact that vascular rays constitute an important part of the secondary body of plants. In this paper we review developmental aspects of the ray system and suggest a general hypothesis for the regulation of ray differentiation and evolution. In studies of ray differentiation, two basic factors should be taken into consideration: 1) the normal gradual increase in ray size in relation to age, distance from the pith, and distance from the young leaves; and 2) the influence of wound effects on the size, structure, and spacing of rays. The relationships between the rate of cambial activity and secondary xylem differentiation are not clearly understood. There are contrasting results on the relationships between ray number and rate of radial growth. The rate of radial growth (= rate of cambial activity) is not the regulating mechanism of ray characteristics. Bünning (1952, 1965) proposed that rays are distributed regularly in the tissue, as the outcome of an inhibitory influence expressed by them. However, Bünning’s hypothesis contradicts a basic feature of the vascular ray system, namely, fusion of rays. Detailed histological studies of the secondary xylem revealed that proximity to and contact with rays plays a major role in the survival of fusiform initials in the cambium (Bannan, 1951, 1953). Such evidence led Ziegler (1964) to suggest that since the cambium is supplied predominantly via the rays, this is an effective feedback regulative system for an equidistant arrangement of the rays. The hypothesis that rays are induced and controlled by a radial signal flow seems to be the best explanation for the structure and spacing of rays. The formation of a polycentric ray—a special case of “ray” initiation inside a vascular ray—supports the idea that radial signal flow occurs within the rays (Lev-Yadun & Aloni, 1991a). This idea is also supported by findings fromQuercus species in which aggregate rays in the xylem disperse naturally in branch junctions and, following partial girdling, leave a longitudinal narrow bridge of cambium and bark as a result of enhanced axial signal flow (of auxin and other growth regulators) (Lev-Yadun & Aloni, 1991b). The longitudinally elongated shape of rays is their response to axial signal flows (mainly the polar auxin flow). Two methods have been used to study the evolution of the ray system: 1) statistical studies of the relationships between vessel and ray characteristics in many species, when vessel characteristics were the evolutionary standard, and 2) comparison of ray characteristics in fossils originating from several geological eras. We suggest that evolution of the ray system reflects changes in the relations between radial and axial signal flows.     

Gloger's rule in plants: The species and ecosystem levels

Gloger''s rule posits that darker birds are found more often in humid environments than in arid ones, especially in the tropics. Accordingly, desert-inhabiting animals tend to be light-colored. This rule is also true for certain mammalian groups, including humans. Gloger''s rule is manifested at 2 levels: (1) at the species level (different populations of the same species have different pigmentation at different latitudes), and (2) at the species assembly level (different taxa at a certain geography have different pigmentation than other taxa found at different habitats or latitudes). Concerning plants, Gloger''s rule was first proposed to operate in many plant species growing in sand dunes, sandy shores and in deserts, because of being white, whitish, or silver colored, based on white trichomes, because of sand grains and clay particles glued to sticky glandular trichomes, or because of light-colored waxes. Recently, Gloger''s rule was shown to also be true at the intraspecific level in relation to protection of anthers from UV irradiation. While Gloger''s rule is true in certain plant taxa and ecologies, there are others where “anti-Gloger” coloration patterns exist. In some of these the selective agents are known and in others they are not. I present both Gloger and “anti-Gloger” cases and argue that this largely neglected aspect of plant biology deserves much more research attention.     

Does chemical aposematic (warning) signaling occur between host plants and their potential parasitic plants?

Aposematism (warning) signaling is a common defensive mechanism toward predatory or herbivorous animals, i.e., interactions between different trophic levels. I propose that it should be considered at least as a working hypothesis that chemical aposematism operates between certain host plants and their plant predators, parasitic plants, and that although they are also plants, they belong to a higher trophic level. Specific host plant genotypes emit known repelling chemical signals toward parasitic plants, which reduce the level of, slow the directional parasite growth (attack) toward the signaling hosts, or even cause parasitic plants to grow away from them in response to these chemicals. Chemical host aposematism toward parasitic plants may be a common but overlooked defense from parasitic plants.     

Plasticity and variability in the patterns of phytolith formation in Asteraceae species along a large rainfall gradient in Israel

Silicification and phytolith formation in Poaceae species growing in arid and semi-arid regions are commonly thought to be positively correlated with silica and water availabilities and with transpiration. To expand our understanding of this phenomenon, we chose to study species of the Asteraceae, the largest dicotyledonous family. We measured phytolith concentrations in eight Asteraceae species (three non-spiny and five spiny) and one Poaceae species (Avena sterilis), as reference, along a large climatic gradient of 80–900 mm mean annual rainfall in Israel.     

Yield stability: an agronomic perspective on the origin of Near Eastern agriculture

Here we argue that, based on evolutionary, ecological and agronomic considerations, climate change could not have been a suitable background nor a probable cause of plant domestication in the Near East. This thesis is developed based on the year-to-year yield dynamics in traditional rainfed grain farming in semi-arid environments, on the genetic basis that underlies temporal yield dynamics in natural wild cereal populations as well as in traditional farming systems, and upon the recognition that prior to elaborate high capacity and long-range trade networks, yield stability was more important than yield maximization. We also briefly discuss the likely social and cultural responses to subtle and real climatic changes vs. responses to rapid directional environmental trends. Taking into account the agronomic, ecological and genetic aspects discussed, it is suggested that the Near Eastern founder crop assemblage was chosen to function within the normal east Mediterranean precipitation regime, in which good rainy years create the ‘normal surplus’ that sustains farming communities during drought years, and the different crop types provide the system with its compensating ability. A slow (but real) climatic change is unlikely to induce major (revolutionary) cultural changes. Nor would a prominent environmental change provide the proper background for the origins of agriculture because it would abolish the buffering capacity of the system. Therefore, farming cannot function as a sustainable ‘buffering mechanism’ to counterbalance climatic instability causing natural resource depletion.