Niche theory and plant growth form

Plant growth form diversity (GFD) is high in the vegetation of North American deserts, and increases from north (Great Basin Desert) to south (Sonoran Desert). While abiotic features (annual temperature, precipitation, and seasonality) appear to limit the range of desert plant GFD, biotic features associated with the coexisting plants at a site, and their GF distribution, add further constraints. Climate may constrain the GF options at certain sites and select for some degree of GF convergence there, but within sites other species in the vegetation select for GF segregation that fosters the local coexistence of species. In this paper GF variation is viewed along structural niche axes, and related to classical niche theory; several corollaries of the theory are examined in the light of plant GF patterns. These are: a) regular spacing of species on the structural niche axis, and the concept of limiting similarity; b) niche axis complementarity, such that species dissimilar in position on one axis, e.g. GF, are similar in position on other axes, e.g. habitat or substrate, and vice versa; c) niche shifts in GF within species are expected, and occur, as the suite of coexisting species varies among sites with similar climate; d) in some desert plant guilds species with very similar GF do not coexist at a site, but act as geographical replacements in different sites.     

Chaetetid growth form and its controlling factors

Chactetid sponge morphology is examined to provide details on growth styles and their controlling factors. Chactetid growth forms range from laminar to domical. bulbous. columnar and complex branching in a variety of sizes. The chactetid skeleton began as a laminar unit comprising growth of many calicles across the substrate at the same time. Several styles of early growth. involving differential calicle growth rates and varying directions of adjacent calicle growth. are recognized. and result in complex arrangements of caliclcs in the skeleton. Despite this. the cross-sectional protile of the gross morphology at any stage of growth is usually a simple outline. implying that internal complexities of calicle development are modulated to produce an optimum cross-sectional outline for the individual chactetid. The morphological range of chactetids is similar to stromatoporoids. some tabulate. heliolitid and colonial rugose corals. some bryozoans. stromatolites. encrusting foraminifera and calcareous algae: the common environmental controlling factors of sedimentation and turbulence profoundly influenced growth form in all these organisms by virtue of their common sessile shallow marine habit. Chactetid growth forms show a general relationship to the environment: columnar and branching forms grew in quiet water. while laminar and domical were better adapted to environments of higher energies. The environmental adaptations of laminar forms. however. remain problematic. because they are found in both high and low energy facies. and interpretation depends strongly on facies study. Also. interpretation of all growth forms is suspected to relate to taxonomic aspects. as has been recognized for other groups. Unfortunately. chaetetid taxonomy is in need of revision. and at present no certain relationship has been demonstrated between taxonomy and growth form. Some modern calcareous sponges with a chaetetiform architccture also show similarities in growth form to fossil types. and may be subject to similar controls. □Chaetetid. calcified sponge. growth form. Pennsyloanian. North America.     

The growth and form of bacterial colonies.

A simple method is described for measuring the profile of bacterial colonies. Profiles were determined for colonies of Bacillus cereus, Escherichia coli and Staphylococcus albus of different ages. In spite of differences in cell morphology, the colony profiles had a common basic structure consisting of steeply rising leading edge connected by a ridge to an interior region where height also rose, though less steeply, to a flat or domed centre. The colony mass increased exponentially through part of the growth phase. It is suggested that net colony growth consists of a combination of leading edge growth, which is unrestricted and approaches the maximum specific growth rate of the organism, and diffusion-limited growth in the colony interior. Common elements of profiles from each species may be a consequence of such differences in growth rate.     

Shell form and growth of the bivalveScapharca broughtoni

Linear growth rates and age-related changes in shell form are analyzed in the bivalveScapharca broughtoni from several areas of Peter the Great Bay, Sea of Japan. Mollusks grow fast during the first 4 to 5 years of life; at the age of 10–12 years, the annual growth increment in shell size does not usually exceed 1–3 mm. Irrespective of habitat, the shell valve convexity ofS. broughtoni increases with age, but the most significant changes in shell form occur during the first year of life. The peculiarities of growth and age-related changes in shell form ofS. broughtoni are discussed from the standpoint of the functional morphology of burrowing bivalve mollusks, which, at the postlarval stage, change from an attached to a free-living mode of life.     

The growth and form of tunnelling networks in ants

Many biological networks grow under strong spatial constraints, where the large-scale structure emerges from the extension, the branching and intersection of growing parts of the network. One example is provided by ant tunnelling networks, which represent the most common nest architecture in ants. Our goal was to understand how these network structures emerge from the tunnel growth dynamics. We used a standardized two-dimensional set-up shaped as a disk and studied the characteristics of tunnel growth in terms of initiation, propagation and termination of new digging sites and found that they can be described with simple probabilistic laws. We show that a model based on these simple laws and for which parameters were measured from the sand disks experiments can account for the emergence of several topological properties that were observed in experimental networks. In particular, the model accurately reproduced an allometric relation between the number of edges and the number of nodes, as well as an invariance of the node degree distribution. The model was then used to make predictions about the resulting networks' topology when the geometry of the sand substrate was shaped as a square. Experiments aimed at testing the model's predictions showed that the predictions were indeed validated. Both in the model and in the experiments, there was a similar trend for the node degree distribution tail to be steeper in the square sand patch than in the disk sand patch, while other characteristics such as the meshedness (i.e. how densely the network is internally connected) remained constant. Because network growth based on branching/fusion events is widespread in biological systems, this general model might provide useful insights for the study of other systems and, more generally, the evolution of spatial networks in biological systems.     

Phloem loading,plant growth form,and climate

Plasmodesmatal frequencies in the phloem of leaf minor veins vary considerably, suggesting that photoassimilate is loaded into the phloem by different strategies. The ecophysiological basis for multiple loading types is unknown. We updated the analysis of van Bel and Gamalei (Plant Cell Environ 15: 265–270, 1992) with more current phylogenetic data and by treating separately two symplastic loading types, those that load actively by polymer trapping (synthesis of raffinose family oligosaccharides—RFOs), and those that load passively, by diffusion. The results indicate a stronger association between passive, symplastic loading and the tree growth form than previously recognized. Apoplastic loading is highly correlated with the herbaceous habit. There is no correlation between RFO families and growth form. At the family level, there are no correlations between minor vein types and climate that cannot be explained by the dearth of woody plants in the arctic for reasons unassociated with phloem loading. However, at the species level, a floristic analysis uncovered a correlation between the RFO trait and species frequency in tropical and subtropical regions of the world. The correlations between loading types and both growth form and climate are subtle, probably indirect, and poorly understood.     

Massive aerial roots affect growth and form of Dracaena draco

Key message

Large aerial roots grow out from the branches of injured Dracaena draco trees. They integrate with the trunk or cause the branches to break off the tree and deform it.

Abstract

Dracaena draco, the dragon tree, is an iconic monocot of the Canary Islands with a tree-like growth habit and some distinctive features that are unique in the plant kingdom. We report about the massive aerial roots in this tree. They appear on trees that are injured or under environmental stress and affect growth form and the whole life of the plant. We analysed the growth of these roots and tested our findings in experiments on plants. Clusters of these roots emerge from the bases of the lowest branches and growing down they may reach the soil. Descending along the trunk, they cling tightly to the trunk, integrate with it and contribute to its radial growth. This may explain (1) why the trunk of a mature D. draco tree looks fibrous, as if made of many individual strands, and (2) how some trees reach enormous radial dimensions. Alternately, a large, 2–5 m high, multi-segmented branch with aerial roots at its base, may break off the tree and grow on its own, as a mammoth off-cut, perhaps the largest known in the plant kingdom. This detachment would cause a significant reduction in the size of the crown and deform its original, highly organized pattern of branching. In the extreme condition this may result in the destruction of the mother plant.     

DNA from soil mirrors plant taxonomic and growth form diversity

Ecosystems across the globe are threatened by climate change and human activities. New rapid survey approaches for monitoring biodiversity would greatly advance assessment and understanding of these threats. Taking advantage of next-generation DNA sequencing, we tested an approach we call metabarcoding: high-throughput and simultaneous taxa identification based on a very short (usually <100 base pairs) but informative DNA fragment. Short DNA fragments allow the use of degraded DNA from environmental samples. All analyses included amplification using plant-specific versatile primers, sequencing and estimation of taxonomic diversity. We tested in three steps whether degraded DNA from dead material in soil has the potential of efficiently assessing biodiversity in different biomes. First, soil DNA from eight boreal plant communities located in two different vegetation types (meadow and heath) was amplified. Plant diversity detected from boreal soil was highly consistent with plant taxonomic and growth form diversity estimated from conventional above-ground surveys. Second, we assessed DNA persistence using samples from formerly cultivated soils in temperate environments. We found that the number of crop DNA sequences retrieved strongly varied with years since last cultivation, and crop sequences were absent from nearby, uncultivated plots. Third, we assessed the universal applicability of DNA metabarcoding using soil samples from tropical environments: a large proportion of species and families from the study site were efficiently recovered. The results open unprecedented opportunities for large-scale DNA-based biodiversity studies across a range of taxonomic groups using standardized metabarcoding approaches.     

Plant classification by growth form for field use

This simple classification system for terrestrial plants, based mainly on growth forms and therefore avoiding the need for identification to genus or species, has been used successfully in studies of colonization and succession on derelict land, but also has other applications