On Arborescence in Gahnia clarkei and Gahnia sieberiana

Specimens of Gahnia sieberiana from Brisbane, Queensland, andof Gahnia clarkei from near Orbost, Victoria, were collectedand examined both morphologically and anatomically. The speciesgrow in wet areas and are of interest because they representthe largest arborescent species known in the Cyperaceae. Stemdiameters up to 120 mm and stems up to 10 m long have been observed.Such long stems tend to be supported by nearby vegetation. Althoughfresh stems are tough and woody, they are brittle. Branchingof the stems is sympodial, and numerous branches are producedby plants growing in exposed habitats. There is less branchingin plants from shaded habitats. Basal shoots may also occur.Adventitious roots develop basally on most plants, but withG. sieberiana, some adventitious roots form near the shoot apexand grow in and around leaf bases. Anatomical features of interestare an endodermoid layer composed of sclereids with elongate,undulated, outer tangential walls that are lignified and suberized,short vessel elements with horizontal to oblique simple perforationplates, and relatively short sclereids surrounding vessel elementsin the vascular bundles. Some vascular bundles are bipolar.The presence of short vessel elements here is in marked contrastto the longer tracheary elements in other arborescent monocotyledons. Arborescence, stem anatomy, Cyperaceae, Gahnia, saw sedge, Monocotyledon, bipolar bundles, morphology, endodermoid layer     

Biomass: Is it a useful tool in paleocommunity reconstruction?

In general, more of the biomass of the community is preserved than is its numerical abundance. Thus, the paleontologist, on the average, works with more of the community when biomass is used. Community characteristics such as taxon dominance and habitat proportions are at least as accurately derived from biomass as numerical abundance. The use of biomass is clearly more appropriate in describing energy flow and trophic proportions. Whenever possible, biomass should be used as a complement to numerical abundance in future paleoecologic reconstructions.     

Assessing transportation by the covariance of species with comments on contagious and random distributions

The paleoecologist must be able to distinguish a transported assemblage from an in situ one. A method is proposed to assess whether the post-mortem transport of individuals affected their observed spatial (horizontal) distribution. The spatial distribution of a species can be random or contagious. The spatial distribution of individuals of a species in the death assemblage produced by the cumulation of many temporally discrete inputs will be random if the individual inputs are random and contagious if the inputs are contagious. The spatial distribution patterns of several species should not covary in the absence of physical disturbance regardless of their own distributions, however. The degree of covariance between individuals of several species of similar hydrodynamic propensity is dependent on the amount and intensity of postmortem movement. The more species that covary, and the larger the size classes that covary, the more likely that transportation played an important role in the species' distribution patterns. Conversely, the absence of covariance suggests that, for at least some species, biological factors determined the species' spatial distributions. Similarly, covariance of vertical distribution patterns might suggest homogenization. by bioturbational or physical mixing.     

On the Occurrence of Intracellular Blue-green Algae in Cortical Cells of the Apogeotropic Roots of Macrozamia communis L. Johnson

The occurrence of species of the cyanophytes Nostoc and Anabaenain the cortex near the algal zone is reported for apogeotropicroots of Macrozamia communis L. Johnson. Algae were found tooccur both intercellularly and intracellularly in cells of theinner and outer cortex. This is the first record of intracellularalgae in the cycads and only the second report of this phenomenonin vascular plants. By examination of cells at various stagesof invasion by algae, it is interpreted that algal invasionof cortical cells and intercellular spaces is preceded by mucusapparently secreted by algal zone cells of the host, and depositedin intercellular spaces of cortical parenchyma cells nearby.Also algal penetration of cortical cells is preceded by an algalinvasion front of finely granular mucal material which bypassesmucus already deposited in intercellular spaces and may eitherlyse part of the host cell wall or enter through the plasmo-desmata,filling much of the cell cavity. Subsequently, large numbersof the algal symbionts enter the cell and may be enclosed withinhost wall material. Electron microscopic techniques are nowbeing employed to further clarify these invasion processes.