A comparison of canopy evapotranspiration for maize and two perennial grasses identified as potential bioenergy crops

In the Midwestern US, perennial rhizomatous grasses (PRGs) are considered one of the most promising vegetation types to be used as a cellulosic feedstock for renewable energy production. The potential widespread use of biomass crops for renewable energy production has sparked numerous environmental concerns, including the impacts of land‐use change on the hydrologic cycle. We predicted that total seasonal evapotranspiration (ET) would be higher for PRGs relative to maize resulting from higher leaf area and a prolonged growing season. We further predicted that, compared with maize, higher aboveground biomass associated with PRGs would offset the higher ET and increase water‐use efficiency (WUE) in the context of biomass harvests for liquid biofuel production. To test these predictions, ET was estimated during the 2007 growing season for replicated plots of Miscanthus×giganteus (miscanthus), Panicum virgatum (switchgrass), and Zea mays (maize) using a residual energy balance approach. The combination of a 25% higher mean latent heat flux (λET) and a longer growing season resulted in miscanthus having ca. 55% higher cumulative ET over the growing season compared with maize. Cumulative ET for switchgrass was also higher than maize despite similar seasonal‐mean λET. Based on total harvested aboveground biomass, WUE was ca. 50% higher for maize relative to miscanthus; however, when WUE calculated from only maize grain biomass was compared with WUE calculated from miscanthus harvested aboveground biomass, this difference disappeared. Although WUE between maize and miscanthus differed postsenescence, there were no differences in incremental WUE throughout the growing season. Despite initial predictions, aboveground biomass for switchgrass was less than maize; thus WUE was substantially lower for switchgrass than for either maize scenario. These results indicate that changes in ET due to large‐scale implementation of PRGs in the Midwestern US would likely influence local and regional hydrologic cycles differently than traditional row crops.     

Host specificity of insects in a community of three co-dominant Eucalyptus species

In a subalpine association of three Eucalyptus species, phytophagous insects showed strong host preferences even among very closely related Eucalyptus species. Sixty-three per cent of insect species attacked only one eucalypt species, 30% attacked two species and only 8% fed on all three. Ninety-seven per cent of individuals belonged to species using one or two hosts. The results are discussed in relation to the degree of host specificity that might be expected when most potential hosts are members of a single genus, the way in which host specificity is determined, and the potential of insects with host preferences to affect the dynamics of plant communities.     

Tetrapod Limblessness: Evolution and Functional Corollaries

Multiple lines of tetrapods show reduced limbs or their loss.Such patterns are in diverse lines associated with multipleother characteristics. Only bodily elongation represents a commondenominator. Analysis suggests that elongation for traverseof crevices in a sheltering environment and for the utilizationof undulatory locomotion may have provided the initial selectiveadvantage to the system. Limb reduction would then have beensecondary. This hypothesis leads to several interesting implicationsabout the process of diversification in tetrapods.     

Fine Structure of the Mastigont System in Tritrichomonas muris (Grassi)*

SYNOPSIS. Tritrichomonas muris shares many fine-structural details with the previously described members of the family Trichomonadidae, and especially with the organisms belonging to the subfamily Tritrichomonadinae. Among the features which T. muris has in common with all Trichomonadidae and in all probability with other Trichomonadida are the arrangement and structure of: the kinetosomes; many rootlet filaments, including the sigmoid filaments of kinetosome #2; the parabasal apparatus; and the pelta-axostyle complex. The structures which T. muris-type flagellates share with other Tritrichomonadinae, and especially with Tritrichomonas augusta-type species (including T. foetus), but not with Trichomonadinae that have been studied to date, are: the Type A costa; a comb-like structure, which appears to have replaced the costal base of Trichomonadinae and of Hypotrichomonas; the suprakinetosomal body, rudimentary in T. muris; and the infrakinetosomal body. The undulating membrane, like that of T. augusta-type organisms, consists of a proximal and a distal part. The proximal part, which contains the proximal marginal lamella, is less developed in T. muris than in T. augusta-type flagellates, being represented by a relatively low ridge for the entire length of the organism. The distal part of the membrane in T. muris, on the other hand, is more highly developed; it is a heavy cord, with a distal marginal lamella which consists of a large triangular organelle having a highly ordered structure and 2 less well defined cords distal to this organelle. The tubules of the recurrent flagellum occupy the area distal to the cords. The sigmoid filaments of kinetosome #2, unlike those of other Trichomonadidae examined to date, extend posteriorly to the peltar-axostylar junction; they seem to terminate within the cytoplasm near, but not connected to the axostyle. In addition to the Type A costa, there is a small rootlet filament, which appears to be homologous to the rudimentary costa noted in Hypotrichomonas. Some of the paraxostylar and paracostal granules consist of an outer, relatively dense layer and an inner “core” of moderate density; between the 2 there is a lucent ring. The discussion deals in some detail with the possible nature of the paraxostylar and paracostal granules in trichomonads. The taxonomic status of Tritrichomonas cricetus (Wantland) [Tritrichomonas criceti (Wantland) emend. Levine] and Trichomonas criceti Ray & Sen Gupta is discussed in an appendix; it is concluded that both of these names are synonyms of T. muris (Grassi).