Ecophenotypic strategies of dalmanellid brachiopods

General ecophenotypic patterns, of particular interest when they apply to all, or most, taxa of the group concerned, can never be demonstrated until after monophyletic taxa have been recognized, that is, until after the initial stages of phylogeny construction have been carried out. In criticizing certain dalmanellid phylogenies, and based in large part on a study of five 'species subgroups'. Hurst & Watkins (1978; Geologica et Palaeontologica 12 ) postulate ecophenotypic patterns for Isorthis , and Hurst (1978; Palaeontology 21 ) postulates general patterns of ecophenotypic variation for dalmanellid brachiopods. These patterns may be invalid for four reasons: (1) Univariate and 'bivariate' statistical analysis of the samples used to define the five subgroups reveals no significant differences between subgroups, or vertical trends, for the very morphological characters claimed to exhibit the ecophenotypic patterns; (2) Hurst & Watkins' discriminant function analysis contains procedural errors and its results are ambiguous; (3) several of the five subgroups represent mixtures of unrelated taxa; (4) in recognizing the alleged patterns, Hurst & Watkins ignored contrary evidence from many taxa (and from many dalmanellid studies). □ Brachiopoda, Dalmanellidae, Silurian, ecology, evolution, systematics.     

Dissolved carbon leaching from soil is a crucial component of the net ecosystem carbon balance

Estimates of carbon leaching losses from different land use systems are few and their contribution to the net ecosystem carbon balance is uncertain. We investigated leaching of dissolved organic carbon (DOC), dissolved inorganic carbon (DIC), and dissolved methane (CH₄), at forests, grasslands, and croplands across Europe. Biogenic contributions to DIC were estimated by means of its δ¹³C signature. Leaching of biogenic DIC was 8.3±4.9 g m^?2 yr^?1 for forests, 24.1±7.2 g m^?2 yr^?1 for grasslands, and 14.6±4.8 g m^?2 yr^?1 for croplands. DOC leaching equalled 3.5±1.3 g m^?2 yr^?1 for forests, 5.3±2.0 g m^?2 yr^?1 for grasslands, and 4.1±1.3 g m^?2 yr^?1 for croplands. The average flux of total biogenic carbon across land use systems was 19.4±4.0 g C m^?2 yr^?1. Production of DOC in topsoils was positively related to their C/N ratio and DOC retention in subsoils was inversely related to the ratio of organic carbon to iron plus aluminium (hydr)oxides. Partial pressures of CO₂ in soil air and soil pH determined DIC concentrations and fluxes, but soil solutions were often supersaturated with DIC relative to soil air CO₂. Leaching losses of biogenic carbon (DOC plus biogenic DIC) from grasslands equalled 5–98% (median: 22%) of net ecosystem exchange (NEE) plus carbon inputs with fertilization minus carbon removal with harvest. Carbon leaching increased the net losses from cropland soils by 24–105% (median: 25%). For the majority of forest sites, leaching hardly affected actual net ecosystem carbon balances because of the small solubility of CO₂ in acidic forest soil solutions and large NEE. Leaching of CH₄ proved to be insignificant compared with other fluxes of carbon. Overall, our results show that leaching losses are particularly important for the carbon balance of agricultural systems.     

Mass algal culture in outdoor plastic-covered minipond systems

A comparative study was undertaken to evaluate the performance of algal cultures grown in plastic-covered outdoor minipond systems. It was demonstrated that production in enclosed miniponds was higher than in open ones on account of the stimulatory effects of elevated temperatures which developed in the enclosed systems. Although the plastic covering reduced the amount of light which was available for photosynthesis, this had minimal effects on production due to the light saturation characteristics of the algal cells. The practice of enclosing mass algal cultures with transparent plastic appears to show promise in semi-arid regions not only as a procedure to reduce evaporation, but also as one for increasing algal yields.     

Investigations in plant commonness and rarity: a comparison of seed removal patterns in the widespread Jatropha standleyi and the endemic J. chamelensis (Euphorbiaceae)

During early August to late September 1998 we examined seed dispersal in the tree species Jatropha standleyi (widespread) and J. chamelensis (endemic; Euphorbiaceae) at the Estacion de Biologia Chamela, Jalisco, Mexico. Using general linear models, we found that seed removal from beneath the parental canopy did not differ between the two species and that seed removal was correlated with both seed availability on the ground and rodent predation. We inferred that seed removal was largely mediated by rodents and determined that if a seed was not removed within 4d (approx. 16% chance), it was highly unlikely to be removed at all (approx. 3.5% chance) for both species. We note that although differences in patterns of seed removal may not explain the observed differences in range size, differences between the two species in seed crop size arc similar to patterns found in other endemic/widespread species pairs.     

The taxonomy and distribution of Azolla species in southern Africa

The three Azolla species which occur in southern Africa, A. pinnata var. pinnata, A. nilotica and A. filiculoides are identified and their distributions illustrated. The endosymbiotic cyanobacterium Anabaena azollae occurred in dorsal leaf lobe cavities of all three species. The first two species are indigenous to southern Africa, whilst the third, A. filiculoides , is an introduced species from North America. Possible means whereby this species could have been introduced are discussed.