Structure and species richness in wetland continua on sandy soils in subtropical and tropical Australia

Net photosynthetic fixation of wetland plant communities is confined to the period of the year when the surface soil is not waterlogged and is thus well aerated. In the open‐structured vegetation continuum across freshwater wetlands on sandy soils in subtropical and tropical Australia, the sum of the foliage projective covers (FPCs) of the overstorey and understorey strata remains constant, while that of the overstorey decreases to zero as seasonal waterlogging (and anaerobic conditions) in the surface root systems increases. Density and height of the overstorey trees – of only one or two species – and species richness (number of species per hectare) in the understorey decreases along this waterlogging gradient. Melaleuca paperbark trees, possessing surface roots with cortical aerenchyma, may form a closed‐forest at the edge of the wetland continuum wherever there is a continuous flow of aerated water. As global warming progresses, an increase in air temperature in the atmosphere flowing over and through the wetland continuum during the short period of annual foliage‐growth will affect the combined FPCs of overstorey and understorey strata, as well as the leaf‐specific weights of all leaves throughout the plant community. With a reduction in net photosynthetic fixation, species richness of the plant community will slowly decline.     

Cuticular morphology and aspects of the ecology and fossil history of North Queensland rainforest Proteaceae

Cuticles of North Queensland rainforest Proteaceae were examined using light and scanning electron microscopy. The genera of North Queensland rainforest Proteaceae are mostly endemic and composed of one or few species, with greatest diversity in the granitic uplands of the region. Knowledge of cuticular morphology may be an important tool in determining the true affinities of several undescribed taxa in the region and can be used to explore hypotheses relating to the history of the Proteaceae. Some species exhibit purported xeromorphic features of thick cuticles, sunken stomates and dense trichome cover on the abaxial surface. Grevillea , Banksieae and Stenocarpus are believed to have radiated into open, much less mesic environments. In the former two taxa this can be interpreted in terms of xeromorphic features expressed in their cuticular morphologies, whereas in Stenocarpus amphistomaty in species of open habitats suggests an alternative mode of evolution more related to physiological factors. Several Cainozoic proteaceous macrofossils temporally and spatially far removed from North Queensland possess cuticular morphologies very similar or identical to extant rainforest taxa in the region.     

The structure of the ostracode carapace

The carapace ultrastructure of three Recent [Heterocypris incongruens (Ramdohr), Cypridopsis uidua (Müller), and Conchoecia belgica Müller] and one Cretaceous ostracode species [Cypridea propunctata Sylvester-Bradley] has been studied by means of standard electron microscope techniques. The carapace is shown to be an organic structure divisible into an outer epicuticle, a median exocuticle and an inner endocuticle in the three cypridacean ostracodes examined. In Conchoecia belgica only an outer epicuticle and an inner endocuticle were observed, but this may be due to preservation. The chitin structure of the carapace of calcareous ostracodes is shown to be essentially an interlocking lattice, more coarsely developed in the exocuticle; layered (lamellar) chitin is only present in the selvage and in the connective tissue joining the valves at the hinge. The non-calcareous Conchoecia belgica possesses the layered chitin structure common to other crustaceans and to insects. The relationship of the carapace structure to that present in the decapod and insect exoskeleton is discussed. The technical problems met with during this study are considered in order to outline the difficulties associated with the study of organisms of this size.     

Population structure in Mediterranean islands and risk of genetic invasion in Culexpipiens L. (Diptera: Culicidae)

The mosquito Culex pipiens is subjected to organophosphate treatments in both Corsica and southern Sardinia, but the resistance gene A2-B2, which is currently in a worldwide expansion, has only reached Sardinia. In order to understand this situation, the genetic structure of populations sampled in Sardinia and Corsica was assessed using 15 isozymes. Two loci (HK1 and HK2) were not taken into account because of the possibility of selection. For trie other loci, statistical independence was not rejected for all possible pairs, and no deviation from Hardy-Weinberg expectations was apparent. Low but significant genie differentiation was present between Corsica and Sardinia, as well as between northern and southern Sardinia, despite a large number of effective migrants per generation. These results are discussed in the context of the high probability of extinction/recolonization of breeding sites, the flight migration ability of this mosquito, and the pleiotropic cost of insecticide resistances genes. It is concluded that A2-B2 resistance is unlikely to reach Corsica from southern Sardinia, unless accidental human transportation occurs.     

Human TRP-1 Has Tyrosine Hydroxylase but no DOPA Oxidase Activity

Human TRP-1 has been immunopurified from normal human melanocytes cultured from black neonatal subjects and used to investigate the catalytic function of TRP-1 for the two substrates, L-tyrosine and L-DOPA. Immunopurified TRP-1 did not demonstrate DOPA staining on SDS/PAGE nor DOPA oxidase (DO) activity with either routine or modified assays. The purified TRP-1 also demonstrated no tyrosine hydroxylase (TH) activity using the routine Pomerantz assay. However, there was apparent TH activity exhibited by immunopurified TRP-1 under conditions with low tyrosine concentration (≤0.8 μCi/ml of ³H-tyrosine), prolonged incubation time (i.e., overnight) and in the absence of the cofactor L-DOPA. Using these latter specific conditions, TH activity was also detected in cell lysates from a tyrosinase-negative albino melanocyte line which exhibited no TH activity with the routine Pomerantz assay. In addition, TH activity under low substrate assay conditions was not exhibited in a melanocyte line derived from a TRP-1 deficient, Brown albino individual. However, the absence of TH in this Brown albino cell line could be compensated for by the addition of L-DOPA to the assay. These results suggested that TRP-1 has some tyrosine hydroxylase but no DOPA oxidase activity. We propose that one function of TRP-1 is to modulate tyrosinase activity by making DOPA available as a cofactor to perpetuate the initial steps in melanogenesis.