Morphometric differences in the grasshopper Cornops aquaticum (Bruner, 1906) from South America and South Africa

The semi-aquatic grasshopper Cornops aquaticum is native to South America and inhabits lowlands from southern Mexico to Central Argentina and Uruguay. It is host-specific to aquatic plants in the genera Eichhornia and Pontederia. A quarantine population has existed in South Africa for 10 y, and it is planned to release it there as a biological control agent of water hyacinth, E. crassipes. Various studies of C. aquaticum are coordinated under HICWA (www.mpil-ploen.mpg.de). This paper compares the morphometry of the release population and 11 native populations in South America. We tested four hypotheses: 1) South African and South American populations of C. aquaticum differ in morphology; 2) the South African laboratory population is more similar to other isolated populations in South America than to nonisolated populations; 3) morphology differs across sites; 4) morphology differs with host plant. South African populations differed from continental nonisolated populations, but not from continental isolated ones. Isolated populations presented smaller individuals than nonisolated, but there was also a change in male morphology: while in nonisolated populations male wing length was similar to their body length, in isolated populations, male wings were smaller than body length. Females were larger when on Eicchornia azurea than on E. crassipes, while males presented larger wings than their body on E. azurea, and similar lengths on E. crassipes. These morphological changes may have resulted from phenotypic plasticity, selection for small size, or because of a loss of genetic diversity in quantitative traits.Fil: Adis, Joachim. Institute for Limnology; AlemaniaFil: Sperber, Carlos F. Universidade Federal de Viçosa; BrasilFil: Brede, Edward G. Institute for Limnology; AlemaniaFil: Capello, Soledad. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto Nacional de Limnología. Universidad Nacional del Litoral. Instituto Nacional de Limnología; ArgentinaFil: Franceschini, Maria Celeste. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Nordeste. Centro de Ecología Aplicada del Litoral. Universidad Nacional del Nordeste. Centro de Ecología Aplicada del Litoral; ArgentinaFil: Hill, Martin. Rhodes University; SudáfricaFil: Lhano, Marcos G. Universidade Federal de Viçosa; BrasilFil: Marques, Marinê. A;z M.. Universidade Federal de Mato Grosso; BrasilFil: Nunes, Ana L.. Muséu Paraense Emílio Goeldi; BrasilFil: Polar, Perry. CAB International; Trinidad y Tobag

Role of protein kinase C and epidermal growth factor receptor signalling in growth stimulation by neurotensin in colon carcinoma cells

<p>Abstract</p> <p>Background</p> <p>Neurotensin has been found to promote colon carcinogenesis in rats and mice, and proliferation of human colon carcinoma cell lines, but the mechanisms involved are not clear. We have examined signalling pathways activated by neurotensin in colorectal and pancreatic carcinoma cells.</p> <p>Methods</p> <p>Colon carcinoma cell lines HCT116 and HT29 and pancreatic adenocarcinoma cell line Panc-1 were cultured and stimulated with neurotensin or epidermal growth factor (EGF). DNA synthesis was determined by incorporation of radiolabelled thymidine into DNA. Levels and phosphorylation of proteins in signalling pathways were assessed by Western blotting.</p> <p>Results</p> <p>Neurotensin stimulated the phosphorylation of both extracellular signal-regulated kinase (ERK) and Akt in all three cell lines, but apparently did so through different pathways. In Panc-1 cells, neurotensin-induced phosphorylation of ERK, but not Akt, was dependent on protein kinase C (PKC), whereas an inhibitor of the β-isoform of phosphoinositide 3-kinase (PI3K), TGX221, abolished neurotensin-induced Akt phosphorylation in these cells, and there was no evidence of EGF receptor (EGFR) transactivation. In HT29 cells, in contrast, the EGFR tyrosine kinase inhibitor gefitinib blocked neurotensin-stimulated phosphorylation of both ERK and Akt, indicating transactivation of EGFR, independently of PKC. In HCT116 cells, neurotensin induced both a PKC-dependent phosphorylation of ERK and a metalloproteinase-mediated transactivation of EGFR that was associated with a gefitinib-sensitive phosphorylation of the downstream adaptor protein Shc. The activation of Akt was also inhibited by gefitinib, but only partly, suggesting a mechanism in addition to EGFR transactivation. Inhibition of PKC blocked neurotensin-induced DNA synthesis in HCT116 cells.</p> <p>Conclusions</p> <p>While acting predominantly through PKC in Panc-1 cells and via EGFR transactivation in HT29 cells, neurotensin used both these pathways in HCT116 cells. In these cells, neurotensin-induced activation of ERK and stimulation of DNA synthesis was PKC-dependent, whereas activation of the PI3K/Akt pathway was mediated by stimulation of metalloproteinases and subsequent transactivation of the EGFR. Thus, the data show that the signalling mechanisms mediating the effects of neurotensin involve multiple pathways and are cell-dependent.</p

Microbial production of recalcitrant dissolved organic matter: long-term carbon storage in the global ocean

The biological pump is a process whereby CO2 in the upper ocean is fixed by primary producers and transported to the deep ocean as sinking biogenic particles or as dissolved organic matter. The fate of most of this exported material is remineralization to CO2, which accumulates in deep waters until it is eventually ventilated again at the sea surface. However, a proportion of the fixed carbon is not mineralized but is instead stored for millennia as recalcitrant dissolved organic matter. The processes and mechanisms involved in the generation of this large carbon reservoir are poorly understood. Here, we propose the microbial carbon pump as a conceptual framework to address this important, multifaceted biogeochemical problem.National Basic Research Program of China [2007CB815904]; National Natural Science Foundation of China [40632013/40841023]; SOA project [201105021/DY1150243]; Gordon and Betty Moore Foundation ; US National Science Foundation [648116, 0752972, 0851113, MCB-0453993]; French Science Ministry [ANR07 BLAN 016]; Netherlands Organisation for Scientific Research-Earth and Life Science