Gas exchange, growth, yield and beverage quality of Coffea arabica cultivars grafted on to C-canephora and C-congensis

Gas exchange, leaf carbon isotope discrimination, growth, yield and beverage quality were evaluated for two Coffea arabica cultivars (Catuai and Mundo Novo), grafted on to C, canephora and C. congensis progenies growing in open fields. During the years 1994 to 1997, grafting resulted in an average increase in bean yield of 151 and 89% for Catuai and Mundo Novo respectively. As analysed by sensory analyses and by the ratio between the mono-isomers and di-isomers of caffeoylquinic acid, beverage quality of the C. arabica was not altered by grafting. Shoot growth was significantly greater in grafted plants, showing an increase of 52% in total leaf area compared with the non-grafted plants. Under conditions of water excess in the soil there was little difference in the transpiration and stomatal conductance rates between the grafted and non-grafted plants, I,ut the net photosynthesis was higher in grafted plants. With an accentuated water deficit in the soil in the dry period, the grafted plants showed significantly higher transpiration and stomatal conductance rates than the non-grafted plants, and similar values to those of C. canephora. Carbon isotope discrimination was greater in the grafted plants, suggesting greater root hydraulic conductance. The results suggest that the better performance of the grafted plants during the dry period was due to the greater capacity of the root system of C. canephora to provide water to the shoot thereby maintaining greater gas exchange in the leaves and consequently a greater carbon gain.o TEXTO COMPLETO DESTE ARTIGO, ESTARÁ DISPONÍVEL À PARTIR DE AGOSTO DE 2015.37224125

Changes in sea ice cover and ice sheet extent at the Yermak Plateau during the last 160 ka – Reconstructions from biomarker records

The Yermak Plateau is located north of Svalbard at the entrance to the Arctic Ocean, i.e. in an area highly sensitive to climate change. A multi proxy approach was carried out on Core PS92/039-2 to study glacial-interglacial environmental changes at the northern Barents Sea margin during the last 160 ka. The main emphasis was on the reconstruction of sea ice cover, based on the sea ice proxy IP25 and the related phytoplankton - sea ice index PIP25. Sea ice was present most of the time but showed significant temporal variability decisively affected by movements of the Svalbard Barents Sea Ice Sheet. For the first time, we prove the occurrence of seasonal sea ice at the eastern Yermak Plateau during glacial intervals, probably steered by a major northward advance of the ice sheet and the formation of a coastal polynya in front of it. Maximum accumulation of terrigenous organic carbon, IP25 and the phytoplankton biomarkers (brassicasterol, dinosterol, HBI III) can be correlated to distinct deglaciation events. More severe, but variable sea ice cover prevailed at the Yermak Plateau during interglacials. The general proximity to the sea ice margin is further indicated by biomarker (GDGT) - based sea surface temperatures below 2.5 °C

Agalactosylated IgG antibodies depend on cellular Fc receptors for in vivo activity

IgG antibodies are glycoproteins containing a branched sugar moiety attached to the asparagine 297 residue in the antibody constant region (Fc). This glycan is essential for maintaining a functional Fc structure, which is a prerequisite for antibody-mediated effector functions, such as the interaction with cellular Fc receptors or the complement component C1q. Variations in the composition of the sugar moiety can dramatically influence antibody activity. Moreover, humans and mice with autoimmune disorders, such as rheumatoid arthritis, have altered IgG glycosylation patterns with increased levels of antibodies lacking terminal sialic acid and galactose residues (IgG-G0). There is great interest in understanding whether this altered glycosylation pattern influences antibody-mediated effector functions. In vitro studies have suggested that IgG-G0 antibodies gain the capacity to activate the complement pathway via mannose-binding lectin (MBL), which could contribute to antibody-mediated inflammation. We have analyzed the activity of IgG-G0 antibodies in mice with a genetic deletion of MBL (MBL-null mice) and demonstrate that IgG-G0 antibodies are unimpaired in MBL-null mice. In contrast, the activity of these antibody glycovariants is fully dependent on the presence of activating Fc receptors