Carbon stable isotope record in the coral species Siderastrea stellata: A link to the Suess Effect in the tropical South Atlantic Ocean

This is the author accepted manuscript. The final version is available from the publisher via the DOI in this record.Coral skeletons are natural archives whose geochemical signatures provide insights into the tropical ocean history beyond the instrumental record. Carbon stable isotopes from coral skeletons (δ13Ccoral) have been used as a proxy for multiple variables on a seasonal basis. Long-term changes in coral δ13C could be related to the changing isotopic composition of the dissolved inorganic carbon (δ13CDIC). δ13CDIC in turn reflects changes in the δ13C of atmospheric CO2, which in the modern Earth system is governed primarily by anthropogenic injection of CO2 into the atmosphere – a process known as the Suess Effect. Here we report three δ13C coral-based records of Siderastrea stellata from the tropical South Atlantic. U-series dating for the colonies 12SFB-1, 13SS-1 and 13SS-2 suggests these corals lived 13, 57 and 65 years, respectively. Short-term δ13C variations in their skeletal aragonite are dominated by interannual variation. All three δ13C records additionally exhibit an overall decreasing trend, with a depletion of about −0.0243 ± 0.0057‰·yr−1 (12SFB-1), −0.0208 ± 0.0007‰·yr−1 (13SS-1) and −0.0214 ± 0.0013‰·yr−1 (13SS-2). These rates of the coral records from Rocas Atoll are similar to the reported trend for the δ13C of atmospheric CO2 over the years 1960–1990 (−0.023 to −0.029‰·yr−1), and to the decreasing rates of global δ13CDIC. Our findings suggest that multiple δ13C coral-based records are required for confidently identifying local changes in the δ13CDIC of the ocean. This information, in turn, can be used to infer changes in the δ13C of the atmospheric CO2 composition and provide valuable information about recent changes on the carbon biogeochemical cycle during the Anthropocene epoch.NSP acknowledges the National Counsel of Technological and Scientific Development (CNPq) for a Post-Doctoral Scholarship Proc. no 150405/2015-4. We thank the chief of the Biological Reserve of Rocas Atoll, Maurizélia de Brito Silva and the field team Tiago Albuquerque, Miguel Miranda, Mirella B. Costa and Eduardo Macêdo, for the great assistance in this study. We thank Gilsa Santana, Vilma Sobral (NEG-LABISE, Brazil) and Bo Petersen (University of Copenhagen) for assisting in stable isotope measurements. We are thankful for the critical and constructive comments of the anonymous reviewers. The 2013 field work was partially supported by National Geographic Waitt Foundation grant W21-12 to K.H.K. and R.K.P.K. U-Th dating was supported by grants from Ministry of Science and Technology (MOST) (105-2119-M-002-001, 106-2628-M-002-013 to C.-C.S.) and the National Taiwan University (105R7625 to C.-C.S.). This manuscript is the scientific contribution no 288 of the NEG-LABISE, UFPE, a contribution of the Reef Ecosystems Working Group of the INCT Ambientes Marinhos Tropicais (InctAmbTropic – CNPq #565.054/2010-4) and represents contribution 5470 of the University of Maryland Center for Environmental Science

Neonatal anthropometry: a tool to evaluate the nutritional status and predict early and late risks

Neonatal anthropometry is an inexpensive, noninvasive and convenient tool for bedside evaluation, especially in sick and fragile neonates. Anthropometry can be used in neonates as a tool for several purposes: diagnosis of foetal malnutrition and prediction of early postnatal complications; postnatal assessment of growth, body composition and nutritional status; prediction of long-term complications including metabolic syndrome; assessment of dysmorphology; and estimation of body surface. However, in this age group anthropometry has been notorious for its inaccuracy and the main concern is to make validated indices available. Direct measurements, such as body weight, length and body circumferences are the most commonly used measurements for nutritional assessment in clinical practice and in field studies. Body weight is the most reliable anthropometric measurement and therefore is often used alone in the assessment of the nutritional status, despite not reflecting body composition. Derived indices from direct measurements have been proposed to improve the accuracy of anthropometry. Equations based on body weight and length, mid-arm circumference/head circumference ratio, and upper-arm cross-sectional areas are among the most used derived indices to assess nutritional status and body proportionality, even though these indices require further validation for the estimation of body composition in neonates

A Novel Requirement for Janus Kinases as Mediators of Drug Resistance Induced by Fibroblast Growth Factor-2 in Human Cancer Cells

The development of resistance to chemotherapy is a major cause of cancer-related death. Elucidating the mechanisms of drug resistance should thus lead to novel therapeutic strategies. Fibroblast growth factor (FGF)-2 signaling induces the assembly of a multi-protein complex that provides tumor cells with the molecular machinery necessary for drug resistance. This complex, which involves protein kinase C (PKC) ε, v-raf murine sarcoma viral oncogene homolog B1 (B-RAF) and p70 S6 kinase β (S6K2), enhances the selective translation of anti-apoptotic proteins such as B-cell leukaemia/lymphoma-2 (BCL-2) and inhibitors of apoptosis protein (IAP) family members and these are able to protect multiple cancer cell types from chemotherapy-induced cell death. The Janus kinases (JAKs) are most noted for their critical roles in mediating cytokine signaling and immune responses. Here, we show that JAKs have novel functions that support their consideration as new targets in therapies aimed at reducing drug resistance. As an example, we show that the Janus kinase TYK2 is phosphorylated downstream of FGF-2 signaling and required for the full phosphorylation of extracellular signal-regulated kinase (ERK) 1/2. Moreover, TYK2 is necessary for the induction of key anti-apoptotic proteins, such as BCL-2 and myeloid cell leukemia sequence (MCL) 1, and for the promotion of cell survival upon FGF-2. Silencing JAK1, JAK2 or TYK2 using RNA interference (RNAi) inhibits FGF2-mediated proliferation and results in the sensitization of tumor cells to chemotherapy-induced killing. These effects are independent of activation of signal transducer and activator of transcription (STAT) 1, STAT3 and STAT5A/B, the normal targets of JAK signaling. Instead, TYK2 associates with the other kinases previously implicated in FGF-2-mediated drug resistance. In light of these findings we hypothesize that TYK2 and other JAKs are important modulators of FGF-2-driven cell survival and that inhibitors of these kinases will likely improve the effectiveness of other cancer therapies

Redox Regulation of the AMP-Activated Protein Kinase

Redox state is a critical determinant of cell function, and any major imbalances can cause severe damage or death