Fearsome Worlds and Uncanny Children:Gothic Early Childhoods in Condé’s La migration des coeurs and Kincaid’s The Autobiography of My Mother

Gothic depictions of early childhood and its antecedents from conception to childbirth stand to fundamentally shape readers’ understanding of colonialism across the transnational and translinguistic space of the Caribbean. This effect is particularly visible in contemporary novels such as Maryse Condé’s La Migration des coeurs (1995) and Jamaica Kincaid’s The Autobiography of My Mother (1996), which not only have been interpreted as rewritings of Wuthering Heights but also draw on a larger, more multicultural Gothic literary tradition. In their renderings of sexual violence, doomed pregnancies, and motherless infancy, Condé and Kincaid appropriate and edit Gothic conventions, highlighting persisting ramifications of the colonial project for women and children. Gothic youth also functions as a subversive site of resistance with the potential to dismantle imperialist ideologies and systems

Haunting Perennial Girlhoods:Infantilization and the Transnational American Gothic from Gilman to Césaire

The Gothic conceit of American womanhood as a nightmarish form of perennial childhood assumes new layers of meaning when viewed in transnational perspective. Haunting portrayals of infantilized women-children give canonical American works like Gilman’s ‘The Yellow Wallpaper’ an unlikely kinship with postcolonial texts like Paz’s La hija de Rappaccini and Césaire’s Une tempête. While echoing Gilman’s critique of patriarchal superstructures, Paz and Césaire also confront white women’s role in upholding systems of white supremacy, slavery, and (neo-)imperialism. Taken together, Gilman, Paz, and Césaire speak to the shifting significations and the staying power of unending Gothic girlhoods in transnational American literature

A model of the Arctic Ocean carbon cycle

Author Posting. © American Geophysical Union, 2011. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Journal of Geophysical Research 116 (2011): C12020, doi:10.1029/2011JC006998.A three dimensional model of Arctic Ocean circulation and mixing, with a horizontal resolution of 18 km, is overlain by a biogeochemical model resolving the physical, chemical and biological transport and transformations of phosphorus, alkalinity, oxygen and carbon, including the air-sea exchange of dissolved gases and the riverine delivery of dissolved organic carbon. The model qualitatively captures the observed regional and seasonal trends in surface ocean PO4, dissolved inorganic carbon, total alkalinity, and pCO2. Integrated annually, over the basin, the model suggests a net annual uptake of 59 Tg C a−1, within the range of published estimates based on the extrapolation of local observations (20–199 Tg C a−1). This flux is attributable to the cooling (increasing solubility) of waters moving into the basin, mainly from the subpolar North Atlantic. The air-sea flux is regulated seasonally and regionally by sea-ice cover, which modulates both air-sea gas transfer and the photosynthetic production of organic matter, and by the delivery of riverine dissolved organic carbon (RDOC), which drive the regional contrasts in pCO2 between Eurasian and North American coastal waters. Integrated over the basin, the delivery and remineralization of RDOC reduces the net oceanic CO2 uptake by ~10%.This study has been carried out as part of ECCO2 and SASS (Synthesis of the Arctic System Science) projects funded by NASA and NSF, respectively. MM and MJF are grateful for support from the National Science Foundation (ARC-0531119 and ARC-0806229) for financial support. MM also acknowledges NASA for providing computer time, the use of the computing facilities at NAS center and also the Scripps post-doctoral program for further financial support that helped to complete the manuscript. RMK also acknowledges NOAA for support (NA08OAR4310820 and NA08OAR4320752).2012-06-1

Sensitivity of global ocean biogeochemical dynamics to ecosystem structure in a future climate

Terrestrial and oceanic ecosystem components of the Earth System models (ESMs) are key to predict the future behavior of the global carbon cycle. Ocean ecosystem models represent low complexity compared to terrestrial ecosystem models. In this study we use two ocean biogeochemical models based on the explicit representation of multiple planktonic functional types. We impose to the models the same future physical perturbation and compare the response of ecosystem dynamics, export production (EP) and ocean carbon uptake (OCU) to the same physical changes. Models comparison shows that: (1) EP changes directly translate into changes of OCU on decadal time scale, (2) the representation of ecosystem structure plays a pivotal role at linking OCU and EP, (3) OCU is highly sensitive to representation of ecosystem in the Equatorial Pacific and Southern Oceans

Corrigendum to "Evaluating the ocean biogeochemical components of Earth system models using atmospheric potential oxygen and ocean color data" (Biogeosciences, 12, 193–208, 2015)

No abstract available

Ocean biogeochemical response to phytoplankton-light feedback in a global model

Oceanic phytoplankton, absorbing solar radiation, can influence the bio-optical properties of seawater and hence upper ocean physics. We include this process in a global ocean general circulation model (OGCM) coupled to a dynamic green ocean model (DGOM) based on multiple plankton functional types (PFT). We not only study the impact of this process on ocean physics but we also explore the biogeochemical response due to this biophysical feedback. The phytoplankton-light feedback (PLF) impacts the dynamics of the upper tropical and subtropical oceans. The change in circulation enhances both the vertical supply in the tropics and the lateral supply of nutrients from the tropics to the subtropics boosting the subtropical productivity by up to 60 gC m(-2) a(-1). Physical changes, due to the PLF, impact on light and nutrient availability causing shifts in the ocean ecosystems. In the extratropics, increased stratification favors calcifiers (by up to similar to 8%) at the expense of mixed phytoplankton. In the Southern Ocean, silicifiers increase their biomass (by up to similar to 10%) because of the combined alleviation of iron and light limitation. The PLF has a small effect globally on air-sea fluxes of carbon dioxide (CO2, 72 TmolC a(-1) outgassing) and oxygen (O-2, 46 TmolO(2) a(-1) ingassing) because changes in biogeochemical processes (primary production, biogenic calcification, and export production) highly vary regionally and can also oppose each other. From our study it emerges that the main impact of the PLF is an amplification of the seasonal cycle of physical and biogeochemical properties of the high-latitude oceans mostly driven by the amplification of the SST seasonal cycle

An Assessment of CO2 Uptake in the Arctic Ocean From 1985 to 2018

As a contribution to the Regional Carbon Cycle Assessment and Processes phase 2 (RECCAP2) project, we present synthesized estimates of Arctic Ocean sea-air CO2 fluxes and their uncertainties from surface ocean pCO2-observation products, ocean biogeochemical hindcast and data assimilation models, and atmospheric inversions. For the period of 1985–2018, the Arctic Ocean was a net sink of CO2 of 116 ± 4 TgC yr−1 in the pCO2 products, 92 ± 30 TgC yr−1 in the models, and 91 ± 21 TgC yr−1 in the atmospheric inversions. The CO2 uptake peaks in late summer and early autumn, and is low in winter when sea ice inhibits sea-air fluxes. The long-term mean CO2 uptake in the Arctic Ocean is primarily caused by steady-state fluxes of natural carbon (70% ± 15%), and enhanced by the atmospheric CO2 increase (19% ± 5%) and climate change (11% ± 18%). The annual mean CO2 uptake increased from 1985 to 2018 at a rate of 31 ± 13 TgC yr−1 dec−1 in the pCO2 products, 10 ± 4 TgC yr−1 dec−1 in the models, and 32 ± 16 TgC yr−1 dec−1 in the atmospheric inversions. Moreover, 77% ± 38% of the trend in the net CO2 uptake over time is caused by climate change, primarily due to rapid sea ice loss in recent years. Furthermore, true uncertainties may be larger than the given ensemble standard deviations due to common structural biases across all individual estimates

Global and regional emissions estimates for N2O

We present a comprehensive estimate of nitrous oxide (N2O) emissions using observations and models from 1995 to 2008. High-frequency records of tropospheric N2O are available from measurements at Cape Grim, Tasmania; Cape Matatula, American Samoa; Ragged Point, Barbados; Mace Head, Ireland; and at Trinidad Head, California using the Advanced Global Atmospheric Gases Experiment (AGAGE) instrumentation and calibrations. The Global Monitoring Division of the National Oceanic and Atmospheric Administration/Earth System Research Laboratory (NOAA/ESRL) has also collected discrete air samples in flasks and in situ measurements from remote sites across the globe and analyzed them for a suite of species including N2O. In addition to these major networks, we include in situ and aircraft measurements from the National Institute of Environmental Studies (NIES) and flask measurements from the Tohoku University and Commonwealth Scientific and Industrial Research Organization (CSIRO) networks. All measurements show increasing atmospheric mole fractions of N2O, with a varying growth rate of 0.1-0.7% per year, resulting in a 7.4% increase in the background atmospheric mole fraction between 1979 and 2011. Using existing emission inventories as well as bottom-up process modeling results, we first create globally gridded a priori N2O emissions over the 37 years since 1975. We then use the three-dimensional chemical transport model, Model for Ozone and Related Chemical Tracers version 4 (MOZART v4), and a Bayesian inverse method to estimate global as well as regional annual emissions for five source sectors from 13 regions in the world. This is the first time that all of these measurements from multiple networks have been combined to determine emissions. Our inversion indicates that global and regional N2O emissions have an increasing trend between 1995 and 2008. Despite large uncertainties, a significant increase is seen from the Asian agricultural sector in recent years, most likely due to an increase in the use of nitrogenous fertilizers, as has been suggested by previous studies.</p

Evaluating CMIP5 ocean biogeochemistry and Southern Ocean carbon uptake using atmospheric potential oxygen: Present-day performance and future projection

Observed seasonal cycles in atmospheric potential oxygen (APO ~ O2 + 1.1 CO2) were used to evaluate eight ocean biogeochemistry models from the Coupled Model Intercomparison Project (CMIP5). Model APO seasonal cycles were computed from the CMIP5 air-sea O2 and CO2 fluxes and compared to observations at three Southern Hemisphere monitoring sites. Four of the models captured either the observed APO seasonal amplitude or phasing relatively well, while the other four did not. Many models had an unrealistic seasonal phasing or amplitude of the CO2 flux, which in turn influenced APO. By 2100 under RCP8.5, the models projected little change in the O2 component of APO but large changes in the seasonality of the CO2 component associated with ocean acidification. The models with poorer performance on present-day APO tended to project larger net carbon uptake in the Southern Ocean, both today and in 2100

An analysis of the carbon balance of the Arctic Basin from 1997 to 2006

Author Posting. © The Authors, 2010. This is the author's version of the work. It is posted here by permission of John Wiley & Sons for personal use, not for redistribution. The definitive version was published in Tellus B 62 (2010): 455-474, doi:10.1111/j.1600-0889.2010.00497.x.This study used several model-based tools to analyze the dynamics of the Arctic Basin between 1997 and 2006 as a linked system of land-ocean-atmosphere C exchange. The analysis estimates that terrestrial areas of the Arctic Basin lost 62.9 Tg C yr-1 and that the Arctic Ocean gained 94.1 Tg C yr-1. Arctic lands and oceans were a net CO2 sink of 108.9 Tg C yr-1, which is within the range of uncertainty in estimates from atmospheric inversions. Although both lands and oceans of the Arctic were estimated to be CO2 sinks, the land sink diminished in strength because of increased fire disturbance compared to previous decades, while the ocean sink increased in strength because of increased biological pump activity associated with reduced sea ice cover. Terrestrial areas of the Arctic were a net source of 41.5 Tg CH4 yr-1 that increased by 0.6 Tg CH4 yr-1 during the decade of analysis, a magnitude that is comparable with an atmospheric inversion of CH4. Because the radiative forcing of the estimated CH4 emissions is much greater than the CO2 sink, the analysis suggests that the Arctic Basin is a substantial net source of green house gas forcing to the climate system.This study was supported, in part, by the NSF Arctic System Science Program as part of the Arctic Carbon Cycle Synthesis Project (ARC-0531047, 0531082, 0531119, and 0554811)