Trabajar en la niñez : ¿Marcas o cicatrices?

En esta presentación se aborda la cuestión del Trabajo Infantil en dos comunidades vulnerables de la ciudad de La Plata. Las reflexiones y cuestionamientos que se formulan son el resultado de un Proyecto de Investigación, aún en curso. El objetivo principal es indagar las producciones subjetivas que el trabajo de niños y niñas inscribe en ellos y en adultos del barrio. A este fin, se empleó metodología cualitativa; y se utilizaron como técnicas, entrevistas semiestructuradas, focus group con niños, asociación libre de palabras. Entre las conclusiones a las que hemos arribado hasta aquí, señalamos la necesidad de abordar esta cuestión desde las condiciones que habilitan el trabajo infantil como estrategia de supervivencia. También, hemos observado el registro de estos niños y niñas acerca del futuro como una prolongación del presente, sin posibilidad de transformación.

Diferenciación social campesina y señorío episcopal. Zamora, siglos XI-XIII

El presente trabajo indaga acerca de los procesos de diferenciación social campesina temprana en la Zamora medieval. Dicho proceso adquiere características particulares de acuerdo al marco señorial en que se inserten las comunidades. La documentación zamorana ha permitido agrupar los casos empíricos en dos tipos ideales, aquellos que presentan desarrollo de caballería y los que maduran al interior de cotos de abadengo. En cuanto al primer tipo, comprobamos que la caballería que surge de las propias clases campesinas tiende a transformarse en un sector privilegiado en la comunidad. Tal proceso de diferenciación se presenta con importantes disparidades evolutivas en las distintas comunidades. Las comunidades de este tipo que ingresan a la órbita episcopal evidencian conflictos violentos relacionados con la imposición de nuevos derechos señoriales y nuevas pautas de reproducción señorial. En cambio, en las aldeas desarrolladas desde su inicio al interior de cotos monásticos la diferenciación por el ejercicio de la función militar se encuentra negada. La única posibilidad estructural de diferenciación se relaciona con el ejercicio de funciones en representación del señor. El surgimiento de tales sectores evoluciona, entonces, de manera coherente con la construcción del poder señorial a escala local. En las comunidades con presencia de caballería será necesario desmontar las jerarquías preexistentes, proceso que determina que únicamente bien entrado el siglo XIII puedan comenzar a esbozarse nuevas elites locales y condiciones de poblamiento afines a la reproducción del señorío eclesiástico.

La reducción 'Exaltación de la Cruz de los indios Quilmes': un caso de relocalización étnica en Pampa a fines del siglo XVII

Nos proponemos estudiar las transformaciones efectuadas en el seno de las comunidades de indios quilmes y acalianes del Valle Calchaquí, luego de su traslado geográfico al espacio pampeano en 1666 y posterior establecimiento en la reducción "Exaltación de la Cruz de los indios Quilmes". Para ello analizaremos las nuevas formas de organización económica y social impuestas en el sistema de reducción, así como en las relaciones interétnicas establecidas con la sociedad colonial porteña. Nuestro objetivo es conocer las causas de la abrupta caída demográfica en el grupo relocalizado e indagar en las posibles respuestas étnicas -estrategias de resistencia-, generadas frente a la situación de sujeción impuesta en el espacio pampeano.

Indígenas, tierra y política en Colombia : Las comunidades indígenas del Bolívar Grande en la segunda mitad del siglo XIX

Este artículo analiza la población indígena del Bolívar Grande (Colombia) en el tercer cuarto del siglo XIX, en el contexto de formación de la nación y la expansión de la ganadería. Mostramos cómo los elementos discursivos sobre la nación mestiza y la identidad política ciudadana, más el fraccionamiento interno de las comunidades indígenas, facilitaron las acciones de ganaderos y poblaciones mestizas para intentar disolver la propiedad comunal de las tierras de los resguardos. También analizamos las formas de resistencia desplegadas por los indígenas, en especial la instrumentalización que realizaron del discurso liberal, y las negociaciones que establecieron con otros sectores sociales y políticos para defender sus intereses

Alternativas ante el conflicto entre autoridades ambientales y habitantes de áreas protegidas en páramos colombianos

Colombia es uno de los países denominados megadiversos biológica y culturalmente. Presenta a su interior la mayor extensión de páramos del mundo, los cuales son considerados fábricas de agua del planeta y hábitats de rica diversidad biológica. Por otro lado, la ocupación humana de los páramos colombianos ha generado conflictos entre las normativas ambientales vigentes y los usos productivos del suelo. El presente artículo analiza las alternativas aplicadas ante el conflicto entre autoridades ambientales de áreas protegidas y habitantes de los páramos en Colombia. Se encontraron dos tipos de alternativas: la primera plantea la concesión de servicios ecoturísticos en los parques naturales y la compra de tierras por parte de sociedades de economía mixta. La segunda plantea el abandono de las actividades productivas de los agricultores, mediado por procesos educativos o de cumplimiento de las normas ambientales vigentes, so pena de enfrentar acciones punitivas por parte del Estado. Este trabajo presenta una tercera alternativa, que parte de la crítica a las dos anteriores e incluye diferentes estrategias: planes de manejo comunitario con tiempo y financiación institucional pertinente, aplicación de modelos agroecológicos y rescate de la memoria biocultural y cambios en la estructura agraria.

Macrobenthos from the Novaya Zemlya Trough, Kara Sea

During Cruise 54 of R/V Akademik Mstislav Keldysh macrobenthos of the Novaya Zemlya Trough was studied with use of a Sigsby trawl along a submeridional transect near 75°30'N at depth range from 68 to 362 m. In total 140 species of bottom animals were found. Relative role of taxons was assessed using three parameters: abundance, biomass, and energy flow. Similarity of the parameters was used for comparison of samples. New material greatly contributes to data on composition of fauna and structure of communities of the studied region. It was revealed that small scyphozoid polyps and sipunculoids play an important role in the trough's community. Presence of a community dominated by Ophiocten sericeum (with important role of small bivalves) was revealed for the first time not only at the eastern by also at the western slope of the Novaya Zemlya Trough. The sharpest changes in composition and structure of the bottom community were confined to a zone of transition from the trough floor to the slope. These changes are determined by specificity of the macrorelief (of the floor and slope), composition of ground (soft brown silts abound in rhizopods and dense gray silts with admixture of pebbles), and possibly by hydrodynamic processes near the bottom.

Aboveground community and species-specific plant biomass from the Jena Experiment (Dominance Experiment, year 2006)

This data set contains aboveground community plant biomass (Sown plant community, Weed plant community, Dead plant material, and Unidentified plant material; all measured in biomass as dry weight) and species-specific biomass from the sown species of the dominance experiment plots of a large grassland biodiversity experiment (the Jena Experiment; see further details below). In the dominance experiment, 206 grassland plots of 3.5 x 3.5 m were established from a pool of 9 plant species that can be dominant in semi-natural grassland communities of the study region. In May 2002, varying numbers of plant species from this species pool were sown into the plots to create a gradient of plant species richness (1, 2, 3, 4, 6, and 9 species). Plots were maintained by bi-annual weeding and mowing. Aboveground community biomass was harvested twice in May and August 2006 on all experimental plots of the dominance experiment. This was done by clipping the vegetation at 3 cm above ground in two rectangles of 0.2 x 0.5 m per experimental plot. The location of these rectangles was assigned by random selection of coordinates within the central area of the plots (excluding an outer edge of 50cm). The positions of the rectangles within plots were identical for all plots. The harvested biomass was sorted into categories: individual species for the sown plant species, weed plant species (species not sown at the particular plot), detached dead plant material, and remaining plant material that could not be assigned to any category. All biomass was dried to constant weight (70°C, >= 48 h) and weighed. Sown plant community biomass was calculated as the sum of the biomass of the individual sown species. The mean of both samples per plot and the individual measurements are provided in the data file. Overall, analyses of the community biomass data have identified species richness and the presence of particular species as an important driver of a positive biodiversity-productivity relationship.

Aboveground community and species-specific plant biomass from the Jena Experiment (Dominance Experiment, year 2003)

This data set contains aboveground community plant biomass (Sown plant community, Weed plant community, and Dead plant material; all measured in biomass as dry weight) and species-specific biomass from the sown species of the dominance experiment plots of a large grassland biodiversity experiment (the Jena Experiment; see further details below). In the dominance experiment, 206 grassland plots of 3.5 x 3.5 m were established from a pool of 9 plant species that can be dominant in semi-natural grassland communities of the study region. In May 2002, varying numbers of plant species from this species pool were sown into the plots to create a gradient of plant species richness (1, 2, 3, 4, 6, and 9 species). Plots were maintained by bi-annual weeding and mowing. Aboveground community biomass was harvested twice in May and August 2003 on all experimental plots of the dominance experiment. This was done by clipping the vegetation at 3 cm above ground in two rectangles of 0.2 x 0.5 m per experimental plot. The location of these rectangles was assigned by random selection of coordinates within the central area of the plots (excluding an outer edge of 50cm). The positions of the rectangles within plots were identical for all plots. The harvested biomass was sorted into categories: individual species for the sown plant species, weed plant species (species not sown at the particular plot), detached dead plant material, and remaining plant material that could not be assigned to any category. All biomass was dried to constant weight (70°C, >= 48 h) and weighed. Sown plant community biomass was calculated as the sum of the biomass of the individual sown species. The mean of both samples per plot and the individual measurements are provided in the data file. Overall, analyses of the community biomass data have identified species richness and the presence of particular species as an important driver of a positive biodiversity-productivity relationship.

Biogeochemical measurements at the Antarctic Peninsula

Size-fractionated chlorophyll a and photosynthetic carbon incorporation, microbial oxygen production and respiration and particulate vertical flux were measured in January 1996 at three regions, characterized by distinct hydrographic fields and planktonic communities, of the Antarctic Peninsula: (1) a diatom-Phaeocystis sp., dominated community associated with the relatively stratified waters of the Gerlache Strait, (2) a nanoplankton-Cryptomonas sp. dominated assemblage at the Gerlache-Bransfield confluence; and (3) a nano- and picoplankton community in mixed waters of the Bransfield Strait. Despite the marked differences in both community structure and total phytoplankton biomass and primary production, and against predictions from models about trophic control of C export, the lowest respiration rates were measured at Bransfield (pico- and nanoplankton), and no difference was observed between the Gerlache (large diatoms) and Bransfield stations in relative vertical particle flux (6.4 vs. 5.1 % of suspended C; 14.9 vs. 10.4 % of net community production, respectively). Growth and loss rates of the phytoplankton population studied for each community indicate that microbial populations can be explained by in situ growth, but spatial (diatom-Phaeocystis sp., bloom) and temporal (diatom-Phaeocystis sp. bloom and nanoplankton communities) scales of study were shown to be insufficient for addressing the coupling between primary production and biogenic carbon export, especially after the appreciation of the accumulation of dissolved organic carbon in the water column. This would explain the unexpected results and highlights the necessity of including the mechanisms controlling accumulation and consumption of dissolved organic matter into conceptual models about the trophic control of C export.

Macrobenthic abundance, biomass, productivity and production in the deep Arctic ocean

The few existing studies on macrobenthic communities of the deep Arctic Ocean report low standing stocks, and confirm a gradient with declining biomass from the slopes down to the basins as commonly reported for deep-sea benthos. In this study we have further investigated the relationship of faunal abundance (N), biomass (B) as well as community production (P) with water depth, geographical latitude and sea ice concentration. The underlying dataset combines legacy data from the past 20 years, as well as recent field studies selected according to standardized quality control procedures. Community P/B and production were estimated using the multi-parameter ANN model developed by Brey (2012). We could confirm the previously described negative relationship of water depth and macrofauna standing stock in the Arctic deep-sea. Furthermore, the sea-ice cover increasing with high latitudes, correlated with decreasing abundances of down to < 200 individuals/m**2, biomasses of < 65 mg C/m**2 and P of < 75 mg C/m**2/y. Stations under influence of the seasonal ice zone (SIZ) showed much higher standing stock and P means between 400 - 1400 mg C/m**2/y; even at depths up to 3700 m. We conclude that particle flux is the key factor structuring benthic communities in the deep Arctic ocean, explaining both the low values in the ice-covered Arctic basins and the high values along the SIZ.

Aboveground community and species-specific plant biomass from the Jena Experiment (Dominance Experiment, year 2007)

This data set contains aboveground community plant biomass (Sown plant community, Weed plant community, Dead plant material, and Unidentified plant material; all measured in biomass as dry weight) and species-specific biomass from the sown species of the dominance experiment plots of a large grassland biodiversity experiment (the Jena Experiment; see further details below). In the dominance experiment, 206 grassland plots of 3.5 x 3.5 m were established from a pool of 9 plant species that can be dominant in semi-natural grassland communities of the study region. In May 2002, varying numbers of plant species from this species pool were sown into the plots to create a gradient of plant species richness (1, 2, 3, 4, 6, and 9 species). Plots were maintained by bi-annual weeding and mowing. Aboveground community biomass was harvested twice in May and August 2007 on all experimental plots of the dominance experiment. This was done by clipping the vegetation at 3 cm above ground in two rectangles of 0.2 x 0.5 m per experimental plot. The location of these rectangles was assigned by random selection of coordinates within the central area of the plots (excluding an outer edge of 50cm). The positions of the rectangles within plots were identical for all plots. The harvested biomass was sorted into categories: individual species for the sown plant species, weed plant species (species not sown at the particular plot), detached dead plant material, and remaining plant material that could not be assigned to any category. All biomass was dried to constant weight (70°C, >= 48 h) and weighed. Sown plant community biomass was calculated as the sum of the biomass of the individual sown species. The mean of both samples per plot and the individual measurements are provided in the data file. Overall, analyses of the community biomass data have identified species richness and the presence of particular species as an important driver of a positive biodiversity-productivity relationship.

Aboveground community and species-specific plant biomass from the Jena Experiment (Dominance Experiment, time series since 2002)

This data set comprises a time series of aboveground community plant biomass (Sown plant community, Weed plant community, Dead plant material, and Unidentified plant material; all measured in biomass as dry weight) and species-specific biomass from the sown species of the dominance experiment plots of a large grassland biodiversity experiment (the Jena Experiment; see further details below). In the dominance experiment, 206 grassland plots of 3.5 x 3.5 m were established from a pool of 9 species that can be dominant in semi-natural grassland communities of the study region. In May 2002, varying numbers of plant species from this species pool were sown into the plots to create a gradient of plant species richness (1, 2, 3, 4, 6, and 9 species). Plots were maintained by bi-annual weeding and mowing. Aboveground community biomass was harvested twice a year, generally in May and August (in 2002 only once in September) on all experimental plots of the dominance experiment. This was done by clipping the vegetation at 3 cm above ground in two rectangles of 0.2 x 0.5 m per experimental plot. The location of these rectangles was assigned by random selection of new coordinates every year within the central area of the plots (excluding an outer edge of 50cm). The positions of the rectangles within plots were identical for all plots. The harvested biomass was sorted into categories: individual species for the sown plant species, weed plant species (species not sown at the particular plot), detached dead plant material, and remaining plant material that could not be assigned to any category. Biomass was dried to constant weight (70°C, >= 48 h) and weighed. Sown plant community biomass was calculated as the sum of the biomass of the individual sown species. The mean of both samples per plot and the individual measurements are provided in the data file. Overall, analyses of the community biomass data have identified species richness and the presence of particular species as an important driver of a positive biodiversity-productivity relationship.

The Global Plankton Database: an inventory and data from the Former Soviet Union expeditions

At present time, there is a lack of knowledge on the interannual climate-related variability of zooplankton communities of the tropical Atlantic, central Mediterranean Sea, Caspian Sea, and Aral Sea, due to the absence of appropriate databases. In the mid latitudes, the North Atlantic Oscillation (NAO) is the dominant mode of atmospheric fluctuations over eastern North America, the northern Atlantic Ocean and Europe. Therefore, one of the issues that need to be addressed through data synthesis is the evaluation of interannual patterns in species abundance and species diversity over these regions in regard to the NAO. The database has been used to investigate the ecological role of the NAO in interannual variations of mesozooplankton abundance and biomass along the zonal array of the NAO influence. Basic approach to the proposed research involved: (1) development of co-operation between experts and data holders in Ukraine, Russia, Kazakhstan, Azerbaijan, UK, and USA to rescue and compile the oceanographic data sets and release them on CD-ROM, (2) organization and compilation of a database based on FSU cruises to the above regions, (3) analysis of the basin-scale interannual variability of the zooplankton species abundance, biomass, and species diversity.