Variabilidad espacial y temporal en la comunidad de cladóceros de la Ciénaga de Paredes (Santander, Colombia) a lo largo de un ciclo anual

En la Ciénaga de Paredes (73 · 45'-73· 49'W y 7·26'-7·29'N), ubicada en el Departamento de Santander (Colombia), se determinó la composición, la variación espacial y temporal de la estructura de la comunidad de cladóceros, con base en arrastres verticales con malla de 68 μm, en ocho estaciones de muestreo en un ciclo anual (febrero de 1998 a enero de 1999).Para evaluar la estructura, se utilizaron los números de Hill (N0, N1 y N2) y la equidad. El soporte del muestreo fue calculado con los estimadores Chao 1 y 2. La existencia de diferencias significativas de los números de Hill, la equidad, la densidad numérica, la columna de agua, el pH, el OD, y la temperatura, entre campañas y entre estaciones, se realizó a través de un ANDEVA. Las especies y morfoespecies encontradas (31) poseen distribución tropical, subtropical y cosmopolita; pertenecen generalmente a cuerpos de agua temporales, llanuras de inundación o ciénagas. Las mayores abundancias fueron registradas para Moina minuta, Moina cf. micrura, Diaphanosoma brevireme y Ceriodaphnia cornuta, las cuales representaron el 81.9 % del total de individuos colectados. Los resultados obtenidos por los estimadores de riqueza indican que si se aumentara el esfuerzo de muestreo con las técnicas utilizadas, no incrementaría el número de morfoespecies. Con respecto a la variación espacial de la estructura, la estación V presento mayor equidad, riqueza y diversidad, pero menor densidad numérica, esta condición muestra la diferencia de esta estación en comparación con las demás; su tendencia atípica es explicada ya que dicha estación se encuentra cerca del afluente principal de la Ciénaga (Quebrada La Gómez). En la variación temporal, la estructura de la comunidad de cladóceros cambió entre campañas de muestreo ya que la equidad y la riqueza presentaron diferencias significativas, que se evidencian en el cambio de la abundancia relativa de las morfoespecies, mas no en la abundancia de cladóceros. Esto es causado por las fluctuaciones de la precipitación y el alto de la columna de agua.In the Ciénaga de Paredes (73 · 45'-73· 49'W y 7·26'-7·29'N), located in the Department of Santander (Colombia), the composition, and the spatial and temporal variation of the cladoceran community structure was determined with samples taken with a 68 μm vertical-hauled net, at eight sampling stations in an annual cycle (February 1998 to January 1999). To evaluate the structure, Hill numbers (N0, N1 and N2) and evenness were used. The sampling support was calculated with the Chao 1 and 2 estimators. The existence of significant differences for Hill numbers, evenness, numeric density, water column, pH, OD, and temperature among field trips and among stations, was analysed through an ANOVA. The species and morphospecies found (31), had a tropical, subtropical, and cosmopolitan distribution; belonging to temporary water bodies, floodplains or "ciénagas". The highest abundances were registered for Moina minuta, Moina cf. micrura, Diaphanosoma brevireme and Ceriodaphnia cornuta, which represented 81.9 % of the total collected individuals. The results obtained with the richness estimates suggest that if the sampling effort were increased using the same techniques, the morphospecies' number would have not increased. With regard to the structure's spatial variation, the station V showed higher evenness, richness, and diversity, but lower numeric density; this condition shows the difference between this station and the other ones; ical trend is explained by this station being near to the main tributary of the "Ciénaga" ("Quebrada La Gómez").Regarding the temporal variation, the cladocerans' community structure changed between field trips, since the evenness and the richness showed significant differences, reflected by the variation in the relative abundance of the morphospecies but not in the cladocerans' abundance. This was caused by the fluctuations in rainfall and water level

Morphological comparison and geographic distribution of the species Tabellaria fenestrata and Tabellaria flocculosa (Bacillariophyceae) in lotic and lentic systems in Colombia

Este trabajo se desarrolló en el marco de un proyecto más amplio cuyo objetivo fue analizar la distribución geográfica de las diatomeas de Colombia, basados en el estudio de sistemas lóticos ubicados en las zonas biogeográficas de los Andes, el Caribe, la Orinoquía y el Pacífico. Durante la investigación se recolectaron muestras de perifiton en 18 sitios, en los cuales se midió la elevación sobre el nivel del mar, el caudal, la temperatura, el pH, la conductividad eléctrica y el oxígeno disuelto. En este trabajo se presentan los resultados del análisis de los taxones pertenecientes al género Tabellaria: T. fenestrata y T. flocculosa, dos especies morfológicamente similares que han sido confundidas frecuentemente. Se observaron y describieron ejemplares de ambos taxones mediante microscopia óptica y microscopia electrónica de barrido. Asimismo, se recopiló información en la literatura acerca de la distribución geográfica de estas dos especies en el país. Se concluye que Tabellaria flocculosa presenta una distribución geográfica más amplia y pocas restricciones ecológicas para colonizar y establecerse en los sistemas acuáticos, mientras que Tabellaria fenestrata presenta una distribución más restringida.This study was developed within the framework of a project conducted with the aim of analyzing the geographical distribution of diatoms in Colombia. This project was based on analyses of information on lotic systems located in the biogeographic regions of the Andes, Caribbean, Orinoquía and Pacific. During the research, periphyton samples were collected at 18 sampling sites. Current flow rate, temperature, pH, conductivity, dissolved oxygen and elevation were measured in each sampling site. We report the presence of two taxa belonging to the genus Tabellaria: T. fenestrata and T. flocculosa, which are morphologically similar and, therefore, have been frequently misidentified. Specimens of both taxa were observed and described with light microscopy and scanning electron microscopy. We also analyzed the geographical distribution of these taxa in the country. We conclude that T. flocculosa has a broad geographical distribution in Colombia and few ecological restrictions to colonize and settle in aquatic systems, while T. fenestrata has a more restricted distribution.Facultad de Ciencias Naturales y Muse

Why ‘Good Governance’ Fails: Lessons from Regional Economic Development in Colombia

By critically reviewing different strands of literature on institutional change and development, this essay argues that, in order to fully understand subnational economic development, we need to move away from ‘good governance' explanations in which geography‐specific analyses of power structures and elite interests are largely absent. Using findings for Colombia and insights from economic geography and heterodox political economy theories, this essay gives theoretical and conceptual guidelines and approximations for future studies on regional economic development. The contribution provides a place‐based discussion of how the historically evolved distribution of power balances, context‐specific elite interests, and the interaction between place‐bound actors and place‐less dynamics affect subnational institutional arrangements shaping policies and development outcomes. The conclusions drawn are not limited to Colombia and will prove beneficial to researchers studying regional economic development in subnational contexts elsewhere in the world

A Proposed Taxonomy of Anaerobic Fungi (Class Neocallimastigomycetes) Suitable for Large-Scale Sequence-Based Community Structure Analysis

Anaerobic fungi are key players in the breakdown of fibrous plant material in the rumen, but not much is known about the composition and stability of fungal communities in ruminants. We analyzed anaerobic fungi in 53 rumen samples from farmed sheep (4 different flocks), cattle, and deer feeding on a variety of diets. Denaturing gradient gel electrophoresis fingerprinting of the internal transcribed spacer 1 (ITS1) region of the rrn operon revealed a high diversity of anaerobic fungal phylotypes across all samples. Clone libraries of the ITS1 region were constructed from DNA from 11 rumen samples that had distinctly different fungal communities. A total of 417 new sequences were generated to expand the number and diversity of ITS1 sequences available. Major phylogenetic groups of anaerobic fungi in New Zealand ruminants belonged to the genera Piromyces, Neocallimastix, Caecomyces and Orpinomyces. In addition, sequences forming four novel clades were obtained, which may represent so far undetected genera or species of anaerobic fungi. We propose a revised phylogeny and pragmatic taxonomy for anaerobic fungi, which was tested and proved suitable for analysis of datasets stemming from high-throughput next-generation sequencing methods. Comparing our revised taxonomy to the taxonomic assignment of sequences deposited in the GenBank database, we believe that >29% of ITS1 sequences derived from anaerobic fungal isolates or clones are misnamed at the genus level

Fusarium: more than a node or a foot-shaped basal cell

Recent publications have argued that there are potentially serious consequences for researchers in recognising distinct genera in the terminal fusarioid clade of the family Nectriaceae. Thus, an alternate hypothesis, namely a very broad concept of the genus Fusarium was proposed. In doing so, however, a significant body of data that supports distinct genera in Nectriaceae based on morphology, biology, and phylogeny is disregarded. A DNA phylogeny based on 19 orthologous protein-coding genes was presented to support a very broad concept of Fusarium at the F1 node in Nectriaceae. Here, we demonstrate that re-analyses of this dataset show that all 19 genes support the F3 node that represents Fusarium sensu stricto as defined by F. sambucinum (sexual morph synonym Gibberella pulicaris). The backbone of the phylogeny is resolved by the concatenated alignment, but only six of the 19 genes fully support the F1 node, representing the broad circumscription of Fusarium. Furthermore, a re-analysis of the concatenated dataset revealed alternate topologies in different phylogenetic algorithms, highlighting the deep divergence and unresolved placement of various Nectriaceae lineages proposed as members of Fusarium. Species of Fusarium s. str. are characterised by Gibberella sexual morphs, asexual morphs with thin- or thick-walled macroconidia that have variously shaped apical and basal cells, and trichothecene mycotoxin production, which separates them from other fusarioid genera. Here we show that the Wollenweber concept of Fusarium presently accounts for 20 segregate genera with clear-cut synapomorphic traits, and that fusarioid macroconidia represent a character that has been gained or lost multiple times throughout Nectriaceae. Thus, the very broad circumscription of Fusarium is blurry and without apparent synapomorphies, and does not include all genera with fusarium-like macroconidia, which are spread throughout Nectriaceae (e.g., Cosmosporella, Macroconia, Microcera). In this study four new genera are introduced, along with 18 new species and 16 new combinations. These names convey information about relationships, morphology, and ecological preference that would otherwise be lost in a broader definition of Fusarium. To assist users to correctly identify fusarioid genera and species, we introduce a new online identification database, Fusarioid-ID, accessible at www.fusarium.org. The database comprises partial sequences from multiple genes commonly used to identify fusarioid taxa (act1, CaM, his3, rpb1, rpb2, tef1, tub2, ITS, and LSU). In this paper, we also present a nomenclator of names that have been introduced in Fusarium up to January 2021 as well as their current status, types, and diagnostic DNA barcode data. In this study, researchers from 46 countries, representing taxonomists, plant pathologists, medical mycologists, quarantine officials, regulatory agencies, and students, strongly support the application and use of a more precisely delimited Fusarium (= Gibberella) concept to accommodate taxa from the robust monophyletic node F3 on the basis of a well-defined and unique combination of morphological and biochemical features. This F3 node includes, among others, species of the F. fujikuroi, F. incarnatum-equiseti, F. oxysporum, and F. sambucinum species complexes, but not species of Bisifusarium [F. dimerum species complex (SC)], Cyanonectria (F. buxicola SC), Geejayessia (F. staphyleae SC), Neocosmospora (F. solani SC) or Rectifusarium (F. ventricosum SC). The present study represents the first step to generating a new online monograph of Fusarium and allied fusarioid genera (www.fusarium.org)

Long-term thermal sensitivity of Earth’s tropical forests

The sensitivity of tropical forest carbon to climate is a key uncertainty in predicting global climate change. Although short-term drying and warming are known to affect forests, it is unknown if such effects translate into long-term responses. Here, we analyze 590 permanent plots measured across the tropics to derive the equilibrium climate controls on forest carbon. Maximum temperature is the most important predictor of aboveground biomass (−9.1 megagrams of carbon per hectare per degree Celsius), primarily by reducing woody productivity, and has a greater impact per °C in the hottest forests (>32.2°C). Our results nevertheless reveal greater thermal resilience than observations of short-term variation imply. To realize the long-term climate adaptation potential of tropical forests requires both protecting them and stabilizing Earth’s climate

The number of tree species on Earth.

One of the most fundamental questions in ecology is how many species inhabit the Earth. However, due to massive logistical and financial challenges and taxonomic difficulties connected to the species concept definition, the global numbers of species, including those of important and well-studied life forms such as trees, still remain largely unknown. Here, based on global ground-sourced data, we estimate the total tree species richness at global, continental, and biome levels. Our results indicate that there are ∼73,000 tree species globally, among which ∼9,000 tree species are yet to be discovered. Roughly 40% of undiscovered tree species are in South America. Moreover, almost one-third of all tree species to be discovered may be rare, with very low populations and limited spatial distribution (likely in remote tropical lowlands and mountains). These findings highlight the vulnerability of global forest biodiversity to anthropogenic changes in land use and climate, which disproportionately threaten rare species and thus, global tree richness

The number of tree species on Earth.

One of the most fundamental questions in ecology is how many species inhabit the Earth. However, due to massive logistical and financial challenges and taxonomic difficulties connected to the species concept definition, the global numbers of species, including those of important and well-studied life forms such as trees, still remain largely unknown. Here, based on global ground-sourced data, we estimate the total tree species richness at global, continental, and biome levels. Our results indicate that there are ∼73,000 tree species globally, among which ∼9,000 tree species are yet to be discovered. Roughly 40% of undiscovered tree species are in South America. Moreover, almost one-third of all tree species to be discovered may be rare, with very low populations and limited spatial distribution (likely in remote tropical lowlands and mountains). These findings highlight the vulnerability of global forest biodiversity to anthropogenic changes in land use and climate, which disproportionately threaten rare species and thus, global tree richness

The global abundance of tree palms

Aim Palms are an iconic, diverse and often abundant component of tropical ecosystems that provide many ecosystem services. Being monocots, tree palms are evolutionarily, morphologically and physiologically distinct from other trees, and these differences have important consequences for ecosystem services (e.g., carbon sequestration and storage) and in terms of responses to climate change. We quantified global patterns of tree palm relative abundance to help improve understanding of tropical forests and reduce uncertainty about these ecosystems under climate change. Location Tropical and subtropical moist forests. Time period Current. Major taxa studied Palms (Arecaceae). Methods We assembled a pantropical dataset of 2,548 forest plots (covering 1,191 ha) and quantified tree palm (i.e., ≥10 cm diameter at breast height) abundance relative to co‐occurring non‐palm trees. We compared the relative abundance of tree palms across biogeographical realms and tested for associations with palaeoclimate stability, current climate, edaphic conditions and metrics of forest structure. Results On average, the relative abundance of tree palms was more than five times larger between Neotropical locations and other biogeographical realms. Tree palms were absent in most locations outside the Neotropics but present in >80% of Neotropical locations. The relative abundance of tree palms was more strongly associated with local conditions (e.g., higher mean annual precipitation, lower soil fertility, shallower water table and lower plot mean wood density) than metrics of long‐term climate stability. Life‐form diversity also influenced the patterns; palm assemblages outside the Neotropics comprise many non‐tree (e.g., climbing) palms. Finally, we show that tree palms can influence estimates of above‐ground biomass, but the magnitude and direction of the effect require additional work. Conclusions Tree palms are not only quintessentially tropical, but they are also overwhelmingly Neotropical. Future work to understand the contributions of tree palms to biomass estimates and carbon cycling will be particularly crucial in Neotropical forests

A922 Sequential measurement of 1 hour creatinine clearance (1-CRCL) in critically ill patients at risk of acute kidney injury (AKI)

Meeting abstrac