Uso de traçadores para avaliação da hidrodinâmica de sistemas alagados construídos operando sob condições climáticas tropicais Fluorescent dyes for hydrodynamic evaluation of constructed wetlands under tropical conditions

Sistemas alagados construídos (SACs) são, atualmente, importante opção para o tratamento de resíduos e controle da poluição pontual e difusa. O uso de SACs tem aumentado ano a ano, entretanto o nível de entendimento da hidrodinâmica do processo não tem crescido na mesma proporção. Traçadores fluorescentes apresentam-se como opção na determinação de curvas de distribuição de tempos de residência (DTR) e de parâmetros hidrodinâmicos, como número de dispersão e eficiência hidráulica. A pesquisa foi realizada com o objetivo de avaliar dois corantes (rodamina WT e fluoresceína sódica) na determinação das características hidrodinâmicas de SACs com escoamento subsuperficial, operando em região de clima tropical. Os tempos de residência experimentais (&#964;R) para os SACs variaram entre 4,5 e 5,0 dias, e os parâmetros de modelos teóricos foram obtidos para cada sistema, indicando dispersões muito pequenas. Os SACs, que apresentavam relação comprimento/largura (L/B) de 24/1, comportaram-se como sistemas de escoamento próximo ao pistonado. Embora a massa total adicionada não tenha sido recuperada (a adsorção é um dos mecanismos de perda), a pesquisa indicou que a rodamina WT pode ser utilizada com resultados satisfatórios na avaliação do comportamento hidrodinâmico de SACs.<br>Nowadays, constructed wetlands (CW) systems are an important wastewater treatment option. Subsurface flow (SSF) constructed wetlands are one of the main types which are being used, and in researches, these systems dyes tracer experiments are an appropriate tool to determine residence time distribution (RDT) curves and parameters of hydrodynamic models, as a wetland dispersion numbers and hydraulic efficiency. The objectives of this paper are to evaluate and compare the performance of two fluorescent tracers (rhodamine WT and sodium fluorescein) on subsurface-flow CWs hydrodynamic characteristics determination. The cells were operated at actual hydraulic residence time (&#964;R) of a 4.5 d ~ 5.0 d range and the parameters of theoretical models were obtained for each system, indicating very low dispersion. The CWs with length/widths ratio equals to 24 presented as plug flow near systems. Although the recovery of total amount was small (high absorption is one of the loss mechanisms during these types of studies), rhodamine WT is a suitable tracer in mesocosms SSF constructed wetland systems of study

Extinction vulnerability in marine populations

Human impacts on the world's oceans have been substantial, leading to concerns about the extinction of marine taxa. We have compiled 133 local, regional and global extinctions of marine populations. There is typically a 53-year lag between the last sighting of an organism and the reported date of the extinction at whatever scale this has occurred. Most disappearances (80%) were detected using indirect historical comparative methods, which suggests that marine extinctions may have been underestimated because of low-detection power. Exploitation caused most marine losses at various scales (55%), followed closely by habitat loss (37%), while the remainder were linked to invasive species, climate change, pollution and disease. Several perceptions concerning the vulnerability of marine organisms appear to be too general and insufficiently conservative. Marine species cannot be considered less vulnerable on the basis of biological attributes such as high fecundity or large-scale dispersal characteristics. For commercially exploited species, it is often argued that economic extinction of exploited populations will occur before biological extinction, but this is not the case for non-target species caught in multispecies fisheries or species with high commercial value, especially if this value increases as species become rare. The perceived high potential for recovery, high variability and low extinction vulnerability of fish populations have been invoked to avoid listing commercial species of fishes under international threat criteria. However, we need to learn more about recovery, which may be hampered by negative population growth at small population sizes (Allee effect or depensation) or ecosystem shifts, as well as about spatial dynamics and connectivity of subpopulations before we can truly understand the nature of responses to severe depletions. The evidence suggests that fish populations do not fluctuate more than those of mammals, birds and butterflies, and that fishes may exhibit vulnerability similar to mammals, birds and butterflies. There is an urgent need for improved methods of detecting marine extinctions at various spatial scales, and for predicting the vulnerability of species