O objetivo deste estudo foi descrever a riqueza, estrutura e diversidade de espécies arbóreas em áreas de Floresta Estacional e ecótono (Floresta Estacional/Floresta Ombrófila) no estado do Tocantins, buscando subsídios para a conservação, manejo florestal, compensação de reserva legal e recuperação ambiental, além de discutir as identidades fitogeográficas em comparação com outras florestas do Brasil. Em 18 bacias hidrográficas, conduziu-se amostragem da vegetação arbórea (DAP > 5 cm) de 22 áreas (amostras) por meio do inventário de 477 parcelas de 400 m². Foram elaboradas análises de classificação pelo método TWINSPAN, em duas escalas distintas. A primeira avaliou a diversidade beta entre as parcelas amostradas no estado do Tocantins e a segunda buscou analisar a similaridade das florestas do Tocantins em relação a outras florestas do bioma Cerrado e suas áreas de tensão ecológica. As florestas amostradas apresentaram ampla variação em termos de riqueza (33 a 243 espécies), densidade (486 a 1.179 ind.ha-1), área basal (14,04 e 37,49 m².ha-1), índices de diversidade (H´ = 2,75 a 4,59) e de equabilidade (J´= 0,72 a 0,86). As análises de classificação convergiram para resultados comuns, identificando quatro ambientes dissimilares em termos florísticos e estruturais no estado do Tocantins: Floresta Estacional Decidual, Floresta Estacional Semidecidual, ecótono Floresta Estacional Semidecidual/Floresta Ombrófila e ecótono Floresta Estacional Decidual/Floresta Ombrófila. A fim de manter a diversidade de plantas e de ambientes na região de transição Floresta Amazônica e Cerrado, sugere-se que o processo de criação de unidades de conservação no estado do Tocantins deva ser intensificado e tenha como base para seleção das áreas critérios biogeográficos.
BackgroundCardiac tumors are rare, mostly benign with high embolic potential.ObjectivesTo correlate the histological type of cardiac masses with their embolic potential,
implantation site and long term follow up in patients undergoing surgery.MethodsBetween January 1986 and December 2011, we retrospectively analyzed 185
consecutive patients who underwent excision of intracardiac mass (119 females,
mean age 48±20 years). In 145 patients, the left atrium was the origin site. 72%
were asymptomatic and prior embolization was often observed (19.8%). The diagnosis
was established by echocardiography, magnetic resonance and histological
examination.ResultsMost tumors were located in the left side of the heart. Myxoma was the most common
(72.6%), followed by fibromas (6.9%), thrombi (6.4%) and sarcomas (6.4%). Ranging
from 0.6cm to 15cm (mean 4.6 ± 2.5cm) 37 (19.8%) patients had prior embolization,
stroke 10.2%, coronary 4.8%, peripheral 4.3% 5.4% of hospital death, with a
predominance of malignant tumors (40% p < 0.0001). The histological type was a
predictor of mortality (rhabdomyomas and sarcomas p = 0.002) and embolic event
(sarcoma, lipoma and fibroelastoma p = 0.006), but not recurrence. Tumor size,
atrial fibrillation, cavity and valve impairment were not associated with the
embolic event. During follow-up (mean 80±63 months), there were 2 deaths (1.1%)
and two recurrences 1 and 11 years after the operation, to the same cavity.ConclusionMost tumors were located in the left side of the heart. The histological type was
predictor of death and preoperative embolic event, while the implantation site
carries no relation with mortality or to embolic event.
In ascending aorta aneurysms (AscAA) the whole vessel wall dilates, while in aortic dissections (AD) the wall cleaves into two sheets. Both may present fine elastic fragmentation and a decrease in collagen. We analyzed whether alterations in the three-dimensional structure of these fibers could be involved in the pathogenesis of AscAA/AD. Specimens obtained at surgery for these diseases (n = 4 for each) and on coronary artery bypass surgery (controls, n = 4) were submitted to treatments which either preserve collagen or the elastic structure. These samples were examined by scanning electron microscopy. In all groups most of the collagen fibers were packed, forming laminar structures very similar to the elastic lamellae. In AscAA/AD, the fibers showed signs of degradation and/or fragmentation. Elastic tissue was distributed in large sheets with fenestrations, with smaller branches between them. In 1 of the dissection cases and 2 of the aneurysm cases elastic sheet fragmentation, which under light microscopy seems to be located at random, had a pattern of clefts which were irregular but approximately transversal to the main axis of the wall. The recognition of this pattern and the degradation/fragmentation of collagen and elastic fibrils facilitates understanding of why the wall is weak and affected by aneurysms and dissections.
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