Evidence based on sputum culture results suggests that bacterial

Evidence based on sputum culture results suggests that bacterial infection may be responsible for around half of AE-COPD,15 with a clear relationship being demonstrated between sputum purulence and the presence of bacteria.16 and 17 For this reason, current guidelines recommend acute antibiotic therapy for patients with more severe symptoms

of AE-COPD, with treatment typically lasting for 5–7 days.18, 19, 20 and 21 In particular, guidelines issued by the Global Initiative for Chronic Obstructive Lung Disease (GOLD) and the Joint Task Force of the European Respiratory Society and the European Society for Clinical Microbiology and Infectious Diseases advocate antibiotic use for check details those with Anthonisen type I (worsening dyspnoea with increased sputum volume and purulence) or type II (change in any two of these symptoms, particularly if one of these symptoms is increase in sputum purulence) episodes,18, 20 and 21 while the Canadian Thoracic Society suggests that antibiotics are beneficial for severe purulent AE-COPD (i.e. new increased expectoration of mucopurulent sputum and dyspnoea).19 Nevertheless, while such treatment has been shown to reduce the risk of subsequent exacerbations, relapse is common.22 Failure may be

related to learn more inadequate antibiotic efficacy, which through incomplete resolution of the initial exacerbation and persistent bacterial infection is likely to influence risk of relapse.23, 24, 25, 26 and 27 Indeed, confirmed bacterial eradication following antibiotic therapy has been shown to be associated with higher clinical cure rates in patients with AE-COPD.28 Effective treatment of the acute exacerbation and reducing the risk of a subsequent bacterial exacerbation are thus important therapeutic goals for

antimicrobial treatment in COPD that may improve, in addition to other conventional treatments (e.g. long-acting bronchodilators and inhaled corticosteroids), the patients’ quality of life. The rate Resveratrol at which exacerbations occur appears to reflect an independent susceptibility phenotype.5 and 29 Furthermore, exacerbations appear to cluster together, with some patients remaining at high risk for recurrent exacerbation for some weeks after the initial exacerbation,5, 9, 30 and 31 possibly due to ongoing lung and systemic inflammation.32 While acquisition of new strains of respiratory pathogens is an important mechanism underlying acute COPD exacerbations,33 chronic microbial colonisation of the lower respiratory tract is also relevant.34, 35 and 36 This colonisation is likely to contribute to chronic inflammation and progressive loss of lung function in COPD due to increased rate of exacerbations.33, 35, 36, 37, 38 and 39 Treatments aimed at reducing bacterial colonisation, which may be regarded as chronic infection in the presence of an inflammatory response,40 may, therefore, help reduce the progression of the disease.

Fica por esclarecer, neste doente, a data exata de início do quad

Fica por esclarecer, neste doente, a data exata de início do quadro de EE. O diagnóstico é por vezes tardio, principalmente pela semelhança ou coexistência de RGE. A nível histológico ficam ainda por esclarecer

os dados que permitem ao patologista afirmar o grau de eosinofilia20. Importante refletir sobre o objetivo do tratamento. Se pretendemos uma melhoria clínica ou uma melhoria histológica (prevenção de impacto alimentar, prevenção de fibroestenose, risco de infeções HSV)15 and 21. Quais serão os marcadores de maior risco ou maior gravidade da doença. Será que a estenose se traduz numa doença de mais difícil controlo? As complicações major da EE são a remodelação e estreitamento esofágico, que devemos evitar. Para isso são necessárias estratégias para monitorizar a doença. Para já, acompanhamento destes doentes é curto. Não há ainda evidência de associação a malignidade. De salientar a realização de biópsia para o diagnóstico CAL-101 ic50 desta patologia, o tratamento de 8 semanas com IBP, que não só inibe a secreção ácida como também diminui citoquinas (IL‐5 www.selleckchem.com/products/ABT-263.html e eotaxina 3), e posterior repetição de EDA com biópsia. Só aí se chega a conclusões definitivas e se considera a necessidade de estudos adicionais3, 7 and 8. É uma doença com uma boa

correlação clínico‐histológica, questiona‐se assim sobre a necessidade de repetições seriadas de EDA e biópsia no doente assintomático. Ainda por definir nos consensos mundiais os timings para a sua realização 21. Este artigo pretende salientar a importância de pensar neste diagnóstico, para a melhoria da qualidade de vida do doente, redução dos riscos/impactação e prevenção de danos irreversíveis Paclitaxel in vitro (remodelação do tecido). Devemos ponderar esta etiologia em casos de má evolução ponderal e dificuldades alimentares5. A terapêutica de ser adequada ao doente e em articulação com o alergologista7, 11, 12 and 18. Os autores declaram que para esta investigação não se realizaram experiências em seres humanos e/ou animais. Os autores declaram ter seguido os protocolos

do seu centro de trabalho acerca da publicação dos dados de pacientes. Os autores declaram ter recebido consentimento escrito dos pacientes e/ou sujeitos mencionados no artigo. O autor para correspondência deve estar na posse deste documento. Os autores declaram não haver conflito de interesses. “
“Renal cell carcinoma (RCC) has the potential to metastasize to almost any site. Metastatic disease may be present in up to 25% of patients at the time of diagnosis while another 50% develop metastasis during follow-up.1 and 2 Its tendency to vascular spreading as well as expansible ostetolytic skeletal metastization is well known. However, it is less expected that RCC presents as an unpredictable tumour which can manifest with very late metastases at unexpected sites, even a long period after successful resection of early stage lesion.

This is because clinicians face considerable challenges in visual

This is because clinicians face considerable challenges in visually identifying oral neoplasia

at an early stage, leading to many diagnoses occurring late in neoplasia progression BIBW2992 price [3] and [4] Currently disease progression, surgical margins, metastasis and extent of invasion are decided based on diagnostic methods such as X-rays, CT scans or PET images carried out prior to surgery [5] and [6]. These techniques, though clinically useful, have safety concerns, cannot predictably detect tumors less than 1 cm in diameter (equating to greater than 1 million cancerous cells), and cannot be generated in real time to guide the surgeon intra-operatively. In recent years, there have been a number of scientific approaches to the problem of oral lesion detection (i.e. ViziLite, VELscope, Trimira, OralCDx, etc.). However, the effectiveness of these technologies is inconsistent [5] and [7].

The literature suggests that these modalities fail to noticeably improve the detection of oral carcinomas from standard head and neck examinations routinely performed by physicians [7]. A major reason for the inconsistency, find more poor specificity and inability to detect earlier stage cancer is the oversight of these technologies to target advanced stage anatomical changes instead of early stage molecular level alterations. Optical molecular imaging provides a non-invasive, in vivo, rapid and cost effective method to detect early molecular level changes in neoplastic tissue, based on its ability to specifically analyze molecules of interest. More importantly, optical molecular imaging can be performed with minimum training, increasing its potential to be used in the general physicians’ office. Possible targets for optical imaging are the glycoproteins and glycolipids on the cell surface. These cellular glycomolecules are completed during the post-translational event called glycosylation, which is known to be abnormal in human disease progression MG-132 cell line such as carcinogenesis and

metastasis [8], [9] and [10]. This irregular glycosylation results in varying glycosyl residues on the cell surface during pathological changes, highlighting the clinical importance of this alteration as a potential target by which to detect oral cancer. A prime example of aberrant glycosylation in carcinogenesis is the overexpression of sialyl Lewis A and sialyl Tn antigen in cancers of the pancreas, colon, stomach and esophagus [11] and [12]. Moreover, increased sialytransferases and sialic acid content on cell glycoconjugates has long been linked to oral cancer and malignant transformation [13] and [14]. Increased sialic acid content can reach up to 10e+09 sialic acid residues per tumor cell [15]. Further, Rajpura et al. showed statistically significantly higher levels of sialic acid in oral cancer patients compared to normal patients (63.70mg/dl versus 30.

Based on the proportion of runoff that reached the outlet on each

Based on the proportion of runoff that reached the outlet on each of the 5 LDK378 purchase days following a rain or snow melt event, we were able to determine a best-fit Tp which minimized the root-mean-square error between the predicted and observed runoff shape

(see Appendix A for further details). We used the take-one-out approach to evaluate the degree to which any one watershed influenced the relationships between the best-fit Tp and Tc. We performed three independent tests on our model: (1) we used a leave-one-out approach to see how well our model would predict the hydrograph of a watershed that was not used to determine the regional model parameters, (2) we compared our predicted storm runoff locations to shallow water table measurements, and (3) we compared our predicted storm runoff locations to measured soil moisture. To understand how the model would perform in ungauged watersheds, we considered the recalculated relationships between S and SWDd and between Tc and Tp, determined by systematically excluding one watershed in a leave-one-out approach ( Arlot and Celisse, 2010). We then used these relationships to model the excluded watershed and compare the predicted and observed discharge hydrographs; note, in the earlier part of this paper we were only investigating how sensitive the parameters

were to any one watershed and here we are evaluating learn more model performance. The values of the coefficients for the relationships between measured and model parameters when excluding each watershed are reported in Table 2. Modeled results were compared to USGS daily streamflow measurements at each location. In addition to the Nash-Sutcliffe efficiencies (NSE),

we determined the ratio of the root mean square error to the standard deviation of observed streamflow (RSR) and the percent bias (PBIAS) for each watershed (Nash and Sutcliffe, 1970). Moriasi et al. (2007) proposed that a model is satisfactory if NSE > 0.50, RSR < 0.70, and has an absolute PBIAS < 25%. We also calculated NSE on an event basis, where runoff events were initiated by a 1 day rise in the observed USGS hydrograph after at least 2 days of decreasing flows. We created a LIDAR-derived STI (Fig. 3) for comparison to water 3-mercaptopyruvate sulfurtransferase table height measurements from Town Brook Watershed, using: (i) a 3 m LIDAR-derived DEM from the NY Department of Environmental Protection (DEP), (ii) maximum triangular slope (Tarboton, 1997), (iii) the Multiple Triangular Flow Direction method (Seibert and McGlynn, 2007) as per Buchanan et al. (2013). We then binned STI values into equal-area wetness classes, such that low-numbered wetness classes are wetter areas (large STI values) and high wetness classes signify dry areas of the watershed (low STI values). This allowed us to assign a location as “wet” or “dry” during a storm event based on the saturated extent predicted by the model. Lyon et al.

This work presents a study regarding

This work presents a study regarding Z-VAD-FMK solubility dmso total vitamin C and ascorbic acid degradation in acerola pulp during thermal treatment by ohmic and conventional heating. For the ohmic heating technology, the ascorbic acid degradation ranged from 3.08 to 10.63%. The applied voltage and the solids content of the pulp significantly influenced the degradation of the compounds. The voltage gradient had a positive effect, i.e., an increase in the voltage gradient lead to an increase in the AA degradation. The

total vitamin C degradation ranged from 2.0 to 5.1%. The vitamin C degradation was influenced only by the linear and the quadratic effects of the voltage. Ohmic heating, when performed with low voltage gradients, exhibited vitamin C and ascorbic acid degradation similar to conventional heating. However, high voltage gradients increased the degradation of both vitamin C and ascorbic acid. This behavior may be explained by the increase of electrochemical reactions when using high voltage gradients, which can adversely affect the ascorbic acid and catalyze the degradation pathways in the presence

of oxygen. The authors acknowledge the financial support received from CNPq (Conselho Nacional de Desenvolvimento Científico Selleck GSK-J4 e Tecnológico, Brasil), as a scholarship to the first author, from CAPES (Coordenação de Aperfeiçoamento de Pessoal de Nível Superior, Brasil) within the PRODOC project, and Mais Fruta Company for supplying the acerola pulp. “
“Thermal processing is one of the most widely used physical Oxalosuccinic acid methods for food preservation. High temperature inactivates undesired microorganisms and enzymes, but also deteriorates quality and sensorial attributes. Consumer demands for minimally

processed products compel food companies to optimize and redesign the existing technologies. In this context, the assessment of the process impact in terms of food safety and quality is of great importance for process evaluation and design. The in situ evaluation of microbial count or vitamin content is often time-consuming and expensive. Alternatively, the effect of the thermal processing can be evaluated in two ways: from the analysis of the time-temperature history and the residence time distribution coupled with the kinetics of thermal change; and from the use a time-temperature integrator (TTI) as indicator of safety and quality ( Lewis & Heppell, 2000, p. 447; Van Loey, Hendrickx, De Cordt, Haentjens, & Tobback, 1996). The first method requires the time-temperature history, which can be recorded online at the processing plant and also residence time distribution techniques. These results, combined with the knowledge of the thermal change kinetics, allow the calculation of the process impact.

e , RED in blue ink) An advantage of this task over the original

e., RED in blue ink). An advantage of this task over the original Stroop task is that it allows the two types of conflict to be examined separately during development and ageing. The difference

waves of key ERP components can then be analyzed to isolate specific change during stimulus or response conflict processing. Stimulus conflict can be measured by analyzing SC minus congruent conditions; response conflict can be measured by analyzing RC minus SC, finally general conflict (or combined stimulus and response level conflict) can be measured by analyzing RC minus congruent condition. For example the most established ERP measure of Stroop conflict is usually called the N450. The N450 is an enhanced negativity with a latency of 300–500 msec in the incongruent condition

relative to the neutral/congruent conditions over midline electrodes (Eppinger et al., 2007, Alectinib Hanslmayr et al., 2008, Rebai et al., 1997 and West and Alain, 2000b). Recent evidence suggests it represents general conflict detection (Szucs and Soltesz, 2012, Szucs et al., 2009a, West et al., 2004 and West and Schwarb, 2006). Across the lifespan the N450 shows distinct maturational patterns in terms of topography, amplitude, and latency; however the functional significance of these changes has not been determined. Jongen and Jonkman TGF-beta inhibitor (2008) documented the developmental emergence of the N450 around 10–12 years of age. Unlike in adults who had left frontal activity they found that the topography of the N450 was focused over left and right parietal sites in children. Etofibrate The developmental

hemispheric shift over parietal sites may be representative of either reduced ability (e.g., to inhibit responses) or compensatory processes (e.g., the engagement of higher levels of attention) (Jongen & Jonkman, 2008). Some ageing literature suggests the latency and amplitude of the N450 decline with age (West and Alain, 2000a and West et al., 2004). However, others found increased N450 amplitude (Mager et al., 2007). These inconsistent findings could be due to the different age range of participants and slight differences in task manipulations. Here we examined this question and related the modulations of the N450 to the manipulation of stimulus and response conflict. Here our overall objective was to identify developmental asymmetries in conflict processing across the lifespan. First we identified any age-related differences in stages of information processing by examining neural activity representative of stimulus processing (P3a, P3b) as well as response levels of processing (LRP, EMG). Secondly we isolated differences in stimulus (SC minus CON), response (RC minus SC) and general (RC minus CON) conflict processing by examining the main effects of congruency effects and the difference waves of key components during the de Houwer colour word Stroop task.

The caption (allogenic gut microbiota infusion) is incorrectly me

The caption (allogenic gut microbiota infusion) is incorrectly mentioned in the right most row (upper and lower panels). The middle row (upper and lower panels) concerns the allogenic gut microbiota infusion and the right most row (upper and lower panels) is the autologous gutmicrobiota infusion. The corrected figure is presented below. “
“Event Date and Venue Details from * ENTOMOLOGICAL SOCIETY OF AMERICA ANNUAL MEETING, Portland, OR, USA 16–19 November Contact: ESA,

9301 Annapolis Rd., Lanham, MD 20706-3115, USA Email [email protected]. Fax: 1-301-731-4538. http://www.entsoc.org. 2015 *8th INTERNATIONAL IPM SYMPOSIUM, Salt Lake City, UT, USA 24–26 March Contact: E.E. Wolff. Email [email protected]. *18th INTERNATIONAL Selumetinib ic50 PLANT PROTECTION CONGRESS, “Mission Possible: Food for All through Adequate Plant Protection”, Berlin/Dahlem, GERMANY 24–27 August Contact see: http://tinyurl.com/3e96vdr. Cyclopamine supplier * ENTOMOLOGICAL

SOCIETY OF AMERICA ANNUAL MEETING, Minneapolis, MN, USA 14–18 November Contact: ESA, 9301 Annapolis Rd., Lanham, MD 20706-3115, USA. [email protected]. Fax: 1-301-731-4538. http://www.entsoc.org. Full-size table Table options View in workspace Download as CSV “
“Intentional food adulteration can be defined as the unscrupulous act of corrupting a genuine food product for pecuniary profit by admixtures with cheaper products and materials which are difficult to detect by the consumers or by simple routine analytical techniques. High-priced commodities are usually targets for adulteration and roasted coffee, a leading commodity in international markets, is rather vulnerable to it. Ground roasted coffee presents physical characteristics (particle size, texture and color) that are easily reproduced by roasting and grinding a variety of

biological materials (cereals, seeds, parchments, etc), thus, it has been the target of fraudulent admixtures with several materials, including lower quality coffees (Alves, Casal, Alves, & Oliveira, 2009; Craig, Franca, & Oliveira, 2012a) and a variety of spurious materials, such as twigs, coffee berry skin and parchment, spent Fludarabine chemical structure coffee grounds, roasted barley, corn and other cheaper grains (Oliveira, Oliveira, Franca, & Augusti, 2009; Reis, Franca, & Oliveira, 2013). A few recent studies have established suitable parameters and markers for detection of coffee husks and roasted starchy grains in ground roasted coffee and instant or soluble coffee Garcia et al., 2009; Nogueira & Lago, 2009; Oliveira et al., 2009; Pauli, Cristiano, & Nixdorf, 2011). Although effective, the analytical methodologies employed are time demanding, expensive and laborious, and usually not appropriate for routine analysis.

Northward flows were dominant

from January until the midd

Northward flows were dominant

from January until the middle of February, resulting in a 15 km3 water transport from the Gulf of Riga to the Väinameri. From mid-February until late April, the cumulative water exchange through the Suur Strait was small, although the instantaneous velocities were not. From May till mid-June outflow from the Väinameri to the Gulf of Riga was dominant, the corresponding cumulative water exchange being 10 km3. From May to July the currents were less variable than during the rest of the year. During the summer months (June, July, August) the periods of outflow from the Gulf of Riga alternated with inflow. From October until the end of December there was a gross outflow from check details the Gulf of Riga to the Väinameri: the corresponding cumulative water exchange was approximately 20 km3. The annual water exchange was about 23 km3 from the Gulf of Riga to the Väinameri. To conclude, both the flow speed and the water exchange are characterized by considerable variability. A dominant outflow from the Gulf of Riga to the Väinameri from late autumn to early spring is characteristic of mild winters (Otsmann et al. 2001). For instance, the winter of 1994/1995 was stormy and ice free, which resulted in a strong outflow into the Suur Strait. October–December 1996 was also windy, resulting in a persistent outflow. In contrast, the winter of 1995/1996 was cold (ice cover

in the Suur Strait) and the Pexidartinib research buy dominant winds blew from the north. Under these conditions a weak inflow to the Gulf of Riga through the Suur Strait was observed. 1. Field measurements showed a certain asymmetry between along-strait wind forcing, Cyclin-dependent kinase 3 flow speed and significant wave height. Because of the longer fetch of southerly waves, the highest significant wave heights (maximum 1.6 m) were observed during southerly wind events. Further studies are needed to quantify material transport

through the Suur Strait focusing on the cycling of material between sediments and water. We thank the anonymous referees for their valuable comments on the manuscript. “
“The North Aegean Sea is a part of the Aegean Sea (Figure 1) experiencing complex bathymetric and hydrographic conditions (Lykousis et al. 2002). The bottom topography is characterized by a NE-SW oriented deep trough, separated by shallow sills and shelves, constituting the ‘North Aegean Trough’ (Poulos et al. 1997). Within this trough, three main depressions exist: the Lemnos Basin to the north-east (maximum depth 1470 m), the Athos Basin at the centre (maximum depth 1150 m) and the North Sporades Basin to the south-west (maximum depth 1500 m). A series of shallow sills separate these basins from the Skyros Basin to the south (maximum depth 1077 m), and from the Chios Basin to the west and south of Chios Island, with a maximum depth of 1200 m (Velaoras & Laskaratos 2005).

PST001 being neutrally charged and consisting of numerous hydroxy

PST001 being neutrally charged and consisting of numerous hydroxyl groups provide anchors for drug attachment and modification. This enables easy binding with TPP, and further with the positively charged Dox-HCl. This nanoconjugate was previously tested to provide a Dox-encapsulation efficiency of 70% as reported [26]. The release profile of Dox from the PST-Dox nanoparticles and Dox-HCl at different pH levels over time at ambient temperature Ruxolitinib in vivo was also previously evaluated [26]. It was found that doxorubicin hydrochloride showed a burst release within 3–5 hours regardless of the change in pH from 4.5 to 7.4. However, the

PST-Dox nanoparticle showed excellent pH and time dependent Dox release kinetics. Yet, another nanoformulation of PST001 with gold (PST-Gold)

also demonstrated similar kinetic profiles and exhibited superior anticancer potential [24]. To determine the mechanism of cell death induced by the PST-Dox nanoparticles in cancer cells, apoptotic assays were conducted after the administration of 1 μg/ml of nanoparticles for 24 hours. Compared to the controls, acridine orange-ethidium bromide staining in the cells treated with the PST-Dox nanoparticles showed a drastic change in fluorescence from green to yellow/red that was associated with other apoptotic features such as the presence of apoptotic bodies and nuclear condensation. Significant changes in fluorescence GSKJ4 were observed in both DLA and EAC cells upon treatment with PST-Dox nanoparticles (Figure 2C). Morphological and phase contrast microscopy evaluation of cells treated with PST-Dox nanoparticles (1 μg/ml) for

24 hours showed salient features of apoptosis such as distorted shape, membrane blebbing, and the presence of apoptotic bodies compared to the vehicle in DLA and EAC cells ( Figure 2D). Benzatropine Apoptosis is the most appropriate mode of cell death in living systems induced by several polysaccharides [34], anticancer drugs such as doxorubicin [35] and polysaccharide based nanoparticles [24]. Membrane blebbing, one of the hallmarks of apoptosis refers to the irregular bulges in the plasma membrane of the cells caused by localized decoupling of the cytoskeleton from the plasma membrane. PST-Dox also exhibited similar trends of apoptosis in MCF-7, K562 and HCT116 as reported earlier [26]. In the current study, the inhibition of cell proliferation exhibited by the PST-Dox nanoparticles in the lymphoma was confirmed through the induction of apoptosis. The extended efficiency of the PST-Dox nanoparticle compared to PST001 and Dox in inducing apoptosis may have been due to the increased uptake of the particles via endocytosis because of small size and increased surface-to-volume ratio [36]. Although DLA and EAC models exhibited robust anticancer effects, cellular uptake and retention assays were not possible in ascites tumors as per the standardized protocols.

equation(6) LetV=−b=[−0 048+0 0016×H++0 00178×ln(N)+0 0077×ln(CC)

equation(6) LetV=−b=[−0.048+0.0016×H++0.00178×ln(N)+0.0077×ln(CC)],where V is the index of mangrove forest structure. The theoretical line of minimum forest band width

in relation to the vegetation index is shown in Figure 6. The mangrove structure index is classified into 5 levels of wave prevention based on its relation to wave height (Figure 6; Table 2). The required mangrove band width decays exponentially with the vegetation index (V). When the mangrove forest is tall and dense, and the canopy closure high (i.e. a high V index), a narrower forest band is required. When the mangrove forest is short, the tree density and canopy closure low (i.e. a low V index), a wider GSK3235025 in vivo mangrove band is required. – Level I: the V index is less than 0.005. At this level when the V index is increasing, the minimum mangrove band width decreases rapidly quickly from 600 m to 240 m. Applying the threshold V index in Table 3, we have identified the levels of wave prevention for 32 mangrove forest plots. The results show that the levels of wave prevention in the southern

plots are higher than those of the northern plots. This indicates that the southern mangrove forest can protect the coastline better than the northern mangrove forest does (Table 3). Mangrove forests are very important ecosystems located in the upper intertidal zones of the tropics. They are the primary source of energy and nutrients in these environments. They have a special www.selleckchem.com/products/gsk1120212-jtp-74057.html role in stabilizing shorelines, minimizing wave damage and trapping sediments. However, in recent decades mangrove forests in Vietnam have been threatened by conversion to agriculture and aquaculture. The primary objectives of this

study were to define a minimum mangrove band width for coastal protection from waves in Vietnam. We set up 32 plots in 2 coastal regions of Vietnam to measure wave attenuation from the edge to the forest centre (distances). The results show that wave height is closely related to cross-shore distances in an exponential equation. All the single equations are highly significant with P < 0.001 and R2 > Cyclin-dependent kinase 3 0.95. We derived an integrated exponential equation applicable to all cases, in which coefficient a (the intercept in the log transformation of the exponential equation) is a function of initial wave height, and coefficient b (the slope in the log transformation of the exponential equation) is a function of canopy closure, height and density. The integrated equation was used to define appropriate mangrove band widths. On the assumption that the average maximum wave height is 300 cm and the safe wave height behind the forest band is 30 cm, the required mangrove forest band width associated with its structures was defined. The mangrove structure index (V) is classified into 5 levels of protection from waves.