Next Article in Journal
Forests: An International and Interdisciplinary Scientific Open Access Journal
Previous Article in Journal
Resiliency of an Interior Ponderosa Pine Forest to Bark Beetle Infestations Following Fuel-Reduction and Forest-Restoration Treatments
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:

Ecological Variability and Carbon Stock Estimates of Mangrove Ecosystems in Northwestern Madagascar

Trevor G. Jones
Harifidy Rakoto Ratsimba
Lalao Ravaoarinorotsihoarana
Garth Cripps
1 and
Adia Bey
Blue Ventures Conservation, Villa Bella Fiharena, Rue Gambetta, Lot 259, Toliara 601, Madagascar
Integrated Remote Sensing Studio, Department of Forest Resources Management, 2424 Main Mall, University of British Columbia, Vancouver, BC V6T 1Z4, Canada
Department of Forestry, P.O. Box 175, University of Antananarivo, Antananarivo 101, Madagascar
Author to whom correspondence should be addressed.
Forests 2014, 5(1), 177-205;
Submission received: 6 December 2013 / Revised: 3 January 2014 / Accepted: 10 January 2014 / Published: 21 January 2014


Mangroves are found throughout the tropics, providing critical ecosystem goods and services to coastal communities and supporting rich biodiversity. Despite their value, world-wide, mangroves are being rapidly degraded and deforested. Madagascar contains approximately 2% of the world’s mangroves, >20% of which has been deforested since 1990 from increased extraction for charcoal and timber and conversion to small to large-scale agriculture and aquaculture. Loss is particularly prominent in the northwestern Ambaro and Ambanja bays. Here, we focus on Ambaro and Ambanja bays, presenting dynamics calculated using United States Geological Survey (USGS) national-level mangrove maps and the first localized satellite imagery derived map of dominant land-cover types. The analysis of USGS data indicated a loss of 7659 ha (23.7%) and a gain of 995 ha (3.1%) from 1990–2010. Contemporary mapping results were 93.4% accurate overall (Kappa 0.9), with producer’s and user’s accuracies ≥85%. Classification results allowed partitioning mangroves in to ecologically meaningful, spectrally distinct strata, wherein field measurements facilitated estimating the first total carbon stocks for mangroves in Madagascar. Estimates suggest that higher stature closed-canopy mangroves have average total vegetation carbon values of 146.8 Mg/ha (±10.2) and soil organic carbon of 446.2 (±36.9), supporting a growing body of studies that mangroves are amongst the most carbon-dense tropical forests.

1. Introduction

Mangroves are found in inter-tidal areas in over 120 countries between 30° N and S latitude and provide a broad range of important ecosystem goods (e.g., food; fuel; construction materials; medicine) and services (e.g., storm protection; erosive barriers; breeding, nesting, nursing and feeding grounds for marine, pelagic and terrestrial fauna; water filtration) for surrounding coastal communities [1,2,3,4,5,6,7,8,9,10,11]. Mangrove ecosystems also support high floral and faunal biodiversity [9,12,13,14] and sequester significant amounts of CO2 [15,16]. While numerous studies have measured above-ground biomass in mangrove trees (e.g., [17,18,19,20,21,22,23,24,25,26]), comparatively few have quantified above- and below-ground carbon (C) pools, including soil (i.e., [15,27,28,29,30,31,32,33,34]); however, it is the deep, organic material enriched soils that contain the vast majority of C stocks [35,36,37,38]. Factoring in soil, mangroves have been found to be amongst the most carbon-dense forests in the tropics, with similar or greater above- and exceptionally larger below-ground stocks compared with the terrestrial systems reported in several studies [15,27,32,33,34,39]. Collectively, despite representing only about 0.7% of tropical forests, mangroves are thought to collectively store as much as 20 petagrams of C [15,17,40].
Despite their tremendous importance, within the last 50 years, global mangrove loss has been rapid and widespread, with estimates of 30%–50% since 1960 [41], 25%–35% from 1980–2000 [42,43,44] and 36% since 1990 [7]. Annual loss is estimated at around 1%–2%, exceeding the deforestation rates of inland tropical forests [4,42,45,46]. The primary anthropogenic drivers of loss include increasing coastal population and development, mounting economic pressures, small- to industrial-scale conversion to agriculture and aquaculture, over-extraction of forest products, and erosion, sedimentation and siltation from upstream intensive farming and terrestrial deforestation [47,48,49,50,51,52,53,54]. The principal natural drivers of loss include forest succession, hydrological dynamics and the impacts of extreme weather events (e.g., cyclones) and sea-level rise, which are projected to increase in frequency and magnitude, due to climate change [4,8,47,53,55,56,57,58]. Degradation and deforestation result in substantial greenhouse gas emissions if deep organic soil layers are disturbed [15,59,60,61]. Much of the world’s remaining mangroves are already degraded, and if current trends continue, most of the remaining extent could become functionally valueless within the 21st century [41,45,62].
Globally, the collective importance and value of mangrove ecosystems is receiving an increasing amount of attention [16,63,64,65,66,67]. Owing to their value and rate of loss, up-to-date information representing the extent and status is critical for effective management and decision making [11]. Employing remotely sensed data for mapping and monitoring mangrove ecosystems is already well established [11,68]. Maps produced from remotely sensed data can enable the partitioning of mangrove ecosystems by ecological differences and statistically distinct C stock values. Of particular note, Landsat imagery is freely available, offers >40 years of data and has proven critical for both locating and quantifying mangrove extent and loss and partitioning mangrove ecosystems to estimate C stocks [40,69,70,71,72,73,74,75,76,77,78,79].
Madagascar contains Africa’s fourth largest extent of mangroves and, as of 2005, represented 2% of the global distribution, covering approximately 2800 km2 [7,40,80]. In keeping with global trends, Madagascar’s mangroves are being rapidly degraded and, in some areas, completely deforested from logging for commercial timber and charcoal production, land-use conversion to agriculture and commercial small-scale (artisanal) and large-scale aquaculture. Anthropogenic loss is particularly significant in Madagascar’s second largest mangrove ecosystem in the northwestern Ambanja and Ambaro bays. Existing national-level maps include contemporary and historical areal extents for mangroves and provide the information required for quantifying the dynamics; however, these data lack the detail required for comprehensive ecosystem characterization and estimation of C stocks for distinct mangrove types. While there have been several localized mangrove mapping efforts in Madagascar for Mahajamba Bay (i.e., [81,82,83]), Betsiboka Bay [84] and the Mangoky Delta [85], there are none published for Ambanja and Ambaro bays. Additionally, no studies have reported above- and below-ground C stocks, including soil, for any of Madagascar’s mangroves. Here, we use existing national-level maps to calculate the long-term dynamics and employ Landsat data to produce the first ever localized map (circa 2010) of mangrove ecosystems and surrounding terrestrial land-cover types for Ambanja and Ambaro bays. Using the localized map to partition the mangroves in to ecologically meaningful strata, we also present the first estimates of total C stocks for Malagasy mangroves and compare them with published values for other terrestrial forest types.

2. Experimental Section

2.1. Study Area

The area of interest (AOI) includes the combined marine and terrestrial extent of Ambanja and Ambaro bays in northwest Madagascar (centered on latitude 48° 30’ East, longitude 13° 26’ South) (Figure 1). Both bays are lined with extensive mangroves, collectively totaling approximately 26,000 hectares (ha). In Madagascar, the AOI mangroves are surpassed in area only by Mahajamba Bay [86]. In the AOI, the semi-diurnal tidal range varies between maximums of 3–3.5 m, and the climate is sub-humid tropical, typified by a relatively dry and cool period from May–October and comparatively hotter and wetter weather influenced by periodic cyclones from November–April [87]. Alluvial and lake deposits predominantly characterize the underlying geology, and the comparative abundance of rainfall and freshwater contributes to higher stature mangrove trees than further south [80,88]. In the AOI and throughout coastal Madagascar, communities are extremely vulnerable to climate change, and mangroves are vital to their present and future wellbeing. The range, frequency and magnitude of anthropogenic activities within mangroves continue to rise for numerous reasons, including a lack of governance and increasing population.
Figure 1. The area of interest includes the combined marine and terrestrial extent encompassed by a seven kilometer coastal buffer of Ambanja and Ambaro bays. One-hundred ninety-one classification reference areas and 55 mangrove carbon plots are shown. The background image is the near-infrared band (i.e., band 4) from a (Global Land Survey) GLS 2010 Landsat image, projected to Universal Transverse Mercator (UTM).
Figure 1. The area of interest includes the combined marine and terrestrial extent encompassed by a seven kilometer coastal buffer of Ambanja and Ambaro bays. One-hundred ninety-one classification reference areas and 55 mangrove carbon plots are shown. The background image is the near-infrared band (i.e., band 4) from a (Global Land Survey) GLS 2010 Landsat image, projected to Universal Transverse Mercator (UTM).
Forests 05 00177 g001

2.2. Inventory of Existing Mangrove Maps and Assessment of Mangrove Dynamics

National-level datasets providing mangrove coverage over the AOI include maps produced by or described in Mayaux et al. [89], the Critical Ecosystem Partnership Fund (CEPF) Madagascar Mapping Project [90], Harper et al. [91], Giri and Muhlhausen [80] and Giri [86]. Mayaux et al. [89] used 1-km Satellite Pour l’Observation de la Terre (SPOT) data to map six dominant vegetation cover types, including mangroves, representing coverage in 1998/1999. The CEPF [90] used Moderate Resolution Imaging Spectroradiometer (MODIS) and Landsat data to produce a 15-class vegetation map circa 2001, including a mangrove class. Harper et al. [91] used Landsat data to map forest cover, including mangroves, for 1973, 1990 and 2000. Using methods detailed in Giri and Muhlhausen [80], Chandra Giri and colleagues at the United States Geological Survey (USGS) produced Landsat-derived maps representing two classes (i.e., mangrove and non-mangrove) for 1973, 1990, 2000, 2005 and 2010 [86]. To determine which dataset provided the most representative mangrove coverage, all maps were compared with reference to Landsat composites, finer spatial resolution imagery viewable through Google Earth and preliminary field observations. The coverage deemed most representative was used to calculate the estimates for mangrove dynamics (i.e., gain, loss and persistence) within the AOI.

2.3. Acquisition and Pre-Processing of Remotely Sensed Data

A Global Land Survey (GLS) Landsat Enhanced Thematic Mapper (ETM)+ scene (path/row: 159/69) was acquired from the USGS Earth Resources Observation and Science Center [92] providing wall-to-wall coverage over the AOI from June 9 2010. GLS data are prepared by the USGS and the National Aeronautics and Space Administration, providing mostly cloud-free, 30-meter (m) spatial resolution, orthorectified (i.e., to a Shuttle Radar Topography Mission (SRTM) digital elevation model (DEM)) Landsat scenes for multiple eras (e.g., 2000, 2005 and 2010 editions) [93]. The Landsat scene was atmospherically corrected using the Cos(t) model, which estimates the effects of absorption by atmospheric gases and Rayleigh scattering, removes systematic atmospheric haze and converts image units to at-surface reflectance [94].
Based on distance to coastline as a mangrove habitat requirement [75,77,95], a 7-km coastal buffer mask was applied. To further exclude areas where mangrove habitat and associated ecosystems were observed not to exist, portions of the imagery >30 m in elevation were removed using an SRTM DEM height mask. SRTM data have previously been associated with field measurements to provide reasonable estimates of mangrove forest canopy heights (e.g., [96,97,98]). Reducing the extent of the area to be classified through masking has been shown to raise accuracy by decreasing spectral variation and confusion amongst the potential range of mapped classes [39]. Preliminary field-recorded height measurements, existing mangrove maps and finer spatial resolution satellite imagery viewable in Google Earth were utilized to determine the thresholds for isolating low-lying coastal scene components.

2.4. Definition and Refinement of Mangrove and Surrounding Land-Cover Categories

Using Landsat ETM+ bands 1–5 and 7 as input, an unsupervised iterative self-organizing classification algorithm (i.e., ISOCLUST) was employed to group pixels into clusters representing prominent spectral components and remove areas dominated by water and shadow. Unsupervised classification is a common preliminary step in the detection and delineation of mangrove and closely related ecosystem types, having been employed in numerous studies [40,78,80,98,99,100,101]. Existing national-level land-cover and mangrove maps and high spatial resolution imagery viewable through Google Earth were referenced to iteratively aggregate and label clusters according to suspected dominant mangrove and other land-cover types (Table 1). Throughout the remote sensing literature, the definition of “mangrove” is extremely variable, at times referring to individual trees, mangrove-related flora or entire ecosystems [11,102]. Our classes are based on dominance by true mangroves, defined by Tomlinson [103] as salt-tolerant halophytic trees and shrubs occurring exclusively in the tidal/inter-tidal zone. Mangrove sub-class labels were initially assigned based on broad canopy-cover categories thought to represent distinct stature and density characteristics.
Table 1. Mapped classes and descriptions.
Table 1. Mapped classes and descriptions.
ClassDescription of typical constituentsClass can also include
Savannahmosaic of dry grass, exposed soil and extremely sparse trees/shrubssenesced rice; reeds
Woodlandmosaic of dry grass and scattered trees/shrubs; canopy <30% closedorchard agriculture
Active cultivationsugar cane, rice, reeds
Closed-canopy terrestrial forestclosed-canopy terrestrial forest; canopy >60% closed
Open-canopy terrestrial forestopen-canopy terrestrial forest; canopy 30%–60% closed
Closed-canopy mangrovetall, mature stands; canopy >60% closedextremely dense younger stands
Open-canopy mangrove Iyoung, short-medium trees; canopy 30%–60% closed; influenced by background soil/mudnaturally open; very degraded tall
Open-canopy mangrove IIstunted short trees, very sparse; canopy ≥10% closed; dominated by background soil/mud
Deforested mangrovemosaic of stumps, scattered trees; canopy <30% closed; greatly influenced by exposed soil/mud
Exposed soilinactive agri/aquacultural fields; extremely patchy savannah; extremely dry tanne (mud-flats)
Exposed mudmangrove/ocean interface; river sediment; wet tannes (mud-flats); inactive aquaculture ponds
To confirm and refine initial class definitions and ensure representative classification, reference data were acquired in February, 2012, during a field survey conducted using a stratified random sampling design, wherein potential plot locations were randomly targeted within mangrove and surrounding land-cover types. A total of 22 100 × 100 m (i.e., hectare-sized) nested classification reference areas were established within mangroves, wherein height, species dominance, stature, age, density, canopy-cover, micro-relief, level of tidal-inundation and the impact of natural and anthropogenic disturbance were estimated qualitatively. Hectare-sized plots were used to ensure that reference areas representing different mangrove ecosystem types could be confidently located within the Landsat image. Within each reference plot, the diameter at 130 or 30 centimeters (cm) (depending on the tree height), height and crown dimensions were measured using a diameter tape and a Vertex hypsometer for representative examples of each mangrove species present in five systematically located 10 × 10 m sub-plots. In each sub-plot, a densiometer was also used to quantify canopy-cover, and litter, understory, regeneration, stumps and standing dead-wood were inventoried. Additional reference areas were established within all non-mangrove classes (see Table 1), wherein extensive field notes and photographs recorded the variability and level of representation. Within all reference areas, geographic coordinates were recorded using a Garmin GPSmap 62sc global positioning system (GPS) unit, which averaged the location in the center for the duration of sampling. Following the fieldwork, through exploiting the familiarity gained with the appearance and location of target mangrove and surrounding land-cover types, additional areas were located to augment field-collected data with reference to imagery viewable in Google Earth. In total, 71 90 × 90 m (3 × 3 pixel) reference areas representing mangrove types and 120 representing non-mangrove classes were delineated. For all classes, at least 33% of the classification reference data was randomly withheld to assess map accuracy.

2.5. Image Classification

The maximum likelihood (ML) algorithm was employed for pixel-based classification of Landsat bands 1–5 and 7. Numerous studies support ML as an effective and robust algorithm for classifying mangrove habitat with medium spatial resolution remotely sensed data [77,79,81,97,104,105,106,107,108,109]. Accuracy was quantitatively assessed using a confusion matrix to cross-tabulate mapped classes against independent validation data. In addition, the Kappa index of agreement was used to assess the extent to which the classification was better than random [110]. Adopting an approach described by Giri and Muhlhausen [80] and Giri et al. [40], the classified map was also divided into a geographically explicit grid in Google Earth, facilitating comparisons with existing maps and finer spatial resolution satellite imagery to identify additional classification error. The classified map was further compared with the best available mangrove coverage data for the AOI, making reference to Landsat color composites, finer spatial resolution imagery viewable through Google and field observations.

2.6. Mangrove Carbon Stocks

To calculate biomass and, subsequently, to estimate C stocks, field surveys were conducted in April–May and August–September, 2012, using a modified version of the measurement protocol outlined in Kauffman and Donato [39], employing a stratified sampling design, wherein plots were systematically located within dominant mangrove cover types. Mangrove strata were defined based on the results of ML classification. Fine spatial resolution imagery viewable in Google Earth was used to eliminate potential plots based on inaccessibility, proximity to class transitions and map error. A total of 55 rectangular nested carbon plots were established (Figure 1). Plots had a default size of 10 × 10 m, but were enlarged to 20 × 20 m if required, to capture ecological variability. All C plots consisted of an inner plot within the main plot (i.e., nested design). Within the inner plot (5 × 5 or 10 × 10 m, depending on the plot size), all the trees with a diameter <5 cm were measured. Throughout the entire plot (10 × 10 or 20 × 20 m, depending on the plot size), all the trees with a diameter >5 cm were measured. Tree measurements included species type, height, diameter (at 130 or 30 cm, depending on height) and the quality of the lead stem, from which plot-level stature, species dominance, density and biomass were derived. Information about the geomorphology (i.e., location, topography) and site conditions (e.g., salinity) was also collected. Canopy-cover was systematically estimated to further assess mangrove labels. For standing dead trees and stumps, heights and diameters were measured to document degradation. Regeneration (i.e., seedlings and saplings), lying-dead wood, leaf-litter, epiphytes and the understory were inventoried, but not quantitatively sampled, as their carbon pools were considered negligible [27]. Soil depth was measured randomly in each quadrat and at the plot-center with a 3-m metal rod. Soil samples were extracted at the plot-center using a soil corer at 0–15, 15–30, 30–50, 50–100 and 100–150 cm. Plot locations were recorded at the plot center using a Garmin GPSmap 62sc GPS unit.
The strong allometric relationships between tree height, diameter at breast height and biomass were used to estimate above-ground biomass and to calculate carbon stocks [111,112]. Equations were selected following a thorough review of the literature and expert advice (Table 2). The below-ground biomass of trees was calculated using a generalized equation developed by Komiyama et al. [113]. The biomass of standing dead wood was calculated using equations in Kauffman and Donato [39]. The bulk density (i.e., oven dry sample mass(g)/volume of the sample (cm3)) and the organic carbon content of the soil samples were determined by the Laboratoire des Radio Isotopes (LRI) of the University of Antananarivo in Madagascar’s capitol city of Antananarivo. To establish the mass of the soil samples divided by the sample volume (i.e., bulk density: g/cm3), the LRI first placed wet soil samples in a ventilated oven at 105 °C for 24 h. The weight of dried samples and empty soil containers were then recorded and each oven-dried sample’s mass divided by the sample’s volume. To determine soil organic carbon (SOC) content, a modified Walkley–Black method was employed, which involved oxidizing soil organic matter without external heat using an H2SO4 solution and potassium dichromate (K2Cr2O7). Further details on this modified Walkley–Black approach are available in Schumacher [114], Mikhailova et al. [115], De Vos et al. [116], Meersmans et al. [117] and Simpson [118].
Table 2. Allometric equations employed for calculating above-ground biomass (B). dbh refers to diameter at breast height; D represents diameter; H stands for height; p = wood density.
Table 2. Allometric equations employed for calculating above-ground biomass (B). dbh refers to diameter at breast height; D represents diameter; H stands for height; p = wood density.
SpeciesAllometric equationWood density [119]References
Avicennia marinaB = 0.1848 × dbh2.35240.661[120]
Bruguiera gymnorrhiza (leaves)B = 0.0679 × dbh1.49140.741[121]
Bruguiera gymnorrhiza (stem)B = 0.464 × (dbh2 × H)0.94275 × p0.741[22]
Ceriops tagal (dbh 2–18 cm)B = 10−0.7247 × dbh2.33790.803[121]
Ceriops tagal (dbh 18–25 cm)B = 10−0.494 × dbh2.0560.803[122]
Heritiera littoralis (leaves)B = 0.0679 × dbh1.49141.074[121]
Heritiera littoralis (stem)B = 0.464 × (dbh2 × H)0.94275 × p1.074[22]
Lumnitzera racemosaB = 0.0214 × (dbh2 × H)1.05655 × p0.565[22]
Rhizophora mucronata (leaves)B = 0.0139 × D2.10720.867[121]
Rhizophora mucronata (root)B = 0.0068 × dbh3.13530.867[121]
Rhizophora mucronata (stem)B = 0.0311 × (dbh2 × H)1.00741 × p0.867[22]
Sonneratia albaB = 0.0825 × (dbh2 × H)0.89966 × p0.78[22]
Xylocarpus granatumB = 0.0830 × (dbh2 × H)0.89806 × p0.7[22]

3. Results and Discussion

3.1. Overview of Existing Mangrove Maps

Comparisons confirmed that the USGS-produced maps [86] offered the most representative historical and contemporary areal estimates of Ambanja and Ambaro bays’ mangroves. Owing to the use of moderate spatial resolution Landsat data, the USGS maps provided greater detail than those derived from coarse resolution SPOT data by Mayaux et al. [89]. Other national-level assessments involved Landsat data, but their scope included numerous terrestrial forest classes (i.e., [90,91]), resulting in less representative mangrove classes. The USGS products were the only maps to focus solely on mangrove coverage and to provide relatively contemporary (i.e., 2010) coverage; all others represented multiple forest classes for time periods nearly or more than 10 years earlier. For further details associated with comparisons between Madagascar’s existing mangrove datasets, see Giri and Muhlhausen (2008) [80]. Using USGS-produced 1990, 2000 and 2010 maps as input, the analysis of historic dynamics indicated that from 1990–2000, Ambanja and Ambaro bays’ mangroves decreased by 2473 ha (7.7%) and gained 466 ha (1.4%). From 2000–2010, there were 5672 ha of loss (18.7%) and 1104 ha of gain (3.3%). Taken collectively, from 1990–2010, mangroves experienced a loss of 7659 ha (23.7%), a gain of 995 ha (3.1%) and persistence over 24,669 ha (76.3%) (Figure 2).
Figure 2. Mangrove dynamics from 1990–2000 and 2000–2010. Persistence, loss and gain were calculated using national-level mangrove maps produced by the United States Geological Survey (USGS).
Figure 2. Mangrove dynamics from 1990–2000 and 2000–2010. Persistence, loss and gain were calculated using national-level mangrove maps produced by the United States Geological Survey (USGS).
Forests 05 00177 g002

3.2. Spectral Separability and Classification Results

Results indicate that at certain wavelengths, all mapped classes were spectrally distinguishable (Figure 3). The near-infrared (NIR) and short-wave infrared (SWIR) were particularly useful for representing mangrove classes. Established properties of vegetation in the NIR and SWIR help to provide an ecologically meaningful context for the observed separability. In band 4 (i.e., NIR: 0.76–0.90 micrometers (µm)), spectral contrast was likely driven by the transitional red-edge, internal vegetation structure and leaf dry-matter content [11,77,122,123]. Increased reflectance in the NIR due to a higher concentration of vegetation was particularly evident for closed-canopy mangroves. For bands 5 (i.e., SWIR: 1.55–1.75 µm) and 7 (SWIR: 2.08–2.35 µm), spectral differences were likely explained by vegetation and soil moisture content and, to a lesser degree, various other canopy-level biogeochemical constituents [124]. Differences in moisture content, especially in band 7, were able to discern between all mangrove types. In addition to distinguishing amongst mangrove classes, our findings support previous work demonstrating that measurements at SWIR wavelengths can further differentiate mangroves from terrestrial vegetation [125]. In contrast to Kuenzer et al. [11], there were additional differences between all mangrove types in visible band 3 (i.e., red: 0.63–0.69 µm). Open-canopy II mangroves could also be distinguished from other mangrove types using visible bands 1 (i.e., blue: 0.45–0.52 µm) and 2 (i.e., green: 0.53–0.61 µm); however, confusion with exposed soil and mud was high at these wavelengths. Subtle differences in moisture content in the SWIR provided the increased separability required to distinguish open-canopy II and bare soil classes.
Figure 3. The mean spectral value (±1 standard deviation) of mapped classes.
Figure 3. The mean spectral value (±1 standard deviation) of mapped classes.
Forests 05 00177 g003
ML classification results indicate 14,015 ha of closed-canopy, 26,192 ha of open-canopy I and 5473 ha of open-canopy II mangroves, totaling 45,680 ha of mangroves in the AOI (Figure 4). Results further indicate nearly 1000 ha of deforested mangroves found disproportionately near and on the peninsula separating Ambanja and Ambaro bays. Overall map accuracy was 93.4% (Kappa 0.9), with all mangrove classes mapped with producer’s and user’s accuracies ≥85% (Table 3). Mangrove class error was driven by a few incidents of confusion between closed-canopy and open-canopy I. Inter-mangrove class confusion can be explained by the similarities in spectral properties exhibited by extremely dense young and closed-canopy stands and naturally open and/or highly degraded tall and open-canopy I stands. While confusion with other vegetation classes (e.g., terrestrial forest) has been reported as a common source of classification error [68], our results indicate this was, in large part, avoided.
Figure 4. Results from the maximum likelihood classification of Landsat GLS 2010 data.
Figure 4. Results from the maximum likelihood classification of Landsat GLS 2010 data.
Forests 05 00177 g004
Table 3. Confusion matrix for maximum likelihood classification of GLS 2010 Landsat data.
Table 3. Confusion matrix for maximum likelihood classification of GLS 2010 Landsat data.
1234567891011TotalUser’s (%)Commission (%)
Savannah (1)54300000001058937
Woodland (2)039000000000391000
Active crops (3)005100000000511000
Closed-canopy terrestrial forest (4)000540000000541000
Open-canopy terrestrial forest (5)04005400000058937
Closed-canopy mangrove (6)000007990000889010
Open-canopy mangrove I (7)0000011720200858515
Open-canopy mangrove II (8)000000052000521000
Deforested mangrove (9)000000006000601000
Exposed soil (10)083000021530677921
Exposed mud (11)000000000054541000
Producer’s (%)10072941001008889969598100Overall93.4
Omission (%)02860012114520Kappa0.9
A comparison with the 24,669 ha of mangrove coverage provided by the 2010 USGS classification highlights the shortcomings of localized applications for this national-level dataset (Figure 5). While USGS distribution maps provide unprecedented detail and accuracy, they are limited to one mangrove class and provide no information on surrounding land-cover categories. In addition, while comprehensively representing taller, intact, mature stands, the USGS map depicts 21,011 ha less mangroves than our results, underrepresenting the naturally lower stature and more open stands and highly degraded areas and completely omitting most scrub ecosystems. This underrepresentation can lead to exaggerated loss estimates, as field observations confirm that many of the deforested areas identified through analyzing the time series of USGS mangrove maps are occupied by naturally lower stature and more open areas and highly degraded stands.

3.3. Carbon Plot Locations and Ecological Characteristics of Mapped Mangrove Classes

Figure 6 shows the location of C plots established within mangrove strata. Plot-level measurements enabled the summarization of the forest characteristics associated with each mapped mangrove class, including sub-class type ecological summaries (Table 4). Open-canopy II plots were comprised of sparse and stunted low stature Avicennia marina with extremely open (i.e., <30%) canopies. Open-canopy I plots were primarily represented by moderately-dense stands of medium stature Ceriops tagal and Rhizophora mucronata with relatively open canopies. Closed-canopy plots were typified by high stature stands dominated by Rhizophora mucronata and exhibiting variable density, but well-formed canopies. Exceptions to the typical forest characteristics of mapped classes include stands dominated by naturally very open and/or highly degraded high stature trees, which were sometimes mapped as open-canopy I. In addition, extremely dense moderate stature stands sometimes appear as closed-canopy in the imagery.
At the scale of analysis (i.e., ha-level), there is negligible difference in the spectral appearance of areas of relatively open-canopy medium stature trees and those comprised of tall trees that were naturally open or had been heavily harvested and/or naturally degraded. While mangrove conversion (i.e., deforestation) is reliable for mapping using established methods and readily available Landsat data, accurately detecting and tracking subtler modification (i.e., degradation) remains a vexing challenge. Whether naturally-induced (e.g., cyclone damage) or resulting from anthropogenic exploitation, sub-pixel change in forest appearance is difficult to accurately measure using moderate spatial resolution remotely sensed data (e.g., Landsat). This challenge highlights the need to research applying methods developed for mapping selective logging in terrestrial forests [126] to assessing mangrove degradation. In addition, the synergistic combination of Landsat imagery with complimentary remotely sensed datasets, including finer spatial resolution optical imagery and the structural information offered by light detection and ranging (LiDAR), needs to be explored further, bearing in mind that such datasets can be prohibitively expensive and rarely available in wall-to-wall coverage for dates and locations of interest [11]. While further work is needed to allow for partitioning existing classes based on their level of degradation, confidently differentiating between natural and anthropogenic degradation will remain problematic, even if separable from naturally intact stands. Bearing in mind the mangrove class and methodological limitations, observations in forest plots confirmed that our broad canopy-cover classes are ecologically rational and associable with statistically distinct C stocks. While the remote sensing of canopy closure is a major topic of research for terrestrial forests and previous studies have shown that extremely closed-canopies are indicative of forest stands comprised of higher stature trees (e.g., [127]), our results contribute to what Heumann [68] summarizes as a comparative dearth of mangrove canopy-closure studies.
Figure 5. Comparison between GLS 2010 Landsat classification results (top left) and single-class USGS 2010 mangrove coverage (top right) for a sub-set of the area of interest (AOI). A Landsat Enhanced Thematic Mapper (ETM+) color composite, where band 3 is blue, band 5 is green and band 4 is red, is shown for context (bottom left).
Figure 5. Comparison between GLS 2010 Landsat classification results (top left) and single-class USGS 2010 mangrove coverage (top right) for a sub-set of the area of interest (AOI). A Landsat Enhanced Thematic Mapper (ETM+) color composite, where band 3 is blue, band 5 is green and band 4 is red, is shown for context (bottom left).
Forests 05 00177 g005
Figure 6. The location of C plots within classified mangrove strata.
Figure 6. The location of C plots within classified mangrove strata.
Forests 05 00177 g006

3.4. Carbon Stocks of Mapped Mangrove Classes

Plot-level biomass estimates were converted to C stocks and scaled to the hectare-level (Figure 7, Table 5 and Table 6). Closed-canopy mangrove trees had by far the highest vegetation and total biomass values. On average, closed-canopy vegetation (i.e., live and dead, above- (i.e., tree) and below-ground (i.e., roots)) had an estimated C value of 146.8 Mg/ha (±10.2 (i.e., 1 standard error)) (n = 25). The average SOC value for closed-canopy mangroves was 446.2 (±36.9) (n = 22). Open-canopy mangrove I had average C values of 42.9 Mg/ha (±5.9) (vegetation: n = 28) and 324.4 Mg/ha (±36.5) (SOC: n = 24). Open-canopy II values were lower than other classes for vegetation (i.e., 20.9 Mg/ha (±4.6)) (n = 4), but SOC values were the highest of any type (i.e., 517.1 (±76)) (n = 4). The high open-canopy II SOC values are most likely attributable to the smaller sample size (i.e., n = 4) and additional plots are required in this mangrove strata to more robustly estimate C.
Table 4. Class sub-type, species (spp) dominance, average height in meters (m) (±1 standard deviation (SD)), average trees per hectare (ha) (±1 SD) and average diameter (d) in centimetres (cm) (±1 SD). Trees/ha (i.e., density) calculated for intact plots. N represents plots per class sub-type.
Table 4. Class sub-type, species (spp) dominance, average height in meters (m) (±1 standard deviation (SD)), average trees per hectare (ha) (±1 SD) and average diameter (d) in centimetres (cm) (±1 SD). Trees/ha (i.e., density) calculated for intact plots. N represents plots per class sub-type.
ClassSub-typeSpp dominanceHeight (m) (±1 SD)Trees/ha (±1 SD)d (cm) (±1 SD)
Closed-canopy (n = 24)intact, tall, mature standsAvicennia marina8.6 (n = 1)1250 (n = 1)14.9 (n = 1)
intact, tall, mature standsCeriops tagal7.3 (±1.2) (n = 3)2625 (±318) (n = 2)10.1 (±0.5) (n = 3)
intact, tall, mature standsRhizophora mucronata7 (±1.3) (n = 14)4719 (±1133) (n = 12)10.1 (±3) (n = 14)
intact, tall, mature standsSonneratia alba5.6 (n = 1)5300 (n = 1)10.6 (n = 1)
very dense medium-tall standsRhizophora mucronata4.8 (±0.1) (n = 2)5600 (±1838) (n = 2)7.8 (±1.1) (n = 2)
intact, tall, mature standsmixed6.7 (±1.6) (n = 2)1825 (±248) (n = 2)11.3 (±2.5) (n = 2)
Open-canopy I (n = 28)medium standsCeriops tagal4.6 (±0.8) (n = 7)3300 (±849) (n = 2)7.5 (±1.6) (n = 7)
medium standsRhizophora mucronata4.2 (±0.6) (n = 6)2160 (±498) (n = 5)7.3 (±1.3) (n = 6)
naturally open/very degraded tallvariable5.7 (±0.3) (n = 4)1525 (±35) (n = 2)10.1 (±1.2) (n = 4)
very dense short standsCeriops tagal2.5 (±0.3) (n = 9)2780 (±750) (n = 5)5.1 (±0.9) (n = 9)
medium standsmixed4.8 (±0.1) (n = 2)1800 (±141) (n = 2)9.5 (±2) (n = 2)
Open-canopy II (n = 4)stunted, scrub ecosystemsAvicennia marina1.7 (±0.5) (n = 4)1306 (±554) (n = 4)4.6 (±0.2) (n = 4)
Figure 7. Estimated average (±1 standard error) above- and below-ground carbon stocks (ton/hectare (ha)) for mapped mangrove classes in Ambanja and Ambaro bays. Below-ground soil strata depths are in centimeters (cm).
Figure 7. Estimated average (±1 standard error) above- and below-ground carbon stocks (ton/hectare (ha)) for mapped mangrove classes in Ambanja and Ambaro bays. Below-ground soil strata depths are in centimeters (cm).
Forests 05 00177 g007
Table 5. Average hectare (ha)-level carbon (Mg/ha) estimates (±1 standard error) for mangrove vegetation (dead and live, above and roots), soil organic carbon (SOC) and total carbon. Estimates are partitioned by strata. N represents the number of plots per class type, with two n values corresponding to trees and soil, respectively.
Table 5. Average hectare (ha)-level carbon (Mg/ha) estimates (±1 standard error) for mangrove vegetation (dead and live, above and roots), soil organic carbon (SOC) and total carbon. Estimates are partitioned by strata. N represents the number of plots per class type, with two n values corresponding to trees and soil, respectively.
ClassVegetation carbonSoil organic carbonTotal carbon
Closed-canopy (n = 23; 22)146.8(10.2)446.2 (36.9)593 (39)
Open-canopy I (n = 28; 24)42.9 (5.8)324.3 (36.5)367.2 (37.3)
Open-canopy II (n = 4; 4)20.8 (4.6)517.1 (76)537.9 (75.2)
Table 6. Average hectare (ha)-level carbon (%), bulk density (g/cm3) and carbon mass (Mg/ha) estimates ±1 standard error (in brackets). Estimates are partitioned by mapped mangrove class and soil depth strata. N corresponds with the number of plots per class type.
Table 6. Average hectare (ha)-level carbon (%), bulk density (g/cm3) and carbon mass (Mg/ha) estimates ±1 standard error (in brackets). Estimates are partitioned by mapped mangrove class and soil depth strata. N corresponds with the number of plots per class type.
ClassSample depth (cm)Carbon (%)Bulk density (g/cm3)Carbon mass (Mg/ha)
Closed-canopy (n = 22)0–154.8(0.9)0.77(0.08)41.1(3.5)
Open-canopy I (n = 24)0–153.4(2.9)0.78(0.08)32.5(3.8)
Open-canopy II (n = 4)0–150.6(0.1)1.39(0.04)12.1(0.7)
A comparison of our results with existing published C stocks for mangroves indicates that our values are comparatively low. For example, mangroves sampled throughout the Indo-Pacific averaged 1023 Mg/ha, 49%–98% of which were directly associated with organic-rich soils [15]. In western Micronesia, specifically Yap state and the Republic of Palau, mangrove C storage ranged from 479 (seaward) to 1385 (landward) Mg/ha, with 70% of storage in soils [27]. While the C stocks reported here are not nearly as high as those reported in the Indo-Pacific and western Micronesia, Madagascar’s mangroves are typically of a lower stature, and our soil samples were only collected to 1.5 m. In addition, our soil samples were analyzed using the Walkley–Black method, which is known to under-represent SOC [114,115,116,117,118]. However, as there are few professional laboratories in Madagascar that analyze soil, and all employ only this approach, we chose the LRI, given the expense of sending samples abroad to be analyzed and the critical need to build local scientific capacity. Future research requires setting up the equipment required to conduct more accurate soil analysis in Madagascar. Acknowledging the shortcomings of the Walkley–Black, the results provide preliminary conservative SOC estimates, which, compared to other terrestrial forest types (e.g., boreal, temperate, tropical upland), still support a growing body of evidence that mangroves are amongst the most carbon-dense forests in the tropics, with similar above- and larger below-ground stocks than terrestrial systems [15,27,28,29,30,32,33,34,38] (Figure 8). For above-ground carbon, our results further support that closed-canopies are indicative of higher stature trees, which typically sequester significantly larger amounts of C than more open stands [127].
Figure 8. Estimated carbon stocks for Madagascar (±1 standard error) compared with published carbon stocks for different forest types. Carbon stocks for non-mangrove forest types are taken from [15]. Soil organic carbon comparisons are made to a depth of 1 m.
Figure 8. Estimated carbon stocks for Madagascar (±1 standard error) compared with published carbon stocks for different forest types. Carbon stocks for non-mangrove forest types are taken from [15]. Soil organic carbon comparisons are made to a depth of 1 m.
Forests 05 00177 g008

4. Conclusions

Owing to a complex and ever-dynamic scene composition, mangrove mapping is one of the most demanding tasks in remote sensing [11]. While our mapping results are not without their acknowledged shortcomings, they allow for ecologically meaningful stratification associable with distinct C stocks. Our simple, yet effective and replicable classification of moderate spatial resolution remotely sensed data provides improved detail and accuracy over existing mangrove coverage and unprecedented information for surrounding land-cover categories. Our initial C stock estimates are also not without their limitations, most notably the Walkley–Black-based estimation of SOC; however, they are conservative and can be improved over time. To improve these initial SOC estimates, existing samples should be reanalyzed once the equipment necessary to facilitate more robust analysis becomes available in-country. In addition, more plots should be established within the open-canopy II strata. Current above- and below-ground tree-related C estimates could also be improved through destructive sampling and developing Madagascar-specific allometric equations.
Although preliminary, our results support ongoing initiatives investigating the feasibility of and working towards implementing mangrove carbon financing projects (e.g., Reducing Emissions from Deforestation and forest Degradation (REDD)+) and other payments for ecosystem services (PES). In particular, the generation of carbon credits through the conservation, restoration and lower-impact use of mangroves could make vital contributions to alleviating poverty and safeguarding biodiversity in coastal Madagascar. Throughout the tropics, hundreds of REDD+ and PES projects have been initiated, yet in few countries are there projects focusing specifically on mangroves (see [128]).
Our mapping results, supported by extensive field observations, confirm that as of 2010, anthropogenic activities, fueled by a diverse and complex range of drivers, including a lack of governance and increasing population, had driven substantial deforestation (i.e., 970 ha) in Madagascar’s second largest mangrove ecosystem. Ongoing research supports this trend nation-wide, and while natural processes, such as forest succession, linked with sedimentological processes and cyclone impacts, are important causes of change, Madagascar’s mangroves are facing increasing anthropogenic impact. While in certain places, such as the AOI of this study, wide-spread deforestation is apparent, the likelihood and long-term outcome of natural or assisted regeneration remains uncertain. However, continued degradation and deforestation could compromise, if not discontinue, many of the ecosystem services offered by intact mangrove ecosystems. The continued modification and conversion of mangrove habitat, if left to proceed unimpeded, could also continue to influence global climate through increased greenhouse gas emissions and increase the risk for ripple effects that can negatively influence surrounding and closely linked marine and terrestrial ecosystems. The first step towards mitigation is quantifying the extent of and contextualizing the reasons for and consequences of loss. Here, we have advanced this agenda for Madagascar by presenting the first localized land-cover map for Ambanja and Ambaro bays and the country’s first above- and below-ground C stocks.


This research was funded by grants from the Western Indian Ocean Marine Science Association and the John D. and Catherine T. MacArthur Foundation. Thanks to Joseph Langat (Kenya Marine and Fisheries Research Institute) for assistance with adapting field techniques and undertaking carbon stock measurements. Additional thanks to Zo Andriamahenina and Rado Rakotomanana (Blue Ventures), Pierre-Francois Roy (Institut Catholique des Arts et Métiers), and Holy Andriamitantsoa and Tina Haingonirina (Institut Halieutique et des Sciences Marines) for assistance with data collection. Extensive gratitude is owed to numerous local guides and field assistants from the coastal Malagasy communities of Port St Louis, Ampampamena, Antetezambato and Ambolikapiki. Thanks also to Aude Carro and Kate England (Blue Ventures) for socio-economic context and to Leah Glass and Samir Gandhi (Blue Ventures) and Mitchell Vartanian and Anna Yuill (UBC) for assistance with manuscript preparation. Additional thanks to J. Boone Kauffman (Oregon State University) for technical advice, particularly assistance with selecting allometric equations, and to two extremely helpful anonymous reviewers.

Conflicts of Interest

The authors declare no conflict of interest.


  1. Lugo, A.E.; Snedaker, S.C. The ecology of mangroves. Annu. Rev. Ecol. Syst. 1974, 5, 39–64. [Google Scholar]
  2. Blasco, F.; Bellan, M.F.; Chaudhury, M.U. Estimating the extent of floods in bangladesh—Using SPOT data. Remote Sens. Environ. 1992, 39, 167–178. [Google Scholar] [CrossRef]
  3. Marshall, N. Mangrove conservation in relation to overall environmental considerations. Hydrobiologia 1994, 285, 303–309. [Google Scholar] [CrossRef]
  4. Alongi, D.M. Present state and future of world’s mangrove forest. Environ. Conserv. 2002, 29, 331–349. [Google Scholar] [CrossRef]
  5. Dahdouh-Guebas, F.; Jayatissa, L.P.; di Nitto, D.; Bosire, J.O.; Lo Seen, D.; Koedam, N. How effective were mangroves as a defence against the recent tsunami? Curr. Biol. 2005, 15, R443–R447. [Google Scholar] [CrossRef]
  6. Barbier, E.B. Natural barriers to natural disasters: Replanting mangroves after tsunami. Front. Ecol. Environ. 2006, 4, 124–131. [Google Scholar] [CrossRef]
  7. Food and Agricultural Organization (FAO). The World’s Mangroves 1980–2005; FAO Forestry Paper 153; FAO: Rome, Italy, 2007. [Google Scholar]
  8. Alongi, D.M. Mangrove forests: Resilience, protection from tsunamis, and responses to global climate chang. Estuar. Coast. Shelf Sci. 2008, 76, 1–13. [Google Scholar] [CrossRef]
  9. Nagelkerken, I.; Blaber, S.J.; Bouillon, S.; Green, P.; Haywood, M.; Kirton, L.G.; Meynecke, J.-O.; Pawlik, J.; Penrose, H.M.; Sasekumar, A.; et al. The habit function of mangroves for terrestrial and marine fauna: A review. Aquat. Bot. 2008, 89, 155–185. [Google Scholar] [CrossRef]
  10. Alongi, D.M. Carbon payments for mangrove conservation: Ecosystem constraints and uncertainties of sequestration potential. Environ. Sci. Policy 2011, 14, 462–470. [Google Scholar] [CrossRef]
  11. Kuezner, C.; Bluemel, A.; Gebhardt, S.; Quoc, T.V.; Dech, S. Remote sensing of mangrove ecosystems: A review. Remote Sens. 2011, 3, 878–928. [Google Scholar] [CrossRef]
  12. Primavera, J.H. Socio-economic impacts of shrimp culture. Aquac. Res. 1997, 28, 815–827. [Google Scholar] [CrossRef]
  13. Kathiresan, K.; Bingham, B. Biology of mangroves and mangrove ecosystems. Adv. Mar. Biol. 2001, 40, 81–251. [Google Scholar]
  14. Mumby, P.J.; Edwards, A.J.; Arias-Gonzáles, E.; Lindeman, K.C.; Blackwell, P.G.; Gall, A.; Gorczynska, M.I.; Harborne, A.R.; Pescod, C.L.; Renken, H.; et al. Mangrove enhance the biomass of coral reef fish communities in the Caribbean. Nature 2004, 427, 533–536. [Google Scholar] [CrossRef]
  15. Donato, D.C.; Kauffman, J.B.; Murdiyarso, D.; Kumianto, S.; Stidham, M.; Kanninen, M. Mangroves among the most carbon-rich forests in the tropics. Nat. Geosci. 2011, 4, 293–297. [Google Scholar] [CrossRef]
  16. Pendleton, L.; Donato, D.C.; Murray, B.C.; Crooks, S.; Jenkins, W.A.; Sifleet, S.; Craft, C.; Fourqurean, J.W.; Kauffman, J.B.; Marba, N.; et al. Estimating global “blue carbon” emissions from conversion and degradation of vegetated coastal ecosystems. PLoS One 2012, 7, e43542. [Google Scholar] [CrossRef] [Green Version]
  17. Twilley, R.R.; Chen, R.H.; Hargis, T. Carbon sinks in mangroves and their implications to carbon budget of tropical coastal ecosystems. Water Air Soil Pollut. 1992, 64, 265–288. [Google Scholar] [CrossRef]
  18. Kirui, K.B.; Karachi, M.; Kairo, J.G. Allometric equations for estimating aboveground biomass of Rhizophora mucronata at Gazi bay Kenya. West. Indian. Ocean J. Mar. Sci. 2006, 5, 27–34. [Google Scholar]
  19. Komiyama, A.; Ong, J.E.; Poungparn, S. Allometry, biomass, and productivity of mangrove forests: A review. Aquat. Bot. 2008, 89, 128–137. [Google Scholar] [CrossRef]
  20. Alongi, D.M. The Energetics of Mangrove Forests; Springer Science and Business Media BV: New York, NY, USA, 2009. [Google Scholar]
  21. Kairo, J.G.; Bosire, J.; Langat, J.; Kirui, B.; Koedam, N. Allometry and biomass distribution in replanted mangrove plantations at Gazi Bay, Kenya. Aquat. Conserv. 2009, 19, S63–S69. [Google Scholar] [CrossRef]
  22. Kauffman, J.B.; Cole, T.G. Micronesian mangrove forest structure and tree responses to a severe typhoon. Wetlands 2010, 30, 1077–1084. [Google Scholar] [CrossRef]
  23. Camacho, L.D.; Gevana, D.T.; Carandang, A.P.; Sofronio, C.C.; Combalicer, E.A.; Rebugio, L.L.; Youn, Y.-C. Tree biomass and carbon stock of a community-managed mangrove forest in Bohol, Phillipines. For. Sci. Technol. 2011, 7, 161–167. [Google Scholar]
  24. Mitra, A.; Sengupta, K.; Banerjee, K. Standing biomass and carbon storage of above-ground structures in dominant mangrove trees in the Sundarbans. For. Ecol. Manag. 2011, 261, 1325–1335. [Google Scholar] [CrossRef]
  25. Abino, A.C.; Castillo, J.A.A.; Lee, Y.J. Assessment of species diversity, biomass and carbon sequestration potential of a natural mangrove stand in Samar, the Philippines. For. Sci. Technol. 2013. [Google Scholar] [CrossRef]
  26. Hutchison, J.; Manica, A.; Swetnam, R.; Balmford, A.; Spalding, M. Predicting global patterns in mangrove forest biomass. Conserv. Lett. 2013. [Google Scholar] [CrossRef]
  27. Kauffman, J.B.; Heider, C.; Cole, T.G.; Dwire, K.A.; Donato, D.C. Ecosystem carbon stocks of Micronesian mangrove forests. Wetlands 2011, 31, 343–352. [Google Scholar] [CrossRef]
  28. Ray, R.; Ganguly, D.; Chowdhury, C.; Dey, M.; Das, S.; Dutta, M.K.; Mandal, S.K.; Majumder, N.; De, T.K.; Mukhopadhyay, S.K.; et al. Carbon sequestration and annual increase of carbon stock in a mangrove forest. Atmos. Environ. 2011, 45, 5016–5024. [Google Scholar] [CrossRef]
  29. Chen, L.; Zeng, X.; Tam, N.F.Y.; Lu, W.; Luo, Z.; Du, X.; Wang, J. Comparing carbon sequestration and stand structure of monoculture and mixed mangrove plantations of Sonneratia caseolaris and S. apetala in Southern China. For. Ecol. Manag. 2012, 284, 222–229. [Google Scholar] [CrossRef]
  30. Donato, D.C.; Kauffman, J.B.; Mackenzie, R.A.; Ainsworth, A.; Pfleeger, A.Z. Whole-island carbon stocks in the tropical Pacific: Implications for mangrove conservation and upland restoration. J. Environ. Manag. 2012, 97, 89–96. [Google Scholar] [CrossRef]
  31. Matsui, N.; Morimune, K.; Meepol, W.; Chukwamdee, J. Ten year evaluation of carbon stock in mangrove plantation reforested from an abandoned shrimp pond. Forests 2012, 3, 431–444. [Google Scholar] [CrossRef]
  32. Adame, M.F.; Kauffman, J.B.; Medina, I.; Gamboa, J.N.; Torres, O.; Caamal, J.P.; Reza, M.; Herrera-Silveira, J.A. Carbon stocks of tropical coastal wetlands within the Karstic landscape of the Mexican Caribbean. PLoS One 2013, 8, e56569. [Google Scholar] [CrossRef]
  33. Wang, G.; Dongsheng, G.; Peart, M.R.; Chen, Y.; Peng, Y. Ecosystem carbon stocks of mangrove forest in Yingluo Bay, Guangdon Province of South China. For. Ecol. Manag. 2013, 310, 539–546. [Google Scholar] [CrossRef]
  34. Kauffman, J.B.; Heider, C.; Norfolk, J.; Payton, F. Carbon stocks of intact mangroves and carbon emissions arising from their conversion in the Dominican Republic. Ecol. Appl. in press. [CrossRef]
  35. Golley, F.; Odum, H.T.; Wilson, R.F. The structure and metabolism of a Puerto Rican red mangrove forest in May. Ecology 1962, 43, 9–19. [Google Scholar] [CrossRef]
  36. Eong, O.J. Mangroves—A carbon source and sink. Chemosphere 1993, 27, 1097–1107. [Google Scholar] [CrossRef]
  37. Matsui, N. Estimated stocks of organic carbon in mangrove roots and sediments in Hinchinbrook Channel, Australia. Mangroves Salt Marshes 1998, 2, 199–204. [Google Scholar] [CrossRef]
  38. Fujimoto, K.; Imaya, A.; Tabuchi, R.; Kuramoto, S.; Utsugi, H.; Murofushi, T. Belowground C storage of Micronesian mangrove forests. Ecol. Res. 1999, 14, 409–413. [Google Scholar] [CrossRef]
  39. Kauffman, J.B.; Donato, D.C. Protocols for the Measurement, Monitoring and Reporting of Structure, Biomass and Carbon Stocks in Mangrove Forests. Working Paper 86; CIFOR: Bogor, Indonesia, 2012. [Google Scholar]
  40. Giri, C.; Ochieng, E.; Tieszen, L.L.; Zhu, Z.; Singh, A.; Loveland, T.; Masek, J.; Duke, N. Status and distribution of mangrove forests of the world using earth observation satellite data. Glob. Ecol. Biogeogr. 2011, 20, 154–159. [Google Scholar] [CrossRef]
  41. Polidoro, B.A.; Carpenter, K.E.; Collins, L.; Duke, N.C.; Ellison, A.M.; Ellison, J.C.; Farnsworth, E.J.; Fernando, E.S.; Kathiresan, K.; Koedam, N.E.; et al. Mangrove extinction risk and geographic areas of global concern. PLoS One 2010, 5, e10095. [Google Scholar] [CrossRef]
  42. Valiela, I.; Bowen, J.L.; York, J.K. Mangrove forests: One of the world’s threatened major tropical environments. Bioscience. 2001, 51, 807–815. [Google Scholar] [CrossRef]
  43. Wilkie, M.L.; Foruna, S. Status and Trends in Mangrove Area Extent Worldwide; Forest Resources Assessment Working Paper 63; Food and Agriculture Organization of the United Nations: Roma, Italy, 2003. [Google Scholar]
  44. Giesen, W.; Wulffraat, S.; Zieren, M.; Scholten, L. Mangrove Guidebook for Southeast Asia; Food and Agricultural Organisation and Wetlands International: Bangkok, Thailand, 2007. [Google Scholar]
  45. Duke, N.C.; Meynecke, J.O.; Dittmann, S.; Ellison, A.M.; Anger, K.; Berger, U.; Cannicci, S.; Diele, K.; Ewel, K.C.; Field, C.D.; et al. A world without mangroves? Science 2007, 317, 41–42. [Google Scholar]
  46. Spalding, M.; Kainuma, M.; Collins, L. World Atlas of Mangroves; Earthscan: London, UK, 2010. [Google Scholar]
  47. Farnsworth, E.J.; Ellison, A.M. The global conservation status of mangroves. AMBIO 1997, 26, 328–334. [Google Scholar]
  48. Primavera, J.H. Development and conservation of Philippine mangroves: Institutional issues. Ecol. Econ. 2000, 35, 91–106. [Google Scholar] [CrossRef]
  49. Dahdouh-Guebas, F. The use of remote sensing and GIS in the sustainable management of tropical coastal ecosystems. Environ. Dev. Sustain. 2002, 4, 93–112. [Google Scholar] [CrossRef]
  50. Primavera, J.H. Mangroves, fishponds, and the quest for sustainability. Science 2005, 310, 57–59. [Google Scholar] [CrossRef]
  51. Gopal, B.; Chauhan, M. Biodiversity and its conservation in the Sundarban Mangrove Ecosystem. Aquat. Sci. 2006, 68, 338–354. [Google Scholar] [CrossRef]
  52. Primavera, J.H. Overcoming the impacts of aquaculture on the coastal zone. Ocean Coast. Manag. 2006, 49, 531–545. [Google Scholar] [CrossRef]
  53. Gilman, E.L.; Ellison, J.; Duke, N.C.; Field, C. Threats to mangroves from climate change and adaptation options: A review. Aquat. Bot. 2008, 89, 237–250. [Google Scholar] [CrossRef]
  54. Walters, B.B.; Rönnbäck, P.; Kovacs, J.M.; Crona, B.; Hussain, S.A.; Badola, R.; Primavera, J.H.; Barbier, E.; Dahdouh-Guebas, F. Ethnobiology, socio-economics and management of mangrove forests: A review. Aquat. Bot. 2008, 89, 220–236. [Google Scholar] [CrossRef]
  55. Field, C.D. Impact of expected climate change on mangroves. Hydrobiologia 1995, 295, 75–81. [Google Scholar] [CrossRef]
  56. Krauss, K.W.; Lovelock, C.E.; McKee, K.L.; Lopez-Hoffman, L.; Ewe, S.M.L.; Sousa, W.P. Environmental drivers in mangrove establishment and early development: A review. Aquat. Bot. 2008, 89, 105–127. [Google Scholar] [CrossRef]
  57. Chan, H.T.; Baba, S. Manual on Guidelines for Rehabilitation of Coastal Forests Damaged by Natural Hazards in the Asia-Pacific Region; International Society for Mangrove Ecosystems (ISME) and International Tropical Timber Organization (ITTO): Okinawa, Japan, 2009; p. 66. [Google Scholar]
  58. Suzuki, T.; Zijlema, M.; Burger, B.; Meijer, M.C.; Narayan, S. Wave dissipation by vegetation with layer schematization in SWAN. Coast. Eng. 2012, 59, 64–71. [Google Scholar] [CrossRef]
  59. De la Cruz, A.A. Tropical wetlands as a carbon source. Aquat. Bot. 1986, 25, 109–115. [Google Scholar] [CrossRef]
  60. Hooijer, A.; Silvius, M.; Wösten, H.; Page, S. PEAT-CO2: Assessment of CO2 Emissions from Drained Peatlands in SE Asia, Delft Hydraulics, Report Q3943, 1st ed.; Wetlands International, Delft Hydraulics: Delft, The Netherlands, 2006. [Google Scholar]
  61. Grimsditch, G.; Alder, J.; Nakamura, T.; Kenchington, R.; Tamelander, J. The blue carbon special edition—Introduction and overview. Ocean Coast. Manag. 2013, 83, 1–4. [Google Scholar] [CrossRef]
  62. United Nations Environmental Program. Global Environment Outlook Yearbook 2004; United Nations Environment Programme: Nairobi, Kenya, 2004. [Google Scholar]
  63. Laffoley, D.; Grimsditch, G. The Management of Natural COASTAL Carbon Sinks; International Union for Conservation of Nature (IUCN): Gland, Switzerland, 2009; p. 53. [Google Scholar]
  64. Nellemann, C.; Corcoran, E.; Duarte, C.M.; Valdés, L.; de Young, C.; Fonseca, L.; Grimsditch, G. Blue Carbon: The Role of Healthy Oceans in Binding Carbon—A Rapid Response Assessment. United Nations Environment Programme, GRID-Arendal. 2009. Available online: (accessed on 1 December 2012).
  65. Gordon, D.; Murray, B.C.; Pendleton, L.; Victor, B. Financing Options for Blue Carbon: Opportunities and Lessons from the REDD+ Experience; Nicholas Institute Report; Nicholas Institute: Durham, NC, USA, 2011. [Google Scholar]
  66. Ullman, R.; Bilbao-Bastida, V.; Grimsditch, G. Including blue carbon in climate market mechanisms. Ocean Coast. Manag. 2012, 83, 15–18. [Google Scholar]
  67. Jones, T.G. Shining a light on Madagascar’s mangroves. Madag. Conserv. Dev. 2013, 8, 4–6. [Google Scholar]
  68. Heumann, B.W. Satellite remote sensing of mangrove forests: Recent advances and future opportunities. Prog. Phys. Geogr. 2011, 35, 87–108. [Google Scholar] [CrossRef]
  69. Manson, F.J.; Loneragan, N.R.; McLeod, I.M.; Kenyon, R.A. Assessing techniques for estimating the extent of mangroves: Topographic maps, aerial photographs, and Landsat TM images. Mar. Freshw. Res. 2001, 52, 787–792. [Google Scholar] [CrossRef]
  70. Ruiz-Luna, A.; Berlanga-Robles, C.A. Land use, land cover changes and coastal lagoon surface reduction associated with urban growth in northwest Mexico. Landsc. Ecol. 2003, 18, 159–171. [Google Scholar] [CrossRef]
  71. Cornejo, R.H.; Koedam, N.; Luna, A.R.; Troell, M.; Dahdouh-Guebas, F. Remote sensing and ethno- botanical assessment of the mangrove forest changes in the Navachiste-San Ignacio-Macapule lagoon complex, Sinaloa, Mexico. Ecol. Soc. 2005, 10, 16. [Google Scholar]
  72. Beland, M.; Goita, K.; Bonn, F.; Pham, T.T.H. Assessment of land-cover changes related to shrimp aquaculture using remote sensing data: A case study in the Giao Thuy District, Vietnam. Int. J. Remote Sens. 2006, 27, 1491–1510. [Google Scholar] [CrossRef]
  73. Giri, C.; Pengra, B.; Zhu, Z.L.; Singh, A.; Tieszen, L.L. Monitoring mangrove forest dynamics of the Sundarbans in Bangladesh and India using multi-temporal satellite data from 1973 to 2000. Estuar. Coast. Shelf Sci. 2007, 73, 91–100. [Google Scholar] [CrossRef]
  74. Giri, C.; Zhu, Z.; Tieszen, L.L.; Singh, A.; Gillette, S.; Kelmelis, J.A. Mangrove forest distributions and dynamics (1975–2005) of the tsunami-affected region of Asia. J. Biogeogr. 2008, 35, 519–528. [Google Scholar] [CrossRef]
  75. Liu, K.; Li, X.; Shi, X.; Wang, S.G. Monitoring mangrove forest changes using remote sensing and GIS data with decision-tree learning. Wetlands 2008, 28, 336–346. [Google Scholar] [CrossRef]
  76. Paling, E.I.; Kobryn, H.T.; Humphreys, G. Assessing the extent of mangrove change caused by Cyclone Vance in the eastern Exmouth Gulf, northwestern Australia. Estuar. Coast. Shelf Sci. 2008, 77, 603–613. [Google Scholar] [CrossRef]
  77. Alsaaideh, B.; Al-Hanbali, A.; Tateishi, R.; Kobayashi, T.; Hoan, N.T. Mangrove forests mapping in the southern part of Japan using Landsat ETM+ with DEM. J. Geogr. Inf. Syst. 2013, 5, 369–377. [Google Scholar]
  78. Li, M.S.; Mao, L.J.; Shen, W.J.; Liu, S.Q.; Wei, A.I. Change and fragmentation trends of Zhanjiang mangrove forests in southern China using multi-temporal Landsat imagery (1977–2010). Estuar. Coast. Shelf Sci. 2013, 130, 111–120. [Google Scholar] [CrossRef]
  79. Nguyen, H.; McAlpine, C.; Pullar, D.; Johansen, K.; Duke, N. The relationship of spatial-temporal changes in fringe mangrove extent and adjacent land-use: Case study of Ken Giang coast, Vietnam. Ocean Coast. Manag. 2013, 76, 12–22. [Google Scholar] [CrossRef]
  80. Giri, C.; Muhlhausen, J. Mangrove forest distributions and dynamics in Madagascar (1975–2005). Sensors 2008, 8, 2104–2117. [Google Scholar] [CrossRef]
  81. Rasolofoharinoro, M.; Blasco, F.; Bellan, M.F.; Aizpuru, M.; Gauquelin, T.; Denis, J. A remote sensing based methodology for mangrove studies in Madagascar. Int. J. Remote Sens. 1998, 19, 1873–1886. [Google Scholar] [CrossRef]
  82. Pasqualini, V.; Iltis, J.; Dessay, N.; Lointier, M.; Guelorget, O.; Polidori, L. Mangrove mapping in North-Western Madagascar using SPOT-XS and SIR-C radar data. Hydrobiologia 1999, 413, 127–133. [Google Scholar] [CrossRef]
  83. Guillet, M.; Renou, E.; Robin, M.; Debaine, F.; Ratsivalaka, S. Suivi et analyze de l’evolution de la mangrove de Mahajamba (Nord-ouest de Madagascar). In Proceedings of the International Pluridisciplinary Conference, Lille, France, 16–18 January 2008.
  84. Raharimahefa, T.; Kusky, T.M. Environmental monitoring of Bombetoka Bay and the Betsiboka Estuary, Madagascar, using multi-temporal satellite data. J. Earth Sci. 2010, 21, 210–226. [Google Scholar] [CrossRef]
  85. Rakotomavo, A.; Fromard, F. Dynamics of mangrove forests in the Mangoky River delta, Madagascar, under the influence of natural and human factors. For. Ecol. Manag. 2010, 259, 1161–1169. [Google Scholar] [CrossRef]
  86. Giri, C. National-Level Mangrove Cover Data-Sets for 1990, 2000 and 2010; United States Geological Survey: Sioux Falls, SD, USA, 2011. [Google Scholar]
  87. Rasolofo, M.V.; Ramilijaona, O. Variability in the abundance and recruitment of Fenneropenaeus indicus and Metapenaeus monoceros postlarvae and juveniles in Ambaro Bay mangroves of Madagascar. Nat. Faune 2009, 24, 103–109. [Google Scholar]
  88. Rasofolo, M.V. Use of mangroves by traditional fishermen in Madagascar. Mangroves Salt Marshes 1997, 1, 243–253. [Google Scholar] [CrossRef]
  89. Mayaux, P.; Gond, V.; Bartholome, E. A near-real time forest-cover map of Madagascar derived from SPOT-4 VEGETATION data. Int. J. Remote Sens. 2000, 21, 3139–3144. [Google Scholar] [CrossRef]
  90. Critical Ecosystem Partnership Fund (CEPF). Madagascar Vegetation Mapping Project; CEPF: Arlington, VA, USA, 2007. [Google Scholar]
  91. Harper, G.J.; Steininger, M.K.; Tucker, C.J.; Juhn, D.; Hawkins, F. Fifty years of deforestation and forest fragmentation in Madagascar. Environ. Conserv. 2007, 34, 325–333. [Google Scholar]
  92. USGS Earth Explorer. Available online: (accessed on 1 December 2011).
  93. Gutman, G.; Byrnes, R.; Masek, J.; Covington, S.; Justice, C.; Franks, S.; Kurtz, R. Towards monitoring land-cover and land-use changes at a global scale: The Global Land Survey 2005. Photogramm. Eng. Remote Sens. 2008, 74, 6–10. [Google Scholar]
  94. Chavez, P.S. Image-based atmospheric corrections: Revisited and improved. Photogramm. Eng. Remote Sens. 1996, 62, 1025–1036. [Google Scholar]
  95. Kirui, K.B.; Kairo, J.G.; Bosire, J.; Viergever, K.M.; Rudra, S.; Huxham, M.; Briers, R.A. Mapping of mangrove forest land cover change along the Kenya coastline using Landsat imagery. Ocean Coast. Manag. 2013, 83, 19–24. [Google Scholar] [CrossRef]
  96. Simard, M.; Zhang, K.Q.; Rivera-Monroy, V.H.; Ross, M.S.; Ruiz, P.L.; Castaneda-Moya, E.; Twilley, R.R.; Rodriguez, E. Mapping height and biomass of mangrove forests in Everglades National Park with SRTM elevation data. Photogramm. Eng. Remote Sens. 2006, 72, 299–311. [Google Scholar] [CrossRef]
  97. Fatoyinbo, T.E.; Simard, M.; Washington-Allen, R.A.; Shugart, H.H. Landscape-scale extent, height, biomass, and carbon estimation of Mozambique’s mangrove forests with Landsat ETM+ and Shuttle Radar Topography Mission elevation data. J. Geophys. Res. Biogeosci. 2008, 113. [Google Scholar] [CrossRef]
  98. Simard, M.; Rivera-Monroy, V.H.; Mancera-Pineda, J.E.; Castaneda-Moya, E.; Twilley, R.R. A systematic method for 3D mapping of mangrove forests based on Shuttle Radar Topography Mission elevation data, ICEsat/GLAS waveforms and field data: Application to Cienaga Grande de Santa Marta, Colombia. Remote Sens. Environ. 2008, 112, 2131–2144. [Google Scholar] [CrossRef]
  99. Bhattarai, B.; Giri, C. Assessment of mangrove forests in the Pacific region using Landsat imagery. J. Appl. Remote Sens. 2011. [Google Scholar] [CrossRef]
  100. Long, J.B.; Giri, C. Mapping the Philippines’ mangrove forests using Landsat imagery. Sensors 2011, 11, 2972–2981. [Google Scholar] [CrossRef]
  101. Fatoyinbo, T.E.; Simard, M. Height and biomass of mangroves in Africa from ICESat/GLAS and SRTM. Int. J. Remote Sens. 2013, 34, 668–681. [Google Scholar] [CrossRef]
  102. Blasco, F.; Gauquelin, T.; Rasolofoharinoro, M.; Denis, J.; Aizpuru, M.; Caldairou, V. Recent advances in mangrove studies using remote sensing data. Mar. Freshw. Res. 1998, 49, 287–296. [Google Scholar] [CrossRef]
  103. Tomlinson, P.B. The Botany of Mangroves; Cambridge University Press: Melbourne, Australia, 1986. [Google Scholar]
  104. Aschbacher, J.; Ofren, R.; Delsol, J.P.; Suselo, T.B.; Vibulsresth, S.; Charrupat, T. An integrated comparative approach to mangrove vegetation mapping using advanced remote sensing and GIS technologies: Preliminary results. Hydrologica 1995, 295, 285–295. [Google Scholar]
  105. Gao, J.A. Hybrid method toward accurate mapping of mangroves in a marginal habitat from SPOT Multispectral data. Int. J. Remote Sens. 1998, 19, 1887–1899. [Google Scholar] [CrossRef]
  106. Green, E.P.; Clark, C.D.; Mumby, P.J.; Edwards, A.J.; Ellis, A.C. Remote sensing techniques for mangrove mapping. Int. J. Remote Sens. 1998, 19, 935–956. [Google Scholar] [CrossRef]
  107. Gao, J.A. Comparative study on spatial and spectral resolutions of satellite data in mapping mangrove forests. Int. J. Remote Sens. 1999, 20, 2823–2833. [Google Scholar] [CrossRef]
  108. Saito, H.; Bellan, M.F.; Al-Habshi, A.; Aizpuru, M.; Blasco, F. Mangrove research and coastal ecosystem studies with SPOT-4 HRVIR and TERRA ASTER in Arabian Gulf. Int. J. Remote Sens. 2003, 24, 4073–4092. [Google Scholar] [CrossRef]
  109. Tong, P.H.; Auda, Y.; Populus, J.; Aizpura, M.; Habshi, A.A.; Blasco, F. Assessment from space of mangroves evolution in the Mekong Delta, in relation to extensive shrimp farming. Int. J. Remote Sens. 2004, 25, 4795–4812. [Google Scholar] [CrossRef]
  110. Jensen, L.S.; Mueller, T.; Tate, K.R.; Ross, D.J.; Magid, J.; Nielsen, N.E. Soil surface CO2 flux as an index of soil respiration in situ: A comparison of two chamber methods. Soil Biol. Biochem. 1996, 28, 1297–1306. [Google Scholar] [CrossRef]
  111. Fromard, F.; Puig, H.; Mougin, E.; Marty, G.; Betoulle, J.L.; Cadamuro, L. Structure, above-ground biomass and dynamics of mangrove ecosystems: New data from French Guiana. Oecologia 1998, 115, 39–53. [Google Scholar] [CrossRef]
  112. Smith, T.J., III; Whelan, K.R.T. Development of allometric relations for three mangrove species in South Florida for use in the Greater Everglades Ecosystem restoration. Wetl. Ecol. Manag. 2006, 14, 409–419. [Google Scholar] [CrossRef]
  113. Komiyama, A.; Poungparn, S.; Kato, S. Common allometric equations for estimate the tree weight of mangroves. J. Trop. Ecol. 2005, 21, 471–477. [Google Scholar] [CrossRef]
  114. Schumacher, B. Methods for the Determination of Total Organic Carbon (TOC) in Soils and Sediments; Ecological Risk Assessment Support Center, Office of Research and Development. US Environmental Protection Agency: Washington, DC, USA, 2002. [Google Scholar]
  115. Mikhailova, E.A.; Noble, R.R.P.; Post, C.J. Comparison of soil organic carbon recovery by Walkley-Black and dry combustion methods in the Russian Chernozem. Commun. Soil Sci. Plant Anal. 2003, 34, 1853–1860. [Google Scholar] [CrossRef]
  116. De Vos, B.; Letterns, S.; Muys, B.; Deckers, J.A. Walkley-Black analysis of forest soil organic carbon: Recovery, limitations and uncertainty. Soil Use Manag. 2007, 23, 221–229. [Google Scholar] [CrossRef]
  117. Meersmans, J.; van Wesemael, B.; van Molle, M. Determining soil organic carbon for agricultural soils: A comparison between the Walkley & Black and the dry combustion methods (north Belgium). Soil Use Manag. 2009, 25, 346–353. [Google Scholar] [CrossRef]
  118. Simpson, W.T. Method to Estimate Dry-Kiln Schedules and Species Groupings: Tropical and Temperate Hardwoods; US Department of Agriculture, Forest Service, Forest Products Laboratory: Washington, DC, USA, 1996. [Google Scholar]
  119. Dharmawan, I.W.S.; Siregar, C.A. Soil carbon and carbon estimation of Avicennia marina (Forsk.). Vierh. Stand at Ciasem, Purwakarta. J. Penelit. Hutan dan Konservasi Alam. 2008, 5, 317–328. [Google Scholar]
  120. Clough, B.F.; Scott, K. Allometric relationships for estimating above-ground biomass in six mangrove species. For. Ecol. Manag. 1989, 27, 117–127. [Google Scholar] [CrossRef]
  121. Comley, B.W.T.; McGuinness, K.A. Above- and below-ground biomass, and allometry, of four common northern Australian mangroves. Aust. J. Bot. 2005, 53, 431–436. [Google Scholar] [CrossRef]
  122. Sinclair, T.T.; Hoffer, R.M.; Schreiber, M.M. Reflectance and internal structure of leaves from several crops during a growing season. Agron. J. 1971, 63, 864–868. [Google Scholar] [CrossRef]
  123. Elvidge, C.D. Visible and near-infrared reflectance characteristics of dry plant materials. Int. J. Remote Sens. 1990, 11, 1775–1795. [Google Scholar] [CrossRef]
  124. Curran, P.J. Remote sensing of foliar chemistry. Remote Sens. Environ. 1989, 30, 271–278. [Google Scholar] [CrossRef]
  125. Tamura, M.; Kikushima, K. Extraction of mangrove forests using a satellite image and a digital elevation model. In Proceedings of the SPIE 7104, Remote Sensing for Agriculture, Ecosystems, and Hydrology X, Cardiff, UK, 15 September 2008; Volume 7104.
  126. Lippitt, C.D.; Rogan, J.; Zhe, L.; Eastman, R.J.; Jones, T.G. Mapping selective logging in mixed deciduous forest: A comparison of machine learning algorithms. Photogramm. Eng. Remote Sens. 2008, 74, 1201–1211. [Google Scholar] [CrossRef]
  127. Plugge, D.; Baldauf, T.; Ratsimba, H.R.; Rajoelison, G.; Köhl, M. Combined biomass inventory in the scope of REDD (Reducing Emissions from Deforestation and Forest Degradation. Madag. Conserv. Dev. 2010, 5, 23–34. [Google Scholar]
  128. Bredbenner, A. Profiles in Blue Carbon Field Work; Conservation International: Washington, DC, USA, 2013. [Google Scholar]

Share and Cite

MDPI and ACS Style

Jones, T.G.; Ratsimba, H.R.; Ravaoarinorotsihoarana, L.; Cripps, G.; Bey, A. Ecological Variability and Carbon Stock Estimates of Mangrove Ecosystems in Northwestern Madagascar. Forests 2014, 5, 177-205.

AMA Style

Jones TG, Ratsimba HR, Ravaoarinorotsihoarana L, Cripps G, Bey A. Ecological Variability and Carbon Stock Estimates of Mangrove Ecosystems in Northwestern Madagascar. Forests. 2014; 5(1):177-205.

Chicago/Turabian Style

Jones, Trevor G., Harifidy Rakoto Ratsimba, Lalao Ravaoarinorotsihoarana, Garth Cripps, and Adia Bey. 2014. "Ecological Variability and Carbon Stock Estimates of Mangrove Ecosystems in Northwestern Madagascar" Forests 5, no. 1: 177-205.

Article Metrics

Back to TopTop