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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">Front. For. Glob. Change</journal-id>
<journal-title>Frontiers in Forests and Global Change</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. For. Glob. Change</abbrev-journal-title>
<issn pub-type="epub">2624-893X</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.3389/ffgc.2021.732468</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Forests and Global Change</subject>
<subj-group>
<subject>Original Research</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Structural Characteristics of the Tallest Mangrove Forests of the American Continent: A Comparison of Ground-Based, Drone and Radar Measurements</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" corresp="yes">
<name><surname>Castellanos-Galindo</surname> <given-names>Gustavo A.</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
<xref ref-type="aff" rid="aff3"><sup>3</sup></xref>
<xref ref-type="corresp" rid="c001"><sup>&#x002A;</sup></xref>
<uri xlink:href="http://loop.frontiersin.org/people/639665/overview"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Casella</surname> <given-names>Elisa</given-names></name>
<xref ref-type="aff" rid="aff3"><sup>3</sup></xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Tavera</surname> <given-names>Hector</given-names></name>
<xref ref-type="aff" rid="aff4"><sup>4</sup></xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Zapata Padilla</surname> <given-names>Luis Alonso</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Simard</surname> <given-names>Marc</given-names></name>
<xref ref-type="aff" rid="aff5"><sup>5</sup></xref>
<uri xlink:href="http://loop.frontiersin.org/people/1189391/overview"/>
</contrib>
</contrib-group>
<aff id="aff1"><sup>1</sup><institution>WWF Colombia</institution>, <addr-line>Cali</addr-line>, <country>Colombia</country></aff>
<aff id="aff2"><sup>2</sup><institution>Smithsonian Tropical Research Institute (STRI)</institution>, <addr-line>Panama City</addr-line>, <country>Panama</country></aff>
<aff id="aff3"><sup>3</sup><institution>Leibniz Centre for Tropical Marine Research (ZMT)</institution>, <addr-line>Bremen</addr-line>, <country>Germany</country></aff>
<aff id="aff4"><sup>4</sup><institution>Ministerio de Ambiente y Desarrollo Sostenible</institution>, <addr-line>Bogot&#x00E1;</addr-line>, <country>Colombia</country></aff>
<aff id="aff5"><sup>5</sup><institution>Jet Propulsion Laboratory, California Institute of Technology</institution>, <addr-line>Pasadena, CA</addr-line>, <country>United States</country></aff>
<author-notes>
<fn fn-type="edited-by"><p>Edited by: Sigit Sasmito, National University of Singapore, Singapore</p></fn>
<fn fn-type="edited-by"><p>Reviewed by: Juan Felipe Blanco-Libreros, University of Antioquia, Colombia; Fernanda Adame, Griffith University, Australia</p></fn>
<corresp id="c001">&#x002A;Correspondence: Gustavo A. Castellanos-Galindo, <email>gustavoa80@yahoo.com</email></corresp>
<fn fn-type="other" id="fn004"><p>This article was submitted to Tropical Forests, a section of the journal Frontiers in Forests and Global Change</p></fn>
</author-notes>
<pub-date pub-type="epub">
<day>08</day>
<month>10</month>
<year>2021</year>
</pub-date>
<pub-date pub-type="collection">
<year>2021</year>
</pub-date>
<volume>4</volume>
<elocation-id>732468</elocation-id>
<history>
<date date-type="received">
<day>29</day>
<month>06</month>
<year>2021</year>
</date>
<date date-type="accepted">
<day>07</day>
<month>09</month>
<year>2021</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#x00A9; 2021 Castellanos-Galindo, Casella, Tavera, Zapata Padilla and Simard.</copyright-statement>
<copyright-year>2021</copyright-year>
<copyright-holder>Castellanos-Galindo, Casella, Tavera, Zapata Padilla and Simard</copyright-holder>
<license xlink:href="http://creativecommons.org/licenses/by/4.0/"><p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</p></license>
</permissions>
<abstract>
<p>The Panama Bight eco-region along the Pacific coast of central and South America is considered to have one of the best-preserved mangrove ecosystems in the American continent. The regional climate, with rainfall easily reaching 5&#x2013;8 m every year and weak wind conditions, contribute to the exceptionally tall mangroves along the southern Colombian and northern Ecuadorian Pacific coasts (Nari&#x00F1;o Department and Esmeraldas Province areas). Here we evaluate the use of different methods (ground-based measurements, drone imagery and radar data [Shuttle Radar Topography mission-SRTM and TanDEM-X]) to characterize the structure of the tallest of these forests. In November 2019, three mangrove sites with canopy heights between 50 and 60 m, previously identified with SRTM data, were sampled close to the town of Guapi, Colombia. In addition to <italic>in situ</italic> field measurements of trees, we conducted airborne drone surveys in order to generate georeferenced orthomosaics and digital surface models (DSMs). We found that the extensive mangrove forests in this area of the Colombian Pacific are almost entirely composed of <italic>Rhizophora</italic> spp. trees. The tallest mangrove tree measured in the three plots was 57 m. With ca. 900 drone photographs, three orthomosaics (2 cm pixel<sup>&#x2013;1</sup> resolution) and digital surface models (3.5 cm pixel<sup>&#x2013;1</sup>) with average area of 4,0 ha were generated. The field-measured canopy heights were used to validate the drone-derived and radar-derived data, confirming these mangrove forests as the tallest in the Americas. The drone-derived orthomosaics showed significant patches of the Golden Leather Fern, <italic>Acrostichum aureum</italic>, an opportunistic species that can be associated to mangrove degradation, indicating that the mangrove forests investigated here may be threatened from increased selective logging requiring improvements and effective implementation of the current mangrove management plans in Colombia. The techniques used here are highly complementary and may represent the three tiers for carbon reporting, whereby the drone-derived canopy height maps, calibrated with local <italic>in situ</italic> measurements, provides cheap but reliable Tier 3 estimates of carbon stocks at the project level.</p>
</abstract>
<kwd-group>
<kwd>unoccupied aerial vehicles (UAVs)</kwd>
<kwd>Shuttle Radar Topography mission</kwd>
<kwd>mangrove above-ground biomass</kwd>
<kwd>eastern Pacific</kwd>
<kwd>Colombia</kwd>
<kwd>mangrove degradation</kwd>
<kwd>structure from motion (SFM)</kwd>
<kwd><italic>Rhizophora</italic> spp.</kwd>
</kwd-group>
<counts>
<fig-count count="6"/>
<table-count count="2"/>
<equation-count count="2"/>
<ref-count count="55"/>
<page-count count="11"/>
<word-count count="8871"/>
</counts>
</article-meta>
</front>
<body>
<sec sec-type="intro" id="S1">
<title>Introduction</title>
<p>Spaceborne remote sensing (SRS) is nowadays a key tool to understand Earth phenomena including the monitoring of biodiversity on our planet (<xref ref-type="bibr" rid="B35">Pettorelli et al., 2016</xref>). This is the case for the use of SRS in monitoring mangrove ecosystems. Accelerating since 2000 and facilitated by the free availability of satellite products, different global datasets of mangrove cover and loss are now available (<xref ref-type="bibr" rid="B53">Worthington et al., 2020</xref>). These baseline products (e.g., <xref ref-type="bibr" rid="B17">Giri et al., 2011</xref>; <xref ref-type="bibr" rid="B7">Bunting et al., 2018</xref>) have helped to derive global datasets of important properties of mangrove such as above-ground biomass (AGB) and carbon (AGC) after extrapolating or averaging site-specific values (<xref ref-type="bibr" rid="B38">Rovai et al., 2016</xref>; <xref ref-type="bibr" rid="B40">Rovai et al., 2018</xref>; <xref ref-type="bibr" rid="B18">Hamilton and Friess, 2018</xref>). Other SRS products like Lidar and interferometric synthetic aperture radar (InSAR) have been recently used to estimate mangrove heights at national, regional and global scales greatly improving previous AGB estimates (<xref ref-type="bibr" rid="B15">Fatoyinbo and Simard, 2013</xref>; <xref ref-type="bibr" rid="B44">Shapiro et al., 2015</xref>; <xref ref-type="bibr" rid="B23">Lagomasino et al., 2019</xref>; <xref ref-type="bibr" rid="B45">Simard et al., 2019</xref>). Nevertheless, there are still limitations faced when using some of these SRS global products with respect to their resolution (usually &#x003E; 25 m per pixel) and the climatic conditions under which images can be taken (e.g., cloud free conditions).</p>
<p>Ideally, local and national mangrove mapping datasets that use remote sensing products with higher resolutions and that incorporate ground-truth measurements can play an important role in providing training data and validation for many of the on-going global mapping exercises (e.g., Global Mangrove Watch initiative; <xref ref-type="bibr" rid="B53">Worthington et al., 2020</xref>). Hence coordination and integration of global, national, and local datasets are needed to overcome many of the limitations of individual datasets.</p>
<p>Consumer-grade drones, belonging to the unoccupied aircraft systems (UAS) sector, appear to be an appropriate tool to overcome some of the limitations of SRS products in mangrove areas that are &#x003C; 100 ha (<xref ref-type="bibr" rid="B9">Castellanos-Galindo et al., 2019</xref>). Examples of mapping mangrove forest with drones at spatial resolutions with centimeter scale are rapidly appearing in the literature (<xref ref-type="bibr" rid="B34">Otero et al., 2018</xref>; <xref ref-type="bibr" rid="B27">Li et al., 2019</xref>; <xref ref-type="bibr" rid="B32">Navarro et al., 2020</xref>). These finer resolution products provide unique opportunities to understand ecological processes and derive essential biodiversity variables that would not be possible to obtain with SRS at the moment. The use of UAS in mangrove mapping is therefore likely to simplify and complement traditional field inventories and additionally increase the accuracy of AGB and AGC estimates at the local level (e.g., <xref ref-type="bibr" rid="B28">Lucas et al., 2020</xref>). Collecting drone-derived information can therefore greatly benefit the calibration of the regional and global estimates that have been produced so far using SRS products of coarser resolution.</p>
<p>The Panama Bight eco-region in the west coast of Central and South America is considered to have one of the best-preserved mangrove ecosystems in the American continent and is thus a widely recognized conservation hotspot (<xref ref-type="bibr" rid="B47">Spalding et al., 2007</xref>). Highly developed mangrove forests are found along the southern Colombian and northern Ecuadorian Pacific coasts (Nari&#x00F1;o and Esmeraldas areas; <xref ref-type="bibr" rid="B8">Castellanos-Galindo et al., 2015</xref>; <xref ref-type="bibr" rid="B19">Hamilton et al., 2017</xref>). Already in the mid-twentieth century, the American Geographer Robert West referred to these intertidal forests as the &#x201C;most luxuriant mangroves of the world&#x201D; (<xref ref-type="bibr" rid="B50">West, 1956</xref>). A more recent study (<xref ref-type="bibr" rid="B45">Simard et al., 2019</xref>) has identified the southern Colombian Pacific coast (Cauca and Nari&#x00F1;o Departments), together with Gabon and Equatorial Guinea in Africa, as the regions containing the tallest mangroves in the world. A combination of high precipitation (i.e., potentially lower salinity), high temperature and low cyclone landfall frequency plus local geomorphological factors are associated to the observed exceptionally large areas and high canopy heights observed in those regions (<xref ref-type="bibr" rid="B45">Simard et al., 2019</xref>).</p>
<p>Mangroves in the southern Colombian Pacific coast occur in areas with geomorphological features like alluvial plains that form dynamic barrier islands surrounded by tidal channels (<xref ref-type="bibr" rid="B29">Mart&#x00ED;nez et al., 1995</xref>). These mangroves may be the wettest in the world with rainfall easily reaching 5 to ca. 8 m every year. The remoteness of this vast area (with no coastal road and only accessible by long boat journeys or small airplanes) contributes to the relatively pristine nature of some of these forests, but also to the difficulty in obtaining scientific ecological information (<xref ref-type="bibr" rid="B10">Castellanos-Galindo et al., 2021</xref>). This difficulty has prevented so far corroborating most of the information from modeling studies that have highlighted the unique characteristics of the mangrove areas in this coast (e.g., <xref ref-type="bibr" rid="B20">Hutchison et al., 2014</xref>; <xref ref-type="bibr" rid="B40">Rovai et al., 2018</xref>).</p>
<p>To validate previous remote sensed measurements (i.e., <xref ref-type="bibr" rid="B45">Simard et al., 2019</xref>) and to assess the complementarity of different techniques, we compare here mangrove tree height and AGB measurements from ground-based inventories, drone imagery and radar data (from the Shuttle Radar Topography mission-SRTM and the TerraSAR-X add-on for Digital Elevation Measurement-TanDEM-X) taken from a remote area in the Colombian Pacific coast recognized to contain the tallest mangroves in the American continent. The combination of field-based methods (tree DBH and height measurements and drone photogrammetry) with existing SRS products in the most extreme range of mangrove canopy height (&#x223C;50 m) allows for the first time: (1) the validation of previous models that highlighted the ecological value of mangroves in this region and (2) the recognition that these areas are in need of urgent protection due on-going localized alterations.</p>
</sec>
<sec id="S2" sec-type="materials|methods">
<title>Materials and Methods</title>
<sec id="S2.SS1">
<title>Study Site</title>
<p>The Colombian Pacific coast encompasses ca. 1,500 km in the tropical eastern Pacific biogeographic region that extends from the Gulf of California, Mexico to northern Peru. Almost 2/3 of this coastal region is dominated by mangroves, with &#x223C;80% of the total mangrove area of Colombia (<xref ref-type="bibr" rid="B31">Mej&#x00ED;a-Renter&#x00ED;a et al., 2018</xref>). The whole coast presents annual precipitations of &#x003E; 2,000 mm, reaching in some areas 8,000 mm yr<sup>&#x2013;1</sup>. This extreme precipitation translates into year-long low water salinities (&#x003C;30) and permanent brackish areas inside bays, small deltas and tidal channels in what is identified as the Eastern Pacific fresh pool (<xref ref-type="bibr" rid="B1">Alory et al., 2012</xref>). The tidal regime is semi-diurnal, meso- to macro-tidal with amplitudes during spring tides greater than 4 m (<xref ref-type="bibr" rid="B13">Correa and Morton, 2010</xref>). These tidal conditions indicate that mangroves and mudflats are completely exposed at low tides and completely inundated at high tide (during both neap and spring tides).</p>
<p>Nari&#x00F1;o, the southernmost coastal Department along the Pacific coast of Colombia, borders the neighboring Esmeraldas province of Ecuador to the South, and the Colombian Cauca Department in Colombia to the North. Nari&#x00F1;o alone contains 46% of the total mangrove forests of the country (<xref ref-type="bibr" rid="B31">Mej&#x00ED;a-Renter&#x00ED;a et al., 2018</xref>). This tectonically active coast is characterized by the presence of two high water discharge and dynamic deltas (Mira and Pat&#x00ED;a; <xref ref-type="bibr" rid="B36">Restrepo and Cantera, 2013</xref>) and an almost uninterrupted mangrove belt. The coast is also under-developed in terms of infrastructure with the presence of small villages (&#x003C;5,000 inhabitants) scattered in a mangrove-dominated landscape. Nari&#x00F1;o contains the largest mangrove marine protected area (MPA) of the whole tropical eastern Pacific (the Sanquianga National Park with &#x223C;80,000 ha) and a more recently created mangrove MPA bordering Ecuador (Distrito Nacional de Manejo Integrado Cabo Manglares Bajo Mira y Frontera). North of Sanquianga MPA lies the mouth of the Iscuand&#x00E9; River, an estuarine area dominated by extensive mangrove forests and small human settlements that constitute the Afro-Colombian community council of Esfuerzo Pescador. The water discharge of the Iscuand&#x00E9; River is 6.71 km<sup>3</sup> yr<sup>&#x2013;1</sup> (<xref ref-type="bibr" rid="B37">Restrepo and Kjerfve, 2004</xref>).</p>
</sec>
<sec id="S2.SS2">
<title>Field Sampling</title>
<p>In November 2019 (6th&#x2013;8th), three different mangrove sites in the northern coast of the Nari&#x00F1;o Department of the Colombian Pacific coast were visited (<xref ref-type="fig" rid="F1">Figure 1</xref>). The sites are located near the mouth of the Iscuand&#x00E9; River, an estuarine area completely dominated by mangrove forests, tidal creeks and mud-sand flats that emerge during low tides. Circular plots of 15 m-diameter were established at each site. Ground measurements within these plots included the identification of tree species, diameter at breast height (DBH) and top height of selected trees. While DBH measurements were generally made around the trunk of each tree at 1.3 m above the ground surface, several measurements were made above the high prop roots of <italic>Rhizophora</italic> spp. (e.g., <xref ref-type="fig" rid="F2">Figure 2</xref>). To measure DBH, a diameter tape was wrapped around the girth of each tree and a diameter measurement read was made to the nearest 0.1 cm. Heights of selected trees within each plot were collected with the aid of a Nikon Forestry Pro II laser hypsometer. There trees were then geolocated using a handheld GPS (Bad Elf GNSS Surveyor).</p>
<fig id="F1" position="float">
<label>FIGURE 1</label>
<caption><p>Location of the mangrove sites visited in the southern Colombian Pacific coast (Iscuand&#x00E9; River mouth, Nari&#x00F1;o Department; Imagery &#x00A9;2021 Google, Maxar Technologies, Data SIO, NOAA, U.S. Navy, NGA, GEBCO, Landsat/Copernicus, Imagery &#x00A9;2021 Terrametrics, Map data &#x00A9;2021). Three mangrove patches were surveyed in the estuarine complex formed close to the mouth of the Iscuand&#x00E9; River: from left to right, sites are known as: &#x201C;La Punta del Codo,&#x201D; &#x201C;La Rotura,&#x201D; and &#x201C;Madrid.&#x201D;</p></caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="ffgc-04-732468-g001.tif"/>
</fig>
<fig id="F2" position="float">
<label>FIGURE 2</label>
<caption><p>Field surveys performed in mangroves of the southern Colombian Pacific coast (Iscuand&#x00E9;, Nari&#x00F1;o). <bold>(a)</bold> Aerial view of one of the sites surveyed (La Punta del Codo); <bold>(b)</bold> measuring DBH of a gigantic <italic>Rhizophora</italic> spp. tree <bold>(c)</bold> piloting a DJI Mavic consumer-grade drone inside a mangrove forests surrounded by the golden leather fern <italic>Acrostrichum aureum</italic>.</p></caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="ffgc-04-732468-g002.tif"/>
</fig>
</sec>
<sec id="S2.SS3">
<title>Allometric Equations</title>
<p>For each of the plots surveyed, we used the DBH values and two allometric equations to determine tree biomass per hectare. First, we used the allometric equation for <italic>Rhizophora mangle</italic> developed by <xref ref-type="bibr" rid="B16">Fromard et al. (1998)</xref> to estimate tree biomass that only takes into account DBH:</p>
<disp-formula id="S2.Ex1">
<mml:math id="M1" display="block">
<mml:mrow>
<mml:mrow>
<mml:mi>A</mml:mi>
<mml:mo>&#x2062;</mml:mo>
<mml:mi>G</mml:mi>
<mml:mo>&#x2062;</mml:mo>
<mml:mpadded width="+3.3pt">
<mml:mi>B</mml:mi>
</mml:mpadded>
</mml:mrow>
<mml:mo rspace="5.8pt">=</mml:mo>
<mml:mrow>
<mml:mpadded width="+3.3pt">
<mml:mn>0.1282</mml:mn>
</mml:mpadded>
<mml:mo rspace="5.8pt">&#x00D7;</mml:mo>
<mml:msup>
<mml:mi>D</mml:mi>
<mml:mrow>
<mml:mo stretchy="false">(</mml:mo>
<mml:mn>2.6</mml:mn>
<mml:mo stretchy="false">)</mml:mo>
</mml:mrow>
</mml:msup>
</mml:mrow>
</mml:mrow>
</mml:math>
</disp-formula>
<p>We also used the pantropical tree allometric model to estimate AGB proposed by <xref ref-type="bibr" rid="B12">Chave et al. (2014)</xref> which takes into account tree height, DBH and wood specific gravity:</p>
<disp-formula id="S2.Ex2">
<mml:math id="M2" display="block">
<mml:mrow>
<mml:mrow>
<mml:mi>A</mml:mi>
<mml:mo>&#x2062;</mml:mo>
<mml:mi>G</mml:mi>
<mml:mo>&#x2062;</mml:mo>
<mml:mpadded width="+3.3pt">
<mml:msub>
<mml:mi>B</mml:mi>
<mml:mrow>
<mml:mi>e</mml:mi>
<mml:mo>&#x2062;</mml:mo>
<mml:mi>s</mml:mi>
<mml:mo>&#x2062;</mml:mo>
<mml:mi>t</mml:mi>
</mml:mrow>
</mml:msub>
</mml:mpadded>
</mml:mrow>
<mml:mo rspace="5.8pt">=</mml:mo>
<mml:mrow>
<mml:mpadded width="+3.3pt">
<mml:mn>0.0673</mml:mn>
</mml:mpadded>
<mml:mo rspace="5.8pt">&#x00D7;</mml:mo>
<mml:msup>
<mml:mrow>
<mml:mo>(</mml:mo>
<mml:mrow>
<mml:mi mathvariant="normal">&#x03C1;</mml:mi>
<mml:mo>&#x2062;</mml:mo>
<mml:msup>
<mml:mi>D</mml:mi>
<mml:mn>2</mml:mn>
</mml:msup>
<mml:mo>&#x2062;</mml:mo>
<mml:mi>H</mml:mi>
</mml:mrow>
<mml:mo>)</mml:mo>
</mml:mrow>
<mml:mn>0.976</mml:mn>
</mml:msup>
</mml:mrow>
</mml:mrow>
</mml:math>
</disp-formula>
<p>where D is DBH in cm, H is tree height in m and <italic>&#x03C1;</italic> is wood specific gravity in g cm<sup>&#x2013;3</sup>. <italic>&#x03C1;</italic> was computed as the mean value of the wood specific gravity values available for <italic>Rhizophora</italic> spp. in the Central and South America from the Global wood density database (<xref ref-type="bibr" rid="B11">Chave et al., 2009</xref>; <xref ref-type="bibr" rid="B54">Zanne et al., 2009</xref>).</p>
<p>To implement the pantropical tree allometric model of <xref ref-type="bibr" rid="B12">Chave et al. (2014)</xref>, we back-calculated the heights of the trees for which we only had DBH. For that we fitted, a Log-Log model of DBH:H with 26 trees for which we had both DBH and Heights (see <xref ref-type="supplementary-material" rid="TS1">Supplementary Figure 1</xref>). Total living carbon was then calculated using the relationship total living biomass:living carbon of 1:0.464 (<xref ref-type="bibr" rid="B22">Kauffman et al., 2011</xref>, <xref ref-type="bibr" rid="B21">2020</xref>).</p>
</sec>
<sec id="S2.SS4">
<title>Drone Surveys</title>
<p>Drone surveys in the direct vicinity of each plot were carried out at low tide with calm winds. The drone patches surveyed were &#x223C;3 ha in size at each site and always covered the plot areas where ground measurements were taken. Low-altitude (100 m) aerial images were acquired using two UAS, DJI Mavic Pro and Mavic 2 Pro. These drones are equipped with integrated photo cameras. DJI Mavic Pro has a FC220 camera, with a sensor 1/2.3&#x201D; CMOS (effective pixel:12,35 Megapixel), focal length of 5 mm, a pixel size of 1.7 &#x00D7; 1.7 &#x03BC;m and a resolution of 4,000 &#x00D7; 2,250 pixels. The Mavic 2 Pro has a L1D-20c camera with a sensor 1&#x201D; CMOS camera (effective pixel:20 Megapixel), focal length of 10 mm, a pixel size of 2.41 &#x00D7; 2.41 &#x03BC;m and a resolution of 5,472 &#x00D7; 3,648 pixels. Photos are geotagged by the DJI integrated GPS/GLONASS location system with a horizontal and vertical precision of up to &#x00B1; 1.5 and &#x00B1; 0.5 m, respectively.<sup><xref ref-type="fn" rid="footnote1">1</xref></sup> Flights were performed in automated mode and were programmed using the commercial web app &#x201C;Drone Deploy.&#x201D; Due to the nature of the environment, characterized by dense vegetation with lack of large gaps exposing the terrain within the forest, it was not possible to easily place and collect ground control points (GCPs). Although few small gaps are present, they are not easily accessible and lack the necessary sky view to operate GNSS and collect GCPs with acceptable accuracy.</p>
<p>The acquired images were analyzed and processed using the software Agisoft Metashape.<sup><xref ref-type="fn" rid="footnote2">2</xref></sup> Metashape is based on Structure from Motion (SfM) (<xref ref-type="bibr" rid="B49">Ullman, 1979</xref>) and Multi-View Stereo reconstruction (MVS) methods (<xref ref-type="bibr" rid="B42">Scharstein and Szeliski, 2002</xref>; <xref ref-type="bibr" rid="B43">Seitz et al., 2006</xref>). For a comprehensive description of the SfM method implemented in Metashape, the reader is referred to <xref ref-type="bibr" rid="B52">Westoby et al. (2012)</xref>. Metashape gives as outputs an orthorectified photomosaic (orthomosaic) and a Digital Surface Model (DSM) from nadir photos collected during the flight. The output models were georeferenced in Metashape to the WGS84 datum using camera positions. The results of the photogrammetric suite were used in the three locations to estimate different environmental variables. Orthomosaics with 2 cm/pixel resolution allowed detecting the heterogeneity of vegetation and the presence of opportunistic species associated to mangrove degradation. DSMs were used to estimate the heights of trees within the <italic>in situ</italic> sampling areas. Since the ground was not visible within the forest, we used the elevation of mud-sand flats that emerge during low tides as a reference. The observed DSM was vertically shifted to match the elevation of the mud-sand flats. Consequently, the height of the trees was extracted from the vertically shifted DSM.</p>
</sec>
<sec id="S2.SS5">
<title>Satellite Data</title>
<p>To compare our <italic>in situ</italic> and drone generated data, we used two global RS products generated by <xref ref-type="bibr" rid="B45">Simard et al. (2019)</xref>. One of maximum mangrove canopy height for the year 2000 with a resolution of &#x223C;30 m that used the Shuttle Radar Topography Mission (SRTM) global digital elevation model (DEM), and the Geoscience Laser Altimeter System (GLAS) global Lidar altimetry products. The second RS product was an aboveground mangrove biomass map that was generated by <xref ref-type="bibr" rid="B45">Simard et al. (2019)</xref> linking field-measured biomass&#x2013;height allometry with SRTM estimates of basal area weighted height (all RS products available at <ext-link ext-link-type="uri" xlink:href="https://daac.ornl.gov/cgi-bin/dsviewer.pl?ds_id=1665">https://daac.ornl.gov/cgi-bin/dsviewer.pl?ds_id=1665</ext-link>).</p>
<p>We additionally compared our mangrove height field-generated data against the high-resolution data product (12 &#x00D7; 12 m) derived from the TerraSAR-X add-on for Digital Elevation Measurement-TanDEM-X mission (Simard unpublished <italic>data</italic>). We performed a similar procedure as with the drone DSMs and adjusted the TanDEM-X DEM shifting it vertically to match the elevation of the adjacent water. For details about use of the TanDEM-X in mangrove canopy height estimations see <xref ref-type="bibr" rid="B26">Lee and Fatoyinbo (2015)</xref> and <xref ref-type="bibr" rid="B24">Lagomasino et al. (2016)</xref>.</p>
<p>The tree height comparisons between the three methods used was done using the ground height measurements taken at the three sites surveyed (<italic>n</italic> = 21 trees). With the georeferenced location of each of these trees, a vector (&#x223C;5 m radius circle) was created in QGIS and using the zonal statistics, height information (mean, maximum and minimum) from the drone, the SRTM and the TanDEM-X rasters were extracted. We fitted linear regressions between <italic>in situ</italic> maximum tree heights and calculated drone, SRTM and TanDEM-X tree heights. In addition, Pearson, determination coefficients and RMSE (root mean squared error) were computed to assess the fit of the regressions.</p>
</sec>
</sec>
<sec sec-type="results" id="S3">
<title>Results</title>
<p>All surveyed sites were dominated by the red mangrove <italic>Rhizophora</italic> spp. In one of the sites (Madrid; <xref ref-type="fig" rid="F3">Figure 3</xref>), the golden leather fern <italic>Acrostrichum aureum</italic>, a mangrove associate, dominated the understory which in many cases reached up to 4 m (see <xref ref-type="fig" rid="F2">Figures 2</xref>, <xref ref-type="fig" rid="F4">4</xref>). While still difficult to distinguish in the drone orthomosaic, we estimated that at least 5% of the orthomosaic obtained for the Madrid site was completely covereded by <italic>A. aurem</italic> (i.e., gaps with no <italic>Rhizophora</italic> spp. canopies). Moreover, our ground surveys at this site showed that the understory in the remaining 95% of the orthomosaic was completely dominated by this species, which was not captured by the drone orthomosaic (<xref ref-type="fig" rid="F4">Figure 4</xref>).</p>
<fig id="F3" position="float">
<label>FIGURE 3</label>
<caption><p>The three RGB orthomosaics obtained with the drone data showing the geo-referenced location of the trees measured for height using the Nikon Forestry Pro II laser hypsometer.</p></caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="ffgc-04-732468-g003.tif"/>
</fig>
<fig id="F4" position="float">
<label>FIGURE 4</label>
<caption><p>Drone orthomosaic of one of the mangrove sites surveyed in Iscuand&#x00E9;, Colombian Pacific. The transparent delineated areas in the orthomosaic show regions entirely covered by the golden leather fern <italic>Acrostrichum aureum</italic>. Pictures on the right show how the understory of these areas is dominated by <italic>A. aureum</italic>.</p></caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="ffgc-04-732468-g004.tif"/>
</fig>
<p>Mean DBH values were very high at the Madrid site in comparison with the other two surveyed sites. The Madrid site was characterized by the largest trees with a mean DBH of 52.4 cm reaching a DBH and height of 96.7 cm and 57 m, respectively. In contrast, the mean DBH at La Rotura and La Punta del Codo sites, were considerably lower (around 20 cm) with maximum tree heights of 50.8 and 53.6 m, respectively. The low mean DBH values indicate the presence of comparatively smaller trees in those two latter sites. Nonetheless, the total AGB was, as expected, dominated by the presence of the largest trees in all sites. Depending on the allometric equation used (<xref ref-type="bibr" rid="B16">Fromard et al., 1998</xref>; <xref ref-type="bibr" rid="B12">Chave et al., 2014</xref>), the mean AGB across all sites was 862.2 or 626.4 Mg ha<sup>&#x2013;1</sup>, respectively. Similarly, mean above-ground mangrove carbon stocks were estimated in 400.1 or 290.7 Mg C ha<sup>&#x2013;1</sup> (<xref ref-type="table" rid="T1">Table 1</xref>). These values, especially in the Madrid site do not account for the contribution of <italic>A. aurem</italic> to the total biomass and carbon. The mangrove AGB values derived from the ground data were two to three times higher than those estimated with the SRTM data in <xref ref-type="bibr" rid="B45">Simard et al. (2019)</xref>. AGB values for the examined plots derived from SRTM, and based on continental scale allometry, ranged from 296.2 to 413.3 to Mg ha<sup>&#x2013;1</sup>.</p>
<table-wrap position="float" id="T1">
<label>TABLE 1</label>
<caption><p>Summary statistics for the field measurements (diameter at breast height-DBH, maximum height, basal area, and tree density) taken at three mangrove sites in Iscuand&#x00E9;, Colombian Pacific coast.</p></caption>
<table cellspacing="5" cellpadding="5" frame="hsides" rules="groups">
<thead>
<tr>
<td valign="top" align="left">Site</td>
<td valign="top" align="center">Samples (n)</td>
<td valign="top" align="center">Mean DBH (cm)</td>
<td valign="top" align="center">Max DBH (cm)</td>
<td valign="top" align="center">Min DBH (cm)</td>
<td valign="top" align="center">Mean tree height (m)</td>
<td valign="top" align="center">Max tree height (m)</td>
<td valign="top" align="center">Basal area (m<sup>2</sup> ha<sup>&#x2013;1</sup>)</td>
<td valign="top" align="center">Tree density (trees ha<sup>&#x2013;1</sup>)</td>
<td valign="top" align="justify" colspan="2"><xref ref-type="bibr" rid="B12">Chave et al. (2014)</xref> Pantropical equation<hr/></td>
<td valign="top" align="justify" colspan="2"><xref ref-type="bibr" rid="B16">Fromard et al. (1998)</xref> Equation<hr/></td>
</tr>
<tr>
<td valign="top" align="justify"/>
<td valign="top" align="justify"/>
<td valign="top" align="justify"/>
<td valign="top" align="justify"/>
<td valign="top" align="justify"/>
<td valign="top" align="justify"/>
<td valign="top" align="justify"/>
<td valign="top" align="justify"/>
<td valign="top" align="justify"/>
<td valign="top" align="center">AGB (Mg ha<sup>&#x2013;1</sup>)</td>
<td valign="top" align="center">C storage (Mg ha<sup>&#x2013;1</sup>)</td>
<td valign="top" align="center">AGB (Mg ha<sup>&#x2013;1</sup>)</td>
<td valign="top" align="center">C storage (Mg ha<sup>&#x2013;1</sup>)</td>
</tr>
</thead>
<tbody>
<tr>
<td valign="top" align="left">La Punta del Codo</td>
<td valign="top" align="center">27</td>
<td valign="top" align="center">22.7</td>
<td valign="top" align="center">73.9</td>
<td valign="top" align="center">5.0</td>
<td valign="top" align="center">47.0</td>
<td valign="top" align="center">53.6</td>
<td valign="top" align="center">28.4</td>
<td valign="top" align="center">382.0</td>
<td valign="top" align="center">848.0</td>
<td valign="top" align="center">393.5</td>
<td valign="top" align="center">579.4</td>
<td valign="top" align="center">268.8</td>
</tr>
<tr>
<td valign="top" align="left">La Rotura</td>
<td valign="top" align="center">33</td>
<td valign="top" align="center">19.5</td>
<td valign="top" align="center">92.0</td>
<td valign="top" align="center">5.0</td>
<td valign="top" align="center">46.1</td>
<td valign="top" align="center">50.8</td>
<td valign="top" align="center">33.4</td>
<td valign="top" align="center">466.9</td>
<td valign="top" align="center">902.1</td>
<td valign="top" align="center">418.6</td>
<td valign="top" align="center">667.6</td>
<td valign="top" align="center">309.8</td>
</tr>
<tr>
<td valign="top" align="left">Madrid</td>
<td valign="top" align="center">22</td>
<td valign="top" align="center">52.4</td>
<td valign="top" align="center">96.7</td>
<td valign="top" align="center">14.1</td>
<td valign="top" align="center">47.2</td>
<td valign="top" align="center">56.7</td>
<td valign="top" align="center">30.1</td>
<td valign="top" align="center">114.3</td>
<td valign="top" align="center">836.4</td>
<td valign="top" align="center">388.1</td>
<td valign="top" align="center">632.3</td>
<td valign="top" align="center">293.4</td>
</tr>
</tbody>
</table></table-wrap>
</sec>
<sec sec-type="discussion" id="S4">
<title>Discussion</title>
<p>We conducted a field campaign specifically to validate and study the regions with the tallest mangrove forests in the Americas (<xref ref-type="bibr" rid="B45">Simard et al., 2019</xref>). Field measurements of tree DBH and height were used to validate drone- and SRTM- derived maps of mangrove canopy height, confirming the findings of <xref ref-type="bibr" rid="B45">Simard et al. (2019)</xref>. The tallest field-measured tree was 57 m, the drone-derived canopy height revealed maximum heights of 57.6 m and the SRTM data for these sites showed maximum canopy heights of 54.3 m. While our analysis is performed in forest stands that may not be representative of the entire region, we show that <italic>in situ</italic>, drone and spaceborne data provide accurate results in the most extreme range of mangrove canopy height. All the three data sources corroborate the existence of exceptionally tall mangrove forests in this region of the Western American tropics. However, each of the methods used to estimate tree height data presented challenges and associated errors (<xref ref-type="fig" rid="F5">Figure 5</xref> and <xref ref-type="table" rid="T2">Table 2</xref>). As revealed in previous modeling studies (e.g., <xref ref-type="bibr" rid="B38">Rovai et al., 2016</xref>; <xref ref-type="bibr" rid="B18">Hamilton and Friess, 2018</xref>; <xref ref-type="bibr" rid="B40">Rovai et al., 2018</xref>), <italic>in situ</italic> measurements confirmed that these sites are on the upper range of mangrove biomass and carbon per area in the world.</p>
<fig id="F5" position="float">
<label>FIGURE 5</label>
<caption><p>Correlation between different methods to calculate mangrove tree heights in three different sites in Iscuand&#x00E9;, Colombian Pacific. <bold>(A)</bold> Scatter plot of <italic>in situ</italic> Height<sub>max</sub> vs. Drone Height<sub>max</sub>; <bold>(B)</bold> scatter plot of <italic>in situ</italic> Height<sub>max</sub> vs. SRTM Height<sub>max</sub>; <bold>(C)</bold> scatter plot of <italic>in situ</italic> Height<sub>max</sub> vs. TanDEM-X Height<sub>max</sub>.</p></caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="ffgc-04-732468-g005.tif"/>
</fig>
<table-wrap position="float" id="T2">
<label>TABLE 2</label>
<caption><p>Summary statistics showing results of linear regressions and Pearson correlations for the comparison among the three different tree height measurements.</p></caption>
<table cellspacing="5" cellpadding="5" frame="hsides" rules="groups">
<thead>
<tr>
<td valign="top" align="left">Methods compared</td>
<td valign="top" align="center">Pearson coefficient (<italic>r</italic>)</td>
<td valign="top" align="center">Determination coefficient (<italic>R</italic><sup>2</sup>)</td>
<td valign="top" align="center">RMSE (m)</td>
</tr>
</thead>
<tbody>
<tr>
<td valign="top" align="left"><italic>In situ</italic> vs. drone</td>
<td valign="top" align="center">0.25</td>
<td valign="top" align="center">0.06</td>
<td valign="top" align="center">5.69</td>
</tr>
<tr>
<td valign="top" align="left"><italic>In situ</italic> vs. SRTM</td>
<td valign="top" align="center">0.34</td>
<td valign="top" align="center">0.12</td>
<td valign="top" align="center">3.18</td>
</tr>
<tr>
<td valign="top" align="left"><italic>In situ</italic> vs. TanDEM-X</td>
<td valign="top" align="center">0.34</td>
<td valign="top" align="center">0.12</td>
<td valign="top" align="center">3.55</td>
</tr>
</tbody>
</table></table-wrap>
<p>Field tree height data was collected with a laser range finder (Nikon Forestry Pro II laser hypsometer). In a recent study, <xref ref-type="bibr" rid="B41">Saliu et al. (2021)</xref> indicated that this method presents the lowest amount of error (8%) among a variety of methods used to measure mangrove tree heights in Malaysia. <xref ref-type="bibr" rid="B25">Larjavaara and Muller-Landau (2013)</xref> have also identified that both methods (tangent and sine) available when using the laser range finder can incur in high random errors and underestimations in moist tropical forests. A few aspects complicate mangrove tree height calculations with this instrument. For example, in highly dense forests, the identification of the ground and the top of the tree crown can be challenging and thus is not exempt from errors. For a mangrove system in the Colombian Caribbean, <xref ref-type="bibr" rid="B46">Simard et al. (2008)</xref> calculated that the random error of tree height measurements in the field can be &#x223C;10%. In the forests examined here, the presence of a dense understory in some sites plus the stilt root nature of <italic>Rhizophora</italic> trees also complicate the identification of the ground with the laser range finder. While we consider these <italic>in situ</italic> measurements to be the most reliable estimates of tree height, we acknowledge the potentially significant uncertainty associated with this method.</p>
<sec id="S4.SS1">
<title>Mangrove Above-Ground Biomass of the Iscuand&#x00E9; Region in the Global Context</title>
<p>The mean mangrove AGB values obtained here using the <italic>in-situ</italic> data are extremely high varying between 862.2 and 626.4 Mg ha<sup>&#x2013;1</sup> (depending on which allometric equation is used). These values are located in the upper range of the recent global synthesis by <xref ref-type="bibr" rid="B39">Rovai et al. (2021)</xref> and also correspond to the upper range values recently estimated by <xref ref-type="bibr" rid="B48">Trettin et al. (2021)</xref> for a mangrove forest in Gabon where mangrove trees of up to 60 m can be found. Our estimated mean AGB values are generally higher than those obtained using the AGB values calculated by <xref ref-type="bibr" rid="B45">Simard et al. (2019)</xref> for the same areas. This result warrants a re-examination of the relationship between SRTM data and <italic>in situ</italic> inventories considering a larger dataset than the one currently considered in our study. Likewise, it is important to consider that our plots represent very tall mangrove forests within the Iscuand&#x00E9; area. A more representative AGB (and carbon) estimate would need a sampling design that considers the whole range of mangrove type mosaics and patch heterogeneity that are present in this large area (e.g., like the recent work of <xref ref-type="bibr" rid="B48">Trettin et al., 2021</xref> in Gabon). Such a study could yield slightly lower mean AGB values for these mangrove forests but would also contribute to more accurate numbers on carbon stocks of these areas.</p>
</sec>
<sec id="S4.SS2">
<title>Advantages of Drone-Derived Data to Detect Mangrove Degradation</title>
<p>The drone derived data (orthomosaics and DSMs) of these three mangrove sites provided sufficiently detailed information (&#x003C;4 cm pixel<sup>&#x2013;1</sup> resolution) to detect landscape features that are not captured with the ground surveys nor with the SRTM or the TanDEM-X products. Especially important are (1) the heterogeneity in canopy heights observed and also (2) the detection of canopy gaps that are the result of possible deforestation (i.e., selective logging). On one hand, the drone-derived DSMs (3.5 cm pixel<sup>&#x2013;1</sup> resolution) recorded highly variable tree heights within each of the 3 ha patches. On the other hand, the pixels SRTM and TanDEM-X products may include tree crowns of short and tall trees or ground areas, thus these elevation of these mixed pixels represent overall canopy height rather than the height of the tallest tree. This effect may be particularly important in this study (<xref ref-type="fig" rid="F6">Figure 6</xref>), with tree heights measured near forest edges along the shore or around canopy gaps.</p>
<fig id="F6" position="float">
<label>FIGURE 6</label>
<caption><p>Comparison of altimetry products derived from surveys in mangroves of Iscuand&#x00E9; (Colombian Pacific coast). Mangrove patches correspond to &#x201C;La Punta del Codo,&#x201D; &#x201C;La Rotura&#x201D; and &#x201C;Madrid&#x201D; from left to right. The upper row shows the vertically shifted DSMs obtained from the drone data. The middle row depicts canopy heights from the TanDEM-X product (Simard unpublished; &#x00A9; DLR 2020) The lower row corresponds to canopy heights from the <xref ref-type="bibr" rid="B45">Simard et al. (2019)</xref> dataset.</p></caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="ffgc-04-732468-g006.tif"/>
</fig>
<p>On the other hand, the drone orthomosaics were sufficiently detailed to detect the presence of gaps within one of the mangrove patches that were dominated by the golden leather fern <italic>A. aureum</italic>, an opportunistic species associated to mangrove degradation (Madrid patch in <xref ref-type="fig" rid="F4">Figure 4</xref>). <italic>Acrostichum aureum</italic> is a highly resistant fern able to colonize the understory of mangrove areas when facilitated either by the presence of natural canopy gaps (see <xref ref-type="bibr" rid="B2">Amir, 2012</xref>; <xref ref-type="bibr" rid="B3">Amir and Duke, 2019</xref>) or by man-made gaps produced after forest logging. The fern is commonly associated to deforestation and is able to rapidly colonize mangrove areas that have been disturbed, a process that has been defined as cryptic (mangrove) ecological degradation (<xref ref-type="bibr" rid="B14">Dahdouh-Guebas et al., 2005</xref>; <xref ref-type="bibr" rid="B6">Blanco et al., 2012</xref>). Once established, <italic>A. aureum</italic> modifies the geomorphology and hydrology, impeding natural regeneration and hindering animal movement (<xref ref-type="bibr" rid="B30">Medina et al., 1990</xref>; <xref ref-type="bibr" rid="B4">Biswas et al., 2018</xref>). Other aspects of the effects of this fern on ecosystem processes within the mangrove forests are poorly understood. The information provided by the drone products on <italic>A. aureum</italic> can be valuable as it provides evidence at the scale of 10 s of hectares on loss of mangrove ecosystem health that would otherwise be unnoticed when using coarser SRS products. These highly detailed drone products can also aid in the development of complexity indexes, such as those proposed in <xref ref-type="bibr" rid="B5">Blanco et al. (2001)</xref>, that could be used to characterize health status and degradation in mangrove forests. Being able to identify the understory vegetation (e.g., <italic>A. aureum</italic> in this case) of a mangrove area with the drone products implies also that the contribution of this vegetation to the ecosystem biomass and carbon storage, which could become very high, could be accounted for. However, it is unclear how persistent in time <italic>A. aureum</italic> can become in this region. Surprisingly, allometric equations and information on the carbon content and establishment dynamics of this opportunistic fern are scarce and needed.</p>
<p>The mangrove areas examined here, still contain well developed forests. However, historical mangrove timber exploitation has occurred and continues to occur. Although we do not have data on the magnitude of recent and on-going logging, the local communities identify this activity as an increasingly pressing factor on the surrounding mangrove ecosystems. Moreover, unaccounted as a mangrove degradation source remains the effects that the anti-narcotics national program for eradication of coca crops that the Colombian government undertook in the 2000s with aerial aspersion of glyphosate (and currently seeks to continue). One of the few accounts on the use of herbicides in mangrove forests is that of the severe effects that its use caused on Vietnam forests during the second Indochina war (<xref ref-type="bibr" rid="B51">Westing, 1983</xref>). Anecdotical information from locals in Iscuand&#x00E9; reported on the effects that glyphosate had on native flora and fauna around mangroves in the past. The localized effects that both timber logging and glyphosate could have on these exceptionally well-developed mangroves could be studied with the finer resolution products from drones.</p>
</sec>
<sec id="S4.SS3">
<title>Implications for Mangrove Carbon Monitoring in Remote Areas</title>
<p>Our study reveals significant challenges in collecting field and drone data in these mangrove areas. These can be categorized as logistical and geometrical. The access to these sites requires careful travel planning that includes site accessibility by plane and boat in a highly dynamic setting driven by the large tidal range, and close collaboration with local authorities and organizations. The latter facilitates, not only safe passage to sites, but gathering of a wealth of knowledge about local landscapes, cultural practices and customs related to mangroves and water management (see <xref ref-type="bibr" rid="B33">Oslender, 2016</xref>). On the other hand, the geometrical challenges are related to the complex terrain with mangroves roots, litter, and mud that constrains the possibility to collect tree heights in a systematic and time-efficient way. To accurately process the drone data, collecting ground control points-GCPs (ideally with a Real-time kinematic-RTK GPS) is desirable. However, identifying sufficiently clear gaps to place those GCPs inside mangrove forests can prove an unachievable task. Ways to overcome this limitation could include using drones that have incorporated an RTK GPS (although this technique does not completely exclude the need of GCPs) and/or using adjacent ecosystems within the mangrove forest (e.g., mudflats) where placing GCPs is feasible.</p>
<p><xref ref-type="bibr" rid="B55">Zeng et al. (2021)</xref> suggests that mangrove blue carbon projects in Colombia may only be profitable in the southern Colombian Pacific coast, the area where this study was conducted. Our results, therefore provide valuable assessment methodologies and an initial <italic>in situ</italic> assessment of carbon stocks for potential blue carbon projects in an area that has been highlighted by modeling studies as a blue carbon hotspot in the world with much need of effective conservation actions. The techniques are complementary and may represent the three tiers for carbon reporting, whereby the drone-derived canopy height maps, calibrated with local <italic>in situ</italic> measurements, provides affordable and reliable Tier 3 estimates of carbon stocks at the project level. These detailed estimates can in turn help calibrating the coarser Tier 1 and Tier 2 assessments. Additionally, the combination of drone and ground survey data can provide a way to detect and monitor small-scale ecosystem degradation symptoms that so far are not possible to detect with the SRS products currently used for mangrove mapping. This can bring a more detailed understanding of landscape processes occurring within these vulnerable ecosystems that so far have been excessively focused on coarse area measurements.</p>
</sec>
</sec>
<sec sec-type="data-availability" id="S5">
<title>Data Availability Statement</title>
<p>The original contributions presented in the study are included in the article/<xref ref-type="supplementary-material" rid="TS1">Supplementary Material</xref>, further inquiries can be directed to the corresponding author/s.</p>
</sec>
<sec id="S6">
<title>Author Contributions</title>
<p>All authors contributed to the article and approved the submitted version.</p>
</sec>
<sec sec-type="COI-statement" id="conf1">
<title>Conflict of Interest</title>
<p>The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.</p>
</sec>
<sec sec-type="disclaimer" id="s7">
<title>Publisher&#x2019;s Note</title>
<p>All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.</p>
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<title>Funding</title>
<p>Funding for fieldwork was provided by WWF Colombia and WWF US (GLOBAL MANGROVE ALLIANCE 510-51000000&#x2014;4350). Bezos Earth Fund (agreement CN11408) supported article publication costs. GC-G was funded by the Smithsonian Tropical Research Institution postdoctoral fellowship. MS was funded by NASA&#x2019;s LCLUC program.</p>
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<p>We thank the members of the community council Esfuerzo Pescador and its Legal representative (Kennedy Caicedo) in Iscuand&#x00E9; for their hospitality and facilitating logistical resources during our field campaign. We also thank the local experts (Carmelo Castillo and others) that guided us through the marvelous mangrove forests of Iscuand&#x00E9;. Part of the research was carried out at the Jet Propulsion Laboratory, California Institute of Technology, under a contract with the National Aeronautics and Space Administration (LCLUC program). We thank DLR for providing TanDEM-X DEM data through their science program. This project (<italic>Manglares y productividad biol&#x00F3;gica en la regi&#x00F3;n de Iscuand&#x00E9;-Tapaje, Pac&#x00ED;fico colombiano</italic>) was part of those approved within the frame of the II Scientific Expedition to the Colombian Pacific - Bocas de Sanquianga (<italic>Plan Nacional de Expediciones Cient&#x00ED;ficas Pac&#x00ED;fico</italic>) organized by the Colombian Commission for the Oceans (<italic>Comisi&#x00F3;n Colombiana del Oc&#x00E9;ano-CCO</italic>). We thank the comments made by the two reviewers and the guest associate editor that helped to improve the clarity of this manuscript.</p>
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<sec id="S9" sec-type="supplementary-material">
<title>Supplementary Material</title>
<p>The Supplementary Material for this article can be found online at: <ext-link ext-link-type="uri" xlink:href="https://www.frontiersin.org/articles/10.3389/ffgc.2021.732468/full#supplementary-material">https://www.frontiersin.org/articles/10.3389/ffgc.2021.732468/full#supplementary-material</ext-link></p>
<p>Raw forest inventory data are also available at <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.6084/m9.figshare.16509045.v2">https://doi.org/10.6084/m9.figshare.16509045.v2</ext-link>.</p>
<supplementary-material xlink:href="Table_1.DOCX" id="TS1" mimetype="application/vnd.openxmlformats-officedocument.wordprocessingml.document" xmlns:xlink="http://www.w3.org/1999/xlink"/>
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