Introduction
The Philippines is one of the top five global biodiversity hotspots, with 46% species endemism (Lee et al. Reference Lee, Hyun and Kang2012). However, forest cover has fallen from 90% in 1521 to 27% at present and only 11% of what remains is primary forest (Food and Agriculture Organisation of the United Nations 2015). This has been a contributing factor to bird species declines and the country now has the 8th highest number of globally threatened bird species in the world (BirdLife International 2020a). The Philippines is therefore a priority area for global conservation (Paz et al. Reference Paz, Ngoprasert, Nuneza, Mallari and Gale2013).
The Negros Bleeding-heart Gallicolumba keayi is a ‘Critically Endangered’ colombid, found only on the islands of Panay and Negros in the Philippines. The most recent population estimate is from 2001, when 70–370 individuals were thought to remain in the wild (BirdLife International 2017). The species is threatened by habitat loss through forest conversion to agriculture or clearance for timber extraction and charcoal production. From the 1500s to 1988, forest cover on Panay and Negros was reduced by 92% and 96%, respectively, and very little primary forest remains (BirdLife International 2017, 2018b). The dove is also threatened by poaching, as it is trapped and hunted for food, or caught to keep as a pet (Cariño Reference Cariño2007, BirdLife International 2017). Some conservation measures are in place, e.g. patrols by forest rangers to dismantle traps and stop illegal logging in the Northwest Panay Peninsula Natural Park and northern Central Panay Mountain Range (Arkive 2007, PhilinCon 2018). Due to its small population and ongoing threats, the Negros Bleeding-heart urgently requires extensive conservation action (Bristol Zoo Gardens Reference Gardens2017, Gaworecki Reference Gaworecki2018).
Little is known about the biology and resource requirements of the Negros Bleeding-heart, as is the case for most species in its genus, Gallicolumba (Walker Reference Walker2007). It seems to spend most of its time on the forest floor, to only use understorey plants to roost, take cover, or breed (Slade et al. Reference Slade, Villanueva, Tacud and Curio2005). It is cryptic and difficult to observe (Slade et al. Reference Slade, Villanueva, Tacud and Curio2005, Cariño Reference Cariño2007). Its diet consists of seeds, berries, and invertebrates (Slade et al. Reference Slade, Villanueva, Tacud and Curio2005, Cariño Reference Cariño2007), including fruit from Ficus and Pinanga species (Cariño Reference Cariño2007). It is thought to prefer lowland forest at 300–1,000 m (BirdLife International 2017) but it has also been reported at > 1,000 m on Negros, where all forest < 800 m has been cleared (Curio Reference Curio2001), aside from some fragments at 300–900 m around Ban-Ban in the south-east (Biodiversity Management Bureau and Philippines Biodiversity Conservation Foundation Inc 2018). It is thought to prefer primary forest, but its ability to use secondary forest remains unclear; although reportedly detected in secondary forest on Panay, it has not been recorded in secondary forest on Negros (BirdLife International 2017). Understanding more about the species’ resource requirements and habitat preference is key to implementing relevant conservation measures (Bibby et al. Reference Bibby, Marsden, Fielding, Bibby, Jones and Marsden2000, Begehold et al. Reference Begehold, Rzanny and Flade2015). Species presence and environmental data can be used in species distribution modelling to map where a species is most probably present (Morales et al. Reference Morales, Fernández and Baca-González2017), such that priority areas for conservation action can be identified (De Carvalho et al. Reference De Carvalho, Sousa-Neves, Cerqueira, Gonsioroski, Silva, Silva and Santos2017). The most recent study of the Negros Bleeding-heart was commissioned by Bristol Zoological Society and undertaken by the Center for Conservation Innovation (CCI), investigating its population size and habitat preference in south Negros (Bristol Zoological Society pers. comm.). Based on nine observations of this highly cryptic species in March 2016, occupancy modelling found that the dove prefers sites with dense ground vegetation coverage and high proportion of canopy cover. Furthermore, bird-habitat association modelling suggested its preference for old growth forest is likely to be influenced by the presence of ferns, fruiting and flowering trees and high ground and mid-storey vegetation cover (CCI 2016).
The aim of the current study was to investigate the habitat preference of the Negros Bleeding-heart in the Northwest Panay Peninsula Natural Park and to model species distribution across its range to identify the best potential areas for conservation action. Objectives therefore were to (1) survey for the Negros Bleeding-heart using point counts, line transects, playback surveys and camera traps, collect habitat variable measurements, and assess the influence of measured habitat variables on this species’ presence using Generalised Linear Modelling (GLM); (2) identify areas of potentially suitable habitat across Panay and Negros using species distribution modelling; and (3) compare Negros Bleeding-heart predicted distribution against current protected areas and Important Bird and Biodiversity Areas to identify focus areas for future conservation action.
Methods
Study site
The study was undertaken in the forest surrounding Sibaliw field station (latitude 121.9675°, longitude 11.8195°) in the Northwest Panay Peninsula Natural Park, Panay, Philippines (Figure 1). This 5,000-ha reserve encompasses the largest remaining contiguous low elevation forest across Negros and Panay, and at least half is old growth (BirdLife International 2018a). It is a protected area, where shifting cultivation, hunting, trapping or disturbing wild animals, cutting timber or gathering forest products are prohibited (Zabal Reference Zabal2014). Various threatened species have been observed there, such as the Visayan Warty Pig Sus cebifrons (CR) (Meijaard et al. Reference Meijaard, Oliver and Leus2017), Visayan Hornbill Penelopides panini (EN) (BirdLife International 2018a), White-throated Jungle Flycatcher Vauriella albigularis (EN) and Yellow-faced Flameback Chrysocolaptes xanthocephalus (EN) (BirdLife International 2020b). Deforestation, mining, hunting, and poaching have also been observed inside the protected area (Foundation for the Philippine Environment 2018, PhilinCon 2018).
The location of the study site, within the Northwest Panay Peninsula Natural Park, Panay island, Philippines. Map inset shows the location of Sibaliw research station (white circle) on the island of Panay, Philippines.
Surveying for birds
Two expeditions were undertaken in the same location within the Northwest Panay Peninsula Natural Park to survey for the Negros Bleeding-heart. Due to the extreme rarity of the species, all contacts with it, obtained using different methods, were used in this analysis to obtain information about distribution and habitat association. The first expedition was from 9 to 22 May 2018 (total 13 days observation) by Mark Abrahams, Daphne Kerhoas and Jenny Poole from Bristol Zoological Society with guides Arcel Dryden “Potpot” Fernandez and Benjamin “Jun” Tacud. Twenty 500 m-long line transects were surveyed, with 30 point-counts placed at the start and at the end of transects. Point-counts (where an observer records all birds seen and heard from one location; Lloyd et al. Reference Lloyd, Cahill, Jones, Marsden, Bibby, Jones and Marsden2000) lasted for 15 minutes, including a 5-minute settling period. Sightings of Negros Bleeding-heart were also recorded ad libitum, and three playback surveys were undertaken, whereby the Negros Bleeding-heart call was played while walking the transect. The second survey was from 12 July until 6 August 2018 (total 25 days observation) by Holly Mynott and the same two guides, in which 64 10-minute point-counts with no settling period were undertaken, as recommended for cryptic (Bibby et al. Reference Bibby, Marsden, Fielding, Bibby, Jones and Marsden2000) and terrestrial (Lee and Marsden Reference Lee and Marsden2008) bird species. This totals 94 point-counts, of which 80 were laid out every 200 m along transect lines following <1 m wide trails, and 14 were not located on trails but were laid out every 200 m along new routes. Given the narrow width and infrequent human use of trails in this area, it is considered that this would not have overly biased results (Cornils et al. Reference Cornils, Riedl, Fricke, Katz and Schulze2015). The distance between each point count location was at least 200 m, to minimise fly-between and double counting (Lloyd et al. Reference Lloyd, Cahill, Jones, Marsden, Bibby, Jones and Marsden2000, Lee and Marsden Reference Lee and Marsden2008). Point counts, when possible, were conducted within the first five hours after dawn (Reid et al. Reference Reid, Harris and Zahawi2012) and three hours before dusk (Cornils et al. Reference Cornils, Riedl, Fricke, Katz and Schulze2015), when birds are most active (Poulsen and Lambert Reference Poulsen and Lambert2000), and were not conducted in rain, fog or high winds, as this reduces bird detectability and activity (Steadman and Freifeld Reference Steadman and Freifeld1998, Paz et al. Reference Paz, Ngoprasert, Nuneza, Mallari and Gale2013, Española et al. Reference Española, Collar, Mallari and Marsden2016).
GPS co-ordinates of all Negros Bleeding-heart sightings from both expeditions were mapped using ArcMap v.10.4 (ESRI 2016) along with the co-ordinates of habitat measurement points. The Negros Bleeding-heart was marked as associated to any habitat data-points within 60 m of a sighting’s co-ordinates, following protocol for the ground-foraging Grenada Dove Leptotila wellsi (Rivera-Milán et al. Reference Rivera-Milán, Bertuol, Simal and Rusk2015).
Four camera traps (Bushnell 12 MP Trophy Low Glow Essential HD Trail Camera) were placed at knee height above the ground from 21 June 2018 to 14 July 2018, and four more were added from 17 July until 6 August 2018. Camera traps were moved every 7–9 days (Rowcliffe et al. Reference Rowcliffe, Carbone, Jansen, Kays and Kranstauber2011) for a total of 161 camera-days. Camera traps were placed using purposive sampling to evenly cover the accessible areas and also focus on locations at which guides had seen the dove previously (Treves et al. Reference Treves, Mwima, Plumptre and Isoke2010).
Measuring habitat
Ninety-three circular quadrats of 5-m radius (78.54 m2 area) were surveyed to measure habitat variables, a figure assumed to be representative of surrounding rainforest habitat (Peh et al. Reference Peh, Sodhi, de Jong, Sekercioglu, Yap and Lim2006, Posa and Sodhi Reference Posa and Sodhi2006, Reid et al. Reference Reid, Harris and Zahawi2012, Pangau-Adam et al. Reference Pangau-Adam, Mühlenberg and Waltert2015). Sixty-four of these quadrats overlapped with point count locations and 13 with camera trap locations (Figure 1). The remaining 16 did not coincide with another measurement point. All 93 quadrats were associated to any Negros Bleeding-heart sightings recorded within 60 m of them (Rivera-Milán et al. Reference Rivera-Milán, Bertuol, Simal and Rusk2015), as stated in the bird survey methods. At each quadrat, GPS co-ordinates and an elevation reading were taken using a Garmin GPS unit (Garmin eTrex 30x), because altitude can be a major predictor of occurrence in forest bird species (Bibby Reference Bibby, Marsden, Fielding, Bibby, Jones and Marsden2000, Dallimer and King Reference Dallimer and King2007, Paz et al. Reference Paz, Ngoprasert, Nuneza, Mallari and Gale2013). Tree diameter at breast height (DBH) was measured in three categories: 0 to ≤ 25 cm (band 1), > 25 to ≤ 50 cm (band 2), and > 50 cm (band 3), following other bird-habitat studies (Paz et al. Reference Paz, Ngoprasert, Nuneza, Mallari and Gale2013, Zarones et al. Reference Zarones, Colon, Ha and Ha2013). Tree height was measured using a protractor-clinometer and trigonometry (Flinn Scientific 2016). Branching architecture was noted following the guidelines in Bibby et al. (Reference Bibby, Marsden, Fielding, Bibby, Jones and Marsden2000) to indicate recent forest disturbance levels, and proportion of trees with a closed and regenerating forest structure was calculated. Canopy cover was estimated using a spherical densiometer (Forest Densiometers, Rapid City, ND) (Peh et al. Reference Peh, Sodhi, de Jong, Sekercioglu, Yap and Lim2006, Posa and Sodhi Reference Posa and Sodhi2006, Reid et al. Reference Reid, Harris and Zahawi2012), by calculating the mean canopy percentage cover from the north, east, south, and west value. Percentage vegetation cover at ground level (< 1 m) (“percentage ground cover”) and understorey cover at 1.5 m above the ground were estimated by eye by the first author (Posa and Sodhi Reference Posa and Sodhi2006, Pangau-Adam et al. Reference Pangau-Adam, Mühlenberg and Waltert2015). The presence or absence of any species of pandan Pandanus sp. and rattan (Calamus or Daemonorops spp.; Tesoro Reference Tesoro, Dransfield, Tesoro and Manokaran2002) was noted, similar to a previous Negros Bleeding-heart study (CCI 2016). Distance to Sibaliw station was calculated using ArcMap, because it has been shown that species diversity can be higher closer to field stations (Campbell Reference Campbell, Kuehl, Diarrassouba, N'Goran and Boesch2011).
Data Analysis
Habitat preference: Data were analysed with a Binomial Generalised Linear Model (Zuur et al. Reference Zuur, Hilbe and Ieno2013) in R v.3.6.1 (R Core Team 2019), in which the dependent variable was presence/absence of the Negros Bleeding-heart. Following Zuur et al. (Reference Zuur, Hilbe and Ieno2013), no outliers were found in the dataset. Multicollinearity was tested for using variance inflation factor (Zuur et al. Reference Zuur, Hilbe and Ieno2013). Tree height was found to be highly correlated with DBH (R = 0.67) using a pair plot (Zuur et al. Reference Zuur, Hilbe and Ieno2013), hence it was dropped from the model (O’Brien Reference O’Brien2007, Zuur et al. Reference Zuur, Ieno and Elphick2010). All the explanatory variables were scaled to enable model convergence and effect size comparisons (Zuur et al. Reference Zuur, Hilbe and Ieno2013, Abrahams et al. Reference Abrahams, Peres and Costa2017). A full model incorporating all variables was created using the R function glm, following which automated model creation was conducted using the R function dredge, in the R package “MuMIn” version 1.43.6 (Bartoń Reference Bartoń2015). Models with ΔAIC ≤ 2 were averaged using the R function model.avg, as described in Feld et al. (Reference Feld, Segurado and Gutiérrez-Cánovas2016) and used in other bird-habitat studies (e.g. Xu et al. Reference Xu, Lin, He, Xin, Zhang, Jiang and Li2017, Lewis et al. Reference Lewis, Melo, de Lima and Bremner-Harrison2018). The GLM was run using the following covariates: ground cover, understorey cover, canopy cover, elevation, proportion of trees with a closed forest branching structure, proportion of trees with a regenerating forest branching structure, presence of pandan, presence of rattan, distance to Sibaliw research station, and the number of trees in each of DBH band 1, 2 and 3 at each site.
Species distribution modelling: Negros Bleeding-heart distribution was modelled in MaxEnt v.3.4.1 (Phillips et al. Reference Phillips, Dudík and Schapire2017) for maximum entropy species distribution modelling (Merow et al. Reference Merow, Smith and Silander2013, Morales et al. Reference Morales, Fernández and Baca-González2017). Two environmental predictor inputs were used. The first was a map of tree cover, which is defined as canopy closure for all vegetation taller than 5 m, and encoded as a percentage output per grid cell, at 30-m resolution (Hansen et al. Reference Hansen, Potapov, Moore, Hancher, Turubanova, Tyukavina, Thau, Stehman, Goetz, Loveland, Kommareddy, Egorov, Chini, Justice and Townshend2013). The second was an elevation map at 90 m resolution (PhilGIS 2007), as the Negros Bleeding-heart has been reported to occur in lowland forests up to 1,000 m (BirdLife International 2017). While the co-ordinates of all 31 Negros Bleeding-heart sightings were included in the model, due to the tree cover and elevation map resolutions, 17 presence records were used for training and five were used for testing. Feature types, selected automatically by MaxEnt, as is the program default, were hinge, linear and quadratic. The regularization parameter on MaxEnt was set to 1.5, which is a suitable figure to reduce over-fitting compared to the default setting of 1 (Radosavljevic and Anderson Reference Radosavljevic and Anderson2014); lower settings risk loss of predictive ability with independent test data, and higher settings can falsely mark areas as suitable (Radosavljevic and Anderson Reference Radosavljevic and Anderson2014). The threshold rule applied was “maximum test sensitivity plus specificity” (Liu et al. Reference Liu, Berry, Dawson and Pearson2005), and the true skill statistic was calculated in Excel. The background was cropped to include only the islands of the species’ known range (Merow et al. Reference Merow, Smith and Silander2013), Panay and Negros. The model was run with 10,000 background points, which has been evaluated as high-performing number (Phillips and Dudik Reference Phillips and Dudík2008) and used in studies on cryptic insect species (Zhao et al. Reference Zhao, Zhang and Wei2019). Finally, the locations of Important Bird and Biodiversity Areas (IBAs) (BirdLife International 2008) were mapped over the species distribution modelling results to enable informed conservation actions.
Results
The Negros Bleeding-heart was recorded 31 times in total. Camera traps recorded the Negros Bleeding-heart on three separate occasions out of 161 camera-days (21, 22 and 24 June 2018) at the same location. Hunters were also recorded on two occasions at the same location by the camera traps.
Habitat preference
All Negros Bleeding-heart sightings were associated with habitat plots measured (i.e. 31 out of the 93 quadrats). The full averaged GLM results (Tables S1 and S2 in the online supplementary material) showed that understorey cover at 1.5 m above the ground had significant impact on Negros Bleeding-heart presence (P = 0.001), showing a positive association with dense understorey cover. Canopy cover was also found significant (P = 0.003), showing that Negros Bleeding-heart presence had a positive association with dense canopy cover. Coefficients and 95% confidence intervals of the explanatory variables in the GLM were graphed (Figure 2). The predicted effect sizes of significant habitat variables on Negros Bleeding-heart presence for the top-performing model within the ΔAIC ≤ 2 averaged model were graphed (Figure 3), and found to be similar to the other top-performing models of ΔAIC ≤ 1 in the set (Figure S1).
Coefficients and 95% confidence intervals of explanatory variables from Generalised Linear Model.
Effect predictions for significant variables on Negros Bleeding-heart presence from the top-performing Generalised Linear Model before averaging (∆AIC = 0). Shaded areas show upper and lower confidence limits, and dots show data points from which predictions were calculated.
Species distribution modelling
The AUC value of the training and test datasets were 0.969 and 0.984, respectively, and the true skill statistic value was 0.9609, indicating a high level of accuracy in the model prediction (Fielding and Bell Reference Fielding and Bell1997). Response curves showed a positive effect of increasing tree cover on habitat suitability and an optimal elevation peaking around 600 m (figure 4).
Response curves of the two environmental variables, tree cover and elevation, in a Maxent species distribution model for Negros Bleeding-heart.
The species distribution modelling in MaxEnt produced relative habitat suitability probabilities ranging from 0 to 1, with the most suitable habitat on Panay located around the Northwest Panay Peninsula Natural Park and the Central Panay Mountain Range, and the most suitable habitat in Negros found in the North Negros Natural Park, on the slopes of an area just outside the Mt Kanla-on Natural Park, and in an area to the south half-covered by Cuernos de Negros IBA (Figure 5). Most areas seem fragmented and few are highly suitable, particularly on Negros. Furthermore, there are large unsuitable patches in high elevation areas due to this species’ preference for lower elevation forest at the centres of the North Negros Natural Park, Mount Kanla-on Natural Park, Cuernos de Negros and the Central Panay Mountain Range.
Species distribution modelling of the Negros Bleeding-heart on Panay and Negros. Scale is from white to dark grey, with relative suitability for Negros Bleeding-heart from 1 to 0, indicating high and low suitability respectively. Locations of Important Bird Areas are shown as black outlines. On Panay: (A) Northwest Panay Peninsula Natural Park (BirdLife International 2018a), (B) Central Panay Mountain Range (BirdLife International 2018b). On Negros: (C) North Negros Natural Park (BirdLife International 2018c), (D) Mount Kanla-on Natural Park (BirdLife International 2018d), (E) Ban-ban (BirdLife International 2018e), (F) Southwestern Negros (BirdLife International 2018f), (G) Cuernos de Negros (BirdLife International 2018g).
Discussion
Habitat preference
Understorey cover, mostly by herbs, shrubs, and ferns, was significantly associated with Negros Bleeding-heart presence. This association has been found for other bird species, postulated to be because dense understorey provides a balance of both attractive food resources and cover to escape from predators (Lima and Dill Reference Lima and Dill1990, Reid et al. Reference Reid, Díaz, Armesto and Willson2004, Smith et al. Reference Smith, Smith and Downs2017). The Luzon Bleeding-heart Gallicolumba luzonica, a close relative to the Negros Bleeding-heart, is reported to use thick undergrowth to escape predators (Del Hoyo et al. Reference Del Hoyo, Elliott and Sargatal1997), and the Negros Bleeding-heart itself is known to forage on the ground, tossing aside leaf litter in its search for food (Curio Reference Curio2001). However, understorey cover could also relate to forest quality. Dense shrub or herb cover can be characteristic of secondary forests (Cochard et al. Reference Cochard, Van and Ngo2018), therefore suggesting that the Negros Bleeding-heart could be able to inhabit secondary forest, as found in other ground doves which also favour primary forest (Blanvillain et al. Reference Blanvillain, Florent and Thenot2002). However, the present study also identified a preference for closed canopy forest, which is characteristic of primary forest (Shoo et al. Reference Shoo, Freebody, Kanowski and Catterall2016). A preference for primary forest is supported by numerous other studies showing that terrestrial birds like the Negros Bleeding-heart are often the species most affected by loss of primary forest (Sieving et al. Reference Sieving, Willson and De Santo1996, Newmark et al. Reference Newmark, Mkongewa and Sobek2010, Powell et al. Reference Powell, Stouffer and Johnson2013, Bradfer-Lawrence et al. Reference Bradfer-Lawrence, Gardner and Dent2018). Such species are often unable to inhabit secondary forest (Peh et al. Reference Peh, Jong, Sodhi, Lim and Yap2005, Stratford and Stouffer Reference Stratford and Stouffer2013), and even well-developed secondary forest, which also has dense canopy cover, is often less biodiverse than its primary counterparts (Chadzon et al. Reference Chadzon, Peres, Dent, Shiel, Lugo, Lamb, Stork and Miller2009). The ability of the Negros Bleeding-heart to use secondary forest remains unclear (BirdLife International 2017). Some secondary forest patches in this study have been recorded, but they were small and surrounded by primary forest, and therefore the dove might move between patches of both forest types to exploit resources but rely mainly on primary forest, as postulated by Peh et al. (Reference Peh, Jong, Sodhi, Lim and Yap2005) for bird species in a Malaysian forest. Potential inability to use exclusively secondary forest could therefore explain why the dove is not found in some areas of secondary forest on Negros (BirdLife International 2017).
The habitat preference findings of this study are preliminary and could be improved by a greater quadrat size for habitat measurement and more accurate linkage of point count results to habitat plots. While 60-m association distance has been used in other studies on similar species (Rivera-Milán et al. Reference Rivera-Milán, Bertuol, Simal and Rusk2015), it adds uncertainty to the results. However, since little is known about this highly threatened species, the findings are still potentially important in directing conservation action (Huon et al. Reference Huon, Jones, Matthiopoulos, McConnell, Caurant and Vincent2015). Research into the tolerance of secondary forest by Negros Bleeding-heart is strongly recommended, particularly considering how little primary forest remains across its range (BirdLife International 2017).
Species distribution modelling
Species distribution modelling shows that suitable habitat is found in forested, low-elevation areas. Such areas have been reported in previous studies (BirdLife International 2017) to be Negros Bleeding-heart requirements. The suitability of forested areas supports the findings of the GLM in regard to the importance of understorey cover and canopy cover. However, elevation was found not to be a significant variable in the GLM. This may be because the range measured was all suitably low elevation habitat, ranging from 192 to 622 m. The species distribution model also highlights that large proportions of the core areas inside many IBAs and protected areas may be less suitable than previously thought. This is particularly so within the protected areas of the North Negros Natural Park and Mt Kanla-on Natural Park, and the unprotected IBAs of the Central Panay Mountains and Cuernos de Negros, with some edge areas appearing more suitable than within the core areas. This is a particular concern, because the edges of reserves are often subject to abiotic and biotic edge effects that can reduce habitat quality, particularly for understorey birds (Pohlman et al. Reference Pohlman, Turton and Goosem2007, Neate-Clegg et al. Reference Neate-Clegg, Morshuis and Banks-Leite2016), and to greater human pressures, such as encroachment by agriculture, charcoal logging or hunting by those living on the borders (Pedregosa-Hospodarsky et al. Reference Pedregosa-Hospodarsky, Hospodarsky, Castro, Jose, Abalajon, Alpas and Perez2009).
The model shows a significant amount of potentially suitable habitat near the eastern border of the North Negros Natural Park, which is one of the only remaining lowland forest sites on Negros, although largely secondary (BirdLife International 2018c). The tree cover map does not distinguish between primary and secondary forest (Hansen et al. Reference Hansen, Potapov, Moore, Hancher, Turubanova, Tyukavina, Thau, Stehman, Goetz, Loveland, Kommareddy, Egorov, Chini, Justice and Townshend2013). The Negros Bleeding-heart has been reported there (BirdLife International 2018c), but has not been found in bird surveys during the past 20 years (Hamann Reference Hamann2002, Pedregosa-Hospodarsky et al. Reference Pedregosa-Hospodarsky, Hospodarsky, Castro, Jose, Abalajon, Alpas and Perez2009), and the park is under pressure from illegal logging and snare hunting (Pedregosa-Hospodarsky et al. Reference Pedregosa-Hospodarsky, Hospodarsky, Castro, Jose, Abalajon, Alpas and Perez2009). Modelling also shows a small area of suitable habitat along the boundary of Mt Kanla-on Natural Park, where the Negros Bleeding-heart was seen in 1991 (Brooks et al. Reference Brooks, Evans, Dutson, Anderson, Asane, Timmins and Toledo1992), but not since (Cariño Reference Cariño2007). Furthermore, most of the park’s forest is >1,000 m asl. (Brooks et al. Reference Brooks, Evans, Dutson, Anderson, Asane, Timmins and Toledo1992), which exceeds the estimated altitudinal limit of the dove based on previous surveys (BirdLife International 2017). Any populations just outside the boundary would be threatened by the continued deforestation on the lower slopes (BirdLife International 2018d), demonstrating that the current boundaries of Mt Kanla-on Natural Park may not be adequate to protect this species. Of the non-protected IBA sites, the largest indicated suitable area is around the Cuernos de Negros IBA, half within the reserve and the rest just outside the borders. Cariño (Reference Cariño2007) recorded the dove several times near the border, and it was reported inside the IBA in the CCI (2016). It has also been recorded on www.ebird.org by two observers in 2019 at Sibulan, within the IBA. However, the CCI survey lasted only four days in 2016, and another nine-week survey in the same area in 2017 failed to encounter the dove (Cantero-Sanchez Reference Cantero-Sanchez2018). Furthermore, Bristol Zoological Society studied the wider Cuernos de Negros IBA in 2014–2017, obtaining a minimum of 347 camera trap days, and the Negros Bleeding-heart was never sighted (Falcidia Reference Falcidia2017). It is therefore possible that the dove may not occur at high density or even be present in much of the Cuernos de Negros IBA, given the high elevation of this area. Hence, this may not be a priority site in the conservation of Negros Bleeding-heart. As far as we are aware, there are no other recent sightings of this species in Negros, but the recent publication of a conservation action plan for Negros (Biodiversity Management Bureau and Philippines Biodiversity Conservation Foundation Inc 2018) shows promise for future collaboration between NGOs to organise effective conservation initiatives.
Based on the number of sightings obtained in this study compared to other recent studies on Negros, and from the species distribution modelling results, the Northwest Panay Peninsula Natural Park appears to be the most effective currently protected area on Panay and Negros for the Negros Bleeding-heart. It is therefore a critical stronghold for the species, requiring continued conservation action, which is ongoing (PhilinCon 2018). Furthermore, there appear to be large areas of potentially suitable habitat for the Negros Bleeding-heart around and within the Central Panay Mountain Range, although this is not yet a formally protected area (Haribon Foundation 2016). The Negros Bleeding-heart has been reported there by several sources (De Soye Reference De Soye1997, Pedregosa-Hospodarsky Reference Pedregosa-Hospodarsky2008, Masur Reference Masur2010, Schwarz Reference Schwarz2014), but to our knowledge, no population survey has been undertaken. Therefore, this area is a priority for survey effort, particularly considering the likely extreme rarity of the Negros Bleeding-heart on Negros.
Finally, species distribution modelling shows that the suitable habitat patches throughout Panay and Negros are not well connected. Habitat connectivity is important for maintaining small populations (Kramer et al. Reference Kramer, Dennis, Liebhold and Drake2009, Spigler et al. Reference Spigler, Theodorou and Chang2017, Gómez-Sánchez et al. Reference Gómez-Sánchez, Olalde, Sastre, Enseñat, Carrasco, Marques-Bonet, Lalueza-Fox, Leonard, Vilà and Ramírez2018) and therefore the creation of forest corridors to connect fragments (Jansen Reference Jansen2005, Barzan et al. Reference Barzan, Baigorria and Bó2015) could benefit the Negros Bleeding-heart, particularly considering that understorey birds are reluctant to cross non-forested patches (Bradfer-Lawrence et al. Reference Bradfer-Lawrence, Gardner and Dent2018). However, certain fragments are very distant, hence forest corridor creation may not be immediately practical at large scales, and work that can be implemented more quickly may be required. To that end, an option which is increasingly used to support in situ conservation of small animal populations is captive breeding, with the aim of future reintroduction (Braverman Reference Braverman2014). Negros Bleeding-heart is currently bred in captivity at the Centre for Tropical Conservation Studies (CENTROP) in Negros, and by Talarak Foundation Incorporation, with an overall captive population of 88 individuals in June 2020 (Fernando ‘Dino’ Guttierez at Talarak, and Lou-Jean Cerial at CENTROP pers. comm.). We recommend that this work continues alongside in situ conservation measures.
Model comparison
The GLM and species distribution modelling approaches respectively offer fine- and large-scale explorations of Negros Bleeding-heart distribution. We selected tree cover and elevation as variables in the species distribution modelling because the Negros Bleeding-heart has been reported to occur in lowland forests up to 1,000 m (BirdLife International 2017). Ideally, understorey cover, the most significant variable in the GLM, would have been used in the species distribution modelling, but large-scale datasets of understorey cover are not available. Elevation may act as a proxy for other, unmapped, biotic, and abiotic variables, rather than directly impacting the Negros bleeding-heart (Hof et al. Reference Hof, Jansson and Nilsson2012). In addition, the tree cover dataset used does not distinguish forest quality or between primary and secondary forest (Hansen et al. Reference Hansen, Potapov, Moore, Hancher, Turubanova, Tyukavina, Thau, Stehman, Goetz, Loveland, Kommareddy, Egorov, Chini, Justice and Townshend2013). Whilst it is unknown if the Negros Bleeding-heart requires primary forest (BirdLife International 2017), if this is the case, then our species distribution modelling maps (Figure 5), which already indicate very little remaining suitable habitat, may be an optimistic overestimate.
Finally, this survey was designed for habitat preference assessment rather than an occupancy type analysis. We therefore did not utilise repeated sampling in a way that would allow us to make use of species distribution modelling approaches that use known absences (Lahoz-Monfort et al. Reference Lahoz-Monfort, Guillera-Arroita and Wintle2014). The authors recognise that detection of the Negros Bleeding-heart is not perfect and are conducting systematically repeated sampling as part of future research to enable modelling of the detection function and use of occupancy detection modelling.
Conclusion
The Negros Bleeding-heart has a preference for dense understorey vegetation and dense canopy cover, and the largest area of suitable habitat currently seems to be in the Northwest Panay Peninsula Natural Park on Panay. On Negros, Mt Kanla-on Natural Park may contain habitat for the Negros Bleeding-heart, although the elevation is high, and further protection of the North Negros Natural Park’s eastern border is needed. Though law enforcement in remote areas entails logistical and security challenges, it is essential that laws against deforestation and hunting in all remaining population refuges are strictly enforced in order to halt the decline in numbers. In addition, we recommend that future research effort focuses on two areas: 1) to establish the degree to which the Negros Bleeding-heart requires primary rather than secondary forest, and 2) to assess its population status in the Central Panay Mountain Range and the North Negros Natural Park, which may be suitable sites for Negros Bleeding-heart conservation.
Supplementary Material
To view supplementary material for this article, please visit http://dx.doi.org/10.1017/S0959270920000611.
Acknowledgements
The authors thank everyone at PhilinCon for making this study possible: guides Potpot Fernandez and Jun Tacud, Rhea Santillan for helping organise the logistics, the Sibaliw research station staff, and porters, including Momel, Ulysses and Dudong, Professor Dr Eberhard Curio (PhilinCon President) and Justine Magbanua. Our thanks go to Christian Schwarz (PhilinCon) for helpful comments on the manuscript, and to Dr Tim Bray for species distribution modelling advice. We especially thank D. Hending (University of Bristol/Bristol Zoological Society), for cleaning the xeno-canto calls for the playbacks. We are grateful to the local barangays and the Department of Environment and Natural Resources (DENR) for permission to conduct research in the Northwest Panay Peninsula Natural Park. We also thank two anonymous reviewers for their thoughtful and helpful comments and suggestions. This research was financially supported by Bristol Zoological Society, Airbus and the University of the West of England.
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