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Forest Plant and Bird Communities in the Lau Group, Fiji

  • Janet Franklin ,

    Janet.Franklin@asu.edu

    Affiliation School of Geographical Sciences and Urban Planning and School of Life Sciences, Arizona State University, Tempe, Arizona, United States of America

  • David W. Steadman

    Affiliation Florida Museum of Natural History, University of Florida, Gainesville, Florida, United States of America

Abstract

Background

We examined species composition of forest and bird communities in relation to environmental and human disturbance gradients on Lakeba (55.9 km2), Nayau (18.4 km2), and Aiwa Levu (1.2 km2), islands in the Lau Group of Fiji, West Polynesia. The unique avifauna of West Polynesia (Fiji, Tonga, Samoa) has been subjected to prehistoric human-caused extinctions but little was previously known about this topic in the Lau Group. We expected that the degree of human disturbance would be a strong determinant of tree species composition and habitat quality for surviving landbirds, while island area would be unrelated to bird diversity.

Methodology/Principal Findings

All trees >5 cm diameter were measured and identified in 23 forest plots of 500 m2 each. We recognized four forest species assemblages differentiated by composition and structure: coastal forest, dominated by widely distributed species, and three forest types with differences related more to disturbance history (stages of secondary succession following clearing or selective logging) than to environmental gradients (elevation, slope, rockiness). Our point counts (73 locations in 1 or 2 seasons) recorded 18 of the 24 species of landbirds that exist on the three islands. The relative abundance and species richness of birds were greatest in the forested habitats least disturbed by people. These differences were due mostly to increased numbers of columbid frugivores and passerine insectivores in forests on Lakeba and Aiwa Levu. Considering only forested habitats, the relative abundance and species richness of birds were greater on the small but completely forested (and uninhabited) island of Aiwa Levu than on the much larger island of Lakeba.

Conclusions/Significance

Forest disturbance history is more important than island area in structuring both tree and landbird communities on remote Pacific islands. Even very small islands may be suitable for conservation reserves if they are protected from human disturbance.

Introduction

The 25,000+ islands in the tropical Pacific Ocean represent discrete terrestrial habitats that vary greatly in size, isolation, origin, and age [1], [2]. Not surprisingly, the region has major geographical gaps in quantitative studies of the terrestrial biotic communities [1], [3]. This paper addresses one of those gaps in West Polynesia (WP), a region that includes Fiji, Tonga, Samoa, and the outlying islands of Rotuma, Wallis & Futuna, and Niue. People have occupied WP for nearly 3000 years [4], [5], resulting in the prehistoric reduction of forest cover [6], [7], [8], the introduction of non-native plants and animals [9], and the loss of populations (extirpations) and species (extinctions) of reptiles, bats, and birds [1], [9], [10], [11]. These impacts must be considered when interpreting the modern diversity and distribution of plants and animals, and thus are informative in conservation planning and management [12], [13], [14].

This paper concerns the Lau Group in Eastern Fiji (Figure 1), which lies between the much larger and geologically older Fijian islands 100–200 km to the west and the more remote Tongan islands 300–350 km to the east. Excluding the geologically unrelated, eroded volcanic islands of Moala, Totoya, and Matuku, the Lau Group consists of 54 named islands (35 of them >1 km2) totaling 376 km2 of land. The plant communities of the Lau Group have been described qualitatively [e.g.], [ 15,16], although no quantitative forest composition data have previously been reported. Birds of the Lau Group have been, until recently, perhaps the most poorly known in WP. Mentioned in a very general way in Watling [17], [18], Clunie [19], and Pratt et al. [20], the relative abundance and habitat relationships were unstudied until our first point-count surveys on Lakeba in 1999 [1], [21]. During 2000 and 2001, we made additional point counts on Lakeba, and on Nayau and Aiwa Levu, allowing us to consider variation in bird community abundance and composition among seasons, islands and habitats.

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Figure 1. Map of Fiji.

Box shows location of the islands surveyed in Central Lau.

https://doi.org/10.1371/journal.pone.0015685.g001

Quantitative descriptions of WP forest communities exist for Tonga [22], [23], [24], [25], Samoa [26], [27], [28], [29], and western Fiji [30], [31], and in a few cases have been related to habitat quality for vertebrates [32], [33], [34]. In this paper we examine variation in species composition of woody plant and bird communities in forests on the Lau islands of Lakeba, Nayau, and Aiwa Levu. We analyze tree abundance data from forest plots to characterize variation in native forest habitats in relation to topographic and human disturbance gradients, examine differences in landbird abundance and community composition among tree-dominated habitats (including pine plantation and agroforestry), islands, and seasons, and then compare our results with those from similar studies elsewhere in WP and other tropical forest communities.

Because prehistoric and historic deforestation has been a major driver of vertebrate extirpations and extinctions in WP [1], we expected that the human disturbance gradient (agroforestry, plantation forestry, and native forest at varying stages of secondary succession) would be a strong determinant of habitat quality for landbirds [32], [33], [35] as well as tree species composition [22]. Those previous studies found that on oceanic islands with long histories of human impact, the composition of ecological communities varies to a greater degree as a function of the intensity of human disturbance than it does along environmental gradients (substrate, topography), especially when those environmental gradients are short.

We also expected, based on our previous findings in Tonga [36] and other archipelagos [1], that island area might not be positively related to bird species richness over the range of island sizes considered. A null model for species-area relationships of landbirds in Oceania [1] states that every species known to inhabit an island group should occur on each high island (non-atoll) of a certain minimum land area within that archipelago, and the findings in [36] were consistent with this null model. As noted in [36] and references therein, nonsignificant correlations between species number and area may be underreported in the literature, although they would be as informative about species-area relationships as positive correlations.

Methods

Study Area

Lakeba (18°14′ S, 178°48′ W; 55.9 km2; Figure 1) has an andesitic volcanic center of Miocene age [37] that is over 200 m maximum elevation, with uplifted limestone exposed on its western (leeward) side that covers ca. 4% of the island [16]. Deforestation for subsistence agriculture probably began soon after people first arrived about 2800 years ago [38]. As a result, nearly all forest in the volcanic uplands has been replaced by talasiga (a fire-degraded, herbaceous and shrubby community dominated by ferns and grasses) or, in recent decades, by pine plantations [15], [16]. Remnant native forest covers ca. 10% (<6 km2) of Lakeba in patches on coastal limestone outcrops and in small ravines on the volcanic hillsides [16], [39].

Nayau (17°58′ S, 179°03′ W; 18.4 km2) is 28 km NW of Lakeba (Figure 1). Also a composite of exposed volcanic rock and weathered limestone [37], Nayau has the “wedding cake” profile of many raised limestone islands [2]. The central plateau is a shallow depression (<100 m elevation) with cultivated volcanic soils [40]. This plateau is surrounded by a discontinuous ring of tiered, uplifted limestone (160 m maximum elevation) that sustains most of the remaining forest on Nayau.

Lying at 18°19′ S, 178°42′ W (12 km SSE of Lakeba) are the twin islets of Aiwa Levu (1.2 km2, ∼50 m elevation) and Aiwa Lailai (∼1 km2, ∼30 m elevation). They are composed entirely of limestone, surrounded by extensive reefs, and separated from each other by a narrow (∼100 m), shallow passage [41]. These islets are currently uninhabited and completely forested, although the forest understory is very disturbed by goats, with likely impacts on forest regeneration [42]. We were able to survey the vegetation and birds on Aiwa Levu but not Aiwa Lailai.

With slightly more than 2000 mm mean average rainfall at Tubou village, Lakeba, the climate in this part of Lau is transitional between “tropical wet” and “wet seasonal” [43]. Mean monthly rainfall is <100 mm only for the three winter months (June-August), with large interannual variation [16]; the forests are dominated by evergreen rather than deciduous species [e.g.], [ 30,44]. Tracking the rainfall pattern, the “small island” forests [3] of Lau are transitional in structure and composition between tropical rain forest and tropical dry forest. Of the 449 species of plants recorded thus far from Lakeba, Nayau, and Aiwa Levu, 161 (36%) are introduced and 41 (14% of the 288 indigenous species) are endemic to Fiji [39]. In this study we quantified the compositional variation of native forest (the numbered groups in Table 1), and then examined the landbird communities in tree-dominated habitats including successional stages of native forest and semi-natural and cultural (agroforestry, plantation forestry) forests, as in our preliminary study [21].

The modern avifauna of the Lau Group is dominated by species that are widespread in WP. The Lau Group lacks most of the species of landbirds found on the six largest, western Fijian islands. Only two (Mayrornis lessoni, Myzomela jugularis) of the 21 species that occur on Lakeba, the largest island in Lau and the tenth largest in Fiji, are endemic to Fiji. Of the 24 species of landbirds that inhabit the entire Lau Group today, the only one endemic to Lau is Mayrornis versicolor, a monarch confined to Ogea Levu [1: Table 6–5].

Forest Community Data and Analysis

In 1999–2001, we established 23 vegetation plots in coastal and lowland forests [sensu 39], including 12 on Lakeba, seven on Nayau, and four on Aiwa Levu. Although vegetation sampling was not even among islands, it was roughly proportional to their forested area. The plots on Lakeba were located in two main areas of coastal limestone outcrops – Tarakua (SE of Tubou village) and Vagadra (SW of Nasaqalau village). The plots on Nayau were located on limestone escarpments on the eastern, southern, and western sides of the island, in the vicinities of the three villages. The plots on Aiwa Levu were located in the central and eastern portions of the island. Difficulties with logistics of travel, accommodation, and health limited our data collection in these remote islands.

Plot locations reflected gradients of human disturbance (different distances from habitation and cultivation) and environment (with varying slopes, rockiness and elevations). The plot size of 500 m2 (10×50 m) is adequate to capture patterns of tree species composition in small forest patches, and is similar to the plot size used in forest vegetation sampling elsewhere in Polynesia [22], [29], [45]. Data collection methods were also very similar to those used in the region [24]. All tree stems with diameter at breast height (DBH; 1.3 m) >5 cm were measured and identified to species. For each plot, we also recorded: a) elevation (m) from 1∶25,000 topographic maps; b) slope aspect (degrees), the direction that the slope faces measured by compass and converted to a northness index for analysis using a cosine transform; c) slope angle (degrees), the steepness of the slope measured by clinometer; d) rockiness (% of ground covered by exposed limestone); and, e) canopy height, estimated by averaging the height of 3–5 tall trees measured using a clinometer and tape measure.

Tree species accumulation with total surveyed area was examined to estimate the extent to which the sample (23 plots) captured the forest community species pool, in order to confirm that the small sample is representative of compositional variation. An asymptotic species accumulation curve would suggest that the sample adequately described the community. Clustering [46] was applied to the species-by-plot matrix to detect groups of plots with similar species composition based on Bray-Curtis distance calculated from relative abundance (percent basal area by species), using group averaging as the linkage method [47]. The multi-response permutation procedure [MRPP; 48] tested for the significance of differences in composition among groups of plots delineated by clustering. Then, in order to interpret and describe the composition of the resulting forest groups, indicator species analysis [49] was carried out to identify those species uniquely associated with, and thus characterizing, each group. The significance of each identified indicator species' indicator values (the average of relative abundance and relative frequency) was determined by simulation.

Species and environmental data were then subjected to constrained multivariate ordination using partial Canonical Correspondence Analysis [pCCA], [ 50,51] in order to identify environmental correlates of compositional variation among plots and groups of plots. The effect of island (treated as a covariable) was first removed from the species-by-plot community matrix because a comparable range of environmental conditions did not occur on each island. Then the residual community matrix was subjected to ordination constrained by the environmental variables.

Bird Community Data and Analysis

Our point-count methods were identical or very similar to those used elsewhere in the region [35], [52]. During 9–15 May 1999 (dry season, Lakeba), 21 February – 6 March 2000 (wet season, Lakeba and Aiwa Levu), and 23–24 October 2001 (dry season, Nayau), we recorded each bird seen or heard within a fixed 50-m radius over a five-minute period at 42 points on Lakeba, 16 points on Nayau, and 15 points on Aiwa Levu. These points were located in the six tree-dominated cultural and native habitats listed in Table 1 (last column). The point counts done on Lakeba in May 1999 [published in 21] were repeated in February-March 2000, whereas only a single count was done at each point on Nayau and Aiwa Levu. Most point counts were done jointly by DWS and JF; a few were by DWS alone. Birds detected at distances >50 m were noted but not included in the analyses. The point-count transects in anthropogenic habitats (Coastal Coconut Plantation, Pure Pine Woodland; Table 1) followed trails or dirt roads to allow rapid, quiet travel between stations. Point-count stations in native forest were not along trails; walking through this rugged limestone terrain was noisier than in other habitats, so we waited two minutes at each station in forest before beginning the count period. Because the swiftlet Collocalia spodiopygia vocalizes irregularly and is much easier to detect (visually) in open habitats than in forests, we do not include its data in the total relative abundance values.

Each point-count station was at least 150 m apart from any other. Each point count was done within ca. 3 hr of sunrise (0552-0857 hr on Lakeba, 0531-0734 hr on Nayau, and 0620-0834 hr on Aiwa Levu). While we report all of these data, we provide interisland comparisons only for the February-March 2000 (wet season) data of Lakeba vs. Aiwa Levu, thereby eliminating the potential effects of seasonality and interannual variability. Avian taxonomy and nomenclature follow that of Steadman (2006).

We examined the variation in species richness and abundance of landbirds by season (fixed effect) and habitat type (nested within seasons) for Lakeba using generalized linear mixed effects Poisson models (for count data). Because these estimates of species richness per habitat are biased by unequal sample sizes (point counts per habitat), we also carried out rarefaction analysis to interpolate estimated species richness to equal sample sizes. We used the function rarefy in the package vegan of the R software [53]. This function is based on Hurlbert's formulation [54], and the standard errors on Heck et al. [55].

We also compared abundances of functional (feeding) guilds of landbirds, including columbid frugivores/granivores, passerine insectivores, and nectarivores, between seasons (fixed effect) and among habitats (nested within season) on Lakeba using Poisson generalized linear mixed effects models for count data. Then we compared the species richness and abundance of forest-obligate guilds (passerine insectivores and columbids) on Lakeba vs. Aiwa Levu based only on the 2000 wet season data (collected during the same months on both islands) and only for point counts in native forest habitat (roughly equal samples and therefore not requiring rarefaction), using non-parametric Kruskal-Wallis tests.

These were the only statistical comparisons of bird data we made owing to the unbalanced sampling (over islands, habitats and time); other patterns are described qualitatively. Although the comparisons of abundances of species or guilds among habitats and islands may be affected by species-specific detectability that can vary by habitat [56], we did not estimate detectability [as in 57] given our small sample. Nevertheless, based on our double-observer approach to estimate relative abundance [see 58] and our familiarity with WP landbirds (surveys on 50+ islands in Fiji, Tonga, and Samoa), the only common species that is vocally inconspicuous is the forest is the swiftlet Collocalia spodiopygia which, as already mentioned, was excluded from the comparisons.

Results

Tree Community Composition

We recorded 85 species of trees >5 cm DBH in the 23 Lau forest plots, including eight of indeterminate identity (Supplementary Table S1). Based on the asymptotic pattern of species accumulation in the plots (Supplementary Figure S1), we concluded that the sample was reasonably adequate to describe forest composition; the estimated number of species in the sampled forests is 112-127 using first- and second-order jackknife estimates [59].

Clustering identified four groups of plots, although they overlap somewhat in species composition (Table 2). MRPP indicates, however, that the groups are distinctive (P≪0.001), having within-group homogeneity typical of plant community data (A = 0.207). Partial CCA showed that the contribution to the mean square contingency coefficient of the conditioning factor, Island, was 16% and of the constraining environmental variables was 17%. The percent contribution of the first three pCCA axes to the contingency coefficient, after removing the contribution of Island, was 7%, 7% and 3%, respectively. pCCA Axis 1 is significantly (α = 0.1) positively correlated with slope angle and negatively with elevation, Axis 2 is negatively correlated with rockiness, and Axis 3 is correlated canopy height (Table 3). However, a permutation test showed the overall effect of the environmental variables to be insignificant. These results suggest that variation in forest composition among plots is only weakly related to the measured gradients of forest structure and topography, although some differences among groups are suggested by the data (Table 4) and will be described.

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Table 2. Basal area (BA; m2/ha) of selected species in groups of plots within Forest types (Table 1).

https://doi.org/10.1371/journal.pone.0015685.t002

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Table 3. Correlations (intra-set) of environmental variables with partial Canonical Correspondence Analysis (pCCA) ordination axes 1-3.

https://doi.org/10.1371/journal.pone.0015685.t003

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Table 4. Mean values (and standard deviation) of environmental and forest structural characteristics of four groups of forest plots in Lau.

https://doi.org/10.1371/journal.pone.0015685.t004

Aiwa Levu supports a unique forest type, distinctive from those on the other two islands. Group 1 corresponds to Coastal Forest and includes four plots (all from Aiwa Levu) with shorter canopies, and occurring at lower elevations and on gentler slopes than in the other plots (Table 4). Group 1 has a diverse overstory (Table 2), with several species (Xylosma simulans, Dysoxylum richii, Pouteria grayana, Maniltoa floribunda) of large size (up to 60 cm DBH; up to 100 cm DBH for Pisonia grandis; Figure 2). Important smaller trees include Aglaia saltatorum and Diospyros elliptica. Because Aiwa Levu is so small (1.2 km2) and low (∼50 m elevation), a strong littoral (coastal) component to this forest is seen in the occurrence of species such as Guettarda speciosa, Neisosperma oppositifolium, Pandanus tectorius, and Barringtonia asiatica.

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Figure 2. Coastal forest on Aiwa (Group 1).

Large Pisonia grandis in center of photo. Photo by JF 11 Mar 2000.

https://doi.org/10.1371/journal.pone.0015685.g002

Group 2, Secondary Forest (Table 1), consists of three plots from Lakeba (Tarakua) and six from Nayau (Figure 3), all dominated by Alphitonia zizyphoides, Dysoxylum richii, and Pleiogynium timoriense, with Melicope cucullata abundant only in one plot (Table 2). Alangium vitiense, Cryptocarya hornei, and Maniltoa floribunda were regenerating in the understory. The dominant A. zizyphoides is an early-successional tree, as is the less common pioneer Macaranga spp. [60], [61]. These plots appeared to be disturbed from selective logging, cyclones, or regeneration following cultivation based on the occurrence of tree stumps, coppicing, and cultivated tree species. Cultivated or preserved trees noted in or near Group 2 plots include Annona muricata, Barringtonia edulis, Cocos nucifera, Citrus spp., Mangifera indica, Pometia pinnata, and Bischofia javanica. The Secondary Forest plots have slightly greater canopy height than the other groups (Table 4); they were found on somewhat less rocky sites than the Mid-successional Forest plots (Groups 3), and therefore were more likely to have been cleared for cultivation in the past.

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Figure 3. Secondary Forest on Nayau (Group 2).

View of coastal plain of Nayau from escarpment at Korobuca, showing Secondary forest (smooth canopy texture) interspersed with Coastal Coconut Plantation. Photo by JF 24 Oct 2001.

https://doi.org/10.1371/journal.pone.0015685.g003

Group 3 represents Mid-successional Forest (Table 1) and includes seven plots on Lakeba and one on Nayau. These plots are dominated by a few very large Gyrocarpus americanus, with abundant Dysoxylum richii and/or D. tenuiflorum (Figure 4; Table 2). Cryptocarya hornei and Pouteria grayana are shade-tolerant species [61] that were regenerating in these plots. This forest occurs on rocky sites (Table 4). The two Group 4 plots, found in the Tarakua and Vagadra areas of Lakeba, also have abundant D. tenuiflorum but are distinguished from Group 3 by the presence of the large banyan, Ficus prolixa (Figure 5), as well as Buchanania vitiensis and Phaleria pubiflora (Table 2). Group 4 plots (also Mid-successional Forest) have shorter canopy height and extremely high basal area (owing to the banyans), and are found at somewhat lower elevations (nearer the coast), than those of Groups 2 or 3 (Table 4).

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Figure 4. Mid-successional Forest (Group 3).

View upward through Dysoxylum-dominated canopy at Vagadra, Lakeba. Photo by JF 7 Nov 2000.

https://doi.org/10.1371/journal.pone.0015685.g004

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Figure 5. Mid-successional Forest (Group 4).

View upward through canopy of a large banyan (Ficus prolixa) at Vagadra, Lakeba. Photo by JF 20 Feb 2000.

https://doi.org/10.1371/journal.pone.0015685.g005

Landbird Community Composition, Habitat Association, and Abundance

The relative abundance of landbirds on Lakeba (Table 5) was not significantly different between seasons (fixed effect; P = 0.652) but differed among habitat types (nested within seasons; P≪0.001). This was primarily because abundance was lower in Pure Pine Woodland than in Mid-successional Forest (Figure 6). Although seasonal differences in total abundance were not significant overall, the data suggest that in modified habitats (Coastal Coconut Plantation and Pure and Mixed Pine Woodland) we detected more species in the wet season than the dry season (Table 5).

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Figure 6. Box plots showing frequency distribution of abundance and richness of landbird communities in habitats on Lakeba.

Frequency distribution of overall abundance, abundance of nectarivores (point counts), and overall species richness (number of species per point) per habitat (wet and dry season surveys lumped). Boxplots show the median (heavy line), quartiles (box) and 5th/95th percentiles (whiskers). Habitat categories are: Coconut  =  Coastal Coconut Plantation; MidFor  =  Mid-successional Forest; MixedPine  =  Mixed Pine Woodland; PurePine  =  Pure Pine Woodland; SecFor  =  Secondary Forest (see Table 1).

https://doi.org/10.1371/journal.pone.0015685.g006

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Table 5. Relative abundance of forest birds during the wet (18 February-6 March 2000) and dry season (10-15 May 1999) on Lakeba (five habitats) and Aiwa Levu (single habitat, single season).

https://doi.org/10.1371/journal.pone.0015685.t005

Differences in the abundance of columbid frugivores and granivores (pigeons and doves, i.e., Ducula pacifica, Ptilinopus perousii, P. porphyraceus, Gallicolumba stairi) were marginally significant among seasons (P = 0.083) and highly significantly among habitat types on Lakeba (P≪0.001), with more individuals recorded in the dry season, and more found in Mid-successional Forest than in any of the more disturbed habitats including Secondary Forest (Figure 7; Table 5). Similarly, the abundance of passerine insectivores (Mayrornis lessoni, Myiagra vanikorensis) was significantly greater in the dry season (P = 0.020), with more found in Mid-successional Forest than in either Pure Pine Woodland or Coastal Coconut Plantation (Figure 7). The relative abundance of passerine nectarivores (Myzomela jugularis, Foulehaio carunculata) was not significantly different between seasons (P = 0.53) but significant differences among habitats (P≪0.001) were the result of much higher abundance in Coastal Coconut Plantation than in any other habitat on Lakeba (Figure 6).

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Figure 7. Box plots showing frequency distribution of abundance of guilds in habitats on Lakeba in the dry versus wet season.

Passerine insectivores and columbid frugivores/granivores (point counts) in habitats for Lakeba in the dry season (May, top row) vs. wet season (Feb-Mar, bottom row). Habitat categories are defined and box plots explained in the caption of Figure 6 (see also Table 1). Note different scales on y-axes.

https://doi.org/10.1371/journal.pone.0015685.g007

Although overall species richness was not significantly different between seasons on Lakeba (P = 0.66), average richness per point differed among habitats (P≪0.001) with a pattern that mirrored overall abundance (Figure 6), i.e., richness was greater in habitats with native trees than in purely anthropogenic habitats (Coastal Coconut Plantation, Pure Pine Woodland). This conclusion is unaffected by unequal sampling among habitats on Lakeba; total species richness estimated by rarefaction based on data pooled by seasons was lowest in Coastal Coconut Plantation (5.76±0.45) and Pure Pine Woodland (7), intermediate in Secondary Forest (8.50±0.61), and highest in Mixed Pine Woodland (9.88±1.08) and Mid-successional Forest (10.87±0.84) where richness was estimated for the lowest pooled abundance of 57 individuals detected (for Pure Pine Woodland). Average abundance (P<0.001) and species richness (P<0.001) were significantly greater on tiny Aiwa Levu than on much larger Lakeba when only forested habitats surveyed at the same time (wet season, Feb-Mar 2000) were compared (Table 5; Figure 8).

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Figure 8. Box plots showing frequency distributions of forest birds of Lakeba versus Aiwa Levu in the wet season.

Overall landbird abundance, abundance of columbid frugivores/granivores, abundance of passerine insectivores (point counts), and species richness (number of species) are shown (both islands sampled in Feb-Mar 2000). This comparison only includes points counts within native forest; 15 in Coastal Forest on Aiwa Levu, and 16 in Secondary Forest (12) + Mid-successional Forest (4) on Lakeba (Table 2). Note differences in scales on y-axes.

https://doi.org/10.1371/journal.pone.0015685.g008

The overall relative abundance of birds among habitats on Nayau could not be analyzed statistically owing to limited sampling. Only three species were common in Mid-successional Forest on Nayau (the dove Ptilinopus porphyraceus, swiftlet Collocalia spodiopygia, and honeyeater Foulehaio carunculata). The latter was abundant in Coastal Coconut Plantation (75% of all individual birds detected on Nayau) because the coconut trees were flowering heavily in October. The overall scarcity of birds in Mid-successional Forest on Nayau stands in stark contrast to the situations in similar habitats on Lakeba and Aiwa Levu (Table 5 vs. Table 6).

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Table 6. Relative abundance of birds on Nayau, Lau Group, Fiji.

https://doi.org/10.1371/journal.pone.0015685.t006

Discussion

Forest Communities

The composition of forests surveyed on Lakeba and Nayau varied somewhat with topographic gradients, but much more with degrees of human disturbance, i.e., stages of secondary succession after clearing for agriculture or settlement, or other less intensive forms of forest disturbance, such as selective logging. Agricultural people settled these islands nearly 3000 years ago, and inland fortified sites were occupied for several periods as recently as 200 years ago [38], [40]. Thus forests were cleared even in upland rocky areas that are not agriculturally productive, and that now support relatively mature forest, such as at Vagadra on Lakeba [38]. Long-term cultivation in tropical forest sites affects community composition [62], [63]. With a multi-millenial agricultural history, forests in West Polynesia (WP) that retain old-growth characteristics occur in patches only in the most remote, inaccessible sites [23], [30], [32].

All of the 19 plots surveyed on Lakeba and Nayau fall within the Limestone Forest community (Table 1). We differentiated three forest types by the dominance of either Alphitonia zizyphoides (Secondary Forest; Group 2), Gyrocarpus americanus and Dysoxylum spp. (Mid-successional Forest; Group 3), or Ficus prolixa (Mid-successional Forest; Group 4). Alphitonia zizyphoides is an important early-successional tree in the region [61], [64], [65]. The widespread occurrence of Cryptocarya hornei, in contrast with the low frequency of Macaranga spp., suggests that Group 2 Secondary Forest sites have been regenerating for at least several decades. Species of Cryptocarya are typically shade tolerant [65], [66], [67] and do not establish in WP forests immediately following large scale disturbance; species of Macaranga are short lived, fast growing pioneers, and dominate only in the first decade or two after disturbance [61], [66], [68], [69], [70]. Lacking Alphitonia, Cryptocarya, and Macaranga, the two Group 4 plots represent the most mature forest sampled on Lakeba. Group 3 Mid-successional Forest shares its strong dominance by deciduous Gyrocarpus americanus with dry forest described for western Fiji [34].

While it is commonly recognized that forests on small islands can sustain endemic and endangered species of vertebrates [21], [71], the importance of such forests for endangered or even undescribed species of plants is less well appreciated. Even our limited sampling in Lau turned up two putative new species of Syzygium (Myrtaceae) [Table 2, and see 39]. Large forest trees including Intsia bijuga, Burckella richii, and Callophyllum vitiense are selectively cut on Nayau for house and boat building, so the forest there continues to lose its old growth characteristics.

Inter-island Comparisons of Bird Communities in Lau

The relative abundance and species richness of birds on Lakeba are greatest in Mid-successional Forest, the habitat least affected by people. This is mostly due to increased numbers of columbids and passerine insectivores. By contrast, the relative abundance of passerine nectarivores is greatest in disturbed habitats with many coconut trees [cf. [72]]. In the two habitats most affected by people (Coastal Coconut Plantation, Pure Pine Woodland), we detected more individuals and species in the wet season than the dry season. In the Mid-successional Forest, by contrast, more individuals and species were detected in the dry season, in part because of increased vocalization by columbids, as has been reported in Samoa [33]. This may be only a seasonal difference in detectability rather than an actual population increase of columbids during the dry season.

Habitat quality influenced the landbird communities more than island area. Both richness and abundance of birds in forest were greater on very small Aiwa Levu than on Lakeba. This is in spite of the fact that Aiwa Levu's forest is more coastal in composition than Lakeba's (Table 2), and typically WP landbird abundance and diversity is lower in coastal forest with more littoral characteristics than in inland lowland forest [35]. Lakeba is mostly deforested and has 2500 people as well as chickens (Gallus gallus), Pacific rats (Rattus exulans), black rats (R. rattus), cats (Felis catus), dogs (Canis familiaris), horses (Equus caballus), pigs (Sus scrofa), and cows (Bos taurus). Aiwa Levu is uninhabited, 100% forested, and lacks non-native mammals except Pacific rats and goats (Capra hircus). To what extent the differences in non-native vertebrates affects the abundance and diversity of landbirds is not known. Columbids and passerine insectivores are more abundant per unit area on Aiwa Levu than on Lakeba (Table 5; Figure 8). Two species found on Aiwa Levu (Falco peregrinus, Clytorhynchus vitiensis) seem to be extirpated on Lakeba; Myzomela jugularis is the only species found in native forest on Lakeba that we did not detect on Aiwa Levu.

Nayau is mostly deforested and has 430 people as well as chickens, rats (species uncertain), cats, dogs, horses, pigs, and cows. From our brief visit in October 2001, the most distinctive aspects of Nayau's landbird fauna are the presence of the pigeon Ducula latrans (absent on Lakeba and Aiwa Levu) and an apparent island-wide absence or rarity of the passerines Lalage maculosa, Mayrornis lessoni, Clytorhynchus vitiensis, and Myiagra vanikorensis, which inhabit the other islands (except that we did not detect C. vitiensis on Lakeba).

Many bird populations on Pacific islands have been extirpated as a result of prehistoric human impacts [1], [73]. Because contemporary bird communities are also influenced by human impacts, which affect some islands more than others, we would expect prehistoric avifaunas to have been more similar in composition among the Lau islands than they are now [e.g., [1]]. Some data on prehistoric bird bones are available from our study islands although these data are compromised by large inter-island differences in the number of identified fossils and the ages of the sites [40]. Nevertheless, prehistoric bones increase the landbird fauna from 21 to 27 species on Lakeba, 18 to 20 species on Nayau, and 18 to 26 species on Aiwa Levu [1: Tables 6–5, 6–8]. On no single island in Lau is the fossil record nearly as thorough as that from the seven Tongan islands, ranging in size from 2–260 km2, where the prehistoric number of bird species varied little with island area before human impact [shown by rarefaction–based species–area calculations; [36]]. Therefore, it is not yet possible to say anything conclusive about the relationship between bird species richness and island area in central Lau, especially given that only on these three islands have modern or prehistoric avaifuanas been sampled. We note, however, that prehistoric species richness values are nearly identical on relatively large Lakeba and small Aiwa Levu.

Conclusions

We identified variation in the composition of forest in Lau that corresponds to a gradient of habitat quality and degree of human disturbance. We discovered that the level of forest maturity is more important than island area in shaping the forest landbird communities of Lau. This effect is especially strong for pigeons and doves (which are important seed dispersers in Oceania [74], [75]) and passerine insectivores (the foraging ecology of which is not well known). Species richness and relative abundance of birds in the most mature forest types were higher on very small Aiwa Levu than on nearby Lakeba, which is more than an order of magnitude larger than Aiwa Levu and has ca. five times as much native forest cover today, but has experienced several millennia of human occupation resulting in extensive forest clearing and fragmentation. This supports the notion that conservation of vertebrates on tropical oceanic islands relies not only on identification of critical habitat for extant and translocated populations [12], [34], but also on protection from contemporary threats including habitat loss and disturbance and introduced predators [14], [76], [77].

While it has been recognized that even small islands can sustain endemic and endangered species of vertebrates, such forests are also important sites for endangered or even undiscovered species of plants, as further exploration of the remote islands of Lau will undoubtedly confirm. Such a plea for new field work may be time-limited; although the forests here still consist primarily of native species, without the problem of invasive trees as in parts of Samoa [28] and large islands of western Fiji [78], the appearance of invasive non-native trees could occur at any time.

Supporting Information

Figure S1.

Species accumulation curve. Estimated rate of accumulation of new species for 23 vegetation plots on Lakeba, Nayau and Aiwa Levu islands, Lau Group, Fiji. Note that the number of species accumulates rapidly from 1 to ∼10 plots and then begins to level off (the rate of accumulation slows). The estimated number of species in the sampled forests is 112-127 using first and second-order jackknife estimates (see text).

https://doi.org/10.1371/journal.pone.0015685.s001

(DOC)

Table S1.

Basal area by species (square m/ha) and environmental and stand variables for 23 forest plots in Lau, each 500 m2 in area.

https://doi.org/10.1371/journal.pone.0015685.s002

(DOC)

Acknowledgments

We are grateful to the late Right Honorable Ratu Sir Kamisese Mara for granting permission to work in Lau. We owe a great deal to many people who supported and assisted with this research, especially G. Keppel, R. and K. Thaman (University of the South Pacific), M. Tuiwawa (South Pacific Regional Herbarium), T. Sarovi-Vunidilo (The Fiji Museum), J. and S. Qica, N. B. and A. Rawaico, P. Nunn, S. Matararaba, Tui Naro, Tui Liku, S. and A. Guvaki, Rusila, Colati, Vatu, Tiko, G. K. Pregill, S. Hathaway, J. A. Oswald, P. O'Day, S. Jones, and W. A. Whistler. For comments that improved the manuscript we thank S. K. Robinson, E. L. Webb and an anonymous reviewer.

Author Contributions

Performed the experiments: JF DWS. Analyzed the data: JF DWS. Wrote the paper: JF DWS.

References

  1. 1. Steadman DW (2006) Extinction and biogeography of tropical Pacific birds. Chicago: University of Chicago Press. 594 p.
  2. 2. Nunn PD (1994) Oceanic islands. Oxford, UK: Blackwell. 413 p.
  3. 3. Mueller-Dombois D, Fosberg FR (1998) Vegetation of the tropical Pacific islands. Berlin: Springer-Verlag. 733 p.
  4. 4. Burley DV, Dickinson WR (2001) Origin and significance of a founding settlement in Polynesia. Proceedings of the National Academy of Science, USA 98: 11829–11831.
  5. 5. Kirch PV (2000) On the road of the winds: an archaeological history of the Pacific Islands before European contact. Berkeley, CA: University of California Press. 424 p.
  6. 6. Kirch PV, Ellison J (1994) Paleoenvironmental evidence for human colonization of remote Oceanic islands. Antiquity 68: 310–321.
  7. 7. Athens JS (1997) Hawaiian native lowland vegetation in prehistory. In: Kirch PV, Hunt TL, editors. Historical ecology in the tropical Pacific. New Haven, CT: Yale University Press. pp. 248–270.
  8. 8. Fall P (2005) Vegetation change in the coastal-lowland rainforest at Avai'o'vuna Swamp, Vava'u, Kingdom of Tonga. Quaternary Research 64: 451–459.
  9. 9. Steadman DW, Pregill GK, Burley DV (2002) Rapid prehistoric extinction of iguanas and birds in Polynesia. Proceedings of the National Academy of Sciences 99: 3673–3677.
  10. 10. Pregill GK (1993) Fossil lizards from the late Quaternary of `Eua, Tonga. Pacific Science 47: 101–114.
  11. 11. Koopman KF, Steadman DW (1995) Extinction and biogeography of bats on `Eua, Kingdom of Tonga. American Museum Novitates 3125: 1–13.
  12. 12. Franklin J, Steadman DW (1991) The potential for conservation of Polynesian birds through habitat mapping and species translocation. Conservation Biology 5: 506–521.
  13. 13. Harlow PS, Biciloa PN (2001) Abundance of the Fijian crested iguana (Brachylophus vitiensis) on two islands. Biological Conservation 98: 223–231.
  14. 14. Robertson HA, Karika I, Saul EK (2006) Translocation of Rarotonga Monarchs Pomarea dimidiata within the southern Cook Islands. Bird Conservation International 16: 197–215.
  15. 15. Garnock-Jones PJ (1978) Plant communities on Lakeba and southern Vanua Balavu, Lau Group. Fiji. Royal Society of New Zealand Bulletin 17: 95–117.
  16. 16. Latham M, Brookfield HC (1983) The Eastern Islands of Fiji, General Report No. 3 of the UNESCO/UNFPA Project Population and Environment in the Eastern Islands of Fiji. Paris: UNESCO. 184 p.
  17. 17. Watling D (1982) Birds of Fiji, Tonga and Samoa. Wellington, NZ: Millwood Press. 176 p.
  18. 18. Watling D (2001) A guide to the birds of Fiji and Western Polynesia. Suva, Fiji: Environmental Consultants (Fiji) Ltd. 272 p.
  19. 19. Clunie F (1984) Birds of the Fiji bush. Suva, Fiji: Fiji Museum.
  20. 20. Pratt HD, Bruner PL, Berrett DG (1987) A field guide to the birds of Hawaii and the Tropical Pacific. Princeton, NJ: Princeton University Press.
  21. 21. Steadman DW, Franklin J (2000) A preliminary survey of landbirds on Lakeba, Lau Group, Fiji. Emu 100: 227–235.
  22. 22. Franklin J, Wiser SK, Drake DR, Burrows LE, Sykes WR (2006) Environment, disturbance history and rain forest composition across the islands of Tonga, Western Polynesia. Journal of Vegetation Science 17: 233–244.
  23. 23. Drake DR, Whistler WA, Motley TJ, Imada CT (1996) Rain forest vegetation of `Eua Island, Kingdom of Tonga. New Zealand Journal of Botany 34: 65–77.
  24. 24. Franklin J, Drake DR, Bolick LA, Smith DS, Motley TJ (1999) Rain forest composition and patterns of secondary succession in the Vavàu island group, Tonga. Journal of Vegetation Science 10: 51–64.
  25. 25. Wiser SK, Drake DR, Burrows LE, Sykes WR (2002) The potential for long-term persistence of forest fragments on Tongatapu, a large island in western Polynesia. Journal of Biogeography 29: 767–787.
  26. 26. Webb EL, Stanfield BJ, Jensen ML (1999) Effects of topography on rainforest tree community structure and diversity in American Samoa, and implications for frugivore and nectarivore populations. Journal of Biogeography 26: 887–897.
  27. 27. Webb EL, Fàaumu S (1999) Diversity and structure of tropical rain forest of Tutuila, American Samoa: effects of site age and substrate. Plant Ecology 144: 257–274.
  28. 28. Webb EL, van de Bult M, Chutipong W, Kabir ME (2006) Composition and structure of lowland rain-forest tree communities on Ta'u, American Samoa. Pacific Science 60: 333–354.
  29. 29. Whistler WA (1980) The vegetation of eastern Samoa. Allertonia 2: 45–190.
  30. 30. Keppel G, Tuiwawa MV (2007) Dry zone forests of Fiji: species composition, life history traits, and conservation. New Zealand Journal of Botany 45: 545–563.
  31. 31. Keppel G, Buckley YM, Possingham H (2010) Drivers of lowland rain forest community composition, diversity and structure on islands in the tropical South Pacific. Journal of Ecology 98: 87–95.
  32. 32. Steadman DW, Franklin J, Drake DR, Freifeld HB, Bolick LA, et al. (1999) Conservation status of forests and vertebrate communities in the Vavàu Island Group, Tonga. Pacific Conservation Biology 5: 191–207.
  33. 33. Freifeld HB (1999) Habitat relationships of forest birds on Tutuila Island, American Samoa. Journal of Biogeography 26: 1191–1213.
  34. 34. Morrison C, Keppel G, Thomas N, Rounds I, Harlow PS (2009) Critically endangered Fijian crested Iguana (Brachylophus vitiensis) shows habitat preference for globally threatened tropical dry forest. Pacific Science 63: 223–242.
  35. 35. Steadman DW (1998) Status of land birds on selected islands in the Hàapai Group, Kingdom of Tonga. Pacific Science 52: 14–34.
  36. 36. Franklin J, Steadman DW (2008) Prehistoric species richness of birds on oceanic islands. Oikos 117: 1885–1891.
  37. 37. Ladd HS, Hoffmeister JE (1945) Geology of Lau. Bernice P Bishop Museum Bulletin 181: 190.
  38. 38. Best SB (2002) Lapita: A view from the east. 24. Auckland, NZ: New Zealand Archaeological Society Monograph.
  39. 39. Franklin J, Keppel G, Whistler WA (2008) The vegetation and flora of Lakeba, Nayau and Aiwa islands, central Lau Group, Fiji. Micronesica 40: 169–225.
  40. 40. O'Day SJ, O'Day P, Steadman DW (2004) Defining the Lau context: Recent findings on Nayau, Lau Islands, Fiji. New Zealand Journal of Archaeology 25: 31–56.
  41. 41. Jones S, Steadman DW, O'Day PM (2007) Archaeological investigations on the small islands of Aiwa Levu and Aiwa Lailai, Lau Group, Fiji. Journal of Island and Coastal Archaeology 2: 72–98.
  42. 42. Coblentz BE (1978) The effects of feral goats Capra hircus on island ecosystems. Biological Conservation 41: 253–268.
  43. 43. Richards PW (1996) The tropical rain forest, an ecological study. Cambridge: Cambridge University Press. 575 p.
  44. 44. Keppel G, Rounds IA, Thomas NT (2006) The flora, vegetation, and conservation value of mesic forest at Dogotuki, Vanua Levu, Fiji Islands. New Zealand Journal of Botany 44: 273–292.
  45. 45. Franklin J, Merlin M (1992) Species-environment patterns of forest vegetation of the uplifted reef limestone of Atiu, Mangaia, Màuke and Mitìaro, Cook Islands. Journal of Vegetation Science 3: 3–14.
  46. 46. Greig-Smith P (1983) Quantitative plant ecology. Oxford: Blackwell Scientific Publications. 359 p.
  47. 47. van Tongeren OFR (1995) Cluster analysis. In: Jongman RHG, ter Braak CJF, van Tongeren OFR, editors. Data analysis in community and landscape ecology. 2nd ed. Cambridge: Cambridge University Press. pp. 174–212.
  48. 48. Mielke PW Jr (1984) Meteorological applications of permutation techniques based on distance functions. In: Krishnaiah PR, Sen PK, editors. Handbook of statistics. Amsterdam: Elsevier Science Publishing. pp. 813–830.
  49. 49. Dufrêne M, Legendre P (1997) Species assemblages and indicator species: the need for a flexible asymmetrical approach. Ecological Monographs 67: 345–366.
  50. 50. ter Braak CJF (1995) Ordination. In: Jongman RHG, Ter Braak CJF, Van Tongeren OFR, editors. Data analysis in community and landscape ecology. Cambridge: Cambridge University Press. pp. 91–173.
  51. 51. ter Braak CJF (1987) The analysis of vegetation-environment relationships by canonical correspondence analysis. Vegetatio 69: 69–77.
  52. 52. Steadman DW, Freifeld HB (1998) Distribution, relative abundance, and habitat relationships of landbirds in the Vavàu Group, Kingdom of Tonga. Condor 100: 609–628.
  53. 53. R Development Core Team (2007) R: A language and environment for statistical computing. Vienna, Austria: R Foundation for Statistical Computing.
  54. 54. Hurlbert SH (1971) Nonconcept of species diversity - critique and alternative parameters. Ecology 52: 577–586.
  55. 55. Heck KL, Vanbelle G, Simberloff D (1975) Explicit calculation of rarefaction diversity measurement and determination of sufficient sample size. Ecology 56: 1459–1461.
  56. 56. MacKenzie DI, Nichols JD, Lachman GB, Droege S, Royle A, et al. (2002) Estimating site occupancy rates when detection probabilities are less than one. Ecology 83: 2248–2255.
  57. 57. Simons TR, Alldredge MW, Pollock KH, Wettroth JM (2007) Experimental analysis of the auditory detection process on avian point counts. Auk 124: 986–999.
  58. 58. Nichols JD, Hines JE, Sauer JR, Fallon FW, Fallon JE, et al. (2000) A double-observer approach for estimating detection probability and abundance from point counts. Auk 117: 393–408.
  59. 59. Palmer MW (1991) Estimating species richness: the second-order jackknife reconsidered. Ecology 71: 1195–1198.
  60. 60. Franklin J, Drake DR, McConkey KR, Tonga F, Smith LB (2004) The effects of Cyclone Waka on the structure of lowland tropical rain forest in Vava'u, Tonga. Journal of Tropical Ecology 20: 409–420.
  61. 61. Franklin J (2003) Regeneration and growth of pioneer and shade-tolerant rain forest trees in Tonga. New Zealand Journal of Botany 41: 669–684.
  62. 62. Burslem DFRP, Whitmore TC, Brown GC (2000) Short-term effects of cyclone impact and long-term recovery of tropical rain forest on Kolombangara, Solomon Islands. Journal of Ecology 88: 1063–1078.
  63. 63. Laurence D (2004) Erosion of tree diversity during 200 years of shifting cultivation in Bornean rain forest. Ecological Applications 14: 1855–1869.
  64. 64. Straatmans W (1964) Dynamics of some Pacific island forest communities in relation to the survival of the endemic flora. Micronesica 1: 113–122.
  65. 65. Hopkins MS, Graham AW (1983) The species composition of soil seed banks beneath lowland tropical rainforests in North Queensland, Australia. Biotropica 15: 90–99.
  66. 66. Hjerpe J, Hedenås H, Elmqvist T (2001) Tropical rain forest recovery from cyclone damage and fire in Samoa. Biotropica 33: 249–259.
  67. 67. Grubb PJ, Metcalfe DJ (1996) Adaptation and inertia in the Australian tropical lowland rain-forest flora: Contradictory trends in intergeneric and intrageneric comparisons of seed size in relation to light demand. Functional Ecology 10: 512–520.
  68. 68. Flenley JR (1969) The vegetation of the Wabag Region, New Guinea Highlands: A numerical study. Journal of Ecology 57: 465–490.
  69. 69. Franklin J (2007) Recovery from clearing, cyclone and fire in rain forests of Tonga, South Pacific: Vegetation dynamics 1995-2005. Austral Ecology 32: 789–797.
  70. 70. Hyndman DC, Menzies JI (1990) Rain forests of the Ok Tedi headwaters, New Guinea: An ecological analysis. Journal of Biogeography 17: 241–273.
  71. 71. Morrison C, Osborne T, Harlow PS, Thomas N, Biciloa P, et al. (2007) Diet and habitat preferences of the Fijian crested iguana (Brachylophus vitiensis) on Yadua Taba, Fiji: implications for conservation. Australian Journal of Zoology 55: 341–350.
  72. 72. Lasky JR, Keitt TH (2010) Abundance of Panamanian dry-forest birds along gradients of forest cover at multiple scales. Journal of Tropical Ecology 26: 67–78.
  73. 73. Steadman DW (1995) Prehistoric extinctions of Pacific Island birds: biodiversity meets zooarchaeology. Science 267: 1123–1131.
  74. 74. Steadman DW, Freifeld HB (1999) The food habits of Polynesian pigeons and doves: a systematic and biogeographic review. Ecotropica 5: 13–33.
  75. 75. McConkey KR, Meehan HJ, Drake DR (2004) Seed dispersal by Pacific Pigeons (Ducula pacifica) in Tonga, Western Polynesia. Emu 104: 369–376.
  76. 76. Kuehler C, Lieberman A, Varney A, Unitt P, Sulpice RM, et al. (1997) Translocation of Ultramarine Lories Vini ultramarina in the Marquesas Islands: Ua Huka to Fatu Hiva. Bird Conservation International 7: 69–80.
  77. 77. Harlow PS, Fisher M, Tuiwawa M, Biciloa PN, Palmeirim JM, et al. (2007) The decline of the endemic Fijian crested iguana Brachylophus vitiensis in the Yasawa and Mamanuca archipelagos, western Fiji. Oryx 41: 44–50.
  78. 78. Keppel G, Navuso JC, Naikatini A, Thomas NT, Rounds IA, et al. (2005) Botanical diversity at Savura, a lowland rain forest site along the PABITRA Gateway Transect, Viti Levu, Fiji. Pacific Science 59: 175–191.