- freely available
Biology 2012, 1(3), 736-765; doi:10.3390/biology1030736
Abstract: Species endemic to mountains on oceanic islands are subject to a number of existing threats (in particular, invasive species) along with the impacts of a rapidly changing climate. The Lord Howe Island endemic palm Hedyscepe canterburyana is restricted to two mountains above 300 m altitude. Predation by the introduced Black Rat (Rattus rattus) is known to significantly reduce seedling recruitment. We examined the variation in Hedyscepe in terms of genetic variation, morphology, reproductive output and demographic structure, across an altitudinal gradient. We used demographic data to model population persistence under climate change predictions of upward range contraction incorporating long-term climatic records for Lord Howe Island. We also accounted for alternative levels of rat predation into the model to reflect management options for control. We found that Lord Howe Island is getting warmer and drier and quantified the degree of temperature change with altitude (0.9 °C per 100 m). For H. canterburyana, differences in development rates, population structure, reproductive output and population growth rate were identified between altitudes. In contrast, genetic variation was high and did not vary with altitude. There is no evidence of an upward range contraction as was predicted and recruitment was greatest at lower altitudes. Our models predicted slow population decline in the species and that the highest altitude populations are under greatest threat of extinction. Removal of rat predation would significantly enhance future persistence of this species.
Oceanic island floras are of high conservation value as they are isolated, geographically diverse and support endemic plant species that have evolved in situ and distinctive assemblages [1,2]. More than half of all palm species are endemic to islands, with the Pacific Ocean particularly high in palm genus endemism [3,4]. There are four palm species in three endemic genera on Lord Howe Island (LHI) in the western Pacific Ocean, (tribe Areceae, Arecoideae), which are thought to have arrived in three colonisation events [5,6].
Islands of volcanic origin, such as LHI, can feature steep mountain gradients, causing adiabatic cooling and orographic cloud formation at higher elevations . Under such clouds, microclimates with reduced radiation and daily temperature range, combined with increased moisture can occur [7,8]. Cloud forest ecosystems can form in such conditions and component species may be adapted to conditions within a specific elevational range. For example, gradations in physiology, morphology and development may occur in response to the environmental conditions, due to different gene frequencies or phenotypic plasticity that have developed over time [9,10,11].
Lord Howe Island is a small (1,455 Ha) volcanic landmass in the South Pacific Ocean approximately 570 km from Australia (Figure 1) . The island has a unique floristic assemblage, with 44% of plant species endemic to the island . Extensive orographic cloud forms over two mountains that dominate the island, Mt Gower (875 m) and Mt Lidgbird (777 m) . Mossy cloud forest, which alone supports 34% of the island’s endemic plant species including two palms , occupies less than 0.5 km2 on LHI including the summit of Mt Gower. One of these palms, Hedyscepe canterburyana (C. Moore & F. Muell) H. Wendl & Drude, is listed as “vulnerable” on the IUCN Red List and occurs between 300–850 m altitude into the cloud forest on Mt Lidgbird and Mt Gower as well as their upper slopes [3,15]. Hedyscepe canterburyana is a monoecious palm with insect-pollinated protandrous inflorescences and large red fruits (~3 × 4.4 cm) that are potentially dispersed by the Lord Howe Pied Currawong (Strepera graculina crissalis) .
Species with small or isolated geographic ranges and narrow environmental tolerances are most at risk under climate change [16,17]. In response to climatic warming, species at particular altitudes are expected to migrate upwards [18,19,20]. Such range shifts may be characterised by reduced population growth at lower altitudes and have already been reported in the northern hemisphere [21,22,23]. The four LHI endemic palm species are distributed along an elevation gradient . Howea forsteriana occurs on calcareous and basaltic soils at lower altitudes (to 350 m), Howea belmoreana occurs on basaltic soils only at lower altitudes (to 400 m) and Lepidorrhachis mooreana is restricted to the mountain summits (750–875 m). The topic of this study, Hedyscepe canterburyana, co-occurs with Howea belmoreana and Lepidorrachis mooreana [3,24]. Climate change may alter the pattern of cloud formation or cloud height over montane habitats [7,25,26] and is thought to be the most critical threat to the survival of endemic flora on Lord Howe Island due to its limited scope for migration [27,28]. Demographic structure and population dynamic modelling studies are easily undertaken on palms and have potential to be used for gauging climate effects on populations [29,30,31].
Where geography limits the possibility of adaptive migration, survival of a species may depend on their ability to adjust to the changed climatic conditions in situ . Isolated species with low genetic variation are at high risk [33,34]. High levels of genetic diversity and strong directional selection pressures facilitate adaptation [34,35]. However, selection acts over generations, and for long lived species this may be slower than the rate of current climatic changes [36,37].
The possession of phenotypic plasticity may buffer individuals against the short term effects of climate change [32,36,38,39]. Morphology has been found to vary across the distribution of several palm species suggesting some plasticity in this group of plants [40,41]. Timing of plant flowering is known to vary across elevation gradients, due to adiabatic temperature changes and temperature-specific flowering initiation . Where flowering is asynchronous, restricted gene flow has resulted in genetic structuring [43,44]. Phenological changes have been reported in some species in response to recent climatic changes [45,46] which may affect long term gene exchange [42,47].
In addition to the potential impacts of climate change, many island plants are already vulnerable to predation by invasive species [48,49]. Rats such as Black Rats (Rattus rattus) cause “recruitment depression” for many plants on islands and may be the cause of extinction of some species [50,51,52,53]. Island endemic palms may be affected by synergies between climate change and seed predation by rats. Black rats arrived on LHI in 1918 and quickly became widespread and abundant. Rat control measures are currently undertaken on a small part of the island . Consumption of fruit by invasive black rats has been documented to severely reduce the levels of recruitment of H. canterburyana seedlings in unbaited areas .
Conservation actions for the next several decades urgently require guidance based on a defendable scientific understanding of the potential impacts posed by a suite of threats to plant communities [55,56]. This study aims to test likely impacts of climate change on a highly restricted plant species occurring over an elevation gradient. Specifically we examined if genetic variation, morphology, reproductive output and demographic structure for the Lord Howe Island endemic palm H. canterburyana varied across an altitude gradient and what impacts this may have on its long-term viability and persistence. In addition, factors such as aspect, protection in shade and site differences were also investigated for potential association with genetic composition and demographic structure. To inform predictions of climate changes we quantified simple elevation lapse rates (adiabatic temperature change) and examined evidence of climatic changes on LHI in the last century using historical climatic records. Population models were used to compare the risk of extinction at different elevations as an indicator of potential upward movement in the species distribution due to climatic changes. This incorporated the impact of possible rat control measures.
2. Results and Discussion
2.1. Climatic Conditions
Lord Howe Island has experienced a variable annual climate in the last 70 years, with the 2000–2009 decade experiencing the lowest mean annual rainfall (1,362 mm; Figure 2), in line with droughts experienced during the same time-frame across the east of Australia. Annual minimum and maximum temperatures significantly increased across decades (p < 0.01, rs = 0.082; rs = 0.026; Table 1; Figure 2). Mean minimum temperatures increased by 0.6 °C in total since 1940 with the period of greatest increase occurring between the 1960s and 1970s. Maximum temperatures increased by 0.025 °C on average each decade (r2 = 0.02). Annual rainfall was negatively correlated with time (p < 0.01, f = 2.647, rs = −0.281). The rates of change found for LHI in this study concur with worldwide climatic changes since the mid-twentieth century reported on a regional scale [20,57,58]. The annual variability in the climate data reported here are common in Australia and New Zealand, partially due to El Niño influences .
As expected, temperature varied significantly between altitudes, decreasing significantly with increasing altitude (p < 0.01; mean rs = −0.546; min. rs = −0.567; max. rs = −0.457). The adiabatic lapse rate for Mt Gower was estimated to be −0.9 °C per 100 m increase in altitude (t = 38.514, p < 0.01, r2 = 0.383). This is greater than adiabatic temperature lapse rates reported for Hawaii, Borneo and Madagascar which range from 0.4 to 0.6 °C decrease per 100 m increase in elevation [20,60,61]. Our figures are consistent with estimations by the Lord Howe Island Board  and those reported for the Krakatau Islands . Simulations predict cloud formation lifting to higher altitudes and for cloud forest areas to experience reduced water availability, increased temperature and daily temperature variation [7,14,26,63]. Based on the current temperatures at low elevations and climatic changes already experienced on LHI, the future warm temperature limit for H. canterburyana is predicted to rise to elevations of 426–500 m by 2030 and 451–710 m by 2070. Thus an upslope range shift in the last half century may already be occurring for H. canterburyana and would be shown by current recruitment failure or increased mortality at lower elevations.
|Mean Max. Temperature||Mean Min. Temperature|
|decade (rs)||decades (f)||decade (rs)||decade (f)|
|January||−0.050 **||16.525 **||0.199 **||23.580 **|
|February||−0.005||18.309 **||0.212 **||20.365 **|
|March||−0.063 **||18.37 **||0.131 **||15.877 **|
|April||0.029||6.683 **||0.106 **||14.894 **|
|May||0.134 **||11.679 **||0.151 **||21.133 **|
|June||0.181 **||20.095 **||0.103 **||4.054 **|
|July||0.153 **||21.768 **||0.119 **||8.096 **|
|August||0.124 **||14.156 **||0.113 **||8.596 **|
|September||0.172 **||24.201 **||0.168 **||13.155 **|
|October||0.052 **||6.541 **||0.122 **||8.385 **|
|November||−0.074 **||17.621 **||0.111 **||7.679 **|
|December||−0.041||29.192 **||0.158 **||16.540 **|
|Annual||0.026 **||30.058 **||0.082 **||41.473 **|
2.2. Population Demography
The mean density (D) of H. canterburyana individuals was 1,644 plants/Ha, with an average distance to nearest neighbour of 1.2 m (NND1; Table 2). Density (D) of trunked H. canterburyana increased with increasing elevation (D rs = 0.655; NND1 rs = −0.675; p < 0.05; Table 2). Individuals were more sparsely distributed in sites shaded by Mt Lidgbird (Table 2).
Population structure varied between sites, but generally there were greater numbers of adults than juveniles with some apparent historical pulses of recruitment (Figure 3). The presence and abundance of a non-trunked palm “juvenile bank” is a key measure of regeneration to maintain population size [6,24,64]. On average, one new seedling results from every three reproductively active individuals (0.33 seedlings per RITable 3). Much greater recruitment and a larger juvenile bank is reported for wild populations of close relative Rhopalostylis sapida . Ex-situ germination of H. canterburyana is reported to have a 70% success rate , while in the wild, the juvenile bank has been shown to be greatly enhanced in sites that are baited to control rats compared to unbaited sites . Thus, it could be rationalised that the low recruitment levels are due in part to invasive black rats.
We expected that there would be greater seedling recruitment at higher altitudes due to moister conditions. In contrast to expectations, regeneration was greater at low altitudes in H. canterburyana (rs= −0.542, t = 3.278, p < 0.05). There was a significant positive correlation between altitude and “Sub-Adults” (rs = 0.629). Altitude was negatively correlated with the abundance of tallest trunked individuals (>6 m tall; p < 0.01, rs = −0.642).
|Total/mean||Mt Gower||Mt Lidgbird||Altitude (rs)||Aspect (rs)||Mountain (t)||Exposure (t)||Aspect (f)||Altitude (f)|
|Non trunked & trunked|
|1,182 (173)||0.418||−0.282||2.966 **||1.721||2.233||−2.214 *|
|−0.588 *||0.373||−4.428 ***||−2.767 *||1.927||2.834 *|
|0.655 **||−0.417||3.940 **||2.410 *||4.749 *||−4.212 **|
|−0.674 **||0.513 *||−2.683 **||−1.111||3.086||2.357 *|
|0.511 *||−0.818 **||−3.750 **||−1.968||2.018||3.013 **|
|−0.220 **||0.239 **||−6.466 ***||−8.868 ***||4.944 ***||4.055 ***|
|−0.078||−0.046||0.539||0.415||5.495 ***||−2.454 *|
|−0.252 **||0.219 **||−3.570 ***||−3.935 ***||14.553 ***||2.269 *|
|Total||Mt Gower||Mt Lidgbird||Altitude (rs)||Altitude (t)||Aspect (rs)||Mountain (t)||Exposure (t)||Aspect (f)|
|RI (%)||44.3||41.52 |
|0.295 **||−3.499 **||−0.221 **||2.780 **||2.748 **||5.342 ***|
|0.187||−3.255 **||−0.311||2.149 *||2.184 *||0.729|
|Developing Splade||0.48||5.97 |
|Half-Sized Green Fruit||28.47||29.06 |
|0.643 *||−5.637 ***||0.083||1.882||0.708||4.401 *|
|Full-Sized Green Fruit||39.23||28.97 |
|−0.416||2.563 *||0.095||−1.856||−2.359 *||2.243|
|Full-Sized Mottled Fruit||4.07||1.12 |
|Full-Sized Red Fruit||0.48||0.21 |
There was a weak yet significant correlation (rs = 0.380, p < 0.001) between the population structure and environmental attributes. A significantly greater proportion of “Adult” trunked individuals 4–4.5 m in height were found in sites with a northwest aspect (p < 0.05, f = 5.480) and the proportion of “mature adults” was significantly greater (Table 3) in sites in the protection of Mt Lidgbird. Low altitude sites, in the protection of Mt Lidgbird, with a south-east or east aspect displayed most continuous recruitment and individuals here had greater DBH and inferred longer plant ages (Table 2). Svenning  notes that a few hundred metres of change in altitude affects palm distribution in Ecuador, possibly due to frequent cloud formation at high altitudes. The lower altitude slopes of Mt Gower and Mt Lidgbird are steep (>29°) and composed of rock-fall debris which may aid drainage. Well drained forests have been known to increase prevalence of palm seedlings and juveniles in some species [66,67]. The potential role of differential seed predation by rats at different altitudes is unknown.
We expected plants to respond to temperature change by growing more slowly at higher altitudes, have a greater DBH, and shorter trunk heights, as reported for other plant species [11,68]. Consistent with this hypothesis, trunked heights for H. canterburyana were weakly but significantly correlated with altitude (Table 2). However, individuals at high altitude sites had significantly smaller DBH (Table 2). Growth rate, measured by the number of rings per metre (R/m), averaged 43 rings per metre, but was highly variable within and among sites. In contrast to expectations, growth rate was significantly greater (fewer rings per metre) in individuals at high altitude sites compared to low altitude sites (Table 2). Hedyscepe canterburyana individuals at higher altitudes subject to increased cloud cover were also found at higher densities, indicating individual adults survive well in this environment. The palm may be more responsive to moisture in a micro-climate than to temperature, or alternatively, the lower altitude sites may be near the upper temperature tolerance of the species. Temperature is the main factor controlling palm distribution worldwide, but moisture also influences palm distribution and growth [3,69].
2.3. Fecundity and Phenology
The abundance of fruit produced, percentage of the population flowering, and the number of infructescences produced per individual, are variable amongst palms [68,70,71]. An average of two inflorescences were produced per reproductively active H. canterburyana individual (Inf). There were no significant correlations (p > 0.05) between inflorescence and population structure or environmental matrices. The number of inflorescences produced on each plant was correlated with the trunk height (H1; rs = 0.509; Table 2). Hedyscepe canterburyana individuals begin producing inflorescences once their trunk reaches 0.5 m, multiple inflorescence production commences above 1.5 m, peaks at 4.01–5 m (when individuals produce up to seven inflorescences) and declines at 5 m (Figure 4). The number of infructescences produced per individual in a year for H. canterburyana was comparable to that of close relative Rhopalostylis sapida . Hedyscepe canterburyana has a comparable, though slightly greater proportion of individuals with reproductive structures present than the other Lord Howe Island palms [6,72]. Reproduction was variable between years with 24% of the H. canterburyana individuals (RI) having reproductive structures in 2008, compared with 44% in 2010. This may relate to variation in climatic conditions between those years. The effective population size for H. canterburyana, based on reproductive variability, is estimated to be approximately 50% of the census population, lower than that based on genetic estimates (Ne = 74%).
In H. canterburyana, higher elevation sites had significantly (p < 0.01) more mature sized fruits (mMRO) and greater overall reproductive output (MRO, mMRO; Table 3) compared to lower altitude sites. The abundance of unripe, half sized green fruit significantly increased with altitude (Table 3). Fruit produced, percentage of population flowering and the number of infructescences are measures of reproductive success, affecting recruitment [68,70,71]. Overall we found that reproductive output was greater at higher altitudes. Given that seedling abundance was lower at higher altitudes this would suggest lower seed germination and survival at higher altitudes. We predicted that H. canterburyana would have asynchronous reproduction across elevations due to flowering commencement triggered by temperature [14,73]. Our studies indicated that reproductive output and timing was variable for plants both within and among sites at different altitudes, which has similarly been reported across the environmental range of a Seychelles palm . Asynchrony in flowering across altitudes is hypothesised as a potential barrier to gene flow, resulting in genetic structuring or clustering along altitude gradients [43,44,74].
2.4. Population Genetics
Genetic diversity was relatively high (A 3.7, P 97.5%, He 0.433) but with little variation across the sites; 50 alleles were recorded across the ten loci tested (Table 4). There was no significant correlation (p > 0.05) between growth rate similarity and genetic similarity among individual plants (Table 2). However, there were significant negative correlations between aspect and Shannon’s diversity index (I; rs = −0.812; p < 0.05). There were no other significant correlations (p > 0.05) or differences in genetic diversity between the mountains, high and low altitudes, aspect or exposed and sheltered sites that could explain variation in the data. The genetic diversity in H. canterburyana is comparable, though moderately higher, than has been reported for endemic palms from the Seychelles, Vanuatu and Canary Islands [41,75]. Hedyscepe canterburyana has similar levels of genetic diversity compared with the other Lord Howe Island endemic palms [5,6,72] and also widespread Mexican palms that are considered to have higher levels of variation compared to other tropical plants [76,77].
There was also very little evidence of genetic differentiation across the island distribution, with low FST (0.030) and only 2% of the species genetic diversity distributed among sites, (Table 5). Consistent with high gene flow estimates (Nm 8.4; Table 5), 80% of the samples were assigned to a different site than their true location in the population assignment test indicating weak genetic provenance. The Principle Coordinates Analysis also demonstrated no clear genetic clustering of individuals associated with sites (Figure 5). Thus, the species appears to be acting as one panmictic population or as a metapopulation of connected subpopulations.
Low genetic differentiation reported here is similar to palms sampled across small spatial distances in Mexico and Brunei [76,78]. The other LHI palms have similarly low levels of genetic differentiation [6,72]. Hedyscepe canterburyana is abundant on LHI with good connectivity throughout its distribution. This suggests dispersal of either pollen or seeds over the entire distribution on the island. Lord Howe Pied Currawongs are expected to be an important seed disperser for this species . Navascues et al.  hypothesised that stepping-stone gene flow along a continuous elevation gradient could counter balance the gene flow restrictions of asynchronous flowering. Such a mechanism may explain our results.
|Variation among populations||2%|
|Variation within populations||98%|
Despite evidence of gene flow across the island, all sites were moderately inbred (F 0.355; Table 4). At each site, six loci on average deviated significantly from Hardy-Weinberg expectations (H-W; p < 0.05). Sites with a north-west aspect (HC1, HC4) were more inbred (F; rs = −0.913) suggesting wind may play a role. This species is thought to be pollinated by insects with restricted ,movements which may lead to the formation of family clusters resulting in effective inbreeding . However, there was no significant correlation (p > 0.05) between geographic and genetic distances within any site and very little evidence for spatial clustering of like genotypes within sites, suggesting little evidence of family genetic structuring. Thus, alternative scenarios provide more plausible explanations for inbreeding in H. canterburyana. Inbred yet genetically diverse populations of Belize palm Chamaedorea ernesti-augusti were explained by thrip pollinators movement among different groups of inflorescences in different years . Inbreeding may also be due to a mixed mating system, pollination between close relatives or self-pollination between male and female flowers on the same plant [72,82]. Self-compatibility may enable a selection advantage whereby the frequency of genotypes that are successful under strong climate change selection can be increased . We found that higher levels of inbreeding in H. canterburyana were correlated with reduced genetic diversity.
2.5. Population Growth Models
Population dynamic models and observational studies are extremely useful for quantifying recent climate induced upslope range shifts [19,22,84]. There were some limitations to the population model used in this study, including intrinsic restrictions by using static population data and the partially unequal distribution of individuals within stage classes . Overall carrying capacity (K) and the initial stage abundance and residence estimations differed between “low altitude” and “rat management” models, and the “high altitude” models based on the input data (Table 6; Figure 6). Transition between stages (S) and survival likelihood varied depending on development stage and the model, reflecting the population structure and grow rate characteristics (Figure 6). The “high altitude” model had the greatest “Mature Adult” Fec, reflecting the observed greater reproductive output, at high altitudes (Figure 6). Thus, we believe the models provide a reasonable representation of population dynamics for H. canterburyana, given the evidence of low recruitment in comparison to other palms, and are therefore appropriate for use in evaluating population growth differences at different altitude [30,86].
Our model matrices predicted slow population declines for H. canterburyana with the “high altitude” model indicating considerably greater declines in numbers compared to the low altitude model (Table 6). We predict that the high altitude populations will start to significantly decline after approximately 30 years and could be reduced to as low as 8% of the current population size after 200 years, with a 69% chance that they will become locally extinct from the high altitude part of their distribution within 180 years if there is no effective reduction in rat predation (Table 6; Figure 7). In contrast to expectations, the models predict a slower population decline at lower altitudes, with these sites potentially retaining 55% of the initial population size after 200 years . Low altitude sites had and only a 3% risk of extinction at lower altitudes within 200 years (Table 6; Figure 7). While upward expansion of plant taxa may occur at different rates, altering community composition , Crimmins et al.  suggest that range could also shift, expand or contract to low altitudes, evidenced by increased population growth at the lower end of a species elevation range. This is more consistent with our results. Hedyscepe canterburyana has an overlapping distribution with Howea belmoreana at the lower end of its elevation range, thus there is potential for increased competition between these species.
|Model||Low altitude||High altitude||Low altitude rat control||High altitude rat control|
|Starting population (/Ha)||1,886||1,109||1,886||1,109|
|Final population (n + t) (/Ha)||652|
|% remaining @200 years||55%||8%||66%||50%|
|Quasi extinction probability||0.030|
|Time to Quasi extinction||>200 years |
(p = 0.01)
|181.1 years |
(p = 0.02)
|>200 years |
(p = 0.01)
|>200 years |
(p = 0.01)
Rat control measures are currently undertaken on eight % of LHI . Seedling survival value (S + Ss) and fecundity values were greater for the “rat management” simulations, consistent with Auld et al. . Our models predict that rat management has considerable positive impacts for the species population survival at both altitudes (Table 6). The most striking impacts were in the “high altitude rat management” simulations where the probability of quasi extinction was reduced to only 8% (from 69% where there is no rat management) and population decline slowed to 50% (as opposed to 92% for no rat management) (Table 6; Figure 7). Negative growth rates have also been found for South American palm Geonoma schottiana due to herbivore predation . Significantly increased seedling recruitment of Rhopalos tylis sapida after Pacific rats were eradicated from several small islands, revealed a previous underestimation of rat predation on that species . The moderate reduction in population decline in these models following real-life rat management actions on islands is sufficient to boost population growth and recovery [88,89].
2.6. Climate Change and In Situ Persistence
Phenotypic plasticity may buffer individuals against the short term effects of climate change [32,34,38,39]. Growth rate of some palms species varies between individuals in a plastic response to environmental conditions [41,90]. Variation in leaf scar interval occurred within H. canterburyana sites across its altitude range but was not correlated with genetic similarity (p > 0.05) and hence, growth rate variation seems more likely a plastic response to the local environment.
Climate linked genetic variation in natural populations may increase the likelihood that some individuals may be pre-adapted to future climatic conditions [35,36,37]. Isolated island endemics that have survived through historical climatic changes potentially have climatically adapted genotypes . Hedyscepe canterburyana or an ancestor has persisted on LHI for at least 4 million years, through several periods of climatic change [5,92]. The moderate to high levels of genetic variation and diversity for H. canterburyana were well dispersed across elevation, therefore individuals potentially exist within current populations that are genetically pre-adapted to a varying climate .
3. Experimental Section
3.1. Field Methods
Samples of H. canterburyana for genetic analysis were collected in 2007 from eight sites across the species distribution on Lord Howe Island (Figure 1). There were four sites per mountain (Mt Lidgbird and Mt Gower) with four sites at both high altitudes (776–875 m) and low altitudes (428–479 m; Figure 1). Geographic location was recorded for each site using a Garmin Etrex GPS. Thirty plants were sampled from each site (total 240). Within each site, plants were randomly sampled from all size classes present, with every second or third plant encountered being sampled. Fresh leaf material was collected and dried in silica gel. The relative locations of the individuals sampled within each site were determined by measuring the compass bearing and distance between plants and later converting these to X and Y coordinates.
In November 2008 several temperature I-buttons (Thermodata Pty Ltd.) were installed along an altitude gradient of 10–800 m in the Erskine Valley to the summit of Mt Gower. Temperature was recorded every three hours for a nine-month period to July 2009, however, reliable data were only received for the first eight months for I-buttons at eight locations.
In 2008, permanent plots were established to monitor the Hedyscepe canterburyana–Howea belmoreana intergrade at three locations (Figure 1). At each site, three transects of 5 m wide × 40 m long were run perpendicular to the slope at different elevations representing: (i) upper dominated by H. canterburyana; (ii) lower dominated by H. belmoreana; and (iii) intermediate both species. Within each transect, locations of each individual of the two study species was noted and its height (cm) recorded . Circumference of the trunk at 50 cm height, number of inflorescences and stage (new, old or fruiting) number of leaf scars for individuals with a trunk or the number of leaf scars in a two metre section was recorded as per Auld et al. . Many palms are characterised by easily counted leaf scars, which can be used to estimate growth rate and plant age [24,29,64].
To measure variation in demographic structure sixteen sites were sampled in 2010 over the full elevation range (316–850 m), with seven sites on Mt Lidgbird and nine sites on Mt Gower (Figure 1) outside of rat control areas. Six sites were at the approximate location of genetic sampling in 2007 (HC1-6). Six sites utilised the long term monitoring plots (HC9-14; Figure 1).
Each of the 16 sites were systematically surveyed in 10 m wide belt transects perpendicular to the slope. Data for all H. canterburyana individuals were recorded until 30 individuals with an emergent trunk were sampled from the site. Locations of all individual plants were mapped as XY coordinates (m) relative to the start point using a Laser Distance meter (Leica DISTO D5, Leica Geosystems) as this provides more accurate relative location than a hand held GPS under canopy cover and on steep slopes. For each H. canterburyana, the height of individuals with no emergent trunk was measured to the tip of the tallest leaf, for plants with a trunk, the presence of a trunk was recorded and height measured to the base of the leaf sheath using the Laser Distance meter. The number of leaf sheath scars (rings) on the trunk were counted as per Auld et al. , and diameter at breast height (DBH) was measured using a diameter tape. The number of reproductive structures were recorded in categories: newly developing, half sized green fruit, full size green fruit, full sized mottled fruit, full sized red fruit or aborted. The abundance of fruit on each infructescence was estimated in abundance classes of: less than 10 fruits, 11–20 fruits, 21–50 fruits, 51–100 fruits.
The following data were recorded at each site: altitude (Alt), cardinal direction of the aspect of the slope (Asp), and transect using a compass (Suunto Co., Finland), slope of land (degrees) using a hand held manual inclinometer (Suunto Co.) and the location at the start and end of the transect using a Garmin Etrex GPS. Orographic cloud cover often forms at altitudes above 550 m ; thus sites greater than 550 m were designated as high populations experiencing more frequent orographic cloud cover (H), the remainder designated as low populations (L). Whilst undertaking fieldwork, it was observed that there is considerable shade cast on some Erskine Valley sites by Mt Lidgbird to the north.Sites in the Erskine Valley were therefore designated as protected from sun exposure in this manner (Pro) or exposed (Ex).
3.2. Genetic Analysis
Leaf tissue was frozen in liquid nitrogen then ground and DNA was extracted using a DNeasy Plant Mini-kit (QIAGEN) . Thirty-six published microsatellite primers developed for palm species were tested for cross-amplification in H. canterburyana [94,95,96,97]. DNA samples from the original species for which they were developed (positive control) and a blank sample (negative control) were used to enable identification of artefacts. Only loci that amplified in the original test species size range were considered.
Ten microsatellite primer pairs were used for H. canterburyana in this study: from Phoenix dactylifera by Billotte et al.  mPdCIR25 (Pd25), mPdCIR050 (Pd50), mPdCIR032 (Pd32), mPdCIR090 (Pd90); Euterpe edulis by Gaiotto et al.  mEe15 (Ee15), mEe03 (Ee3), mEe54 (Ee54); Elaeis guineensis by Billotte et al.  mEgCIR0476 (Eg476), mEgCIR0391 (Eg391); and Oenocarpus bataua (Ob7) . The forward primer was end-labelled with a fluorescent dye (HEX, FAM or NED), except for Ob7, which was end-labelled with HEX following the universal florescent labelling method of Shimizu et al. .
PCR was performed using reaction volumes of 12.5 µL containing, 1× PCR buffer (Fisher Biotech), 200 µM of each dNTP, 1.5 mM MgCl2 (Fisher Biotech), 0.2 µM forward primer, 0.2 µM reverse primer and 0.5 U F1 Taq polymerase (Fisher Biotech), optimised for individual loci as follows: Eg476 2 mM MgCl2; Pd90 125 mM dNTP, 2 mM MgCl2; Ob7 125 mM of dNTP, 2.5 mM MgCl2, 0.4 µM forward primer, 0.1 µM reverse primer and 0.1 µM HEX; Ee03 0.52 µM forward primer and reverse primer; Ee54 and Ee15 250 µM dNTP.
The PCR cycling conditions for Pd25, Pd50, Pd32, Eg391, Eg476 and Pd90 were): 95 °C for 1 min; 35 cycles of 94 °C for 30 s, 52 °C for 1 min, 72 °C for 1 min; 72 °C for 8 min [94,95]. Optimised of cycling conditions for individual loci as follows: annealing temperature for: Pd50 and Eg391 49 °C; Eg476 56 °C; Pd90 48.6 °C. The PCR conditions for Ee03, Ee15 and Ee54 followed Gaitto et al. : 96 °C for 2 min; 30 cycles of 94 °C for 1 min, 59 °C for 1 min, 72 °C for 1 min, 72 °C for 7 min. For Ee54, annealing temperature was 56 °C. The PCR conditions for Ob7 followed Montufar et al. : 96 °C for 2 min; 35 cycles of 95 °C for 30 s, 55 °C for 30 s, 72 °C for 45 s, 72 °C for 10 min.
PCR products of Pd25, Eg 476, Ob7 and Ee3 were run on a Gelscan 2000 (Corbett Research) fragment analyser, using the CR Gelscan program v 7.2.7 (Corbett Research 2001) to visualise the results. The scored bands were assigned to alleles using the oneD Scan v2.05 program (Scanalytics Inc). The PCR products from the remaining six loci were run on a AB3500 Genetic Analyser (Applied Biosystematics 2010). Fragments were scored into alleles at each locus using the ABI Gene Mapper v.4.1 program (Applied Biosystematics 2010) and cross-checked manually.
3.3. Statistical Analysis
The allelic frequencies, and measures of genetic diversity, mean number alleles per locus (A), the effective number of alleles (Ae), the number of private alleles (Ap), percentage polymorphic loci (P), mean expected heterozygosity (He), mean observed heterozygosity, (Ho), the information index (I) and the inbreeding coefficient (F) were calculated. A chi-square analysis was undertaken at each loci to determine significant deviation from Hardy-Weinberg equilibrium in GenAlEx V6.4 .
Spatial analysis was undertaken to determine the density (D; plants/Ha) of H. canterburyana at each site; average distance to nearest neighbour (NND1) and three nearest neighbours (NND3) and pairwise geographic distance within sites between each individual sampled for genetics was calculated using GenAlEx V.6. Carrying capacity (K) per Ha for the high and low altitude population growth models was estimated by doubling the mean density (D) for high altitude sites (HC5, 6, 15–18) and low altitude sites (HC1-4, 9–14), based on the assumption that H. canterburyana was not occupying the full potential carrying capacity and that twice the current density was a conservative yet realistic estimate of the increase sites could accommodate. Number of leaf scars (H2) for trunked individuals was extrapolated using the mean number of rings in 1 m multiplied by mean trunk height (H1). Average growth rate (number of rings per metre; R/m) for each population was calculated as: H2/H1. Growth progression rate (rR/m) for high sites relative to low sites the formula (R/ml)/(R/mh) was used, where R/mh was mean growth at high and R/ml low altitudes sites.
Individuals were assigned to fifteen size classes; three size classes for non-trunked individuals using height increments of 0.6 m and crown size increments of 0.6 m and twelve size classes for trunked individuals using trunk height increments of 0.5 m. The proportion of individuals in height classes for each site and across the whole distribution was plotted. The number of inflorescences was plotted against height classes and the correlation between number of multiple inflorescences on each reproductive individual and DBH, H1 and H2 was tested using Spearman’s correlations. The strongest significant correlation H1 was determined to be the best indicator of reproductive age.
Developmental stages for later use in the population growth models were calculated based on the number of inflorescences for each height class, the approximate height of reproduction commencement and peaks in reproduction . Thus, stages were defined as: Seedlings (S; non-reproductive plants <60 cm), Juveniles (J; non-reproductive plants >60 cm), Adolescents (Ad; non-reproductive individuals trunk <0.5 m), Sub Adults (SA; trunk height 0.5–1.5 m, ≤2 inflorescences), Adults (A; trunk height 1.5–5 m, >2 inflorescences) and Mature Adults (MA; trunk >5 m).
The mean number of inflorescences per reproductive individual (Inf) was calculated for each site and overall (Infp). The percentage of reproductive individuals per site (% Inf), the proportion of individuals of reproductive age (RI) with reproductive structures present per site, and the effective population size based on reproduction  were calcualted. The mean number of seedlings per RI (nS/RI) was calculated for each site and for entire population. Fecundity values (Fec) for the population growth models were derived from the mean nS/RI for high (nS/RIh) and low (nS/RIl) sites. The proportion of inflorescences at each stage of maturity was calculated for each site. Thus, maximum reproductive output (MRO) for each RI was calculated as the sum of the maximum value for each abundance class of all inflorescences. In addition, MRO for immature (iMRO) and mature sized (mMRO) fruit was calculated to enable testing for evidence of potential rat predation.
Significant differences in demographic and genetic measures among sites and among Asp were tested using Analysis of Variance (ANOVA) in SPSS v.19 (IBM 2010). Differences in demographic, growth (R/m and DBH) reproductive (MRO and mMRO) and genetic measures between mountains, H and L, and Ex and Pro sites were tested for significance using ANOVA or Independent T-tests. Spearman’s rank correlations were used to test for significant relationships of Alt and Asp with demographic, growth rates (R/m, DBH), reproductive (MRO and mMRO) and genetic measures in SPSS v.19 (IBM 2010).
Measures of partitioning of genetic diversity in the species (FST; FIS; FIT), were calculated using Wright’s F statistics  and measures of gene flow (Nm) were calculated based on FST. The significance of the genetic partitioning among populations within the species was statistically tested by AMOVA (9999 permutations). Genetic effective population size (Ne) for the species was calculated, using the GenAlEx v.6.4.
Nei’s genetic distance was calculated between individuals and the sites and Principal Coordinates Analysis (PCoA) was used to investigate the major patterns in genetic relationships among all individuals sampled, using 9999 bootstrap permutations GenAlEx V6.4. The genetic distinctiveness of sites was tested using a frequency-based population assignment test undertaken using 9999 bootstrap permutations. A Mantel test between genetic distance (Nei) and geographic distance using and a spatial autocorrelation analysis were used to test for spatial genetic structure within sites, using 9999 permutations using GenAlEx V6.4. Within sites, spatial autocorrelation analysis was undertaken using three annulus distance classes (5 m, 10 m, 15 m), based on general average seed dispersal .
Mean daily minimum and maximum temperature was calculated for each altitude. Differences between altitudes were tested using ANOVA, and the strength of the relationship with altitude was tested with Spearman’s Rank correlations in SPSS v.19. Where correlations were significant, they were regressed to estimate adiabatic decline in temperature.
Long term historical climatic data for Lord Howe Island were obtained from the Australian Bureau of Meteorology (BOM). Climatic data for 1960 to 1987 were obtained from the original Lord Howe Island Meteorology Station (200440); and for 1988–2010, from the Lord Howe Island Aero Meteorology Station (200839). Only years with a BOM “100% completeness” rating were utilised. To ensure that weather records between the two weather stations were not affected by microclimatic variation, records for the daily, mean, maximum and minimum temperatures and rainfall at the two stations were compared in the month of overlap (November 1988). While some differences were noted in the records, they were not greater than ±0.01 °C for temperatures or ±1 mm for rainfall, and therefore were not regarded to contribute to any error in the statistical analysis of long term weather records for LHI.
To estimate the climatic changes on LHI 1940–2010, mean daily temperatures (minimum and maximum) were calculated for each month and year, and total annual rainfall was calculated for each year. Decadal differences in mean annual and monthly minimum and maximum temperatures, and mean annual rainfall, were tested with ANOVA. The strength of climatic changes over time were tested using a Spearman’s rank correlation and regressed against decade.
A Euclidian resemblance (similarity) matrix was created based on the environmental attributes (Alt, Asp, Mountain, mountain shade) of the sites and two Bray-Curtis similarity matrices were created using Hedyscepe population structure attributes (1NND, 3NND, development stage proportions), and inflorescence attributes (RI, Ip, MRO) in PRIMER v.6.1.5 (PRIMER-ELtd 2006). For each resemblance matrix, multi-dimensional scaling analysis was undertaken. The strength of the relationship between the Euclidian resemblance matrix and each Bray-Curtis similarity matrix was tested with a rank correlation in randomly permuted samples (999 permutations) using the RELATE analysis (equivalent to a Mantels test) in PRIMER v.6.1.5 (PRIMER-ELtd 2006). In addition, Euclidian distance was used to calculate a distance measure between individual trunked plants growth rates based on the number of leaf scars per metre. This was then tested for correlation with genetic distance among the same plants as above using PRIMER v.6.1.5.
3.4. Population Growth Models
Four stage matrix models with a time step of one year were constructed for H. canturburyana (Figure 5) . These were: a “low altitude” model based on static population parameters at low altitudes; a “high altitude” model based on static population parameters at high altitudes, and “rat management” models for high and low altitudes with increased fecundity and seedling survival to simulate the removal of rats. Initial stage abundances were calculated for a one hectare (Ha) population sample based on the mean proportion of individuals in each stage and the mean number of individuals per hectare across “L” sites for “low altitude” and “rat management” models and “H” sites for the “high altitude” model.
Stage transition rates were estimated using paired height class data from repeated surveys in established permanent plots. The average time spent in each class (Ayhc) was estimated based on differences in the proportion of the individuals in each class over a three-year timeframe. This was converted to number of years of residence in each stage (y). A frequency table was constructed to estimate for each stage, the transition probability values for survival, the probability of moving to the next stage (pSn) in one year (one time step), and the probability of stage specific survival (pSsn) in one year. These values were used for “low population” model. The average time spent in each height class for the “high population” model was calculated using rR/m × Ayhc, and a frequency table of transition probability values was constructed for “high population”.
The combined static height class structure (2010) was utilised to calculate the overall survivorship from one stage to the next stage (NS), the using the formula NS = (N(t + 1)/N(t))1/y which accounts for mortality. Transition survival rate (Sn) was estimated using the formula: Sn = NS × pSn. Stage specific survival (Ssn) was estimated using the formula: Sn = NS × pSsn.
Relative reproductive output (RRO) was calculated for each reproductive development stage using the total MRO. Fecundity (Fec) for each stage was calculated using the formula: Fecn = RROn × nS/RIn. Fecundity values for the “rat management” model were calculated using the Fec values as above ×37% for both high and low altitude, as this is the median for observed fruit loss . Survivorship from “Seedling” to “Juvenile” stage for the “rat control” simulations was increased by 10%, based on Auld et al. . This was then incorporated into the stage matrix section of the model. Average stage residencies were examined as a result a second adult stage was incorporated into each model (“Adult 2”) with the same stage matrix values as the “Adult” stage, to best reflect relative residency times for each stage in the population modelling algorithms.
RAMAS GIS metapopulation v.5.0 software (Applied Biomathematics 2005) was used to develop stage-structured stochastic models of the potential population growth of the “low altitude”, “high altitude”, and “rat management” populations. Matrix models with seven stages were based on the stage matrices table . The standard deviation of the matrix and of K was set at ±10%, to allow for measurement errors . Density dependence in population dynamics was modelled with scramble type (logistic, Ricker) to effect all vital rates, weighted for seedlings = 0.0001, juveniles = 0.001, adolescent = 0.25, sub-adults, adults and mature adults = 1. Within the model framework, demographic stochasticity was selected and environmental stochasticity was designated ‘lognormal’. Dispersal was set to zero. Maximum growth rate (Rmax) was set to a neutral value of 1 and quasi-extinction thresholds were set at 100 individuals. Each population model projected the abundance over 200 time steps (200 years), outputs of the mean of 100 replications. Predicted population growth (lambda λ), differences between starting population size and mean final population size, and time to quasi extinction, were compared between models.
We found that Lord Howe Island is getting warmer and drier and quantified the degree of temperature change with altitude (0.9 °C per 100 m), which is greater than rates often used to make climate change predictions. For H. canterburyana, differences in development rates, population structure, reproductive output and population growth rate were identified between altitudes. In contrast to expectations, the highest recruitment was at low altitudes and we found no evidence of upward range contraction of Hedyscepe canterburyana in response to recent climate change. We found that trunked H. canterburyana individuals had smaller diameter at breast height and were shorter at higher altitudes. Conversely, reproductive output was higher at higher altitudes under cloud cover. Hedyscepe canterburyana has relatively high genetic diversity distributed across the island, increasing its effective population size and its potential for persistence through environmental change. Genetic composition was not correlated with individual growth rate variation, suggesting the species has a plastic growth response. The presence of both genetic diversity and phenotypic plasticity indicates some potential for both a short-term buffer to climatic variability and the potential for genetic adaptation to occur in the long term.
High and low altitude populations of the species are predicted to slowly decline under ongoing rat predation with high altitude sites affected the most. We predict that the high altitude populations under current conditions will start to decline significantly in approximately 30 years, and there is a 70% chance of extinction within 180 years. However, the low altitude populations are not predicted to become extinct within the next two hundred years. We found that rat control would lead to a significant reduction in population decline particularly at high altitudes, and is likely to be more important for survival of this species than climate change. Thus, long term management aimed at rat control will be the most effective action to benefit this species. While rat eradication would be the most effective action, an alternative of rotating rat control measures around the island over time should enable cohorts of seedlings to establish in different environments.
This project was funded by the Department of Environment, Climate Change and Water NSW and the University of the Sunshine Coast. We wish to thank the Lord Howe Island Management Board especially B. Thompson, C. Hasleton and S. & H. Bower. We would also like to thank H. Hipperson (Imperial College London), J. Shick, R. Byrne, L. Wilson, J. Trehy, A. Denham and M. Ooi for field assistance, D. Hiscox for climbing expertise.
- MacArthur, R.H.; Wilson, E.O. The Theory of Island Biogeography; Princeton University Press: Princeton, NJ, USA, 1967. [Google Scholar]
- Simberloff, D. Extinction-proneness of island species-Causes and management implications. Raffles Bull. Zool. 2000, 48, 1–9. [Google Scholar]
- Dransfield, J.; Uhl, N.W.; Asmussen, C.B.; Baker, W.J.; Harley, M.M.; Lewis, C.E. Genera Palmarum: The Evolution and Classification of Palms; Royal Botanic Gardens, Kew: Richmond, Surry, UK, 2008. [Google Scholar]
- Kissling, W.D.; Baker, W.J.; Balslev, H.; Barfod, A.S.; Borchsenius, F.; Dransfield, J.; Govaerts, R.; Svenning, J.-C. Quaternary and pre-Quaternary historical legacies in the global distribution of a major tropical plant lineage. Glob. Ecol. Biogeogr. 2012, 21, 909–921. [Google Scholar] [CrossRef]
- Savolainen, V.; Anstett, M.C.; Lexer, C.; Hutton, I.; Clarkson, J.J.; Norup, M.V.; Powell, M.P.; Springate, D.; Salamin, N.; Baker, W.J. Sympatric speciation in palms on an oceanic island. Nature 2006, 441, 210–213. [Google Scholar]
- Babik, W.; Butlin, R.K.; Baker, W.J.; Papadopulos, A.S.T.; Boulesteix, M.; Anstett, M.C.; Lexer, C.; Hutton, I.; Savolainen, V. How sympatric is speciation in the Howea palms of Lord Howe Island? Mol. Ecol. 2009, 18, 3629–3638. [Google Scholar] [CrossRef]
- Still, C.J.; Foster, P.N.; Schneider, S.H. Simulating the effects of climate change on tropical montane cloud forests. Nature 1999, 398, 608–610. [Google Scholar]
- Hamilton, L.S. Mountain Cloud Forest Conservation and Research: A Synopsis. Mt. Res. Dev. 1993, 15, 259–266. [Google Scholar] [CrossRef]
- Bradshaw, A.D. Evolutionary Significance of Phenotypic Plasticity in Plants. Adv. Genet. 1965, 13, 115–155. [Google Scholar] [CrossRef]
- Guo, H.; Mazer, S.J.; Du, G.Z. Geographic variation in seed mass within and among nine species of Pedicularis (Orobanchaceae): Effects of elevation, plant size and seed number per fruit. J. Ecol. 2010, 98, 1232–1242. [Google Scholar] [CrossRef]
- Takahashi, K. Effects of altitude and competition on growth and mortality of the conifer Abies sachalinensis. Ecol. Res. 2010, 25, 801–812. [Google Scholar] [CrossRef]
- Green, P.S. Norfolk Island and Lord Howe Island; Australian Government Publishing Service: Canberra, Australia, 1994; Volume 49 Oceanic Islands 1. [Google Scholar]
- LHIB. Draft Review of the Permanent Park Preserve Plan of Management; Report to the Lord Howe Island Board: Lord Howe Island, Australia, 2002.
- Harris, R.; Cassis, G.; Auld, T.; Hutton, I. Floristics and structure of the mossy cloud forest of Mt Gower summit, Lord Howe Island. Pac. Conserv. Biol. 2005, 11, 246–256. [Google Scholar]
- Hedyscepe canterburyana. IUCN Red List of Threatened Species. Version 2010.4. International Union for Conservation of Nature and Natural Resources. Available online: http://www.iucnredlist.org/ (accessed on 19/08/2011).
- Thomas, C.D.; Cameron, A.; Green, R.E.; Bakkenes, M.; Beaumont, L.J.; Collingham, Y.C.; Erasmus, B.F.N.; Ferreira de Siqueira, M.; Grainger, A.; Hannah, L.; et al. Extinction risk from climate change. Nature 2004, 427, 145–148. [Google Scholar]
- Schwartz, M.W.; Iverson, L.R.; Prasad, A.M.; Matthews, S.N.; O’Connor, R.J. Predicting extinctions as a result of climate change. Ecology 2006, 87, 1611–1615. [Google Scholar] [CrossRef]
- Huntley, B. How Plants Respond to Climate Change: Migration Rates, Individualism and the Consequences for Plant Communities. Ann. Bot. (Lond.) 1991, 67, 15–22. [Google Scholar]
- Lenoir, J.; Gégout, J.C.; Pierrat, J.C.; Bontemps, J.D.; Dhôte, J.F. Differences between tree species seedling and adult altitudinal distribution in mountain forests during the recent warm period (1986-2006). Ecography 2009, 32, 765–777. [Google Scholar] [CrossRef]
- Chen, I.C.; Shiu, H.J.; Benedick, S.; Holloway, J.D.; Chey, V.K.; Barlow, H.S.; Hill, J.K.; Thomas, C.D. Elevation increases in moth assemblages over 42 years on a tropical mountain. Proc. Natl. Acad. Sci. USA 2009, 106, 1479–1483. [Google Scholar]
- Walther, G.R.; Gritti, E.S.; Berger, S.; Hickler, T.; Tang, Z.; Sykes, M.T. Palms tracking climate change. Glob. Ecol. Biogeogr. 2007, 16, 801–809. [Google Scholar] [CrossRef]
- Le Roux, P.C.; McGeoch, M.A. Rapid range expansion and community reorganization in response to warming. Glob. Change Biol. 2008, 14, 2950–2962. [Google Scholar] [CrossRef]
- Dang, H.S.; Zhang, Y.J.; Jiang, M.X.; Zhang, Q.F. Growth performance and range shift of the subalpine fir (Abies fargesii) in the Qinling Mountains, China. Int. J. Sustain. Dev. World Ecol. 2010, 17, 162–171. [Google Scholar] [CrossRef]
- Auld, T.D.; Hutton, I.; Ooi, M.K.J.; Denham, A.J. Disruption of recruitment in two endemic palms on Lord Howe Island by invasive rats. Biol. Invasions 2010, 12, 1–11. [Google Scholar] [CrossRef]
- Markham, A. Potential impacts of climate change on tropical forest ecosystems. Clim. Change 1998, 39, 141–143. [Google Scholar] [CrossRef]
- Foster, P. The potential impacts of global climate change on tropical montane cloud forests. Earth Sci. Rev. 2001, 55, 73–106. [Google Scholar] [CrossRef]
- Auld, T.D.; Hutton, I. Conservation Issues for the vascular flora of Lord Howe Island. Cunninghamia 2004, 8, 490–500. [Google Scholar]
- Implications of climate change for Australia’s World Heritage properties: A preliminary assessment. Technical Report for Department of the Environment, Water, Heritage and the Arts: Fenner School of Environment and Society, the Australian National University, Canberra, Australia, June 2009.
- Enright, N.J.; Watson, A.D. Population dynamics of the nikau palm, Rhopalostylis sapida (Wendl. et Drude), in a temperate forest remnant near Auckalnd, New Zealand. N. Z. J. Bot. 1992, 30, 29–43. [Google Scholar] [CrossRef]
- Rodríguez-Buriticá, S.; Orjuela, M.A.; Galeano, G. Demography and life history of Geonoma orbignyana: An understory palm used as foliage in Colombia. For. Ecol. Manag. 2005, 211, 329–340. [Google Scholar] [CrossRef]
- Widyatmoko, D.; Burgman, M.A.; Guhardja, E.; Mogea, J.P.; Walujo, E.B.; Setiadi, D. Population status, demography and habitat preferences of the threatened lipstick palm Cyrtostachys renda Blume in Kerumutan Reserve, Sumatr. Acta Oecol. 2005, 28, 107–118. [Google Scholar] [CrossRef]
- Gienapp, P.; Teplitsky, C.; Alho, J.S.; Mills, J.A.; Merilä, J. Climate change and evolution: Disentangling environmental and genetic responses. Mol. Ecol. 2008, 17, 167–178. [Google Scholar] [CrossRef]
- Lande, R. Genetics and demography in biological conservation. Science 1988, 241, 1455–1460. [Google Scholar]
- Jump, A.S.; Marchant, R.; Peñuelas, J. Environmental change and the option value of genetic diversity. Trends Plant Sci. 2009, 14, 51–58. [Google Scholar] [CrossRef]
- Bradshaw, A.D.; McNeilly, T. Evolutionary Response to Global Climatic Change. Ann. Bot. (Lond.) 1991, 67, 5–14. [Google Scholar]
- Jump, A.S.; Peñuelas, J. Running to stand still: Adaptation and the response of plants to rapid climate change. Ecol. Lett. 2005, 8, 1010–1020. [Google Scholar] [CrossRef]
- Davis, M.B.; Shaw, R.G. Range shifts and adaptive responses to quaternary climate change. Science 2001, 292, 673–679. [Google Scholar] [CrossRef]
- Pfennig, D.W.; Wund, M.A.; Snell-Rood, E.C.; Cruickshank, T.; Schlichting, C.D.; Moczek, A.P. Phenotypic plasticity’s impacts on diversification and speciation. Trends Ecol. Evol. 2010, 25, 459–467. [Google Scholar] [CrossRef]
- De Jong, G. Evolution of phenotypic plasticity: Patterns of plasticity and the emergence of ecotypes. New Phytol. 2005, 166, 101–118. [Google Scholar] [CrossRef]
- Zizumbo-Villarreal, D.; Fernández-Barrera, M.; Torres-Hernández, N.; Colunga-GarcíaMarín, P. Morphological variation of fruit in Mexican populations of Cocos nucifera L. (Arecaceae) under in situ and ex situ conditions. Genet. Res. Crop Evol. 2005, 52, 421–434. [Google Scholar] [CrossRef]
- Fleischer-Dogley, F.; Kettle, C.J.; Edwards, P.J.; Ghazoul, J.; Määttänen, K.; Kaiser-Bunbury, C.N. Morphological and genetic differentiation in populations of the dispersal-limited coco de mer (Lodoicea maldivica): Implications for management and conservation. Divers. Distrib. 2011, 17, 235–243. [Google Scholar] [CrossRef]
- Crimmins, T.M.; Crimmins, M.A.; Bertelsen, C.D. Flowering range changes across an elevation gradient in response to warming summer temperatures. Glob. Change Biol. 2009, 15, 1141–1152. [Google Scholar] [CrossRef]
- Sander, T.; König, S.; Rothe, G.M.; Janßen, A.; Weisgerber, H. Genetic variation of European beech (Fagus sylvatica L.) along an altitudinal transect at mount Vogelsberg in Hesse, Germany. Mol. Ecol. 2000, 9, 1349–1361. [Google Scholar] [CrossRef]
- Bellusci, F.; Pellegrino, G.; Palermo, A.M.; Gargano, D.; Musacchio, A. Genetic differentiation of the endemic orophyte Campanula pollinensis along an altitudinal gradient. Plant Biosyst. 2005, 139, 349–356. [Google Scholar] [CrossRef]
- Walther, G.R.; Post, E.; Convey, P.; Menzel, A.; Parmesan, C.; Beebee, T.J.C.; Fromentin, J.M.; Hoegh-Guldberg, O.; Bairlein, F. Ecological responses to recent climate change. Nature 2002, 416, 389–395. [Google Scholar]
- Minorsky, P.V. The Hot and the Classic. Plant Physiol. 2002, 129, 1421–1422. [Google Scholar] [CrossRef]
- Frankham, R. Genetics and extinction. Biol. Conserv. 2005, 126, 131–140. [Google Scholar] [CrossRef]
- Pullin, A.S. Conservation Biology; Cambridge University Press: Cambridge, New York ,NY, USA, 2002. [Google Scholar]
- Caujapé-Castells, J.; Tye, A.; Crawford, D.J.; Santos-Guerra, A.; Sakai, A.; Beaver, K.; Lobin, W.; Vincent Florens, F.B.; Moura, M.; Jardim, R.; et al. Conservation of oceanic island floras: Present and future global challenges. Perspect. Plant Ecol. 2010, 12, 107–129. [Google Scholar] [CrossRef]
- Campbell, D.J.; Atkinson, I.A.E. Effects of kiore (Rattus exulans Peale) on recruitment of indigenous coastal trees on northern offshore islands of New Zealand. J. Roy. Soc. N. Z. 1999, 29, 265–290. [Google Scholar] [CrossRef]
- Campbell, D.J.; Atkinson, I.A.E. Depression of tree recruitment by the Pacific rat (Rattus exulans Peale) on New Zealand’s northern offshore islands. Biol. Conserv. 2002, 107, 19–35. [Google Scholar] [CrossRef]
- Chapin, M.H. Rat Damage on Native Hawaiian Palms. Palms 2004, 48, 153–155. [Google Scholar]
- Meyer, J.Y.; Butaud, J.F. The impacts of rats on the endangered native flora of french Polynesia (Pacific Islands): Drivers of plant extinction or coup de grâce species? Biol. Invasions 2009, 11, 1569–1585. [Google Scholar] [CrossRef]
- Billing, J.; Harden, B. Control of introduced Rattus rattus L. on Lord Howe Island. I. The response of mouse populations to warfarin bait used to control rats. Wildl. Res. 2000, 27, 655–658. [Google Scholar] [CrossRef]
- Williams, S.E.; Shoo, L.P.; Isaac, J.L.; Hoffmann, A.A.; Langham, G. Towards an integrated framework for assessing the vulnerability of species to climate change. PLoS Biol. 2008, 6, e325. [Google Scholar] [CrossRef]
- Thomas, C.D. Translocation of species, climate change, and the end of trying to recreate past ecological communities. Trends Ecol. Evol. 2011, 26, 216–221. [Google Scholar] [CrossRef]
- Climate Change 2007: Synthesis Report. Contribution of Working Groups I, II and III to the Fourth Assessment Report of the Intergovernmental Panel on Climate Change. In Intergovernmental Panel on Climate Change; Core Writing Team, Pachauri, R.K., Resinger, A., Eds.; IPCC: Geneva, Switzerland, 2007.
- CSIRO. BOM State of the Climate; CSIRO & Australian Bureau of Meteorology: Canberra, Australia, 2012.
- Rotstayn, L.D.; Collier, M.A.; Dix, M.R.; Feng, Y.; Gordon, H.B.; O’Farrell, S.P.; Smith, I.N.; SSyktus, J. Improved simulation of Australian climate and ENSO-related rainfall variability in a global climate model with an interactive aerosol treatment. Int. J. Climatol. 2010, 30, 1067–1088. [Google Scholar]
- Loope, L.L.; Giambelluca, T.W. Vulnerability of island tropical montane cloud forests to climate change, with special reference to East Maui, Hawaii. Clim. Change 1998, 39, 503–517. [Google Scholar] [CrossRef]
- Raxworthy, C.J.; Pearson, R.G.; Rabibisoa, N.; Rakotondrazafy, A.M.; Ramanamanjato, J.B.; Raselimanana, A.P.; Wu, S.; Nussbaum, R.A.; Stone, D.A. Extinction vulnerability of tropical montane endemism from warming and upslope displacement: A preliminary appraisal for the highest massif in Madagascar. Glob. Change Biol. 2008, 14, 1703–1720. [Google Scholar] [CrossRef]
- Whittaker, R.J.; Bush, M.B.; Richards, K. Plant recolonization and vegetation succession on the Krakatau Islands, Indonesia. Ecol. Monogr. 1989, 59, 59–123. [Google Scholar] [CrossRef]
- Pounds, J.A.; Fogden, M.P.L.; Campbell, J.H. Biological response to climate change on a tropical mountain. Nature 1999, 398, 611–615. [Google Scholar]
- Pettit, N.E.; Dowe, J.L. Distribution and population structure of the vulnerable riparian palm Livistona lanuginosa A. N. Rodd (Arecaceae) in the Burdekin River catchment, north Queensland. Pac. Conserv. Biol. 2003, 9, 207–214. [Google Scholar]
- Wilson, L. Personal communication, Lord Howe Island: NSW, Australia, 2010.
- Svenning, J.C. Environmental heterogeneity, recruitment limitation and the mesoscale distribution of palms in a tropical montane rain forest (Maquipucuna, Ecuador). J. Trop. Ecol. 2001, 17, 97–113. [Google Scholar] [CrossRef]
- Widyatmoko, D.; Burgman, M. Influences of edaphic factors on the distribution and abundances of a rare palm (Cyrtostachys renda) in a peat swamp forest in eastern Sumatra, Indonesia. Aust. Ecol. 2006, 31, 964–974. [Google Scholar] [CrossRef]
- Tomlinson, P.B. The Structural Biology of Palms; Oxford University Press: Oxford, UK, 1990. [Google Scholar]
- Blach-Overgaard, A.; Svenning, J.C.; Dransfield, J.; Greve, M.; Balslev, H. Determinants of palm species distributions across Africa: The relative roles of climate, non-climatic environmental factors, and spatial constraints. Ecography 2010, 33, 380–391. [Google Scholar]
- Otero-Arnaiz, A.; Oyama, K. Reproductive phenology, seed-set and pollination in Chamaedorea alternans, an understorey dioecious palm in a rain forest in Mexico. J. Trop. Ecol. 2001, 17, 745–754. [Google Scholar]
- Adler, G.H.; Lambert, T.D. Spatial and temporal variation in the fruiting phenology of palms in isolated stands. Plant Species Biol. 2008, 23, 9–17. [Google Scholar] [CrossRef]
- Shapcott, A.; Hutton, I.; Baker, W.J.; Auld, T. Conservation genetics and ecology of an endemic montane palm on Lord Howe Islandand potential for resilience. Conserv. Genet. 2012, 13, 257–270. [Google Scholar] [CrossRef]
- Menzel, A.; Sparks, T.H.; Estrella, N.; Roy, D.B. Altered geographic and temporal variability in phenology in response to climate change. Glob. Ecol. Biogeogr. 2006, 15, 498–504. [Google Scholar]
- Bradshaw, W.E.; Holzapfel, C.M. Genetic response to rapid climate change: It’s seasonal timing that matters. Mol. Ecol. 2008, 17, 157–166. [Google Scholar] [CrossRef]
- Dowe, J.L.; Benzie, J.; Ballment, E. Ecology and genetics of Carpoxylon macrospermum H Wendl & Drude (Arecaceae), an endangered palm from Vanuatu. Biol. Conserv. 1997, 79, 205–216. [Google Scholar] [CrossRef]
- Eguiarté, L.E.; Perez-Nasser, N.; Piñero, D. Genetic structure, outcrossing rate and heterosis in Astrocaryum mexicanum (tropical palm): Implications for evolution and conservation. Heredity 1992, 69, 217–228. [Google Scholar] [CrossRef]
- Luna, R.; Epperson, B.K.; Oyama, K. High levels of genetic variability and inbreeding in two Neotropical dioecious plams with contrasting life histories. Heredity 2007, 99, 466–476. [Google Scholar] [CrossRef]
- Shapcott, A. Comparison of the population genetics and densities of five Pinanga palm species at Kuala Belalong, Brunei. Mol. Ecol. 1999, 8, 1641–1654. [Google Scholar] [CrossRef]
- Navascues, M.; Vendramin, G.G.; Emerson, B.C. The Effect of Altitude on the Pattern of Gene Flow in the Endemic Canary Island Pine, Pinus canariensis. Silvae Genet. 2008, 57, 357–363. [Google Scholar]
- Hartl, D.L. A Primer of Population Genetics, 3rd ed; Sinauer Associates: Sunderland, MA, USA, 2000. [Google Scholar]
- Cibrián-Jaramillo, A.; Bacon, C.D.; Garwood, N.C.; Bateman, R.M.; Thomas, M.M.; Russell, S.; Bailey, C.D.; Hahn, W.J.; Bridgewater, S.G.M.; DeSalle, R. Population genetics of the understory fishtail palm Chamaedorea ernesti-augusti in Belize: High genetic connectivity with local differentiation. BMC Genet. 2009, 10, 65. [Google Scholar]
- Scariot, A.; Lleras, E.; Hay, J.D. Reproductive biology of the palm Acrocinua aculeata in Central Brazil. Biotropica 1991, 23, 12–22. [Google Scholar] [CrossRef]
- Ghazoul, J. Pollen and seed dispersal among dispersed plants. Biol. Rev. Camb. Philos. 2005, 80, 413–443. [Google Scholar] [CrossRef]
- Gimenez-Benavides, L.; Albert, M.J.; Iriondo, J.M.; Escudero, A. Demographic processes of upward range contraction in a long-lived Mediterranean high mountain plant. Ecography 2011, 34, 85–93. [Google Scholar]
- Vandermeer, J.H. 377: On the Construction of the Population Projection Matrix for a Population Grouped in Unequal Stages. Biometrics 1975, 31, 239–242. [Google Scholar] [CrossRef]
- Silva Matos, D.M.; Freckleton, R.P.; Watkinson, A.R. The role of density dependence in the population dynamics of a tropical palm. Ecology 1999, 80, 2635–2650. [Google Scholar]
- Sampaio, M.B.; Scariot, A. Effects of stochastic herbivory events on population maintenance of an understorey palm species (Geonoma schottiana) in riparian tropical forest. J. Trop. Ecol. 2010, 26, 151–161. [Google Scholar] [CrossRef]
- Towns, D.R. Eradications as reverse invasions: Lessons from Pacific rat (Rattus exulans) removals on New Zealand islands. Biol. Invasions 2009, 11, 1719–1733. [Google Scholar] [CrossRef]
- Smith, D.G.; Shiinoki, E.K.; VanderWerf, E.A. Recovery of native species following rat eradication on Mokoli'i Island, O'ahu, Hawai'i. Pac. Sci. 2006, 60, 299–303. [Google Scholar] [CrossRef]
- Ratsirarson, J.; Silander, J.A., Jr.; Richard, A.F. Conservation and management of a threatened Madagascar palm species, Neodypsis decaryi, Jumele. Conserv. Biol. 1996, 10, 40–52. [Google Scholar]
- Whittaker, R.J.; Fernández-Palacios, J.M. Island Biogeography: Ecology, Evolution, and Conservation, 2nd ed; Oxford University Press: New York, NY, USA, 2007. [Google Scholar]
- Irvine, I. Late-Pliocene-Quaternary Biostratigraphy and Climatic Changes in DSDP 208, Lord Howe island Rise. Bull. Aust. Soc. Explor. Geophys. 1978, 9, 146–148. [Google Scholar] [CrossRef]
- Bijlsma, R.; Loeschcke, V. Environmental stress, adaptation and evolution: An overview. J. Evol. Biol. 2005, 18, 744–749. [Google Scholar]
- Billotte, N.; Marseillac, N.; Brottier, P.; Noyer, J.L.; Jacquemoud-Collet, J.P.; Moreau, C.; Couvreur, T.; Chevallier, M.H.; Pintaud, J.C.; Risterucci, A.M. Nuclear microsatellite markers for the date palm (Phoenix dactylifera L.): Characterization and utility across the genus Phoenix and in other palm genera. Mol. Ecol. Notes 2004, 4, 256–258. [Google Scholar] [CrossRef]
- Billotte, N.; Risterucci, A.M.; Barcelos, E.; Noyer, J.L.; Amblard, P.; Baurens, F.C. Development, characterisation, and across-taxa utility of oil palm (Elaeis guineensis Jacq.) microsatellite markers. Genome 2001, 44, 413–425. [Google Scholar]
- Gaiotto, F.A.; Brondani, R.P.V.; Grattapaglia, D. Microsatellite markers for heart of palm-Euterpe edulis and E. oleracea Mart. (Arecaceae). Mol. Ecol. Notes 2001, 1, 86–88. [Google Scholar] [CrossRef]
- Montufar, R.; Mariac, C.; Pham, J.L.; Pintaud, J.C. Isolation of 23 polymorphic microsatellite loci in the Neotropical palm Oenocarpus bataua Martius (Arecaceae). Mol. Ecol. Notes 2007, 7, 75–78. [Google Scholar]
- Shimizu, M.; Kosaka, N.; Shimada, T.; Nagahata, T.; Iwasaki, H.; Nagai, H.; Shiba, T.; Emi, M. Universal fluorescent labeling (UFL) method for automated microsatellite analysis. DNA Res. 2002, 9, 173–178. [Google Scholar]
- Peakall, R.; Smouse, P.E. GENALEX 6: Genetic analysis in Excel. Population genetic software for teaching and research. Mol. Ecol. Notes 2006, 6, 288–295. [Google Scholar]
- Frankham, R. Conservation genetics. Annu. Rev. Genet. 1995, 29, 305–327. [Google Scholar] [CrossRef]
- Wright, S. The Interpretation of Population Structure by F-Statistics with Special Regard to Systems of Mating. Evolution 1965, 19, 395–420. [Google Scholar] [CrossRef]
- Peakall, R.; Ruibal, M.; Lindenmayer, D.B. Spatial autocorrelation analysis offers new insights into gene flow in the Australian bush rat, Rattus fuscipes. Evolution 2003, 57, 1182–1195. [Google Scholar]
- Akçakaya, H. Population viability analyses with demographically and spatially structured models. Ecol. Bull. 2000, 48, 23–38. [Google Scholar]
- Akçakaya, H.; Atwood, J.L. A habitat-based metapopulation model of the California Gnatcatcher. Conserv. Biol. 1997, 11, 422–434. [Google Scholar]
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