Volume 100, Issue 4 p. 958-968
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Tree cover–fire interactions promote the persistence of a fire-sensitive conifer in a highly flammable savanna

Clay Trauernicht

Corresponding Author

Clay Trauernicht

School of Plant Science, Private Bag 55, University of Tasmania, Hobart Tas. 7001, Australia

Correspondence author. E-mail: [email protected]Search for more papers by this author
Brett P. Murphy

Brett P. Murphy

School of Plant Science, Private Bag 55, University of Tasmania, Hobart Tas. 7001, Australia

Geographic Information Science Center of Excellence, South Dakota State University, 1021 Medary Ave., Wecota Hall Box 506B, Brookings, SD 57007, USA

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Talia E. Portner

Talia E. Portner

School of Plant Science, Private Bag 55, University of Tasmania, Hobart Tas. 7001, Australia

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David M. J. S. Bowman

David M. J. S. Bowman

School of Plant Science, Private Bag 55, University of Tasmania, Hobart Tas. 7001, Australia

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First published: 04 April 2012
Citations: 65


1. Callitris intratropica is a long-lived, obligate-seeding, fire-sensitive overstorey conifer that typically occurs in small groves (<0.1 ha) of much higher tree densities than the surrounding, eucalypt-dominated tropical savanna in northern Australia. We used C. intratropica groves of varying canopy cover to examine the role of feedbacks between fire and tree cover in the persistence of a fire-sensitive tree species and the maintenance of habitat heterogeneity in a highly flammable savanna.

2. We examined the population structure and floristic composition of C. intratropica groves and conducted controlled burns with Aboriginal landowners to test the prediction that groves of C. intratropica with closed canopies inhibit savanna fires by physically altering the fuel arrays below trees. We measured pre- and post-burn fuel availability, the probability of burning and fire intensity along transects (55–75 m) spanning entire C. intratropica groves and extending into the surrounding savanna matrix.

3. We found that closed-canopy groves of C. intratropica had higher densities of seedlings and saplings than open-canopy groves and supported a distinct plant community. Closed-canopy groves also had a lower probability of burning and less severe fires due to a lower availability of fine fuels than the surrounding savanna.

4. Synthesis. Our results suggest that the observed regeneration within closed-canopy C. intratropica groves within frequently burnt savanna reflects a vegetation–fire feedback. A significant, negative relationship between canopy cover and the probability of burning provides strong evidence that closed-canopy C. intratropica groves are capable of excluding low-intensity savanna fires, thereby enabling the persistence of patches of fire-sensitive forest or woodland amid open, highly flammable savanna vegetation. We present our findings as evidence that alternative stable state dynamics may play a role in determining savanna diversity and structure.


The diversity in size and age of habitat patches within an ecosystem is closely linked to the heterogeneity of disturbance across the landscape (Denslow 1995; Hobbs 1996; Turner 2005; Collins & Smith 2006; Peterson & Reich 2008). Thus, in flammable ecosystems, the ecological interactions that influence burning heterogeneity have important implications for understanding broader patterns of biological diversity and composition. While climate-driven factors such as short-term fire weather, rainfall seasonality and fuel productivity shape the general conditions under which fire occurs in ecosystems, positive and negative feedbacks among plants, animals and their environment further modulate patterns of burning. For instance, high herbivore densities can reduce fuel loads, while high graminoid productivity increases fuel availability, consequently affecting ecosystem flammability at different temporal and spatial scales (de Knegt et al. 2008; Fuhlendorf et al. 2009; Setterfield et al. 2010; Mayer & Khalyani 2011). Contrasting fire regimes observed across habitat boundaries also suggest that overstorey woody plant composition and abundance play an important role in altering a system’s propensity to burn (Peterson & Reich 2008; Hoffmann et al. 2009; Warman & Moles 2009; Staver, Archibald & Levin 2011). Trees and shrubs display a wide range of adaptations that have the potential to facilitate or inhibit fire at the individual level (Bond & Midgley 1995; Schwilk 2003; Kane, Varner & Hiers 2008). How woody plant-fire interactions scale up to affect flammability and burning heterogeneity at the patch, community or ecosystem scale is therefore an important aspect of savanna and forest ecology (Mourik et al. 2007; Nowacki & Abrams 2008; Beckage, Platt & Gross 2009; Engber et al. 2011; Mandle et al. 2011; Kitzberger et al. 2012).

In this study, we examine the potential of a fire-sensitive savanna tree species to exclude fires and thereby contribute to habitat heterogeneity and the persistence of other fire-sensitive species in an Australian tropical savanna. Callitris intratropica R.T. Baker & H.G. Smith (syn. Callitris collumellaris var. intratropica Silba) is a long-lived (>200 years), obligate-seeding conifer of Gondwanan origin that is widespread throughout northern Australia. The persistence of C. intratropica in one of the most fire-prone ecosystems on earth (Russell-Smith et al. 2007) is a key question concerning the composition of these savannas. Region-wide declines in the species’ abundance had been noted by biologists as early as the 1920s and continue into the present across much of northern Australia (Easton 1922; Bowman & Panton 1993). These, as well as recent and dramatic declines in other species assemblages, notably small mammals and granivorous birds, have been attributed to the shift in fire regimes from Aboriginal patch burning to unmanaged, higher intensity wildfires within the past century (Franklin 1999; Bowman et al. 2001; Woinarski et al. 2010). Aboriginal landowners have long recognized high C. intratropica mortality as a sign of poor fire management (Haynes 1985). Thus, adapting this traditional knowledge and using C. intratropica as an indicator of ecologically beneficial fire regimes is of great interest to contemporary management and conservation programmes in Aboriginally owned Arnhem Land and World Heritage Kakadu National Park.

In northern Australian savannas, C. intratropica can occur as isolated, mature trees but commonly forms small (typically <0.1 ha), discrete groves with higher tree densities than the scattered eucalypts, which otherwise dominate the savanna overstorey. Callitris intratropica groves vary in canopy cover and can be broadly delineated into two types – open- and closed-canopy groves (Fig. 1). Aside from differences in canopy cover, open-canopy groves appear to differ from closed-canopy groves in their lack of seedling and sapling regeneration and the continuity of the grass understorey. Despite these distinct spatial patterns in C. intratropica distribution, the mechanisms and temporal dynamics that maintain these groves remain unclear. It is well established that frequent savanna fires limit the establishment and recruitment of woody plants (Mourik et al. 2007; Hoffmann et al. 2009) – especially if they are obligate-seeding species (i.e. incapable of resprouting after fire) like C. intratropica (Cohn et al. 2011; Prior et al. 2011). Conversely, high rates of C. intratropica recruitment have been observed in savannas where fire has been excluded (Bowman, Wilson & Davis 1988). Callitris intratropica is a long-lived species, and larger trees appear capable of surviving decades of high-frequency surface fires typical of Australian savannas (Prior, Bowman & Brook 2007). We therefore suspect that these open-canopy groves represent a state in which the grove structure has been degraded by one or several severe fires; however, demonstrating a longitudinal degradation from closed- to open-canopy groves to individuals is beyond the temporal scope of this study. Rather, we suggest that groves with varying canopy cover (open versus closed) provide important clues to the mechanisms behind both the persistence of C. intratropica and broader patterns of heterogeneity and diversity in these savannas. Our objective is therefore to provide a clear ecological description of these two grove types and examine the fine-scale interaction between C. intratropica and savanna fires.

Details are in the caption following the image

The context of the study system. (a) Closed-canopy groves of Callitris intratropica form clearly defined habitat boundaries with the matrix of open savanna dominated by Eucalyptus tetrodonta and Eucalyptus miniata and are clearly distinguishable from (b) open-canopy C. intratropica groves. (c) Canopy cover distributions (derived from hemispherical photographs) illustrate differences among plots in closed-canopy groves, open-canopy groves and open eucalypt savanna. (d) A map of Arnhem Land shows the study site in relation to Kakadu National Park and the Arnhem Plateau (shaded grey).

The spatial clumping of C. intratropica parallels patterns in other fire-prone systems, including congeners elsewhere in Australia (Cohn et al. 2011; Prior et al. 2011), Pinus and Quercus species dynamics in North American grasslands (Guerin 1993; Platt 1999; Nowacki & Abrams 2008), shola forests of India (Mohandass & Davidar 2009) and tree groves or bush islands in African and South American savannas (Couteron & Kokou 1997; Furley 2007). It has been argued that the persistence of vegetation boundaries under identical climatic and edaphic conditions is due to alternative stable state dynamics. Alternative stable state theory essentially attributes vegetation with the potential to alter abiotic conditions, thereby deterministically maintaining distinct ecological ‘regimes’ (Scheffer et al. 2001; Folke et al. 2004). In the context of fire, for example, the theory has been proposed to explain abrupt ecosystem boundaries between savanna and rain forest (Hoffmann et al. 2009; Warman & Moles 2009; Staver, Archibald & Levin 2011) and sclerophyllous shrubland and forest (Perry & Enright 2002; Odion, Moritz & DellaSala 2010). But alternative stable state theory also has conceptual implications for habitat composition at smaller spatial scales, whereby feedbacks between vegetation and disturbance by fire may shape patch-level heterogeneity (Laycock 1991). The classic example of a positive feedback is the grass–fire cycle (D’Antonio, Hughes & Vitousek 2001). Yet fire-impeding species (e.g. Kane, Varner & Hiers 2008) as invaders in flammable systems may alter the probability of disturbance at the patch level, thereby creating a self-promoting negative feedback (Buckley, Bolker & Rees 2007; Stevens & Beckage 2009). Therefore, examining the patterns of burning across the boundary between open- and closed-canopy vegetation within savannas may help elucidate whether and how fire feedbacks affect the persistence of fire-sensitive vegetation at the local scale and habitat heterogeneity at the landscape scale.

Here, we first describe the floristic composition and community and population structure of open- and closed-canopy groves of C. intratropica in relation to the surrounding matrix of eucalypt savanna. Using controlled burns conducted with Aboriginal landowners, we then empirically test the prediction that closed-canopy groves of C. intratropica inhibit savanna burning by physically altering the habitat below trees. We specifically address the following hypotheses:

  • 1

    The composition and structure of woody understorey vegetation in closed-canopy groves of C. intratropica differ from that of open-canopy C. intratropica groves and savanna.

  • 2

    Callitris intratropica regeneration is greater in closed- than in open-canopy groves.

  • 3

    Fine fuel cover and biomass are lower within closed-canopy groves of C. intratropica than in the surrounding savanna.

  • 4

    The probability of burning and fire intensity are lower within closed-canopy groves of C. intratropica.

Materials and Methods

Study Site

Surveys of C. intratropica groves and experimental savanna fires were conducted at Dukladjarranj along the Cadell River on the northern rim of the Arnhem Plateau, within the Djelk Indigenous Protected Area of north-central Arnhem Land, Northern Territory (Fig. 1d). The Arnhem Plateau is a low massif (<400 m) of deeply dissected Middle Proterozoic quartzose sandstone and is a regional centre of species endemism (Woinarski et al. 2006). The region is characterized by very short fire return times (1–3 years), and 40–60% of the landscape may burn annually (Gill et al. 2000; Edwards & Russell-Smith 2009). A general trend within the past century towards unmanaged, higher intensity wildfires occurring in the late dry season is widely attributed to the decline of Aboriginal patch burning across most of the region (Bowman et al. 2001; Yibarbuk et al. 2001; Russell-Smith et al. 2007). Our study site Dukladjarranj is a Gunei language group Aboriginal clan estate comprising an area of c. 90 km2 and has been under nearly continuous management since before European colonization. Detailed descriptions of the study area are provided by Yibarbuk et al. (2001) and Murphy & Bowman (2007).

Survey of Callitris Groves

In the mid-dry season (July–August) 2010, a total of 21 discrete C. intratropica groves were randomly selected at Dukladjarranj ranging in size from 100 to 650 m2. Ten closed-canopy (>50% canopy cover) and five open-canopy groves were situated east of the Cadell River in an area of open savanna, which had last burned in 2008. In addition, three groves of each type were located to the west of the Cadell River among more rocky country, which had experienced a late dry season, intense burn in October 2009. LANDSAT-derived fire history for the study site is currently available only as far back as 2006. Vegetation surrounding groves in both areas consisted of open savanna-woodland dominated by Eucalyptus tetrodonta and Eucalyptus miniata [mean basal area = 7.5 m2 ha−1 ±0.7 (SE); mean density = 168 stems ha−1 ± 18 (SE)].

Sampling at C. intratropica groves consisted of between two and five adjacent 5-m-wide transects, depending on the size of the grove. Transects ran from 25 m outside the grove, completely through the grove, and extended 25 m beyond the far side of the grove into the eucalypt savanna matrix. Hence, transect length varied from 55 to 75 m, and all transects ran parallel to the prevailing south-easterly trade winds, which spread dry season fires. In each transect, we recorded the diameter at breast height (d.b.h.) and x- and y-coordinates of all trees ≥130 cm tall.

A line was marked down the centre of each transect at 5-m intervals beginning at 2.5 m, effectively defining a plot centre for adjacent 5 × 5 m plots along the length of each transect. In alternating 5 × 5 m plots, we recorded the species and counted all shrubs and small trees (<5 cm d.b.h.) in each of two size classes (50–200 cm and ≥ 200 cm). Vouchers were collected and identified at the Northern Territory Herbarium in Darwin. At each 5 × 5 m plot centre, hemispherical canopy photographs were taken 1 m above ground level using a fish-eye lens (Pentax DA 10–17 mm; Pentax Ricoh Imaging, Ltd, Denver, CO, USA) mounted on a tripod. For sites consisting of only two parallel transects, photographs were taken every 5 m along the centre line joining the two transects due to the time constraints of taking canopy photographs at dawn and dusk to prevent sun flares. Canopy cover was measured from each photograph as the percentage of closed-canopy pixels using the Gap Light Analyzer software (Frazer, Canham & Lertzman 1999). Tree coordinates were plotted in a GIS database to derive tree counts for each 5 × 5 m plot and the distance of the C. intratropica individual nearest to each plot centre.

Burning Heterogeneity and Experimental Fires

The heterogeneity of habitat burning was measured at all 21 C. intratropica groves by recording the centre of each 5 × 5 m plot as burnt or unburnt after fires had passed around and/or through the grove. We also recorded scorch heights (maximum height of damaged, browned foliage) on 12 trees in the savanna matrix around each C. intratropica grove, a metric that has been shown to be correlated with fire intensity in this region (Williams, Gill & Moore 1998; Setterfield et al. 2010). However, it is important to note that scorch height may better reflect the effect of fire on vegetation (i.e. fire damage) than the actual behaviour of the fire (Hood 2010). Burn measurements at the 15 groves east of the Cadell River were recorded within several days of fires, which occurred during the course of the study, whereas measurements at the six groves west of the river were recorded approximately 8 months after a late fire in the previous dry season.

Variation in fuels and fire behaviour across the boundary between savanna and closed-canopy C. intratropica groves was examined in greater detail by intentionally setting fires under the supervision of Aboriginal landowners at seven of the 21 C. intratropica groves. One additional grove was accidentally burned from helicopter by local rangers in our absence, and we were therefore able to record fuel data but not aspects of fire behaviour and fire intensity. The area of savanna surrounding all eight of these groves last burned in 2008.

At each of the eight groves, per cent cover was estimated and mean height measured for available fuels within 1 × 1 m quadrats at each 5 × 5 m plot centre before burning and immediately after fires had passed the transects. Fuel categories included tree litter (the leaf litter layer above humus and soil horizons), live graminoids, dead graminoids, shrubs <50 cm tall and coarse fuels (woody debris >0.64 cm diameter). Three 10-g samples of litter and grass fuels were also collected and sealed in plastic bags inside and outside each C. intratropica grove. Samples were weighed before and after oven-drying to determine fuel moisture. In addition, before burning at each grove, the standing biomass of litter, dead graminoids and live graminoids was cut and weighed from three, randomly placed 1 × 1 m quadrats inside the C. intratropica grove and three quadrats outside the grove.

These fires enabled us to measure fire behaviour and fuels before, during and after burning. Fires were lit as an arc of patch fires c. 50 m upwind from each C. intratropica grove, so that the fires connected into a single front moving parallel with the transects. As fires approached C. intratropica groves, rate of spread was measured at three locations and height of the flame front was measured at five locations. Wind speed was measured with a hand-held anemometer, while temperature and humidity were derived from observations at Jabiru and Maningrida airports, the nearest meteorological stations located c. 150 and 65 km from the field site, respectively. During the burns, we used the amount of water vaporized from open calorimeters to measure the energy released by the fire as a proxy for fire intensity (Perez & Moreno 1998). Aluminium cans were filled with 50 g of water, weighed to the nearest 0.01 g and placed at ground level at each 5 × 5 m plot centre before burning. Five control cans were placed outside the burn area to account for ambient evaporation. Cans were collected and reweighed immediately after the fire passed, and water loss due to vaporization was determined by subtracting the mean water loss in the control cans from the water loss of the burnt cans.


All data modelling employed linear and generalized linear models (GLMs) with model selection based on Akaike Information Criterion (AICc) as outlined in the information-theoretic framework (Anderson & Burnham 2002). We used mixed models wherever possible, incorporating site (i.e. each C. intratropica grove) as a random effect to account for the slight random variation in both environmental conditions and fire events among groves (Bolker et al. 2009). For all response variables that produced normal errors, we employed spatially explicit linear mixed models (LMMs), which incorporated the x- and y-coordinates of all sample points to account for spatial autocorrelation (Crawley 2007) using the ‘lme’ function in the ‘nlme’ package in R (Pinheiro et al. 2009). For analyses of data with binomial and Poisson distributed errors, we used GLMs or generalized LMMs (GLMMs; ‘lmer’ package in R), which do not allow for spatial structure to be incorporated into the analyses. For clarification, all model types, data transformations and global parameterizations are listed for each response variable in Table S1 (See Supporting Information).

The hypothesis that woody plant composition differs among open- and closed-canopy C. intratropica groves and the eucalypt savanna matrix was explored using non-metric multidimensional scaling (NMDS) as part of the ‘vegan’ package in R (Oksanen et al. 2011). The ordination used 3-dimensions (based on scree plots of NMDS stress values) and Bray–Curtis dissimilarities to model the differences among all 5 × 5 m plots based on the composition and abundance of 59 plant species (excluding C. intratropica). We also tested the strength of this separation as a function of plot location (eucalypt savanna versus open-canopy versus closed-canopy C. intratropica groves) with a permutational multivariate analysis of variance (permanova) also based on Bray–Curtis dissimilarities using the ‘vegan’ package in R.

We tested for structural differences in the woody plant community among closed-canopy groves, open-canopy groves and savanna by modelling the total count of shrubs and small trees in each plot as a function of grove type (open- versus closed-canopy) and plot location using a GLMM with log-normal Poisson errors for overdispersed data (Elston et al. 2001). Plot location was based on the distance of each plot centre to the nearest C. intratropica individual to group plots into three categories: (i) inside grove (<5 m); (ii) grove edge (5–10 m); and (iii) outside grove (<10 m). We selected a categorical over a continuous distance variable in this and subsequent analyses because we expected our dependent variables to display a threshold rather than a continuous response across the habitat boundary.

We tested the hypothesis that open- and closed-canopy C. intratropica groves differ in regeneration patterns by examining population structures based on tree size classes. We calculated the mean and standard error of stem density among C. intratropica groves of each type (open- versus closed-canopy groves) for 5 cm d.b.h. classes, beginning with 0–4.9 cm.

To test the hypothesis that closed-canopy groves of C. intratropica have lower fine fuel availability, we employed LMMs to examine the importance of plot location to the following fuel measurements: (i) index of grass fuel abundance: total grass cover × height; (ii) litter cover; (iii) cover of shrubs <50 cm tall; and (iv) index of coarse fuel abundance: coarse fuel cover × height. We used a least-squares linear model (‘lm’ function in R) of fuel moisture as a function of fuel type, site and sample location (inside versus outside grove) to determine fuel moisture content for estimates of fuel biomass. Biomass of live graminoids, dead graminoids and litter were modelled as a function of sample location (inside versus outside grove) using non-spatial LMMs with site as a random factor.

To test the hypothesis that closed-canopy groves of C. intratropica are capable of reducing the spread of savanna fires, we used a binomial GLMM to examine the importance of canopy cover to the proportion of plot centres burnt, a binary response variable. Using canopy cover as a single, continuous explanatory variable in this analysis captured the key ecological feature distinguishing closed-canopy groves of C. intratropica from both open-canopy groves and eucalypt savanna (Fig. 1c).

The hypothesis that closed-canopy groves of C. intratropica reduce the intensity of fires was tested by modelling the amount of water vaporized from calorimeters as a function of plot location using LMMs. To see which of the fuel measurements were important to fire intensity, we also used LMMs to model water loss as a function of net change in fuel cover (i.e. fuel consumed) for the fuel variables described above.


Compositional Differences among C. intratropica Groves

Plotting the first two dimensions of the NMDS ordination illustrated a clear distinction between plots in closed-canopy groves and plots within the eucalypt savanna matrix, with those in open-canopy groves intermediate (Fig. 2a). The NMDS reached a stress level of 0.20, which suggested a ≤ 1% chance of the ordination having a random structure (Sturrock & Rocha 2000). The permanova also supported this pattern, with plot location supported as a significant factor explaining the separation of points (F = 18.6, P <0.01). Callitris intratropica groves and eucalypt savanna also differed structurally in their associated woody plant community, with higher stem counts of shrubs and small trees inside closed-canopy groves than inside open-canopy groves or outside groves (wi > 0.99; Fig. 2b). In terms of regeneration patterns, closed- and open-canopy groves of C. intratropica showed clear differences with notably lower densities of C. intratropica individuals among smaller size classes in open-canopy groves (Fig. 3). Despite this difference, the mean total basal area of C. intratropica was similar between the two grove types [closed groves: 19.4 ± 2.9 (SE); open groves: 23.3 ± 3.8 (SE)].

Details are in the caption following the image

The structural and compositional aspects of the woody plant community among closed-canopy and open-canopy Callitris intratropica groves and the surrounding eucalypt savanna matrix. (a) A scatterplot of the first two axes of an ordination using non-metric multidimensional scaling (stress = 0.20) is based on woody plant species composition (excluding C. intratropica) from 25-m2 plots sampled among closed-canopy groves, open-canopy groves and eucalypt savanna. (b) GLMM predictions of counts of shrubs >50 cm tall are presented as a function of plot location relative to C. intratropica and C. intratropica grove type. Error bars represent standard errors, and the Akaike weight (wi) relative to the null model is presented.

Details are in the caption following the image

Mean Callitris intratropica stem densities per diameter at breast height (d.b.h.) size class are shown for closed- and open-canopy groves. Error bars represent standard errors.

Negative Feedback between C. intratropica Cover and Fire

Fire weather and fuel conditions during our experimental burns resulted in low-intensity surface fires. Mean wind speed during the fires was moderate, ranging from 15 to 20 km h−1 from the east to southeast; mean relative humidity was 38%; and temperature was 31 °C. anovas of fuel moisture predicted differences among fuel types with no differences among sites [live graminoids: 57% ± 2 (SE); dead graminoids: 27% ± 2 (SE); litter: 15% ± 2 (SE)]. anovas of rate of spread [mean = 1.4 ms−1 ± 0.1(SE)] and flame height [mean = 0.81 m ± 0.15(SE)] indicated no significant differences among the seven fires intentionally lit at C. intratropica groves. The mean intensity along fire fronts outside C. intratropica stands was 640 kW m−1 (Byram 1959) based on rate of spread data, estimates of graminoid fuel consumption [mean = 261 kg ha−1 ± 74 (SE)] from cover and biomass measurements along transects, and mean heat of combustion for grass fuels (17 781 kJ kg−1; Trollope 1984). This estimate falls within the range of low-intensity savanna fires that are typical of the mid-dry season for the region (Russell-Smith & Edwards 2006).

The fuels data supported the hypothesis that closed-canopy groves of C. intratropica reduce the availability of fine fuels. LMMs predicted lower graminoid fuel abundance (% cover × height) and lower graminoid biomass inside closed-canopy groves (Fig. 4a, d, e; abundance: wi = 0.98; dead biomass: ***wi > 0.99; live biomass: wi > 0.99). Our analyses indicated an increase in the abundance of coarse fuels (% cover × height; Fig. 4c; wi > 0.99) and a decrease in low shrub cover inside closed-canopy groves (Fig. 4b; wi > 0.99). Although no relationship was found between litter cover and the presence of a C. intratropica canopy, our analyses demonstrated higher litter biomass within closed-canopy C. intratropica groves (Fig. 4f; wi > 0.99). Analyses of calorimeter water loss as a function of fuel consumed found the change in cover of low shrubs and litter were both important to fire intensity measurements (wi = 0.99, R2 =0.29).

Details are in the caption following the image

Relationships between available fuels (i.e. before burning) and plot locations relative to Callitris intratropica groves. The upper panels present spatially explicit linear mixed model (LMM) predictions for fuel cover measurements taken along transects for (a) graminoid abundance, (b) low shrub cover and (c) coarse fuel abundance. The lower panels present LMM predictions based on biomass collected from 1 × 1 m plots inside and outside closed-canopy groves for (d) live graminoids, (e) dead graminoids and (f) litter. Error bars represent the standard error of model predictions, and Akaike weights (wi) relative to the null model are presented.

Our analyses showed that the probability of habitat burning decreases with increasing canopy cover based on the GLMM (Fig. 5a; wi > 0.99; R2 =0.32), thus supporting our hypothesis that closed-canopy C. intratropica groves are able to limit the spread of fire. We present R2 values calculated from model deviances based on log-likelihood (Nagelkerke 1991); however, it is important to note that deriving R2 for models with random effects is problematic (e.g. Xu 2003). The analyses of the calorimeter data also supported the hypothesis that fire intensity is lower inside closed-canopy C. intratropica groves relative to open savanna (Fig. 5b; wi = 0.97).

Details are in the caption following the image

Relationships between Callitris intratropica groves and savanna fires. Panel (a) presents the relationship between the proportion of plots burnt (binned in 5% cover increments) and canopy cover, which is a key factor distinguishing closed-canopy C. intratropica groves from open-canopy groves and the eucalypt savanna matrix. Dashed vertical lines show median canopy cover values for closed-canopy groves, open-canopy groves and eucalypt savanna. Panel (b) presents linear mixed model (LMM) predictions of fire intensity, measured by water loss from open calorimeters, as a function of plot location relative to closed-canopy C. intratropica groves. Error bars represent standard errors, and Akaike weights (wi) are presented relative to the null model.


Fire is considered a principal driver of habitat heterogeneity in savannas (e.g. Scholes & Archer 1997; Sankaran et al. 2005), yet the ways in which feedbacks between fire and woody vegetation affect the spatial patterns of disturbance within plant communities and ecosystems remain unclear. Here, we focussed on the occurrence of open- and closed-canopy groves of C. intratropica (Fig. 1), a fire-sensitive savanna conifer, in a highly fire-prone ecosystem to better understand the mechanisms that shape and maintain savanna heterogeneity. Our results showed marked differences in the floristics and community and population structures between closed-canopy groves and both open-canopy groves and the surrounding savanna matrix. For example, the NMDS ordination (Fig. 2a) illustrates a clear pattern of separation among plots into closed-canopy C. intratropica groves and eucalypt savanna, indicating that the boundary between closed-canopy groves and savanna (Fig. 1a) is also characterized by differences in the woody plant community. These compositional patterns are mirrored by differences in the stem counts of woody plants over 50 cm tall (Fig. 2b), which was highest in closed-canopy groves and, importantly, very similar for open-canopy groves and eucalypt savanna.

Fire is the primary disturbance limiting woody plant establishment in Australian savannas, and therefore, the lack of juveniles and saplings (<15 cm d.b.h.) in open-canopy groves may be an indication that these groves are more likely to burn than groves with closed canopies (Fig. 3). Of course, fire can affect tree establishment in other ways, for example, by altering fecundity (Quintana-Ascencio & Menges 2000; Caddy & Gross 2006). However, high counts of C. intratropica seedlings have been observed to establish between fire events in both grove types (C. Trauernicht, unpublished data), indicating adult trees in open-canopy groves maintain their reproductive capacity. Callitris intratropica seedlings take many years to reach maturity and are much more vulnerable to fire than adult trees (C. Trauernicht, unpublished data; Russell-Smith 2006). Therefore, we argue that the population structure of open groves is ultimately shaped by higher rates of seedling and sapling mortality due to fire. Although an admittedly static representation of demography, the lower densities in smaller size classes for both open- and closed-canopy groves suggest that, at the patch scale, these populations may be declining (Rubin, Manion & Faber-Langendoen 2006). Gaps in size class structures may also reflect the fact that C. intratropica is a mast seeder and relies on episodic recruitment (e.g. Stocker 1966; Drewa et al. 2008; Prior et al. 2010). However, the temporal variability among the processes limiting seedling recruitment can make population structures difficult to interpret and a forthcoming paper will examine C. intratropica demography in greater detail. Modelling long-term population stability at the patch scale will be critical in determining whether C. intratropica groves are expanding and/or whether the species relies on the initiation of new patches in a meta-population context. Given the longevity of C. intratropica adults (>200 years), population dynamics may also provide a strong indication of the degree to which current fire regimes have changed since extant groves established. Yet the key aspect of the data we present here is that the higher density of seedlings and saplings in closed-canopy groves (Fig. 3) strongly implies that some kind of feedback mechanism is reducing the likelihood of disturbance within these groves (e.g. Stevens & Beckage 2009), thereby allowing smaller trees to escape mortality.

Previous anecdotal descriptions have linked fire exclusion by C. intratropica to the litter layer forming within groves (Stocker & Mott 1981; Bowman & Wilson 1988). Our results support this assertion with closed-canopy groves having greater litter biomass than the surrounding savanna (Fig. 4f). However, it is more likely the reduction in fine fuel cover and biomass – specifically graminoids and low shrubs (Fig. 4a, b, d, f) – within groves that ultimately reduces the probability of habitat burning. Grasses are the primary fuel source for fires in these savannas (e.g. Setterfield et al. 2010), and our analyses found low shrubs to be an important factor driving observed fire intensities. Increased litter cover has been shown to negatively affect grass establishment (Schramm & Ehrenfeld 2010; Scott et al. 2010; Viard-Cretat et al. 2010). Alternatively, multiple studies have found shading to be a limiting factor to the growth and survival of C4 grasses, which are dominant fuels in temperate and tropical savannas (Veenendaal, Shushu & Scurlock 1993; Lett & Knapp 2003; Scott et al. 2010). Light limitation is an obvious physical effect of closed-canopy C. intratropica groves on the local environment (Fig. 1c). However, it is difficult to disentangle the effects of shading and litter on fuels with our data and both processes may be important. Regardless of the mechanism, the reduction in grass biomass within C. intratropica groves has direct consequences for limiting both fire intensity, critical for adult survival and stand persistence, and fire occurrence, critical for juvenile recruitment (e.g. Thaxton & Platt 2006; Engber et al. 2011).

We examined the potential for a feedback between fire and C. intratropica more explicitly by measuring the extent of habitat burnt along transects extending across the boundary of eucalypt savanna and closed- and open-canopy groves after fires had passed through our field sites. Our data provide compelling evidence that closed-canopy groves of C. intratropica have a lower probability of being burnt (Fig. 5a). In addition, calorimeter measurements suggest that those areas that do burn within closed-canopy C. intratropica groves experience fires of lower intensity than outside or along the edges of groves (Fig. 5b). These results have important implications for understanding how C. intratropica persists in such a flammable ecosystem. The apparent feedback between closed-canopy C. intratropica groves and fire has the potential to maintain long fire-free intervals within groves even under frequent, low-intensity, ambient fire conditions. From a demographic perspective, the ability of these groves to exclude fires would be critical to maintaining recruitment among smaller, highly fire-sensitive size classes (Russell-Smith 2006). This not only provides an explanation of observed differences in population structure among grove types (Fig. 3), but also suggests the mechanism by which the species self-organizes into groves. The persistence of C. intratropica in the landscape requires further examination to determine the ultimate fate of damaged groves, as well as the degree to which the species depends on the tree cover–fire feedback we describe versus the initiation of new groves. Nonetheless, our results suggest the decline and degradation of C. intratropica groves are due to increases in fire intensity rather than in fire frequency (Russell-Smith et al. 2010), although establishing specific thresholds for fire impacts on canopy cover and tree survival would require observations of fires at varying intensities (e.g. Cohn et al. 2011).

A growing body of literature has explored the potential of woody plants to both facilitate and impede fire in flammable ecosystems (Bond & Midgley 1995; Schwilk 2003; Kane, Varner & Hiers 2008). On broader scales, alternative stable state theory has been invoked to explain how vegetation–fire feedbacks maintain contrasting disturbance regimes across ecosystem boundaries (Hoffmann et al. 2009; Odion, Moritz & DellaSala 2010; Staver, Archibald & Levin 2011). We argue that the potential for a feedback between fire and closed-canopy groves of C. intratropica suggests a similar mechanism may be operating at the patch level and community level in savannas. A canopy cover–fire feedback has obvious and direct implications for the demography and persistence of C. intratropica. However, the community composition data (Fig. 2a, b) also suggest that fire exclusion by C. intratropica has implications for broader patterns of vegetation structural complexity and diversity. At larger spatial scales, the persistence of closed-canopy C. intratropica groves essentially maintains a mosaic of small-scale forest or woodland patches within the wider eucalypt savanna matrix. Unfortunately, establishing a longitudinal decline due to fire damage from closed-canopy to open-canopy groves and eventually to isolated, individual trees is beyond the temporal scope of the present study. However, we hypothesize that open-canopy groves provide evidence of a state change, in terms of canopy cover (Fig. 1c), community structure (Fig. 2b) and habitat flammability (Fig. 5a), from C. intratropica woodland to eucalypt savanna conditions, despite the survival of C. intratropica adults.

While the fire feedback we describe is critical to the persistence of C. intratropica and potentially other fire-sensitive species, continued regional declines in C. intratropica abundance suggest that this mechanism cannot withstand the high-intensity fires typical of current fire regimes (Bowman & Panton 1993; Edwards & Russell-Smith 2009; Cohn et al. 2011). There is a strong case that the prevailing pattern of landscape-scale habitat degradation in northern Australia (Russell-Smith et al. 1998; Bowman et al. 2001; Franklin et al. 2005; Woinarski et al. 2010) is related to the breakdown of Aboriginal fire management. The life histories of extant C. intratropica groves in this region span the transition across much of the region from >50 000 years of Aboriginal management to what can be aptly described as modern wilderness (Bowman et al. 2001). Thus, the spatial patterns of C. intratropica groves and their potential to tolerate frequent, low-intensity burning likely hold further clues to disentangling the complex relationships between people and savanna landscapes (e.g. Price & Bowman 1994). We hope that by establishing the mechanism by which C. intratropica can exclude fire, we can better understand the species’ potential as an indicator of fine-grain landscape heterogeneity, the availability of long-unburnt habitat and the system’s response to changing fire regimes. Although still a contentious issue, the maintenance of habitat heterogeneity by fire is currently thought to be crucial for the integrity of communities across multiple guilds of species (Schwilk, Keeley & Bond 1997; Bradstock et al. 2005; Van Dyke et al. 2007; Yarnell et al. 2007; Clarke 2008; Fuhlendorf et al. 2009). Our research on vegetation–fire feedbacks at the patch scale provides further insight into the processes driving habitat complexity in Australian savannas and raises the question of how alternative stable state dynamics may shape patterns of savanna structure and burning world-wide.


We are very grateful to the Rostron family, Wesley Campion and the Djelk Aboriginal Ranger group for their support. Many thanks to the staff at the Northern Territory Herbarium for help with plant identification. The comments of Thomas Kitzberger, Dick Williams and two anonymous referees greatly improved earlier versions of the manuscript. Grants from the ANZ Holsworth Endowment, Australian Geographic, the Ecological Society of Australia and the Australian Research Council (Linkage project LP110200006) funded this research.