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27 February 2020 Spatial Ecology of the Introduced Chinese Water Dragon Physignathus cocincinus in Hong Kong
Wai-Ho Chan, Anthony Lau, Paolo Martelli, Danielle Tsang, Wing-Ho Lee, Yik-Hei Sung
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Abstract

Basic ecological understanding is important for effective management of introduced species. If the species is rare or threatened in its native ranges, ecological knowledge gained from its introduced ranges may offer useful information for conservation. We radio-tracked 12 adult Physignathus cocincinus in Hong Kong, where it is introduced, to investigate their home range, movements, and habitat use. The home range of all P. cocincinus covered the stream, but 66% of relocations occur >5 m away from the stream. Movements did not differ between sexes and seasons. Females stayed at a longer distance from the stream than males. Lizards preferred woodland and concrete structures over orchards. For microhabitats, they preferred wider streams, greater height, and denser canopy cover. This infers the high association of this species with streams and riparian forests, which may be crucial for the establishment of introduced populations. To effectively manage the introduced populations through eradication efforts, areas away from streams (5–100 m) needs to be covered.

Introduction

Invasive species are one of the greatest threats to biodiversity worldwide (Wilcove et al., 1998; Clavero and Garcıa-Berthou, 2005). In many cases, if timely and effective erradication is not implemented, the spread of introduced species becomes uncontrollable and can harm local ecosystems (Wiles et al., 2003; Phillips et al., 2006). Basic ecological knowledge can guide effective management of introduced species. For example, applying knowledge on spatial use to evaluate plans for eradication and to predict the likelihood of further establishment of populations (Klug et al., 2015).

The Chinese water dragon, Physignathus cocincinus, is a semi-aquatic lizard that is native to southern China, Thailand, Myanmar, Vietnam, Laos, and Cambodia (Uetz et al., 2017). It is a popular species in the pet trade and has been introduced to Taiwan and Malaysia (Grismer, 2011). In Hong Kong, it was first recorded in 2005, which may be attributed to religious release or abandoned pets (To, 2005). It has been recorded in over 10 localities in Hong Kong (Y.-H. Sung, personal observations). Some populations appear to be robust and studies on the impacts of these introduced populations on the local ecosystem are overdue.

While some populations of P. cocincinus are robust in Hong Kong, a recent study found that native populations in Vietnam are severely threatened by harvesting for the local food market and the international pet market (Nguyen et al., 2018). Detailed studies on their basic ecology, either in its native or introduced ranges, are lacking, which may hinder effective conservation measures.

In this study, we sought to gather ecological information of the introduced populations of P. cocincinus in Hong Kong. Specifically, we (1) determine the home range size; (2) examine movement patterns; and (3) investigate habitat use and identify potential habitat parameters that influence use. The results may provide useful information for the management of introduced populations and the conservation of native populations.

Materials and Methods

Study area

We conducted this study in Tsing Yi Road West Park (22°21.170′ N, 114°05.985′ E), an urban park in the Hong Kong Special Administrative Region, China. Although this study was conducted in an urban park, the stream and riparian vegetation are similar to locations within protected areas where P. cocincinus has established in Hong Kong. Hong Kong has a subtropical climate, which is characterized by two distinctive seasons, a wet and hot summer (May to August), and a dry and cold winter (November to February) (Dudgeon and Corlett, 2004). The study stream section is approximately 200 m long, and the average stream width is 3.6 m. Both sides of the stream are dominated by dense riparian trees, including Sterculia lanceolate and Ficus variegate, and orchards that are actively managed, where Musa paradisiaca, Dimocarpus longan, Litchi chinensis, Artocarpus heterophyllus, Citrofortunella mitis, and Citrus maxima are planted.

Radio-tracking

Between August and November 2015, we searched along the stream at night and captured adult P. cocincinus by hand or using a noose and fishing rod. Upon capture, lizards were kept temporarily and transferred to Ocean Park, Hong Kong within 24 hours for transmitter implantation. We anesthetized the lizards using vaporized Isoflurane and surgically implanted a transmitter with coiled antenna (Model: BD-2H, expected battery life=3 months, Holohil System Ltd, Carp, Ontario, Canada) into the coelomic cavity. The weight of the transmitters was <5% of the weight of all radio-tracked lizards. We released lizards at the locations of capture within 48 hours after attachment. We collected relocation data one week after release using a flexible three-element Yagi antenna (Model: F172-3FB 02145, Wildlife Materials Inc., Illinois, USA) and a receiver (Model: IC-R20, ICOM Inc., Tokyo, Japan). We located each lizard twice a week during daytime hours (7:00–18:00). To account for nocturnal habitat use, we located each lizard once per two weeks during nighttime hours (19:00–23:00). We located each lizard by triangulation except for the lizards that were visually observed. We tracked all individuals until we could not detect the signal from the transmitters.

To determine habitat use, we recorded the habitat type (woodland, shrubland, orchard, concrete structure, and stream), substrate type (concrete/rock, woody debris/tree branch, and leaf litter/soil), height above ground, distance to stream, and percentage of canopy cover for each sighting. We measured the height above ground using a laser distance measurer (Model: DISTO D2, Leica Geosystems Inc., Heerbrugg, Switzerland). The distance to the stream was measured using a range finder or calculated using GIS program with the locations recorded using a GPS unit (Model: GPSMAP 64s, Garmin, Olathe, Kansas, USA). For lizards that were found in or within five meters from the stream, we also recorded the in-stream microhabitat type (pool, run, and riffle), stream width, and proportion of different types of substrate in the stream (boulder [>25.6 cm], cobble [6.4–25.6 cm], pebble [2.0–6.4 cm], and gravel [<2.0 cm]). For every relocation point, a random point was selected where habitat type and habitat parameters were recorded to indicate habitat availability. The random points were selected by picking two numbers randomly, one between 1 and 20 and the other between 1 and 360, representing distance (in meters) and bearing, respectively.

Data analysis

We used ArcMap 10.1 (ESRI, Redlands, California, USA) to estimate the home range of each lizard by calculating 100% minimum convex polygon (MCP) as MCP is recognized as a better method than kernel density estimation in estimating home range of reptiles (Row and Blouin-Demers, 2006). We calculated mean daily displacement by dividing the distances moved between relocations by the time interval (in days) between successive relocations. As P. cocincinus are active during the day, we excluded tracking data collected at night in movement calculation. We included the lizards that were tracked for more than four weeks in a season in the analysis, nine and eight lizards were tracked in the wet (August to October) and dry (November to January) season, respectively (Appendix 1). We compared the home range sizes, mean daily displacements, and distance to stream between sexes and seasons using Generalized Linear Mixed Models (GLMM) (Bolker et al., 2009) in software R (R Core Team, 2004). Sex and season were set as fixed effects while the lizard ID was considered as a random effect to account for individual variations. We used linear regression to examine correlations between home range size, daily displacements, and distance to stream with body size.

We calculated log ratios of used and available habitat types and in-stream microhabitat types in wet and dry seasons for compositional analysis and tested for non-random use of habitats using t-test (Aebischer et al., 1993). For compositional analysis of habitat types, we arbitrarily chose stream as the reference habitat against other habitat types. For the proportion of habitat types, we replaced 0 values with 0.0001 following Aebischer et al. (1993). For compositional analysis of in-stream microhabitat types, we arbitrarily chose riffle as the reference microhabitat against other microhabitats.

We used GLMM with binomial distribution to test which terrestrial and stream habitat variables were related to the occurrence of lizards, puting presence or absence of lizards as the response variable (Zuur et al., 2009). Prior to model building, we tested for multicollinearity by calculating variance inflation factors (VIF) for each habitat variable, and removed factors with VIF >4 (Fox, 1997). Proportion of gravels correlates with proportion of pebbles, boulders, and cobbles, and thus was removed from the analysis. For terrestrial habitat variables, we included relocations that were >5 m away from the stream. We set height above ground, substrate type, distance to stream, and canopy cover as fixed factors. For stream habitat variables, we included relocations that were in or ≤5 m away from the stream. We set height above ground, distance to stream, canopy cover, stream width, proportion of cobble, proportion of pebble, and proportion of boulder as fixed factors. For all models for terrestrial and stream habitat variables, we set lizard ID and season as random effects to account for individual and seasonal variations. We tested multicollinearity using package car (Fox et al., 2012) in software R before model building. We used package lme4 for model building (Bates, 2010), and function dredge of package MuMIn (Barton, 2011) in software R to select the best models based on the corrected form of Akaike's Information Criterion for small sample sizes (AICc) (Burnham and Anderson, 2002; Barton, 2011). Models that best explained the difference between used and available habitats were selected based on the comparison of AICc values between the most parsimonious (“best”) model (minimum AICc value) and other models. Models with AICc values within two of the best model were regarded as having similar support as the best model (Burnham and Anderson, 2002). We averaged the variables from models with similar support to obtain final estimates and standard errors for predictor variables.

Fig. 1.

Relocation points of 5 female and 7 male Physignathus cocincinus in the wet and dry season in Tsing Yi, Hong Kong between August 2015 and January 2016.

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Results

We attached radio transmitters to 12 lizards (5 females and 7 males; Fig. 1). All lizards were tracked for over one month (mean 74±27 days, range 37–113 days; Appendix 1). Among the 229 relocations made, we observed the lizards directly in 121 occasions (52.8%) while estimations of locations were made according to the signals in the remaining 108 occasions (47.2%). Lizards were found >5 m away from streams in 148 relocations (64.6%) while being found ≤5 m from the streams in 81 occasions (35.4%). Mean (±SD; range) 100% MCP of all tracked lizards was 1793 m2 (±1604; 469–5159). In the wet season, mean 100% MCP of males and females were 397 m2 (±423; 85–1020) and 1436 m2 (±1776; 469–4586), respectively (Fig. 2A). In the dry season, mean 100% MCP of males and females were 1825 m2 (±1835; 489–5159; Fig. 2B) and 663 m2 (±650; 203–1123), respectively. Home range (MCP) sizes did not differ significantly between seasons (Z=–1.31, P=0.21; Fig. 3A) and sexes (Z=–0.62, P=0.55).

Fig. 2.

Home ranges (100% minimum convex polygon) of 12 radio-tracked Physignathus cocincinus in Tsing Yi, Hong Kong in the (A) wet season, (B) dry season, and (C) at night between August 2015 and January 2016. Numbers indicate lizard ID and red and orange polygons indicate ranges of males and females, respectively.

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Fig. 3.

(A) Home ranges (100% minimum convex polygon), (B) mean daily displacement, and (C) mean distance to stream of 5 female and 7 male Physignathus cocincinus in wet and dry seasons in Tsing Yi, Hong Kong between August 2015 and January 2016.

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Mean daily displacements in the wet season and the dry season were 5.13 m (±3.68; 3.45–7.20 and 4.11 m (±4.88; 2.96–5.89), respectively (Appendix 2). Mean daily displacements of females and males were 3.77 m (±4.31; 3.77–7.30) and 4.34 m (±4.59; 3.30–6.01), respectively. Mean daily displacements did not differ significantly between seasons (Z=0.18, P=0.86) and sexes (Z=–1.61, P=0.13) (Fig. 3B).

Mean distance to stream of males and females were 10.18 m (±10.40; 4.13–20.25) and 19.77 m (±21.55; 3.22–31.20), respectively (Appendix 2). Mean distance to stream in wet season and dry season were 13.16 m (±18.04; 2.42–31.21) and 13.67 m (±13.81; 3.49–28.8), respectively. Mean distances to the stream differed significantly between seasons (Z=–2.153, P=0.032; Fig. 3C) and sexes (Z=2.412, P=0.017). Body size of lizards (snout-vent length) was not correlated with home range size (P=1.00), daily displacement (P=0.90), or distance to the stream (P=0.27).

In the wet season, lizards showed nonrandom selection of habitat types with preferences for woodlands (t=2.853, P=0.03) and concrete structures (t=–2.573, P=0.04) over orchards (Table 1). However, in the dry season, lizards exhibited random selection of habitats (P>0.1 in all comparisons). For stream microhabitat types, we found random selection in both seasons (P>0.15 in all comparisons) (Table 1).

For terrestrial habitat variables, the best models included canopy cover and height above ground (Appendix 3). The probability of occurrence increased with canopy cover and height above ground (Table 2 and 3). For stream habitat variables, the best models included canopy cover, stream width, and proportion of boulders (Appendix 3). The probability of occurrence increased with canopy cover and stream width for lizards that were relocated ≤5 m away from the stream (Table 3).

Discussion

The introduced populations of P. cocincinus established in Hong Kong provide an opportunity for filling knowledge gaps of their basic ecology. We found that P. cocincinus prefers woodland, and taller microhabitats with denser canopy cover. More mature forests with tall trees and dense canopy cover provide more shelters and food for arboreal lizards (Ober and Hayes, 2008; Perry et al., 2009). In Hong Kong, P. cocincinus has been recorded in over ten locations, all of which include streams with riparian forests, suggesting that riparian forests and streams are crucial for the establishment of introduced populations.

Table 1.

Mean percentage (SD) of habitats and in-stream microhabitats used by 12 Physignathus cocincinus and available within home ranges in wet and dry season in Tsing Yi, Hong Kong between 2015 and 2016.

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Table 2.

Terrestrial and stream habitat parameters (mean and SD in parentheses) in habitats used by 12 Physignathus cocincinus and available within home ranges in wet and dry season in Tsing Yi, Hong Kong between 2015 and 2016.

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Table 3.

Terrestrial and stream habitat variables that best explained (GLMM) probability of occurrence of 12 Physignathus cocincinus in Tsing Yi, Hong Kong between 2015 and 2016. Bold indicates significant variables.

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The home range of all tracked P. cocincinus encompassed the stream (Fig. 1 and 2), however, over 60% of relocations were made at >5 m away from the stream, supporting extensive use of nearby habitats away from streams. In addition, one female lizard (lizard ID 11) stayed away from the stream (maximum distance=85 m) for more than 35 days before the signal from the transmitter was lost. This provides an implication for the management of introduced populations: terrestrial forests away from streams (5–100 m) may need to be included for eradication or control of this species.

Lizards may choose microhabitats to obtain thermal benefits, and reduce disturbance and risk of predation. On land, despite the association of P. cocincinus with trees, they preferred rock and concrete structures over orchard. Rock and concrete structures retain heat, allowing effective thermoregulation (Webb and Whiting, 2005; Croak et al., 2008). Crevices in rocks and concrete structures provide shelters to P. cocincinus for escaping from predators (Campbell, 2015), whereas the sparse vegetation in orchards may not provide secure shelters. Frequent visitation by people to the orchards may also deter usage by the lizards.

Territoriality is probably pronounced in P. cocincinus, concordant to the studies on the closely related species, Australian water dragons Intellagama (formerly Physignathus) lesueurii (Baird et al., 2012). The home range at night of most males, except two individuals, did not overlap (Fig. 2C). In the field, we seldom observed males in close proximity to each other at any time, further supporting the existence of male-male territoriality. Between sexes, we found that males, the larger sex, stayed closer to the stream than females did. Males were often observed staying on trees above streams, where they could dive into the water when disturbed. Dominant males may defend deeper and larger pools, which are better refuges to escape from predators. This also explains their preference for wider streams.

It was surprising that we observed similar home range sizes and movements between the wet and dry season, given that seasonal differences in movements have been shown in many reptile species which become inactive during the dry season (Huey and Pianka, 1977). The dry season covered in the present study (November 2015 to January 2016) was exceptionally hot and wet: the highest average temperature in November and the highest monthly rainfall in January were recorded (Hong Kong Observatory 2018). Therefore, in this study, movements may be abnormal in this dry season and further study is needed to investigate the impacts of climatic condition on movement patterns.

We supplement an example that studying introduced populations can benefit the conservation of native populations (Gibson and Yong, 2017). The population density in the study site (114.3 individuals/100 m along the stream [Y.-H. Sung, unpublished data]) is considerably higher than that of the native populations in Vietnam (1.98–2.64 individuals/100 m), which has been under harvesting pressure (Nguyen et al., 2018). Little is known about the conservation status of other native populations. The robust population in Hong Kong might be of conservation value, acting as a source for captive breeding or reintroduction in the future (Gibson and Yong, 2017).

Although the sample size (12 individuals were tracked) of this study is relatively small, we found that P. cocincinus exhibits extensive use of habitats away from streams, an observation that may assist in targeting habitat for eradication of populations. To conserve native populations of P. cocincinus, preservation of riparian forests within 100 m from the stream may be necessary. For the management of introduced populations, the ecological impacts of the introduction of P. cocincinus has not been studied in Hong Kong. However, in Taiwan, the introduced P. cocincinus preys upon a high diversity of invertebrates, potentially competing with endemic lizard species (Ciao, 2015). For effective control, for example eradication, we suggest including riparian forests approximately 100 m away from streams.

Acknowledgments

We are grateful for financial support from the Environment and Conservation Fund, HKSAR Government (ECF 2015-85). We thank David Dudgeon for providing radio-transmitters and Nancy Karraker for the support of this project. We thank Pui Ting Chan, Wing Yue Tang and Chun Kit Ng for assistance in the field. Permission for using a noose to capture lizards was obtained from the Agriculture, Fisheries and Conservation Department, HKSAR Government. The Committee on the Use of Human & Animal Subjects, Hong Kong Baptist University granted approval for use of animals (HASC/ 15-16/0010).

Literature Cited

1.

Aebischer, N. J., Robertson, P. A., and Kenward, R. E. 1993. Compositional analysis of habitat use from animal radio-tracking data. Ecology 74: 1313–1325. Google Scholar

2.

Baird, T. A., Baird, T. D., and Shine, R. 2012. Aggressive transition between alternative male social tactics in a long-lived Australian dragon (Physignathus lesueurii) living at high density. PlosOne 7: e41819. Google Scholar

3.

Barton, K. 2011. MuMIn: Multi-model Inference. R package version 1.0.0.  http://CRAN.Rproject.org/package/MuMIn/ (accessed 20 August 2016) Google Scholar

4.

Bates, D. M. 2010. lme4: Mixed-effects modeling with R . Springer.  http://lme4.r-forge.r-project.org/book (accessed 10 April 2015) Google Scholar

5.

Bolker, B. M., Brooks, M. E., Clark, C. J., Geange, S. W., Poulsen, J. R., Stevens, M. H. H., and White, J.-S. S. 2009. Generalized linear mixed models: a practical guide for ecology and evolution. Trends in Ecology & Evolution 24: 127–135. Google Scholar

6.

Burnham, K. P. and Anderson, D. R. 2002. Model Selection and Multimodel Inference: A Practical Information-theoretic Approach , 2nd Edition . Springer-Verlag, New York. Google Scholar

7.

Campbell, A. B. 2015. An Analysis of the Demography and Habitat Usage of Roatán's Spiny-tailed Iguana, Ctenosaura oedirhina. Unpublished Ph.D. thesis. Florida Atlantic University, Boca Raton. Google Scholar

8.

Ciao, B.-K. 2015. Study on Food Habits of the Invasive Asian Water Dragon Physignathus cocincinus in Taiwan. Unpublished master's thesis. National Taipei University of Education, Taipei. Google Scholar

9.

Clavero, M. and García-Berthou, E. 2005. Invasive species are a leading cause of animal extinctions. Trends in Ecology & Evolution 20: 110. Google Scholar

10.

Croak, B. M., Pike, D. A., Webb, J. K., and Shine, R. 2008. Three-dimensional crevice structure affects retreat site selection by reptiles. Animal Behaviour 76: 1875–1884. Google Scholar

11.

Dudgeon, D. and Corlett, R. T. 2004. The Ecology and Biodiversity of Hong Kong , 1st Edition . Agriculture Fisheries and Conservation Department, Government of Hong Kong SAR & Joint Publishing Company, Hong Kong. Google Scholar

12.

Fox, J. 1997. Applied Regression Analysis, Linear Models, and Related Methods. Sage, Thousand Oaks. Google Scholar

13.

Fox, J., Weisberg, S., Bates, D., and Fox, M. 2012. Package ‘car '.  http://cran-r.project.org/web/packages/car/car.pdf (accessed 15 March 2017) Google Scholar

14.

Gibson, L. and Yong, D. L. 2017. Saving two birds with one stone: solving the quandary of introduced, threatened species. Frontiers in Ecology and the Environment 15: 35–41. Google Scholar

15.

Grismer, L. L. 2011. Lizards of Peninsular Malaysia, Singapore, and Their Adjacent Archipelagos: Their Description, Distribution, and Natural History. Edition Chimaira, Frankfurt am Main. Google Scholar

16.

Hong Kong Observatory 2018. Climatological Information Services .  http://www.hko.gov.hk (accessed 7 June 2018) Google Scholar

17.

Huey, R. B. and Pianka, E. R. 1977. Seasonal variation in thermoregulatory behavior and body temperature of diurnal Kalahari lizards. Ecology 58: 1066–1075. Google Scholar

18.

Klug, P. E., Reed, R. N., Mazzotti, F. J., McEachern, M. A., Vinci, J. J., Craven, K. K., and Yackel Adams, A. A. 2015. The influence of disturbed habitat on the spatial ecology of Argentine black and white tegu (Tupinambis merianae), a recent invader in the Everglades ecosystem (Florida, USA). Biological Invasions 17: 1785–1797. Google Scholar

19.

Nguyen, T. Q., Ngo, H. N., Pham, C. T., Van, H. N., Ngo, C. D., van Schingen, M., and Ziegler, T. 2018. First population assessment of the Asian water dragon (Physignathus cocincinus Cuvier, 1829) in Thua Thien Hue Province, Vietnam. Nature Conservation 26: 1–14. Google Scholar

20.

Ober, H. K. and Hayes, J. P. 2008. Influence of forest riparian vegetation on abundance and biomass of nocturnal flying insects. Forest Ecology and Management 256: 1124–1132. Google Scholar

21.

Perry, R. W., Rudolph, D. C., and Thill, R. E. 2009. Reptile and amphibian responses to restoration of fire - maintained pine woodlands. Restoration Ecology 17: 917–927. Google Scholar

22.

Phillips, B. L., Brown, G. P., Webb, J. K., and Shine, R. 2006. Invasion and the evolution of speed in toads. Nature 439: 803. Google Scholar

23.

R Core Team 2014. R: A Language and Environment for Statistical Computing . R Foundation for Statistical Computing, Vienna, Austria.  http://www.R-project.org/ (accessed 7 November 2017) Google Scholar

24.

Row, J. R. and Blouin-Demers, G. 2006. Kernels are not accurate estimators of home-range size for herpetofauna. Copeia 2006: 797–802. Google Scholar

25.

To, A. 2005. Another alien has landed: the discovery of a wild population of water dragon, Physignathus cocincinus, in Hong Kong. Porcupine 33: 3–4. Google Scholar

26.

Uetz, P., Hošek, J., and Hallermann, J. 2017. The Reptile Database .  http://www.reptiledatabase.org/ (accessed 11 May 2018) Google Scholar

27.

Webb, J. K. and Whiting, M. J. 2005. Why don't small snakes bask? Juvenile broad - headed snakes trade thermal benefits for safety. Oikos 110: 515–522. Google Scholar

28.

Wilcove, D. S., Rothstein, D., Dubow, J., Phillips, A., and Losos, E. 1998. Quantifying threats to imperiled species in the United States. BioScience 48: 607–615. Google Scholar

29.

Wiles, G. J., Bart, J., Beck, R. E., and Aguon, C. F. 2003. Impacts of the brown tree snake: patterns of decline and species persistence in Guam's avifauna. Conservation Biology 17: 1350–1360. Google Scholar

30.

Zuur, A. F., Ieno, E. N., Walker, N. J., Saveliev, A. A., and Smith, G. M. 2009. Mixed Effects Models and Extensions in Ecology with R , 1st Edition . Springer, New York. Google Scholar

Appendices

Appendix 1

Home range sizes of 5 female and 7 male Physignathus cocincinus in the wet and dry season in Tsing Yi, Hong Kong between August 2015 and January 2016.

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Appendix 2

Daily displacement and distance to stream of 5 female and 7 male Physignathus cocincinus in the wet and dry season in Tsing Yi, Hong Kong between August 2015 and January 2016.

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Appendix 3

The best GLMM models, based on corrected Akaike's Information Criterion (AICc) examining the relationship between terrestrial and stream habitat variables, and probability of occupancy of 12 Physignathus cocincinus in Tsing Yi, Hong Kong between 2015 and 2016. Bold indicates models with similar support to the best model (≤2 ΔAICc).

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© 2020 by The Herpetological Society of Japan
Wai-Ho Chan, Anthony Lau, Paolo Martelli, Danielle Tsang, Wing-Ho Lee, and Yik-Hei Sung "Spatial Ecology of the Introduced Chinese Water Dragon Physignathus cocincinus in Hong Kong," Current Herpetology 39(1), 55-65, (27 February 2020). https://doi.org/10.5358/hsj.39.55
Accepted: 22 January 2020; Published: 27 February 2020
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habitat use
home range
invasive species
movement
radio-tracking
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