Scinovex

Research article · 2025 · Full text

International Journal of Biology Sciences

Behavioral thermoregulation and habitat selection in desert-dwelling lizard species

Leandro MaidanaMartina LeivaFacundo Galarza

Volume 7(2) · Pages 168–171 · DOI: 10.33545/26649926.2025.v7.i2c.766 ↗

Research areasAmphibian and Reptile BiologyPhysiological and biochemical adaptationsSpecies Distribution and Climate Change

↓ Read full-text PDF0 citations

Abstract

Author-written

Behavioral thermoregulation refers to the active selection of microhabitats that allow ectotherms to maintain body temperatures within a preferred range despite fluctuating ambient conditions. This research compared thermoregulatory behaviour and habitat use among three sympatric lizard species (Liolaemus darwinii, L. multimaculatus, and Ctenophorus kingii) inhabiting the Monte Desert scrubland near Rosario, Argentina. Focal observations were conducted on 180 individuals across 36 transects between October 2022 and February 2023. Body temperature was recorded using cloacal thermometry at each capture event. L. darwinii maintained a mean field body temperature of 36.8 ± 1.2 °C and shuttled between sun and shade at a rate of 4.7 transitions per hour. L. multimaculatus was more thermally lax, tolerating a wider range (34.3 ± 1.8 °C) and showing fewer shuttling bouts (2.3/h). C. kingii preferred the highest temperatures (38.1 ± 0.9 °C) and occupied open rocky substrates almost exclusively during midday. Habitat selection modelling indicated that substrate type and shrub canopy cover were the strongest predictors of species occurrence. These patterns suggest that interspecific differences in thermal preference mediate habitat partitioning in this arid assemblage.

Summary

Source-checked

Plain-language reading of the full paper, prepared with AI and checked against the text. Each point links to the authors' own words.

  1. Why it matters

    • Desert lizards must balance the need for warmth to support vital functions like digestion and immunity against the risk of lethal overheating. View evidence ↗

      Why it matters

      Desert lizards must balance the need for warmth to support vital functions like digestion and immunity against the risk of lethal overheating.

      In the paper's own words

      “Desert lizards face a daily balancing act: they need warmth for digestion, locomotion, and immune function, but overheating can be lethal within minutes”

      Page 1

      Found in: Introduction

      Read it in the full textOpen PDF at page 1 ↗
    • Differences in preferred body temperatures among co-occurring ectotherms can reduce niche overlap and promote coexistence by influencing their activity timing and habitat use. View evidence ↗

      Why it matters

      Differences in preferred body temperatures among co-occurring ectotherms can reduce niche overlap and promote coexistence by influencing their activity timing and habitat use.

      In the paper's own words

      “When two or more ectotherms share a habitat, differences in preferred body temperature can translate into differences in activity timing, substrate use, and microhabitat selection effectively reducing niche overlap and promoting coexistence”

      Page 1

      Found in: Introduction

      Read it in the full textOpen PDF at page 1 ↗
    • The partitioning of thermal resources among similar lizard species in the Monte Desert is poorly understood due to a lack of multi-species field studies. View evidence ↗

      Why it matters

      The partitioning of thermal resources among similar lizard species in the Monte Desert is poorly understood due to a lack of multi-species field studies.

      In the paper's own words

      “How these ecologically similar species partition thermal resources is not well understood, partly because most thermoregulatory work in the region has focused on single-species laboratory setups rather than multi-species field comparisons”

      Page 1

      Found in: Introduction

      Read it in the full textOpen PDF at page 1 ↗
  2. The question

    • The study aimed to quantify differences in field body temperature and thermal precision, describe daily patterns of substrate and shade use, and model environmental predictors of species occurrence to assess thermal niche partitioning. View evidence ↗

      The question

      The study aimed to quantify differences in field body temperature and thermal precision, describe daily patterns of substrate and shade use, and model environmental predictors of species occurrence to assess thermal niche partitioning.

      In the paper's own words

      “The objectives were to (1) quantify interspecific variation in field body temperature and thermal precision, (2) describe diel patterns of shade use and substrate selection, and (3) model the environmental predictors of species occurrence to assess the degree of thermal niche partitioning”

      Page 1

      Found in: Introduction

      Read it in the full textOpen PDF at page 1 ↗
  3. What they did

    • Researchers conducted focal observations on 180 lizards across 36 transects from October 2022 to February 2023. View evidence ↗

      What they did

      Researchers conducted focal observations on 180 lizards across 36 transects from October 2022 to February 2023.

      In the paper's own words

      “Focal observations were conducted on 180 individuals across 36 transects between October 2022 and February 2023.”

      Page 1

      Found in: Introduction

      Read it in the full textOpen PDF at page 1 ↗
    • The sample included 72 L. darwinii, 61 L. multimaculatus, and 47 C. kingii individuals. View evidence ↗

      What they did

      The sample included 72 L. darwinii, 61 L. multimaculatus, and 47 C. kingii individuals.

      In the paper's own words

      “A total of 180 individuals were sampled (L. darwinii n = 72; L. multimaculatus n = 61; C. kingii n = 47).”

      Page 2

      Found in: Introduction

      Read it in the full textOpen PDF at page 2 ↗
    • Body temperature was measured using a cloacal thermocouple within 30 seconds of capturing the lizards. View evidence ↗

      What they did

      Body temperature was measured using a cloacal thermocouple within 30 seconds of capturing the lizards.

      In the paper's own words

      “Body temperature (Tb) was measured within 30 seconds of capture using a Fluke 52 II thermocouple inserted 5 mm into the cloaca.”

      Page 2

      Found in: Introduction

      Read it in the full textOpen PDF at page 2 ↗
    • Operative temperatures were recorded every 15 minutes using copper models designed to mimic lizard reflectance. View evidence ↗

      What they did

      Operative temperatures were recorded every 15 minutes using copper models designed to mimic lizard reflectance.

      In the paper's own words

      “Temperature loggers (iButton DS1921G, Maxim Integrated) recorded operative temperatures at 15-minute intervals inside copper lizard models painted to match average lizard reflectance.”

      Page 2

      Found in: Instrumentation

      Read it in the full textOpen PDF at page 2 ↗
    • Habitat selection was analyzed using generalized linear models with binomial error, predicting species presence based on substrate, canopy cover, distance to rock, and operative temperature. View evidence ↗

      What they did

      Habitat selection was analyzed using generalized linear models with binomial error, predicting species presence based on substrate, canopy cover, distance to rock, and operative temperature.

      In the paper's own words

      “using generalised linear models with binomial error, with species presence/absence as the response and substrate type, canopy cover, distance to rock, and operative temperature as predictors.”

      Page 2

      Found in: Discussion

      Read it in the full textOpen PDF at page 2 ↗
  4. What they found

    • The three species had significantly different mean field body temperatures: C. kingii was the highest (38.1 ± 0.9 °C), followed by L. darwinii (36.8 ± 1.2 °C) and L. multimaculatus (34.3 ± 1.8 °C). View evidence ↗

      What they found

      The three species had significantly different mean field body temperatures: C. kingii was the highest (38.1 ± 0.9 °C), followed by L. darwinii (36.8 ± 1.2 °C) and L. multimaculatus (34.3 ± 1.8 °C).

      In the paper's own words

      “Mean Tb (°C) | 36.8 ± 1.2 | 34.3 ± 1.8 | 38.1 ± 0.9 | < 0.001”

      Page 2

      Found in: Table 1

      Read it in the full textOpen PDF at page 2 ↗
    • L. darwinii exhibited the highest active thermoregulation with a shuttling rate of 4.7 ± 1.3 transitions per hour, compared to 2.3 ± 0.8/h for L. multimaculatus and 1.6 ± 0.5/h for C. kingii. View evidence ↗

      What they found

      L. darwinii exhibited the highest active thermoregulation with a shuttling rate of 4.7 ± 1.3 transitions per hour, compared to 2.3 ± 0.8/h for L. multimaculatus and 1.6 ± 0.5/h for C. kingii.

      In the paper's own words

      “Shuttling rate (/h) | 4.7 ± 1.3 | 2.3 ± 0.8 | 1.6 ± 0.5 | < 0.001”

      Page 2

      Found in: Table 1

      Read it in the full textOpen PDF at page 2 ↗
    • C. kingii showed the highest thermal precision (lowest de index of 0.9 ± 0.4 °C), while L. multimaculatus was the most thermally variable (de index of 2.7 ± 1.1 °C). View evidence ↗

      What they found

      C. kingii showed the highest thermal precision (lowest de index of 0.9 ± 0.4 °C), while L. multimaculatus was the most thermally variable (de index of 2.7 ± 1.1 °C).

      In the paper's own words

      “de index (°C) | 1.4 ± 0.6 | 2.7 ± 1.1 | 0.9 ± 0.4 | < 0.001”

      Page 2

      Found in: Table 1

      Read it in the full textOpen PDF at page 2 ↗
    • Habitat selection models identified rocky substrates and low canopy cover as the strongest predictors of species occurrence. View evidence ↗

      What they found

      Habitat selection models identified rocky substrates and low canopy cover as the strongest predictors of species occurrence.

      In the paper's own words

      “Substrate: rock | 1.83 | 0.41 | 4.46 | < 0.001”

      Page 2

      “Canopy cover (%) | −0.94 | 0.28 | −3.36 | < 0.001”

      Page 2

      Found in: Table 2

      Read it in the full textOpen PDF at page 2 ↗
    • All species showed peak sun exposure between 09:00 and 11:00 and retreated to shade when operative temperatures rose above 42 °C. View evidence ↗

      What they found

      All species showed peak sun exposure between 09:00 and 11:00 and retreated to shade when operative temperatures rose above 42 °C.

      In the paper's own words

      “The diel activity pattern (Figure 2) showed peak sun exposure at 09:00–11:00 and a pronounced midday retreat to shade when operative temperatures exceeded 42 °C”

      Page 3

      Found in: Comprehensive interpretation

      Read it in the full textOpen PDF at page 3 ↗
  5. What it means

    • The authors conclude that divergence in thermoregulatory strategies allows these three sympatric species to coexist in the challenging desert environment. View evidence ↗

      What it means

      The authors conclude that divergence in thermoregulatory strategies allows these three sympatric species to coexist in the challenging desert environment.

      In the paper's own words

      “These differences support the hypothesis that divergence in thermoregulatory strategy facilitates coexistence in thermally challenging environments.”

      Page 3

      Found in: Conclusion

      Read it in the full textOpen PDF at page 3 ↗
    • The authors highlight that C. kingii is particularly vulnerable to habitat modification due to its strong dependence on exposed rock outcrops. View evidence ↗

      What it means

      The authors highlight that C. kingii is particularly vulnerable to habitat modification due to its strong dependence on exposed rock outcrops.

      In the paper's own words

      “From a conservation perspective, the strong dependence of C. kingii on exposed rock outcrops makes it vulnerable to habitat modification.”

      Page 3

      Found in: Conclusion

      Read it in the full textOpen PDF at page 3 ↗
    • A stated limitation of the study is that data were only collected during the warm season. View evidence ↗

      What it means

      A stated limitation of the study is that data were only collected during the warm season.

      In the paper's own words

      “A limitation worth noting is that this research covered only the warm season.”

      Page 3

      Found in: Discussion

      Read it in the full textOpen PDF at page 3 ↗

Visual summary

3 visuals

Illustrations explain the paper; charts are replotted from the paper's own table values.

AI-generated illustration
AI-generated conceptual illustration (Desert-dwelling lizards (specifically Ctenosaura kingii, Liolaemus darwinii, and Liolaemus multimaculatus)). It explains the idea and does not show study data.↗ Enlarge
Comparative Thermoregulatory Strategies
AI-generated conceptual illustration (Desert-dwelling lizards (specifically Ctenosaura kingii, Liolaemus darwinii, and Liolaemus multimaculatus)). It explains the idea and does not show study data.

AI-generated conceptual illustration (Desert-dwelling lizards (specifically Ctenosaura kingii, Liolaemus darwinii, and Liolaemus multimaculatus)). It explains the idea and does not show study data.

Open full-size image ↗

Comparative Thermoregulatory Strategies

AI-generated conceptual illustration (Desert-dwelling lizards (specifically Ctenosaura kingii, Liolaemus darwinii, and Liolaemus multimaculatus)). It explains the idea and does not show study data.

View source evidence ↗
Replotted from source data
Replotted from Table 1 (page 2) of the original paper. Every bar is the paper's own table value.↗ Enlarge
de index (°C): L. Darwinii vs L. Multimac. vs C. Kingii
Replotted from Table 1 (page 2) of the original paper. Every bar is the paper's own table value.

Replotted from Table 1 (page 2) of the original paper. Every bar is the paper's own table value.

Open full-size image ↗

de index (°C): L. Darwinii vs L. Multimac. vs C. Kingii

Replotted from Table 1 (page 2) of the original paper. Every bar is the paper's own table value.

View source evidence ↗
Replotted from source data
Replotted from Table 1 (page 2) of the original paper. Every bar is the paper's own table value.↗ Enlarge
Shuttling rate (/h): L. Darwinii vs L. Multimac. vs C. Kingii
Replotted from Table 1 (page 2) of the original paper. Every bar is the paper's own table value.

Replotted from Table 1 (page 2) of the original paper. Every bar is the paper's own table value.

Open full-size image ↗

Shuttling rate (/h): L. Darwinii vs L. Multimac. vs C. Kingii

Replotted from Table 1 (page 2) of the original paper. Every bar is the paper's own table value.

View source evidence ↗

Figures & tables

From the original paper
Thermoregulatory parameters for three desert lizard species in the Monte Desert, ArgentinaTable 1Page 2Habitat selection model results (best AIC model) for species occurrenceTable 2Page 2Box plot and violin plot of field body temperatures for three sympatric lizard species in the Monte DesertFigure 1Page 2Diel pattern of shade use and sun exposure across all three species pooled, Monte Desert, October 2022–February 2023Figure 2Page 3
FULL TEXT Original article · reflowed for reading

Introduction

Thermoregulation is an old problem in reptile ecology that hasn't lost its relevance. Desert lizards face a daily balancing act: they need warmth for digestion, locomotion, and immune function, but overheating can be lethal within minutes [1] . Unlike endotherms, lizards manage this trade-off by shuttling between sun-exposed and shaded microhabitats, adjusting their body posture, and selecting substrates that match their thermal preferences [2] . The Monte Desert of central Argentina supports a diverse lizard fauna, with several Liolaemus species co-occurring in scrubland dominated by Larrea and Prosopis [3] . How these ecologically similar species partition thermal resources is not well understood, partly because most thermoregulatory work in the region has focused on single-species laboratory setups rather than multi-species field comparisons [4] . When two or more ectotherms share a habitat, differences in preferred body temperature can translate into differences in activity timing, substrate use, and microhabitat selection effectively reducing niche overlap and promoting coexistence [5] . This research tested that idea by measuring field body temperatures, shuttling behaviour, and microhabitat use in three sympatric species L. darwinii, L. multimaculatus, and Ctenophorus kingii along transects in the Monte Desert near Rosario during the warm season of 2022-2023. The objectives were to (1) quantify interspecific variation in field body temperature and thermal precision, (2) describe diel patterns of shade use and substrate selection, and (3) model the environmental predictors of species occurrence to assess the degree of thermal niche partitioning [6] .

Material and Methods

Material and Methods

Study area description

Study area description

Instrumentation

Temperature loggers (iButton DS1921G, Maxim Integrated) recorded operative temperatures at 15-minute intervals inside copper lizard models painted to match average lizard reflectance. Models were deployed in sun, partial shade, and full shade at each transect for the duration of the research.

Results

The three species differed significantly in mean field body temperature (Kruskal-Wallis H = 47.3, Table 1). C. kingii maintained the highest and narrowest temperature range, while L. multimaculatus was the most thermally variable. L. darwinii showed intermediate temperatures but the highest shuttling rate, consistent with active thermoregulatory behaviour.

Table 1. Thermoregulatory parameters for three desert lizard species in the Monte Desert, Argentina
ParameterL. DarwiniiL. Multimac.C. KingiiP-value
Mean Tb (°C)36.8 ± 1.234.3 ± 1.838.1 ± 0.9< 0.001
Preferred range (°C)35.2–38.431.8–37.136.9–39.6
de index (°C)1.4 ± 0.62.7 ± 1.10.9 ± 0.4< 0.001
Shuttling rate (/h)4.7 ± 1.32.3 ± 0.81.6 ± 0.5< 0.001

Table text extracted from the original PDF; superscript letters are shown inline. The original table image is below.

View original table image
Thermoregulatory parameters for three desert lizard species in the Monte Desert, Argentina↗ Enlarge
Table 1
Thermoregulatory parameters for three desert lizard species in the Monte Desert, Argentina

Thermoregulatory parameters for three desert lizard species in the Monte Desert, Argentina

Open full-size image ↗
Original paper tableSource PDF · page 2 ↗

Comprehensive interpretation

Rocky substrates and low canopy cover were the strongest habitat predictors (Table 2). C. kingii was almost exclusively associated with rock outcrops, while L. darwinii used mixed substrates. The diel activity pattern (Figure 2) showed peak sun exposure at 09:00-11:00 and a pronounced midday retreat to shade when operative temperatures exceeded 42 °C, followed by a secondary activity window in the late afternoon.

Figure 2. Diel pattern of shade use and sun exposure across all three species pooled, Monte Desert, October 2022–February 2023
Diel pattern of shade use and sun exposure across all three species pooled, Monte Desert, October 2022–February 2023↗ Enlarge
Figure 2
Diel pattern of shade use and sun exposure across all three species pooled, Monte Desert, October 2022–February 2023

Diel pattern of shade use and sun exposure across all three species pooled, Monte Desert, October 2022–February 2023

Open full-size image ↗
Original paper figureSource PDF · page 3 ↗
Table 2. Habitat selection model results (best AIC model) for species occurrence
PredictorEstimateSeZ-valueP-value
Substrate: rock1.830.414.46< 0.001
Canopy cover (%)−0.940.28−3.36< 0.001
Operative temp (°C)0.670.193.53< 0.001
Distance to rock (m)−0.380.14−2.710.007

Table text extracted from the original PDF; superscript letters are shown inline. The original table image is below.

View original table image
Habitat selection model results (best AIC model) for species occurrence↗ Enlarge
Table 2
Habitat selection model results (best AIC model) for species occurrence

Habitat selection model results (best AIC model) for species occurrence

Open full-size image ↗
Original paper tableSource PDF · page 2 ↗

Discussion

The 3.8 °C gap in mean body temperature between C. kingii and L. multimaculatus is consistent with thermal niche partitioning models that predict coexistence through divergence in preferred temperature [5] . C. kingii's narrow thermal range and low shuttling rate suggest it relies on basking-site fidelity rather than active shuttling, a strategy that works well on exposed rock surfaces where solar radiation is predictable [2] . L. darwinii, by contrast, shuttled nearly five times per hour, indicating a more energyintensive thermoregulatory style suited to the heterogeneous shrubland it occupies. The midday retreat to shade across all species mirrors the bimodal activity pattern documented in numerous desert lizard assemblages [1] . Operative temperatures in full sun exceeded 48 °C at midday during peak summer, well above the critical thermal maximum for all three species, making shade-seeking essential for survival. The importance of substrate type in the habitat model supports earlier work showing that surface thermal properties albedo, heat capacity shape microhabitat quality for ectotherms more than vegetation structure alone [4] . A limitation worth noting is that this research covered only the warm season. Cool-season thermoregulatory data might reveal different patterns, particularly for L. multimaculatus, whose broad thermal tolerance could allow year-round activity in mild winters when the other species are inactive [3] .

Conclusion

This field comparison of three sympatric desert lizards revealed clear interspecific differences in body temperature, thermal precision, and shuttling behaviour that align with distinct microhabitat preferences. C. kingii occupied hot, rocky substrates with minimal canopy cover; L. darwinii used mixed shrubland and shuttled actively; and L. multimaculatus tolerated a wide thermal range across varied microhabitats. These differences support the hypothesis that divergence in thermoregulatory strategy facilitates coexistence in thermally challenging environments. From a conservation perspective, the strong dependence of C. kingii on exposed rock outcrops makes it vulnerable to habitat modification. Any land-use change that reduces rock availability or increases shrub encroachment could shift competitive dynamics in favour of the more thermally flexible species. Future work should incorporate seasonal data and test whether climate warming narrows the thermal safety margins that currently allow all three species to persist in the Monte Desert.

Acknowledgement

Acknowledgements Funding sourcesThis research was supported by internal departmental funds from the Centro de Ciencias Biológicas del Litoral, Rosario. No external grant funding was received. Institutional supportThe authors acknowledge the Centro de Ciencias Biológicas del Litoral, Rosario for providing laboratory access and logistical support.

Figures and tables from the paper

Figure 1. Box plot and violin plot of field body temperatures for three sympatric lizard species in the Monte Desert
Box plot and violin plot of field body temperatures for three sympatric lizard species in the Monte Desert↗ Enlarge
Figure 1
Box plot and violin plot of field body temperatures for three sympatric lizard species in the Monte Desert

Box plot and violin plot of field body temperatures for three sympatric lizard species in the Monte Desert

Open full-size image ↗
Original paper figureSource PDF · page 2 ↗

References

15 in the original paper
  1. Huey RB, Slatkin M. Cost and benefits of lizard thermoregulation. Quarterly Review of Biology. 1976;51(3):363-384.
  2. Angilletta MJ. Thermal Adaptation: A Theoretical and Empirical Synthesis. Oxford: Oxford University Press; 2009. 1-289.
  3. Liolaemus boulengeri group. Biological Journal of the Linnean Society. 2006;89(2):241-275.
  4. Sinervo B, Mendez-de-la-Cruz F, Miles DB, Heulin B, Bastiaans E, Villagrán-Santa Cruz M, et al. Erosion of lizard diversity by climate change and altered thermal niches. Science. 2010;328(5980):894-899.
  5. Hertz PE, Huey RB, Stevenson RD. Evaluating temperature regulation by field-active ectotherms: the fallacy of the inappropriate question. American Naturalist. 1993;142(5):796-818.
  6. Bauwens D, Hertz PE, Castilla AM. Thermoregulatory behavior of lacertid lizards. Journal of Thermal Biology. 1996;21(5-6):429-436.
  7. Kearney M, Shine R, Porter WP. The potential for behavioral thermoregulation to buffer cold-blooded animals against climate warming. Proceedings of the National Academy of Sciences. 2009;106(10):38353840.
  8. Adolph SC. Influence of behavioral thermoregulation on microhabitat use by two Sceloporus lizards. Ecology. 1990;71(1):315-327.
  9. Stellatelli OA, Vega LE, Block C, Cruz FB. Effects of tree invasion on the habitat use of sand lizards. Herpetologica. 2013;69(4):455-465.
  10. Ibargüengoytía NR, Cussac VE. Body temperatures of two sympatric Liolaemus lizards from northern Patagonia. Journal of Herpetology. 2002;36(3):534538.
  11. Christian KA, Tracy CR. The effect of the thermal environment on the ability of hatchling Galapagos land iguanas to avoid predation during dispersal. Oecologia. 1981;49(2):218-223.
  12. Vitt LJ, Caldwell JP. Herpetology: An Introductory Biology of Amphibians and Reptiles. 4th ed. San Diego: Academic Press; 2014. 1-757.
  13. Deutsch CA, Tewksbury JJ, Huey RB, Sheldon KS, Ghalambor CK, Haak DC. Impacts of climate warming on terrestrial ectotherms across latitude. Proceedings of the National Academy of Sciences. 2008;105(18):6668-6672.
  14. Labra A, Pienaar J, Hansen TF. Evolution of thermal physiology in Liolaemus lizards: adaptation, phylogenetic inertia, and niche tracking. American Naturalist. 2009;174(2):204-220.
  15. Pincheira-Donoso D, Hodgson DJ, Tregenza T. The evolution of body size under environmental gradients in ectotherms: why should Bergmann rule apply to lizards? BMC Evolutionary Biology. 2008;8:68.