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Marginated tortoise

The marginated tortoise (Testudo marginata) is a medium-sized species of in the Testudinidae, notable as the largest member of its with a straight length typically reaching up to 40 cm (exceptionally 47.5 cm). It is characterized by a dark featuring flared posterior marginal scutes that give the shell a serrated appearance, along with yellow chevron-like markings on the plastron. Native to rocky, Mediterranean habitats, this herbivorous reptile plays a key ecological role in and soil aeration within its range. Endemic to , the marginated tortoise's natural distribution spans mainland , southern Albania, and various Ionian and , with introduced populations established in northeastern Sardinia, . It inhabits warm, dry environments such as shrubby macchia, phrygana scrub, olive groves, and rocky hillsides, often at elevations up to 1,600 m in (though limited to 600 m in Sardinia). As a generalist , its diet consists primarily of grasses, leaves, flowers, and fruits from like spp. and Dianthus multipunctatus, supplemented occasionally by fungi, carrion, or even feces during scarcity. The species demonstrates adaptability to seasonal extremes, hibernating in burrows or leaf litter during winter and tolerating brief freezing temperatures. Reproduction occurs in two mating periods—September to October and April to May—with females producing 1–3 clutches annually of 4–9 eggs (up to 15) in shallow nests during May–June; incubation lasts 90–120 days, yielding hatchlings measuring 30–40 mm in carapace length. Males are slightly larger than females on average (mean SCL 30.2 cm vs. 28.0 cm) and exhibit a more plastron and longer . A smaller ecotype, sometimes recognized as T. m. weissingeri, reaches only up to 25 cm and is found in specific island populations. Despite its Least Concern status on the due to a stable, widespread population, the species faces ongoing threats from due to , , and ; wildfires; road mortality; and illegal collection for the pet trade, with historical exports exceeding hundreds of individuals annually to . It is protected under Appendix II and EU Annexes II and IV, emphasizing the need for continued monitoring and .

Taxonomy

Nomenclature and classification

The marginated tortoise was first scientifically described by Johann David Schoepff in 1793 as marginata in his work Historia Testudinum Iconibus Illustrata, although older sources sometimes cite 1789 due to publication discrepancies in fascicles. An earlier non-binomial name, Testudo tabulata campanulata by Walbaum in 1782, is considered unavailable under modern nomenclatural rules. The specific epithet "marginata" derives from the Latin for "bordered" or "margined," referring to the distinctive flared posterior margins of the that characterize the species. Systematically, marginata is placed in the Testudinidae and the Testudo, where it is the sister to Testudo kleinmanni, with the two diverging approximately 11 million years ago; the broader Testudo , including the T. graeca , diverged around 14 million years ago, based on recent estimates calibrated against fossil records. The synonymy of T. marginata includes historical names such as Testudo graja Hermann 1804, Testudo campanulata Walbaum 1862 (a later binomialization), Peltastes marginatus melas Gray 1870, and Testudo nemoralis Schreiber 1875, reflecting early taxonomic confusion with related forms. Reclassifications occurred through the , with some proposed like T. m. sarda Mayer 1992 and T. m. weissingeri Bour 1996 later debated, but the current consensus in the 2023 Chelonian Research Monographs recognizes T. marginata as monotypic without valid . Karyological studies have confirmed the diploid number for T. marginata as 2n=52, comprising 14 pairs of macrochromosomes (divided into 9 in group A and 5 in group B) and 12 pairs of microchromosomes (group C), with no identifiable sex chromosomes. This chromosomal configuration aligns with other Testudo species, supporting the genus-level classification.

Subspecies and phylogeny

The marginated tortoise ( marginata) is traditionally divided into two : the nominate T. m. marginata, distributed across mainland and the , and T. m. sarda, occurring in , with the latter exhibiting smaller average size and less pronounced shell flaring. However, the validity of these is debated, as analyses reveal insufficient to support their separation, indicating substantial overlap with mainland populations. Recent taxonomic checklists, including the 2023 IUCN assessment, question full subspecific status due to this genetic continuity and morphological variability attributable to environmental factors rather than distinct evolutionary lineages. A proposed extinct subspecies, T. m. cretensis, was described from Pleistocene fossils on , characterized by purportedly distinct shell features such as a larger size and altered shapes. Modern re-examination of type specimens and additional fossils from Cretan cave sites, however, demonstrates that these traits fall within the natural intraspecific variation and potential of T. marginata, refuting its recognition as a separate . Phylogenetically, T. marginata occupies a position as the sister species to T. kleinmanni within the genus Testudo, diverging approximately 11 million years ago; the clade further diverged from the closest relative group including T. graeca around 14 million years ago, according to molecular clock estimates calibrated against fossil records. A 2022 study on niche diversification highlights low genetic divergence among Mediterranean Testudo species, including T. marginata, with interspecific splits occurring primarily during the late Miocene to Pliocene, underscoring limited molecular differentiation despite ecological adaptations.

Description

Morphology and size

The marginated tortoise (Testudo marginata) is the largest species of tortoise native to , with adults typically attaining a straight length (SCL) of 32–34 cm and weights ranging from 2–5 kg. Individuals commonly reach up to 40 cm in SCL, with exceptional cases up to 47.5 cm (particularly in ). The is highly domed and elongated, forming a trapezoidal shape with 13 scutes arranged in the typical vertebral (5) and costal (8) pattern; its posterior margin features distinctive flared and saw-toothed projections formed by the enlarged marginal scutes, providing a serrated appearance. The plastron is solid and unhinged, consisting of 12 scutes that enclose the underside without flexibility for retraction. The limbs are robust and adapted for and burrowing, with forelimbs bearing five claws and covered in large, imbricate scales suitable for digging into soil; hindlimbs have four claws. Hatchlings measure 3–4 in SCL and weigh approximately 12 g, with juveniles exhibiting growth until the posterior flaring develops around 12–14 SCL. is reached at 6–8 years for males and 10–12 years for females, typically when individuals are 15–20 in SCL or females exceed 2.3 kg in mass. Growth slows significantly after maturity, with minimal increase beyond 20 years of age. Marginated tortoises can live over 50 years in the wild and up to 100 years or more in captivity. in size and shape becomes evident after maturity, with males often developing a more concave plastron and longer tail.

Coloration and sexual dimorphism

The of the marginated tortoise ( marginata) is characteristically black or dark brown, adorned with yellow or orange radiating lines emanating from the centers of the scutes, particularly on the costal, vertebral, and posterior marginal scutes. The plastron contrasts with a yellowish background featuring dark central markings, typically arranged in symmetrical patterns along the longitudinal axis. The head is predominantly black in adults, with dark scales, while the overall coloration darkens with maturity. Juveniles display more vibrant coloration, with a lighter brownish-yellow to café-au-lait outlined by dark horseshoe-like patterns on the costal and vertebral scutes; the marginal scutes are pale with faint dark patterns, and the plastron shows blurred markings on a brighter base. The head in young individuals is with diffuse dark spots, which intensify and darken as the tortoise ages, leading to a gradual fading of the yellow highlights across the shell. Geographic variation in coloration and shell features occurs across populations, notably in the Sardinian group (previously classified as the subspecies T. m. sarda, though not currently recognized as valid). Individuals from Sardinia exhibit less intensely black carapaces, resulting in more pronounced yellow markings compared to the mainland Greek populations, where the black dominates more fully; additionally, the posterior marginal scutes in Sardinian specimens are smoother and more rounded with reduced serration and steeper flaring, contrasting the longer, deeply serrated flares typical of Greek forms. Intraspecific variation is primarily tied to these regional populations rather than additional color-based subspecies, with no further validated distinctions beyond the nominal T. marginata and the debated Sardinian form. Sexual dimorphism in the marginated tortoise manifests in several morphological traits beyond overall body structure. Males possess longer and thicker tails than females, with the vent positioned closer to the tip to aid in reproduction. The male plastron features a deeper concavity in the abdomino-femoral region and a wider anal notch, adaptations for mounting during courtship, whereas females have a flatter plastron. Rear carapace flaring is more pronounced in males, contributing to a steeper "skirt-like" posterior margin that is less marked in females. Although adult sizes overlap, males are slightly larger on average, with mean straight carapace lengths of 30.2 cm compared to 28.0 cm in females; this pattern holds across populations, including smaller ecotypes like the southern Peloponnese weissingeri form (males 21.3 cm, females 20.9 cm). Coloration itself shows no sexual differences in adults.

Distribution and habitat

Geographic range

The marginated tortoise (Testudo marginata) is native to , occurring primarily in the southern —specifically mainland and island populations across and extreme southern . Introduced populations have established in northeastern (), with occasional records but no naturalized populations in mainland (e.g., ). Its distribution spans diverse terrains within these regions, from coastal lowlands to inland areas. The species inhabits elevations ranging from to approximately 1,600 m in the mountainous (limited to below 600 m on ). Historically, its range extended farther, including now-extinct populations on the islands of , , and during the Pleistocene and early periods. Recent surveys, including records from 2023, have confirmed its occurrence in additional sites within , such as highland areas near Gjirokastra and zones around Saranda and Delvina, highlighting ongoing efforts to map fragmented distributions. Overall population estimates indicate a stable but fragmented status per the 2004 IUCN assessment (Least Concern), reflecting densities that vary from 3 to over 20 individuals per hectare in key Greek and Italian sites. Within this range, the tortoise occupies a mix of open woodlands, scrublands, and grasslands, though specific habitat selections are detailed elsewhere.

Habitat preferences

The marginated tortoise (Testudo marginata) primarily inhabits Mediterranean scrublands, including macchia formations of sclerophyllous shrubs (1.5–3.5 m tall) and phrygana of low aromatic shrubs (<60 cm), as well as rocky hillsides and open woodlands with sparse vegetation that facilitate through exposure to . These environments provide the open, shrubby conditions essential for the tortoise's activity patterns, with individuals often found on sunny, rocky outcrops or at the margins of (Quercus spp.) and coniferous forests. The species requires loose, well-drained soils for burrowing and nesting—typically excavating bell-shaped chambers up to 15 cm deep—and relies on elevated basking sites such as rocks or low vegetation to achieve preferred body temperatures of 26.8–31.6°C. It actively avoids dense forests, thick vegetation, and wetlands, where mobility is restricted and suitable microhabitats for basking or burrowing are scarce. Recent ecological analyses indicate low habitat niche segregation among mesic Mediterranean tortoise species, with T. marginata exhibiting substantial overlap in resource use with Testudo graeca and Testudo hermanni, particularly in areas with moderate moisture and vegetation cover driven by shared thermal requirements. However, T. marginata demonstrates a narrower niche breadth and a preference for higher elevations compared to its congeners, often occurring up to 1,600 m in , where cooler microclimates at altitude support its thermoregulatory needs. This elevational preference aligns with its distribution in hilly, open terrains rather than lowland plains dominated by T. graeca. Seasonally, T. marginata shifts its habitat use to cope with variability, favoring more exposed, arid slopes during active periods in spring and early summer for foraging and basking, before entering estivation from mid-June to September in shaded or buried refuges to avoid peak heat. In winter, individuals seek sheltered valleys or south-facing slopes for , typically from mid-December to late , where milder conditions prevail and risk is lower. The species tolerates hot, dry summers with air temperatures reaching 40°C—remaining active between 30–37°C—and mild winters with average temperatures around 13.6°C above freezing. While adapted to periodic dry conditions through behaviors like consuming drought-resistant bulbs (e.g., Asphodelus spp.), prolonged droughts can exacerbate food scarcity and stress, potentially impacting population viability in altered climates.

Behaviour

Diet and foraging

The marginated tortoise (Testudo marginata) is primarily herbivorous, consuming a diverse array of plant material in its Mediterranean , including grasses, herbs, leaves, flowers, stems, buds, fruits, seeds, and occasionally succulents. Common food plants include species from the (such as dandelion-like rosettes), , Leguminosae (), and various shrubs like Cistus spp., Salvia pomifera, and Quercus spp., with selective grazing to avoid toxic or resinous plants such as Euphorbia spp. and Pinus halepensis unless in nutritional distress. Occasional opportunistic intake of fungi, mosses, carrion, or has been observed in T. marginata, though this is not a primary component of the . The diet exhibits strong seasonal variation aligned with habitat productivity. In spring, tortoises prioritize fresh shoots, seedlings, and protein-rich legumes like Calicotome villosa and dandelions (Taraxacum spp.) to support post-hibernation recovery and growth. Summer foraging shifts to flower buds, dry plant parts, seeds, and occasional wild fruits such as figs (Ficus carica), with tortoises climbing low vegetation to access resources during drier periods. By autumn, following post-rain germination, they consume emerging young plants to build fat reserves before hibernation. Foraging is diurnal, with unimodal activity patterns in and autumn (peaking at 40-47% feeding observations) and bimodal in summer to avoid midday heat, covering typical daily distances of 50-100 in a manner while selectively to maximize intake and minimize toxins. This promotes gut health through continuous low-volume feeding. Some populations exhibit reduced activity or short periods during mid-summer heat. Nutritionally, the diet emphasizes high calcium (from and of calcium-rich soils or ) to maintain a Ca:P ratio of approximately 3.5:1 to 5:1, preventing , alongside low protein levels (2-6% wet basis) to avoid shell deformities and renal strain. High fiber content supports slow transit times of 3-8 days, essential for efficient extraction. Digestive adaptations include a slow suited to low-energy matter, with microbial fermentation in the breaking down fibrous via symbiotic gut , enabling energy recovery from otherwise indigestible components; this process is enhanced by coprophagy of to inoculate beneficial microbes.

Social behaviour

The marginated tortoise (Testudo marginata) is generally solitary, with limited social interactions outside of the season. Individuals exhibit strong site fidelity, often remaining in the same area for years, which contributes to their and low levels of inter-individual contact. However, they display territorial behavior, particularly males who defend burrows and home ranges during the period using visual displays such as head extensions and posturing. These tortoises follow a diurnal activity pattern, emerging in the morning to bask and becoming most active from to in their Mediterranean , with during winter months. Their daily routine typically involves basking in the early morning to raise body temperature, followed by midday , and retreating to shade or burrows in the hot afternoons to avoid overheating; activity is unimodal in spring and autumn but bimodal in summer, with peaks in before reduced activity or short in mid-June to September for some populations. Aggression is primarily observed among males, who ram or bite rivals to establish dominance, especially during encounters over or resources. A 2025 study on the closely related (Testudo hermanni) found that social interactions in adults are shaped more by sex than by familiarity, suggesting sex-based territorial motivations drive aggressive behaviors over recognition of prior associates. Communication relies mainly on visual and tactile signals, with rare vocalizations limited mostly to grunts during physical interactions; tactile cues include shell vibrations produced during confrontations or mounting attempts. Head movements and body posturing serve as primary visual signals for displays of dominance or submission. In optimal habitats with abundant resources, marginated tortoises form loose aggregations, sometimes sharing refuges during periods, but they lack any true or cooperative behaviors. Population densities can reach up to 20.7 individuals per in favorable areas, facilitating occasional non-aggressive encounters without forming stable groups.

Reproduction

The mating season for marginated tortoises (Testudo marginata) in the wild occurs primarily in and , with a secondary period in April and May shortly after emergence from . During , males pursue females aggressively, approaching with head oscillations, encircling them, biting their limbs or , and ramming to position for mounting; copulation lasts 5-30 minutes and is often accompanied by male . Success in mating is influenced by male size and vocalization intensity, with —such as longer tails and concave plastrons in males—facilitating the process. Females lay eggs from late April to August, producing 1-3 clutches per season in shallow, bell-shaped nests excavated to about 15 deep in loose, sunny . Each clutch typically contains 4-9 eggs, though up to 15 have been recorded, with smaller clutches (2-4 eggs, 1-2 per season) in the weissingeri . Eggs are elongated and white, measuring approximately 33-34 mm in length and 29-30 mm in width. Incubation lasts 60-70 days at temperatures of 30-35°C, though periods of 90-120 days have been reported at 28-32°C. Sex determination is temperature-dependent (TSD pattern Ia), with at 26-28°C producing males and temperatures above 30°C yielding females. Hatching occurs in September and October, when neonates emerge measuring 34-36 mm (up to 42 mm in some ecotypes) in straight length and weighing about 12 g; they are independent immediately but highly vulnerable to predation. There is no after egg-laying, contributing to elevated juvenile mortality rates from predators such as birds, mammals, and reptiles.

Hibernation

The marginated tortoise (Testudo marginata) enters a state of brumation, a form of dormancy akin to , involving reduced activity typically from mid-December to late depending on local conditions. During this period, individuals seek shallow refuges in rock crevices or accumulations of leaf litter to insulate against cold, with no soil burial or excavation reported; some individuals may even bask at temperatures as low as 8°C. Preparation for brumation begins in summer, when tortoises accumulate body fat reserves through increased , providing essential energy, vitamins, and hydration to sustain the dormant phase. Physiologically, metabolic rate decreases dramatically as body temperature equilibrates with the environment, typically dropping to 10-15°C; slows to 3-4 beats per minute, facilitating and enabling survival through winter. favors sheltered locations on south-facing slopes, which minimize risk from winter rains and allow passive warming upon emergence. Emergence is triggered by rising ambient temperatures exceeding 15°C in , prompting to resume activity around or . Incomplete brumation, often due to fluctuating winter temperatures, poses risks such as and excessive depletion, potentially leading to weakened upon waking. Regional variations influence brumation duration; in milder Sardinian climates, the period is shorter, with tortoises emerging as early as mid-February compared to later in continental .

Conservation

Status and threats

The marginated tortoise (Testudo marginata) is classified as Least Concern on the , with a stable global population trend despite localized declines due to and other pressures. Populations remain widespread and robust across its native range in and , as well as in introduced areas like northeastern , though the species faces ongoing risks that could affect long-term viability in fragmented habitats. The primary threats to wild populations include and alteration driven by intensive , , and development, which reduce available dry, rocky preferred by the species. Wildfires pose a significant acute , causing over 20% mortality in monitored populations within affected sites. Road mortality further compounds these impacts, as tortoises crossing paved areas are frequently killed by vehicles, exacerbating population declines in human-modified landscapes. Illegal collection for the pet trade represents another major danger, with T. marginata listed on Appendix II to regulate international commerce; however, illegal exports persist, particularly from and . A 2025 analysis of global trade highlighted continued prevalence of T. marginata specimens in European markets, underscoring enforcement challenges despite regulatory measures. Additional risks include predation by introduced mammals such as foxes and dogs, as well as parasitic infections; a 2024 study in reported oxyurid prevalence of 74.4% in examined Testudines, including T. marginata individuals. The introduced Sardinian population, while viable, remains isolated and potentially more vulnerable due to its smaller size and limited with mainland groups.

Protection and research

The marginated tortoise (Testudo marginata) is protected under the EU in Annexes II and IV, which require the designation of Special Areas of Conservation and strict protection measures, respectively. It is also listed on Appendix II of the Bern Convention, mandating conservation of habitats and regulation of exploitation, and on Appendix II of since the convention's entry into force in 1975, controlling to prevent . These protections apply across its range in , , , and introduced populations like . Conservation efforts include habitat restoration and monitoring programs in , such as those led by Pelargos Natura, which initiated telemonitoring of individuals in southern to track movement, shelter use, and mortality factors like fires since 2020. Headstarting programs for juveniles involve captive rearing and release to boost survival rates, as implemented in 's Riserva Naturale Gran Bosco della Mesola for reintroduction into suitable habitats. In , patrols and enforcement actions by authorities, including seizures of illegally traded , help address threats. Recent research highlights include a 2025 study on habitat partitioning among Mediterranean tortoises, which used (EVI) metrics to assess niche overlap with congeners like Testudo graeca and Testudo hermanni, revealing low segregation in mesic environments. Distribution records from 2023 confirmed the species' presence in , with limited occurrences near the Greek border, informing range mapping efforts. A 2025 morphometric analysis of eggs from captive T. marginata ecotypes evaluated size and shape variations to assess viability for reintroduction programs. Population monitoring involves annual surveys in protected areas, such as Brijuni National Park in , where introduced populations are tracked to evaluate and . Genetic studies have confirmed low in isolated groups, such as those in , attributed to historical introductions and fragmentation, underscoring the need for connectivity measures. Future conservation requires advanced climate modeling to predict range shifts, emphasizing proactive habitat management.

In captivity

Housing and care

Marginated tortoises in captivity require spacious enclosures to accommodate their active nature and growth potential, with adults reaching up to 40 in length. Outdoor pens are ideal for individuals in suitable , providing a minimum of 4 x 4 meters of secure, predator-proof space with solid walls buried at least 30 underground to prevent escapes and burrowing out. These enclosures should include a well-drained such as a 50/50 mix of and , at least 7.5 deep, to allow natural burrowing behavior, along with varied terrain featuring rocks, slopes, and planted areas for enrichment. Indoor housing is suitable for juveniles or during inclement weather, using open-top tortoise tables or large vivaria with good , starting at 0.9 x 0.6 meters for hatchlings and scaling up to at least 2.4 x 1.2 meters for subadults. A must be maintained, with a basking spot of 32-35°C under a UVB-emitting heat source and cooler areas around 24-28°C during the day, dropping to 15°C at night; full-spectrum UVB lighting (10-12% UVB output, such as T5 tubes) is essential for at least 12-14 hours daily to support and prevent deficiencies. The diet should mimic natural foraging patterns, consisting of approximately 80% high-fiber weeds and grasses such as dandelion, , and , supplemented with 20% leafy vegetables like or , while fruits should be limited to occasional treats to avoid digestive issues. High-protein foods, including commercial tortoise pellets or animal products, must be avoided to prevent shell pyramiding, a deformation caused by rapid growth; daily dusting on food, combined with vitamin D3 supplements 2-3 times weekly, supports healthy development. Shallow soaks in lukewarm 2-3 times per week aid and . Health management involves annual veterinary examinations by a specialist to screen for common parasites, particularly oxyurid nematodes like those in the Tachygonetria, which are prevalent in up to 43% of captive pet tortoise populations, including species, and often but require fecal testing and treatment if burdens are high. simulation is optional in temperate regions, involving a gradual cooling to 4-10°C for 8-12 weeks in a insulated with monitoring to ensure body temperature does not drop below 1°C, though many keepers opt for year-round activity with proper heating to reduce risks. Enrichment is crucial for , incorporating hiding spots like caves or stacked rocks, dense for cover, and live plants such as mulberry or globe mallow to encourage natural exploration and reduce stress; varied terrain promotes exercise and . Group housing can be feasible in large enclosures (e.g., 4.5 x 7.6 meters for up to a dozen adults) but carries risks of , particularly among males, which may lead to injuries or dominance hierarchies, so single housing or careful sex-balanced groups with ample space are recommended. Common health issues include (MBD), resulting from inadequate UVB exposure or calcium imbalance, manifesting as soft shells or deformities; prevention through proper lighting and diet is key. Recent studies emphasize natural setups, such as integrating edible weeds into enclosures, to enhance behavioral health and reduce risks in captive marginated tortoises.

Breeding in captivity

Breeding marginated tortoises (Testudo marginata) in captivity requires careful pairing to mitigate male aggression, with a recommended ratio of one male to three to five females to distribute mating pressure and reduce injury risk. must comply with Appendix II regulations to ensure legal and ethical practices. behaviors closely mimic those in the wild, typically occurring in spring from to May following , where males pursue females, ram their shells with extended gular scutes, and bite their limbs before mounting with vigorous rocking motions. Females produce one to three clutches per season, each containing 4 to 12 hard-shelled eggs, laid in flask-shaped nests dug into loose ; eggs are then carefully removed for artificial . Incubation setups maintain temperatures of 30-32°C and humidity levels of 40-70% using substrates like , with the process lasting 60-80 days; a 2025 morphometric study of captive-raised ecotypes revealed that T. marginata eggs are significantly larger than those of T. graeca, averaging 36.65 mm in length and 16.57 g in weight compared to 33.34 mm and 14.92 g (p<0.05). Hatching success in controlled environments reaches 70-90% with optimal and minimal disturbance, though mortality can occur if temperatures fluctuate. Hatchlings, measuring 30–35 mm and weighing 10-14 g, absorb their sacs over 24 hours in the before transfer to separate rearing enclosures to prevent injury or rare instances of among juveniles. Effective genetic management emphasizes avoiding inbreeding by periodically introducing unrelated individuals from verified captive lineages, supporting conservation headstarting programs that bolster wild populations with reared juveniles. Key challenges include reduced fertility in adults recently imported from the wild due to transport stress and acclimation issues, as well as potential sex ratio biases from incubation temperatures, since Testudo species exhibit temperature-dependent sex determination with warmer conditions (above 31°C) favoring female offspring.

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