The sun warms lichen growing on the fallen rocks, carved out by the sea and populated with wild seeds from landscapes distant in space and time. Here nature has found harmonious solutions to distressed land forms, eroding them into a velvet green carpet that catches the eye before it lands on the sea. Bushes of mastic (Pistacia lentiscus), myrtle (Myrtus communis) and cade juniper (Juniperus oxycedrus), are shaped by the Mediterranean Sirocco winds, in shades of green that host modest fauna, while the intermittent screech of a cicadas keeps time: it is the heartbeat of a land in constantly growing, despite the actions of man.
In prehistoric times a vast forest covered the majority of the Salento peninsula. Various human activities gradually modified local plant life over time, at a rhythm dictated largely by demographic growth.
In the 3rd century BCE, the Roman occupation brought about a collapse of agriculture due to the extermination of the Apulian people, signaling the beginning of a comeback for spontaneous vegetation and the reformation of wooded areas. In fact, according to Giuseppe Palmieri, “the long stay of armies in this region and the continued devastation, rendered the area empty of inhabitants.” (G. Palmieri, Pensieri economici relativi al Regno di Napoli, Naples, Editore Vincenzo Flauto, 1789).
In the 18th century, a law imposed taxes for the owners of wooded lands, causing them to seek to be rid of them, even by means of fire. An important contribution to the phytohistorical study of southern Italy is represented by the Geographic Atlas of the Kingdom of Naples by Antonio Rizzi Zannoni, based on geographical measurements most likely from 1798. This volume included maps that illustrate the majority of wooded areas from that period, including “the dense macchia of the Arneo,” located near the Giardini d’Acqua (G.A. Rizzi Zannoni, Atlante geografico del Regno di Napoli, Naples, Istituto Geografico Militare, 1808).
Five, six centuries ago in Apulia many wooded areas and forests were under the control of feudal lords, who claimed exclusive rights.To maintain such control, an armed force was created including foresters. It was the king (Kingdom of Naples) who named the master foresters and who listed all of the forests of the Kingdom with their respective number of custodians.
To defend the “Forest of Nardò,” once referred to as Nerito, where the Giardini d’Acqua are located, there was just a single forester assigned.
According to 20th century marine biologist Pietro Parenzan (who discovered the novel Iris revoluta Colas. on the tiny Mojuso island nearby) there over 130 species in the spunnulate protected from the dry winds and the attack of salt spray, mere meters below the surface. Even today, clinging to the “cuti” (rocky cliffs) beneath one’s feet, we can experience the “slow explosion of seeds” as Bruno Munari described trees. Lying in wait since spring, they distribute colorful plant life among the fissures of the coastline, where “algae and aquatic plants green as soft glass,” in the words of the Parenzan, fill these grand limestone vases.
The predominance of holm oaks (Quercus ilex), know locally as the leccio (hence, the toponym Lecce), protected inside the sinkholes from the salt-laced winds beyond, supports the hypothesis that the site was previously a leccio forest, disturbed over time by the presence of man and by wildfires.
In 1978 the local flora the spunnulate of Torre Castiglione, was classified by Giovanni Caniglia in the Carta della vegetazione di Torre Colimena, as “vegetation of a saline wetland (paludi salse).”
The humid micro climate created inside the spunnulate favors, in particular, the development of vegetation that is totally different from that of the nearby terrain, often completely bare, functioning like islands of wild flora in a “sea” of land eroded over time by cultivation and the grazing of livestock. Therefore, it is not difficult to find singular vegetative associations and relicts of flora in these karstic formations or close nearby. This is due to the peculiar micro climate created inside the spunnulate, protected from the sea winds laden with salt, fed by humidity and spring water, and, most of all, not affected by the intense grazing activities or the damaging interference of human activity over past centuries.
In the largest sinkholes, with ponds visible at the bottom, there are distinct zones of plant life that can be elaborated:
Along the upper edges of the spunnulate we find: branched asphodel (Asphodelus ramosus), sea squill (Urginea maritima) and numerous grass plants.
Along the walls and terraces: bird’s foot (Lotus commutatus), Clematis cirrhosa, flax-leaved daphne (Daphne gnidium), myrtle (Myrtus communis), mock privet (Phillyrea latifolia), mastic (Pistacia lentiscus), holm oak (Quercus ilex), and other elements of the Quercion ilicis ecosystem, common smilax (Smilax aspera), caper bush (Capparis spinosa), and navelwort (Cotyledon umbicus veneris);
Along the bottom: grasses like spiral ditchgrass (Ruppia cirrhosa), Potamogeton pectinatus, and occasional tufts of softstem bulrush (Schoenoplectus tabernaemontani).
Underwater: common reed (Phragmites australis), sea rush (Juncus maritimus), spiny rush (Juncus acutus), black bog-rush (Schoenus nigricans), sea lavender (Limonium serotinum), golden samphire (Inula crithmoides), sea aster (Aster tripolium).
“Banal” Flora: A phrase coined by local author Michele Mainardi, these are species introduced by man due to improper use of the spunnulate, therefore disrupting previously existing vegetation. These include annual mercury (Mercurialis annua), herb-Robert (Geranium robertianum), longstalk cranesbill (Geranium columbinum), dovesfoot geranium (Geranium molle), sourgrass (Oxalis pes caprae) ,common stork’s-bill (Erodium cicutarium), petty spurge (Euphorbia peplus), common mallow (Malva sylvestris), and many others.
Garrigue, or surface flora: The area around the spunnulate has suffered extreme degradation; millennia of anthropic activity, grazing of livestock, fires, and agriculture have modified the vegetation over time. At present the plant life that dominates the areas surrounding the sinkholes is made up of geophytes, plants that form bulbs and disappear during periods of unfavorable meteorological conditions, their underground organs in a state of dormancy. There are also numerous thorny plants, whose spines take the place of leaves, reducing transpiration and the need for water. Many common examples of these two types of plants are myrtle (Myrthus communis), barbary nut (Iris sisyrinchium sisyrinchium), Apulian satureja (Satureya cuneifolia), alkanet (Alkanna tinctoria), wild fennel (Foeniculum vulgare), Montpellier rockrose (Cistus monspeliensis), three-horned stock (Matthiola tricuspidata), coastal medick (Medicago marina), broom (Calicotome infesta), pink butterfly orchid (Anacamptis papilionacea), bumblebee orchid (Ophrys bombyliflora), yellow bee-orchid (Ophrys lutea), sawfly orchid (Ophrys tenthredinifera), Bertoloni’s bee orchid (Ophrys bertolonii), several species of ornitholgalum, cade juniper (Juniperus macrocarpa), and Silene colorata.
The genus name comes from ancient Greek (a = not, spodos = ash, elos = valley), as the tubers of this plant are capable of resisting heat created during wildfires.
Named uluzzi in the local dialect, branched asphodel plants have a bitter component that makes them undesirable for grazing livestock, which contributes to their spreading in disproportion.
In flower: from March until May
Commonly called bird’s foot, there are nearly 150 related species, 22 of which are present in Italy: L. commutatus, in particular, is found in central and southern Italy, including the regions of Sicily, and Liguria.
In flower: from March until June
The genus name for the common reed derives from ancient Greek (phragma tos= fence, palisade, hedge) meaning suitable for creating hedges, perhaps due in part to its hollow stem shape divided by several diaphragms. The species designation comes from the Latin auster, the name for the god of the south wind in ancient Rome, indicating it as plant from southern climes.
In flower: from July until September
The barbary nut (Moraea sisyrinchium), a plant with a sweet bulb cited by Theophrastus, most likely gets its name from ancient Greek sys (pig) and rynchos (snout), as they are particularly beloved by swine.
In flower: from April until May
Alkanna tinctoria (alkanet) derives its name from the Arabic word alkenneh, meaning root, and the Latin term tinctorius meaning “dyer.” The roots were used in the past to give wool and other fabrics a red mahogany color.
In flower: from March until June
The flowers of the Montpellier rockrose last only one day. However, to make up for it, the plant continues to flower for several weeks.
In flower: from March until May
The three-horned stock has flowers with four purple petals fading to white in the center and gets its genus name from the 16th century botanist Pietro Andrea Mattioli.
The fruit of this species form extremities with three horns, hence the Latin name “tricuspidata.”
In flower: from April until July
Coastal medick is a Mediterranean species, whose genus name comes from the belief of the Greek philosopher Theophrastus that this plant originally came from the ancient Persian region of Media. The species name refers instead to its coastline habitat.
In flower: from March until August
The bumblebee orchid gets its epithet from the ancient Greek bombýlios, due to the similarity between the labellum (bottom petal) of the flower and the Bombus genus of the Hymenoptera order.
In flower: from February until May
The yellow bee orchid has yellow-bordered labellum with a brown spot in the middle that features a butterfly-shaped design. The scientific name comes from the Latin term luteus meaning yellow, the dominant color of this particular species.
In flower: from February until May
The sawfly orchid owes its epithet tenthredinifera (bearer of wasps) to the Latin tenthredo, for “wasp” (fellow member of the Hymenoptera order), and the suffix -fera, meaning “bearer of”.
In flower: from March until May
The name Ophrys comes from the ancient Greek for “eyebrow,” as these plants in this genus were possibly used to create pigment for dying eyebrows. This particular species of wild orchid is named for the 19th century botanist Antonio Bertoloni.
In flower: from March until June
Ornithogalum is derived from ancient Greek and means “hen’s milk,” referring to the white color of its tepals. The flowers, when closed, resemble a cock’s comb, and open around 11 o’clock in the morning.
In flower: from March/April until June
The name possibly derives from the Sileno, the potbellied friend of Dionysus in ancient Greek mythology; or from sialon, meaning saliva, due to the sticky liquid that these plants have on their stems.
In flower: from April until June
The pink butterfly orchid (Orchis papilionacea) extends across Italian territory with the exception of the Val d’Aosta and Trentino regions. Pollination takes place thanks to small wasps, whose males are tricked by pheramones (in reality this flower doesn’t have nectar) into landing on the flower’s labellum, which look like females of the same species. The species name refers to the butterfly shape of the flowers (papilio = butterfly in Latin).
In flower: from March until June
In the summer, the Giardini d’Acqua are enveloped by a constellation of sounds, from the fluttering of little bittern wings, to the subtle murmur of mastic leaves brushed up against by slithering ratsnake and the chirping of crickets and cicadas, while the sea acts as the orchestra conductor.
When the sun is high, warming rocky ravines and timid geckos, the tepid air becomes heavy, capturing echoes of hidden life.
Then, at night the cicada song abates into silence on an endlessness of the horizon, with jagged shadows painted by the full moon around ancient boulders and the scampering of crabs inside small pools of water and salt.
In antique maps up until the beginning of the 19th century the greater Terra d’Arneo was referred to as “the dense macchia of Arneo,” a maquis shrubland populated by wild boar, deer, fox, hares and aquatic animals. The doctor and author Girolamo Marciano (1571-1628) in his 16th century encyclopedic tome, “Description, Origin and Successes of the Province of Otranto,” affirmed that near Torre di Castiglione there was already:
The fauna of the spunnulate are particularly interesting during the spring and autumn migration periods, especially from mid-March until the end of May.
The most representative avifauna of the coastline includes the common kingfisher, mallard ducks, black-winged stilts, and little turns. Along the rocky coastlines, and among the wellsprings in the sinkholes, it is possible to observe gray heron, purple heron, little egret, black-crowned night heron, great and little bittern, as well as squacco heron.
Occasionally visitors include Eurasian stone-curlew, collared pratincole, common rock thrush, hoopoes and common cuckoos, who stop here looking to rest and feed before continuing their journeys elsewhere.
This rich array of fauna makes the spunnulate of Torre Castiglione even more strategic for bird-watching than other well-known areas like Messina, Gibilterra and the Dardanelli. It is also interesting to note towards the end of the spring the migration of the painted lady, while, around the end of the summer and the beginning of autumn the red admiral and small tortoiseshell arrive in Salento, respectively.
These butterflies, while a common sight, are difficult to capture in still images, as they flee at the slightest movement.
In Italy, a migrant and nest builder. Frequents diverse typologies of wetlands with shallow water and low vegetation. Social in nature, they form small colonies during nesting, and are known for their loud call and for bobbing their heads back and forth when agitated.
They feed on aquatic insects and their larvae, nesting only once a year and laying their eggs sometime between the end of April and the months of May and June.
Credits photo: “Piano Comunale delle coste di Porto Cesareo”
In Italy, a migrant and nest builder. Frequents diverse typologies of wetlands with shallow water and low vegetation. Social in nature, they form small colonies during nesting, and are known for their loud call and for bobbing their heads back and forth when agitated.
They feed on aquatic insects and their larvae, nesting only once a year and laying their eggs sometime between the end of April and the months of May and June.
Credits photo: “Piano Comunale delle coste di Porto Cesareo”
In Italy, sedentary nest builders, regular and wintering migrants. In the reproductive phase they prefer environments with small, deep bodies of water rich in vegetation; during the fall and the winter they also rest in the sea, not far from the coast. They are social, except during the breeding period, and primarily eat algae, shoots, seeds, berries, insects and larvae. Egg laying takes place between February and the beginning of July, with a second nesting possible after a failed attempt.
Photo AMP
A solitary, sedentary nest builder, and regular migrant that frequents salty wetlands.
Feeds on small fish, aquatic insects, and mollusks, balancing above the water before diving in headlong to hunt. In a single year, they are capable of nesting three times, and begin laying between April and May.
Demonstrates a typical zigzag flight pattern. In Italy, up to three generations are possible per year, with adults appearing at the beginning of spring. After mating, the females deposit their eggs on Carduus genus plants and others in the Composite family. Caterpillars once hatched take up residence among the leaves, completing their development and undergoing metamorphosis in a relatively brief period, allowing for a second and third generation.
Period of flight: starting in April
Demonstrates a typical zigzag flight pattern. In Italy, up to three generations are possible per year, with adults appearing at the beginning of spring. After mating, the females deposit their eggs on Carduus genus plants and others in the Composite family. Caterpillars once hatched take up residence among the leaves, completing their development and undergoing metamorphosis in a relatively brief period, allowing for a second and third generation.
Period of flight: from May until October
Period of flight: from May until July
Relatively common along the coast of the Salentine peninsula, this species was discovered for the first time in the Zinzalusa Grotto located in the town of Castro and is named for the researcher Filippo Bottazzi.
A small omnivorous crustacean, similar to shrimp, they live in very deep water and can be found in cave environments along a section of the coast between Gallipoli and Porto Cesareo. It is between 6,5 and 13mm in length, and is capable of adapting to environments of variable salinity.
This species was introduced during the 1920’s as part of an anti-malarial initiative, as at that time they were considered fervent consumers of the larvae of the genus Anopheles of mosquito, a malarial vector. Mosquitofish are voracious and aggressive predators, who is some cases attack animals larger than themselves. Reproducing between 3 and 6 times per year, they begin in the spring, and do not deposit eggs, but rather a large number of juvenile fish, already similar to the adults. Mosquitofish are invasive and a threat to autochthonous species.
Capable of reaching up to 70cm in length and weighing up to 8 kilos, they frequent coastal waters up to 30 meters in depth. Schools in small groups, and, as an omnivore, eats micro-algae, plankton, and insect larvae. They reproduce in the sea between July and September, mating in groups composed of 1 female and 3-5 males. Each female produces from 100,000 to 300,000 eggs per kilo of body weight, and the eggs contain an oily component enabling them to float.
Possessing a serpent-shaped body, they can reach up to 1 meter in length. Eel eggs are deposited in the Sargasso Sea (a region of the Atlantic Ocean near Central America and the Caribbean); the larvae begin their trip towards the European coast and Mediterranean sea where they arrive after 1-3 years, white in color, for which they are called “glass eels.” After 8 to 9 years, they return to the Sargasso Sea to reproduce. Feeding on small fish, and their blood is toxic if it comes in contact with a wound
The seabed of the Torre Castiglione sinkholes is home to sea fauna such as mullet (Mugilcephalus), western mosquitofish (Gambusia affinis) and eels (Anguilla anguilla), evidence of their past connection with the greater sea.
The mosquito fish, however, were introduced in the past to combat malaria. Because of the extreme isolation created by these peculiar habitats, there are also ancient, rare, and sometimes unique cave dwelling inhabitants, including invertebrates like Spelaemysis bottazzii, endemic to Apulia, Metaingolfiella and Diamisi camassai (endemic specifically to the sinkholes of Torre Castiglione).
These species are representative of paleo-mediterranean life, which colonized the subterranean waters in Apulia nearly 160 million years ago.
Mammals have been documented along the edges of the sinkholes and on nearby roads, including numerous red fox (Vulpes vulpes), least weasels (Mustela nivalis), beech martens (Martes foina), and hedgehogs (Erinaceus europaeus), who leave their dens during the dusk and nocturnal hours in the search of food. Here these mammals tend to abandon their places of refuge during the summer months due to the intensification of human activity.
In terms of reptiles and amphibians, the spunnulate have a significant variety despite the modest area they cover. Among the reptiles present are European pond turtles (Emys orbicularis), four-lined snakes (Elaphe quatuorlineata) and European ratsnakes (Elaphe situla).
The red fox is a carnivore that resorts when necessary to berries and wild fruit. Nearly nocturnal, they are shy and avoid contact.
Present in a wide variety of habitats, a credit to its adaptability, rather than give chase, when hunting foxes leap a meter into the air and land in a nosedive on their prey using their front paws to pin it down.
In periods of abundance, they dig numerous small holes where they hide their food.
Females give birth once a year in a den located inside the fox burrow after a gestational period of 52-53 days, with 3 to 8 kits per litter.
The least weasel is a from the Mustelidae family, with short limbs and thick fur. It lives in cultivated land, woods, and near abandoned homes.
Especially active at night, it also moves during the day, living either alone or in small groups and taking shelter in burrows dug by other animals.
They feed primarily on rodents, but also hares, rabbits, amphibians, reptiles, birds and bird eggs, living up to 4 years in the wild, or 8-10 years in captivity.
The beech marten, also from the Mustelidae family, has an elongated body about the size of cat. It leaves paw prints with only four toes, despite having five, mimicking those of a cat. The preferred habitats for this species are woods, rural grounds with wooded areas, hedges and farmland. The beech marten in an omnivore, with a preference for small rodents and voles, but depending on the season, they can also consume a large amount of fruit. This is a solely nocturnal species, for the most part solitary, with males and females interacting only during the reproductive period. Life expectancy can easily go up to as high as 20 years.
These mammals possess large claws designed for digging and about 6,000 spines. Being very shortsighted, hedgehogs use their olfactory sense, smelling the ground to locate their pray while. During the day they hide under decaying wood or dry leaves, preferring bushy areas and the underbrush and borders of woodlands. They feed on insects, worms, small rodents, and slugs, but will resort when necessary to acorns, berries and fruit.
A local Salentine legend tells the story of a hedgehog who loved grapes: not able to arrive at the height of the grapes, he would shake the vine to make the fruit fall, then roll over to skewer them with his spines, so as to bring them back to his burrow and divvy up the spoils.
Photo credit: AMP
The ideal habitat for the European pond turtle is made up of canals with slow moving water, abundant aquatic vegetation, banks and ponds. It is a primarily carnivorous species that feeds on insects, annelids, slugs, crustaceans, mollusks and even aquatic plants, occasionally eating small amphibians and fish carcasses. The females deposit their eggs at night, in a hole dug between plant roots, where the ground is softer, positioned so as to guarantee exposure to the sun. When the hatchlings emerge, they are armed with an “egg tooth” used initially to break out of their egg shell that will eventually disappear. The sex of the newly hatched is determined by the incubation temperature: between 23° – 27° degrees for males and 30 °- 33° for females.
Photo credit: AMP
This species has light brown skin with four distinct black lines, hence its scientific name in Latin, quatuorlineata. A diurnal reptile, during the winter season they prefer to occupy abandoned rodent tunnels.
They feed on small mammals such as rabbits, weasels and mice, while occasional pray include pigeons, eggs and sometimes lizards.
Despite their noteworthy size, reaching up to 220 centimeters in length, it is mild-mannered species.
According to local legends they are gluttons for milk, bringing about the name “sacara pasturavacche,” (loosely translating to “sucker of hobbled cows”) because of stories where of them found attached to cow’s and sheep’s udders, or even more dramatically, attempting to drink milk left on the lips of newborns, or breast of feeding mothers. In reality, this species has no attraction to milk whatsoever.
This reptile has a yellow-green coloring with striking irregular rust-colored spots bordered in black. The ratsnake can reach up to 90 cm in length and is a capable hunter of small rodents. However, they will also turn to lizards, frogs, small birds and their eggs when necessary. Being without fangs or poisonous venom, they kill their pray using constriction, or, alternatively, by swallowing their pray whole.
They prefer arid and sunny environments like dry stone walls, stone quarries, Mediterranean macchia, the edges of fields, and waterways. Mostly active during the day, it is good at climbing and an excellent swimmer.
Photo credit: Amp