Katak / Frog

Frogs are amphibians in the order Anura (meaning "tail-less", from Greek an-, without + oura, tail), formerly referred to as Salientia (Latin salere (salio), "to jump"). Most frogs are characterized by long hind legs, a short body, webbed digits (fingers or toes), protruding eyes and the absence of a tail. Frogs are widely known as exceptional jumpers, and many of the anatomical characteristics of frogs, particularly their long, powerful legs, are adaptations to improve jumping performance. Due to their permeable skin, frogs are often semi-aquatic or inhabit humid areas, but move easily on land. They typically lay their eggs in puddles, ponds or lakes, and their larvae, called tadpoles, have gills and develop in water. Adult frogs follow a carnivorous diet, mostly of arthropods, annelids and gastropods. Frogs are most noticeable by their call, which can be widely heard during the night or day, mainly in their mating season.
The distribution of frogs ranges from tropic to subarctic regions, but most species are found in tropical rainforests. Consisting of more than 5,000 species described, they are among the most diverse groups of vertebrates. However, populations of certain frog species are declining significantly.
A distinction is often made between frogs and toads on the basis of their appearance, caused by the convergent adaptation among so-called toads to dry environments; however, this distinction has no taxonomic basis. The only family exclusively given the common name "toad" is Bufonidae, but many species from other families are also called "toads," and the species within the toad genus Atelopus are referred to as "harlequin frogs".
The name frog derives from Old English frogga, (compare Old Norse frauki, German Frosch, older Dutch spelling kikvorsch), cognate with Sanskrit plava (frog), probably deriving from Proto-Indo-European praw = "to jump"

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Rusa / Deer

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Deer are the ruminant mammals forming the family Cervidae. They include for example Moose, Red Deer, Reindeer, Roe and Chital. Animals from related families within the order Artiodactyla (even-toed ungulates) are often also considered to be deer – these include muntjac and water deer. Male deer of all species but the Chinese Water deer and female reindeer grow and shed new antlers each year. In this they differ from permanently horned animals such as antelope; these are in the same order as deer and may bear a superficial resemblance. The musk deer of Asia and Water Chevrotain (or Mouse Deer) of tropical African and Asian forests are not usually regarded as true deer and form their own families, Moschidae and Tragulidae, respectively.

he word "deer" was originally quite broad in meaning, but became more specific over time. In Middle English der (O.E. dēor) meant a wild animal of any kind (as opposed to cattle, which then meant any domestic livestock, from the idea of ownership and related to chattle and capital).^[1] This general sense gave way to the modern sense by the end of the Middle English period, around 1500. Cognates of English "deer" in several other languages still have the general sense of "animal" – for example German Tier, Dutch dier, and Scandinavian djur, dyr, dýr. "Deer" is the same in the plural as in the singular.
For most deer the male is called a buck and the female is a doe, but the terms vary with dialect, and especially according to the size of the species. For many larger deer the male is a stag and the female a hind, while for other larger deer the same words are used as for cattle: bull and cow. Terms for young deer vary similarly, with that of most being called a fawn and that of the larger species calf; young of the smallest kinds may be a kid. A group of deer of any kind is a herd.The adjective of relation pertaining to deer is cervine; like the family name "Cervidae" this is from Latin: cervus, "deer".
The word 'hart' is an old alternative word for "stag", especially in a (British) Medieval hunting context.
Deer are widely distributed, and hunted, with indigenous representatives in all continents except Antarctica and Australia, though Africa has only one native species, the Red Deer, confined to the Atlas Mountains in the northwest of the continent.
Deer live in a variety of biomes ranging from tundra to the tropical rainforest. While often associated with forests, many deer are ecotone species that live in transitional areas between forests and thickets (for cover) and prairie and savanna (open space). The majority of large deer species inhabit temperate mixed deciduous forest, mountain mixed coniferous forest, tropical seasonal/dry forest, and savanna habitats around the world. Clearing open areas within forests to some extent may actually benefit deer populations by exposing the understory and allowing the types of grasses, weeds, and herbs to grow that deer like to eat. Additionally, access to adjacent croplands may also benefit deer. However, adequate forest or brush cover must still be provided for populations to grow and thrive.
Small species of brocket deer and pudús of Central and South America, and muntjacs of Asia generally occupy dense forests and are less often seen in open spaces, with the possible exception of the Indian Muntjac. There are also several species of deer that are highly specialized, and live almost exclusively in mountains, grasslands, swamps, and "wet" savannas, or riparian corridors surrounded by deserts. Some deer have a circumpolar distribution in both North America and Eurasia. Examples include the caribou that live in Arctic tundra and taiga (boreal forests) and moose that inhabit taiga and adjacent areas. Huemul Deer (taruca and Chilean Huemul) of South America's Andes fill an ecological niche of the ibex or Wild Goat, with the fawns behaving more like goat kids.
The highest concentration of large deer species in temperate North America lies in the Canadian Rocky Mountain and Columbia Mountain Regions between Alberta and British Columbia where all five North American deer species (White-tailed deer, Mule deer, Caribou, Elk, and Moose) can be found. This region has several clusters of national parks including Mount Revelstoke National Park, Glacier National Park (Canada), Yoho National Park, and Kootenay National Park on the British Columbia side, and Banff National Park, Jasper National Park, and Glacier National Park (U.S.) on the Alberta and Montana sides. Mountain slope habitats vary from moist coniferous/mixed forested habitats to dry subalpine/pine forests with alpine meadows higher up. The foothills and river valleys between the mountain ranges provide a mosaic of cropland and deciduous parklands. The rare woodland caribou have the most restricted range living at higher altitudes in the subalpine meadows and alpine tundra areas of some of the mountain ranges. Elk and Mule Deer both migrate between the alpine meadows and lower coniferous forests and tend to be most common in this region. Elk also inhabit river valley bottomlands, which they share with White-tailed deer. The White-tailed deer have recently expanded their range within the foothills and river valley bottoms of the Canadian Rockies owing to conversion of land to cropland and the clearing of coniferous forests allowing more deciduous vegetation to grow up the mountain slopes. They also live in the aspen parklands north of Calgary and Edmonton, where they share habitat with the moose. The adjacent Great Plains grassland habitats are left to herds of Elk, American Bison, and pronghorn antelope.
The Eurasian Continent (including the Indian Subcontinent) boasts the most species of deer in the world, with most species being found in Asia. Europe, in comparison, has lower diversity in plant and animal species. However, many national parks and protected reserves in Europe do have populations of Red Deer, Roe Deer, and Fallow Deer. These species have long been associated with the continent of Europe, but also inhabit Asia Minor, the Caucasus Mountains, and Northwestern Iran. "European" Fallow Deer historically lived over much of Europe during the Ice Ages, but afterwards became restricted primarily to the Anatolian Peninsula, in present-day Turkey. Present-day Fallow deer populations in Europe are a result of historic man-made introductions of this species first to the Mediterranean regions of Europe, then eventually to the rest of Europe. They were initially park animals that later escaped and reestablished themselves in the wild. Historically, Europe's deer species shared their deciduous forest habitat with other herbivores such as the extinct tarpan (forest horse), extinct aurochs (forest ox), and the endangered wisent (European bison). Good places to see deer in Europe include the Scottish Highlands, the Austrian Alps, and the wetlands between Austria, Hungary, and Czech Republic. Some fine National Parks include Doñana National Park in Spain, the Veluwe in the Netherlands, the Ardennes in Belgium, and Białowieża National Park of Poland. Spain, Eastern Europe, and the Caucasus Mountains still have virgin forest areas that are not only home to sizable deer populations but also for other animals that were once abundant such as the wisent, Eurasian Lynx, Spanish lynx, wolves, and Brown Bears.

The highest concentration of large deer species in temperate Asia occurs in the mixed deciduous forests, mountain coniferous forests, and taiga bordering North Korea, Manchuria (Northeastern China), and the Ussuri Region (Russia). These are among some of the richest deciduous and coniferous forests in the world where one can find Siberian Roe Deer, Sika Deer, Elk, and Moose. Asian Caribou occupy the northern fringes of this region along the Sino-Russian border.
Deer such as the Sika Deer, Thorold's deer, Central Asian Red Deer, and Elk have historically been farmed for their antlers by Han Chinese, Turkic peoples, Tungusic peoples, Mongolians, and Koreans. Like the Sami people of Finland and Scandinavia, the Tungusic peoples, Mongolians, and Turkic peoples of Southern Siberia, Northern Mongolia, and the Ussuri Region have also taken to raising semi-domesticated herds of Asian Caribou.
The highest concentration of large deer species in the tropics occurs in Southern Asia in Northern India's Indo-Gangetic Plain Region and Nepal's Terai Region. These fertile plains consist of tropical seasonal moist deciduous, dry deciduous forests, and both dry and wet savannas that are home to Chital, Hog Deer, Barasingha, Indian Sambar, and Indian Muntjac. Grazing species such as the endangered Barasingha and very common Chital are gregarious and live in large herds. Indian Sambar can be gregarious but are usually solitary or live in smaller herds. Hog Deer are solitary and have lower densities than Indian Muntjac. Deer can be seen in several national parks in India, Nepal, and Sri Lanka of which Kanha National Park, Dudhwa National Park, and Chitwan National Park are most famous. Sri Lanka's Wilpattu National Park and Yala National Park have large herds of Indian Sambar and Chital. The Indian sambar are more gregarious in Sri Lanka than other parts of their range and tend to form larger herds than elsewhere.
The Chao Praya River Valley of Thailand was once primarily tropical seasonal moist deciduous forest and wet savanna that hosted populations of Hog Deer, the now-extinct Schomburgk's Deer, the Eld's Deer, Indian Sambar, and Indian Muntjac. Both the Hog Deer and Eld's Deer are rare, whereas Indian Sambar and Indian Muntjac thrive in protected national parks such as Khao Yai.
Many of these South Asian and Southeast Asian deer species also share their habitat with various herbivores such as Asian Elephants, various Asian rhinoceros species, various antelope species (such as nilgai, Four-horned Antelope, blackbuck, and Indian gazelle in India), and wild oxen (such as Wild Asian Water Buffalo, gaur, banteng, and kouprey). How different herbivores can survive together in a given area is each species have different food preferences, although there may be some overlap.
Australia has six introduced species of deer that have established sustainable wild populations from acclimatisation society releases in the 19th century. These are Fallow Deer, Red Deer, Sambar Deer, Hog Deer, Rusa deer, and Chital. Red Deer introduced into New Zealand in 1851 from English and Scottish stock were domesticated in deer farms by the late 1960s and are common farm animals there now. Seven other species of deer were introduced into New Zealand but none are as widespread as Red Deer.

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Burung Helang / Eagle

Eagle

Eagles are large birds of prey which are members of the bird family Accipitridae, and belong to several genera which are not necessarily closely related to each other. Most of the more than 60 species occur in Eurasia and Africa.^[1] Outside this area, just two species (the Bald and Golden Eagles) can be found in the United States and Canada, nine more in Central and South America, and three in Australia.

Eagles are different from many other birds of prey mainly by their larger size, more powerful build, and heavier head and beak. Even the smallest eagles, like the Booted Eagle (which is comparable in size to a Common Buzzard or Red-tailed Hawk), have relatively longer and more evenly broad wings, and more direct, faster flight. Most eagles are larger than any other raptors apart from the vultures. Species named as eagles range in size from the South Nicobar Serpent-eagle, at 500 g (1.1 lb) and 40 cm (16 in), to the 6.7 kg (14.7 lbs) Steller's Sea Eagle and the 100 cm (39 in) Philippine Eagle.
Like all birds of prey, eagles have very large powerful hooked beaks for tearing flesh from their prey, strong muscular legs, and powerful talons. They also have extremely keen eyesight which enables them to spot potential prey from a very long distance.^[2] This keen eyesight is primarily contributed by their extremely large pupils which ensure minimal diffraction (scattering) of the incoming light.
Eagles build their nests, called eyries, in tall trees or on high cliffs. Many species lay two eggs, but the older, larger chick frequently kills its younger sibling once it has hatched. The dominant chick tends to be the female, as they are bigger than the male. The parents take no action to stop the killing.
Major new research into eagle taxonomy suggests that the important genera Aquila and Hieraaetus are not composed of nearest relatives, and it is likely that a reclassification of these genera will soon take place, with some species being moved to Lophaetus or Ictinaetus.^[3]

• Bonelli's Eagle, the Booted Eagle and the Little Eagle have been moved from Hieraaetus to Aquila.
• Either the Greater Spotted Eagle and Lesser Spotted Eagle should move from Aquila to join the Long-crested Eagle in Lophaetus, or, perhaps better, all three of these species should move to Ictinaetus with the Black Eagle.
• The Steppe Eagle and Tawny Eagle, once thought to be conspecific, are not even each other's nearest relatives.

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Merak / Peafowl

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The term peafowl can refer to the two species of bird in the genus Pavo of the pheasant family, Phasianidae. The African Congo Peafowl is placed in its own genus Afropavo and is not dealt with here. Peafowl are best known for the male's extravagant tail, which it displays as part of courtship. The male is called a peacock, and the female a peahen,^[1] although it is common to hear the female also referred to as a "peacock" or "female peacock". The female peafowl is brown or toned grey and brown. The two species are:

• Indian Peafowl, Pavo cristatus (Asiatic)
• Green Peafowl, Pavo muticus (Asiatic)

The Indian Peafowl is a resident breeder in the Indian subcontinent. The peacock is designated as the national bird of India and the provincial bird of the Punjab (Pakistan).
The Green Peafowl breeds from Burma east to Java. The IUCN lists the Green Peafowl as vulnerable to extinction due to hunting and a reduction in extent and quality of habitat.

Plumage

The male (peacock) Indian Peafowl has iridescent blue-green or green colored plumage. The so-called "tail" of the peacock, also termed the "train," is not the tail quill feathers but highly elongated upper tail coverts. The train feathers have a series of eyes that are best seen when the tail is fanned. Both species have a crest atop the head.
The female (peahen) Indian Peafowl has a mixture of dull green, brown, and grey in her plumage. She lacks the long upper tail coverts of the male but has a crest. The female can also display her plumage to ward off female competition or danger to her young.
The Green Peafowl is different in appearance from the Indian Peafowl. The male has green and gold plumage and has an erect crest. The wings are black with a sheen of blue.
Unlike the Indian Peafowl, the Green Peahen is very similar to the male, only having shorter upper tail coverts and less iridescence. It is very hard to tell a juvenile male from an adult female.
Many of the brilliant colours of the peacock plumage are due to an optical interference phenomenon, Bragg reflection, based on (nearly) periodic nanostructures found in the barbules (fiber-like components) of the feathers.
Different colours correspond to different length scales of the periodic structures. For brown feathers, a mixture of red and blue is required: one colour is created by the periodic structure, and the other is a created by a Fabry–Pérot interference peak from reflections off the outermost and innermost boundaries of the periodic structure. White peafowls are sometimes bred.
Such interference-based structural colour is especially important in producing the peacock's iridescent hues (which shimmer and change with viewing angle), since interference effects depend upon the angle of light, unlike chemical pigments.

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Burung Tiong Mas / Common Hill Myna (Gracula religiosa)

The Common Hill Myna (Gracula religiosa), sometimes spelled "mynah" and formerly simply known as "Hill Myna", is the myna bird most commonly seen in aviculture, where it is often simply referred to by the latter two names. It is a member of the starling family (Sturnidae), resident in hill regions of South Asia and Southeast Asia. The Sri Lanka Hill Myna, a former subspecies of G. religiosa, is generally accepted as a separate species G. ptilogenys nowadays. The Enggano Hill Myna (G. enganensis) and Nias Hill Myna (G. robusta) are also widely accepted as specifically distinct, and many authors favor treating the Southern Hill Myna (G. r. indica) from the Nilgiris and elsewhere in the Western Ghats of India as a separate species also.

This is a stocky jet-black myna, with bright orange-yellow patches of naked skin and fleshy wattles on the side of its head and nape. At about 29 cm length, it is somewhat larger than the Common Myna (Acridotheres tristis).^[1]
It is overall green-glossed black plumage, purple-tinged on the head and neck. There are large white wing patches which are obvious in flight but mostly covered when the bird is sitting. The bill and strong legs are bright yellow, and there are yellow wattles on the nape and under the eye. These differ conspicuously in shape from the naked eye-patch of the Common Myna and Bank Myna (A. ginginianus), and more subtly vary between the different hill mynas from South Asia: in the Common Hill Myna they extend from the eye to the nape, where they join, while the Sri Lanka Hill Myna has a single wattle across the nape and extending a bit towards the eyes. In the Southern Hill Myna, the wattles are separate and curve towards the top of the head. The Nias and Enggano Hill Mynas differ in details of the facial wattles, and size, particularly that of the bill.^[1]
Sexes are similar; juveniles have a duller bill.^[1]
With the Southern, Nias and Enggano Hill Mynas as separate species, the Common Hill Myna has seven or eight subspecies which differ only slightly. They are:^[2]

• Gracula religiosa andamanensis Beavan 1867 – Andaman Hill Myna. Andaman Islands, Central (Nancowry) group of the Nicobar Islands
• Gracula religiosa batuensis – Batu and Mentawai Islands.
• Gracula religiosa halibrecta Oberholser 1926 – Great Nicobar Hill Myna. Great Nicobar Little Nicobar and adjacent islets in the Nicobar Islands. Doubtfully distinct from andamanensis.
• Gracula religiosa intermedia – North-western Indochina and adjacent north-eastern India and southern China.
• Gracula religiosa palawanensis – Palawan in the Philippines.
• Gracula religiosa peninsularis – Bastar Hill Mynah. Central India.
• Gracula religiosa religiosa – Greater Sundas (except Sulawesi) and Peninsular Malaysia.
• Gracula religiosa venerata – Western Lesser Sundas.

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Biawak Air / Water Monitor

The Water monitor, (Varanus salvator) is a large species of monitor lizard capable of growing to 3.21 metres (10.5 ft) in length, with the average size of most adults at 1.5 metres (4 ft 11 in) long.^[1] Maximum weight of Varanus salvator can be over 25 kilograms (55 lb), but most are half that size. Their body is muscular with a long, powerful, laterally compressed tail. Water monitors are one of the most common monitor lizards found throughout Asia, and range from Sri Lanka, India, Indochina, the Malay Peninsula and various islands of Indonesia, living in areas close to water.

Etymology
The generic name Varanus is derived from the Arabic waral (ورل), which translates as "monitor" in English. The specific name is the Latin word for "Saviour" denoting a possible religious connotation.^[2] The Water monitor is occasionally confused with the Crocodile monitor (V. salvadorii) because of their similar scientific names.^[3]
In Thailand, the word water monitor or actually local word 'เหี้ย' (hia) is used as an insulting word for bad and evil things including a bad person. Its name is also considered a word bringing a bad luck, so some people prefer to call them 'ตัวเงินตัวทอง' which means 'silver and gold' in Thai to avoid the jinx.
The origin of this offensive meaning can be traced back to a time when more people lived in rural areas in close proximity to monitor lizards. Traditionally, Thai villagers lived in 2-story houses, the top floor was for living while the ground floor was designed to be a space for domestic animals such as pigs, chickens, and dogs. Water monitors would enter the ground floor and eat or maim the domestic animals, also hence the other name 'ตัวกินไก่' (Tua kin kai - chicken eater).

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Labah-labah / Spider

Spiders (order Araneae) are air-breathing chelicerate arthropods that have eight legs, and chelicerae modified into fangs that inject venom. They are the largest order of arachnids and rank seventh in total species diversity among all other groups of organisms.^[1] Spiders are found world-wide on every continent except for Antarctica, and have become established in nearly every ecological niche with the exception of air and sea colonization. As of 2008, approximately 40,000 spider species, and 109 families have been recorded by taxonomists;^[2] however, there has been confusion within the scientific community as to how all these genera should be classified, as evidenced by the over 20 different classifications that have been proposed since 1900.^[3]
Anatomically, spiders differ from other arthropods in that the usual body segments are fused into two tagmata, the cephalothorax and abdomen, and joined by a small, cylindrical pedicel. Unlike insects, spiders do not have antennae. In all except the most primitive group, the Mesothelae, spiders have the most centralized nervous systems of all arthropods, as all their ganglia are fused into one mass in the cephalothorax. Unlike most arthropods, spiders have no extensor muscles in their limbs and instead extend them by hydraulic pressure.
Their abdomens bear appendages that have been modified into spinnerets that extrude silk from up to six types of silk glands within their abdomen. Spider webs vary widely in size, shape and the amount of sticky thread used. It now appears that the spiral orb web may be one of the earliest forms, and spiders that produce tangled cobwebs are more abundant and diverse than orb-web spiders. Spider-like arachnids with silk-producing spigots appear in the Devonian period about 386 million years ago, but these animals apparently lacked spinnerets. True spiders have been found in Carboniferous rocks from 318 to 299 million years ago, and are very similar to the most primitive surviving order, the Mesothelae. The main groups of modern spiders, Mygalomorphae and Araneomorphae, first appear in the Triassic period, before 200 million years ago.
A vegetarian species was described in 2008,^[4] but all other known species are predators, mostly preying on insects and on other spiders, although a few large species also take birds and lizards. Spiders use a wide range of strategies to capture prey: trapping it in sticky webs, lassoing it with sticky bolas, mimicking the prey to avoid detection, or running it down. Most detect prey mainly by sensing vibrations, but the active hunters have acute vision, and hunters of the genus Portia show signs of intelligence in their choice of tactics and ability to develop new ones. Spiders' guts are too narrow to take solids, and they liquidize their food by flooding it with digestive enzymes and grinding it with the bases of their pedipalps, as they do not have true jaws.
Male spiders identify themselves by a variety of complex courtship rituals to avoid being eaten by the females. Males of most species survive a few matings, limited mainly by their short life spans. Females weave silk egg-cases, each of which may contain hundreds of eggs. Females of many species care for their young, for example by carrying them around or by sharing food with them. A minority of species are social, building communal webs that may house anywhere from a few to 50,000 individuals. Social behavior ranges from precarious toleration, as in the aggressive widow spiders, to co-operative hunting and food-sharing. Although most spiders live for at most two years, tarantulas and other mygalomorph spiders can live up to 25 years in captivity.
While the venom of a few species is dangerous to humans, scientists are now researching the use of spider venom in medicine and as non-polluting pesticides. Spider silk provides a combination of lightness, strength and elasticity that is superior to that of synthetic materials, and spider silk genes have been inserted into mammals and plants to see if these can be used as silk factories. As a result of their wide range of behaviors, spiders have become common symbols in art and mythology symbolizing various combinations of patience, cruelty and creative powers.

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Mentadak / Mantis

Mantodea or mantises is an order of insects which contains approximately 2,200 species in 9 families^[1] worldwide in temperate and tropical habitats. Most of the species are in the family Mantidae. Historically, the term "mantid" was used to refer to any member of the order because for most of the past century, only one family was recognized within the order; technically, however, the term only refers to this one family, meaning the species in the other eight recently-established families are not mantids, by definition (i.e., they are empusids, or hymenopodids, etc.), and the term "mantises" should be used when referring to the entire order. A colloquial name for the order is "praying mantises", because of the typical "prayer-like" stance, although the term is often misspelled as "preying mantis" since mantises are notoriously predatory. The word mantis is Greek for "prophet" or "fortune teller". In Europe, the name "praying mantis" refers to Mantis religiosa. The closest relatives of mantises are the orders Isoptera (termites) and Blattodea (cockroaches), and these three groups together are sometimes ranked as an order rather than a superorder. They are sometimes confused with phasmids (stick/leaf insects) and other elongated insects such as grasshoppers and crickets.

Description

Praying Mantises are exclusively predatory. Larger species have been known to prey on small lizards, frogs, birds, snakes, and even rodents, basically anything that it can successfully capture and devour. Most species are known to engage in cannibalism. The majority of mantises are ambush predators, waiting for prey to stray too near. The mantis then lashes out at remarkable speed. Some ground and bark species, however, pursue their prey rather quickly. Surprisingly, though, praying mantises are particularly susceptible to an enzyme found in the mucus excreted by slugs, and thus, their primary enemy is the slug. Prey items are caught and held securely with grasping, spiked forelegs ("raptorial legs"); the first thoracic segment, the prothorax, is commonly elongated and flexibly articulated, allowing for greater range of movement of the front limbs while the remainder of the body remains more or less immobile. The articulation of the head is also remarkably flexible, permitting nearly 300 degrees of movement in some species, allowing for a great range of vision (their compound eyes have a large binocular field of vision) without having to move the remainder of the body. As their hunting relies heavily on vision, they are primarily diurnal, but many species will fly at night.

Reproduction and life history

Sexual cannibalism is common among mantises in captivity, and under some circumstances may also be observed in the field. The female may start feeding by biting off the male’s head (as with any prey), and if mating had begun, the male’s movements may become even more vigorous in its delivery of sperm. Early researchers thought that because copulatory movement is controlled by ganglion in the abdomen, not the head, removal of the male’s head was a reproductive strategy by females to enhance fertilisation while obtaining sustenance. Later, this behaviour appeared to be an artifact of intrusive laboratory observation. Whether the behaviour in the field is natural, or also the result of distractions caused by the human observer, remains controversial. Mantises are highly visual creatures, and notice any disturbance occurring in the laboratory or field such as bright lights or moving scientists. Research by Liske and Davis (1987) and others found (e.g. using video recorders in vacant rooms) that Chinese mantises that had been fed ad libitum (so that they were not starving) actually displayed elaborate courtship behavior when left undisturbed. The male engages the female in courtship dance, to change her interest from feeding to mating. Courtship display has also been observed in other species, but it does not hold for all mantises.
The reason for sexual cannibalism has been debated, with some considering submissive males to be achieving a selective advantage in their ability to produce offspring. This theory is supported by a quantifiable increase in the duration of copulation among males who are cannibalized, in some cases doubling both the duration and the chance of fertilization. This is further supported in a study where males were seen to approach hungry females with more caution, and were shown to remain mounted on hungry females for a longer time, indicating that males actively avoiding cannibalism may mate with multiple females. The act of dismounting is one of the most dangerous times for males during copulation, for it is at this time that females most frequently cannibalize their mates. This increase in mounting duration was thought to indicate that males would be more prone to wait for an opportune time to dismount from a hungry female rather than from a satiated female that would be less likely to cannibalize her mate. Some consider this to be an indication that male submissiveness does not inherently increase male reproductive success, rather that more fit males are likely to approach a female with caution and escape.^[2]
The mating season in temperate climates typically begins in autumn. To mate following courtship, the male usually leaps onto the female’s back, and clasps her thorax and wing bases with his forelegs. He then arches his abdomen to deposit and store sperm in a special chamber near the tip of the female’s abdomen. The female then lays between 10 and 400 eggs, depending on the species. Eggs are typically deposited in a frothy mass that is produced by glands in the abdomen. This froth then hardens, creating a protective capsule with a further protective coat, and the egg mass is called an ootheca. Depending on the species these can be attached to a flat surface, wrapped around a plant or even deposited in the ground. Despite the versatility and durability of the eggs, they are often preyed on, especially by several species of parasitic wasps. In a few species, the mother guards the eggs.
As in related insect groups, mantises go through three stages of metamorphosis: egg, nymph, and adult (mantises are among the hemimetabolic insects). The nymph and adult insect are structurally quite similar, except that the nymph is smaller and has no wings or functional genitalia. The nymphs are also sometimes colored differently from the adult, and the early stages are often mimics of ants. A mantis nymph increases in size (often changing its diet as it does so) by replacing its outer body covering with a sturdy, flexible exoskeleton and molting when needed. This can happen up to five to ten times, depending on the species. After the final molt most species have wings, though some species are wingless or brachypterous ("short-winged"), particularly in the female sex.
In tropical species, the natural lifespan of a mantis in the wild is about 10–12 months, but some species kept in captivity have been sustained for 14 months. In colder areas, females will die during the winter (as well as any surviving males).

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Ulat Gonggok / Millipede

Millipedes, known as shongololos in South African English, are arthropods that have two pairs of legs per segment (except for the first segment behind the head which does not have any appendages at all, and the next few which only have one pair of legs). Each segment that has two pairs of legs is a result of two single segments fused together as one. Most millipedes have very elongated cylindrical bodies, although some are flattened dorso-ventrally, while pill millipedes are shorter and can roll into a ball, like a pillbug.

Millipedes are detritivores and slow moving. Most millipedes eat decaying leaves and other dead plant matter, moisturising the food with secretions and then scraping it in with the jaws. However they can also be a minor garden pest, especially in greenhouses where they can cause severe damage to emergent seedlings. Signs of millipede damage include the stripping of the outer layers of a young plant stem and irregular damage to leaves and plant apices.

This class contains around 10,000 species. There are 13 orders and 115 families.

The giant African millipede (Archispirostreptus gigas) is the largest species of millipede.

Millipedes can be easily distinguished from the somewhat similar and related centipedes (Class Chilopoda), which move rapidly, and have a single pair of legs for each body segment.

Unlike centipedes however, millipedes are by nature not predators, and due to their slow, non-aggressive behavior and simple diet of decomposing leaves, are easy to keep and ideal as pets.

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Bunga Bawang / Zephyranthes

Zephyranthes is a genus of about 70 species in the Amaryllis family. Common names for species in this genus include fairy lily, rainflower, zephyr lily, magic lily and rain lily.

According Meerow et al., cladistics suggests that they are native to the Americas. This is important to mention since several species have become naturalized (sometimes unintentionally) in distant places like Hawaii, Indonesia, and Thailand. The species that are native to the higher altitudes in Mexico (e.g. Z. lindleyana) and parts of North America (e.g. Z. longifolia) or Argentina (e.g. Z. candida) represent the species having the greatest potential for cold hardiness.

These perennial geophytes are remarkable for the many ecological niches they tolerate (periodically wet soil to desert conditions), and have many ornamental characteristics worth preserving. Care should be taken with the plants since many of the parts, leaves, bulbs etc. are toxic. Although the genus has been evaluated for possible medicinal properties the biochemically toxic compounds are things like alkaloids. (Kojima et al. 1997.)

Species in the genus which are listed in this article, vary in morphology. Characteristics such as bulb size, tunic color, and leaf morphology help to identify the species. Foliage in the wild is often ephemeral, but under cultivation becomes more persistent. Leaf color ranges from the bright grassy green of Z. candida (shown in the photo) to rather broad glaucous colored foliage such as Z. drummondii. A few of the species have distinct bronze tints in the foliage when grown in bright light. Size of leaves in these species, ranges from dark green and tiny grassy leaves in species like Z.jonesi or Z. longifolia, to broader, glaucous leaves in species like Z. drummondii, and perhaps largest of all, the cultivar commonly known as "Horsetail Falls" which has handsome broad leaves almost like a Hippeastrum.

Flower color in the species ranges from white to yellow (various tints of this color from lemon to sulfur) and pink. Zephyranthes have erect flower stalks which support a flower that may be upward facing or slightly nodding. The funnel-shaped, flowers with six petals can be crocus shaped, but may also open flat such as in Z.jonesii or even reflex slightly. The flowers of some species have a sweet, pleasant fragrance. Fragrance appears to be recessive in crosses, but there are a few species or hybrids, Z. drummondii (white), Z. morrisclintae (pink)and Z.jonesii (light yellow), that all carry the trait. At least 2 of these open their flowers at night and are attractive to nocturnal insects. The flowers typically last only for a day or two; but new flowers may appear in a succession of blooms, especially during humid or rainy weather. Various members of the genus may bloom spring only or repeat and continue into autumn, often a few days after rainstorms thus one of the common names, rainlilies. Periods of synchronous bloom, which breeders have dubbed 'blitzes', are part of their ornamental value, but also times breeders exploit for the purpose of producing new hybrids. (Marta 2005)

Most species under cultivation will bloom without the naturally imposed drought and wet that occurs in nature. Greenhouse grown plants bloom very freely but cycle through periods of bloom. One of the longest blooming of all the species is Z. primulina which blooms from April until October. Although it is apomictic, it is a choice parent for crosses because of its rapid repeat flowering trait and long bloom season. Some other species such as Z. Morrisclintae appear to bloom only in the spring season. Most of these species are easily propagated vegetatively via offsets or twin scaling. A few of them such a Z.clintae are slow to produce increase. Unusual phenotypes can be preserved vegetatively. Sexual reproduction is via seed. The apomictic species freely set seed and faithfully reproduce the maternal phenotype. Sterility in hybrids can be problematic;reasons for this are mentioned below. Seed usually is best sown quickly after harvest, although short term storage can be successful. Maiden seedling can be brought into bloom for some of the hybrid in 8-12 after sowing in ideal conditions. This is great for doing necessary checks for apomixis. Currently these plants are grown in the garden in USDA zones 7 and higher. Hopefully with some attention from breeders new cultivar might increase the plants' cold hardiness. Often the plants are sold in nurseries already potted up, this is a great benefit since the growth cycle is not interrupted. Dried bulbs are marketed wholesale and rarely may be slow to rebloom. Such bulbs usually recover once they have a long growing season after rooting out.

Breeding with these species has some inherent difficulties summarized by M. RoyChowdhury (2006 JAAS) as ranging from pseudogamy and apomixis, differences in chromosome number and varying times of flowering. In spite of these drawbacks interesting breeding work is being done to enhance the value of the plants as ornamentals. Because of the nature botanical restriction breeding programs often encounter impediments. Reciprocal crosses may be difficult because the apomictic parent cannot be used as female parents. However interspecific crosses are well documented (RoyChowdhury 2006). There are tri-hybrids and quad hybrids being produced. (Crossing 3 or 4 distinct species.) Such work indicates that complex hybrids should be possible. One constraint remains that seedlings may still carry the apomictic trait, and it is necessary to have progeny from a test cross to determine this. Mr. John Fellers, Mr. Fadjar Marta and Mr. Tony Avent are just a few of the talented breeders currently working today to increase the potential for these plants. Their work has come to the attention of connoisseurs of the these plants. Colors in man-made crosses currently include red, orange, tan, salmon, blends, picotees and stripes. Floral types such as goblet shaped, wavy petal edges, narrow petals and doubles have been bred (Marta 2005). Complex hybrids may have advantages in holding their flowers open longer, up to three days. While difficult, there have been a few attempts to cross some of these species with related species in the genus Habranthus. Currently it appears that a few crosses with large flowered Habranthus species have been possible for example the cultivar, 'Normal Pearl' which is an intergeneric cross.

The name Zephyranthes comes from Zephyrus, the god of the west wind in Greek mythology.Therefore one translation for a common name might be Westwind Flower. The west wind presumably brings rain that these plants revel in.

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