Myriapods contain arthropods such as millipedes and centipedes. The group contains about 13,000 species, all of them terrestrial.

The fossil record of myriapods reaches back into the late Wenlock epoch of the late Silurian, although molecular evidence suggests a diversification in the Cambrian Period, and Cambrian fossils exist which resemble myriapods. 

Myriapods have a single pair of antennae and, in most cases, simple eyes. Exceptions are the two classes symphylans and pauropods, and the millipede order Polydesmida and the centipede order Geophilomorpha, which are all eyeless. The house centipedes (Scutigera) on the other hand, have large and well-developed compound eyes. The mouthparts lie on the underside of the head, with an “epistome” and labrum forming the upper lip, and a pair of maxillae forming the lower lip. A pair of mandibles lie inside the mouth. Myriapods breathe through spiracles that connect to a tracheal system similar to that of insects. There is a long tubular heart that extends through much of the body, but usually few, if any, blood vessels.

Malpighian tubules excrete nitrogenous waste into the digestive system, which typically consists of a simple tube. Although the ventral nerve cord has a ganglion in each segment, the brain is relatively poorly developed.

During mating, male myriapods produce a packet of sperm (spermatophore), which they must transfer to the female externally. This process is often complex and highly developed. The female lays eggs which hatch as much-shortened versions of the adults, with only a few segments and as few as three pairs of legs. The young add additional segments and limbs as they repeatedly molt to reach the adult form.

The process of adding new segments during postembryonic growth is known as anamorphosis, of which there are three types: euanamorphosis, emianamorphosis, and teloanamorphosis. In euanamorphosis, every molt is followed by addition of new segments, even after reaching sexual maturity; in emianamorphosis, new segments are added until a certain stage, and further molts happen without addition of segments; and in teloanamorphosis, where the addition of new segments stops after the adult form is reached, after no further molts occur.

Myriapods are most abundant in moist forests, where they fulfill an important role in breaking down decaying plant material, although a few live in grasslands, semi-arid habitats or even deserts. A very small percentage of species are littoral (found along the seashore). The majority are detritivorous, except for centipedes, which are chiefly nocturnal predators.

A few species of centipedes and millipedes can produce light and are therefore bioluminescent. Millipedes differ from the other groups in having their body segments fused into pairs, giving the appearance that each segment bears two pairs of legs, while the other groups have a single pair of legs on each body segment.

Although not generally considered dangerous to humans, many millipedes produce noxious secretions (often containing benzoquinones) which in rare cases can cause temporary blistering and discolouration of the skin. Large centipedes, however, can bite, and although the bite may cause intense pain and discomfort, fatalities are extremely rare.

Source: Wikipedia

Chilopoda (Centipedes)

Family Schendylidae

Schendylidae 0F1A0784
(Singapore)
Schendylidae 0F1A2512
(Singapore)
Schendylidae 086A7222
(Singapore)

Family Scolopendridae (Scolopendrid Centipedes)

Subfamily Otostigminae

Edentistoma octosulcatum
(Sabah, Malaysia)
Otostigmus sp. 086A4679
(Singapore)

Subfamily Scolopendrinae

Scolopendra subspinipes (Singapore)

Family Scutigeridae (Typical House Centipedes)

Subfamily Thereuoneminae

Thereuopoda longicornis
(Singapore)
Thereuopoda sp. 0F1A3183
(Doi Inthanon, Thailand)
Thereuopoda sp. 0F1A2798
(Sarawak, Malaysia)
Thereuopoda sp. 0F1A8646
(Khao Sok NP, Thailand)
Thereuopoda sp. 0F1A0470
(Tawau Hills, Sabah, Malaysia)
Thereuopoda sp. 0F1A6049
(Sarawak, Malaysia)

Diplopoda (Milipedes)

Family Andrognathidae

Subfamily Bazillozoniinae

Pseudodesmus sp. 0F1A7967
(Sarawak, Malaysia)

Family Arthrosphaeridae (Malagasy and Indian Pill Millipedes)

Zoosphaerium neptunus (Andasibe, Madagascar)

Family Pachybolidae

Leptogoniulus sorornus
(Singapore)
Trigoniulus corallinus
(Singapore)
Pachybolidae 086A5650
(Singapore)
Pachybolidae 0F1A5908
(Sumaco, Ecuador)
Pachybolidae 0F1A8600
(Sarawak, Malaysia)

Family Paradoxosomatidae

Paradoxosomatidae
(Sarawak, Malaysia)
Paradoxosomatidae 0F1A6930
(Sarawak, Malaysia)
Paradoxosomatidae 0F1A8316
(Sabah, Malaysia)
Paradoxosomatidae 0F1A9656
(Phuket, Thailand)
Paradoxosomatidae IMG_2148
(Doi Inthanon NP, Thailand)
Paradoxosomatidae 0F1A2776
(Khao Yai NP, Thailand)

Subfamily Paradoxosomatinae

Tribe Orthomorphini

Orthomorpha murphyi
(Singapore)

Tribe Sulciferini

Anoplodesmus saussurii
(Singapore)

Tribe Sundaninini

Opisthodolichopus scandens
(Singapore)

Tribe Tectoporini

Helicorthomorpha holstii
(Singapore)

Family Platyrhacidae

Platyrhacidae 0F1A9305
(Sarawak, Malaysia)
Platyrhacidae 0F1A8632
(Khao Sok NP, Thailand)
Platyrhacidae 0F1A4583
(Singapore)

Subfamily Barydesminae

Barydesmus sp. 0F1A1245
(Tandayapa, Ecuador)
Barydesmus sp. 0F1A5554
(Sumaco, Ecuador)

Subfamily Platyrhacinae

Platyrhacus sp. 0F1A1908
(Doi Inthanon NP, Thailand)

Family Zephroniidae (Southeast Asian Pill Millipedes)

Zephronia sp. 0F1A2517
(Kaeng Krachan NP, Thailand)
Zephroniidae 0F1A8577
(Sabah, Malaysia)
Zephroniidae 086A6017
(Singapore)
Zephroniidae 0F1A4124
(Sarawak, Malaysia)
Zephroniidae 0F1A9405
(Sarawak, Malaysia)
Zephroniidae 0F1A7688
(Sarawak, Malaysia)
Zephroniidae 0F1A1810
(Doi Inthanon NP, Thailand)