The millipede family Conotylidae in northwestern North America, with a complete bibliography of the family (Diplopoda, Chordeumatida, Heterochordeumatidea, Conotyloidea).

The center of diversity for the chordeumatidan millipede family Conotylidae is northwestern North America, where five of six subfamilies and ten of fourteen previously described genera occur; in this paper, seven additional new genera and 33 new species from the region are described. New species in the genus Taiyutyla Chamberlin, 1952 are: Taiyutyla tillamook, Taiyutyla acuphora, and Taiyutyla amicitia; in the genus Bollmanella Chamberlin, 1941: Bollmanella bombus, Bollmanella washingtonensis and Bollmanella leonardi; in the genus Brunsonia Loomis Schmitt, 1971: Brunsonia pulchra, Brunsonia digitata, Brunsonia wenatchee, Brunsonia chelanoparva, Brunsonia chelanomagna, Brunsonia selwayana and Brunsonia benewah. Vancouvereuma n. gen. is described with the type species Taiyutyla shawi Shear 2004. Calityla n. gen. includes the new species Calityla siskiyou, Calityla ubicki, Calityla trinitaria, Calityla essigi, and Calityla humboldtensis. Ovaskella, n. gen. includes the new species Ovaskella ovaskae and Ovaskella sinuosa. Karagama, n. gen. includes the new species Karagama ladybird. Complicatella, n. gen. includes the new species Complicatella pectenifera and Complicatella neili. Bifurcatella n. gen. includes the new species Bifurcatella olympiana, Bifurcatella hoh, Bifurcatella angulata, Bifurcatella pacifica, Bifurcatella germania, Bifurcatella uniclada, Bifurcatella inflata and Bifurcatella hobo. Loomisiella, n. gen. includes the new species Loomisiella evergreen and Loomisiella pylei. New distribution records are provided for numerous previously described species of conotylids. A complete bibliography of the family Conotylidae of the world is also included.

Natural history of the social millipede Brachycybe lecontii Wood, 1864.

The millipede Brachycybe lecontii Wood, 1864 is a fungivorous social millipede known for paternal care of eggs and forming multi-generational aggregations. We investigated the life history, paternal care, chemical defence, feeding and social behaviour of B. lecontii and provided morphological and anatomical descriptions, using light and scanning electron microscopy. Based on observations of B. lecontii from 13 locations throughout its distribution, we report the following natural history aspects. The oviposition period of B. lecontii lasted from mid-April to late June and the incubation period lasted 3-4 weeks. Only males cared for the eggs and subsequent care of juveniles was not observed. In one case, the clutches of two males became combined and they were later cared for by only one of the males. The defensive compound of B. lecontii is stored in large glands occupying a third of the paranotal volume and were observed only in stadia II millipedes and older. We observed B. lecontii feeding on fungi of the order Polyporales and describe a cuticular structure on the tip of the labrum that may relate to fungivory. We found that their stellate-shaped aggregations (pinwheels) do not form in the absence of fungus and suggest the aggregation is associated with feeding. We describe and illustrate a previously undescribed comb-like structure on the tibia and tarsi of the six anterior-most leg-pairs and measure the colour and spectral reflectance of the B. lecontii exoskeleton.

Structure and pigment make the eyed elater's eyespots black.

Surface structures that trap light leading to near complete structural absorption creates an appearance of "super black." Well known in the natural world from bird feathers and butterfly scales, super black has evolved independently from various anatomical structures. Due to an exceptional ability to reduce specular reflection, these biological materials have garnered interest from optical industries. Here we describe the false eyes of the eyed elater click beetle, which, while not classified as super black, still attains near complete absorption of light partly due to an array of vertically-aligned microtubules. These cone-shaped microtubules are modified hairs (setae) that are localized to eyespots on the dorsum of the beetle, and absorb 96.1% of incident light (at a 24.8° collection angle) in the spectrum between 300-700 nm. Filled with melanin, the setae combine structure and pigment to generate multiple reflections and refractions causing light to travel a greater distance. This light-capturing architecture leaves little light available to receivers and the false eyes appear as deep black making them appear more conspicuous to predators.