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Fig. 1 in Reinstatement of the New Zealand cave wētā genus Miotopus Hutton (Orthoptera: Rhaphidophoridae) and description of a new species

Fig. 1. Apical spine numbering, terminology and position on Rhaphidophoridae, after Fitness et al. (2015). Dorsal view, showing cross-sectional relationship of each potential spine on femora and tibiae. Positions are indicated as prolateral (anterior facing), retrolateral (posterior facing), inferior (ventral facing) and superior (dorsal facing) orientations are indicated.

Fig. 3 in Reinstatement of the New Zealand cave wētā genus Miotopus Hutton (Orthoptera: Rhaphidophoridae) and description of a new species

Fig. 3. Phylogenetic relationship of Pleioplectron Hutton, 1896 and Miotopus Hutton, 1898 inferred from Bayesian Inference of 1435bp mtDNA COI sequence alignment with four 4 × 106 MCMC chains, sampling every 2 × 103 generations.

Fig. 8 in Reinstatement of the New Zealand cave wētā genus Miotopus Hutton (Orthoptera: Rhaphidophoridae) and description of a new species

Fig. 8. Female terminalia of Miotopus Hutton, 1898 cave wētā. A–C. Miotopus diversus (Hutton, 1896) (MPN CW3596). A. Ventral. B–C. Lateral views. D–F. Miotopus richardsi sp. nov. (MPN CW3543). D. Ventral. E–F. lateral views. Scale bars = 3 mm.

Fig. 7 in Reinstatement of the New Zealand cave wētā genus Miotopus Hutton (Orthoptera: Rhaphidophoridae) and description of a new species

Fig. 7. Male terminalia of Miotopus Hutton, 1898 cave wētā. A–B. Miotopus diversus (Hutton, 1896) (MPN CW3601). A. Lateral. B. Ventral. C–F. Miotopus richardsi sp. nov. (MPN CW3542). C. Lateral. D. Ventral. E. Close dorsal. F. Ventral views of named structures. Scale bars = 2 mm.

Fig. 7 in New bryozoan species from the Pleistocene of the Wanganui Basin, North Island, New Zealand

Fig. 7. Frequency distribution of zooidal size (mean ZL in mm) in 56 Microporella species known to possess ovicells and for which zooidal size has been reported in the literature.

Fig. 6 in New bryozoan species from the Pleistocene of the Wanganui Basin, North Island, New Zealand

Fig. 6. Microporella hyadesi (Jullien, 1888) sensu Brown 1952 (NHMUK D36796 and D36797), Southland, Waianan, Middle Miocene, base of the uppermost Mt. Brown "E" Limestone, Junction of Weka Creek, Weka Pass Stream, Waipara, Canterbury, New Zealand. Two colony fragments including autozooids and ovicellate zooids. Scale bars = 200 µm.

Fig. 5. Microporella ordo Brown, 1952. A–C in New bryozoan species from the Pleistocene of the Wanganui Basin, North Island, New Zealand

Fig. 5. Microporella ordo Brown, 1952. A–C. Holotype (NHMUK D36809), Wanganui, Castlecliffian Horizon CU3, Pleistocene, NZGS Loc. 4013 Castlecliff, New Zealand. A. Frontal view of the linear colony fragment. B. Close-up of an autozooid. C. Close-up of the orifice and ascopore. D. Paratype (NHMUK D36806), same provenance as holotype, view of the linear colony fragment. Scale bars: A, D = 200 µm; B = 100 µm; C = 20 µm.

Fig. 3 in New bryozoan species from the Pleistocene of the Wanganui Basin, North Island, New Zealand

Fig. 3. Parkermavella columnaris sp. nov. A–C. Paratype (NHMUK PI BZ 7832), Castlecliffian, Pleistocene, Upper Kai-Iwi Shellbed, New Zealand. A. View of a small colony. B. Group of autozooids. C. Two ovicellate zooids. D. Paratype (NHMUK PI BZ 7833), same provenance as preceding, inner view of the frontal shield showing part of the ring scar bordering the umbonuloid area. Scale bars: A = 500 µm; B–C = 100 µm; D = 50 µm.

Fig. 1 in New bryozoan species from the Pleistocene of the Wanganui Basin, North Island, New Zealand

Fig. 1. Buskia waiinuensis sp. nov., holotype (GNS BZ 335), Nukumaruan, Pleistocene, Nukumaru Limestone, Waiinu Beach, New Zealand. A. General view of the bioimmured colony, showing the regular development of the stolonal pattern. B. Close-up of a sector of the colony. C. Close-up of a zooid with oval orifice. Note the cystid appendage lateral to the orifice and the concentric lines on the zooidal and stolonal surface. D. Close-up of a zooid with a circular orifice and two cystid appendages lateral to the orifice. Scale bars: A = 1 mm; B = 200 µm; C = 50 µm; D = 100 µm.

Fig. 2 in New bryozoan species from the Pleistocene of the Wanganui Basin, North Island, New Zealand

Fig. 2. Parkermavella columnaris sp. nov., holotype (NIWA 97418), Recent, inferred greater Cook Strait, New Zealand. A. Group of ovicellate zooids. B. Tilted close-up of an autozooid showing the broadly cleithridiate (keyhole shaped) orifice, four distal oral spines, two of which coalescent, and the suboral avicularium with complete cross-bar. C. Lateral view of the columnar peristome bearing the suboral avicularium. D. Inner view of the frontal shield showing the umbonuloid area and ring scar. Scale bars: A = 250 µm; B = 100 µm; C–D = 50 µm.

Fig. 4. A–D in Descriptions of species of Stegelleta Thorne, 1938 (Nematoda, Rhabditida, Cephalobidae) from California, New Zealand and Senegal, and a revision of the genus

Fig. 4. A–D. Stegelleta ophioglossa Andrássy, 1967. A. Pharyngeal region. B. Anterior end, surface view. C. Female gonad. D. Female tail. E–G. Stegelleta tuarua Yeates, 1967. E. Pharyngeal region. F. Anterior end, surface view. G. Male tail. Scale bar = 20 µm.

Fig. 2 in Descriptions of species of Stegelleta Thorne, 1938 (Nematoda, Rhabditida, Cephalobidae) from California, New Zealand and Senegal, and a revision of the genus

Fig. 2. Stegelleta incisa (Thorne, 1937), SEM micrographs. A–B. Anterior end, left lateral view. C. Anterior part of lateral field. D. Deirid (arrow). E. Vulval region. F. Female tail, subventral view. G. Female tail, left sublateral view (arrow points at phasmid). H. Female tail, lateral view. Scale bars = 5 µm.

Fig. 3 in Descriptions of species of Stegelleta Thorne, 1938 (Nematoda, Rhabditida, Cephalobidae) from California, New Zealand and Senegal, and a revision of the genus

Fig. 3. Stegelleta laterocornuta sp. nov., SEM micrographs. A. Vulval opening. B. Anal opening. C–D. Anterior end, left subventral view. E. Anterior end, left lateral view (arrows in C–E point at the long acute tine extending along the primary axil on the lateral lips). Scale bars = 2 µm.

Fig. 1. A–E in Descriptions of species of Stegelleta Thorne, 1938 (Nematoda, Rhabditida, Cephalobidae) from California, New Zealand and Senegal, and a revision of the genus

Fig. 1. A–E. Stegelleta incisa (Thorne, 1937). A. Pharyngeal region. B. Female gonad. C. Anterior end, surface view. D. Female tail. E. Male tail. F–J. Stegelleta laterocornuta sp. nov. F. Pharyngeal region. G. Female gonad. H. Anterior end, surface view. I. Female tail. J. Male tail. Scale bar = 20 µm.

Fig. 9. A in An inquiline deep-water bryozoan/amphipod association from New Zealand, including the description of a new genus and species of Chevaliidae

Fig. 9. A. Optical view of the abfrontal side of a distal marginal autozooid (polypide reduced to a residual brown body, bb) adjacent to a lateral kenozooid in which there is a distally tapered (i.e., apically developing) intracoelomic calcareous rod (arrow). B. SEM of a similar view to A but of skeletal elements only, showing the distal tip of the calcareous rod (white arrow) and the communication pores (blue arrowhead) that allow nutrient connectivity between the feeding autozooid and non-feeding kenozooid in which the coelomic cavity comes to be filled by the calcareous rod. C. Fractured transverse section of a calcareous rod showing alternating thick and thin wall-perpendicular prismatic fabric. D. Part of C magnified. Scale bars: A = 200 μm; B = 100 μm; C = 25 μm; D = 5 μm.

Fig. 7 in An inquiline deep-water bryozoan/amphipod association from New Zealand, including the description of a new genus and species of Chevaliidae

Fig. 7. Bryoconversor tutus gen. et sp. nov., paratype, ♂, NIWA 52919, 0.64 mm long. A. Habitus. B. Head. C. Epimeron. D. Urosome. E. Uropod 2 and uropod 1. F. Telson. Scale bars: A = 300 μm; B-D = 100 μm; E = 20 μm; F = 10 μm.

Fig. 6 in An inquiline deep-water bryozoan/amphipod association from New Zealand, including the description of a new genus and species of Chevaliidae

Fig. 6. Bryoconversor tutus gen. et sp. nov., holotype, ♀, NIWA 88918, 1.72 mm long. A. Pereopod 5. B. Pereopod 6. C. Pereopod 7. D. Pleopod 1. Scale bars = 100 μm.

Fig. 8 in An inquiline deep-water bryozoan/amphipod association from New Zealand, including the description of a new genus and species of Chevaliidae

Fig. 8. Bryoconversor tutus gen. et sp. nov., paratype, ♂, NIWA 52919, 0.64 mm long. A. Detail of serrated surface on telson. B. Gnathopod 1 and larger gnathopod 2. C. Dactylus gnathopod 1. D. Dactylus gnathopod 1. E. Dorsal view telson, uropod 3 and uropod 2. F. Flat-topped projections on telson. Scale bars: A = 1 μm; B = 100 μm; C-D = 10 μm; E = 20 μm; F = 2 μm.

Fig. 5 in An inquiline deep-water bryozoan/amphipod association from New Zealand, including the description of a new genus and species of Chevaliidae

Fig. 5. Bryoconversor tutus gen. et sp. nov., holotype, ♀, NIWA 88918, 1.72 mm long. A. Gnathopod 1. B. Gnathopod 2. C. Pereopod 3. D. Pereopod 4. Scale bars = 100 μm.

Fig. 4 in An inquiline deep-water bryozoan/amphipod association from New Zealand, including the description of a new genus and species of Chevaliidae

Fig. 4. Bryoconversor tutus gen. et sp. nov., holotype, ♀, NIWA 88918, 1.72 mm long. A. Hypopharynx. B. Maxilla 2. C. Maxilla 1. D. Maxilliped. Scale bars = 100 μm.