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Fig. 7 in Deep-sea shrimps of the genus Glyphocrangon A. Milne-Edwards, 1881 (Decapoda: Caridea: Glyphocrangonidae) collected by the SJADES 2018 expedition off Java, Indonesia, with description of one new species

Fig. 7. Glyphocrangon serratirostris, new species, holotype ovigerous female (cl 22.0 mm), MZB Cru5055. A, carapace and cephalic appendages, dorsal view; B, rostrum, dorsal view; C, proximal part of rostrum, dorsolateral view, showing armature; D, distal part of rostrum, ventral view; E, pleon, telson, and left uropod, dorsal view; F, telson, dorsal view.

Fig. 5 in Factors limiting the current distribution of the introduced Java sparrow (Lonchura oryzivora) in Bangkok, Thailand

Fig. 5. Four nest localities of Java sparrow in the study area; nurse dormitory of Bhumipol Hospital (1), Air Force Youth Club (2), Air Force Museum (3) and Phaholyothin 69/1 alley (4). Java sparrows were mostly found nesting in (1) and (3). All sites were located <1.5 km from Don Muang Airport. (1), (2) and (3) were located on the eastern side of Don Muang Airport and (4) was located to the south-west.

Fig. 6. There were 39 in Factors limiting the current distribution of the introduced Java sparrow (Lonchura oryzivora) in Bangkok, Thailand

Fig. 6. There were 39 nest sites at Bhumibol Hospital, 22 sites at the Royal Thai Air Force Museum, 3 at the Thai Air Force Youth Club and 3 at Phahonyothin Soi 69/1. Birds mostly located their nests in cavities in the ceilings of buildings or in openings of air ducts.

Fig. 3. Within the 15 occupied cells, 6 cells had a in Factors limiting the current distribution of the introduced Java sparrow (Lonchura oryzivora) in Bangkok, Thailand

Fig. 3. Within the 15 occupied cells, 6 cells had a percentage of paddyfield cover <1%, 6 cells had 1–20% paddyfield cover and 3 cells had 20–40% paddyfield cover. For the 26 cells with no detections, 16 had a percentage of paddyfield cover <1%, 7 cells had 1–20% paddyfield cover and 3 cells had 20–40% paddyfield cover.

Fig. 2. Forty-one grid cells randomly set within a 10 in Factors limiting the current distribution of the introduced Java sparrow (Lonchura oryzivora) in Bangkok, Thailand

Fig. 2. Forty-one grid cells randomly set within a 10-km radius around Don Muang airport, Bangkok, Thailand, used for surveying Java sparrows. Don Muang was the site where Java sparrows were first recorded in Thailand in 1924. The study area includes three provinces; Bangkok, Pathum Thani, and Nonthaburi. The primary land use was urban, while paddyfields were mostly located on the eastern side of the study area. Different symbols (circles, squares and triangles) represent the number of occasions (out of 5 possible visits to a location) on which the sparrow was detected. Size of symbols of Java sparrow detection points was related to the number of birds detected; smallest size indicated only 1 bird was detected, medium size indicated 2–10 birds were detected, and largest size indicated a group of more than 40 birds was detected.

Fig. 1. 101 in Factors limiting the current distribution of the introduced Java sparrow (Lonchura oryzivora) in Bangkok, Thailand

Fig. 1. 101 grid cells (400 ha each) were overlaid on the study area (40,000 ha). We randomly selected approximately 40% (41) (green) of 98 accessible grid cells in total. Access to three grid cells (red) in the middle of study area including Don Muang International Airport were restricted by the Thai Air Force.

Fig. 4 in Factors limiting the current distribution of the introduced Java sparrow (Lonchura oryzivora) in Bangkok, Thailand

Fig. 4. Number of Java sparrows counted at the two main roosting sites in Bangkok, Thailand, each site was counted once per month from August 2016 to July 2017. Lowest and highest counts (33 and 2132 individuals) were obtained from the Kan Kheha Thung Song Hong (KKTSH) roost (dashed line). Lowest counts at KKTSH were in August–September 2016. The roosting site at Chaeng Wattana (solid line) had a lower number of birds but may have received some birds from KKTSH during the first two months of the count.

Fig. 21 in A First Epigean Species Of Stygophrynus Kraepelin (Amblypygi: Charontidae) From Java And Adjacent Islands, Indonesia With Notes On S. Dammermani Roewer, 1928

Fig. 21. Distributions of Stygophrynus species in Java and the Sunda Strait. (Note: circles: Stygophrynus dammermani, triangles = Stygophrynus sunda).

Figs. 13–20 in A First Epigean Species Of Stygophrynus Kraepelin (Amblypygi: Charontidae) From Java And Adjacent Islands, Indonesia With Notes On S. Dammermani Roewer, 1928

Figs. 13–20. Stygophrynus dammermani, male (MZB.Ambl. 052): 13, cheliceral dentition, internal view; 14, cheliceral dentition, external view. Syntype female (MZB.Ambl.002): 15, pedipalpal tibia of left pedipalp. Male (MZB.Ambl.104): 16, left leg IV showing trichobothria; 17, left tarsus IV; 18, ventral view of male genitalia; 19, dorsal view. Female (MZB.Ambl.101): 20, dorsal view female genitalia. Scale bars = 1 mm.

Figs. 3–12 in A First Epigean Species Of Stygophrynus Kraepelin (Amblypygi: Charontidae) From Java And Adjacent Islands, Indonesia With Notes On S. Dammermani Roewer, 1928

Figs. 3–12. Stygophrynus sunda, paratype male (MZB.Ambl.021): 3, left chelicera, internal view; 4, left chelicera, external view. Holotype male (MZB.Ambl.109): 5, left pedipalp, dorsal view; 6, left pedipalp, ventral view; 7, left pedipalpal tibia; 8, left leg IV showing trichobothria; 9, left leg IV, tarsal segments; 10, male genitalia, ventral view; 11, male genitalia, dorsal view. Paratype female (MZB.Ambl.022): 12, female genitalia. Scale bars = 1mm.

Figs. 1–2 in A First Epigean Species Of Stygophrynus Kraepelin (Amblypygi: Charontidae) From Java And Adjacent Islands, Indonesia With Notes On S. Dammermani Roewer, 1928

Figs. 1–2. Stygophrynus from Java: 1, Male holotype of Stygophrynus sunda new species collected from Ujung Kulon National Park. 2, Stygophrynus dammermani, female from Buniayu Cave (MZB.Ambl.118). (Photo. C. Rahmadi). Scale bars: 1 = 4 mm; 2 = 7 mm.

Fig. 26 in Haemosporozoan Parasites Found In Birds In Peninsular Malaysia, Singapore, Sarawak And Java

Fig. 26. Haemoproteus fallisi from Turdus obscurus, Malaysia (from left: microgametocyte and two macrogametocytes).

Fig. 25 in Haemosporozoan Parasites Found In Birds In Peninsular Malaysia, Singapore, Sarawak And Java

Fig. 25. Plasmodium (Giovannolaia) ninoxi, from Ninox scutulata, Singapore (from left: two meronts, microgametocyte, macrogametocyte).

Fig. 18 in Haemosporozoan Parasites Found In Birds In Peninsular Malaysia, Singapore, Sarawak And Java

Fig. 18. Haemoproteus rhipiduris from Rhipidura albicollis, Malaysia (from left: microgametocyte and macrogametocyte).

Fig. 14 in Haemosporozoan Parasites Found In Birds In Peninsular Malaysia, Singapore, Sarawak And Java

Fig. 14. Leucocytozoon sp. 8 from Malacopteron magnum, Sarawak (from left: microgametocyte and two macrogametocytes).

Fig. 15 in Haemosporozoan Parasites Found In Birds In Peninsular Malaysia, Singapore, Sarawak And Java

Fig. 15. Leucocytozoon pittae from Pitta guajana, Java (from right: macrogametocyte, microgametocyte and macrogametocyte).

Fig. 9 in Haemosporozoan Parasites Found In Birds In Peninsular Malaysia, Singapore, Sarawak And Java

Fig. 9. Leucocytozoon sakharoffi from Corvus splendens, Singapore (from left: macrogametocyte and microgametocyte).

Fig. 13 in Haemosporozoan Parasites Found In Birds In Peninsular Malaysia, Singapore, Sarawak And Java

Fig. 13. Lecocytozoon sp. 7, macrogametocyte, from Leiohtrix argentauris (right), Leucocytozoon sp. 10, macrogametocyte from Oriolus cruentus (left), Malaysia.

Fig. 6 in Haemosporozoan Parasites Found In Birds In Peninsular Malaysia, Singapore, Sarawak And Java

Fig. 6. Leucocytozoon sp. 3 from Alcippe peracensis, Malaysia (from left: microgametocyte and two macrogametocytes).

Fig. 10 in Haemosporozoan Parasites Found In Birds In Peninsular Malaysia, Singapore, Sarawak And Java

Fig. 10. Haemoproteus cf. pallidus from Ficedula solitaria, Malaysia (from left: multiple juvenile infection; elongated macrogametocyte folded around the host nucleus, seemingly merged gametocytes with conspicuous macrogametocyte nucleus; same but with conspicuous microgametocyte features.