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Figure 4 in Horsehair worms (Nematomorpha) from the Baltic island Bornholm (Denmark), with notes on the biology of Gordius albopunctatus

Figure 4. Six dissected larvae and praepupae of Pomatophylax cingulatus (Trichoptera), parasitized by Gordius albopunctatus (note that worms are white in colour except for the one to the right which is light brown).

Figure 1 in Horsehair worms (Nematomorpha) from the Baltic island Bornholm (Denmark), with notes on the biology of Gordius albopunctatus

Figure 1. Gordius albopunctatus. (A) Details of three males with different coloration, white spots are not visible on the lightest specimen (top); (B) ventral view of male posterior end showing tail lobes, cloacal opening, and postcloacal crescent; (C, D) cuticle with regular polygonal areoles. (B–D) SEM. Scale bars: 100 mm (B); 20 mm (C, D).

Figure 2 in Horsehair worms (Nematomorpha) from the Baltic island Bornholm (Denmark), with notes on the biology of Gordius albopunctatus

Figure 2. Gordionus violaceus. (A, B) Ventral view of male posterior end showing tail lobes, cloacal opening surrounded by spines, and anterolateral rows of bristles (arrows in A); (C) cuticle with rounded areoles which are surrounded by short bristles; (D) magnification of one areole. All SEM. Scale bars: 50 mm (A, B); 10 mm (C); 5 mm (D).

Figure 3 in Horsehair worms (Nematomorpha) from the Baltic island Bornholm (Denmark), with notes on the biology of Gordius albopunctatus

Figure 3. Outline of the Baltic island Bornholm with location of investigated streams and relation of species found in those streams. White, Gordius albopunctatus; black, Gordionus violaceus.

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Figure 1 in Breeding biology of Phyllomedusa azurea Cope, 1862 and P. sauvagii Boulenger, 1882 (Anura) from the Cerrado, Central Brazil

Figure 1. Number of individuals present in monthly samples from October 2000 to September 2001 and total rainfall per month at the study site. Black bars, number of Phyllomedusa sauvagii; dotted white bars, number of P. azurea; black circles, total rainfall during the study; black triangles, rainfall recorded during 4 days by month of study.

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Figure 2 in Breeding biology of Phyllomedusa azurea Cope, 1862 and P. sauvagii Boulenger, 1882 (Anura) from the Cerrado, Central Brazil

Figure 2. Females of Phyllomedusa azurea (A) and P. sauvagii (B, C) collected at the study site from October 2000 to September 2001. Correlations between: (A) SVL versus NME (NME56.411SVL2173.22); (B) SVL versus OM (OM50.403SVL221.79); (C) BM versus OM (OM50.3043BM25.41).

opencc-by-4.0Nov 2006View details →

Figure 2 in Ecology and reproductive biology of two species of Aplastodiscus (Anura: Hylidae) in the Atlantic forest, Brazil

Figure 2. Number of courtship displays observed for Aplastodiscus leucopygius (grey columns) and A. arildae (black columns) in the Serra do Japi, municipalty of Jundiai, State of São Paulo, Brazil.

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Figure 1 in Ecology and reproductive biology of two species of Aplastodiscus (Anura: Hylidae) in the Atlantic forest, Brazil

Figure 1. (A) Maximum number of males of Aplastodiscus arildae in calling activity in the studied stream; (B) maximum number of males of A. leucopygius in calling activity in three habitats (stream, swamp, and lake) in the Serra do Japi, municipality of Jundiaı´, State of São Paulo, Brazil.

Figs 54 in Taxonomy and biology of the bromeliad-inhabiting genus Lachnodacnum (Coleoptera: Hydrophilidae: Sphaeridiinae)

Figs 54í62. First instar larva of Lachnodacnum luederwaldti Orchymont, 1937. 54í55 – antenna (54 – dorsal view, 55 – ventral view); 56í57 – maxilla (56 – ventral view, 57 – dorsal view); 58í59 – labium (58 – ventral view, 59 – dorsal view); 60 – right mandible, dorsal view; 61 – prosternum; 62 – mesothoracic leg, anterior view.

Figs 29 in Taxonomy and biology of the bromeliad-inhabiting genus Lachnodacnum (Coleoptera: Hydrophilidae: Sphaeridiinae)

Figs 29í32.Adult morphology of Lachnodacnum luederwaldti Orchymont, 1937, SEM micrographs. 29 – mesofemur; 30 – apical portion of elytra; 31 – microsculpture of the clypeus; 32 – trichobothrium on the elytron.

Figs 18 in Taxonomy and biology of the bromeliad-inhabiting genus Lachnodacnum (Coleoptera: Hydrophilidae: Sphaeridiinae)

Figs 18í23. Biology of Lachnodacnum luederwaldti Orchymont, 1937. 18 – micropool in the rosette of Neoregelia sp., a typical habitat; 19 – egg cases attached at the inner face of a bromeliad leaf; 20 – third instar larva and pupa in the detritus accumulated in the bromeliad rosette; 21í22 – pupa in the broken pupal chamber (21 – dorsal view; 22 – ventral view); 23 – adults staying submerged among bromeliad leaves in the rearing box. Figs 18í19, 23: photo B. Clarkson in Ubatuba Municipality, São Paulo; Figs 20í22: photo by F. F. Albertoni in Florianopolis, Santa Catarina.

Figs 15 in Taxonomy and biology of the bromeliad-inhabiting genus Lachnodacnum (Coleoptera: Hydrophilidae: Sphaeridiinae)

Figs 15 í17. Aedeagus. 15 – Lachnodacnum luederwaldti Orchymont, 1937; 16 – L. saundersi Orchymont, 1937; 17 – Phaenostoma urichi (Scott, 1912).

Figs 11 in Taxonomy and biology of the bromeliad-inhabiting genus Lachnodacnum (Coleoptera: Hydrophilidae: Sphaeridiinae)

Figs 11í14. Morphological details of Lachnodacnum Orchymont, 1937 and Phaenostoma Orchymont, 1937. 11í12 – hind wings (11 – Lachnodacnum luederwaldti Orchymont, 1937; 12 – Phaenostoma urichi (Scott, 1912)). 13í14 – detail of spiracular atrium of the third instar larva of L. luederwaldti.

Figs 1 in Taxonomy and biology of the bromeliad-inhabiting genus Lachnodacnum (Coleoptera: Hydrophilidae: Sphaeridiinae)

Figs 1í10. General habitus of adults and larvae of Lachnodacnum Orchymont, 1937. 1í3 – adults of L. luederwaldti Orchymont, 1937 (1 – dorsal view, 2 – lateral view, 3 – dorsal view of the head). 4í8 – larva of L. luederwaldti (4 – third instar larva in dorsal view; 5 – same in ventral view; 6 – ¿rst instar in dorsal view; 7 – detail of head and thorax of third instar, dorsal view; 8 – same, ventral view). 9í10 – adults of L. saundersi Orchymont, 1937 (9 – dorsal view, 10 – lateral view).

Fig. 5 in Biology and morphology of immature stages of Coniocleonus nigrosuturatus (Coleoptera: Curculionidae: Lixinae)

Fig. 5. Adult, host plant and habitats of Coniocleonus nigrosuturatus (Goeze, 1777). A – adult beetle; B – host plant Erodium cicutarium (L.) L'Hér.; C – an excavated host plant with larval feeding marks; D–E: habitats in Romania (Sfânta Elena); F – habitat in Slovakia (KolíĖany).

Fig. 4 in Biology and morphology of immature stages of Coniocleonus nigrosuturatus (Coleoptera: Curculionidae: Lixinae)

Fig. 4. Immature stages and feeding marks of Coniocleonus nigrosuturatus (Goeze, 1777). A – mature larva; B – earthen cell with mature larva; C – pupa (removed from the earthen cell); D – opening of larval tunnel in the soil; E – opening of the larval tunnel and feeding marks; F – detail of larval feeding marks.

Fig. 2 in Biology and morphology of immature stages of Coniocleonus nigrosuturatus (Coleoptera: Curculionidae: Lixinae)

Fig. 2. Coniocleonus nigrosuturatus (Goeze, 1777), mature larva habitus:A – shape of the body (lateral view), B – lateral view of thoracic segments, C – lateral view of abdominal segment II., D – lateral view of abdominal segments VII–X (prns – pronotal seta(e), prs – prodorsal s., pds – postdorsal s., as – alar s., ss – spiracular s., dpls – dorsopleural s., vpls – ventropleural s., pda – pedal s., dls – dorsolateral s., lsts – laterosternal s., msts – mesosternal s., ds – dorsal s., ls – lateral s., sts – sternal s., ts – terminal s.; Th1-3, Ab1-10 – number of thoracic or abdominal segment).

Fig. 1 in Biology and morphology of immature stages of Coniocleonus nigrosuturatus (Coleoptera: Curculionidae: Lixinae)

Fig. 1. Coniocleonus nigrosuturatus (Goeze, 1777), mature larva head, antenna and mouth parts:A – dorsal view (des – dorsal epicranial seta(e), fs – frontal s., les – lateral epicranial s., st – stemmata, at – antenna); B – right maxilla and labium (both ventral view) (dms – dorsal malae s., vms – ventral malae s., mpxs – maxillary palps s., mbs – basiventral s., pfs – palpiferal s., stps – stipal s., plbs – prelabial s., pslbs – postlabial s., ligs – ligular s.); C – right mandible (mds – mandible dorsal s.); D – antenna; E – labrum and clypeus (cls – clypeal s., lrms – labral s.); F – epipharynx (ams – anteromedial s., als – anteriolateral s., mes – median s., lr – labral rods).

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Fig. 19 in Confirmed occurrence of Hydroscapha granulum in Iran, with notes on its biology (Coleoptera: Myxophaga: Hydroscaphidae)

Fig. 19. Known distribution of West-Palaearctic Hydroscapha derived from the published data (see the text for details). Asian records are mapped by full circles, Spanish record of H. granulum (Motschulsky, 1855) by JÄCH et al. (1999) by an empty circle. Species whose synonymy with H. granulum requires revision are mapped in dotted line.