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Fig. 1 in A new glimpse on trophic interactions of 100-million-year old lacewing larvae
Fig. 1. Neuropteran larvae from Hukawng Valley, Kachin State, Myanmar; Turonian–Cenomanian, Cretaceous, 90–100 mya. A. SNSB-BSPG 2020 XCIII 19 with assemblage of neuropteran stylets; A1, overview; A2, close-up image of enclosed stylets; A3, stylets, with five clearly visible (1–5) and possibly three additional stylets (6?–8?); A4, close-up image of representative of Hymenoptera. B. SNSB-BSPG 2020 XCIII 26 (previously BUB 033 in Haug et al. 2019c); B1, head of neuropteran larva with stylets pair in situ; B2, drawing of a single stylet of the specimen in B1; note the high number of teeth, similar to that of stylets 1 and 2 in A3.
Figs 82-94 in Australian Dragonfly (Odonata) Larvae: Descriptive history and identification
Figs 82-94. Larvae of Australian Odonata: (82) Synlestes weyersii (Synlestidae); (83) Griseargiolestes intermedius (Argiolestidae); (84) Xanthagrion erythroneurum (Coenagrionidae); (85, 86) Aeshnidae: (85) Anax papuensis; (86) Notoaeschna sagittata; (87- 90) Gomphidae: (87) Ictinogiomphus australis; (88) Antipodogomphus acolythus; (89) Austroepigomphus (Xerogomphus) turneri; (90) Hemigomphus heteroclytus; (91) Eusynthemis virgula (Synthemistidae); (92, 93) Libellulidae: (92) Nannophya dalei; (93) Orthetrum caledonicum; (94) Pseudocordulia sp. (Libelluloidea genera incertae sedis).
Figs 37-48 in Australian Dragonfly (Odonata) Larvae: Descriptive history and identification
Figs 37-48. Final instar larvae of Australian Anisoptera: (37-44) Synthemistidae (with insert of frontal plate): (37) Archaeosynthemis leachii; (38) Austrosynthemis cyanitincta; (39) Choristhemis flavoterminata; (40) Eusynthemis ursula; (41) Parasynthemis regina; (42) Synthemiopsis gomphomacromioides; (43) Synthemis eustalacta; (44) Tonyosynthemis claviculata; (45) Macromia tillyardi (Macromiidae); (46-48) Corduliidae: (46) Hemicordulia tau; (47) Pentathemis mebranulata; (48) Procordulia jacksoniensis.
Figs 73-81 in Australian Dragonfly (Odonata) Larvae: Descriptive history and identification
Figs 73-81. Final instar larvae of Australian Libelluloidea of genera incertae sedis: (73) Archaeophya adamsi; (74) Cordulephya pygmaea; (75) Apocordulia macrops; (76) Austrocordulia leonardi; (77) Austrophya mystica; (78)?Austrophya sp.; (79) Hesperocordulia berthoudi; (80) Lathrocordulia metallica; (81) Micromidia convergens.
Figs 13-24 in Australian Dragonfly (Odonata) Larvae: Descriptive history and identification
Figs 13-24. Final instar larvae/exuviae of Australian Anisoptera: (13, 14) Austropetaliidae: (13) Archipetalia auriculata; (14) Austropetalia patricia; (15-23) Aeshnidae: (15) Adversaeschna brevistyla; (16) Anax gibbosulus; (17) Austrogynacantha heterogena; (18) Dendroaeschna conspersa; (19) Acanthaeschna victoria; (20) Austroaeschna (Pulchaeschna) muelleri; (21) Austrophlebia costalis; (22) Spinaeschna tripunctata; (23) Telephlebia brevicauda; 24) Petalura hesperia (Petaluridae).
Map 1 in Australian Dragonfly (Odonata) Larvae: Descriptive history and identification
Map 1. The regions of Australia referred to in text and table (from Watson et al. (1991). SWA = south-western Australia; SES = south-eastern South Australia; VIC = Victoria; TAS = Tasmania; SEN = south-eastern New South Wales; NEN = north-eastern New South Wales; SEQ = south-eastern Queensland; NEQ = north-eastern Queensland; CY = Cape York Peninsula; NNT = top end of Northern Territory; KIM = Kimberley region; NWA = north-western Australia; IN = inland New South Wales; SIQ = southern inland Queensland; NIQ = northern inland Queensland; IA = inland Australia.
Figs 1-12 in Australian Dragonfly (Odonata) Larvae: Descriptive history and identification
Figs 1-12. Final instar larvae of Australian Zygoptera: (1) Hemiphlebia mirabilis (Hemiphlebiidae); (2) Synlestes weyersii (Synlestidae); (3) Austrolestes annulosus (Lestidae); (4) Diphlebia euphoeoides (Lestoideidae); (5-8) Argiolestidae: (5) Archiargiolestes parvulus; (6) Austroargiolestes icteromelas; (7) Griseargiolestes griseus; (8) Miniargiolestes minimus; (9) Austrosticta soror (Isostictidae); (10) Nososticta pilbara (Platycnemididae); (11, 12) Coenagrionidae: (11) Caliagrion billinghursti; (12) Ischnura heterosticta.
Figs 61-72 in Australian Dragonfly (Odonata) Larvae: Descriptive history and identification
Figs 61-72. Final instar larvae of Australian Libellulidae: (61) Nannophya sp. (from Barcaldine); (62) Neurothemis stigmatizans; (63) Orthetrum caledonicum; (64) Pantala flavescens; (65) Potamarcha congener; (66) Rhodothemis lieftincki; (67) Rhyothemis princeps; (68) Tetrathemis irregularis; (69) Tholymis tillarga; (70) Tramea stenoloba; (71) Urothemis aliena; (72) Zyxomma elgneri.
Figure 6 in Vertical distribution and migration of planktonic polychaete larvae in Onagawa Bay, north-eastern Japan
Figure 6. Box plots of vertical distribution of two spionid larvae: a, Pseudopolydora achaeta and b, Prionospio spp. The central line in the box represents the median, the upper and lower boundaries of the box represent the quartiles, and the vertical bar represents the 95% range of larval distribution (left axes). The dashed wavy lines and dark shaded areas represent the tidal level (right axes) and night-time, respectively.
Figure 5 in Vertical distribution and migration of planktonic polychaete larvae in Onagawa Bay, north-eastern Japan
Figure 5. Diel changes in vertical distribution of planktonic spionid larvae at St. 1 in Onagawa Bay from 8:00 a.m. on 20 August to 5:00 a.m. on 21 August 2012.
Figure 4 in Vertical distribution and migration of planktonic polychaete larvae in Onagawa Bay, north-eastern Japan
Figure 4. Diel changes in vertical distribution of planktonic polychaete (upper axes) and chlorophyll fluorescence (ppb) (lower axes) larvae at St. 1 in Onagawa Bay from 8:00 a.m. on 20 August to 5:00 a.m. on 21 August, 2012.
Figure 3 in Vertical distribution and migration of planktonic polychaete larvae in Onagawa Bay, north-eastern Japan
Figure 3. Vertical distribution of each species or genus of planktonic spionid larvae at St. 1 in Onagawa Bay from January to December 2012.
Figure 2 in Vertical distribution and migration of planktonic polychaete larvae in Onagawa Bay, north-eastern Japan
Figure 2. Vertical distribution of each family of planktonic polychaete larvae (upper axes) and chlorophyll a concentration (µg L−1) (lower axes) at St. 1 in Onagawa Bay from January to December 2012.
Figure 95 in Australian Dragonfly (Odonata) Larvae: Descriptive history and identification
Figure 95. Accumulation curve illustrating the increase in descriptive information for Australian odonate larvae between 1880 and 2014.
Figs 49-60 in Australian Dragonfly (Odonata) Larvae: Descriptive history and identification
Figs 49-60. Final instar larvae of Australian Libellulidae: (49) Aethriamanta nymphaeae; (50) Agrionoptera longitudinalis; (51) Austrothemis nigrescens; (52) Brachydiplax denticauda; (53) Camacinia gigantea; (54) Crocothemis nigrifrons; (55) Diplacodes haematodes; (56) Huonia melvillensis; (57) Hydrobasisleus brevistylus; (58) Macrodiplax cora; (59) Nannodiplax rubra; (60) Nannophlebia risi.
Map 2 in Australian Dragonfly (Odonata) Larvae: Descriptive history and identification
Map 2. Map of eastern Australia showing relevant localities (from Watson & Theischinger (1984). NSW = New South Wales; NT = Northern Territory; QLD = Queensland; SA = South Australia; VIC = Victoria; 1 = Paluma Range; 2 = Eungella; 3 = Carnarvon Gorge; 4 = Barrington Tops; 5 = Blue Mountains; 6 = Canberra. The PalumaEungella gap (marked with +, ca. 19ºS) spans between 1 and 2.
Fig. 2 in Larva and Life History of Togashia horii (Hymenoptera, Tenthredinidae) Feeding on Cornus controversa (Cornaceae) in Honshu, Japan
Fig. 2. Togashia horii, female adult (A), host leaf with eggs deposited inside (B–E) host leaf with larval exit holes (F) and early instar larvae (G–I). A, June 12; B, upper surface, arrows showing rows of eggs inside, June 14; C, same leaf, underside, June 14; D, same leaf, upper surface, showing inflated eggs inside, June 18; E, same leaf, underside, June 18; F–H, June 26; I, June 28. All photographed indoors in Nagano by Kojima in 2023.
Fig. 1 in Larva and Life History of Togashia horii (Hymenoptera, Tenthredinidae) Feeding on Cornus controversa (Cornaceae) in Honshu, Japan
Fig. 1. Togashia horii, late instar larvae (A–C), damage of host leaves (D), eaten leaf with larval exuviae (E) and mature larvae entering dead branch (F). A, B, D, E, Tsugaike, September 14, 2014; C, Sasagamine, August 31, 2022; F, Nagano, September 9, 2022. Photographed by Shinohara (A, B, D, E) and Kojima (C, F).
Supplementary material for "Cretaceous lacewing larvae with binocular vision demonstrate the convergent evolution of sophisticated simple eyes" by Haug C. et al.
<p>Supplementary matereial including R-Code and data for elliptic Fourier analysis for the publication: "<span>Cretaceous lacewing larvae with binocular vision demonstrate the convergent evolution of sophisticated simple eyes" </span></p> <p><span>Carolin Haug, Roland R. Melzer, Florian Braig, Simon J. Linhart, Derek E. G. Briggs, Alejandro Caballero, Yanzhe Fu, Gideon T. Haug, Marie K. Hörnig, Joachim T. Haug</span></p> <p> </p> <p><span>Abstract: </span></p> <p><span>Many insects and their relatives are renowned for sophisticated compound eyes, which are also preserved in the fossil record. Yet there are also other types of eyes, notably the so-called stemmata of holometabolans, such as beetles, bees, and butterflies. Stemmata are not as effective as compound eyes, except in some predatory larvae. Here we report three lacewing larvae with large forward-directed stemmata from Cretaceous Kachin amber, Myanmar. The stemmata are large relative to those of other fossil lacewing larvae, comparable to the simple eyes of modern larvae capable of image formation. The head is very wide in one larva, representing a new type of morphology as demonstrated by a quantitative comparison of the head and stylets of over 400 fossil and extant lacewing larvae. The arrangement of the exceptionally large stemmata of the larvae reported here provides stereoscopic vision. These new specimens demonstrate the convergent evolution of highly developed simple eyes in at least two additional lineages of lacewings, showcasing the enormous diversity of lacewing larvae in the Cretaceous.</span></p>
Fig. 1 in Early-Spring Floods Decrease The Survival Of Hibernating Larvae Of A Wetland-Inhabiting Population Of Neptis Rivularis (Lepidoptera: Nymphalidae)
Fig. 1. Map of the central part of Třeboň Basin (along Lužnice river) with colonies of Neptis rivularis () and records of stray adults of the butterfly (), as encountered during 1996 season. The gray
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
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