Find research datasets worth reusing

Fig. 5. A–B in Two new species of Engertia Dalla Torre, 1913 and Philacelota Heller, 1900 from Indonesia and the Philippines with a revised identification key (Coleoptera: Scarabaeidae: Melolonthinae)

Fig. 5. A–B. Philacelota leucothea sp. nov., holotype, ♂ (MNHN). A. Aedeagus, lateral view. B. Parameres, dorsal view. — C–D. P. submaculata Heller, 1900, from Kema, Sulawesi, ♂ (MNHN). C. Aedeagus, lateral view. D. Parameres, dorsal view. Scale bars: A–B = 1.5 mm; C–D = 2 mm.

Fig. 3 in Two new species of Engertia Dalla Torre, 1913 and Philacelota Heller, 1900 from Indonesia and the Philippines with a revised identification key (Coleoptera: Scarabaeidae: Melolonthinae)

Fig. 3. Philacelota leucothea sp. nov., habitus. A. ♂, holotype (MNHN). B. ♀, paratype (MNHN). Scale bars: 2.5 mm.

Fig. 4 in Two new species of Engertia Dalla Torre, 1913 and Philacelota Heller, 1900 from Indonesia and the Philippines with a revised identification key (Coleoptera: Scarabaeidae: Melolonthinae)

Fig. 4. Philacelota leucothea sp. nov., holotype, ♂ (MNHN) (A–C) and paratype, ♀ (MNHN) (D– G). A. Antenna, lateral view. B. Propygidium. C. Pygidium. D. Antenna, lateral view. E. Antenna, dorsolateral view showing relative size of club antennomeres. F. Propygidium. G. Pygidium. Scale bars: A, C–E = 1.5 mm; B = 2 mm; F–G = 2.5 mm.

Fig. 2. A–G in Two new species of Engertia Dalla Torre, 1913 and Philacelota Heller, 1900 from Indonesia and the Philippines with a revised identification key (Coleoptera: Scarabaeidae: Melolonthinae)

Fig. 2. A–G. Engertia allolepis sp. nov., holotype, ♂ (MNHN). A. Antenna. B. Lateral part of the elytron. C. Apical margin of elytra and propygidium. D. Pygidium. E. Abdominal ventrites 2–4. F. Parameres, dorsal view. G. Aedeagus, lateral view. — H–J. E. papuana (Moser, 1913), ♂, from Sentani (cAP). H. Lateral part of elytron. I. Apical margin of elytra and propygidium. J. Aedeagus, lateral view. — K. E. amboinae (Brenske, 1897), ♂, from Ambon (MNHN), lateral part of elytron. — L. E. setifera (Moser, 1913), ♂, from Seram, pygidium (cAP). Scale bars are in common for B, H and K, and for F–G and J. Scale bars: A–B, H, K = 1.5 mm, C–G, I–J, L = 2.5 mm.

Fig. 6 in Two new species of Fridericia (Annelida: Enchytraeidae) from Hungarian caves

Fig. 6. Maximum likelihood (ML) trees of studied Fridericia species based on the ITS region (A), CO1 (B) and H3 genes (C). Bootstrap values greater than 50 are shown at the nodes. Sequences from new species described here appear in bold. A. ML tree of the ITS region based on 821 nucleotide positions. B. ML tree of the CO1 gene based on 388 nucleotide positions. C. ML tree of the H3 gene based on 202 nucleotide positions.

Fig. 1. A–D in Two new species of Fridericia (Annelida: Enchytraeidae) from Hungarian caves

Fig. 1. A–D. Fridericia baradlana sp. nov. A–B. Spermathecae. C. Oesophageal appendage. D. Coelomocytes. E–F. Fridericia spelaeophila sp. nov. E. Coelomocytes. F. Spermathecae. Scale bars: 50 μm.

Fig. 2 in Two new species of Fridericia (Annelida: Enchytraeidae) from Hungarian caves

Fig. 2. Micrograph of Fridericia baradlana sp. nov. A. Brain. B–D. Coelomocytes (C. several large lenticytes). E. Detached chaetae in coelom. F. Thick body wall, thin cuticle. G. Pharyngeal glands (marked with arrows). H. Subneural glands in XIII–XIV (marked with arrows). I–K. Sperm funnels (funnel's body marked with black arrows, sperm head marked with white arrows). (B–C, F, I–K in vivo, A, F, H fixed, stained, D, G fixed, not stained. Scale bars: 50 μm, in D 20 μm. B, E from holotype.)

Fig. 5 in Two new species of Fridericia (Annelida: Enchytraeidae) from Hungarian caves

Fig. 5. Micrograph of Fridericia spelaeophila sp. nov. A. Sperm funnel. B, H. Spermathecal ampullae (sperm in ampulla marked with arrows). C–G. Spermathecae. (In C, diverticula marked with black arrows, ectal glands with white arrow. D–E. Fused proximal parts marked with white arrows, ectal glands with black arrows. F. Ectal duct marked with white arrow, ectal glands with black arrows. G. Ectal glands marked with white arrow, the refractive sperm in ampullar distal part marked with black arrow). All pictures fixed and stained. E from holotype. Scale bars: 50 μm.

Fig. 7 in Two new species of Fridericia (Annelida: Enchytraeidae) from Hungarian caves

Fig. 7. Concatenated phylogenetic tree of the two new and other Fridericia species based on 1447 nucleotid positions (which comprise the CO1, H3 genes and the ITS region). Posterior probabilities greater than 50 are shown at the nodes. Sequences from new species described here appear in bold.

Fig. 4 in Two new species of Fridericia (Annelida: Enchytraeidae) from Hungarian caves

Fig. 4. Micrograph of Fridericia spelaeophila sp. nov. A. Brain. B. Head pore (marked with arrow). C. Chaetae in V–VII. D. Clitellar glands, dorsal view. E. Chaetae in VII–VIII. F. Detached chaetae in coelom. G. Coelomocytes. H. Nephridium at 7/8 (pre- and postseptale marked with arrows). I. Fragments of decaying wood in the intestine (marked with arrow). J. Male copulatory organs, lateral view. K–L. Sperm funnels. (A, K in vivo, B–J, L fixed, stained. Scale bars: 50 μm. B, G from holotype, K from DNA 1283.)

Fig. 3 in Two new species of Fridericia (Annelida: Enchytraeidae) from Hungarian caves

Fig. 3. Micrograph of Fridericia baradlana sp. nov. A. Sperm funnels (marked with arrows). B–C. Male copulatory organs (marked with arrows). D. Bursal slit (marked with arrow). E–H, K–L. Spermathecae. I–J. Spermathecal ectal glands (marked with arrows). (A, C, E–F in vivo, B, J, K–L fixed, stained, D, G, H–I fixed, not stained). Scale bars: 50 μm, in H, J–L 20 μm, J–L from holotype.

Data and code for figures in "Two-tone optomechanical instability and its fundamental implications for backaction-evading measurements"

Here we prepare the data and process scripts to reconstruct figure 4 of the paper (Two-tone optomechanical instability and its fundamental implications for backaction-evading measurements). The folder contains several subfolders and files: “Raw data”: In this folder, you can find the raw data recorded by measurement devices during the experiment. It follows the hierarchical structure. We have three pairs of folders corresponding to three cooperativities (3.5, 7, 14). One folder of each pair contains raw data files in text format (.dat) and the other one contains plots and a Numpy dictionary of the extracted parameter for each cooperativity (superdict.npy). If you need to redo the extraction process from the raw data you can simply run “181031_CXX_Final_NOQT_BAE_2D_post_processeing.py” (XX: 3.5 or 7 or 14) python code to rewrite superdict.npy files and replot all plots in the Raw data folder. “NRBcodes”: A side package for the circle fit (Lorentzian fitting) in the complex plane. “Dicts”: A folder containing Numpy dictionaries needed for the final plot. “superdictXX.npy” are copies of Numpy dictionaries in the Raw data folder. “powers_XX.npy” and “Ds_nor_XX.npy” are Numpy dictionaries needed for the theory plots. You can reproduce them by the uncommenting first part of the “Final_plot.py” and correcting the corresponding cooperativity. “getdata.py” and “postprocessing_libs.py”: Side packages help to read the raw data files.   All post-processes are done on the raw data and you just need to run the “Final_plot.py” to reproduce the plot. If you want to access the post-processed data you can simply read “superdictXX.npy” in the Dicts folder.  Please do not hesitate to contact us in case of any questions.  amir.youssefi@epfl.ch

Fig. 14 in Two new species of Lepidocyrtus Bourlet s. lat. (Collembola: Entomobryidae) from China

Fig. 14. Lepidocyrtus (S.) wanningensis sp. nov., chaetotaxy of Abd. I−III (right side). Scale bar: 70 μm.

Fig. 2 in Two new species of Lepidocyrtus Bourlet s. lat. (Collembola: Entomobryidae) from China

Fig. 2. Lepidocyrtus (A.) huizhouensis sp. nov. A. Apex of Ant. IV (left side). B. Distal part of Ant. III (lateral side). C. Distal part of Ant. II (left side). D. Lateral process of labial palp (right side). E. Maxillary outer lobe (left side). F. Labial and mental chaetotaxy (right side). G. Labial palp and labium (right side). Scale bars: 20 μm.

Fig. 5 in Two new species of Lepidocyrtus Bourlet s. lat. (Collembola: Entomobryidae) from China

Fig. 5. Lepidocyrtus (A.) huizhouensis sp. nov., dorsal chaetotaxy (right side). A−B. Abd. I. C−D. Abd. II. Scale bars: 50 μm.

Fig. 9 in Two new species of Lepidocyrtus Bourlet s. lat. (Collembola: Entomobryidae) from China

Fig. 9. Lepidocyrtus (A.) huizhouensis sp. nov. A. Distal part of ventral manubrium (right side). B–C. Manubrial plaque and proximal part of dens (lateral view). D–E. Distal part of dens and mucro (lateral view). Scale bars: 20 μm.

Fig. 4 in Two new species of Lepidocyrtus Bourlet s. lat. (Collembola: Entomobryidae) from China

Fig. 4. Lepidocyrtus (A.) huizhouensis sp. nov. A. Chaetotaxy of Th. II−III (right side). B. Trochanteral organ. C. Hind foot complex (anterior view). Scale bars: 30 μm.

Fig. 13 in Two new species of Lepidocyrtus Bourlet s. lat. (Collembola: Entomobryidae) from China

Fig. 13. Lepidocyrtus (S.) wanningensis sp. nov. A. Coxal macrochaetal formula of fore leg. B. Coxal macrochaetal formula of middle leg. C. Coxal macrochaetal formula of hind leg. D. Trochanteral organ. E. Hind foot complex (anterior view). Scale bars: 20 μm.

Fig. 12 in Two new species of Lepidocyrtus Bourlet s. lat. (Collembola: Entomobryidae) from China

Fig. 12. Lepidocyrtus (S.) wanningensis sp. nov. A. Labrum. B. Dorsal chaetotaxy of head (partially, right side). C. Chaetotaxy of Th. II−III (right side). Scale bars: 20 μm.

Fig. 8 in Two new species of Lepidocyrtus Bourlet s. lat. (Collembola: Entomobryidae) from China

Fig. 8. Lepidocyrtus (A.) huizhouensis sp. nov. A–B. Chaetotaxy of Abd. V (right side). C. Anterior face of ventral tube (right side). D. Posterior face of ventral tube (apically). E. Lateral flap of ventral tube. Scale bars: A−B = 15 μm; C−E = 20 μm.