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Figure 16 from: Cumming RT, Le Tirant S, Teemsma SN, Hennemann FH, Willemse L, Büscher TH (2020) Lost lovers linked at long last: elusive female Nanophyllium mystery solved after a century of being placed in a different genus (Phasmatodea, Phylliidae). ZooKeys 969: 43-84. https://doi.org/10.3897/zookeys.969.56214
Figure 16 Notable known Nanophyllium females scaled to relative size ANanophyllium chitoniscoides comb. nov. Coll FHBNanophyllium suzukii comb. nov. CNanophyllium frondosum comb. nov. DNanophyllium keyicum comb. nov. (RMNH).
Figure 13 from: Cumming RT, Le Tirant S, Teemsma SN, Hennemann FH, Willemse L, Büscher TH (2020) Lost lovers linked at long last: elusive female Nanophyllium mystery solved after a century of being placed in a different genus (Phasmatodea, Phylliidae). ZooKeys 969: 43-84. https://doi.org/10.3897/zookeys.969.56214
Figure 13 Alae wing venation of males for the two species groups, dorsal ANanophyllium rentzi (pygmaeum species group) BNanophyllium stellae (stellae species group). Abbreviations used: C (costa); Sc (subcosta); R (radius); R1 (radius 1); Rs (radial sector); M (media); MA (media anterior); MP (media posterior); Cu (cubitus); Cu+1AA (cubitus and first anterior anal); 1AA–7AA (first through seventh anterior anal); 1PA–6PA (first through fifth posterior anal).
Figure 10 from: Cumming RT, Le Tirant S, Teemsma SN, Hennemann FH, Willemse L, Büscher TH (2020) Lost lovers linked at long last: elusive female Nanophyllium mystery solved after a century of being placed in a different genus (Phasmatodea, Phylliidae). ZooKeys 969: 43-84. https://doi.org/10.3897/zookeys.969.56214
Figure 10 Side by side Nanophyllium males of the two species groups Apygmaeum species group, Nanophyllium asekiense male from Morobe Province, Papua New Guinea Bstellae species group, Nanophyllium stellae HT from Jayapura, Indonesia.
Figure 15 from: Cumming RT, Le Tirant S, Teemsma SN, Hennemann FH, Willemse L, Büscher TH (2020) Lost lovers linked at long last: elusive female Nanophyllium mystery solved after a century of being placed in a different genus (Phasmatodea, Phylliidae). ZooKeys 969: 43-84. https://doi.org/10.3897/zookeys.969.56214
Figure 15 Distribution map showing the undetermined Nanophyllium specimens with mappable localities.
Figure 1 from: Cumming RT, Le Tirant S, Teemsma SN, Hennemann FH, Willemse L, Büscher TH (2020) Lost lovers linked at long last: elusive female Nanophyllium mystery solved after a century of being placed in a different genus (Phasmatodea, Phylliidae). ZooKeys 969: 43-84. https://doi.org/10.3897/zookeys.969.56214
Figure 1 Live Nanophyllium asekiense (Größer, 2002), comb. nov. females, three primary color forms photographed in Morobe Province, Papua New Guinea.
Figure 4 from: Kang I, Long KD, Sharkey MJ, Whitfield JB, Lord NP (2020) Orientocardiochiles, a new genus of Cardiochilinae (Hymenoptera, Braconidae), with descriptions of two new species from Malaysia and Vietnam. ZooKeys 971: 1-15. https://doi.org/10.3897/zookeys.971.56571
Figure 4 A Distribution map of Orientocardiochiles joeburrowi sp. nov. in Wang Kelian B distribution map of O. joeburrowi sp. nov. in Malaysia.
Figure 2 from: Kang I, Long KD, Sharkey MJ, Whitfield JB, Lord NP (2020) Orientocardiochiles, a new genus of Cardiochilinae (Hymenoptera, Braconidae), with descriptions of two new species from Malaysia and Vietnam. ZooKeys 971: 1-15. https://doi.org/10.3897/zookeys.971.56571
Figure 2 Orientocardiochiles joeburrowi sp. nov., holotype. A Lateral habitus B dorsal habitus C ventral metasoma; arrow: hypopygium D dorsal propodeum and metasomal terga 1–3; arrow: plateau-like projection E dorsal mesonotum F anterior head G claws.
Figure 6 from: Kang I, Long KD, Sharkey MJ, Whitfield JB, Lord NP (2020) Orientocardiochiles, a new genus of Cardiochilinae (Hymenoptera, Braconidae), with descriptions of two new species from Malaysia and Vietnam. ZooKeys 971: 1-15. https://doi.org/10.3897/zookeys.971.56571
Figure 6 A Distribution map of Orientocardiochiles nigrofasciatus sp. nov. in Cat Tien NP B distribution map of O. nigrofasciatus sp. nov. in Vietnam.
Figure 5 from: Kang I, Long KD, Sharkey MJ, Whitfield JB, Lord NP (2020) Orientocardiochiles, a new genus of Cardiochilinae (Hymenoptera, Braconidae), with descriptions of two new species from Malaysia and Vietnam. ZooKeys 971: 1-15. https://doi.org/10.3897/zookeys.971.56571
Figure 5 Orientocardiochiles nigrofasciatus sp. nov. A Lateral habitus (holotype, female) B head (dorsal view) C head (anterior view) D head (lateral view) E dorsal mesonotum F lateral mesonotum G metasoma (dorsal view) H forewing I hind wing J propodeum K hamuli on hind wing L hind tarsal claw M ventro-lateral mesonotum N ventral metasoma O apex of ovipositor sheath (lateral view).
Figure 1 from: Kang I, Long KD, Sharkey MJ, Whitfield JB, Lord NP (2020) Orientocardiochiles, a new genus of Cardiochilinae (Hymenoptera, Braconidae), with descriptions of two new species from Malaysia and Vietnam. ZooKeys 971: 1-15. https://doi.org/10.3897/zookeys.971.56571
Figure 1 Austerocardiochiles pollinator, paratype. A Lateral habitus B dorsal habitus C ventral metasoma; arrow: median enfold on hypopygium D dorsal propodeum and metasomal terga 1 to 3; arrow: lens-shaped area E dorsal mesonotum F anterior head G claws.
Figure 2 from: Migliorini D, Luchi N, Pepori AL, Pecori F, Aglietti C, Maccioni F, Munck I, Wyka S, Broders K, Wingfield MJ, Santini A (2020) Caliciopsis moriondi, a new species for a fungus long confused with the pine pathogen C. pinea. MycoKeys 73: 87-108. https://doi.org/10.3897/mycokeys.73.53028
Figure 2 Morphological differences between Caliciopsis moriondi and C. pineaA–CCaliciopsis moriondi: A four-week-old colonies grown at 20 °C on MEA B, C ascomata growing from a canker of Pinus radiataD–FCaliciopsis pinea: D four-week-old colonies grown at 20 °C on MEA E, F ascomata growing from a canker of P. radiata.
Supplementary material 1 from: Migliorini D, Luchi N, Pepori AL, Pecori F, Aglietti C, Maccioni F, Munck I, Wyka S, Broders K, Wingfield MJ, Santini A (2020) Caliciopsis moriondi, a new species for a fungus long confused with the pine pathogen C. pinea. MycoKeys 73: 87-108. https://doi.org/10.3897/mycokeys.73.53028
Figure S1. One of the most parsimonious trees from EF1-α sequence datasets
Figure 1 from: Migliorini D, Luchi N, Pepori AL, Pecori F, Aglietti C, Maccioni F, Munck I, Wyka S, Broders K, Wingfield MJ, Santini A (2020) Caliciopsis moriondi, a new species for a fungus long confused with the pine pathogen C. pinea. MycoKeys 73: 87-108. https://doi.org/10.3897/mycokeys.73.53028
Figure 1 Caliciopsis moriondi structures A cankers on a Pinus radiata trunk B–D ascomata growing from a canker B image of C. pinea ascigerous columns from an archive of 1970 (provided by Prof. Paolo Capretti) E–G asci H ascospores I ascigerous, terminal portion L four weeks colony grown at 20 °C on MEA. Scale bars: 2.5 µm (F–H), 5 µm (I).
Figure 5 from: Migliorini D, Luchi N, Pepori AL, Pecori F, Aglietti C, Maccioni F, Munck I, Wyka S, Broders K, Wingfield MJ, Santini A (2020) Caliciopsis moriondi, a new species for a fungus long confused with the pine pathogen C. pinea. MycoKeys 73: 87-108. https://doi.org/10.3897/mycokeys.73.53028
Figure 5 Polymorphic nucleotides from aligned sequence data of ITS, EF1-α and Bt1 loci showing the variation between isolates of Caliciopsis pinea from US and isolates of C. moriondi from the US and EU. Different colours demark variation in bases found in the sequences. Variation type is reported in the bottom part: "Sb" is the abbreviation for base's substitution; "In" is the abbreviation for base's insertion. Fix polymorphisms are signalled with "/". Sequences US232b, US67 and IT1 are respectively marked with *1, *2, *3 as representative for the following groups of sequences not reported in the figure: *1 (US151, US199, US238, US240, US232b); *2 (US52, US100, US81, US110, US149, US161, US163, US167, US172, US206, US220, US225a, US230d, US234a, US252); *3 (IT2, IT4, IT5, IT6, IT7, IT9, IT11, IT13, IT14, IT15, IT20, IT22, US66, US65)
Figure 4 from: Migliorini D, Luchi N, Pepori AL, Pecori F, Aglietti C, Maccioni F, Munck I, Wyka S, Broders K, Wingfield MJ, Santini A (2020) Caliciopsis moriondi, a new species for a fungus long confused with the pine pathogen C. pinea. MycoKeys 73: 87-108. https://doi.org/10.3897/mycokeys.73.53028
Figure 4 One of the most parsimonious trees of aligned ITS dataset (length = 168, CI = 0.721154, RI = 0.922043, RC = 0.762881, HI = 0.664935). The MP and Bayesian posterior probability are indicated next to the branches.
Supplementary material 2 from: Migliorini D, Luchi N, Pepori AL, Pecori F, Aglietti C, Maccioni F, Munck I, Wyka S, Broders K, Wingfield MJ, Santini A (2020) Caliciopsis moriondi, a new species for a fungus long confused with the pine pathogen C. pinea. MycoKeys 73: 87-108. https://doi.org/10.3897/mycokeys.73.53028
Figure S2. One of the most parsimonious trees from Bt1 sequence datasets
Figure 3 from: Migliorini D, Luchi N, Pepori AL, Pecori F, Aglietti C, Maccioni F, Munck I, Wyka S, Broders K, Wingfield MJ, Santini A (2020) Caliciopsis moriondi, a new species for a fungus long confused with the pine pathogen C. pinea. MycoKeys 73: 87-108. https://doi.org/10.3897/mycokeys.73.53028
Figure 3 One of the most parsimonious trees (length = 137) from the combined sequence datasets of the ITS rDNA, Bt1 and EF1-α loci is shown (CI = 0.9444, RI = 0.99633, RC = 0.98178, HI = 0.94098). MP bootstraps and Bayesian posterior probabilities are indicated alongside the branches. C. pseudotsugae and C. orientalisEF1-α were selected as outgroup taxa.
Australian long-finned pilot whales (Globicephala melas) emit stereotypical, variable, biphonic, multi-component, and sequenced vocalisations, similar to those recorded in the northern hemisphere
<p>While in the northern hemisphere, many studies have been conducted on the vocal repertoire of long-finned pilot whales (<i>Globicephala melas</i>), no such study has been conducted in the southern hemisphere. Presented here, is the first study on the vocalisations of long-finned pilot whales along the southern coast of mainland Australia. Multiple measures were taken of<b> </b>2 028 vocalisations recorded over five years in several locations. These vocalisations included tonal sounds with and without overtones, sounds of burst-pulse character, graded sounds, biphonations, and calls of multiple components. Vocalisations were further categorised based on spectrographic features into 18 contour classes. Altogether, vocalisations ranged from approximately 200 Hz to 25 kHz in fundamental frequency and from 0.03 s to 2.07 s in duration. These measures compared well with those from northern hemisphere pilot whales. Some call types were almost identical to northern hemisphere vocalisations, even though the geographic ranges of the two populations are far apart. Other call types were unique to Australia. Striking similarities with calls of short-finned pilot whales (<i>Globicephala macrorhynchus</i>) and sometimes sympatric killer whales (<i>Orcinus orca</i>) were also found. Theories for call convergence and divergence are discussed.</p>
Data and code for: Dietzel et al. Long-term shifts in the colony size structure of coral populations along the Great Barrier Reef
<p>The age or size structure of a population has a marked influence on its demography and reproductive capacity. While declines in coral cover are well documented, concomitant shifts in the size frequency distribution of coral colonies are rarely measured at large spatial scales. Here we document major shifts in the colony size structure of coral populations along the 2,300km length of the Great Barrier Reef over the past two decades. Coral colony abundances on reef crests and slopes have declined sharply across all colony size classes and in all coral taxa compared to historical baselines. Declines were particularly pronounced in the Northern and Central regions of the Great Barrier Reef, following mass coral bleaching in 2016 and 2017. The relative abundances of large colonies remained relatively stable, but this apparent stability masks steep declines in absolute abundance. The potential for recovery of older fecund corals is uncertain given the increasing frequency and intensity of disturbance events. The systematic decline in smaller colonies across regions, habitats and taxa, suggests that a decline in recruitment has further eroded the recovery potential and resilience of coral populations.</p>
Data and code from: Long-term effects of colonization-extinction dynamics of generalist versus specialist wodd-decaying fungi
<p>Data and scripts required to fit colonization-extinction models and to run simulations presented in Moor et al. 2020 J Ecol.</p> <p>Scripts use RData files; data is also available i CSV file format.</p>
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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)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
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.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.