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311 results for “Terry Erwin”

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Figure 9 from: Belousov IA, Kabak II (2021) Yalongaphaenops erwini gen. et sp. nov., the world's most high-altitude hypogean trechine beetle from China (Coleoptera, Carabidae, Trechinae). In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 197-220. https://doi.org/10.3897/zookeys.1044.62572

Figure 9 Male genitalia of Yalongaphaenops erwini gen. et sp. nov. A lateral view (holotype) B dorsal view (paratype).

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Figure 3 from: Tsafack N, Wang X, Xie Y, Fattorini S (2021) Niche overlap and species co-occurrence patterns in carabid communities of the northern Chinese steppes. In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 929-949. https://doi.org/10.3897/zookeys.1044.62478

Figure 3 Histograms of expected values (blue bars) for species co-occurrence (c-scores) in carabid beetle communities of Central Asian steppes using the fixed-fixed algorithm to generate 10,000 null matrices. Investigated ecosystems were a desert steppe (a), a typical steppe (b), a meadow steppe (c), three sectors within the typical steppe (d–f), and two sectors within the meadow steppe (g, h). In each graph, the vertical red line indicates the observed value, long-dash lines indicate the one-tailed 95% limits, and the short-dash lines the two-tailed 95% limits.

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Supplementary material 1 from: Riley Peterson KN, Browne RA, Erwin TL (2021) Carabid beetle (Coleoptera, Carabidae) richness, diversity, and community structure in the understory of temporarily flooded and non-flooded Amazonian forests of Ecuador. In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 831-876. https://doi.org/10.3897/zookeys.1044.62340

Geolocation data for sampling sites at Tiputini Biodiversity Station

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Figure A1 from: Riley Peterson KN, Browne RA, Erwin TL (2021) Carabid beetle (Coleoptera, Carabidae) richness, diversity, and community structure in the understory of temporarily flooded and non-flooded Amazonian forests of Ecuador. In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 831-876. https://doi.org/10.3897/zookeys.1044.62340

Figure A1 Water height for the Tiputini River at Tiputini Biodiversity Station, Ecuador. (A) Monthly values represent overall mean river height and the mean maxima and minima based on data from 2009–2014 (B) three years before and after the sampling period for this study. Monthly river height values during the sampling periods, 2011 (B) and 2012 (C) for mean river height in addition to water height maxima and minima.

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Figure 5 from: Riley Peterson KN, Browne RA, Erwin TL (2021) Carabid beetle (Coleoptera, Carabidae) richness, diversity, and community structure in the understory of temporarily flooded and non-flooded Amazonian forests of Ecuador. In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 831-876. https://doi.org/10.3897/zookeys.1044.62340

Figure 5 Number of Cicindelini (tiger beetles) collected from FP and TF forests. Significantly more tiger beetle individuals were collected in TF forest (P = 0.011).

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Figure 2 from: Tsafack N, Wang X, Xie Y, Fattorini S (2021) Niche overlap and species co-occurrence patterns in carabid communities of the northern Chinese steppes. In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 929-949. https://doi.org/10.3897/zookeys.1044.62478

Figure 2 Histograms of expected values (blue bars) for niche overlap in carabid beetle communities of Central Asian steppes using the RA2 algorithm to generate 10,000 null matrices. Investigated ecosystems were a desert steppe (a), a typical steppe (b), a meadow steppe (c), three sectors within the typical steppe (d–f), and two sectors within the meadow steppe (g, h). In each graph, the vertical red line indicates the observed value, long-dash lines indicate the one-tailed 95% limits, and the short-dash lines the two-tailed 95% limits.

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Map 2 from: Belousov IA, Kabak II (2021) Yalongaphaenops erwini gen. et sp. nov., the world's most high-altitude hypogean trechine beetle from China (Coleoptera, Carabidae, Trechinae). In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 197-220. https://doi.org/10.3897/zookeys.1044.62572

Map 2 Relief map of the area nearby the type locality of Y. erwini gen. et sp. nov. The yellow line shows the closest distance to the upper forest limit

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Figure 1 from: Tsafack N, Wang X, Xie Y, Fattorini S (2021) Niche overlap and species co-occurrence patterns in carabid communities of the northern Chinese steppes. In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 929-949. https://doi.org/10.3897/zookeys.1044.62478

Figure 1 Histograms of expected values (blue bars) for niche overlap in carabid beetle communities of Central Asian steppes using the RA3 algorithm to generate 10,000 null matrices. Investigated ecosystems were a desert steppe (a), a typical steppe (b), a meadow steppe (c), three sectors within the typical steppe (d–f), and two sectors within the meadow steppe (g, h). In each graph, the vertical red line indicates the observed value, long-dash lines indicate the one-tailed 95% limits, and the short-dash lines the two-tailed 95% limits.

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Figure 11 from: Liebherr JK, Porch N, Shaw M, Sinclair BE, Maddison DR (2021) Systematic revision of the trans-Bassian moriomorphine genus Theprisa Moore (Coleoptera, Carabidae). In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 339-373. https://doi.org/10.3897/zookeys.1044.62335

Figure 11 Female reproductive tract of Theprisa darlingtoni, ventral view; scale bar = 0.50 mm. Abbreviations: bc, bursa copulatrix; co, common oviduct; gc, gonocoxa; hg, hindgut; hs, helminthoid sclerite; sd, spermathecal duct; sg, spermathecal gland; sgd, spermathecal gland duct; sgs, spermathecal gland stem; sp, spermatheca; v, vagina.

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Figure 12 from: Liebherr JK, Porch N, Shaw M, Sinclair BE, Maddison DR (2021) Systematic revision of the trans-Bassian moriomorphine genus Theprisa Moore (Coleoptera, Carabidae). In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 339-373. https://doi.org/10.3897/zookeys.1044.62335

Figure 12 Strict consensus of two equally parsimonious, 380-step cladograms including Theprisa spp. and cladistically neighboring moriomorphine taxa of the subtribe Tropopterina (see text); consensus cladogram length 382 steps, CI = 0.43, RI = 0.66. Character numbers are shown above cladogram edges, character states below. Cladogram root placed so tree topology is compatible with the more inclusive cladogram of Liebherr (2020: fig. 1). Filled squares represent unique state transformations on cladogram, open squares indicate state transformations that occur more than once on cladogram. Clades of this analysis previously recovered in Liebherr (2020) are indicated by pointers numbered 1; the clade subtended by Pterogmus reported in Liebherr (2019) indicated by the pointer numbered 2. Decay indices (i.e., Bremer Support values) shown beneath cladogram edges for all internal edges of the cladogram. Geographic distributions of species are indicated by abbreviations following species epithets: EOZ, southeastern Australia; i.e., A. C. T., New South Wales and Victoria; NNZ, North Island, New Zealand; NZ, New Zealand; SNZ, South Island, New Zealand; QOZ, Queensland; Tas, Tasmania; WOZ, Western Australia

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Figure 10 from: Liebherr JK, Porch N, Shaw M, Sinclair BE, Maddison DR (2021) Systematic revision of the trans-Bassian moriomorphine genus Theprisa Moore (Coleoptera, Carabidae). In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 339-373. https://doi.org/10.3897/zookeys.1044.62335

Figure 10 Distributional records for Theprisa spp.: T. australis (circle);  T. darlingtoni (square).

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Figure 1 from: Liebherr JK, Porch N, Shaw M, Sinclair BE, Maddison DR (2021) Systematic revision of the trans-Bassian moriomorphine genus Theprisa Moore (Coleoptera, Carabidae). In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 339-373. https://doi.org/10.3897/zookeys.1044.62335

Figure 1 Dorsal habitus illustrations of Theprisa spp.; range of standardized body lengths indicated AT. otway female BT. convexa female CT. montana female.

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Figure 18 from: Maddison DR, Porch N (2021) A preliminary phylogeny and review of the genus Tasmanitachoides, with descriptions of two new species (Coleoptera, Carabidae, Bembidarenini). In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 153-196. https://doi.org/10.3897/zookeys.1044.62253

Figure 18 Elytral microsculpture of Tasmanitachoides, dorsal view AT. baehri, voucher V101484 BT. erwini, voucher V101483. Scale bar: 100 µm.

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Figure 16 from: Maddison DR, Porch N (2021) A preliminary phylogeny and review of the genus Tasmanitachoides, with descriptions of two new species (Coleoptera, Carabidae, Bembidarenini). In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 153-196. https://doi.org/10.3897/zookeys.1044.62253

Figure 16 Left elytron of TasmanitachoidesAT. sp. "Lerderderg R", voucher V101049 BT. erwini, voucher V101469 CT. hobarti, voucher V101463 DT. leai, voucher V101467 ET. rufescens, voucher V101478 FT. sp. "River Forth", voucher DNA5555 GT. sp. "Angle Crossing #2", voucher DNA5678 HT. flindersianus, paratype JT. bicolor, voucher V101472 KT. fitzroyi, voucher V101471 LT. maior, voucher DNA5508 MT. arnhemensis, voucher V101476. NT. murrumbidgensis, voucher V101464 PT. minor, voucher V101474 QT. sp. "Tambo R", voucher V101465.

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Supplementary material 1 from: Hayashi M, Sugiura S (2021) Shell-breaking predation on gastropods by Badister pictus (Coleoptera, Carabidae) with strikingly asymmetric mandibles. In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 815-830. https://doi.org/10.3897/zookeys.1044.62293

Movie 1. Badister pictus attacking a dextral snail Zonitoides arboreus.

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Figure 4 from: Hayashi M, Sugiura S (2021) Shell-breaking predation on gastropods by Badister pictus (Coleoptera, Carabidae) with strikingly asymmetric mandibles. In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 815-830. https://doi.org/10.3897/zookeys.1044.62293

Figure 4 Shell morphology and bite traces of Badister pictusA dextral shell B sinistral shell C dextral shell with an operculum D–F bite traces on dextral shells G, H bite traces on sinistral shells I broken part (shaded area) on a sinistral shell A–D, G front view E, H, I back view F dorsal view. Red circles indicate the positions where the shell (aperture) thickness was measured. Red arrows indicate the starting point of shell breaking by B. pictus. Broken lines indicate the bite traces by B. pictus.

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Figure 13 from: Maddison DR, Porch N (2021) A preliminary phylogeny and review of the genus Tasmanitachoides, with descriptions of two new species (Coleoptera, Carabidae, Bembidarenini). In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 153-196. https://doi.org/10.3897/zookeys.1044.62253

Figure 13 Adults of TasmanitachoidesAT. rufescens, voucher V101478 BT. sp. "River Forth", voucher DNA5555 CT. sp. "Angle Crossing #2", voucher DNA5678 DT. flindersianus, paratype ET. bicolor, voucher V101472 FT. balli, holotype. Scale bars: 1.0 mm.

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Figure 2 from: Maddison DR, Porch N (2021) A preliminary phylogeny and review of the genus Tasmanitachoides, with descriptions of two new species (Coleoptera, Carabidae, Bembidarenini). In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 153-196. https://doi.org/10.3897/zookeys.1044.62253

Figure 2 Habitats of TasmanitachoidesA Australia: ACT: Murrumbidgee River at Angle Crossing, 35.5825°S, 149.1100°E, 598 m. This and similar areas a few meters upstream are habitat of T. murrumbidgensis, T. sp. " Tambo R", T. cf. gerdi, T. sp. "Angle Crossing #1", T. wilsoni, T. maior, T. sp. "Angle Crossing #2", and T. rufescensB Australia: Victoria: Flat Rock Creek at highway B23, 37.2835°S, 149.2223°E, 256 m. Habitat of T. lutus, T. leai, and T. angulicollisC Australia: Tasmania: mouth of Machinery Creek into the River Forth at C136, 41.4712°S, 146.1366°E, 126 m. Habitat of T. leai, T. kingi, T. erwini, and T. sp. "River Forth" D Australia: Tasmania: Lake St Clair, 42.1121°S, 146.2051°E, 741 m. Habitat of T. hobarti.

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Figure 12 from: Maddison DR, Porch N (2021) A preliminary phylogeny and review of the genus Tasmanitachoides, with descriptions of two new species (Coleoptera, Carabidae, Bembidarenini). In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 153-196. https://doi.org/10.3897/zookeys.1044.62253

Figure 12 Adults of the wattsensis group and other TasmanitachoidesAT. wattsensis, voucher DNA5758; NSW: Leatherbarrel Creek u/s Alpine Way BT. sp. "Lerderderg R", voucher V101049; VIC: Lerderderg River, 6.8 km N. Bacchus Marsh CT. erwini, voucher V101469 DT. leai, voucher V101467 ET. hobarti, voucher V101463 FT. glabellus, paratype. Scale bars: 1.0 mm.

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Figure 10 from: Maddison DR, Porch N (2021) A preliminary phylogeny and review of the genus Tasmanitachoides, with descriptions of two new species (Coleoptera, Carabidae, Bembidarenini). In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 153-196. https://doi.org/10.3897/zookeys.1044.62253

Figure 10 Adults of the Tasmanitachoides kingi species group as well as T. lutusAT. kingi, voucher V101468 BT. angullicollis, voucher DNA5515. CT. hendrichi, holotype. DT. wilsoni, voucher V101470. ET. baehri, voucher V101479. FT. lutus, voucher V101462. Scale bars: 1.0 mm.

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