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Fig. 8 in Distribution Of The Carabid Species (Coleoptera, Carabidae) In Woodlands Of The Protected And Urban Areas (North Of Ukraine)

Fig. 8. The ratios of forest carabid species according to their geographical ranges in the studied territories. Codes of geographical range given in table 2.

Fig. 7 in Distribution Of The Carabid Species (Coleoptera, Carabidae) In Woodlands Of The Protected And Urban Areas (North Of Ukraine)

Fig. 7. Average of activity density (± 95 %CI) of the five abundant forest species in the Polisky Nature Reserve and in the urban parks.

Fig. 4 in Distribution Of The Carabid Species (Coleoptera, Carabidae) In Woodlands Of The Protected And Urban Areas (North Of Ukraine)

Fig. 4. The ordination (non-metric multidimensional scaling using the Bray-Curtis index similarity and the square root transform method) of the total species compositions in the forests of the Polisky Nature Reserve and the urban parks during the study years. The stress of the two-dimensional configuration is 4 %. Site name abbreviations are the same as in fig. 3.

Fig. 3 in Distribution Of The Carabid Species (Coleoptera, Carabidae) In Woodlands Of The Protected And Urban Areas (North Of Ukraine)

Fig. 3. Cluster analysis of Bray-Curtis similarity measure and the group average linkage method of carabid assemblages in the studied areas. Site name abbreviations: R ― Polisky Nature Reserve, T ― Teremky and F ― Theofania urban parks; the numbers after the letter are indicate the study year.

Fig. 3 in Species Composition And Biotopical Distribution Of Blackflies (Diptera, Simuliidae) On The South-Western Macroslope Of The Ukrainian Carpathians

Fig. 3. Correlation of different groups of blackflies in hydrobiocoenoses on the south-western macroslope of the Ukrainian Carpathians.

Fig. 6 in Distribution Of The Carabid Species (Coleoptera, Carabidae) In Woodlands Of The Protected And Urban Areas (North Of Ukraine)

Fig. 6. Plot ordination of detrending correspondent analysis (66 % of the variance) of the forest species compositions in forests of the Nature Reserve and the urban parks during the study years. Symbols represent: plus — species which found only in parks, cross — species which found only in Reserve and column — shared species in both territories. Site name abbreviations are the same as in fig. 3.

Fig. 2 in Species Composition And Biotopical Distribution Of Blackflies (Diptera, Simuliidae) On The South-Western Macroslope Of The Ukrainian Carpathians

Fig. 2. Correlation Simuliidae species developing in rivers on the south-western macroslope of the Ukrainian Carpathians.

Fig. 6 in Species Composition And Biotopical Distribution Of Blackflies (Diptera, Simuliidae) On The South-Western Macroslope Of The Ukrainian Carpathians

Fig. 6. Species diversity of blackflies (according to Simpson's index) on the south-western macroslope of the Ukrainian Carpathians. (The numeration of altitudinal vegetative groups corresponds to that one given in fig. 4.)

Fig. 5 in Species Composition And Biotopical Distribution Of Blackflies (Diptera, Simuliidae) On The South-Western Macroslope Of The Ukrainian Carpathians

Fig. 5. Cluster analysis of similarity of blackflies species composition in altitudinal vegetation groupings on the south-western macroslope of the Ukrainian Carpathians. (The numeration of altitudinal vegetative groups corresponds to that one given in fig. 4).

Fig. 4 in Species Composition And Biotopical Distribution Of Blackflies (Diptera, Simuliidae) On The South-Western Macroslope Of The Ukrainian Carpathians

Fig. 4. Geobotanical subdivision of the Ukrainian Carpathians (Holubets, 2003). І — subdivision of oak-beech and oak submontane Transcarpathian forests (1): 1a — district of beech-oak and oak-beech submontane forests of the Volcanic Range, 1b — district of oak-beech and beech-oak forests of Marmaros basin; ІІ — subdivision of beech Carpathian forests: 2 — district of fur-beech Verkhouzhotski forests, 3 — district of hornbeam-beech and beech Dubrynychi-Svaliava forests, 4 — districts of the beech forests of southern megaslope of the Polonynian Beskyd, 5 — Mizhhirskiy (Intermountain) and 6 — Rakhiv subdistricts in the district of spruce-fir-beech, spruce-beech-fir and spruce-beech Transcarpathian forests; III — subdivision of spruce Carpathian mountain forests: 7 — subdistrict of the Upper Tysa beech-fir-spruce forests of the district of Chornohora-Marmaros forests. • — places of sample collection.

Fig. 5 in Distribution Of The Carabid Species (Coleoptera, Carabidae) In Woodlands Of The Protected And Urban Areas (North Of Ukraine)

Fig. 5. Plots of the distribution of carabids species (A) and their density (B) according to dispersal ability (B — brachypterous, D — dimorphic, M — macropterous) in three habitat affinity groups in the Polisky Nature Reserve and in the urban parks.

Fig. 2 in Distribution Of The Carabid Species (Coleoptera, Carabidae) In Woodlands Of The Protected And Urban Areas (North Of Ukraine)

Fig. 2. Estimated species richness of carabid beetles collected in the investigated territories using rarefaction analysis (bars are 95 % CI).

Fig. 1 in Distribution Of The Carabid Species (Coleoptera, Carabidae) In Woodlands Of The Protected And Urban Areas (North Of Ukraine)

Fig. 1. Geographic location of the investigated areas is shown in arrows (indicating the position of the Polisky Nature Reserve (PNR) and the urban parks in Kyiv City, in the Ukraine). The study area is marked by the red flags.

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Data from: Fauxcurrence: simulating multi-species occurrences for null models in species distribution modelling and biogeography

<p>This dataset contains GPS coordinates of occurrences from 22 species from Sulawesi, Indonesia. It was used in the manuscript "Fauxcurrence: simulating multi-species occurrences for null models in species distribution modelling and biogeography" to demonstrate the utility of the fauxcurrence R package (<a href="https://github.com/ogosborne/fauxcurrence">https://github.com/ogosborne/fauxcurrence)</a>.</p>

dryad32/100

Data from: A data-driven geospatial workflow to map species distributions for conservation assessments

<p>We developed a geospatial workflow that refines the distribution of a species from its extent of occurrence (EOO) to area of habitat (AOH) within the species range map. The range maps are produced with an inverse distance weighted (IDW) interpolation procedure using presence and absence points derived from primary biodiversity data (GBIF and eBird hotspots respectively). Here we provide sample data to run the geospatial workflow for nine forest species across Mexico and Central America.</p>

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Subspecies and Distribution. M.f.fimbriatusPeters,1871—E&SEChina(Shandong,Jiangsu,Anhui,Zhejiang,Jiangxi,Fujian,andGuangdong). M. f. taiwanensis Arnback-Christie-Linde, 1908 — Taiwan. Specimens from Yunnan, SC China and possibly specimens from Sichuan and Guizhou represent an undescribed species. in Vespertilionidae

Subspecies and Distribution. M.f.fimbriatusPeters,1871—E&SEChina(Shandong,Jiangsu,Anhui,Zhejiang,Jiangxi,Fujian,andGuangdong). M. f. taiwanensis Arnback-Christie-Linde, 1908 — Taiwan. Specimens from Yunnan, SC China and possibly specimens from Sichuan and Guizhou represent an undescribed species.

Subspecies and Distribution. M.g.guilleniSoisooketal.,2013—Penin-sularThailand. M. g. nicobarensis Soisook et al., 2013 — Nicobar Is (Tillangchong, Bompuka, Camorta, Trinket and Great Nicobar); individuals similar to this species were also captured on Teressa, Katchal, and Nancowry Is. in Vespertilionidae

Subspecies and Distribution. M.g.guilleniSoisooketal.,2013—Penin-sularThailand. M. g. nicobarensis Soisook et al., 2013 — Nicobar Is (Tillangchong, Bompuka, Camorta, Trinket and Great Nicobar); individuals similar to this species were also captured on Teressa, Katchal, and Nancowry Is.

Distribution. Tsushima Is (Japan); a specimen collected on Yakushima (Osumi Is) has been claimed to be this species, but most probably is the Ussuri Tube-nosed Bat (M. ussuriensis). in Vespertilionidae

Distribution. Tsushima Is (Japan); a specimen collected on Yakushima (Osumi Is) has been claimed to be this species, but most probably is the Ussuri Tube-nosed Bat (M. ussuriensis).

Distribution. Manus, New Britain, Duke of York, and Umboi Is; a specimen from Wetar I was identified as this species, but specific status of this specimen needs to be confirmed. in Vespertilionidae

Distribution. Manus, New Britain, Duke of York, and Umboi Is; a specimen from Wetar I was identified as this species, but specific status of this specimen needs to be confirmed.

One of the first cryptic mammal species discovered, when it was separated from the morphologically similar R. tumida (= R. bickhami) based on karyological studies. Karyotype of 2n = 42 of R. genowaysi is identical to that observed in R. velilla, but these species are genetically distinct; their ranges do not overlap. R. genowaysi is morphologically very similar to other species within the R. tumida complex and is sympatric with R. bickhami (2n = 34). Monotypic. Distribution. Two nearby localities in Pacific lowlands of S Chiapas, S Mexico. in Vespertilionidae

One of the first cryptic mammal species discovered, when it was separated from the morphologically similar R. tumida (= R. bickhami) based on karyological studies. Karyotype of 2n = 42 of R. genowaysi is identical to that observed in R. velilla, but these species are genetically distinct; their ranges do not overlap. R. genowaysi is morphologically very similar to other species within the R. tumida complex and is sympatric with R. bickhami (2n = 34). Monotypic. Distribution. Two nearby localities in Pacific lowlands of S Chiapas, S Mexico.