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184 results for “diversity and invasibility”

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Supplementary material 1 from: Spafford R, Lortie C, Butterfield B (2013) A systematic review of arthropod community diversity in association with invasive plants. NeoBiota 16: 81-102. https://doi.org/10.3897/neobiota.16.4190

Supplementary material 1 from: Spafford R, Lortie C, Butterfield B (2013) A systematic review of arthropod community diversity in association with invasive plants. NeoBiota 16: 81-102. https://doi.org/10.3897/neobiota.16.4190

opencc-by-4.0Apr 2013View details →
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Supplementary material 2 from: Spafford R, Lortie C, Butterfield B (2013) A systematic review of arthropod community diversity in association with invasive plants. NeoBiota 16: 81-102. https://doi.org/10.3897/neobiota.16.4190

Supplementary material 2 from: Spafford R, Lortie C, Butterfield B (2013) A systematic review of arthropod community diversity in association with invasive plants. NeoBiota 16: 81-102. https://doi.org/10.3897/neobiota.16.4190

opencc-by-4.0Apr 2013View details →
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FIGURE 4 in Drastic reduction of the functional diversity of native ichthyofauna in a Neotropical lake following invasion by piscivorous fishes

FIGURE 4 | Temporal changes in species richness (dashed lines) and functional richness (FRic; continous lines) of the ichthyofauna from Carioca Lake, Middle Rio Doce basin, state of Minas Gerais, considering two scenarios: "all species", including native and non-native; and "only native species" (left figures). Plotted values expressed as a proportion to the maximum richness. The arrows represent the first records of the introduced piscivorous Cichla kelberi (in 1985) and Pygocentrus nattereri (in 1992) in the system. The upper plots represent the functional space (only two dimensions for simplify visualization), with polygons indicating the proportion filled by the set of species (FRic) in each year. Right figures illustrate the functional space showing the position of each species. Green and blue colors indicate, respectively, the native and introduced species, and crosses indicate native species extirpated from the lake. Codes at the ends of the arrows are the most important ecomorphological traits for each axis of the PCA (for functional trait and species codes, see Tab. 1 and Tab. S2).

opencc-by-4.0Sep 2021View details →
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FIGURE 3 in Drastic reduction of the functional diversity of native ichthyofauna in a Neotropical lake following invasion by piscivorous fishes

FIGURE 3 | Compositional change of the ichthyofauna from Carioca Lake, Middle Rio Doce basin state of Minas Gerais, southeastern Brazil. Green and blue squares indicate, respectively, the presence of native and introduced species in each year.

opencc-by-4.0Sep 2021View details →
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FIGURE 1 in Drastic reduction of the functional diversity of native ichthyofauna in a Neotropical lake following invasion by piscivorous fishes

FIGURE 1 | The lacustrine system of the Middle Rio Doce basin, state of Minas Gerais, Brazil. The green polygon delimits the area of the Rio Doce State Park (PERD) and the white circle indicates the location of Carioca Lake.

opencc-by-4.0Sep 2021View details →
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FIGURE 2 in Drastic reduction of the functional diversity of native ichthyofauna in a Neotropical lake following invasion by piscivorous fishes

FIGURE 2 | Morphometric measures taken from digital pictures: CPd – caudal-peduncle minimal depth, CFd – caudal-fin maximum depth, CFs – caudal-fin surface, PFi – distance from pectoral-fin insertion to the bottom of the body, PFb – body depth at the level of the pectoral-fin insertion, PFl – pectoral-fin length, PFs – pectoral-fin surface, Hd – head depth along the vertical axis of the eye, Ed – eye diameter, Eh – distance from the center of the eye to the bottom of the head, Mo – distance from the tip of the upper jaw to the bottom of the head along the head depth axis. Adapted from Leitão et al. (2016).

opencc-by-4.0Sep 2021View details →
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Figure 1. A in Structural and diversity changes in coastal dunes from the Mexican Caribbean: the case of the invasive Australian pine (Casuarina equisetifolia)

Figure 1. A) Location of Cozumel Island within the Yucatán Peninsula. B) Study area on the north side of Cozumel Island. C) The distribution of Casuarina equisetifolia, shown as dark gray polygons and the sampling plots (numbered circles). Plots 1, 6–9 are the invaded, while plots 2–5, 10 are non-invaded.

opencc-by-4.0Jan 2022View details →
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Figure 3 in Structural and diversity changes in coastal dunes from the Mexican Caribbean: the case of the invasive Australian pine (Casuarina equisetifolia)

Figure 3. Grouping of invaded (triangles) and non-invaded (squares) sampling plots according to their species composition similarity (PERMANOVA). The numbers close to the symbols are the assigned sampling plot number. The dotted lines represent the scores' standard deviation of each group. The solid black lines represent the distance (similarity) between sampling plots.

opencc-by-4.0Jan 2022View details →
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Figure 1 in Invasions of two estuarine gobiid species interactively induced from water diversion and saltwater intrusion

Figure 1. The East Route of South-to-North Water Transfer Project, showing the five major lakes along the route (shadow areas) as storages, the Grand Canal as conveyance, and geographic relationships of the major rivers (i.e., the Yangtze River, the Huai River, and the Yellow River) with the route. The Nansi Lake is separated into the Lower Nansi Lake and Upper Nansi Lake by the Erji Dam. The year of the first record of the two invasive species, Taenioides cirratus and Tridentiger bifasciatus, in each of these lakes was indicated to show their invasion patterns.

opencc-by-4.0Feb 2019View details →
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Fig. 2 in Analysis of propagule pressure and genetic diversity in the invasibility of a freshwater apex predator: the peacock bass (genus Cichla)

Fig. 2. Structure bar plots of probabilities of assignment of each individual from populations of CP in green (1 - TOC, 2 - ITU, 3 - ML and 4 - FU) and CK in red (5 - TOC, 6 - ITU, 7 - TRM, 8 - RD). Probabilities of assignment (q) of each individual to each cluster are shown along the x-axis.

opencc-by-4.0Mar 2014View details →
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Fig. 7 in Proliferation of the invasive termite Coptotermes gestroi (Isoptera: Rhinotermitidae) on Grand Cayman and overall termite diversity on the Cayman Islands

Fig. 7. Plot for the Single Linkage clustering method for distances to the nearest marine dockage of Coptotermes gestroi over Grand Cayman Island.

opencc-by-4.0Sep 2016View details →
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Fig. 6 in Proliferation of the invasive termite Coptotermes gestroi (Isoptera: Rhinotermitidae) on Grand Cayman and overall termite diversity on the Cayman Islands

Fig. 6. Plot for the Single Linkage clustering method for Coptotermes gestroi over Grand Cayman Island.

opencc-by-4.0Sep 2016View details →
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Fig. 8 in Proliferation of the invasive termite Coptotermes gestroi (Isoptera: Rhinotermitidae) on Grand Cayman and overall termite diversity on the Cayman Islands

Fig. 8. Distribution of mean nearest neighbor distance obtained from Monte- Carlo simulation with 102 randomized points placed in built areas within suitable habitats.

opencc-by-4.0Sep 2016View details →
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Fig. 5 in Proliferation of the invasive termite Coptotermes gestroi (Isoptera: Rhinotermitidae) on Grand Cayman and overall termite diversity on the Cayman Islands

Fig. 5. Termite sampling localities from UF Termite Collection (for purposes of space, the geographic positions of Little Cayman and Cayman Brac are not related to that of Grand Cayman).

opencc-by-4.0Sep 2016View details →
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Fig. 9 in Proliferation of the invasive termite Coptotermes gestroi (Isoptera: Rhinotermitidae) on Grand Cayman and overall termite diversity on the Cayman Islands

Fig. 9. Areas predicted as infested by the simulation model for Coptotermes gestroi over Grand Cayman Island. Sampled termite locations in 2014 are mapped (points). Yellow, orange, and red cells indicate the>0%, ≥50%, and 100% occupancy envelopes, respectively.

opencc-by-4.0Sep 2016View details →
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Fig. 10 in Proliferation of the invasive termite Coptotermes gestroi (Isoptera: Rhinotermitidae) on Grand Cayman and overall termite diversity on the Cayman Islands

Fig. 10. Caribbean basin survey localities for all termites (blue dots) and for Microcerotermes species only (orange dots) (Source: UF Termite Collection).

opencc-by-4.0Sep 2016View details →
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Fig. 2. Hierarchical cluster analysis with 2 in Proliferation of the invasive termite Coptotermes gestroi (Isoptera: Rhinotermitidae) on Grand Cayman and overall termite diversity on the Cayman Islands

Fig. 2. Hierarchical cluster analysis with 2 (a), 3 (b), 4 (c), and 5 (d) clusters for Coptotermes gestroi over Grand Cayman Island.

opencc-by-4.0Sep 2016View details →
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Fig. 4 in Proliferation of the invasive termite Coptotermes gestroi (Isoptera: Rhinotermitidae) on Grand Cayman and overall termite diversity on the Cayman Islands

Fig. 4. Vector-type layers used to obtain a surface of unsuitable habitat for Coptotermes gestroi on Grand Cayman Island.

opencc-by-4.0Sep 2016View details →
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Fig. 3. Collection localities for Coptotermes gestroi over Grand Cayman Island and 102 in Proliferation of the invasive termite Coptotermes gestroi (Isoptera: Rhinotermitidae) on Grand Cayman and overall termite diversity on the Cayman Islands

Fig. 3. Collection localities for Coptotermes gestroi over Grand Cayman Island and 102 random points.

opencc-by-4.0Sep 2016View details →
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Fig. 1 in Proliferation of the invasive termite Coptotermes gestroi (Isoptera: Rhinotermitidae) on Grand Cayman and overall termite diversity on the Cayman Islands

Fig. 1. Coptotermes gestroi localities in the greater Caribbean Basin (Source: UF Termite Collection).

opencc-by-4.0Sep 2016View details →

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International Brain Laboratory public data

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OpenNeuro

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