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Figure 5 in Ionic homeostasis, biochemical components and yield of Italian zucchini under nitrogen forms and salt stress

Figure 5. Italian zucchini plants fertilized with different forms of nitrogen and irrigated with saline waters.

Figure 2 in Ionic homeostasis, biochemical components and yield of Italian zucchini under nitrogen forms and salt stress

Figure 2. Accumulation of nitrogen (N) (A), phosphorus (P) (B), potassium (K) (C), calcium (Ca) (D) and magnesium (Mg) (E) in Italian zucchini plants irrigated with saline waters. * - Significant at 0.05 probability level (p<0.05).

Figure 4. Chlorophyll b in Ionic homeostasis, biochemical components and yield of Italian zucchini under nitrogen forms and salt stress

Figure 4. Chlorophyll b content (A) and electrolyte leakage (B) in Italian zucchini plants nourished with different forms of nitrogen and irrigated with saline waters. Means followed by different letters indicate significant difference by Tukey test at 0.05 probability level.

Figure 3 in Ionic homeostasis, biochemical components and yield of Italian zucchini under nitrogen forms and salt stress

Figure 3. Accumulation of sodium (Na+) (A), sodium/potassium ratio (Na+/K+) (B), sodium/calcium ratio (Na+/Ca++) (C and D) and sodium/ magnesium ratio (Na+/Mg++) (E and F) in Italian zucchini plants nourished with different forms of nitrogen and irrigated with saline waters. Means followed by different letters indicate significant difference by Tukey test at 0.05 probability level. * and ns - Significant at 0.05 probability level (p<0.05) and not significant (p>0.05), respectively.

Figure 1 in Ionic homeostasis, biochemical components and yield of Italian zucchini under nitrogen forms and salt stress

Figure 1. Accumulation of nitrogen - N (A), phosphorus - P (B), potassium - K (C), calcium - Ca (D) and magnesium - Mg (E) in Italian zucchini plants fertilized with different forms of nitrogen and irrigated with saline water. Means followed by different letters indicate significant difference by Tukey test at 0.05 probability level.

opencc-by-4.0May 2022View details →

Fig. 1 in First record of Aphaereta difficilis Nixon, 1939 from Italy with a key to the Italian species of the genus (Hymenoptera: Braconidae, Alysiinae)

Fig. 1 – Aphaereta difficilis Nixon, 1939 (female). A, Habitus, lateral view; B, Head and mesosoma, lateral view; C, Antenna, basal segments; D, Head, frontal view; E, Head and mesonotum, dorsal view; F, Legs, metasoma and ovipositor, lateral view.

Fig. 15 in New records of Adelidae from forested habitats of Calabria (South Italy) with an update of the Italian ckecklist (Lepidoptera: Adeloidea)

Fig. 15 – Distribution of Adelidae in the Calabria region. Map created with SimpleMappr (http://www.simplemappr.net).

Figs 11-12 in New records of Adelidae from forested habitats of Calabria (South Italy) with an update of the Italian ckecklist (Lepidoptera: Adeloidea)

Figs 11-12 – Comparison of antennae in the genus Nematopogon. 11, N. robertella, Pietra del Signore; 12, N. garganellus, Bosco dei Gesuiti.

Fig. 10 in New records of Adelidae from forested habitats of Calabria (South Italy) with an update of the Italian ckecklist (Lepidoptera: Adeloidea)

Fig. 10 – Male genitalia of Nematopogon robertella, Pietra del Signore (microscope slide: CREA-0237).

Figs 1-8 in New records of Adelidae from forested habitats of Calabria (South Italy) with an update of the Italian ckecklist (Lepidoptera: Adeloidea)

Figs 1-8 – Adults of Adelidae. 1, Nemophora metallica, Croce di Magara, 17mm; 2, Nemophora scopolii, Croce di Magara, 21mm; 3, Adela mazzolella, Righio, 12mm; 4, Adela reaumurella, Passo della Crocetta, 15mm; 5, Nematopogon robertella, Pietra del Signore, 15mm; 6, Nematopogon sericinellus, Carraci, 14mm; 7, Nematopogon swammerdamella, Timpone Magara, 22mm; 8, Nematopogon garganellus, Bosco Gesuiti, 19mm.

Fig. 5 in Morphological disparity in Plio-Pleistocene large carnivore guilds from Italian peninsula

Fig. 5. Disparity values computed for morphospace of each extant and Plio−Pleistocene large carnivore guild. Lines define 95% confidence interval under 999 randomizations. Extant is for all living taxa (N = 34) while Plio−Pleistocene stand for all fossil taxa (N = 23). Kruger, Africa is for Africa, Gunung Lensung, Indonesia for Indonesia, Otishi for South America,, Yellowstone for North America, Krokonose for Czech Republic. Fossil communities are ordered from the youngest to the oldest: Aurelian, 0.3 Ma; Galerian 3, 0.45 Ma; Galerian 2, 0.6 Ma; Galerian 1, 0.8 Ma; Pirro, 1.1 Ma; Valdi− Chiana, 1.5 Ma; Up Valdarno, 1.9 Ma; Montopoli, 2.6 Ma; Triversa, 3.2 Ma.

Fig. 3 in Morphological disparity in Plio-Pleistocene large carnivore guilds from Italian peninsula

Fig. 3. Scatter plots of RW1 (X axis, scale −0.40 / +0.40) versus RW2 (Y axis, scale −0.40 / +0.40). Each extant large carnivore guild is highlighted by closed circles. The Kruger, Africa guild represents Africa, Krokonose is for Czech Republic, Gunung Lensung, Indonesia Lensung for Indonesia, Otishi for South America and Yellowstone for North America.

Fig. 4 in Morphological disparity in Plio-Pleistocene large carnivore guilds from Italian peninsula

Fig. 4. Scatter plots of RW1 (X axis, scale −0.40 / +0.40) versus RW2 (Y axis, scale −0.40 / +0.40). Each Plio−Pleistocene carnivore guild is highlighted by closed circles. Guild are representative of distinct Paleo−Communities trough time: Triversa, 3.2 Ma; Montopoli, 2.6 Ma; Up Valdarno, 1.9 Ma; ValdiChiana, 1.5 Ma; Pirro, 1.1 Ma; Galerian 1, 0.8 Ma; Galerian 2, 0.6 Ma; Galerian 3, 0.45 Ma; and Aurelian, 0.3 Ma.

Fig. 6 in Morphological disparity in Plio-Pleistocene large carnivore guilds from Italian peninsula

Fig. 6. Scatter plot of log number of artiodactyls vs. large carnivore disparity values. Open circles, extant ecosystems; closed, fossil ecosystems. A linear trendline is placed on extant data points. Open circles represent extant ecosystem including Kruger, Africa, Africa; Gunung Lensung, Indonesia Lensung, Indonesia; Otishi, South America; Yellowstone, North America; Krokonose, Czech Republic. Closed circles are fossil communities: Triversa, 3.2 Ma; Montopoli, 2.6 Ma; Up Valdarno, 1.9 Ma; Valdi− Chiana, 1.5 Ma; Pirro, 1.1 Ma; Galerian 1, 0.8 Ma; Galerian 2, 0.6 Ma; Galerian 3, 0.45 Ma; and Aurelian, 0.3 Ma.

opencc-by-4.0Dec 2020View details →

Fig. 2 in Records of Solenosthedium bilunatum (Lefèbvre, 1827) on the Italian island of Ustica and the Spanish island of Ibiza (Hemiptera: Heteroptera: Scutelleridae).

Fig. 2.- Adult of Solenosthedium bilunatum (Lefèbvre, 1827), Sant Antoni de Portmany, Ibiza, Spain. (Photo: Juan Pérez).

opencc-by-4.0Apr 2024View details →

Fig. 2 in Short Communication A new record of the rare Hypleurochilus bananensis (Poll 1959) (Actinopterygii: Blenniidae) with a review of its distribution and ecology in Italian seas

Fig. 2 - Individuals of H. bananensis observed in the Tyrrhenian Sea in the present study observed on 30th December 2023 (A and C) and on 29th December 2023 (B). / Individui di Hypleurochilus bananensis osservati il 30 dicembre 2023 (A e C) e il 29 dicembre 2023 (B) e riportati nel presente studio (Mar Tirreno).

opencc-by-4.0Apr 2024View details →

Fig. 1 in Short Communication A new record of the rare Hypleurochilus bananensis (Poll 1959) (Actinopterygii: Blenniidae) with a review of its distribution and ecology in Italian seas

Fig. 1 - Known distribution of Hypleurochilus bananensis in Italian waters updated to January 2024 (records of this study are included). Black circles indicate areas where the species was recorded. For details see Table 1. / Distribuzione nota di Hypleurochilus bananensis nelle acque italiane aggiornata al gennaio 2024 (sono incluse le registrazioni di questo studio). I cerchi neri indicano le aree in cui la specie è stata registrata. Per i dettagli si veda la Tabella 1.

opencc-by-4.0Oct 2022View details →

Fig. 1 in Short Communication Contribution to the knowledge of Ypsolophidae from forested habitats of Southern Italy with an update of the Italian checklist of the genus Ypsolopha Latreille 1796 (Lepidoptera: Yponomeutoidea)

Fig. 1 - Species of the genus Ypsolopha found in Calabria. / Specie del genere Ypsolopha trovate in Calabria. a) Y. alpella, 01.X.2019, Campanella, Sellia, Catanzaro. b) Y. mucronella, 10.V.2016, Il Palmento, Serra San Bruno, Vibo Valentia. c) Y. nemorella, 7.VIII.2013, Fosso Cucolo, Donnici, Cosenza. d) Y. parenthesella, 31.VIII.2016, Piano del minatore, Saracena, Cosenza. e) Y. persicella, 9.XI.2015, Glicarello, Montalto Uffugo, Cosenza. f) Y. scabrella, 17.VIII.2017, Sciortaglie, Alessandria del Carretto, Cosenza. g) Y. sequella, 19.VII.2017, Sciortaglie, Alessandria del Carretto, Cosenza. h) Y. ustella, 25.IX.2019, Coturelle, Albi, Catanzaro. i) Y. vittella, 5.VIII.2013, Pianette, Dipignano, Cosenza.

opencc-by-4.0Oct 2022View details →

Fig. 2 in The western European hedgehog Erinaceus europaeus L. 1758 on San Pietro Island (southern Sardinia, Italy) and an updated review of its presence on the Italian small islands

Fig. 2 - The small Italian islands with evidence of western European hedgehog presence. Thick-bordered circles: probable occurrence of stable populations; thin-bordered circles: only occasional presence of individuals (low probability of short-term persistence). See Tab. 2 for details. / Evidenze di presenza di riccio europeo occidentale nelle piccole isole italiane. Cerchi con bordo spesso: probabile presenza di popolazioni stabili; cerchi con bordo sottile: probabile presenza di singoli individui (bassa probabilità di persistenza a breve termine). Vedasi Tab. 2 per dettagli. 1) Elba; 2) Capraia; 3) Pianosa; 4) Alicudi; 5) Salina; 6) Favignana; 7) Ustica; 8) Procida; 9) Vivara; 10) Capraia; 11) La Maddalena; 12) Asinara; 13) San Pietro.