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370 results for “seasonal forest”
Figure 2 from: Sánchez-Reyes UJ, Niño-Maldonado S, Clark SM, Barrientos-Lozano L, Almaguer-Sierra P (2019) Successional and seasonal changes of leaf beetles and their indicator value in a fragmented low thorn forest of northeastern Mexico (Coleoptera, Chrysomelidae). ZooKeys 825: 71-103. https://doi.org/10.3897/zookeys.825.30455
Figure 2 - Successional gradient of low thorn forest in northeastern Mexico, and location of the sampling plots.
Figure 3 from: Sánchez-Reyes UJ, Niño-Maldonado S, Clark SM, Barrientos-Lozano L, Almaguer-Sierra P (2019) Successional and seasonal changes of leaf beetles and their indicator value in a fragmented low thorn forest of northeastern Mexico (Coleoptera, Chrysomelidae). ZooKeys 825: 71-103. https://doi.org/10.3897/zookeys.825.30455
Figure 3 - Seasonal variation of community parameters of Chrysomelidae in a successional gradient of low thorn forest in northeastern Mexico. Different letters between bars indicate significant differences.
Figure 7 from: Sánchez-Reyes UJ, Niño-Maldonado S, Clark SM, Barrientos-Lozano L, Almaguer-Sierra P (2019) Successional and seasonal changes of leaf beetles and their indicator value in a fragmented low thorn forest of northeastern Mexico (Coleoptera, Chrysomelidae). ZooKeys 825: 71-103. https://doi.org/10.3897/zookeys.825.30455
Figure 7 - Suggested species of Chrysomelidae for evaluating successional time and environmental monitoring of low thorn forest in northeastern Mexico. A Centralaphthona diversa (Baly, 1877) B Cyclotrypema furcata (Olivier, 1808) C Heterispa vinula (Erichson, 1847) D Acrocyum dorsalis Jacoby, 1885.
Figure 5 from: Sánchez-Reyes UJ, Niño-Maldonado S, Clark SM, Barrientos-Lozano L, Almaguer-Sierra P (2019) Successional and seasonal changes of leaf beetles and their indicator value in a fragmented low thorn forest of northeastern Mexico (Coleoptera, Chrysomelidae). ZooKeys 825: 71-103. https://doi.org/10.3897/zookeys.825.30455
Figure 5 - Chrysomelidae species with significant indicator value of successional time in a low thorn forest fragment in northeastern Mexico. A Acallepitrix sp. 1 B Epitrix sp. 5 C Acrocyum dorsalis Jacoby, 1885 D Alagoasa jacobiana (Horn, 1889) E Asphaera sp. 1 F Babia tetraspilota texana Schaeffer, 1933 G Brachycoryna pumila Guérin-Méneville, 1844 H Centralaphthona diversa (Baly, 1877) I Chaetocnema sp. 1 J Colaspis townsendi Bowditch, 1921 K Cryptocephalus trizonatus Suffrian, 1858 L Cyclotrypema furcata (Olivier, 1808). Scale bar: 1 mm.
Figure 11 in Soldier flies (Diptera: Stratiomyidae) on semideciduous seasonal forest fragments, with a list of species for São Paulo State, Brazil, and two new records of species for the country
Figure 11 Species accumulation curve and performance of the richness estimators of the Stratiomyidae collected at Reserva Ecológica e Biológica Augusto Ruschi, Sertãozinho, São Paulo, Brazil, from May 2010 to December 2011 and in September 2014.
Figure 10 in Soldier flies (Diptera: Stratiomyidae) on semideciduous seasonal forest fragments, with a list of species for São Paulo State, Brazil, and two new records of species for the country
Figure 10 Climate and seasonal data of soldier flies collected using white roof Malaise traps at the Reserva Ecológica e Biológica de Sertãozinho, São Paulo, Brazil.
Figure 7 in Soldier flies (Diptera: Stratiomyidae) on semideciduous seasonal forest fragments, with a list of species for São Paulo State, Brazil, and two new records of species for the country
Figure 7 Stratiomyids from the Reserva Ecológica e Biológica Augusto Ruschi, Sertãozinho, São Paulo, Brazil. (a) Chloromelas sp. 1, male; (b) Myxosargus sp. 1, male; (c) Myxosargus sp. 2, male; (d) Eidalimus sp. 1, male; (e) Manotes sp. 1, male; (f) Panacris lucida, male; (g) Popanomyia sp. 1, female; (h) Psephiocera sp. 1, female; (i) Strobilapsis sp. 1, female. Scale bar, 1 mm.
Figure 6 in Soldier flies (Diptera: Stratiomyidae) on semideciduous seasonal forest fragments, with a list of species for São Paulo State, Brazil, and two new records of species for the country
Figure 6 Stratiomyids from the Reserva Ecológica e Biológica Augusto Ruschi, Sertãozinho, São Paulo, Brazil. (a) Merosargus nebulifer James, 1971 in James & McFadden, 1971, male; (b) M. opaliger Lindner, 1931, female. (c) M. tripartitus James, 1971 in James & McFadden, 1971, female; (d) Microchrysa bicolor (Wiedemann, 1830), female; (e) Pteticus testaceus (Fabricius, 1805), male; (f) Sargus fasciatus Fabricius, 1805, male; (g) S. thoracicus Macquart, 1834, male; (h) S. thoracicus, female; (i) Sargus sp. 1, male; (j) Sargus sp. 1, female; (k) Sargus sp. 2, female; (l) Glariopsis sp. 1, female. Scale bar, 1 mm.
Figure 3 in Soldier flies (Diptera: Stratiomyidae) on semideciduous seasonal forest fragments, with a list of species for São Paulo State, Brazil, and two new records of species for the country
Figure 3 Stratiomyids from the Reserva Ecológica e Biológica Augusto Ruschi, Sertãozinho, São Paulo, Brazil. (a) Heteracanthia ruficornis Macquart, 1850, female; (b) Oplachantha sp. 1, male; (c) Oplachantha sp. 1, female; (d) Barbiellinia sp. 1, male; (e) Chiromyza sp. 1, male; (f) Chiromyza sp. 1, female; (g) Cyphomyia aurifrons Wiedemann, 1830, male; (h) C. aurifrons, female; (i) C. gracilicornis Gerstaecker, 1857, male; (j) C. gracilicornis, female; (k) C. leucocephala Wiedemann, 1819, female; (l) Cyphomyia sp. 1, male. Scale bar, 1 mm.
Figure 1 in Soldier flies (Diptera: Stratiomyidae) on semideciduous seasonal forest fragments, with a list of species for São Paulo State, Brazil, and two new records of species for the country
Figure 1 Map of the area of study, with limits of all municipalities of the state of São Paulo.(a) Limits of the municipality of Sertãozinho and studied area; (b) Satellite image of the Reserva Ecológica e Biológica Augusto Ruschi, with head office and research buildings outlined in white, larger fragments outlined in red, and numbers 1 and 2 represent the areas of sampling.
Figure 2 in Soldier flies (Diptera: Stratiomyidae) on semideciduous seasonal forest fragments, with a list of species for São Paulo State, Brazil, and two new records of species for the country
Figure 2 Sampling sites at the Reserva Ecológica e Biológica Augusto Ruschi, Sertãozinho, São Paulo, Brazil. (a-c) Areas near an artificial lake, fragment 2; (d) Bottle traps set up in the field; (e) Black roof Malaise trap; (f) White roof Malaise trap.
Fig. 1 in Seasonal Variations in the Assembly of Dung Beetles (Coleoptera: Geotrupidae and Scarabaeidae) Attracted to Macaque Feces in Temperate Forests in Japan
Fig. 1. Map of the study sites in Japan.
FIGURE 3 in A new species of Anthurium Schott (Araceae) in a seasonal semideciduous forest in Espírito Santo State, Brazil
FIGURE 3. Type locality of A. cachoeirense. Adapted from Brasil (2007).
FIGURE 1 in Biogeographical identity of the Mesoamerican dominion with emphasis on seasonally dry tropical forests
FIGURE 1. Geographical extension of the Mesoamerican dominion.
Seasonality affects specialisation of a temperate forest herbivore community
<p>Understanding spatiotemporal trends on insect-plant interaction networks is essential to unveil the ecological and evolutionary processes driving herbivore specialisation. However, community studies accounting for temporal dynamics in host-plant specialisation of herbivorous insects are surprisingly scarce.</p> <p>Here, we provide the background data which were used to investigate how seasonality affects specialisation of a temperate forest herbivore community. This dataset results from a comprehensive sampling of more than 4,700 folivorous caterpillars associated with 16 deciduous tree species in eastern North America. Specifically, we provide three abundance-based plant-caterpillar interaction matrices. Each interaction matrix represents a six-week period of the growing season. These time periods are defined as follow: early season, midseason, and late season.</p> <p>We observed a significantly less specialised herbivore fauna in the early season than in the two subsequent summer seasons. We further found that the seasonal increase in specialisation was driven by a remarkable turnover in species composition rather than by shifts in guild structure or intraspecific changes in diet breadth of the herbivores.</p>
Fig. 1 in Spatial, seasonal and ontogenetic variation in the diet of Astyanax aff. fasciatus (Ostariophysi: Characidae) in an Atlantic Forest river, Southern Brazil
Fig. 1. Monthly average precipitation and temperature for the rio das Pedras region, Guarapuava, PR, Brazil. (Data refer to the period of January 1976 to December 2000). Source: SIMEPAR.
Fig. 7 in Spatial, seasonal and ontogenetic variation in the diet of Astyanax aff. fasciatus (Ostariophysi: Characidae) in an Atlantic Forest river, Southern Brazil
Fig. 7. Mean ± S.D. Intestinal quotient (I q) of the three established standard length classes for Astyanax aff. fasciatus at two sites on the rio das Pedras. (SL1: <50 mm; SL2: 51-75 mm and SL3:> 76 mm).
Cross-scale assessment of the impacts of chronic seasonal drought and episodic typhoons on subtropical montane cloud forests
<p>The data that support the findings of this study.</p>
Data for: Long-term surveys support declines in early-season forest plants used by bumble bees
Open the record for dataset details and reuse information.
Data from: Tough fishing and severe seasonal food insecurity in Amazonian flooded forests
Open the record for dataset details and reuse information.
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International Brain Laboratory public data
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OpenNeuro
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