Wildlife farming: an alternative to unsustainable hunting and deforestation in Neotropical forests?

2011 ◽  
Vol 20 (7) ◽  
pp. 1385-1397 ◽  
Author(s):  
Selene S. C. Nogueira ◽  
Sérgio L. G. Nogueira-Filho
Oikos ◽  
1994 ◽  
Vol 71 (2) ◽  
pp. 279 ◽  
Author(s):  
S. Joseph Wright ◽  
Matthew E. Gompper ◽  
Bonifacio DeLeon

2001 ◽  
Vol 12 (1-2) ◽  
pp. 37-60 ◽  
Author(s):  
Florencia Montagnini ◽  
Bryan Finegan ◽  
Diego Delgado ◽  
Beatriz Eibl ◽  
Lilian Szczipanski ◽  
...  

Biotropica ◽  
2004 ◽  
Vol 36 (1) ◽  
pp. 7-19 ◽  
Author(s):  
Saara J. DeWalt ◽  
Jerome Chave
Keyword(s):  

2013 ◽  
Vol 27 (1) ◽  
pp. 129
Author(s):  
Edilson Caron ◽  
Cibele S. Ribeiro-Costa ◽  
Alfred F. Newton

Rove beetles of the genus Piestus Gravenhorst, 1806 are commonly captured under the bark of or inside decaying logs from Neotropical forests. Piestus belongs to the subfamily Piestinae, historically an ill-defined dumping-ground for Staphylinidae defined by plesiomorphic characters, but which has gradually been restricted in concept and currently includes only six additional extant genera worldwide. Piestinae in this restricted sense has been considered a probably monophyletic subfamily, but its status and phylogenetic position, as a possible sister-group of Osoriinae within the recently proposed Oxyteline group of staphylinid subfamilies, are uncertain and need confirmation. The main aim of the present study was to provide a morphological cladistic analysis and complete taxonomic revision of Piestus, which, as the type and most speciose genus of Piestinae, is critical for future phylogenetic studies involving the subfamily. In our study, the monophyly of Piestus is established and phylogenetic relationships among its species are proposed based on 70 adult morphological characters. Piestus is supported by 11 synapomorphies and high branch support. All species of Piestus are revised and the genus is redefined. The genus contains 43 species, including 13 species described here for the first time. The previously proposed subgenera Antropiestus Bernhauer, 1917, Eccoptopiestus Scheerpeltz, 1952, Elytropiestus Scheerpeltz, 1952, Lissopiestus Scheerpeltz, 1952, Piestus s. str., Trachypiestus Scheerpeltz, 1952 and Zirophorus Dalman, 1821 have not been confirmed, as they were found to be poly- or paraphyletic, or are here removed from Piestus, and therefore subgenera are not used. The main taxonomic changes are as follows. Lissopiestus, syn. nov. is proposed as new synonym of Eleusis Laporte, 1835 and its species, E. interrupta (Erichson, 1840), comb. rest., is transferred again to that genus. Antropiestus, syn. nov. and Eccoptopiestus, syn. nov. are proposed as new synonyms of Hypotelus Erichson, 1839 and their species, H. laevis (Solsky, 1872), comb. nov. and H. andinus (Bernhauer, 1917), comb. nov., are transferred to Hypotelus. Fourteen new synonymies are proposed (valid species listed first): P. lacordairei Laporte, 1835 = Z. furcatus Sharp, 1887, syn. nov.; P. capricornis Laporte, 1835 = P. frontalis Sharp, 1876, syn. nov.; P. pennicornis Fauvel, 1864 = P. plagiatus Fauvel, 1864, syn. nov.; P. rectus Sharp, 1876, syn. nov.; P. pygialis Fauvel, 1902, syn. nov.; P. surinamensis Bernhauer, 1928, syn. nov.; P. minutus Erichson, 1840 = P. nigrator Fauvel, 1902, syn. nov.; P. sulcatus Gravenhorst, 1806 = P. sanctaecatharinae Bernhauer, 1906, syn. nov.; P. condei Wendeler, 1955, syn. nov.; P. gounellei Fauvel, 1902 = P. wasmanni Fauvel, 1902, syn. nov.; P. mexicanus Laporte, 1835 = P. alternans Sharp, 1887, syn. nov.; P. aper Sharp, 1876 = P. schadei Scheerpeltz, 1952, syn. nov.; P. angularis Fauvel, 1864 = P. crassicornis Sharp, 1887, syn. nov.; H. andinus (Bernhauer, 1917) = P. strigipennis Bernhauer, 1921, syn. nov. One species is revalidated: P. fronticornis (Dalman, 1821), stat. rev., and one synonym is restored: P. penicillatus (Dalman, 1821) = P. erythropus Erichson, 1840, syn. rest. Neotypes are designated for P. lacordairei Laporte, 1835 and Oxytelus bicornis Olivier, 1811, and lectotypes are designated for P. puncticollis Fauvel, 1902, P. capricornis variety muticus Fauvel, 1902, P. zischkai Scheerpeltz, 1951, P. pennicornis Fauvel, 1864, P. plagiatus Fauvel, 1864, P. pygmaeus Laporte, 1835, P. niger Fauvel 1864, P. minutus Erichson, 1840, P. nigratror Fauvel, 1902, P. sulcatus Gravenhorst, 1806, P. sanctaecatharinae Bernhauer, 1906, P. sulcipennis Scheerpeltz, 1952, P. aper Sharp, 1876, P. schadei Scheerpeltz, 1952 and P. andinus Bernhauer, 1917.


2015 ◽  
Vol 75 (4 suppl 1) ◽  
pp. 126-135 ◽  
Author(s):  
T. N. Thel ◽  
P. H. R. Teixeira ◽  
R. M. Lyra-Neves ◽  
W. R. Telino-Júnior ◽  
J. M. R. Ferreira ◽  
...  

Abstract Guans are large frugivorous birds that inhabit Neotropical forests and play a fundamental role in seed dispersal and forest regeneration. Despite their ecological importance, the natural populations of these birds are increasingly threatened by deforestation and hunting pressure. The present study was conducted in the Araripe National Forest, Ceará (Brazil), with the objective of estimating population parameters (density and total population size) in the Rusty-margined Guan (Penelope superciliaris) and the White-browed Guan (Penelope jacucaca), as well as providing data on their feeding ecology, including seasonal variation and fruit morphology. The study was based on the monthly collection of data between November, 2011, and October, 2012. Population parameters were estimated using line transect surveys, while feeding ecology was studied by direct observation, and the collection of plant and fecal samples. The estimated population density of P. superciliaris was 19.17 individuals/km2 (CV=13.98%), with a mean of 0.13 sightings per 10 km walked. Penelope jacucaca was not encountered during the surveys. A total of 14 plant species were recorded in the diet of P. superciliaris, 12 by direct observation, and two from fecal samples. Fruit diameter varied from 6.3±1.35 mm (Miconia albicans) to 29.9±1.7 mm (Psidium sp.). Yellow was the most frequent fruit color (41.6%, n=5), with two species each (16.6%) providing black, green, and red fruits. Fleshy fruits of the baccate (50.0%, n=6) and drupe (33.3%, n=4) types were the most consumed. The data on population parameters and feeding ecology collected in the present study provide an important database for the development of effective management strategies by environmental agencies for the conservation of the populations of the two guan species.


2002 ◽  
Vol 357 (1421) ◽  
pp. 667-681 ◽  
Author(s):  
Ricard V. Solé ◽  
David Alonso ◽  
Alan McKane

Why are some ecosystems so rich, yet contain so many rare species? High species diversity, together with rarity, is a general trend in neotropical forests and coral reefs. However, the origin of such diversity and the consequences of food web complexity in both species abundances and temporal fluctuations are not well understood. Several regularities are observed in complex, multispecies ecosystems that suggest that these ecologies might be organized close to points of instability. We explore, in greater depth, a recent stochastic model of population dynamics that is shown to reproduce: (i) the scaling law linking species number and connectivity; (ii) the observed distributions of species abundance reported from field studies (showing long tails and thus a predominance of rare species); (iii) the complex fluctuations displayed by natural communities (including chaotic dynamics); and (iv) the species–area relations displayed by rainforest plots. It is conjectured that the conflict between the natural tendency towards higher diversity due to immigration, and the ecosystem level constraints derived from an increasing number of links, leaves the system poised at a critical boundary separating stable from unstable communities, where large fluctuations are expected to occur. We suggest that the patterns displayed by species–rich communities, including rarity, would result from such a spontaneous tendency towards instability.


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