Understanding how environmental heterogeneity and elevation drives the distribution of woody communities across vegetation types within the campo rupestre in South America

2021 ◽  
Vol 18 (5) ◽  
pp. 1192-1207
Author(s):  
Marcelo Leandro Bueno ◽  
Vanessa Leite Rezende ◽  
Luiza Fonseca A. De Paula ◽  
João Augusto Alves Meira-Neto ◽  
José Roberto Rodrigues Pinto ◽  
...  
Phytotaxa ◽  
2021 ◽  
Vol 486 (1) ◽  
pp. 1-105
Author(s):  
LAURA C. DE LANNOY ◽  
AYRTON I. DE OLIVEIRA ◽  
RENATO GOLDENBERG ◽  
DUANE F. LIMA

Myrtaceae is one of the largest families in number of species within the order Myrtales and one of the richest families in Brazil. Myrcia is the fourth largest genus of Myrtaceae, with approximately 770 species distributed from Central America and the Caribbean to southern South America. In Brazil Myrcia is represented by 397 species, of which 309 are endemic. In this study, we present the taxonomic treatment for all species of Myrcia that occur in Paraná state, Brazil. Analyses of herbarium specimens, online databases, and bibliography were performed. Fifty-three species of Myrcia occur in Paraná, distributed in all vegetation types. Twenty-three names were excluded from previous lists of species or listed as doubtful species. Neither of the recorded species is endemic to Paraná, but this state is the southern and northern limit of distribution of six and two species, respectively. We present an identification key, taxonomic descriptions, figures, maps, and comments on phenology, habitat, and morphology for each species.


2014 ◽  
Vol 11 (3) ◽  
pp. 4591-4636 ◽  
Author(s):  
E. M. Veenendaal ◽  
M. Torello-Raventos ◽  
T. R. Feldpausch ◽  
T. F. Domingues ◽  
F. Gerard ◽  
...  

Abstract. Through interpretations of remote sensing data and/or theoretical propositions, the idea that forest and savanna represent "alternative stable states" is gaining increasing acceptance. Filling an observational gap, we present detailed stratified floristic and structural analyses for forest and savanna stands mostly located within zones of transition (where both vegetation types occur in close proximity) in Africa, South America and Australia. Woody plant leaf area index variation was related in a similar way to tree canopy cover for both savanna and forest with substantial overlap between the two vegetation types. As total woody plant canopy cover increased, so did the contribution of middle and lower strata of woody vegetation to this total. Herbaceous layer cover also declined as woody cover increased. This pattern of understorey grasses and herbs being progressively replaced by shrubs as canopy closure occurs was found for both savanna and forests and on all continents. Thus, once subordinate woody canopy layers are taken into account, a less marked transition in woody plant cover across the savanna-forest species discontinuum is observed compared to that implied when trees of a basal diameter > 0.1m are considered in isolation. This is especially the case for shrub-dominated savannas and in taller savannas approaching canopy closure. An increased contribution of forest species to the total subordinate cover is also observed as savanna stand canopy closure occurs. Despite similarities in canopy cover characteristics, woody vegetation in Africa and Australia attained greater heights and stored a greater concentration of above ground biomass than in South America. Up to three times as much aboveground biomass is stored in forests compared to savannas under equivalent climatic conditions. Savanna/forest transition zones were also found to typically occur at higher precipitation regimes for South America than for Africa. Nevertheless, coexistence was found to be confined to a well-defined edaphic/climate envelope consistent across all three continents with both soil and climate playing a role as the key determinants of the relative location of forest and savanna. Taken together these observations do not lend support the notion of alternate stable states mediated through fire-feedbacks as the prime force shaping the distribution of the two dominant vegetation types of the tropical lands.


Author(s):  
Kenneth R. Young ◽  
Paul E. Berry

South America’s shape, size, and geographic position, now and in the past, have acted to influence the development of diverse coverings of land surfaces with plants of different sizes, adaptations, and origins. Underlying geologic structures have been exposed to weathering regimes, thereby resulting in a multiplicity of landforms, soil types, and ecological zones. The most notable large-scale features are the Andes, which curl along the western margin of the continent, and the broad swath of the Amazon lowlands in the equatorial zone. However, there are also extensive, more ancient mountain systems in the Brazilian Shield of east-central Brazil and the Guiana Shield in northern South America. The interplay of environmental factors has given rise to a panoply of vegetation types, from coastal mangroves to interior swamplands, savannas, and other grasslands, deserts, shrublands, and a wide array of dry to moist and lowland to highland forest types. The narrower southern half of South America is also complex vegetationally because of the compression of more vegetation types into a smaller area and the diverse climatic regimes associated with subtropical and temperate middle latitudes. Alexander von Humboldt began to outline the major features of the physical geography of South America in his extensive writings that followed his travels in the early nineteenth century (von Humboldt, 1815–1832). For example, he first documented the profound influences of contemporary and historical geologic processes such as earthquakes and volcanoes, how vegetation in mountainous areas changes as elevation influences the distributions of plant species, and the effect of sea surface temperatures on atmospheric circulation and uplift and their impacts on precipitation and air temperatures (Botting, 1973; Faak and Biermann, 1986). His initial insights, in combination with modern observations (Hueck and Seibert, 1972; Cabrera and Willink, 1973; Davis et al., 1997; Lentz, 2000), still serve to frame our synthesis of the major vegetation formations of South America. In this chapter, we relate vegetation formations to spatial gradients of soil moisture and elevation in the context of broad climatic and topographic patterns.


2012 ◽  
Vol 12 (4) ◽  
pp. 125-129 ◽  
Author(s):  
Rafael Vieira Nunes ◽  
Marina Regina Frizzas ◽  
Fernando Zagury Vaz-de-Mello

Our aim was to characterize the Scarabaeinae fauna from a rupestrian field formation at APA de Cafuringa, DF, Brazil. We made seven samples between 2007 and 2009 using baited pitfall traps. We collected 602 individuals belonging to 27 species and 13 genera, of which 17 were identified at species level. The majority of species caught has wide geographical distribution in Brazil and South America and do not seem to be specialized in 'campo rupestre' formation. Two species, Canthidium marseuli and Canthon lamproderes have restricted geographical distribution, being present in the central Brazilian highlands. C. marseuli and C. lamproderes are probably restricted to rupestrian fields since they have been registered only for this formation in Brazil, which indicates that these species need attention in relation to the conservation of theirs populations and habitats.


Oecologia ◽  
2019 ◽  
Vol 192 (1) ◽  
pp. 191-200 ◽  
Author(s):  
Vanessa Leite Rezende ◽  
Vanessa Pontara ◽  
Marcelo Leandro Bueno ◽  
Eduardo van den Berg ◽  
Ary Teixeira de Oliveira-Filho

Zootaxa ◽  
2021 ◽  
Vol 4964 (3) ◽  
pp. 401-442
Author(s):  
MARYSOL TRUJANO-ORTEGA ◽  
CURTIS J. CALLAGHAN ◽  
ARTURO ARELLANO-COVARRUBIAS ◽  
ARMANDO LUIS-MARTÍNEZ ◽  
OMAR ÁVALOS-HERNÁNDEZ ◽  
...  

We present a synthesis of the existing information on the genus Emesis Fabricius in Mexico concerning biogeographical patterns and taxonomical aspects. Emesis is the most diverse genus of Emesidini with 57 species and subspecies, with Mexico as the northern limit of this Neotropical genus. We analyzed 5434 specimens of the Lepidoptera Collection of the MZFC, UNAM and compared them with specimens from collections of Mexico, Central and South America. Taxonomic determination and corroboration were made by analysis of wing patterns and genitalia. Geographic distribution and phenology were obtained from the database MARIPOSA. We present an updated list of Emesis of Mexico, with 17 species and subspecies. For each species, we provide information on phenology, geographic, altitudinal, and vegetation distributions. We discuss taxonomic and undersampling concerns for some species, as well as spatial and temporal patterns with special reference to vegetation types and biogeographic provinces in Mexico. 


1989 ◽  
Vol 5 (3) ◽  
pp. 309-322 ◽  
Author(s):  
Jaime Cavelier ◽  
Guillermo Goldstein

ABSTRACTFog interception and rainfall were measured during one year in three elfin cloud forests on small mountains along the Caribbean coast of South America and one in the Venezuelan Andes. (1) While rainfall increases from west to east in the small mountains along the coast, fog interception decreases. In 1985, the total annual rainfall and fog interception were 853 mm and 796 mm in the cloud forest of Serrania de Macuira, 1630 mm and 518 mm in Cerro Santa Ana and, 4461 mm and 480 mm in Cerro Copey. In the Andean forest of El Zum-bador, the 1985 rainfall was 1983 mm and the annual fog interception was only 72 mm. (2) Fog interception seems to be an important source of water to the elfin cloud forests of the small mountains which are surrounded by dry vegetation types and where the rainfall regime is highly seasonal. (3) Fog interception increases with altitude (in the same mountain), exposure (windward slopes) and leaf inclination. These variations of fog interception could partially explain the observed distribution of epiphytic flora in some of these cloud forests.


1993 ◽  
Vol 6 (5) ◽  
pp. 457 ◽  
Author(s):  
PJ Garnock-Jones

The southern segregates of Veronica (Hebe, Parahebe, Chionohebe, Dementia, and Detzneria) form a monophyletic assemblage of c. 144 species found in New Guinea, Australia, New Zealand, Rapa, and South America. Most of the species occur in New Zealand, where Hebe is the largest genus and a characteristic member of many vegetation types. Cladistic analysis of the Hebe complex, based on 45 characters and 22 terminal taxa, indicates that: (1) Hebe is monophyletic if Hebe 'Paniculatae' is excluded and H. formosa is included; (2) Parahebe is paraphyletic; (3) Chionohebe is monophyletic, but is part of a larger clade which includes alpine Parahebe and possibly the monotypic Detzneria; (4) Hebe 'Paniculatae', Derwentia, and New Guinea Parahebe are monophyletic basal groups in the complex. According to this study, recognition of monophyletic genera would require six genera in the complex, supporting the recognition of Derwentia and separation of Hebe 'Paniculatae' from Hebe. Leonohebe Heads is considered polyphyletic and is not accepted; new combinations are provided for two species of Leonohebe with no name at species rank in Hebe. Competing biogeographic hypotheses have implied (1) a Gondwanan origin, or (2) migration from South-east Asia via New Guinea. An origin in Australasia from Asian ancestors best explains the topology of the basal parts of the cladogram, but at least seven dispersal events from New Zealand are postulated to explain the occurrence of species of Hebe in South America and Rapa and Parahebe, Hebe, and Chionohebe in Australia. An hypothesis which did not allow dispersal would require that nearly all the evolution in the complex occurred before the Tertiary, and hardly any since.


2015 ◽  
Vol 12 (10) ◽  
pp. 2927-2951 ◽  
Author(s):  
E. M. Veenendaal ◽  
M. Torello-Raventos ◽  
T. R. Feldpausch ◽  
T. F. Domingues ◽  
F. Gerard ◽  
...  

Abstract. Through interpretations of remote-sensing data and/or theoretical propositions, the idea that forest and savanna represent "alternative stable states" is gaining increasing acceptance. Filling an observational gap, we present detailed stratified floristic and structural analyses for forest and savanna stands located mostly within zones of transition (where both vegetation types occur in close proximity) in Africa, South America and Australia. Woody plant leaf area index variation was related to tree canopy cover in a similar way for both savanna and forest with substantial overlap between the two vegetation types. As total woody plant canopy cover increased, so did the relative contribution of middle and lower strata of woody vegetation. Herbaceous layer cover declined as woody cover increased. This pattern of understorey grasses and herbs progressively replaced by shrubs as the canopy closes over was found for both savanna and forests and on all continents. Thus, once subordinate woody canopy layers are taken into account, a less marked transition in woody plant cover across the savanna–forest-species discontinuum is observed compared to that inferred when trees of a basal diameter > 0.1 m are considered in isolation. This is especially the case for shrub-dominated savannas and in taller savannas approaching canopy closure. An increased contribution of forest species to the total subordinate cover is also observed as savanna stand canopy closure occurs. Despite similarities in canopy-cover characteristics, woody vegetation in Africa and Australia attained greater heights and stored a greater amount of above-ground biomass than in South America. Up to three times as much above-ground biomass is stored in forests compared to savannas under equivalent climatic conditions. Savanna–forest transition zones were also found to typically occur at higher precipitation regimes for South America than for Africa. Nevertheless, consistent across all three continents coexistence was found to be confined to a well-defined edaphic–climate envelope with soil and climate the key determinants of the relative location of forest and savanna stands. Moreover, when considered in conjunction with the appropriate water availability metrics, it emerges that soil exchangeable cations exert considerable control on woody canopy-cover extent as measured in our pan-continental (forest + savanna) data set. Taken together these observations do not lend support to the notion of alternate stable states mediated through fire feedbacks as the prime force shaping the distribution of the two dominant vegetation types of the tropical lands.


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