Ecological Studies on the Rain Forest of Southern Nigeria: I. The Structure and Floristic Composition of the Primary Forest

1939 ◽  
Vol 27 (1) ◽  
pp. 1 ◽  
Author(s):  
P. W. Richards
2021 ◽  
Vol 8 (1) ◽  
Author(s):  
Francesco Maria Sabatini ◽  
Hendrik Bluhm ◽  
Zoltan Kun ◽  
Dmitry Aksenov ◽  
José A. Atauri ◽  
...  

AbstractPrimary forests, defined here as forests where the signs of human impacts, if any, are strongly blurred due to decades without forest management, are scarce in Europe and continue to disappear. Despite these losses, we know little about where these forests occur. Here, we present a comprehensive geodatabase and map of Europe’s known primary forests. Our geodatabase harmonizes 48 different, mostly field-based datasets of primary forests, and contains 18,411 individual patches (41.1 Mha) spread across 33 countries. When available, we provide information on each patch (name, location, naturalness, extent and dominant tree species) and the surrounding landscape (biogeographical regions, protection status, potential natural vegetation, current forest extent). Using Landsat satellite-image time series (1985–2018) we checked each patch for possible disturbance events since primary forests were identified, resulting in 94% of patches free of significant disturbances in the last 30 years. Although knowledge gaps remain, ours is the most comprehensive dataset on primary forests in Europe, and will be useful for ecological studies, and conservation planning to safeguard these unique forests.


2003 ◽  
Vol 19 (2) ◽  
pp. 209-214 ◽  
Author(s):  
Jean-François Mauffrey ◽  
François Catzeflis

Stable isotopes are commonly used in ecological studies to infer food resources (Ambrose & DeNiro 1986, Bocherens et al. 1990,1991,1994;Yoshinaga et al. 1991) since isotopic composition is conserved during the feeding process. Moreover,for herbivorous (sensu lato) species, it is often possible to identify the main resource because different photosynthetic pathways generate different values of carbon isotope ratios (Park & Epstein 1961, Sternberg et al. 1984). This allows the characterization of broad biota such as savannas or forest and discrimination of grazers from sympatric folivorous species (DeNiro & Epstein 1978).


2002 ◽  
Vol 32 (2) ◽  
pp. 277-277 ◽  
Author(s):  
João Olegário Pereira de CARVALHO

Changes in the floristic composition over an eight-year period in a logged area at the Tapajós National Forest in Brazilian Amazonia arc discussed. Two treatments of different intensities of logging were compared with an undisturbed (control) forest. Data were collected from permanent sample-plots. The effects of logging on floristic composition were stronger in the more heavily logged treatment. The number of species decreased immediately after logging, but started to increase before the fifth year after logging and was higher at the end of the study period than before logging. The more heavily logged plots responded more to disturbances, as judged by the increase in the number of species during the period after logging. This forest appears to recover its initial floristic composition after disturbance without intervention.


1995 ◽  
Vol 73 (6) ◽  
pp. 817-826 ◽  
Author(s):  
D. J. Metcalfe ◽  
P. J. Grubb

Seed mass values are given for 140 species of primary lowland rain forest and associated secondary forests in Singapore. Among shade-tolerant species of primary forest there is a trend for a decrease in mean seed mass with tall trees > woody climbers > small trees > shrubs > herbs; the differences between tall trees and small trees or shrubs or herbs, and between herbs and small trees or woody climbers are significant. There are a few light-demanding herbs or shrubs in the primary forest; among small trees, light demanders have significantly lower seed mass values than shade tolerators. In 9 out of 13 comparisons within taxa including both shade tolerants and light demanders the former had appreciably larger seeds than the latter. Two out of 13 comparisons involved very small seeded shade tolerators, and one a notably large-seed light demander. Many shade-tolerant herbs, shrubs, and trees have seed mass values much smaller than those of trees of secondary forest conventionally regarded as small seeded, and exploit moist, litter-free sites, e.g., steep microslopes. The trees of secondary forests on degraded soils do not differ significantly in seed mass from those on nondegraded soils. Key words: seed mass, light requirement, regeneration, tropical rain forest, phylogenetic analysis.


1999 ◽  
Vol 15 (4) ◽  
pp. 399-413 ◽  
Author(s):  
T. Ganesh ◽  
Priya Davidar

Fruit biomass and frugivore abundance were quantified over 3 y in a rain forest of the south Western Ghats, India. Fruit biomass was estimated by sampling fruit fall in the primary forest, and frugivore abundance by a 2.5-km transect. A total of 645 kg ha−1 of fruit was produced annually in the forest. Only 49% of this is edible to the frugivores and the remaining 51% is in the form of non-edible husks. Mammalian frugivores outnumbered avian frugivores and the majority of the mammals were seed predators. The total fruit biomass produced at Kakachi is lower than in the lowland forest and mountain forests in the neotropics but higher than in the wet sclerophyll forest of Australia. Lower diversity of trees and edaphic factors at Kakachi could be some of the reasons for these differences. On the other hand, paucity of fleshy fruits, low density of trees producing fleshy fruits and irregular fruiting of these species, account for the low number of obligate avian frugivores at Kakachi.


2003 ◽  
Vol 19 (4) ◽  
pp. 387-395 ◽  
Author(s):  
Tomoya Iwata ◽  
Mikio Inoue ◽  
Shigeru Nakano ◽  
Hitoshi Miyasaka ◽  
Atsushi Doi ◽  
...  

Microhabitat use and habitat-abundance relationships of four freshwater shrimps, Atyopsis moluccensis, Macrobrachium pilimanus, Macrobrachium trompii and Macrobrachium neglectum, were surveyed in tropical streams running through primary and secondary forests in Borneo, East Malaysia. Underwater observations revealed that A. moluccensis preferred relatively high water velocity and a boulder substrate. Macrobrachium pilimanus also preferred high water velocity and a cobble substrate, whereas M. trompii occupied stream margins with slow current and fine substrates (from POM (particulate organic matter) to pebbles). In contrast, M. neglectum was distributed relatively evenly through the stream channel. The abundance of A. moluccensis, M. pilimanus and M. trompii in the stream reaches was best explained by the abundance of boulders, cobbles and POM, respectively, suggesting that the amount of preferred microhabitat is an important factor affecting shrimp abundances in the tropical rain-forest streams. The primary-forest reaches were dominated by coarse substrates, such as cobbles and boulders, while a great proportion of the streambeds in the secondary-forest reaches were covered with sand. Owing probably to such habitat differences, the abundance of both A. moluccensis and M. pilimanus, which preferred coarse substrates, was less in the secondary- than in the primary-forest reaches. These suggested that loss of preferred habitat, namely decreased coarse substrate availability, by sedimentation resulting from riparian deforestation had altered the shrimp assemblage structures.


Sign in / Sign up

Export Citation Format

Share Document