scholarly journals Use of the flooded forest by fish assemblages in lakes of the National Park of Anavilhanas (Amazonas, Brazil)

2012 ◽  
Vol 42 (4) ◽  
pp. 561-566 ◽  
Author(s):  
Janette Noveras ◽  
Kedma C. Yamamoto ◽  
Carlos E.C. Freitas

We evaluated diversity and distribution of fish species in two habitats: flooded forest and open water of lakes of Rio Negro. Each of four lakes within the Anavilhanas Archipelago was sampled three times from 2009-2010. Species diversity generally was higher in flooded forests and at night, according to correspondence analysis. Predators were most active at night, but showed no preference between the flooded forest and open water habitats. Omnivores, filter feeders, and detritivores were most active during the day.

2021 ◽  
Vol 52 (1) ◽  
Author(s):  
Kuo-Shu Chen ◽  
Hsu-Sen Chen ◽  
Chiee-Young Chen ◽  
Yan-Lin Su ◽  
Pei-Jie Meng ◽  
...  

AbstractTo understand the spatial species diversity of demersal fish assemblages in Taijiang National Park (TJNP) of Taiwan, fishes from 44 demersal trawl hauls and environmental data were collected in the nearshore and offshore areas of TJNP from April 2016 to May 2019. In total, fishes of 47 families, 84 genera, and 113 species were recorded. The nearshore and offshore demersal fish assemblages in TJNP exhibited significant variability in species composition assessed via beta diversity. Using distance-based redundancy analysis, we demonstrated that bottom depth and substrate type were significant explanatory variables of spatial species diversity and identified three habitat types (I: shallow soft bottom; II: deeper soft bottom; III: deeper bottom with mixed sand and gravel substrates). The nearshore assemblage was characterized by type I, where Tarphops oligolepis (flounder), Trachinocephalus myops (snakefish), and Liachirus melanospilos (carpet sole) dominated in terms of abundance. The offshore assemblage was characterized by either type II or type III because differences in substrate types among sampling sites were noticeable. At the offshore sites characterized by a deeper soft bottom (type II), Johnius distinctus (croaker), Cynoglossus kopsii (shortheaded tonguesole), and Coelorinchus formosanus (Formosa grenadier) predominated. In contrast, the westernmost sampling site, characterized by type III habitat, exhibited relatively high Shannon indices, and Scorpaena miostoma (scorpionfish), Urolophus aurantiacus (sepia stingray), and Parabothus taiwanensis (lefteye flounder) predominated. Our results provide the first baseline information on the environmental characteristics and spatial species diversity of demersal fish assemblages in TJNP and have implications for biodiversity conservation in existing spatial management areas.


2013 ◽  
Vol 13 (4) ◽  
pp. 260-268 ◽  
Author(s):  
Philip Wesley Willink ◽  
Eustace Alexander ◽  
Christopher Campbell Jones

The Upper Essequibo Conservation Concession is a reserve in central-eastern Guyana managed by Conservation International. The site is uninhabited by people and poorly studied. The first scientific fish survey was in 2007 in conjunction with the filming of the BBC nature documentary Lost Land of the Jaguar. Aquatic habitats were primarily flowing water, ranging from the main channel of the Essequibo River to small forest creeks. Ponds and seasonally flooded forests were uncommon. Large predatory fishes were abundant in the Essequibo River. Fishes tolerant of low oxygen levels were common in flooded forests and small forest creeks. There was zero similarity between the fish assemblages of the Essequibo River and flooded forests / small forest creeks. The rest of the habitats and fish assemblages formed a continuum between these extremes. Imminent threats to the Upper Essequibo Conservation Concession include logging, mining, and over-fishing. Because of the heterogeneous distribution of fish assemblages, and because each threat will differentially affect different habitats, a two-pronged approach focusing on the ends of the habitat / fish assemblage continuum should be implemented in order to conserve the entire fish biodiversity of the Upper Essequibo Conservation Concession.


Koedoe ◽  
1998 ◽  
Vol 41 (1) ◽  
Author(s):  
K.N. De Kock ◽  
C.T. Wolmarans

Most of the previous records of the freshwater molluscs from the Kruger National Park date back prior to and up to 1966. On account of several droughts between 1966 and 1995 it was decided to do a survey of the freshwater mollusc population in 1995 to evaluate the effect of these droughts. The traditional mollusc intermediate hosts were also screened for trematode parasites to establish whether or not they were infected. No infected molluscs were found. Eight of the 19 species reported up to 1966 were not found during the 1995 survey. Three new mollusc species were collected in 1995. The consequences of the drought are clearly visible when the species diversity found in the dams in the 1995 survey, is compared to what was previously recorded.


Author(s):  
Richard K.F. Unsworth ◽  
James J. Bell ◽  
David J. Smith

The present study considered the influence of the tide on shallow water fish assemblages within the Wakatobi Marine National Park, Indonesia. Timed underwater visual observations were made across a gradient of intertidal to subtidal habitats from near-shore to reef crest at different tidal heights. Transient fish were found to dominate shallow water fish assemblages and the assemblage composition varied with tidal state. Fish assemblages were more diverse and abundant at higher tides in both coral and sea grass habitats, however, this was more pronounced within sea grass habitats. A tidal reduction from ≈2.0m to ≈0.8m (above chart datum) corresponded to a 30% reduction in fish abundance, while species richness also significantly decreased from 13.5 to 10.8 species per standardized timed observation. Fifty fish groups were reported from sea grass habitats with the most abundant being from the Engraulidae family and Lethrinus harak, which form important local subsistence fisheries. This research confirms the importance of tidal changes in structuring the fish fauna of Indonesian sea grass habitats and underlines the connectivity that exists between these habitats and nearby coral reefs.


Koedoe ◽  
2001 ◽  
Vol 44 (2) ◽  
Author(s):  
I.A. Russell

Fish assemblages were sampled at six sites in the Breede River in the Bontebok National Park during 1999 and 2000. A total of 380 fish from 12 species was recorded. Indigenous fish collected included one freshwater species (Barbus andrewi), two catodromous species (Anguilla mossambica, Myxus capensis). and three estuarine species (Gilchris- tella aestuaria, Monodactylusfalciformis, Mugil cephalus). Four of the species recorded were aliens (Tinea tinea, Lepomis macrochirus, Micropterus salmoides, Micropterus dolomieu) and two species translocated from other South African rivers (Tilapia sparrmanii, Clarias gariepinus). A further two indigenous species (Sandelia capensis, Pseudobarbus biirchelli) could potentially occur within the park, though the high abundance of alien predators means that there is little chance for recolonisation from tributaries higher in the Breede River system. There is little opportunity to meaningfully conserve most indigenous freshwater fish in Bontebok National Park.


2017 ◽  
Vol 15 (3) ◽  
Author(s):  
Francisco S. Álvarez ◽  
Wilfredo A. Matamoros ◽  
Francisco A. Chicas

ABSTRACT The ichthyofauna of the Río Acahuapa was analyzed sampling 17 sites that included the basin main channel and its tributaries. Fish were collected using dip-nets, seine-nets and electrofishing. Fish standard length and species abundance were recorded. Species origin and salinity tolerance criteria were used to classify fish species. Water physicochemical variables, habitat structure and sampling sites elevation were recorded. A total of 33 fish species were registered, 12.1% are primary, 45.5% are secondary and 42.4% are of marine derivation. Fish species richness declined with increase of elevation (R2=0.55, p=0.0006). Two assemblages of fishes were identified: the first one associated to sites of low elevations (19-184 masl), composed mainly of secondary and marine-estuarine fish species related with high temperature, water velocity, river width, dissolved oxygen and low sand and silt substrate cover; the second one associated to sites of middle and higher elevations (185-519 masl), composed by primary and secondary freshwater fishes related with high pH, logs and rocks substrate cover. In summary, elevation and environmental variables contributed to the composition and distribution of fish in the Río Acahuapa.


1970 ◽  
Vol 18 (1) ◽  
pp. 11-17 ◽  
Author(s):  
Shalik Ram Sigdel

Study on plant community structure was undertaken in different altitudinal ranges of Shivapuri National Park. The general objective of this study is to analyse different plant community structure in Shivapuri National Park with regards to altitudinal variation. The forest was divided into three distinct altitudinal ranges on the basis of dominancy. In each altitudinal range standard quadrats method was applied for vegetation analysis. The highest number of species was found in site II. All the ecological parameters of the plant species were higher in site II except Basal Area of tree that was highest in site III. The pattern of distribution of plant species was not uniform according to altitude. At higher elevation, the forest was mature with almost closed canopy and trees were large; so the tree density was low. Species richness was highest in site II. Species diversity among tree and shrub species was higher in site I. But for herb species diversity was higher in site II for both seasons. Such type of variations may be due to nature of soil i.e. acidity, nutrient availability and other micro-climatic factors. The most noteworthy thing was that variation in flower colour of Rhododendron arboreum i.e. deep scarlet at low altitude, but it gradually changed into pinkish white as altitude increased. Key words: Altitude, Density, Plant community, Species diversity doi: 10.3126/banko.v18i1.2161 Banko Janakari, Vol. 18, No. 1, 11-17


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