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  • 1. Justifying the designation of protected areas often depends on the ability to select areas in good ecological conditions, with high taxonomic richness, and unique habitats or species assemblage characteristics.
  • 2. The ecology of scleractinian coral and prosobranch snails were examined along the Masoala Peninsula of north‐eastern Madagascar using rapid assessment methods to evaluate the correspondence between unique invertebrate faunal characteristics and park designation.
  • 3. The reefs along this peninsula are in good ecological condition and have a coral and snail fauna similar to most of the western Indian Ocean, with no indications of local endemism in these groups. There was no relationship between the taxonomic richness of snails and corals. Corals were better at distinguishing locations based on taxonomic richness while snails were better based on unique faunal characteristics.
  • 4. Corals had the highest taxonomic richness on the extreme windward north and south and the lowest richness on the leeward side of the peninsula. The leeward side did, however, have an unusual habitat of corals growing on granite rock with a unique coral and snail fauna. A northern and southern assemblage characterized snail fauna on the windward side of the peninsula.
  • 5. The composite findings indicate that the currently designated park areas cover two of the three areas that have either high diversity or unique faunas.
Copyright © 2006 John Wiley & Sons, Ltd.  相似文献   

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  • 1. Marine protected areas (MPAs) are set up to conserve biodiversity, but their design is not always based on strictly scientific considerations. Ideally, an MPA should protect all key habitats necessary for a marine species to complete its life cycle. The identification of these key habitats is complex, especially during the early life of marine fishes.
  • 2. A widely distributed tropical and important low trophic‐level fish species, Spratelloides delicatulus (Clupeidae), was used to evaluate the significance of various coastal habitats for its larvae and juveniles in the Con Dao Archipelago MPA in Vietnam. Early stages (larvae and juveniles) were sampled monthly over one year (June 2016 to May 2017) using light traps in three main habitats (seagrass beds, coral reefs and harbour). The species was identified using morphometry and DNA barcoding. Age and growth variables were estimated using otolith daily growth increments.
  • 3. A total of 3,581 fish were caught. The species was not found in captures between January and February, directly linked to the decrease in seawater temperature and was most abundant from April to June. For a subsample of 248 fish (7–38 mm standard length), ages ranged from 7 to 108 days.
  • 4. Captures and back‐calculated birthdates using otolith daily increments showed that S. delicatulus spawns during the period of high seawater temperature, from March to October. The species colonizes all three habitats during the early stages (0–26 days old), with growth rate lowest on the seagrass beds. Nevertheless, the species occupies seagrass beds exclusively during the older stages.
  • 5. The conservation of seagrass beds in the Con Dao archipelago is essential for protection of juvenile stages of this species but this habitat is presently not included in the MPA patches. Establishment of a continuum of protected areas linking habitats, rather than the existing patches is needed to conserve the complete life cycle of this species in the Con Dao MPA.
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  • 1. The identification and protection of known breeding grounds is a high priority for the conservation of marine biodiversity. Here, we examine the intertidal habitats used by marine gastropods for the deposition of benthic egg masses along a wave‐exposed coastline in New South Wales, Australia.
  • 2. A total of 200 surveys were conducted on 13 intertidal reefs. The egg masses of 46 species were identified, with a further eight distinct types recorded but remaining unidentified. Over half of the gastropods were found to deposit egg masses exclusively on the underside of boulders. Other intertidal substrata used for gastropod egg mass deposition included vertical and horizontal exposed rock surfaces, algal fronds and sand. Only eight species were found to attach their egg masses to more than one type of substratum.
  • 3. Twelve reefs were classified into three categories according to exposure to wave action and habitat diversity. The mean number of species found depositing egg masses was compared using a standard eight surveys from each site. Sub‐maximally wave‐exposed reefs with maximal habitat diversity were found to support a significantly higher species richness of gastropod egg masses, compared with maximally wave‐exposed reefs with either maximal or sub‐maximal habitat diversity (p=0.000).
  • 4. Gastropods that deposit egg masses on the underside of boulders were more likely to be found on sub‐maximally wave‐exposed reefs, whereas species that deposit egg masses in all other microhabitats were equally likely to be found breeding on sub‐maximally or maximally exposed reefs.
  • 5. Gastropods with pelagic larvae tended to occur at a greater number of sites than those that hatch post‐metamorphosis. A significant difference was found between species grouped according to these two developmental modes for the mean number of sites at which egg masses were recorded (p=0.008).
  • 6. Variation in the species richness of gastropods found depositing egg masses on different intertidal reefs appears to be influenced by the availability of suitable boulders and exposure to wave action. These factors should be taken into consideration during the selection of locations for intertidal protected areas.
Copyright © 2004 John Wiley & Sons, Ltd.  相似文献   

6.
  • 1. Growing concern associated with threats to the marine environment has resulted in an increased demand for marine reserves that conserve representative and adequate examples of biodiversity. Often, the decisions about where to locate reserves must be made in the absence of detailed information on the patterns of distribution of the biota. Alternative approaches are required that include defining habitats using surrogates for biodiversity. Surrogate measures of biodiversity enable decisions about where to locate marine reserves to be made more reliably in the absence of detailed data on the distribution of species.
  • 2. Intertidal habitat types derived using physical properties of the shoreline were used as a surrogate for intertidal biodiversity to assist with the identification of sites for inclusion in a candidate system of intertidal marine reserves for 17 463 km of the mainland coast of Queensland, Australia. This represents the first systematic approach, on essentially one‐dimensional data, using fine‐scale (tens to hundreds of metres) intertidal habitats to identify a system of marine reserves for such a large length of coast. A range of solutions would provide for the protection of a representative example of intertidal habitats in Queensland.
  • 3. The design and planning of marine and terrestrial protected areas systems should not be undertaken independently of each other because it is likely to lead to inadequate representation of intertidal habitats in either system. The development of reserve systems specially designed to protect intertidal habitats should be integrated into the design of terrestrial and marine protected area systems.
Copyright © 2005 John Wiley & Sons, Ltd.  相似文献   

7.
  • 1. Current selection of marine protected areas in South Africa is based on objective criteria including biogeographic representation and habitat heterogeneity. This paper specifically examines rocky shores on the west coast of South Africa to determine whether they are divisible into discrete ‘habitats’ that need independent conservation.
  • 2. Seventeen rocky shores spanning the full spectrum of wave exposure were compared in terms of maximum wave forces, biomass, species richness and diversity among zones and sites. Three biotic assemblages were identified, characterizing sheltered, semi‐exposed to exposed, and very exposed habitats. Differences among these were clear‐cut low on the shore but disappeared at the top of the shore where wave action was attenuated and desiccation uniformly intense.
  • 3. The recognition of three discrete biologically‐defined habitats means that rocky shores cannot be regarded as a uniform habitat for conservation purposes. All three components need protection if the full spectrum of rocky‐shore communities is to be conserved.
  • 4. It is argued that this approach allows habitats to be defined in an objective manner, and that once this has been done, habitat heterogeneity constitutes a better measure of conservation value of an area than a ‘hotspot’ approach based on species richness and endemism.
Copyright © 2008 John Wiley & Sons, Ltd.  相似文献   

8.
  • 1. If marine environments are to be systematically protected from the adverse effects of human activities, then identification of the types of marine habitats and the communities they contain, and delineation of their boundaries utilizing a consistent classification is required. Human impacts on defined communities can then be assessed, the ‘health’ of these communities can be monitored, and marine protected areas can be designated as appropriate.
  • 2. Schemes to classify habitats at local and regional scales, according to their geophysical properties, may identify different factors as determinants, and/or use them in different sequences in a hierarchical classification. We examined the reasons for these differences in local and regional applications of a global concept, and argue that a common set of factors could be applied in a defined and defensible sequence to produce a common hierarchy of habitat types among geographic regions.
  • 3. We show how simple mapping and GIS techniques, based on readily available data, can lead to the identification of representative habitat types over broad geographic regions. We applied a geophysical framework first to the entire Canadian coastline and second to the Scotian Shelf of Atlantic Canada to establish broad scale marine natural regions and ‘seascapes’, respectively. This ecosystem level approach — which defines representative habitat types — is a fundamental prerequisite for many purposes. It can form the basis for further analyses including: definition of community types from habitat — community relationships; evaluation of the potential roles of focal species in marine conservation; evaluation of candidate marine protected areas; definition of unaffected reference areas against which the effects of human activities can be gauged; guidance for water quality monitoring studies; management of marine resources.
Copyright © 2003 John Wiley & Sons, Ltd.  相似文献   

9.
  1. Intertidal macroalgal communities are economically and ecologically important and, with a likely increase in anthropogenic pressures, there is need to evaluate and monitor these diverse habitats. Efforts to conserve and sustainably manage these habitats must be underpinned by accurate, cost‐effective, and efficient data collection methods. The high spatial and temporal resolution of unmanned aerial vehicles (UAVs), compared with satellites and aircraft, combined with the development of lightweight sensors, provides researchers with a valuable set of tools to research intertidal macroalgal communities.
  2. The ability of multispectral sensors, mounted on a satellite, an aircraft, and a UAV, to identify and accurately map the intertidal brown fucoid Ascophyllum nodosum (Fucales, Ochrophyta) at a site with a low species diversity of macroalgae were compared.
  3. Visual analysis confirmed that the spatial resolution of satellite imagery was too coarse to map intertidal macroalgae as it could not capture the fine spatial patterns of the macroalgal community. High‐resolution RGB (colour) imagery, taken during the aircraft and UAV surveys, was used to collect training and reference data through the visual identification and digital delineation of species. Classes were determined based on the level of taxonomic detail that could be observed, with higher levels of taxonomic detail observed in the UAV imagery over the aircraft imagery. Data from both were used to train a maximum‐likelihood classifier (MLC).
  4. The UAV imagery was able to more accurately classify a distinct A. nodosum class, along with other macroalgal and substratum classes (overall accuracy, OA, 92%), than the aerial imagery, which could only identify a lower taxonomic resolution of mixed A. nodosum and fucoid class, achieving a lower OA (78.9%). This study has demonstrated that in a coastal site with low macroalgal species diversity, and despite the spectral similarity of macroalgal species, UAV‐mounted multispectral sensors proved the most accurate for focused assessments of individual canopy‐forming species.
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  • 1. Conservation efforts have traditionally been directed to ‘flagship’ species (whales, seals, migratory birds, etc.) that capture public attention. Often these flagship species occupy distinctive habitats. Distinctive habitats appear to be distinguished because of anomalous physical structures and unique oceanographic processes occurring within them, whereas representative habitats are not notable in this way. Distinctive habitats are found in areas of various physical anomalies described primarily by temperature, chlorophyll and topography.
  • 2. Several different kinds of distinctive habitats can be defined by their anomalous physical structures and oceanographic and biological processes. Species diversity may be either higher or lower in distinctive than in representative habitats. Distinctive habitats predominantly belong to a class of environments called ‘ergoclines’, and are typically associated with elevated resources at some ‘trophic level’.
  • 3. These elevated resources may be either the product of true production (i.e. they are generated (in situ), or they are the product of physical accumulation due to circulation mechanisms. These processes lie at the heart of the ecology of distinctive habitats, and are fundamental to maintenance of ecosystem health, ecological integrity, distributions, abundances and recruitment of species, patterns of animal migrations, and potential or actual fisheries yields.
  • 4. Conservation strategies need to examine the relationships between distinctive and representative habitats and species diversity. A strategy, leading from studies on flagship or other focal species, could have several advantages. It should rejuvenate the inherent appeal and significance of ‘species’ approaches to marine conservation, provide a rationale for human interest and a new foundation for examination of marine ecological interactions. It would also require a novel synthesis of relationships between ‘species’ and ‘spaces’ approaches to marine conservation by asking how we can take the best advantage of both approaches, rather than seeing them as in conflict.
Copyright © 2002 John Wiley & Sons, Ltd.  相似文献   

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  • 1. Three classes of habitat used by groups of fish species classified as conservation and management priorities were developed for the Gerua River (also known as the Girwa River, Karnali River) in the Ganges river basin. This river is large (mean annual discharge ca 1500 m3 s?1, up to 900 m wide), surrounded by protected lands of India and Nepal, and upstream of major diversions and river alterations.
  • 2. Fish and habitat sampling was conducted at 45 sites from 2000 to 2003. Data were analysed for 2172 fish of 14 species. Species and life stages found occupying a statistically distinct subset of the river habitats were grouped to identify classes of river habitat for conservation.
  • 3. Most species and life‐stage groups specialized on specific habitat conditions revealed by multivariate analyses of variance and a principal component analysis. The most numerous and diverse group (six species, 15 life stages) was associated with deep depositional habitats with sandy substrate. Two species covering three life stages were primarily oriented to erosional habitat marked by fast current velocity with pebble and cobble substrate. A third group of three species of adults and juveniles were intermediate in habitat use.
  • 4. River conservation for fish faunas should maintain both erosional and depositional channel habitats with depths, substrates, and current velocity inclusive of the ranges reported. The erosional and depositional nature of the key habitats requires that rivers be maintained with flows capable of channel‐forming functions.
Copyright © 2006 John Wiley & Sons, Ltd.  相似文献   

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  • 1. Since most of the natural habitats critical for freshwater fish survival have been adversely affected by human disturbance, the effectiveness of artificial structures in providing new and suitable habitats for fish has been increasingly investigated.
  • 2. This paper evaluates the role of artificial structures as fish habitat in a structureless 30 km2 Brazilian reservoir, through underwater surveys conducted monthly from April 1999 to March 2000.
  • 3. In total, 5759 fish in nine species were recorded, but only three cichlid species—one native, Geophagus brasiliensis and two non‐native, Cichla kelberi and Tilapia rendalli—showed consistent association with the artificial habitats, suggesting that this family reacts to submerged structures.
  • 4. The absence of fish at control sites compared with high occurrences in sites provided with a physically complex structure suggests that artificial structures can play an important ecological role for cichlids smaller than 150 mm TL, probably related to shelter and/or feeding benefits.
  • 5. The level of structural complexity and position in the water column influenced fish use of artificial structures. C. kelberi was associated with highly complex structures, whereas moderately complex bottom structures were more effective in harbouring G. brasiliensis. Bottom structures are apparently more important than midwater structures in harbouring T. rendalli, but structural complexity seemed to play a secondary role.
  • 6. This study is the first in demonstrating that adding complex artificial structures can expand habitats for small fish (<150 mm TL), especially cichlids, in a neotropical impoundment. It seems reasonable to expect that deploying physically complex structures in other oligotrophic, structureless and cichlid‐dominated impoundments in Brazil will lead to similar results to those found in this work.
Copyright © 2008 John Wiley & Sons, Ltd.  相似文献   

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  • 1. Data from fishing surveys employing bottom long‐lines were analysed to characterize the diversity, assemblages and distribution patterns of demersal fish along the Brazilian outer shelf and upper slope, between latitudes 13°S and 22°S.
  • 2. Non‐metric multi‐dimensional scaling (MDS) and cluster analysis indicate three distinct species assemblages separated primarily by depth (the 200 m isobath) and secondarily by latitude (19°S), suggesting a continual transition along the depth and latitudinal gradients in the study area. Species richness was negatively correlated with depth, but with no clear relationship with latitude.
  • 3. Results suggest the existence of reef formations on the shelf‐edge zone (40–200 m) and slope down to 500 m depth off the eastern Brazilian coast. More than 75% of the catches recorded were reef fish species from the families Serranidae, Lutjanidae, Malacanthidae, Muraenidae, Sparidae, Balistidae, Carangidae, Haemulidae, Scorpaenidae and Priacanthidae.
  • 4. The maximum depth of occurrence for 20 reef species was extended from limits previously recorded.
  • 5. The findings reinforce the hypothesis of a faunal corridor for species associated with deep reef formations along the shelf‐edge zone (40–200 m), in the South American continental margin, connecting the south‐western Atlantic and the Caribbean provinces.
  • 6. The shelf‐edge reefs support important multi‐species fisheries and harbour critical habitats for the life cycle of many reef fish species, including spawning aggregation sites that are extremely vulnerable to human pressures, such as intensive fishing, shipping and offshore oil and gas exploitation; all activities currently expanding off the Brazilian coast.
  • 7. Results reveal the biological importance of deep shelf‐edge reefs as a critical ecological area. Despite their importance, shelf edge reefs are not currently included in any marine protected area network in the tropical south‐western Atlantic. There is now an urgent need to enhance knowledge, implement adequate management strategies and consider these deeper habitats as priority areas for conservation. Copyright © 2011 John Wiley & Sons, Ltd.
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