首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献,搜索用时 15 毫秒
1.
To bridge the gaps between restoration as a science and as a practice, restoration ecology has to broaden its scope toward transdisciplinarity in close cooperation with landscape ecologists and other holistic environmentally oriented scientists, professionals, practitioners, and stakeholders. For restoration, the ongoing transdisciplinary scientific revolution has opened new insights to cope with the complex bio‐hydro‐ and human‐ecological network relations. The Total Human Ecosystem (THE), integrating humans with all other organisms and their total environment at the highest level of the global hierarchy, should become the unifying holistic paradigm for all synthetic “eco‐disciplines.” These should link ecological knowledge, wisdom, and ethics with their scientific and professional expertise from the natural and social sciences and the humanities. As the tangible matrix for all organisms, including humans, our industrial Total Human Landscape is the concrete spatial and functional system of the THE. It forms a closely interlaced network of solar energy–powered natural and seminatural biosphere landscapes and fossil energy–powered urban and agro‐industrial technosphere landscapes. The self‐organizing and self‐creative restoration capacities of biosphere landscapes are driven by mutually amplifying auto‐ and cross‐catalytic feedback loops, but the rapidly expanding technosphere landscapes are driven by destabilizing “run‐away” feedback loops. To prevent a global breakdown and to ensure the sustainable future for both humankind and nature, these positive feedbacks have to be counteracted by restraining, cultural feedbacks of environmental planning and management, conservation, and restoration. As the theme of this special issue alludes to, this template should become an integral part of an urgently needed sustainability revolution, to which the transdisciplinary landscape restoration could contribute its important share.  相似文献   

2.
3.
There is increasing recognition of the importance for local biodiversity of post-mining sites, many of which lie near communities that have suffered significant social and economic deprivation as the result of mine closures. However, no studies to date have actively used the knowledge of local communities to relate the history and treatment of post-mining sites to their current ecological status. We report a study of two post-mining sites in the Yorkshire coalfield of the UK in which the local community were involved in developing site histories and assessing plant and invertebrate species composition. Site histories developed using participatory GIS revealed that the sites had a mixture of areas of spontaneous succession and technical reclamation, and identified that both planned management interventions and informal activities influenced habitat heterogeneity and ecological diversity. Two groups of informal activity were identified as being of particular importance. Firstly, there has been active protection by the community of flower-rich habitats of conservation value (e.g. calcareous grassland) and distinctive plant species (e.g. orchids) which has also provided important foraging resources for butterfly and bumblebee species. Secondly, disturbance by activities such as use of motorbikes, informal camping, and cutting of trees and shrubs for fuel, as well as planned management interventions such as spreading of brick rubble, has provided habitat for plant species of open waste ground and locally uncommon invertebrate species which require patches of bare ground. This study demonstrates the importance of informal, and often unrecorded, activities by the local community in providing diverse habitats and increased biodiversity within a post-mining site, and shows that active engagement with the local community and use of local knowledge can enhance ecological interpretation of such sites and provide a stronger basis for successful future management.  相似文献   

4.
5.
Developing and strengthening a more mutualistic relationship between the science of restoration ecology and the practice of ecological restoration has been a central but elusive goal of SERI since its inaugural meeting in 1989. We surveyed the delegates to the 2009 SERI World Conference to learn more about their perceptions of and ideas for improving restoration science, practice, and scientist/practitioner relationships. The respondents' assessments of restoration practice were less optimistic than their assessments of restoration science. Only 26% believed that scientist/practitioner relationships were “generally mutually beneficial and supportive of each other,” and the “science–practice gap” was the second and third most frequently cited category of factors limiting the science and practice of restoration, respectively (“insufficient funding” was first in both cases). Although few faulted practitioners for ignoring available science, many criticized scientists for ignoring the pressing needs of practitioners and/or failing to effectively communicate their work to nonscientists. Most of the suggestions for bridging the gap between restoration science and practice focused on (1) developing the necessary political support for more funding of restoration science, practice, and outreach; and (2) creating alternative research paradigms to both facilitate on‐the‐ground projects and promote more mutualistic exchanges between scientists and practitioners. We suggest that one way to implement these recommendations is to create a “Restoration Extension Service” modeled after the United States Department of Agriculture's Cooperative Extension Service. We also recommend more events that bring together a fuller spectrum of restoration scientists, practitioners, and relevant stakeholders.  相似文献   

6.
7.
Toxinogenic endobacteria were isolated from a collection of Rhizopus spp. representing highly diverse geographic origins and ecological niches. All endosymbionts belonged to the Burkholderia rhizoxinica complex according to matrix-assisted laser desorption ionization-time of flight biotyping and multilocus sequence typing, suggesting a common ancestor. Comparison of host and symbiont phylogenies provides insights into possible cospeciation and horizontal-transmission events.Bacterial symbionts and their metabolic potential play essential roles for many organisms. They may benefit from improved fitness, survival, and even acquired virulence (7, 12, 22). In the course of our studies of the biosynthesis of rhizoxin, the causative agent of rice seedling blight (10), we found that the phytotoxin is produced not by the fungus Rhizopus microsporus but by symbiotic bacteria (Burkholderia rhizoxinica) that reside within the fungus cytosol (13, 15, 23). Furthermore, cloning and sequencing of the rhizoxin biosynthesis gene cluster revealed the molecular basis of bacterial toxin production (14). In sum, this represents an unparalleled example for a symbiosis in which a fungus harbors bacteria for the production of a virulence factor. In analogy, we found that the first reported “mycotoxins” from lower fungi, the highly toxic cyclopeptides rhizonin A and B (25, 28), are also produced by symbiotic bacteria (Burkholderia endofungorum) and not by the fungus (16). While both rhizoxins and rhizonins have been believed to promote zygomycoses (21), there is no indication for toxin-producing endosymbiotic bacteria in clinical isolates (18).In nature, toxin production plays a pivotal role in the development of the fungus-bacterium association. Studies of the evolution of host resistance indicate that the association resulted from a pathogenicity mutualism shift in insensitive zygomycetes (24). The fungus lost its ability to sporulate independently and became totally dependent on endobacteria for reproduction through spores, thus warranting the persistence of the symbiosis and its efficient distribution through vegetative spores (17).To gain a broader view of the occurrence, biosynthetic potential, and relationship of toxinogenic endofungal bacteria, we investigated a collection of Rhizopus spp. consisting of 20 isolates classified as R. microsporus (of which 13 belong to R. microsporus var. microsporus, four to R. microsporus var. chinensis, two to R. microsporus var. oligosporus, and one to R. microsporus var. rhizopodiformis), one isolate classified as Rhizopus sp., and one Rhizopus oryzae strain. We initially monitored the presence of bacterial symbionts by PCR using universal primers (16S rRNA genes) and rhizoxin production in all available Rhizopus strains. Liquid cultivation of fungi in production medium with and without antibiotic followed by organic solvent extraction yielded crude extracts that were analyzed by high-performance liquid chromatography (HPLC) and mass spectrometry (MS). In total, eight fungal strains were identified or confirmed as rhizoxin positive and thus expected to harbor endosymbionts. In all cases, this assumption was verified by PCR and confocal scanning microscopy. By means of an optimized protocol, we finally succeeded in the isolation and cultivation of all eight bacterial symbiont strains in pure cultures (isolates B1 to B8) (Table (Table11).

TABLE 1.

Fungal strains and their bacterial endosymbionts
TaxonStrain designationaOriginBacterial endosymbiont (isolate)
Rhizopus microsporus van TieghemATCC 62417Rice seedlings, JapanBurkholderia rhizoxinica HKI-0454 (B1)
Rhizopus sp. strain F-1360ATCC 20577Soil, JapanBurkholderia sp. strain HKI-0512 (B2)
Rhizopus microsporus Tieghem var. microsporusCBS 111563Sufu starter culture, rice wine tablet, VietnamBurkholderia sp. strain HKI-0455 (B3)
Rhizopus microsporus Tieghem var. microsporusCBS 699.68Soil, UkraineBurkholderia sp. strain HKI-402 (B4)
Rhizopus microsporus TieghemCBS 112285Ground nuts, MozambiqueBurkholderia endofungorum HKI-0456 (B5)
Rhizopus microsporus var. chinensis (Saito) Schipper & StalpersCBS 261.28Not specified, United States of AmericaBurkholderia sp. strain HKI-0513 (B6)
Rhizopus microsporus Tieghem var. microsporusCBS 700.68Forest soil, GeorgiaBurkholderia sp. strain HKI-0403 (B7)
Rhizopus microsporus Tieghem var. microsporusCBS 308.87Man, from deep necrotic tissue within the hand following a spider bite, AustraliaBurkholderia sp. strain HKI-0404 (B8)
Open in a separate windowaATCC, American Type Culture Collection, Manassas, VA; CBS, Centraalbureau voor Schimmelcultures, Utrecht, The Netherlands.Notably, the eight Rhizopus isolates are from geographically distinct collection sites, covering all five continents (Africa, America, Asia, Australia, and Europe) and representing diverse ecological niches of the host (plants, soil, food, and necrotic tissue) (Fig. (Fig.1;1; Table Table1).1). HPLC and MS analyses of the metabolic profiles and comparison with authentic references revealed that all endofungal bacterial strains are capable of producing considerable amounts of rhizoxin derivatives 1 to 7 (23) (Fig. (Fig.2).2). Among the rhizoxin derivatives, rhizoxin S2 (derivative 3) is the main product formed by all isolates, followed by compounds WF-1360F (derivative 6) (11), rhizoxin Z1 (derivative 4), and rhizoxin S1 (derivative 1) (23), while derivatives 2, 5, and 7 are formed only in minor amounts. Significant differences in production of rhizoxins were not found among the isolates (see Fig. S1 in the supplemental material). Only one isolate, Burkholderia endofungorum HKI-0456 (isolate B5), also produces the hepatotoxic cyclopeptides rhizonin A (derivative 8) and B (derivative 9) under laboratory conditions (16).Open in a separate windowFIG. 1.Survey of collection sites of toxinogenic R. microsporus strains used in this study.Open in a separate windowFIG. 2.Structures of the main rhizoxin derivatives (derivatives 1 to 7) produced by all eight fungal endosymbionts (isolates B1 to B8) and structures of rhizonin A and B (derivatives 8 and 9), produced by the symbiont B. endofungorum HKI-0456 (isolate B5).A preceding phylogenetic analysis of the 16S rRNA gene of the type strains B. rhizoxinica HKI-0454 (B1) and B. endofungorum HKI-0456 (B5) showed that both isolates belong to the genus Burkholderia (13). Although the two strains resemble each other in terms of endofungal lifestyle and physiology, DNA-DNA hybridization experiments enforced the division of the two isolates into two distinct species. To establish the taxonomic positions of all eight bacterial symbionts, we isolated genomic DNA from the recovered strains and obtained full-length 16S rRNA gene sequences by PCR using 16S universal primers (15). Sequence comparisons revealed that all isolated endosymbiotic bacteria are closely related to species of the genus Burkholderia.However, the close relationship of the symbionts is particularly intriguing considering the highly diverse collection localities of the host strains (Table (Table1).1). Despite the clear grouping of the bacteria associated with Rhizopus, the phylogenetic relationship within the endofungal symbiont complex could not be resolved by 16S rRNA gene data alone (see Fig. S2 in the supplemental material). Several computational methods failed to infer a statistically meaningful phylogeny. To overcome uncertainties in the 16S rRNA gene and biotyping analyses and to further characterize the genotypes of the eight isolates of the B. rhizoxinica complex, we performed a multilocus sequence typing (MLST) analysis. Seven conserved gene loci from all isolates were amplified by PCR, sequenced, and phylogenetically analyzed. To facilitate the comparison with an MLST study of the related bacterium Burkholderia pseudomallei (8), fragments of the following genes were chosen: ace (acetoacetyl-coenzyme A reductase), gltB (glutamate synthase, large subunit), gmhD (ADP-l-glycero-d-manno-heptose-6-epimerase), lepA (GTP-binding protein), lipA (lipoate synthase), and ndh (NADH:ubiquinone oxidoreductase). Shotgun sequencing of the genomes of two symbiont isolates indicated that the narK locus used in the B. pseudomallei study is obviously not present in the endofungal Burkholderia strains (G. Lackner, L. P. Partida-Martinez, and C. Hertweck, unpublished results). Therefore, as a characteristic feature of the ecotype, a locus from the rhizoxin biosynthesis gene cluster, rhiE (14), was sequenced in all isolates. The rhiE locus codes for a part of the polyketide synthase involved in rhizoxin biosynthesis in endofungal bacteria (14). It should be mentioned that a homologous rhizoxin biosynthesis gene cluster has been identified in the phylogenetically distant strain Pseudomonas fluorescens Pf-5 (3, 19).All loci were analyzed independently to test for incongruence between the data sets. The majority of the single-locus trees yielded a topology similar to that shown in Fig. S3 in the supplemental material. Only the ace locus resulted in a different tree: it showed a split (Eurasian, B8) (B5, others) different from the split (Eurasian, B5) (B8, others) found in the majority of single-locus trees (gltB, gmhD, and lipA) (see Fig. S3 in the supplemental material). The remaining loci (lepA, ndh, and rhiE) failed to infer statistically supported clades containing the strain B5 or B8. The phi test for recombination implemented in the program SplitsTree4 (5, 9a) indicated evidence for recombination, if the ace locus was included in the data set (P = 0.044). The removal of the ace locus abolished the signal. We conducted concatenated analyses including gltB, gmhD, lipA, lepA, ndh, and rhiE in the presence and absence of the ace locus. The resulting phylogenetic trees were recovered using distance matrix, maximum-parsimony, and Bayesian methods (see Fig. S3 and S4 in the supplemental material). We found that the tree topology is independent from the presence or absence of the ace locus. An alternative way to illustrate the phylogenetic groupings is in a network (9) (Fig. (Fig.3).3). The type strain B. rhizoxinica HKI-0454 (isolate B1) and isolate B6 share identical alleles in all sequenced loci and thus could be considered the same species. This high degree of similarity is supported by matrix-assisted laser desorption ionization protein profiling (see Fig. S5 in the supplemental material). However, it is remarkable that the geographic origins of isolates B1 and B6 (Japan and the United States, respectively) are different. Another member of this “Pacific group,” isolate B2 from Japan, is the closest relative. This observation strongly suggests that the Japanese and U.S. isolates have a common ancestor. Another highly supported clade, the “Eurasian group,” consists of the isolates B3 (Vietnam), B4 (Ukraine), and B7 (Georgia). Again, strain B3 and B7 are highly similar at the nucleotide level despite their geographic distance. Although related to this clade, the B. endofungorum type strain HKI-0456 (isolate B5), isolated from ground nuts in Mozambique, is unique in both genotypic and phenotypic aspects. Isolate B8 from Australia is related even more remotely to all other strains. The phylogenetic data obtained in this study suggest that all Burkholderia symbiont strains found in Rhizopus have a common ancestor.Open in a separate windowFIG. 3.Phylogenetic network of the endofungal symbiont complex (isolates B1 to B8) and B. pseudomallei (BPS), based on MLST. The graph was obtained by the neighbor-net method, implemented with the SplitsTree4 program. Uncertainties in the data are visualized by the network structure in the center.To test whether the phylogenetic data obtained from the MLST analysis contain further information about the evolution of the endofungal symbiosis, we analyzed the extent of detectable recombination in the data set. The presence of recombination could be explained by the exchange of genetic material between bacterial lineages that might have occurred during horizontal transmission of endosymbionts. Less likely, recombination could mean that the mutualistic association was established several times in some of the lineages.The number of incompatible splits in the center of the phylogenetic-network structure (Fig. (Fig.3)3) leaves some uncertainty about the correct placement of the strains B8 and B5, and the phi test for recombination indicated evidence for recombination if the ace locus was included. However, recombination does not appear to be a dominant factor in the evolution of the core genome of the known endosymbionts. Notably, the strong congruence between the trees retrieved from the symbiont data is in stark contrast to the recently reported high rate of recombination in free-living Burkholderia spp. (2, 6). Presumably, this is not due to a lack of recombination machinery, as homologous recombination works fine in at least three of the strains under laboratory conditions. Rather, we assume that the mainly vertically transmitted and geographically separated symbionts have evolved primarily separately from each other. Remaining traces of recombination might be hints of coinfection events in the early history of the symbiosis.Another genetic feature of the endosymbionts presented here is their relatively low GC content compared to that for related, but free-living Burkholderia species. The bacterial endosymbiont of aphids, Buchnera aphidicola, is known to have some mutational bias toward low GC content (26). Indeed, all of the endosymbionts have significantly lower GC contents than their sequenced free-living relatives, e.g., B. pseudomallei, Burkholderia thailandensis, and Burkholderia cenocepacia, in all conserved loci (see Fig. S6 in the supplemental material). Although the data obtained in this study are only preliminary evidence and future studies at the whole-genome level could certainly provide more insights into the nucleotide evolution of fungal endosymbionts, it is possible that mechanisms similar to those for Buchnera species are responsible for the reduced GC content in the fungal endosymbionts. The observation that the reduction in GC content is not as striking as that in Buchnera species is then well in accordance with the expectation that the fungus-bacterium endosymbiosis is young compared to the Buchnera-aphid mutualistic relationship.To obtain hints about possible cospeciation or horizontal-transmission events, we compared the phylogenetic relationships between the endobacteria and their fungal hosts. Nucleotide sequences of the 18S ribosomal DNA (rDNA), 28S rDNA, and internal transcribed spacer (ITS) regions were chosen to elucidate phylogenetic relationships between fungal hosts (1). These attempts were hampered since 18S rDNA sequences were highly conserved among the fungal isolates. The only variable site distinguished symbiotic from nonsymbiotic R. microsporus strains (see Fig. S7 in the supplemental material). 28S rDNA sequences are known to accumulate single nucleotide changes at a relatively low rate as well (27). Our 28S rDNA data set, with a total length of 604 nucleotides, contained only eight variable sites. With three of them being parsimony informative, no meaningful phylogram could be inferred from the 28S rDNA sequences. The ITS region is known to evolve more rapidly and is used to provide discrimination within species (27). The curated ITS alignments consisted of 621 sites, 14 being variable and 10 being parsimony informative. Four short insertions or deletions, which are mostly ignored by phylogeny inference software, were found. The phylogram based on both ITS data sets was juxtaposed with the endosymbiont tree determined by MLST (Fig. (Fig.4).4). The host strains of the Burkholderia sp. isolates B1, B2, and B6 (ATCC 62417, ATCC 20577, and CBS 261.28, respectively) were identical and reproduced the Pacific group of endobacteria. Strikingly, in contrast to their bacterial partners, the fungal host strains CBS 308.87 (Burkholderia sp. isolate B8) from Australia and CBS 111563 (Burkholderia sp. isolate B3) from Vietnam are members of the Pacific group as well. The strains CBS 700.08 (Burkholderia sp. isolate B7) from Georgia and ATCC 699.68 (Burkholderia sp. isolate B4) from Ukraine appeared to represent the Eurasian branch. This group was known from the bacterial phylogeny, but the fungal clade missed the close relationship to CBS 111563 (Burkholderia sp. isolate B3). Again, the African branch, consisting exclusively of CBS 112285 (Burkholderia sp. isolate B5), shared a common ancestor with the Eurasian group. These results are in accordance with cospeciation of some fungal hosts and their endosymbionts, especially for Burkholderia sp. isolates B1, B2, and B6 and B5, B4, and B7 (Fig. (Fig.4).4). However, there might be first evidence for some host switching events in the history of the endofungal bacteria (Burkholderia sp. isolates B3 and B8). Although this hypothesis is based mainly on a few informative sites within the ITS data set, three insertion or deletion events within the alignment support the extended Pacific group (Burkholderia sp. isolates B1, B2, B6, B3, and B8), indicating the horizontal transfer of symbionts and/or genetic material between strains. While it is possible that multiple events led to this unusual symbiosis, a scenario in which all symbiont strains are derived from an ancestral association seems to be more likely. The endosymbiont-dependent sporulation of the host strain indicates that the fungus-bacterium interaction is highly specialized. Furthermore, vertical transmission of the symbionts through spores is an efficient strategy for rapid distribution (4, 20). Nonetheless, our data suggest that the horizontal transmission of symbionts might also have played a role during the evolution of the endofungal bacteria.Open in a separate windowFIG. 4.Juxtaposition of phylogenetic trees derived from the MLST data of the endofungal symbiont complex (isolates B1 to B8) and the ITS sequence data of the fungal host (strain designations of fungal isolates of the genus Rhizopus are given). Dashed lines are representative of a symbiotic relationship. The numbers on top of the branches indicate the clade probability values. Shading designates similar clade affiliations for the bacterial symbiont and the fungal host.In conclusion, we have investigated eight bacterial endosymbiont strains isolated from toxinogenic R. microsporus strains in pure culture. All isolates are representatives of the same unique “endofungal” ecotype, albeit the hosts'' origins cover all five continents and occur in highly diverse niches. The bacterial endosymbionts share characteristic phenotypic traits, like secondary metabolite production and protein profile, as demonstrated by HPLC-MS and matrix-assisted laser desorption ionization-time of flight biotyping, respectively. Phylogenetic analyses (16S rRNA genes) provide strong evidence that all symbiont strains originate from a common ancestor and form a new complex within the genus Burkholderia. This observation is strongly supported by MLST, according to which all eight symbiont isolates can be grouped into continental branches. Results revealing both similar and deviating geographical groupings of fungal isolates in comparison to bacterial endosymbionts allow hypothesizing about the possible cospeciation of fungal and bacterial symbionts and some extent of horizontal-transmission events. All bacterial strains investigated seem to have evolved mainly separately from each other, not showing extensive recombination. In addition, we present preliminary evidence that there might be a mutational bias toward high AT contents, as is known for other endosymbiotic bacteria.  相似文献   

8.
The Human Elder in Nature, Culture and Society. David Gutmann. Boulder, CO: Westview Press, 1997. 250 pp.  相似文献   

9.
Current and predicted trends indicate that an increasing proportion of the world’s population is living in urban and suburban places. The nature of the urban environment becomes an important factor if we are concerned with the restoration and preservation of biodiversity and ecosystems in and around cities. This article highlights the varied impacts of cities on soils and their implications for restoration planning and expectations of restoration “success.” Urban soils exist in different historical and formational trajectories than their local nonurbanized counterparts due to direct anthropogenic disturbance and indirect environmental impacts from urbanization. Therefore, urban soils often exhibit altered physical, chemical, and biological characteristics in comparison to local nonurbanized soils. Several unique features of urban soils and urban ecosystems pose particular issues for ecological restoration or the improvement of degraded soil conditions in cities. The creation of novel soil types, conditions that promote invasion by non‐natives, the strong influence of past land use on soil properties, and the presence of strong interactions and alternative stable states set up unique difficulties for the restoration of urban soils. Soils in urban restorations are a medium that can be deliberately manipulated to improve site conditions or in the monitoring of soil conditions as indices of ecosystem status. Including an explicit role for strong manipulations of soils in urban ecosystems changes how we approach baselines, management, and reference conditions in urban ecological restoration. With an understanding of urban soil ecological knowledge, we can guide aspects of urban ecological restoration toward successful outcomes.  相似文献   

10.
11.
12.
13.
VA菌根共生的起源和进化   总被引:10,自引:2,他引:10  
VA菌根共生的起源和进化赵之伟(云南大学生物学系,昆明650091)OriginandEvolutionoftheVAMycorrhizalSymbiosis.ZhaoZhiwei(BiologyDepartmentofYunnanUniversit...  相似文献   

14.
The Society for Ecological Restoration (SER) published the second edition of its International Principles and Standards for the Practice of Ecological Restoration in 2019. We conducted a pan-Canadian study using semi-structured interviews with restoration professionals to explore the extent to which restoration practitioners are aware of the document and use it. Overall, we found that direct uptake of the document by practitioners was lower than expected, with approximately 37.7% of all participants that were both aware of and consulting the publication for guidance in their practice of ecological restoration. This is due in part to low awareness of the document itself, with only a small majority (56.5%) of interviewees being aware of it. Other reasons listed by practitioners such as the structure of the publication, its added value, and its suitability for on-the-ground work revealed why some individuals aware of the existence of the document still failed to consult it. Here, we present a more nuanced assessment of these observations and share our findings with the ecological restoration community to address this disconnection. With intensifying pressures to achieve restoration success internationally, SER's guidance is critical. We analyze why it seems guidance from SER is not being taken up as fully as it might, and ways in which future versions may be improved.  相似文献   

15.
While human genetic variation is limited due to a bottleneck on the origin of the species ~200 kya, cultural traits can change more rapidly, and may do so in response to the variation in human habitats. Does cultural diversification simulate a natural experiment in evolution much like biodiversity so that cultural divergences and convergences can be interpreted in terms of the differences and similarities of local environments? Or is cultural diversity simply the result of human behavioral flexibility? Although the majority of cultural data comes from the tips of the hominin phylogeny, anthropologists can follow the example of evolutionary ecologists, who often compare the endpoints of phylogenies when that is all that is available. This article compares 97 contemporary indigenous language communities from around the world, and 24 of their cultural traditions, to help determine whether human cultures and their cultural traits are proportionately dispersed, as predicted by the neutral theory of biodiversity, or whether they show non-proportionalities that could be explained with evolutionary reasoning.  相似文献   

16.
Ecological restoration is practiced by people of diverse backgrounds working at many different levels in a variety of settings. Portraying the human body as a metaphor of a natural ecosystem can be useful in identifying the breadth of strategies used to restore the natural environment. A technical approach, environmental stewardship, and more spiritual traditional attitudes to ecological restoration can be viewed as analogous to restoring health to the human body through an operation in a hospital, administering remedies to oneself from the medicine cabinet, and taking a broader holistic/preventative approach to cultivate the mind–body connection through, e.g., yoga.  相似文献   

17.
18.
鲍沁星  沈瑶 《生物信息学》2018,25(12):30-35
印度灵鹫峰历史悠久、佛教影响深远,是亚洲早期山地景观开发中受人文因素影响的重要案例,然现今园林景观等相关研究领域对其关注不足。从风景园林历史研究的角度,梳理了灵鹫峰文化景观的历史沿革与重要影响,包括佛教文化在王舍城地区的形成过程、灵鹫峰景观建置、灵鹫峰图像史料遗存以及文化景观用典,阐释了其对杭州飞来峰文化景观的深刻影响,并分析了近现代考古研究对印度灵鹫峰再开发与旅游的影响,探讨了灵鹫峰对研究当代山地开发保护与可持续发展的意义。  相似文献   

19.
Human‐induced erosion regularly delivers massive quantities of fine sediments into streams and rivers forming large static bodies of sediment known as sand slugs, which smother in‐stream habitat, alter community structure, and decrease biodiversity. Sand slugs are widespread in parts of southeastern Australia as well as in many other parts of the world, and there is now considerable interest in restoring such affected streams. The reintroduction of large timber is widely suggested as a strategy for restoring habitat complexity, but this has rarely been tested in sand slug–affected streams. We examined the response of fish populations to wood addition to two streams in southeastern Australia that have been impacted by sand slugs. Manipulated sites (three per treatment) had either one or four timber structures added, and these sites were compared with (three) unmanipulated (control) sites before and after the manipulation occurred. Despite a supraseasonal drought during the study, we observed short‐term increases in the abundance of Mountain galaxias (Galaxias olidus) at the four‐structure sites, while both the four‐structure and the one‐structure treatments appeared to buffer against drought‐induced declines in two other species, River blackfish (Gadopsis marmoratus) and Southern pygmy perch (Nannoperca australis), relative to controls. However, drought eventually caused the complete loss of surface water from these streams and the loss of fish from both manipulated and unmanipulated sites. Thus, although the study supports the use of timber structures as a means of increasing local fish abundances, these beneficial effects were, in these streams, contingent upon permanency of flow. Because sedimentation has depleted the number of permanent refuge pools in these creeks, recovery rates of the fauna (i.e., resilience) are likely to be slow. We therefore conclude that in streams subjected to frequent disturbance, restoring refugia may be as, if not more, important as restoring what we term residential habitat.  相似文献   

20.
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号