BioScience ◽  
2020 ◽  
Author(s):  
Benjamin S Halpern ◽  
Eric Berlow ◽  
Rich Williams ◽  
Elizabeth T Borer ◽  
Frank W Davis ◽  
...  

Abstract Synthesis has become ubiquitous in ecology. Despite its widespread application to a broad range of research topics, it remains unclear how synthesis has affected the discipline. Using a case study of publications (n = 2304) from the National Center for Ecological Analysis and Synthesis compared with papers with similar keywords from the Web of Science (n = 320,000), we address several questions about the comparative impact of synthesis, the role of synthesis in driving key research themes, and whether synthesis is focused on different topics than is the broader ecological literature. We found much higher citation rates for synthesis papers overall (fivefold more) and within eleven key topic themes (e.g., species richness, biodiversity, climate change, global change). Synthesis papers often played key roles in driving, redirecting, or resolving core questions and exhibited much greater cross-theme connectivity. Together, these results indicate that synthesis in science has played a crucial role in accelerating and advancing ecological knowledge.


Ecology ◽  
1932 ◽  
Vol 13 (4) ◽  
pp. 408-408

Zootaxa ◽  
2021 ◽  
Vol 4951 (1) ◽  
pp. 80-106
Author(s):  
JOSÉ D. PABLO-CEA ◽  
ANGÉLICO ASENJO ◽  
JOSÉ L. NAVARRETE-HEREDIA ◽  
ALFRED F. NEWTON

This paper is primarily a compilation of published data on the staphylinid beetle species reported for El Salvador. It is based on taxonomic and ecological literature, with inclusion of some new records from different entomological collections. Thirty eight genera and 96 species are reported in the list, including a first country record: Eulissus chalybaeus. Country-level distribution outside of El Salvador, locality references and topographic zones are included for each species. In the list, three endemic species are recorded: Seeversiella badia, S. minima and Stenus salvadorensis. It is remarkable that 14 genera (37%) and 52 species (54%) have only been reported at a country level in the literature, without a specific locality of collection, indicating the need for local inventories of this coleopteran family in the salvadoran territory. 


Ecology ◽  
1933 ◽  
Vol 14 (3) ◽  
pp. 322-322

2017 ◽  
Vol 284 (1849) ◽  
pp. 20162080 ◽  
Author(s):  
Gabriel A. Jamie

‘Mimicry’ is used in the evolutionary and ecological literature to describe diverse phenomena. Many are textbook examples of natural selection's power to produce stunning adaptations. However, there remains a lack of clarity over how mimetic resemblances are conceptually related to each other. The result is that categories denoting the traditional subdivisions of mimicry are applied inconsistently across studies, hindering attempts at conceptual unification. This review critically examines the logic by which mimicry can be conceptually organized and analysed. It highlights the following three evolutionarily relevant distinctions. (i) Are the model's traits being mimicked signals or cues? (ii) Does the mimic signal a fitness benefit or fitness cost in order to manipulate the receiver's behaviour? (iii) Is the mimic's signal deceptive? The first distinction divides mimicry into two broad categories: ‘signal mimicry’ and ‘cue mimicry’. ‘Signal mimicry’ occurs when mimic and model share the same receiver, and ‘cue mimicry’ when mimic and model have different receivers or when there is no receiver for the model's trait. ‘Masquerade’ fits conceptually within cue mimicry. The second and third distinctions divide both signal and cue mimicry into four types each. These are the three traditional mimicry categories (aggressive, Batesian and Müllerian) and a fourth, often overlooked category for which the term ‘rewarding mimicry’ is suggested. Rewarding mimicry occurs when the mimic's signal is non-deceptive (as in Müllerian mimicry) but where the mimic signals a fitness benefit to the receiver (as in aggressive mimicry). The existence of rewarding mimicry is a logical extension of the criteria used to differentiate the three well-recognized forms of mimicry. These four forms of mimicry are not discrete, immutable types, but rather help to define important axes along which mimicry can vary.


The Holocene ◽  
2018 ◽  
Vol 28 (9) ◽  
pp. 1523-1534 ◽  
Author(s):  
Althea L Davies ◽  
Richard Streeter ◽  
Ian T Lawson ◽  
Katherine H Roucoux ◽  
William Hiles

The concept of resilience has become increasingly important in ecological and socio-ecological literature. With its focus on the temporal behaviour of ecosystems, palaeoecology has an important role to play in developing a scientific understanding of ecological resilience. We provide a critical review of the ways in which resilience is being addressed by palaeoecologists. We review ~180 papers, identifying the definitions or conceptualisations of ‘resilience’ that they use, and analysing the ways in which palaeoecology is contributing to our understanding of ecological resilience. We identify three key areas for further development. First, the term ‘resilience’ is frequently defined too broadly to be meaningful without further qualification. In particular, palaeoecologists need to distinguish between ‘press’ vs ‘pulse’ disturbances, and ‘ecological’ vs ‘engineering’ resilience. Palaeoecologists are well placed to critically assess the extent to which these dichotomies apply in real (rather than theoretical) ecosystems, where climate and other environmental parameters are constantly changing. Second, defining a formal ‘response model’ – a statement of the anticipated relationships between proxies, disturbances and resilience properties – can help to clarify arguments, especially inferred causal links, since the difficulty of proving causation is a fundamental limitation of palaeoecology for understanding ecosystem drivers and responses. Third, there is a need for critical analysis of the role of scale in ecosystem resilience. Different palaeoenvironmental proxies are differently able to address the various temporal and spatial scales of ecological change, and these limitations, as well as methodological constraints on inherently noisy proxy data, need to be explored and addressed.


Nature ◽  
1976 ◽  
Vol 259 (5543) ◽  
pp. 446-447 ◽  
Author(s):  
Judith May ◽  
Robert M. May

Ecology ◽  
1932 ◽  
Vol 13 (3) ◽  
pp. 308-308

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