| Literature DB >> 23637740 |
Yohay Carmel1, Rafi Kent, Avi Bar-Massada, Lior Blank, Jonathan Liberzon, Oded Nezer, Gill Sapir, Roy Federman.
Abstract
It is thought that the science of ecology has experienced conceptual shifts in recent decades, chiefly from viewing nature as static and balanced to a conception of constantly changing, unpredictable, complex ecosystems. Here, we ask if these changes are reflected in actual ecological research over the last 30 years. We surveyed 750 articles from the entire pool of ecological literature and 750 articles from eight leading journals. Each article was characterized according to its type, ecological domain, and applicability, and major topics. We found that, in contrast to its common image, ecology is still mostly a study of single species (70% of the studies); while ecosystem and community studies together comprise only a quarter of ecological research. Ecological science is somewhat conservative in its topics of research (about a third of all topics changed significantly through time), as well as in its basic methodologies and approaches. However, the growing proportion of problem-solving studies (from 9% in the 1980s to 20% in the 2000 s) may represent a major transition in ecological science in the long run.Entities:
Mesh:
Year: 2013 PMID: 23637740 PMCID: PMC3634786 DOI: 10.1371/journal.pone.0059813
Source DB: PubMed Journal: PLoS One ISSN: 1932-6203 Impact factor: 3.240
Frequency of domains and topics in ecological research 1980–2010.
| Frequency of Topics (%) | ||||
| Domain | Topic/Type | All Journals | Core Journals | |
|
| Demography | 123 (16.4) | 219 (29.2) | *** |
| Physiology | 230 (30.7) | 154 (20.5) | *** | |
| Distribution | 113 (15.1) | 98 (13.1) | ||
| Behavior | 139 (18.5) | 96 (12.8) | ** | |
| Evolution | 31 (4.0) | 23 (3.0) | ||
| Genetics | 76 (10.1) | 15 (2.0) | *** | |
| Single Species | 532 (70.9) | 498 (66.4) | ||
|
| Grazing | 17 (2.3) | 69 (9.2) | *** |
| Predation | 53 (7.1) | 66 (8.8) | ||
| Mutualism | 12 (1.6) | 16 (2.1) | ||
| Parasitism | 20 (2.7) | 35 (4.7) | * | |
| Competition | 37 (4.9) | 53 (7.1) | ||
| Species Interactions | 132 (17.6) | 224 (29.9) | *** | |
|
| Biodiversity | 72 (9.6) | 58 (7.7) | |
| Community structure | 68 (9.1) | 82 (10.9) | ||
| Community | 124 (16.5) | 127 (16.9) | ||
|
| Food web | 25 (3.3) | 12 (1.6) | * |
| Climate change | 15 (2.0) | 13 (1.7) | ||
| Vegetation dynamics | 30 (4.0) | 89 (11.9) | *** | |
| Biomass and productivity | 60 (8.0) | 28 (3.7) | *** | |
| Biogeochemistry | 81 (10.8) | 63 (8.4) | ||
| Ecosystem | 121 (16.1) | 135 (18.0) | ||
| Others | Scale | 7 (0.9) | 20 (2.7) | * |
| Statistics | 11 (1.5) | 17 (2.3) | ||
Differences between the two surveys are: *** significant at the Bonferroni-adjusted level, p<0.001, ** p<0.01, * p<0.05.
Annual percentage change in the frequency of domains and topics in ecological research 1980–2010.
| Percent of annual average change (95% CI) | ||||
| Domain | Topic | All Journals | Core Journals | |
|
| Demography | NS | −2.0 (−0.2– −3.8)* | |
| Physiology | −3.1 (−5.9– −1.3) | NS | ||
| Distribution | NS | NS | ||
| Behavior | −5.0 (−7.1–−2.8) | NS | ||
| Evolution | NS | 5.9 (0.2–11.9)* | ||
| Genetics | 10.4 (6.9–14.1) | NS | ||
| Single species | NS | NS | ||
|
| Grazing | NS | −3.2 (−6.0–−0.3)* | |
| Predation | NS | NS | ||
| Mutualism | NS | NS | ||
| Parasitism | NS | 5.2 (0.9–9.7)* | ||
| Competition | NS | NS | ||
| Species interactions | NS | NS | ||
|
| Biodiversity | 6.0 (2.8– 9.2) | 4.7 (1.4–8.2)** | |
| Community structure | NS | NS | ||
| Community | 3.6 (1.3–6.0) | 2.9 (0.6–5.3)** | ||
|
| Food web | NS | NS | |
| Climate change | 7.7 (0.8–15.0)* | 13.9 (4.5–24.2) | ||
| Vegetation dynamics | NS | −2.7 (−5.2–−0.1)* | ||
| Biomass and productivity | NS | NS | ||
| Biogeochemistry | NS | NS | ||
| Ecosystem | NS | NS | ||
| Others | Scale | NS | 9.0 (2.7–15.7)** | |
| Statistics | NS | NS | ||
Change is significant at the Bonferroni-adjusted level, p<0.001, ** p<0.01, * p<0.05.
Figure 1Proportions of ecological domains in the last three decades.
White bars denote ‘all journals’ and gray bars denote ‘core journals’. Temporal trend was significant for community studies only (a logistic model, see Table 2).
Figure 2Change in the frequency over time for the topics for which temporal change was significant at the Bonferroni-adjusted level (p<0.001) in at least one of the datasets.
White bars denote ‘all journals’ and gray bars denote ‘core journals’. *** Temporal trend was significant (a logistic model, see Table 2), p<0.001. ** p<0.01. * p<0.05.
Frequency of research types and problem-solving studies, in ecological research 1980–2010.
| Frequency (%) | |||
| Research Type | All Journals | Core Journals | P |
| Observation | 446 (59.4) | 334 (44.5) | *** |
| Experiments | 206 (27.5) | 264 (35.2) | ** |
| Models | 89 (11.9) | 87 (11.6) | |
| Data Analysis | 66 (8.8) | 46 (6.1) | * |
| Problem solving | 127 (17.0) | 113 (15.1) | |
Differences between the two surveys are: *** significant at the Bonferroni-adjusted level, p<0.001, ** p<0.01, * p<0.05.
Annual percentage change in the frequency of research types and problem-solving studies, in ecological research 1980–2010.
| Percent of annual average change (95% CI) | ||
| Research Type | All journals | Core Journals |
| Observation | NS | NS |
| Experiments | NS | NS |
| Models | NS | 3.5 (0.8–6.2)** |
| Data Analysis | 4.9 (1.7–8.1)** | NS |
| Problem Solving | 4.7 (2.3–7.1) | 5.5 (3.0–8.1) |
Change is significant at the Bonferroni-adjusted level, p<0.001, ** p<0.01, * p<0.05.