Hydrobiologia

Naselli-Flores, Luigi; Rossetti, Giampaolo

doi: 10.1007/s10750-010-0340-6pmid: N/A

Thomaz, Sidinei; Michelan, Thaisa; Carvalho, Priscilla; Bini, Luis

doi: 10.1007/s10750-010-0342-4pmid: N/A

In 1959, G.E. Hutchinson provided a general explanation for the diversity of species in his paper “Homage to Santa Rosalia or why are there so many kinds of animals?” To assess the contribution of the ideas Hutchinson introduced in “The Homage” to aquatic ecology research, we performed a bibliometric evaluation of all the articles that cited this paper between 1960 and 2009. The articles were retrieved using the database from Thomson Reuters (ISI Web of Knowledge) in March 2009. For each paper, we first identified the studied environment (terrestrial, marine or freshwater) and whether the study was theoretical or empirical. For marine and freshwater studies, we recorded the journal where the article was published, the year of publication, the number of citations, the taxonomic group (e.g. fish, phytoplankton, zooplankton, macroinvertebrates or macrophytes), the habitat (e.g. wetlands, lakes, rivers, streams or ocean) and the main ideas addressed. A total of 1345 articles cited “The Homage”, and the number of citations increased significantly with time. Most of the articles that cited “The Homage” described research carried out in a terrestrial environment or were theoretical, and a lesser number of citations came from freshwater and marine papers, which used mainly fish and invertebrates as model organisms. In the aquatic sciences, most of the papers discussed the influences of competition and energy (productivity) on diversity. Our results indicate that “The Homage” can still be considered a “citation classic” and a breakthrough contribution, and that it is still having a great impact on different fields of ecology, including limnology and marine ecology.

Litchman, Elena; de Tezanos Pinto, Paula; Klausmeier, Christopher; Thomas, Mridul; Yoshiyama, Kohei

doi: 10.1007/s10750-010-0341-5pmid: N/A

In addition to answering Hutchinson’s question “Why are there so many species?”, we need to understand why certain species are found only under certain environmental conditions and not others. Trait-based approaches are being increasingly used in ecology to do just that: explain and predict species distributions along environmental gradients. These approaches can be successful in understanding the diversity and community structure of phytoplankton. Among major traits shaping phytoplankton distributions are resource utilization traits, morphological traits (with size being probably the most influential), grazer resistance traits, and temperature responses. We review these trait-based approaches and give examples of how trait data can explain species distributions in both freshwater and marine systems. We also outline new directions in trait-based approaches applied to phytoplankton such as looking simultaneously at trait and phylogenetic structure of phytoplankton communities and using adaptive dynamics models to predict trait evolution.

Descy, Jean-Pierre; Tarbe, Anne-Laure; Stenuite, Stéphane; Pirlot, Samuel; Stimart, Johan; Vanderheyden, Julie; Leporcq, Bruno; Stoyneva, Maya; Kimirei, Ismael; Sinyinza, Danny; Plisnier, Pierre-Denis

doi: 10.1007/s10750-010-0343-3pmid:

Padisák, Judit; Hajnal, Éva; Krienitz, Lothar; Lakner, József; Üveges, Viktória

doi: 10.1007/s10750-010-0344-2pmid: N/A

In this article, we attempt to estimate the contemporary phytoplankton species pool of a particular lake, by assessing the rate of floral change over a period of 15 years. Phytoplankton time series data from Lake Stechlin, an oligo-mesotrophic lake in the Baltic Lake District (Germany) were used. Of the 254 algal species recorded during the 15-year of studies with roughly biweekly sampling, 212 species were planktonic. In the individual plankton years, the recorded total number of species changed between 97 and 122, of which the number of dominants (>1% contribution to the annual average of total biomass) was only 10–19. The 15-year cumulative number of species exhibited an almost linear increase after an initial saturation phase. This increase was attributed to two reasons: increase of sample size and immigration of species new to the flora. Based on a probabilistic model developed in this study, we estimated the number of co-existing planktonic species of the lake as some 180, and the rate of floral change as 1–2 species per year. Of these co-existing species, only few maintain the matter–energy processing ecosystem functions in any particular plankton year. Selection of these dominants is probably driven by mesoclimatic cycles, coupled with human-induced forcing, like eutrophication. All others are hiding as an ecological memory, in the sense of the capacity or experiences of past states to influence present or future responses of the community. Data analyses suggest that selection of the ‘memory species’ that show temporary abundance increases over shorter (several years) periods are largely dependent upon the dominants. These results show that interspecific interactions and the particular autecological features of the dominants, together with their effects on the whole ecosystem, act as a major organizing force. Some phytoplankton species, like Planktothrix rubescens, are efficient ecosystem engineers with cascading effects of both a top-down and bottom-up nature. Historical scientific data on Planktothrix blooms in Lake Stechlin suggest cyclic patterns in long-term development of phytoplankton which, as the legend of the Red Cock suggests, dates back much further than scientific archives.

Matthiessen, Birte; Ptacnik, Robert; Hillebrand, Helmut

doi: 10.1007/s10750-010-0349-xpmid: N/A

The evidence for species diversity effects on ecosystem functions is mainly based on studies not explicitly addressing local or regional processes regulating coexistence or the importance of community structure in terms of species evenness. In experimental communities of marine benthic microalgae, we altered the successional stages and thus the strength of local species interactions by manipulating rates of dispersal and disturbance. The treatments altered realized species richness, evenness and community biomass. For species richness, dispersal mattered only at high disturbance rates; when opening new space, dispersal led to maximized richness at intermediate dispersal rates. Evenness, in contrast, decreased with dispersal at low or no disturbance, i.e. at late successional stages. Community biomass showed a non-linear hump-shaped response to increasing dispersal at all disturbance levels. We found a positive correlation between richness and biomass at early succession, and a strong negative correlation between evenness and biomass at late succession. In early succession both community biomass and richness depend directly on dispersal from the regional pool, whereas the late successional pattern shows that if interactions allow the most productive species to become dominant, diverting resources from this species (i.e. higher evenness) reduces production. Our study emphasizes the difference in biodiversity–function relationships over time, as different mechanisms contribute to the regulation of richness and evenness in early and late successional stages.

Muylaert, Koenraad; Pérez-Martínez, Carmen; Sánchez-Castillo, Pedro; Lauridsen, Torben; Vanderstukken, Maarten; Declerck, Steven; Gucht, Katleen; Conde-Porcuna, José-Maria; Jeppesen, Erik; Meester, Luc; Vyverman, Wim

doi:

Rojo, Carmen; Salazar, Guillem

doi: 10.1007/s10750-010-0346-0pmid: N/A

In an attempt to explain ‘Why are there so many kinds of animals?’ G.E. Hutchinson highlighted the food web context to suggest that diversity of primary producers should allow consumer richness to be maintained as a result of their adaptive foraging. Co-existence of consumers is then made possible when species differ in body size and thus only a minor diet overlap occurs. All these ideas are still major topics in ecological research and some have been re-examined in order to provide mechanistic explanations of species richness versus connectance relationships in food web structure. The effect of body size as a determinant of diet, jointly with the assumption that individuals are adapted to switch their diet in order to maximise energy gain, have been combined in recent years to develop the Allometric Diet Breadth Model (ADBM). This model, successful for plankton communities, enables us to determine the specific resource–consumer links and then evaluate the diet breadth and test whether the diet overlaps. Here, we apply the ADBM to infer the feeding linkages within a freshwater planktonic community of a Spanish oligo-mesotrophic lake and three spatial partitions of it. ADBM treats phytoplankton species and bacteria as resources and each consumer species (ciliates, rotifers and crustaceans) as both consumers and resources. We applied ADBM to water-column integrated- and single-layered plankton communities to test the importance of the diet on structuring the plankton. If a given pair of species that co-occur in the whole vertical community overlap their diet more than when they occur in the three layers separately, this means that they will never co-exist and are hence overdispersed (segregated). Not all species pairs that have a weak diet overlap when belonging to the whole water-column community co-exist in water-layered communities. Hence, the richer, whole water-column community would then have lower diet overlap than spatially segregated communities. Therefore, the hypothesis of diet breadth of Hutchinson (The American Naturalist 93: 145–159, 1959) explains community structure throughout the water column, and its deviations may be forced abiotically.

Gliwicz, Z.; Wursbaugh, Wayne; Szymanska, Ewa

doi: 10.1007/s10750-010-0347-zpmid: N/A

Examples from fishless aquatic habitats show that competition among zooplankton for resources instigates rapid exclusion of competitively inferior species in the absence of fish predation, and leads to resource monopolization by the superior competitor. This may be a single species or a few clones with large body size: a cladoceran such as Daphnia pulicaria, or a branchiopod such as Artemia franciscana, each building its population to a density far higher than those found in habitats with fish. The example of zooplankton from two different fish-free habitats demonstrates the overpowering force of fish predation by highlighting the consequences of its absence. Released from the mortality caused by predation, a population of a superior competitor remains at a density equal to the carrying capacity of its habitat, in a steady state with its food resources, consisting of small green flagellate algae, which are successful in compensating high loss rates due to grazing, by fast growth. In such a situation, the high filtering rate of Daphnia or Artemia reduces resources to levels that are sufficient for assimilation to cover the costs of respiration (threshold food concentration) in adults but not in juveniles. This implies long periods of persistence of adults refraining from producing live young, because production of instantly hatching eggs would be maladaptive. Severe competition for limiting resources imposes a strong selective pressure for postponing reproduction or for producing resting eggs until food levels have increased. Offspring can only survive when born in a short time window between such an increase in food levels and its subsequent decline resulting from population growth and intense grazing by juveniles. Such zooplanktons become not only a single-species community, but also form a single cohort with a long-lifespan population. The observations support the notion that diversity may be sustained only where predation keeps densities of coexisting species at levels much below the carrying capacity, as suggested by Hutchinson 50 years ago.

Ordóñez, Jaime; Armengol, Joan; Moreno-Ostos, Enrique; Caputo, Luciano; García, Juan; Marcé, Rafael

doi: 10.1007/s10750-010-0348-ypmid: N/A

Among the topics covered by Hutchinson’s Santa Rosalia article, the question of the shortening and lengthening of food webs occupies a central role. As Hutchinson realized, at the time scales of ecological studies, the impact of invader species on established food webs is the fastest shortcut to the shortening or lengthening of the food webs. The construction of thousands of dams in Spain during the last century has offered ecologists a good opportunity to test the effects of invader fish species on the plankton dynamics of these systems. In this article, a series of data related to the food web structure of Sau Reservoir is analyzed for the period 1997–2005. Parameters such as Secchi depth and chlorophyll concentration, as well as abundance and size structure of zooplankton, have been matched to the zooplankton dynamics in the reservoir. Most of the changes detected within this period are attributed to the introduction of zooplanktivorous fish in the reservoir. The Secchi depth measurements have showed a progressive diminution in the clear-water phase during recent years. These changes have been related to the decrease in the abundance of Daphnia and to the reduction of the size of zooplankton, which help to explain concomitant increases in the chlorophyll concentration in the same period. Other observed changes in the composition of the zooplankton community have been the substitution of Daphnia by Bosmina and the increase in the abundance of rotifers. Thus, the annual average abundance of Bosmina in 1997 was 70% of cladocerans, while in 2005 it reached 98%. In parallel, the percentage occurrence of individual rotifers was 40% of total zooplankton numbers but had risen to 85% at the end of the period. All these changes are attributed to the artificial expansion of the food web through stocking of the reservoir with zooplanktivorous fish (Rutilus rutilus and Alburnus alburnus). This study improves our understanding of the trophic relationships in the food web prior to the introduction of the fish.