scholarly journals Comparison of Natural Abiotic Factors and Pollution Influence on the Soil Enzymative Activity

2022 ◽  
Vol 23 (1) ◽  
pp. 42-48
Author(s):  
Anna Olkova ◽  
Evgeniya Tovstik
Keyword(s):  
Abiotic Factors

Coral husbandry for ocean futures: leveraging abiotic factors to increase survivorship, growth, and resilience in juvenile Montipora capitata

2021 ◽  
Vol 657 ◽  
pp. 123-133
Author(s):  
JR Hancock ◽  
AR Barrows ◽  
TC Roome ◽  
AS Huffmyer ◽  
SB Matsuda ◽  
...  
Keyword(s):  
Abiotic Factors ◽  
Larval Rearing ◽  
Abiotic Conditions ◽  
Montipora Capitata ◽  
Reef Restoration ◽  
Juvenile Corals ◽  
Bleaching Response ◽  
The Face ◽  
Survival And Growth ◽  
Global And Local

Reef restoration via direct outplanting of sexually propagated juvenile corals is a key strategy in preserving coral reef ecosystem function in the face of global and local stressors (e.g. ocean warming). To advance our capacity to scale and maximize the efficiency of restoration initiatives, we examined how abiotic conditions (i.e. larval rearing temperature, substrate condition, light intensity, and flow rate) interact to enhance post-settlement survival and growth of sexually propagated juvenile Montipora capitata. Larvae were reared at 3 temperatures (high: 28.9°C, ambient: 27.2°C, low: 24.5°C) for 72 h during larval development, and were subsequently settled on aragonite plugs conditioned in seawater (1 or 10 wk) and raised in different light and flow regimes. These juvenile corals underwent a natural bleaching event in Kāne‘ohe Bay, O‘ahu, Hawai‘i (USA), in summer 2019, allowing us to opportunistically measure bleaching response in addition to survivorship and growth. This study demonstrates how leveraging light and flow can increase the survivorship and growth of juvenile M. capitata. In contrast, larval preconditioning and substrate conditioning had little overall effect on survivorship, growth, or bleaching response. Importantly, there was no optimal combination of abiotic conditions that maximized survival and growth in addition to bleaching tolerances. This study highlights the ability to tailor sexual reproduction for specific restoration goals by addressing knowledge gaps and incorporating practices that could improve resilience in propagated stocks.

Characterizing the impact of recovering sea otters on commercially important crabs in California estuaries

2020 ◽  
Vol 655 ◽  
pp. 123-137
Author(s):  
TM Grimes ◽  
MT Tinker ◽  
BB Hughes ◽  
KE Boyer ◽  
L Needles ◽  
...  
Keyword(s):  
Abiotic Factors ◽  
Sea Otter ◽  
Dungeness Crab ◽  
Sea Otters ◽  
Elkhorn Slough ◽  
Enhydra Lutris Nereis ◽  
Crab Abundance ◽  
Population Sizes ◽  
Commercially Important ◽  
The Impact

Protective legislation and management have led to an increase in California’s sea otter Enhydra lutris nereis population. While sea otter recovery has been linked to ecosystem benefits, sea otter predation may negatively affect commercially valuable species. Understanding the potential influence of sea otters is of particular importance as their range expands into estuaries that function as nurseries for commercially valuable species like Dungeness crab Metacarcinus magister. We consider how sea otter predation has affected the abundance and size of juvenile Dungeness crab in Elkhorn Slough, California, USA, and analyzed cancrid crab abundance and size across 4 California estuaries with and without sea otters to understand how biotic and abiotic factors contribute to observed variation in crab size and abundance. We compared trends in southern sea otters relative to Dungeness crab landings in California to assess whether increasing sea otter abundance have negatively impacted landings. In Elkhorn Slough, juvenile Dungeness crab abundance and size have declined since 2012, coinciding with sea otter population growth. However, the impact of sea otters on juvenile Dungeness crab size was habitat-specific and only significant in unvegetated habitat. Across estuaries, we found that cancrid crab abundance and size were negatively associated with sea otter presence. While abiotic factors varied among estuaries, these factors explained little of the observed variation in crab abundance or size. Although we found evidence that sea otters can have localized effects on cancrid crab populations within estuaries, we found no evidence that southern sea otters, at recent population sizes, have negatively impacted Dungeness crab landings in California from 2000-2014.

Do habitat size and shape modify abiotic factors and communities in artificial treeholes?

2006 ◽  
Vol 7 (2) ◽  
pp. 211-222 ◽  
Author(s):  
N. Harlan ◽  
C. Paradise
Keyword(s):  
Abiotic Factors ◽  
Habitat Size ◽  
Size And Shape

Effect of Changes in Some Abiotic Factors on Growth, Reproduction, and Energy Metabolism of the Rotifer Euchlanis dilatata Ehrenberg

1998 ◽  
Vol 34 (1) ◽  
pp. 76-83
Author(s):  
A. S. Konstantinov ◽  
N. A. Tagirova ◽  
V. M. Stepanenko ◽  
E. A. Solov'eva
Keyword(s):  
Energy Metabolism ◽  
Abiotic Factors ◽  
Euchlanis Dilatata

Large-scale mapping of the catenas vegetation in Subarctic tundra

1995 ◽  
pp. 3-21
Author(s):  
S. S. Kholod
Keyword(s):  
Spatial Distribution ◽  
Vegetation Cover ◽  
Large Scale ◽  
Block Diagram ◽  
Abiotic Factors ◽  
Ecological Factors ◽  
Spatial Arrangement ◽  
Geological Time ◽  
Ecological Barriers ◽  
Functional Zones

One of the most difficult tasks in large-scale vegetation mapping is the clarification of mechanisms of the internal integration of vegetation cover territorial units. Traditional way of searching such mechanisms is the study of ecological factors controlling the space heterogeneity of vegetation cover. In essence, this is autecological analysis of vegetation. We propose another way of searching the mechanisms of territorial integration of vegetation. It is connected with intracoenotic interrelation, in particular, with the changing role of edificator synusium in a community along the altitudinal gradient. This way of searching is illustrated in the model-plot in subarctic tundra of Central Chukotka. Our further suggestion concerns the way of depicting these mechanisms on large-scale vegetation map. As a model object we chose the catena, that is the landscape formation including all geomorphjc positions of a slope, joint by the process of moving the material down the slope. The process of peneplanation of a mountain system for a long geological time favours to the levelling the lower (accumulative) parts of slopes. The colonization of these parts of the slope by the vegetation variants, corresponding to the lowest part of catena is the result of peneplanation. Vegetation of this part of catena makes a certain biogeocoenotic work which is the levelling of the small infralandscape limits and of the boundaries in vegetation cover. This process we name as the continualization on catena. In this process the variants of vegetation in the lower part of catena are being broken into separate synusiums. This is the process of decumbation of layers described by V. B. Sochava. Up to the slope the edificator power of the shrub synusiums sharply decreases. Moss and herb synusium have "to seek" the habitats similar to those under the shrub canopy. The competition between the synusium arises resulting in arrangement of a certain spatial assemblage of vegetation cover elements. In such assemblage the position of each element is determined by both biotic (interrelation with other coenotic elements) and abiotic (presence of appropriate habitats) factors. Taking into account the biogeocoenotic character of the process of continualization on catena we name such spatial assemblage an exolutionary-biogeocoenotic series. The space within each evolutionary-biogeocoenotic series is divided by ecological barriers into some functional zones. In each of the such zones the struggle between synusiums has its individual expression and direction. In the start zone of catena (extensive pediment) the interrelations of synusiums and layers control the mutual spatial arrangement of these elements at the largest extent. Here, as a rule, there predominate edificator synusiums of low and dwarfshrubs. In the first order limit zone (the bend of pediment to the above part of the slope) one-species herb and moss synusiums, oftenly substituting each other in similar habitats, get prevalence. In the zone of active colonization of slope (denudation slope) the coenotic factor has the least role in the spatial distribution of the vegetation cover elements. In particular, phytocoenotic interactions take place only within separate microcoenoses of herbs, mosses and lichens. In the zone of the attenuation of continualization process (the upper most parts of slope, crests) phytocoenotic interactions are almost absent and the spatial distribution of vegetation cover elements depends exclusively on the abiotic factors. The principal scheme of the distribution of vegetation cover elements and the disposition of functional zones on catena are shown on block-diagram (fig. 1).

Vegetation structure of tundra and taiga on the map of the natural vegetation of Europe

2007 ◽  
pp. 13-22 ◽  
Author(s):  
T. K. Yurkovskaya
Keyword(s):  
Vegetation Cover ◽  
Abiotic Factors ◽  
Self Regulation ◽  
Space Structure ◽  
Middle Taiga ◽  
Russian Plain ◽  
Forest Communities ◽  
The North ◽  
Tundra Vegetation ◽  
Starting Point

I have focused only on some features of structure in the taiga vegetation cover. In conclusion I would like to tell some words about the causes of complicated space structure of the taiga and tundra vegetation cover. The causes of latitudinal differentiation are climatic undoubtedly, but heterogeneity of vegetation cover within the limits of tundra and taiga subzones is accounted for different factors. In tundra abiogenic factors prevail, first of all the permafrost processes. That is the reason why tundra vegetation cover is so sensible to any disturbances and so hard regenerates after various transformations. In taiga the space structure is mostly the result of self-regulation and self- restoration of biota. The abiotic factors, certainly, play significant role, but they recede to the second plan. So we showed that in the north and middle taiga the structure of vegetation cover, during the Holocene up to present time, is determined in many respects by the increasing role of mires. Suffice it to look at the map of distribution of mires in order to estimate their role in vegetation cover of the easteuropean taiga (Yurkovskaya, 1980). So, the increase of mire area on the Russian Plain in m2/year per 1000 ha varies between 200 and 700, the average increas is ca 300—400 m2/year (Elina et all., 2000). The mires favour peniplenization and unite the separate areas of forest communities into the whole by means of forming the buffer paludificated territories (various hydrophilous variants of forest communities). But if mires, at all their stability, after destroying practically don't restore, the forests even after continuous cuttings restore their structure and composition through the series of successional stages unless an ecotope is damaged completely. Hence the space structure of taiga is the result, first of all, self development and self regulation of its vegetation cover. But, as it is known, at present time the process of destruction of natural biota has gone too far that the question arises not only about supporting its state and structure but also about the survival of the mankind itself. In this regard the vegetation map of Europe is the invaluable basis, which gives the starting point for all conservational, ecological and economical measures. But it is important to learn reading and using the map. And this is one of our actual goals.

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