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27 results for “lentic habitat”

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edi56/100

Mid-winter habitat suitability indices for centrarchids in contiguous lentic areas of the Upper Mississippi River System: 1994-2018

This dataset includes raw measurements and calculated bluegill winter habitat suitability indices for depth (HSID), dissolved oxygen (HSIDO), temperature (HSIT), and flow (HSIF), as well as an overall bluegill winter habitat suitability index (HSIO), for 2915 mid-winter, lentic sampling locations across 208 contiguous lentic areas throughout the Upper Mississippi River System (Upper Mississippi and Illinois Rivers) from 1994-2018. This dataset also includes several spatial and temporal climatic and hydrogeomorphic parameters that were used to assess potential drivers of winter habitat suitability.

openCC0Feb 2025View details →
dryad36/100

Data from: Predation drives morphological convergence in the Gambusia panuco species group among lotic and lentic habitats

Fish morphology is often constrained by a trade-off between optimizing steady vs. unsteady swimming performance due to opposing effects of caudal peduncle size. Lotic environments tend to select for steady swimming performance, leading to smaller caudal peduncles, while predators tend to select for unsteady swimming performance, leading to larger caudal peduncles. However, it is unclear which aspect of performance should be optimized across heterogeneous flow and predation environments and how this heterogeneity may affect parallel phenotypic evolution. We investigated this question among four Gambusia species in northeastern Mexico, specifically the riverine G. panuco, the spring endemics G. alvarezi and G. hurtadoi, and a fourth species, G. marshi, found in a variety of habitats with varying predation pressure in the Cuatro Ciénegas basin and Río Salado de Nadadores. We employed a geometric morphometric analysis to examine how body shapes of both male and female fish differ among species and habitats and with piscivore presence. We found that high-predation and low-predation species diverged morphologically, with G. marshi exhibiting a variable, intermediate body shape. Within G. marshi, body morphology converged in high-predation environments regardless of flow velocity, and fish from high-predation sites had larger relative caudal peduncle areas. However, we found that G. marshi from low-predation environments diverged in morphology between sub-basins of Cuatro Ciénegas, indicating other differences among these basins that merit further study. Our results suggest that a morphological trade-off promotes parallel evolution of body shape in fishes colonizing high-predation environments and that changing predation pressure can strongly impact morphological evolution in these species.

opencc-zeroDec 2016View details →
dryad36/100

Introgressive hybridization erodes morphological divergence between lentic and lotic habitats in an endangered minnow

<p>Introgressive hybridization may erode phenotypic divergence along environmental gradients, collapsing locally adapted populations into a hybrid swarm. Alternatively, introgression may promote phenotypic divergence by providing variation on which natural selection can act. In freshwater fishes, water flow often selects for divergent morphological traits in lake versus stream habitats. We tested the effects of introgression on lake-stream morphological divergence in the minnow Owens Tui Chub (<em>Siphateles</em> <em>bicolor</em> <em>snyderi</em>), which has been rendered endangered by introgression from the introduced Lahontan Tui Chub (<em>Siphateles</em> <em>bicolor</em> <em>obesa</em>). Using geometric morphometric analysis of 457 individual Tui Chub from thirteen populations, we found that both the native and introgressing parent taxa exhibited divergent body and caudal fin shapes in lake vs. stream habitats, but their trajectories of divergence were distinct. In contrast, introgressed populations exhibited intermediate body and caudal fin shapes that were not differentiated by habitat type, indicating that introgression has eroded phenotypic divergence along the lentic-lotic gradient throughout the historic range of the Owens Tui Chub. Individuals within hybrid populations were less morphologically variable than those within parent populations, suggesting hybrid adaptation to selective agents other than water flow or loss of variance by drift.</p>

opencc-zeroAug 2022View details →
dryad36/100

Introgressive hybridization erodes morphological divergence between lentic and lotic habitats in an endangered minnow

Open the record for dataset details and reuse information.

publicAug 2022View details →
dryad36/100

Data from: Predation drives morphological convergence in the Gambusia panuco species group among lotic and lentic habitats

Open the record for dataset details and reuse information.

publicDec 2017View details →
zenodo32/100

FIG. 10 in A Lentic Breeder in Lotic Waters: Sierra Nevada Yellow-Legged Frog (Rana sierrae) Habitat Suitability in Northern Sierra Nevada Streams

FIG. 10. Distribution of depth and velocity values over time within cascade (CAS), riffle (LGR), and pool (POO) geomorphic unit types at (A) Lone Rock Creek and (B) South Fork Tributary. Dashed and shaded box in lower left corner of each panel represents high suitability microhabitat for adults (includes subadults) of velocity,0.1 m s–1 and depth,0.3 m.

opennotspecifiedNov 2019View details →
zenodo32/100

FIG. 8 in A Lentic Breeder in Lotic Waters: Sierra Nevada Yellow-Legged Frog (Rana sierrae) Habitat Suitability in Northern Sierra Nevada Streams

FIG. 8. Mean predicted probability of microhabitat use by tadpoles of R. sierrae for all study sites combined for all possible values from a given predictor variable from 1,000 bootstrapped logistic regression models. Shading and bars represent 95% credible intervals. Substrate categories are silt (Slt), sand (Snd), fine gravel (FGrav), coarse gravel (CGrav), cobble (Cob), boulder (Bld), and bedrock (Bed).

opennotspecifiedNov 2019View details →
zenodo32/100

FIG. 6 in A Lentic Breeder in Lotic Waters: Sierra Nevada Yellow-Legged Frog (Rana sierrae) Habitat Suitability in Northern Sierra Nevada Streams

FIG. 6. Mean predicted probability of microhabitat use by adult R. sierrae (includes subadults) for all study sites combined for all possible values from a given predictor variable from the 1,000 bootstrapped logistic regression models. Shading and bars represent 95% credible intervals. Substrate categories are silt (Slt), sand (Snd), fine gravel (FGrav), coarse gravel (CGrav), cobble (Cob), boulder (Bld), and bedrock (Bed).

opennotspecifiedNov 2019View details →
zenodo32/100

FIG. 4 in A Lentic Breeder in Lotic Waters: Sierra Nevada Yellow-Legged Frog (Rana sierrae) Habitat Suitability in Northern Sierra Nevada Streams

FIG. 4. Distribution of use and available microhabitat points within each substrate category for locations of (A) adult (includes subadults) and (B) tadpoles of R. sierrae at each study site. To better visualize the number of points within each substrate category, violin boxplots were overlaid onto jittered points for each substrate category. The overlay shows a mirrored kernel density estimation for all substrate size categories to illustrate the distribution of the data. IND ¼ Independence Creek, LRC ¼ Lone Rock Creek, SFRC ¼ South Fork Rock Creek, SFT ¼ South Fork Tributary, SFTT ¼ South Fork Tadpole Tributary.

opennotspecifiedNov 2019View details →
zenodo32/100

FIG. 3 in A Lentic Breeder in Lotic Waters: Sierra Nevada Yellow-Legged Frog (Rana sierrae) Habitat Suitability in Northern Sierra Nevada Streams

FIG. 3. Hydraulic variables measured for locations and available microhabitat points of (A) adult and (B) tadpoles of R. sierrae in five study sites in the Sierra Nevada. Figures show the relationship between total depth and mid-column velocity at both use and available locations for (A) adults (includes subadults) and (B) tadpoles at each study site. IND ¼ Independence Creek, LRC ¼ Lone Rock Creek, SFRC ¼ South Fork Rock Creek, SFT ¼ South Fork Tributary, SFTT ¼ South Fork Tadpole Tributary.

opennotspecifiedNov 2019View details →
zenodo32/100

FIG. 2 in A Lentic Breeder in Lotic Waters: Sierra Nevada Yellow-Legged Frog (Rana sierrae) Habitat Suitability in Northern Sierra Nevada Streams

FIG. 2. Hydrographs of stream stage (depth) at three of five study sites in the northern Sierra Nevada over the course of the study. (A) South Fork Rock Creek (SFRC) and (B) Lone Rock Creek (LRC) hydrographs show a strong seasonal signal of winter storm events and spring snowmelt recession into low flow in summer, while (C) Independence Creek (IND) shows modified flow releases in spring and augmented flow releases in late summer from the upstream reservoir. Data were collected with pressure transducers placed in pools that remained wet over the summer.

opennotspecifiedNov 2019View details →
zenodo32/100

FIG. 5 in A Lentic Breeder in Lotic Waters: Sierra Nevada Yellow-Legged Frog (Rana sierrae) Habitat Suitability in Northern Sierra Nevada Streams

FIG. 5. Distribution of use and available points within each total cover decile for locations and available microhabitat points of (A) adult (includes subadults) and (B) tadpoles of R. sierrae at each study site. To better visualize the number of points within each decile, points are jittered. Overlay shows a mirrored kernel density estimate for total cover deciles to illustrate the distribution of the data. IND ¼ Independence Creek, LRC ¼ Lone Rock Creek, SFRC ¼ South Fork Rock Creek, SFT ¼ South Fork Tributary, SFTT ¼ South Fork Tadpole Tributary.

opennotspecifiedNov 2019View details →
zenodo32/100

Figure 6 in Predatory insects in lentic freshwater habitats from northwest Patagonia: richness and phenology

Figure 6. Seasonal variations in dominant insect species abundance at four wetlands with different hydroperiods (given between brackets in each figure). In addition, for each wetland, average monthly water temperature recorded between 11.00 and 16.00 h is plotted (grey triangles).

opennotspecifiedJun 2013View details →
zenodo32/100

Figure 5 in Predatory insects in lentic freshwater habitats from northwest Patagonia: richness and phenology

Figure 5. Phenology of predatory insects (black bar = adult stage; white bar = coleopteran larva; single-hatched bar = odonate nymph; double-hatched bar = hemipteran nymph), and climate data (precipitation = black circles; minimum temperatures = white triangles; maximum temperatures = black triangles) from June 2006 to March 2007.

opennotspecifiedJun 2013View details →
zenodo32/100

Figure 4 in Predatory insects in lentic freshwater habitats from northwest Patagonia: richness and phenology

Figure 4. Monthly variation in predatory insect richness in the wetlands studied, showing mean richness (± SE) for the wetlands classified according to their hydroperiod.

opennotspecifiedJun 2013View details →
zenodo32/100

Figure 3 in Predatory insects in lentic freshwater habitats from northwest Patagonia: richness and phenology

Figure 3. Comparison of the richness of predatory insects in three types of wetlands, classified according to the duration of the hydroperiod. Different letters indicate significant differences in species richness (P &lt;0.01).

opennotspecifiedJun 2013View details →
zenodo32/100

Figure 2 in Predatory insects in lentic freshwater habitats from northwest Patagonia: richness and phenology

Figure 2. Predatory insect distribution in the study area. Distribution index was obtained by the ratio: number of wetlands with species i/total number of wetlands sampled.

opennotspecifiedJun 2013View details →
zenodo32/100

Figure 1 in Predatory insects in lentic freshwater habitats from northwest Patagonia: richness and phenology

Figure 1. Map of the study area surrounding the city of San Carlos de Bariloche. Numbers refer to wetland location: 1 = Llao-Llao; 2 = Laguna El Trébol; 3 = Mallín 2 de Agosto; 4 = Laguna Fantasma; 5 = Virgen de las Nieves; 6 = Mallín Pinar de Festa; 7 = Teleférico; 8 = Mallín Ñireco, Ñireco 1 and Ñireco 2; 9 = Laguna Verde; 10 = Mallín Los Patos; 11 = Bernal 1–6; 12 = Ñirihuau 1–4. The triangle indicates the location of the meteorological station.

opennotspecifiedJun 2013View details →
dryad28/100

Data from: Not going with the flow: a comprehensive time-calibrated phylogeny of dragonflies (Anisoptera: Odonata: Insecta) provides evidence for the role of lentic habitats on diversification

Ecological diversification of aquatic insects has long been suspected to have been driven by differences in freshwater habitats, which can be classified into flowing (lotic) waters and standing (lentic) waters. The contrasting characteristics of lotic and lentic freshwater systems imply different ecological constraints on their inhabitants. The ephemeral and discontinuous character of most lentic water bodies may encourage dispersal by lentic species in turn reducing geographical isolation among populations. Hence, speciation probability would be lower in lentic species. Here, we assess the impact of habitat use on diversification patterns in dragonflies (Anisoptera: Odonata). Based on the eight nuclear and mitochondrial genes, we inferred species diversification with a model-based evolutionary framework, to account for rate variation through time and among lineages and to estimate the impact of larval habitat on the potentially nonrandom diversification among anisopteran groups. Ancestral state reconstruction revealed lotic fresh water systems as their original primary habitat, while lentic waters have been colonized independently in Aeshnidae, Corduliidae and Libellulidae. Furthermore, our results indicate a positive correlation of speciation and lentic habitat colonization by dragonflies: speciation rates increased in lentic Aeshnidae and Libellulidae, whereas they remain mostly uniform among lotic groups. This contradicts the hypothesis of inherently lower speciation in lentic groups and suggests species with larger ranges are more likely to diversify, perhaps due to higher probability of larger areas being dissected by geographical barriers. Furthermore, larger range sizes may comprise more habitat types, which could also promote speciation by providing additional niches, allowing the coexistence of emerging species.

opencc-zeroDec 2015View details →
zenodo28/100

Figure 2 from: Silva M, Rezende R, Lopes Ferreira R (2013) Detritus processing in lentic cave habitats in the neotropics. Subterranean Biology 11: 3-14. https://doi.org/10.3897/subtbiol.11.5107

Figure 2 - Remaining weight of plant disks exposed to processing in the 9 mm2 litterbag mesh size in the lentic habitats of Brega and Santuário caves. Mean, Box: Mean±SE, Whisker: Mean±SD.

opencc-by-4.0Apr 2013View details →

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