Stephanie M. Carlson’s research while affiliated with University of California, Berkeley and other places

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Publications (114)


Anatomy of a range contraction: Flow–phenology mismatches threaten salmonid fishes near their trailing edge
  • Article

March 2025

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39 Reads

Proceedings of the National Academy of Sciences

Stephanie M. Carlson

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Climate change is redistributing life on Earth, with profound impacts for ecosystems and human well-being. While repeat surveys separated by multidecadal intervals can determine whether observed shifts are in the expected direction (e.g., poleward or upslope due to climate change), they do not reveal their mechanisms or time scales: whether they were gradual responses to environmental trends or punctuated responses to disturbance events. Here, we document population reductions and temporary range contractions at multiple sites resulting from drought for three Pacific salmonids at their ranges’ trailing edge. During California’s 2012 to 2016 historic multiyear drought, the 2013 to 2014 winter stood apart because rainfall was both reduced and delayed. Extremely low river flows during the breeding season (“flow–phenology mismatch”) reduced or precluded access to breeding habitat. While Chinook ( Oncorhynchus tshawytscha) experienced a down-river range shift, entire cohorts failed in individual tributaries (steelhead trout, O. mykiss ) and in entire watersheds (coho salmon, O. kisutch) . Salmonids returned to impacted sites in subsequent years, rescued by reserves in the ocean, life history diversity, and, in one case, a conservation broodstock program. Large population losses can, however, leave trailing-edge populations vulnerable to extinction due to demographic stochasticity, making permanent range contraction more likely. When only a few large storms occur during high flow season, the timing of particular storms plays an outsized role in determining which migratory fish species are able to access their riverine breeding grounds and persist.


Disparity in the number of weather stations within a ~30 km radius of two ecologically and economically important freshwater lakes: (A) Nahuel Huapi Lake in Patagonia, Argentina, and (B) Lake Tahoe in the Western United States. There are 122 weather stations around Lake Tahoe (https://mesowest.utah.edu/), but only two weather stations around Nahuel Huapí Lake (https://snih.hidricosargentina.gob.ar/Filtros.aspx). Meteorological data around Lake Tahoe are collected and maintained by five separate organizational entities (colored dots): NWS (National Weather Service); CWOP (Citizen Weather Observer Program); RAWS (Remote Automatic Weather Stations); SNOTEL (Snow Telemetry Network); and OLRN (Other Local and Regional Networks).
Sufficient data collection (abundance, coverage, representativeness, and appropriate methodology) and data access (useability, interoperability, availability, and visibility) are crucial for generating useful information to address environmental challenges. Ideally data collection and access increase in tandem, achieving high utility along the shortest path (black arrow). Research and monitoring programs can follow different paths toward generating high‐utility data (dark blue region), but many “stall out” along their trajectory (solid red arrows). In many regions or ecosystem types, data abundance and even more so, data access, remain at low levels, reducing the utility of data that are collected (Scenario A). In highly monitored ecosystems, data abundance often increases more rapidly than data access, resulting in a plateau of low data utility (Scenario B). In another example (Scenario C), data are accessible, but due to sampling biases, data coverage and representativeness is insufficient to achieve high utility. For all three scenarios, solutions may be applied to get them “back on track” toward higher data utility (dashed arrows).
(A) Global distribution of river gaging stations, with longer time series (years) shown in warmer colors, and (B) the historical trajectory in the number of river gages on each continent, standardized by the estimated surface area of rivers and streams (Allen & Pavelsky, 2018), with brown colors showing continents in the northern hemisphere, and turquoise colors showing continents in the southern hemisphere. (C) Stream and river methane flux measurements, with greater number of measurements (days) shown in warmer colors. (D) The monthly distribution of daily methane flux measurements, with brown representing data collected in the northern hemisphere and turquoise representing data collected from the southern hemisphere. Data shown in panels (A and B) were obtained from the Global Runoff Data Center (https://portal.grdc.bafg.de/), accessed September 2023. Trends in panel (B) are shown through 2014 to allow for delay in reporting. Stream and river methane flux data shown in panels (C and D) were obtained from the Global River Methane Database (GRiMe; Stanley et al., 2023).
Too much and not enough data: Challenges and solutions for generating information in freshwater research and monitoring
  • Article
  • Full-text available

March 2025

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295 Reads

Evaluating progress toward achieving freshwater conservation and sustainability goals requires transforming diverse types of data into useful information for scientists, managers, and other interest groups. Despite substantial increases in the volume of freshwater data collected worldwide, many regions and ecosystems still lack sufficient data collection and/or data access. We illustrate how these data challenges result from a diverse set of underlying mechanisms and propose solutions that can be applied by individuals or organizations. We discuss creative approaches to address data scarcity, including the use of community science, remote‐sensing, environmental sensors, and legacy datasets. We highlight the importance of coordinated data collection efforts among groups and training programs to improve data access. At the institutional level, we emphasize the power of prioritizing data curation, incentivizing data publication, and promoting research that enhances data coverage and representativeness. Some of these strategies involve technological and analytical approaches, but many necessitate shifting the priorities and incentives of organizations such as academic and government research institutions, monitoring groups, journals, and funding agencies. Our overarching goal is to stimulate discussion to narrow the data disparities hindering the understanding of freshwater processes and their change across spatial scales.

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Variation in Salmon Migration Phenology Bolsters Population Stability but Is Threatened by Drought

February 2025

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48 Reads

Ecology Letters

Intrapopulation variation in movement is common in nature but its effects on population dynamics are poorly understood. Using movement data from 3270 individually‐marked fish representing nine cohorts of coho salmon (Oncorhynchus kisutch) in California, we show that bimodal intrapopulation variation in the timing of juvenile down‐migration from their natal habitat and subsequent residence in non‐natal habitat affects growth, emigration timing, and the abundance and stability of adult returns. Non‐natal fish (early down‐migrants) exhibited more variable growth and more variable but earlier emigration to the estuary than natal fish (late down‐migrants). While natal rearing was more common, non‐natal fish were overrepresented among adult returns, and total returns were 1.4 times more stable than natal returns alone. Our results demonstrate that variation in migratory behaviour bolsters population stability. However, non‐natal rearing is reduced in low water years, suggesting that drought exacerbates population instability by reducing critical intrapopulation variation.


FIGURE 1 | Spatial configuration of the network used in this analysis based on the Brittany metapopulation. Populations are represented by circles (size scaled to population size, colour based on net migration) and emigration flows between populations are represented by the arrows (width scaled to emigrants' number). Modified from Lamarins, Hugon, et al. (2022) with a dispersal rate of 15% and no exploitation.
FIGURE 3 | Metapopulation performance metrics averaged over the metapopulation and simulations for life-history selectivity (left/right) and spatial selectivity (colours) scenarios of exploitation, for increasing metapopulation exploitation rate (MER) and a dispersal rate of 15% (other rates in Data S1). The local exploitation rates are reported adjacent to the curves (loess regression) for each scenario. (A, B) Abundance of returns (PreFishery Abundance, last 5 years). (C, D) Portfolio effect over the 50 years.
FIGURE 4 | Exploitation metrics averaged over the metapopulation and simulations for life-history selectivity (left/right) and spatial selectivity (colours) scenarios of exploitation, for increasing metapopulation exploitation rate (MER) and a dispersal rate of 15% (other rates in Data S1). The local exploitation rates are reported adjacent to the curves (loess regression) for each scenario. (A, B) Total catch. (C, D) MSW catch (last 5 years).
FIGURE 5 | Adaptive traits (genetic) averaged over the metapopulation and simulations for life-history selectivity (left/right) and spatial selectivity (colours) scenarios of exploitation, for increasing metapopulation exploitation rate (MER) and a dispersal rate of 15% (other rates in Data S1). The local exploitation rates are reported adjacent to the curves (loess regression) for each scenario. (A, B) Average genetic values of growth potential and (C, D) female maturation threshold for philopatric individuals (last 5 years).
Eco‐Evolutionary Consequences of Selective Exploitation on Metapopulations Illustrated With Atlantic Salmon

January 2025

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69 Reads

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1 Citation

Fish and Fisheries

Although the eco‐evolutionary consequences of dispersal and exploitation are increasingly recognised, consideration of these effects and how they interact for management and conservation remains limited. We addressed this gap by examining population exploitation within a metapopulation framework, using Atlantic salmon as a case study. We compared eco‐evolutionary consequences of alternative exploitation strategies by incorporating selective exploitation based on life‐history traits and spatial dimension of exploitation (i.e., whether populations were net exporters or importers of individuals). We used a demo‐genetic agent‐based model to examine demographic and evolutionary consequences of these strategies across a gradient of population‐specific exploitation rates. At the metapopulation scale, we found both lower abundance and earlier sexual maturation with increasing exploitation, particularly when fishing was selective on larger individuals. The spatial selectivity of exploitation had an overall additional detrimental effect on metapopulation performance and fisheries yield, and induced stronger evolutionary changes than when exploitation was evenly spread over all populations. We discuss the implications of metapopulation functioning for species management and how considering dispersal patterns and intensity might change how we apply harvest. Nevertheless, our findings suggest that the safest approach remains to distribute exploitation efforts evenly across all populations, especially in the absence of variation in intrinsic productivity. However, this strategy might not completely prevent negative consequences at the local scale. Therefore, we advise managers to critically assess the relevance of our results and dispersal assumptions in the specific cases they may have to deal with.


Long‐term data reveal widespread phenological change across major US estuarine food webs

December 2024

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141 Reads

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1 Citation

Ecology Letters

Climate change is shifting the timing of organismal life‐history events. Although consequential food‐web mismatches can emerge if predators and prey shift at different rates, research on phenological shifts has traditionally focused on single trophic levels. Here, we analysed >2000 long‐term, monthly time series of phytoplankton, zooplankton, and fish abundance or biomass for the San Francisco, Chesapeake, and Massachusetts bays. Phenological shifts occurred in over a quarter (28%) of the combined series across all three estuaries. However, phenological trends for many taxa (ca. 29–68%) did not track the changing environment. While planktonic taxa largely advanced their phenologies, fishes displayed broad patterns of both advanced and delayed timing of peak abundance. Overall, these divergent patterns illustrate the potential for climate‐driven trophic mismatches. Our results suggest that even if signatures of global climate change differ locally, widespread phenological change has the potential to disrupt estuarine food webs.


Prolonged low flows and non-native fish operate additively to alter insect emergence in mountain streams

November 2024

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60 Reads

Climate-induced flow alteration is subjecting mountain streams to more frequent and severe low-flow periods due to lower snowpack and earlier snowmelt. Yet, anticipating how stream ecosystems respond to prolonged low flows remains challenging because trophic levels can respond differently, and non-native predators could dampen or amplify responses. Here, we conducted a large-scale experiment to examine how early, prolonged low flows projected by the end of the century in California's Sierra Nevada will alter mountain stream food webs and emerging insect flux--a critical stream-to-land cross-ecosystem linkage. Additionally, we tested whether Brown trout (Salmo trutta), a widespread non-native top predator, would change food-web responses to low-flow conditions. We found that early low flows and non-native fish effects were additive rather than synergistic or antagonistic. Early low flows did not alter the overall rate of emerging insects but they did shift community structure and reduce the prevalence of small-sized individuals--possibly reflecting larger size at emergence and faster growth rates due to warming. In contrast, non-native fish presence increased seasonally-aggregated abundance of stream insects up to 12%, mainly by increasing abundance of Chironomidae and small-sized Ephemeroptera and Trichoptera. In channels with fish, benthic algal biomass doubled and scraper-grazer and collector-gatherer insects emerged 60% and 55% more than channels without fish, likely benefiting from trout keeping mesopredators at bay. This experiment illustrates that prolonged low flows and invasions can profoundly alter mountain river food webs even when operating additively; and shows how mesocosm-based research may help understand global-change driven disruption of cross-ecosystem linkages.


Phenology-informed decline risk of estuarine fishes and their prey suggests potential for future trophic mismatches

October 2024

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26 Reads

Conservation scientists have long used population viability analysis (PVA) on species count data to quantify trends and critical decline risk, thereby informing conservation actions. These assessments typically focus on single species rather than assemblages and assume that risk is consistent within a given life stage (e.g., across the different seasons or months of a year). However, if risk is assessed at too broad a temporal or spatial scale, it may overlook diverging population declines between predators and prey that disrupt biotic interactions. In this study, we used time-series based PVA for age-0 forage fishes and their potential zooplankton prey for each month of the year in the San Francisco Estuary, over 1995-2023 (N = 175 time series). We used Multivariate Autoregressive (MAR) models that estimate long-term population trends and variability (i.e., process error) for each population. We found widespread negative population trends across fish species (56.6%) and observed that critical decline risk is often higher in months when species abundances peak compared to ‘shoulder’ months. Although current decline risk is somewhat balanced between predators and their prey (mean 21.8% for fish and 21.4% for zooplankton), our time-series models indicate trophic levels are poised to diverge over the next 10 years, with fish generally accumulating risk faster than their prey. Additionally, zooplankton showed 11.5% higher uncertainty about their near-term critical decline risk relative to fish. These observations suggest strong, previously unreported potential for future trophic mismatches. Our results underscore the need to assess risk over finer temporal scales within and across trophic levels to better understand vulnerability, and thus inform conservation of imperiled species. Our approach is transferable and highlights the benefits of time-series based PVA to understand risk of food-web collapse in the face of climate-induced phenological shifts.


Reintroduction of spring‐run Chinook salmon in the San Joaquin River: Evaluating genetic and phenotypic effects of captive breeding

August 2024

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184 Reads

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1 Citation

Captive‐breeding programs are increasingly implemented to curb population declines but can have unintended negative effects on genetic diversity and phenotypes. Through an analysis of ~10 years of genetic monitoring, pedigree information, and phenotypic data, we evaluated a captive‐breeding program that uses adaptive management to reduce inbreeding and improve captive broodstock performance. A captive‐breeding program was established in 2012 to reintroduce spring‐run Chinook salmon to the southern edge of their range in California's San Joaquin River (SJR), using fish produced each year at the nearby Feather River Hatchery (FRH). We found that the SJR program adequately captured the genetic diversity of the FRH source population and that mate pairings guided by genetic relatedness reduced inbreeding. However, the SJR broodstock reared in captivity had smaller body size at maturity in comparison to the FRH source broodstock which matures at sea, but this effect disappeared when SJR juveniles were released from captivity to mature at sea. Phenotypic traits of SJR female parents also influenced reproductive performance; older mothers and those with smaller eggs had offspring with lower survival. These findings demonstrate that adaptive genetic monitoring and pedigree information can be powerful tools for reducing risks of captive breeding and evaluating program effectiveness.


Location of 84 dry-riverbed sampling sites and their Köppen climate class
The inset illustrates site locations within the most densely sampled area.
Composition of Bacteria and Archaea communities in dry riverbed sediments (n = 84)
Read proportions (square root scale) correspond to the relative abundance of each taxon per sample and were estimated using the 16S marker dataset rarefied to 2311 reads per sample. The vertical bold line within the box represents the median. The upper and lower limits of the box represent the 75th and 25th percentiles. Horizontal dotted lines indicate the range of observed values within 1.5× the interquartile range from the 75th and 25th percentiles. Values outside this range were considered outliers and are indicated as points. Source data are provided as a Source Data file.
Composition of eukaryotic communities in dry riverbed sediments (n = 76)
Read proportions (square root scale) correspond to the relative abundances of each taxon per sample and were estimated using the 18S marker dataset rarefied to 15624 reads per sample. Further details are provided in the Fig. 2 legend. Source data are provided as a Source Data file.
Influence of environmental variables on the bacterial copiotrophic:oligotrophic ratio
Partial dependence plots of the relative abundance of bacterial copiotrophic and oligotrophic operational taxonomic units (OTUs), indicating the contribution of five predictor variables to log10(copiotrophic:oligotrophic [copio:oligo] ratio +1) as a function of the predictors (i.e. when the other contributing predictors are held at their mean). Hash marks on x axes indicate the deciles of the predictor variables. Predictors are shown in order of decreasing importance (%IncMse as defined in Table 1).
Partial correlation network between the beta-diversity of the eight major taxa contributing to dry-riverbed biodiversity and climatic, physicochemical, land-use, and spatial distances between sites, as inferred from a graphical lasso method
Each node represents the turnover component of beta-diversity (calculated using the Bray-Curtis index) of a taxon (yellow) or a spatial (blue), climatic (orange), or environmental (green) distance. Line width is proportional to the partial correlations (indicated on each line) between pairs of nodes.
Unravelling large-scale patterns and drivers of biodiversity in dry rivers

August 2024

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1,983 Reads

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5 Citations

More than half of the world’s rivers dry up periodically, but our understanding of the biological communities in dry riverbeds remains limited. Specifically, the roles of dispersal, environmental filtering and biotic interactions in driving biodiversity in dry rivers are poorly understood. Here, we conduct a large-scale coordinated survey of patterns and drivers of biodiversity in dry riverbeds. We focus on eight major taxa, including microorganisms, invertebrates and plants: Algae, Archaea, Bacteria, Fungi, Protozoa, Arthropods, Nematodes and Streptophyta. We use environmental DNA metabarcoding to assess biodiversity in dry sediments collected over a 1-year period from 84 non-perennial rivers across 19 countries on four continents. Both direct factors, such as nutrient and carbon availability, and indirect factors such as climate influence the local biodiversity of most taxa. Limited resource availability and prolonged dry phases favor oligotrophic microbial taxa. Co-variation among taxa, particularly Bacteria, Fungi, Algae and Protozoa, explain more spatial variation in community composition than dispersal or environmental gradients. This finding suggests that biotic interactions or unmeasured ecological and evolutionary factors may strongly influence communities during dry phases, altering biodiversity responses to global changes.


Dispersal and gene flow in anadromous salmonids: A systematic review

August 2024

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90 Reads

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2 Citations

Ecology of Freshwater Fish

Dispersal is a ubiquitous ecological process that has been extensively studied in many plants and animals. Anadromous salmonids are an interesting system for examining dispersal, in part because of their well‐known philopatric behaviour, but also because of the conservation challenges related to the dispersal of hatchery‐origin fish. Building on earlier work, we provide an updated systematic review of dispersal and gene flow in anadromous salmonids. In particular, we compared studies on the dispersal of anadromous salmonids from wild and hatchery origins, including studies providing estimates of dispersal rates, observations of dispersal and results from modelling studies. We reviewed 228 studies and found these were unevenly distributed among species, with Atlantic salmon, Chinook salmon and sea trout being well‐represented. Our results showcase considerable variability in estimated dispersal rates within and across studies, which is likely related to the different methodologies, dispersal propensities across species and populations, and spatial extents considered. Overall, our results confirmed a higher tendency of hatchery fish to disperse relative to wild fish, but we also found some variation across species that warrants further study. Moreover, we found that dispersal propensity tended to decline exponentially with distance and that the drivers of dispersal varied considerably among studies. Additionally, we highlight various facets of dispersal captured across this suite of studies, including variation in terminology, methods and metrics for characterising dispersal, and the spatio‐temporal scales considered. Finally, our review revealed that few studies considered, and even fewer assessed, the implications of dispersal for the conservation and management of anadromous salmonids.


Citations (77)


... [36,37] treat epidemiological dynamics and antigenic escape together in a well-mixed population, while Ref. [38] explores the evolutionary impact of punctuated antigenic escape. Others treat population structure and epidemic dynamics [35,39] or networks structure and evolutionary impact without a host-disease model [40,41]. Ecologists have studied "eco-evo coupling" with great interest in the past few decades as mounting evidence shows the importance of such phenomena, but often in well-mixed populations and at steady state. ...

Reference:

How host mobility patterns shape antigenic escape during viral-immune co-evolution
Eco‐Evolutionary Consequences of Selective Exploitation on Metapopulations Illustrated With Atlantic Salmon

Fish and Fisheries

... Insofar as such phenological shifts are asynchronous among interacting species, they may alter competitive and trophic dynamics, affecting population performance (Iler et al. 2021) and overall ecosystem function (Beard et al. 2019). In this special issue, Fournier et al. (2024) analyse the covariance of > 2000 long-term time series of Age of major university 50-1000 years monthly data on the seasonal timing of peak abundance of fish, zooplankton and phytoplankton, together with changes in temperature and salinity, across three major estuarine ecosystems in North America over a period of ca. 30 years. They found that over a quarter of the studied taxa showed significant shifts in phenology, the vast majority advancing their phenology over time in response to changing temperature and salinity. ...

Long‐term data reveal widespread phenological change across major US estuarine food webs

Ecology Letters

... From a practical perspective, the effective population size of stocked fish may be improved through a range of measures including increasing the number of broodstock used per consignment of stocked individuals to be released, increasing rates of broodstock rotation both within and among hatcheries and sourcing broodstock from diverse source populations. Genetic information can also be used to limit inbreeding among captive broodstock and equalise family contributions of broodstock to increase the effective population size of fish being stocked (Pregler et al. 2024). Captive breeding software exists that can help guide the selection of mate pairs in a way that minimises relatedness and reduces family structure and over-representation of close kin (e.g., PMx, SWINGER Lacy et al. 2012;Sandoval-Castillo et al. 2017). ...

Reintroduction of spring‐run Chinook salmon in the San Joaquin River: Evaluating genetic and phenotypic effects of captive breeding

... Community assembly may vary across intermittence regimes according to the frequency and duration of drying events. These variations are driven by climatic factors-such as the prolonged and frequent drying events characteristic of Mediterranean climates (Bonada et al. 2007;Tonkin et al. 2017)or by geomorphological differences (Foulquier et al. 2024;Vander Vorste et al. 2021). However, the distinct effects of the frequency versus duration of drying events on the taxonomic and trait structure of macroinvertebrate communities across large spatial scales remain unexplored. ...

Unravelling large-scale patterns and drivers of biodiversity in dry rivers

... Finally, the extent to which dispersal translates into gene flow depends on the strength of local adaptation, which is typically more pronounced in highly philopatric species (Hendry et al. 2003;Mobley et al. 2019;Peterson et al. 2014). Together, these complex interactions yield variable dispersal rates and gene flow across species, with substantial intraspecific variation also observed among populations (Lamarins et al. 2024). ...

Dispersal and gene flow in anadromous salmonids: A systematic review
  • Citing Article
  • August 2024

Ecology of Freshwater Fish

... As the conditions that create distinct, asynchronous patterns of habitat conditions and resource availability diminish, the temporal window for consumers, like juvenile fish, may become constrained ( Figure 6). Such shifts may cascade across habitats in species with complex life histories such as anadromous fishes by reducing the stabilizing portfolio effects of, for example, juvenile life history diversity (Cordoleani et al., 2021;Rossi et al., 2024;Schindler et al., 2010). Future work should quantify the degree to which fish perceive and integrate across physicochemical and resource gradients created by meltwater-and non-meltwater habitat mosaics and the relationships among local resource dynamics, mobile-consumer movement and life history expression, and metapopulation and metacommunity dynamics. ...

Foodscapes for salmon and other mobile consumers in river networks
  • Citing Article
  • August 2024

BioScience

... freshwater residence or precocious maturation) are observed in natura (Birnie-Gauvin et al., 2019). While natural populations generally express an elevated homing rate (Lamarins and Buoro, 2024), studies have shown that salmonid species can exhibit a wide variety of life histories (Erkinaro et al., 2019), and that globally, the role of dispersal has been overlooked (Birnie-Gauvin et al., 2019;Källo et al., 2022a). Yet, the sustainability of this wide and complex diversity (i.e. ...

Dispersal and gene flow in anadromous salmonids: a systematic review

... The relative proportion of source and sink populations (and thus the proportion of total abundance under protection), along with their spatial distribution across the network, may drive the demographic and evolutionary responses of the network to exploitation. These factors have been shown to affect the adaptive capacity and demographic recovery of populations following a perturbation (Lamarins et al. 2024). We therefore advise managers to critically assess the relevance of our assumptions in the specific cases they may have to deal with. ...

The importance of network spatial structure as a driver of eco‐evolutionary dynamics

... For each combination of taxa, sampling location, and estuary, we calculated three Pearson correlation coefficients, capturing: (1) the relationship between phenology (adjusted yearly date of peak abundance) and time (hereafter, PT); (2) the relationship between the climatic variables and time (hereafter, CT); and (3) the relationship between phenology and climate (hereafter, PC). For each taxa and site, the triplet of coefficients was used to calculate Fisher's Z transformed effect sizes that entered a meta-regression model (see raw coefficients; Fournier et al., 2023). Because taxonomic groups might respond to environmental trends across different temporal scales, we compared the models that incorporate climatic trends at annual vs. seasonal scales. ...

Long-term data reveal widespread phenological change across major U.S. estuaries

... Our findings that hatchery fish mature at a younger age than that for natural-origin wild fish are consistent with patterns observed elsewhere, including in Russia and North America (Aruga et al. 2014;McConnell et al. 2018;Chen et al. 2023;Mikheev et al. 2023;McPhee et al. 2024; but see Zelennikov et al. 2023). One reason for this may be the plastic effects of the high initial growth rate for hatchery fish. ...

Age structure of natural versus hatchery-origin endangered Chinook salmon and implications for fisheries management in California
  • Citing Article
  • November 2023

Marine Ecology Progress Series