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River ecosystems host a continuum of various discontinuities, such as dams and tributary inflows, which shape the habitats of aquatic organisms; this makes it important to evaluate the interactions among discontinuities and effects of a single discontinuity point. Herein, we focused on tributaries in dammed rivers to elucidate a manner to mediate discontinuities and hypothesized that the effects of the tributary inflow on the downstream river were mediated by the (1) distance between the dam and tributary inflow, (2) size ratio between the dam and tributary, and (3) ability of the tributary to transport fine sediments, such as sand and gravel. We conducted field investigations to measure 24 environmental factors, including the water column, riverbed, and river topography, along eight dammed rivers to test the three hypotheses. Only five factors differed significantly between the upstream and downstream sites of the tributary confluence, whereas 12 factors differed significantly between the tributary and mainstem. We also classified the variation pattern using principal component analysis (PCA). The correlation between each PCA axis and environmental factors suggests that the modifications of the water quality factors by tributary inflow were significantly correlated with the distance between the dam and the tributary inflow, and that the flux of various riverbed factors, that is, was significantly correlated with the ability to resupply of fine riverbed sediments by the tributary. Overall, tributary‐inflow downstream of a dam has the potential to be applicable in environmental restoration, especially in terms of resupplying fine sediment. [ABSTRACT FROM AUTHOR]

Environmental DNA (eDNA) has recently been developed for detecting the distribution of macroorganisms in aquatic systems and for estimating biomass/abundance. Although positive relationships between eDNA concentrations of species and biomass/abundance have been observed in previous studies, estimation of total biomass in a particular ecosystem based on eDNA concentration has not been investigated.To test this, we sampled eDNA from the littoral and pelagic zones of eight small ponds in Japan. Then, we drained ponds to capture all fish inhabiting each pond. We compared the eDNA copies measured by quantitative real‐time polymerase chain reaction analysis with the captured biomass of three dominant fish species (common carp, bluegill sunfish, and largemouth bass) obtained by direct capture. Differences in eDNA concentrations were compared between the littoral and pelagic zones of each pond.We found positive relationships between the eDNA copies and the whole captured biomass of all target species using Type II logarithmic equations, and the eDNA copies appeared to be saturated at a higher total biomass.We found positive correlations between the total number of eDNA copies and the total captured biomass of three fish species. This demonstrated the first step in estimating the population biomass of target fish species under natural conditions using eDNA measurement. [ABSTRACT FROM AUTHOR]

Dam‐mediated biological invasions are a serious problem all over the world. Once established in reservoirs, the invasive species have catastrophic impacts on the river ecosystems downstream, and thus, rapid monitoring of invasive species is an urgent issue for the effective removal of them and the conservation management of native ecosystems. Here, we verified the utility of environmental DNA (eDNA) analysis as a tool to effectively monitor three invasive fish species (bluegill, largemouth bass, and smallmouth bass) in reservoirs using multiplex real‐time PCR. First, to determine the optimal sampling location and season to detect eDNA from these species, we analyzed the eDNA in water samples from shore and offshore sites in three reservoirs all year around. We found that eDNA detection rates either did not differ between sampling locations or were higher for shore than offshore sites. In addition, eDNA detection rates were higher in spring (breeding season of target species) and/or summer than winter. Second, we extensively surveyed the distribution of the three species in 30 reservoirs in Japan using eDNA analysis. Consequently, a single eDNA‐based surveillance in summer allowed to match approximately 90% of the presence/absence of the invasive fish species known from 27 yr of administrative capture‐based surveillances. Given these results, we recommend collecting the replicated water samples from shore sites in summer or the breeding season for the effective detection of invasive fish eDNA in reservoirs. Our eDNA assays with multiplex real‐time PCR enable the rapid and sensitive monitoring of invasive fish distribution in reservoirs. [ABSTRACT FROM AUTHOR]

The recent development of the environmental DNA (eDNA) technique has dramatically facilitated investigations of the distribution and abundance of macroorganisms in the natural environment. Various real‐time polymerase chain reaction (PCR)‐based methods have been proposed for the detection and quantification of eDNA by independent researchers or groups. Although several eDNA reviews have outlined the critical requirements for experimental processes and provided guidelines for best practice, clear standardization of eDNA protocols is lacking. Here, we collected the PCR conditions of previous eDNA studies using real‐time PCR (n = 190), that is, the volume of the DNA template, PCR cycles, number of PCR replicates and PCR inhibition tests. Then, we synthesized the current development of real‐time PCR techniques for eDNA studies. Our synthesis has identified the critical issues that need to be addressed to design standardized protocols for eDNA monitoring that will enable broader uptake of eDNA technology. [ABSTRACT FROM AUTHOR]

Environmental DNA (eDNA) analysis has seen rapid development in the last decade, as a novel biodiversity monitoring method. Previous studies have evaluated optimal strategies, at several experimental steps of eDNA metabarcoding, for the simultaneous detection of fish species. However, optimal sampling strategies, especially the season and the location of water sampling, have not been evaluated thoroughly. To identify optimal sampling seasons and locations, we performed sampling monthly or at two‐monthly intervals throughout the year in three dam reservoirs. Water samples were collected from 15 and nine locations in the Miharu and Okawa dam reservoirs in Fukushima Prefecture, respectively, and five locations in the Sugo dam reservoir in Hyogo Prefecture, Japan. One liter of water was filtered with glass‐fiber filters, and eDNA was extracted. By performing MiFish metabarcoding, we successfully detected a total of 21, 24, and 22 fish species in Miharu, Okawa, and Sugo reservoirs, respectively. From these results, the eDNA metabarcoding method had a similar level of performance compared to conventional long‐term data. Furthermore, it was found to be effective in evaluating entire fish communities. The number of species detected by eDNA survey peaked in May in Miharu and Okawa reservoirs, and in March and June in Sugo reservoir, which corresponds with the breeding seasons of many of fish species inhabiting the reservoirs. In addition, the number of detected species was significantly higher in shore, compared to offshore samples in the Miharu reservoir, and a similar tendency was found in the other two reservoirs. Based on these results, we can conclude that the efficiency of species detection by eDNA metabarcoding could be maximized by collecting water from shore locations during the breeding seasons of the inhabiting fish. These results will contribute in the determination of sampling seasons and locations for fish fauna survey via eDNA metabarcoding, in the future. [ABSTRACT FROM AUTHOR]

Environmental DNA (eDNA) techniques utilizing DNA fragments from water have recently been developed to investigate the distribution and abundance/biomass of aquatic organisms. The eDNA technique is based on the analysis of DNA fragments in sampled water; thus, an unmanned aerial vehicle (UAV; drone) would be a useful way of collecting water for eDNA sampling, and may consequently allow us to extend eDNA surveys both spatially and temporally. Here, we developed a new method of water collection by using UAV with bleachable equipment, to avoid DNA contamination. To test the performance and contamination risk of UAV water sampling in eDNA surveys, we sampled water from a dam reservoir, detected eDNA from two fish species, and compared the water samples obtained by UAV with those obtained by boat. Additionally, we investigated contamination using blank samples. The results revealed that our UAV water sampling method performed similar to the boat sampling method. No positive signals were detected in the blank samples, including those used for UAV sampling, transportation, filtering, and PCR blanks. Our UAV method can be used to investigate species distributions using eDNA. Combinations of UAV technologies, including remote and thermal sensing, will enable efficient environmental monitoring in various waterbodies. [ABSTRACT FROM AUTHOR]

Environmental DNA (eDNA) has recently been used for detecting the distribution of macroorganisms in various aquatic habitats. In this study, we applied an eDNA method to estimate the distribution of the Japanese clawed salamander, Onychodactylus japonicus, in headwater streams. Additionally, we compared the detection of eDNA and hand-capturing methods used for determining the distribution of O. japonicus. For eDNA detection, we designed a qPCR primer/probe set for O. japonicus using the 12S rRNA region. We detected the eDNA of O. japonicus at all sites (with the exception of one), where we also observed them by hand-capturing. Additionally, we detected eDNA at two sites where we were unable to observe individuals using the hand-capturing method. Moreover, we found that eDNA concentrations and detection rates of the two water sampling areas (stream surface and under stones) were not significantly different, although the eDNA concentration in the water under stones was more varied than that on the surface. We, therefore, conclude that eDNA methods could be used to determine the distribution of macroorganisms inhabiting headwater systems by using samples collected from the surface of the water. [ABSTRACT FROM AUTHOR]

1. The vertical and horizontal distribution of unionoid mussels (Pronodularia japanensis) were examined in spring, late summer and winter for different size classes, including juveniles (<20 mm) and large adults (>50 mm), in an agricultural drainage channel in Central Japan. 2. A large number of small-sized juveniles were found at the surface (0-3 cm depth) in spring, whereas approximately half of the adults remained in the deep layer (3-8 cm depth). Most individuals were found in the surface layer irrespective of size classes in summer, and approximately 70% of all individuals descended to the deep layer in winter. 3. Horizontal distribution did not substantially change across seasons and high density patches were consistently found in the areas where substrate appeared to be stable or hydraulically sheltered. Spatial distribution of small juveniles was relatively well predicted by the abundance of adults. 4. The size-frequency distribution was multi-modal in three seasons and estimated numbers of newly recruited juveniles were highly variable in recent years, suggesting that juveniles were rarely found owing to irregular reproduction and/or recruitment not the overlooked habitat preferred by small-sized juveniles. 5. As P. japanensis is characterized by the behaviour of burrowing down to a depth of ∼10 cm, maintaining the processes of sediment deposition appears to be one of the critical criteria for the conservation of mussel habitats in agricultural drainage channel systems, which are commonly lined with smooth concrete materials. [ABSTRACT FROM AUTHOR]

Climate change is inducing changes in the phenological timings of organisms. Genetic diversity could influence phenological responses to climate change, but empirical evidence is very limited. We estimated the regional variation across Japan in flowering and leaf budburst dates of plants based on a dataset of phenological timings from 1953 to 2005. The observed plants' genetic diversities varied according to human cultivation. The within-species variations of phenological response to temperature as well as regional variations were less in the plant populations with lower genetic diversity. Thus, genetic diversity influences the variation in phenological responses of plant populations. Under increased temperatures, low variation in phenological responses may allow drastic changes in the phenology of plant populations with synchronized phenological timings. Our findings indicate that we should pay attention to maintaining genetic diversity of populations to alleviate changes in phenology due to future climate change. [ABSTRACT FROM AUTHOR]

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Copyright of Basic & Applied Ecology is the property of Urban & Fischer Verlag and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Environmental DNA (eDNA) is a powerful tool for monitoring the distribution of aquatic macro-organisms. However, environmental factors, including the water temperature and water quality, can affect the inhibition and/or degradation of eDNA, which complicates accurate estimations of eDNA concentrations and the detection of the presence/absence of species in natural habitats. Further very few eDNA studies have been conducted for reptiles, especially with respect to estimating their biomass and/or abundances. Here we examined the relationship between the visually-observed number of red-eared sliders ( Trachemys scripta elegans ) and eDNA concentrations across 100 ponds. Additionally, we evaluated the effect of water quality on red-eared slider eDNA concentration in these ponds. We found that there was a significant positive correlation between the observed number of red-eared sliders and the eDNA concentration in the ponds. On comparing various water quality indicators, including dissolved nitrogen, dissolved phosphorous, organic matter, and chlorophyll a (Chl. a ), we found that only Chl. a had a negative correlation with the red-eared slider eDNA concentration, while we did not find any inhibition in the quantitative PCR. We conclude that concentrations of eDNA can potentially be used for estimating the abundance of the red-eared slider. Additionally, Chl. a might indirectly influence the degradation of eDNA through the microorganisms bonded to the phytoplankton in the ponds, as microbial activity is thought to decrease eDNA persistence., Competing Interests: Rio Souma is an employee of IDEA Consultants Inc., (©2019 Kakuda et al.)

Background: Grazing activity on periphytic mats determines mat structure and spatial heterogeneity. Spatial complexity in stream periphyton is highly divergent and may depend on the functional traits of the different primary consumers species (i.e., grazers) such as mouthpart morphology, feeding behavior, and feeding activity. We evaluated the effect of grazing by three species having different functional traits on periphytic mat structure with a focus on mohthpart morphology., Methods: An enclosure experiment was conducted in a stream located in the Nara Prefecture of Japan using two caddisflies with scraping mouthparts, Micrasema quadriloba and Glossosoma , and one mayfly, Epeorus , with brushing mouthparts. The spatial heterogeneity of chlorophyll a (Chl a ) was evaluated, and the periphytic mat was analyzed using scanning electron microscopy (SEM) after a 12-d feeding experiment., Results: Our results showed the differences in the spatial heterogeneity of the periphytic mats, such as differences in Chl a levels, grazed by the different grazing species. The strongest effect on the spatial heterogeneity and periphytic abundance was observed for Micrasema quadriloba , a caddisfly species with scraping mouthparts. Epeorus mayfly, with brushing mouthparts and high-mobility behavior, produced the weakest effect on spatial heterogeneity. Glossosoma caddisflies had moderate effects on periphytic spatial heterogeneity and abundance. Our results suggest that differences in grazing effects are largely dependent on grazer mouthparts and behavior., Competing Interests: The authors declare there are no competing interests.

The use of environmental DNA (eDNA) has recently been employed to evaluate the distribution of various aquatic macroorganisms. Although this technique has been applied to a broad range of taxa, from vertebrates to invertebrates, its application is limited for aquatic insects such as aquatic heteropterans . Nepa hoffmanni (Heteroptera: Nepidae) is a small (approx. 23 mm) aquatic heteropteran that inhabits wetlands, can be difficult to capture and is endangered in Japan. The molecular tool eDNA was used to evaluate the species distribution of N. hoffmanni in comparison to that determined using hand-capturing methods in two regions of Japan. The eDNA of N. hoffmanni was detected at nearly all sites (10 eDNA-detected sites out of 14 sites), including sites where N. hoffmanni was not captured by hand (five eDNA-detected sites out of six captured sites). Thus, this species-specific eDNA technique can be applied to detect small, sparsely distributed heteropterans in wetland ecosystems. In conclusion, eDNA could be a valuable technique for the detection of aquatic insects inhabiting wetland habitats, and could make a significant contribution to providing distribution data necessary to species conservation., Competing Interests: We declare we have no competing interests.

Stream grazers have a major impact on food web structure and the productivity of stream ecosystems; however, studies on the longitudinal (upstream versus downstream) and temporal changes in their drift dynamics and resulting distributions remain limited. Here, we investigated the longitudinal and temporal distributions and drift propensity of a trichopteran grazer, the caddisfly, Micrasema quadriloba , during its life cycle in a Japanese stream. The distribution of larvae significantly shifted downstream during the fifth instar larval stage during late winter; with periphyton abundance (i.e. their food source) showing similar shifts downstream. Therefore, our results show that the drift dispersal the caddisfly occurs in response to decline in available food resources (i.e. food-resource scarcity) and an increase in food requirements by growing individuals. Furthermore, our results show that this observed longitudinal shift in larval distribution varies through their life cycle, because the drift dispersal of fifth instar larvae was greater than that of immature larvae. The correlation between periphyton abundance and drift propensity of fourth instar larvae was not statistically significant, whereas that of fifth instar larvae was significantly negative. In conclusion, we detected an ontogenetic shift in drift propensity, which might explain the longitudinal and temporal distributions of this species.

This study aimed to determine the association between herbivore behavior and cues from producers. We used stream grazer Glossosoma larvae and determined their crawling direction in relation to chemical and visual cues from microalgae. The experimental treatments included control (no cue), particulate (chemical and particulate cues), and dissolved (chemical cue) cues from microalgae. The experimental water samples were randomly placed into either arm of a Y-shaped channel, and the crawling direction of the grazers was determined. Although the grazers crawled toward the arm containing either particulate or dissolved cues, they preferred the arm with particulate cues. This suggested that grazers responded well to both particulate (i.e., drifting algal cells) and chemical (algal smell) cues, and that particulate cues were more important for foraging. In natural habitats, grazers detect cues from producers and change their behaviors to maintain a balance between top-down and bottom-up cues.