This paper describes the Hubble Space Telescope imaging data products and data reduction procedures for the Cosmic Assembly Near-IR Deep Extragalactic Legacy Survey (CANDELS). This survey is designed to document the evolution of galaxies and black holes at z ∼ 1.5 − 8, and to study Type Ia SNe beyond z > 1.5. Five premier multi-wavelength sky regions are selected, each with extensive multiwavelength observations. The primary CANDELS data consist of imaging obtained in the Wide Field Camera 3 / infrared channel (WFC3/IR) and UVIS channel, along with the Advanced Camera for Surveys (ACS). The CANDELS/Deep survey covers ∼ 125 square arcminutes within GOODS-N and GOODS-S, while the remainder consists of the CANDELS/Wide survey, achieving a total of ∼ 800 square arcminutes across GOODS and three additional fields (EGS, COSMOS, and UDS). We summarize the observational aspects of the survey as motivated by the scientific goals and present a detailed description of the data reduction procedures and products from the survey. Our data reduction methods utilize the most up to date calibration files and image combination procedures. We have paid special attention to correcting a range of instrumental effects, including CTE degradation for ACS, removal of electronic bias-striping present in ACS data after SM4, and persistence effects and other artifacts in WFC3/IR. For each field, we release mosaics for individual epochs and eventual mosaics containing data from all epochs combined, to facilitate photometric variability studies and the deepest possible photometry. A more detailed overview of the science goals and observational design of the survey are presented in a companion paper.

Early approaches to surgical implantation of electronic tags in fish were often through trial and error, however, in recent years there has been an interest in using scientific research to identify techniques and procedures that improve the outcome of surgical procedures and determine the effects of tagging on individuals. Here we summarize the trends in 108 peer-reviewed electronic tagging effect studies focused on intracoleomic implantation to determine opportunities for future research. To date, almost all of the studies have been conducted in freshwater, typically in laboratory environments, and have focused on biotelemetry devices. The majority of studies have focused on salmonids, cyprinids, ictalurids and centrarchids, with a regional bias towards North America, Europe and Australia. Most studies have focused on determining whether there is a negative effect of tagging relative to control fish, with proportionally fewer that have contrasted different aspects of the surgical procedure (e.g., methods of sterilization, incision location, wound closure material) that could advance the discipline. Many of these studies included routine endpoints such as mortality, growth, healing and tag retention, with fewer addressing sublethal measures such as swimming ability, predator avoidance, physiological costs, or fitness. Continued research is needed to further elevate the practice of electronic tag implantation in fish in order to ensure that the data generated are relevant to untagged conspecifics (i.e., no long-term behavioural or physiological consequences) and the surgical procedure does not impair the health and welfare status of the tagged fish. To that end, we advocate for (1) rigorous controlled manipulations based on statistical designs that have adequate power, account for inter-individual variation, and include controls and shams, (2) studies that transcend the laboratory and the field with more studies in marine waters, (3) incorporation of knowledge and techniques emerging from the medical and veterinary disciplines, (4) addressing all components of the surgical event, (5) comparative studies that evaluate the same surgical techniques on multiple species and in different environments, (6) consideration of how biotic factors (e.g., sex, age, size) influence tagging outcomes, and (7) studies that cover a range of endpoints over ecologically relevant time periods.

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Many biological, hydrological, and geological processes are interactively linked in ecosystems. These ecological phenomena normally vary within bounded ranges, but rapid, nonlinear changes to markedly different conditions can be triggered by even small differences if threshold values are exceeded. Intrinsic and extrinsic ecological thresholds can lead to effects that cascade among systems, precluding accurate modeling and prediction of system response to climate change. Ten case studies from North America illustrate how changes in climate can lead to rapid, threshold-type responses within ecological communities; the case studies also highlight the role of human activities that alter the rate or direction of system response to climate change. Understanding and anticipating nonlinear dynamics are important aspects of adaptation planning since responses of biological resources to changes in the physical climate system are not necessarily proportional and sometimes, as in the case of complex ecological systems, inherently nonlinear. Published by Elsevier B.V.

Thermal stratification occurred in pools of three rivers in northern California when inflow of cold water was sufficiently great or currents were sufficiently weak to prevent thorough mixing of water of contrasting temperatures. Surface water temperatures in such pools were commonly 3-9°C higher than those at the bottom. Cold water entered pools from tributaries, intergravel flow through river bars, and streamside subsurface sources. In Redwood and Rancheria Creeks, cold water was protected where gravel bars encroached into pools that were scoured along bedrock banks, creating isolated backwaters. Sixty-five percent of the juvenile steelhead Oncorhynchus mykiss found in the Rancheria Creek study reaches moved into adjacent stratified pools during periods of high ambient stream temperatures (23-28°C). Fish showed a decline in forage behavior and increased agonistic activity just before movement into stratified pools. In the Middle Fork Eel River, pools deeper than 3 m stratified when surface flow decreased to less than 1 m 3 /s. Summer-run steelhead adults were found in deep stratified pools on the Middle Fork Eel River throughout summer when midday ambient stream temperatures ranged from 26 to 29°C and coldwater pockets averaged 3.5°C cooler. Thermally stratified pools provided refuge habitat for significant numbers of young-of-the-year, yearling, and adult steelhead in marginal river habitats where stream temperatures reach upper incipient lethal levels.

Observations of behavior were made on marked juvenile coho salmon Oncorhynchus kisutch in pools in Huckleberry Creek, Washington. Fish exhibited two distinct types of forage behavior during observations made from May to August 1988 and from June to August 1989. Some coho salmon formed dominance hierarchies wherein fish defended forage stations in ranks determined by an individualˈs ability or willingness to defend access to drifting food. Other coho salmon foraged as nonhierarchical floaters. Eight percent of marked individuals changed their foraging behavior class during their first summer. Focal point velocity (FPV) differentiated specific microhabitats used by these two foraging behavior classes. Coho salmon in dominance hierarchies (FPV > 0.06 m/s) fed most frequently on drifting invertebrates, which contributed 81% of their energy intake. Floaters (FPV ≤ 0.06 m/s) fed by patrolling large forage arenas, where they fed opportunistically on items delivered by aerial drop and instream drift. Energy contribution from large aerially delivered food items represented 69% of floatersˈ total energy intake. Dominant fish in the hierarchy grew faster than subdominants and subdominants grew faster than floaters. Growth rates in specific microhabitats were directly related to relative food availabilities in the different foraging behavior classes.

We use the Wide-field Infrared Survey Explorer (WISE) and the Sloan Digital Sky Survey (SDSS) to confirm a connection between dust-obscured active galactic nuclei (AGNs) and galaxy merging. Using a new, volume-limited (z ≤ 0.08) catalog of visually-selected major mergers and galaxy-galaxy interactions from the SDSS, with stellar masses above 2 × 10 10 M , we find that major mergers (interactions) are 5-17 (3-5) times more likely to have red [3.4]−[4.6] colors associated with dust-obscured or 'dusty' AGNs, compared to nonmerging galaxies with similar masses. Using published fiber spectral diagnostics, we map thecolors of different emission-line galaxies and find one-quarter of Seyferts have colors indicative of a dusty AGN. We find that AGNs are five times more likely to be obscured when hosted by a merging galaxy, half of AGNs hosted by a merger are dusty, and we find no enhanced frequency of optical AGNs in merging over non-merging galaxies. We conclude that undetected AGNs missed at shorter wavelengths are at the heart of the ongoing AGN-merger connection debate. The vast majority of mergers hosting dusty AGNs are star-forming and located at the centers of M halo < 10 13 M groups. Assuming plausibly short duration dusty-AGN phases, we speculate that a large fraction of gas-rich mergers experience a brief obscured AGN phase, in agreement with the strong connection between central star formation and black hole growth seen in merger simulations.

The importance of interspecific competition as a mechanism regulating population abundance in offshore marine communities is largely unknown. We evaluated offshore competition between Asian pink salmon and Bristol Bay (Alaska) sockeye salmon, which intermingle in the North Pacific Ocean and Bering Sea, using the unique biennial abundance cycle of Asian pink salmon from 1955 to 2000. Sockeye salmon growth during the second and third growing seasons at sea, as determined by scale measurements, declined significantly in odd‐numbered years, corresponding to years when Asian pink salmon are most abundant. Bristol Bay sockeye salmon do not interact with Asian pink salmon during their first summer and fall seasons and no difference in first year scale growth was detected. The interaction with odd‐year pink salmon led to significantly smaller size at age of adult sockeye salmon, especially among younger female salmon. Examination of sockeye salmon smolt to adult survival rates during 1977–97 indicated that smolts entering the ocean during even‐numbered years and interacting with abundant odd‐year pink salmon during the following year experienced 26% (age‐2 smolt) to 45% (age‐1 smolt) lower survival compared with smolts migrating during odd‐numbered years. Adult sockeye salmon returning to Bristol Bay from even‐year smolt migrations were 22% less abundant (reduced by 5.9 million fish per year) compared with returns from odd‐year migrations. The greatest reduction in adult returns occurred among adults spending 2 compared with 3 years at sea. Our new evidence for interspecific competition highlights the need for multispecies, international management of salmon production, including salmon released from hatcheries into the ocean.