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Systematic studies of Oryzomyine rodents (Muridae, Sigmodontinae): diagnoses and distributions of species formerly assigned to Oryzomys 'capito'

We describe the morphological species-boundaries and geographic distributions of ten Neotropical Oryzomys based on analyses of museum specimens (skins and skulls, examples preserved in fluid, chromosomal spreads, and information about collection sites from skin tags, field catalogs, and other sources). These species have been regarded as members of an Oryzomys capito complex and for a long time were consolidated into a single entity identified as O. capito. Our study documents the following: 1. Defining the limits of species within the O. capito complex first requires a comprehensive review and rigorous definition of O. capito itself. We consider Fischer's (1814) Mus megacephalus to be valid and available, designate a neotype to bear the name, and reinstate it as a senior synonym of capito Olfers (1818). We then provide a working definition of O. megacephalus and its close relative, O. laticeps, derived from analyses of morphometric variation, estimates of geographic distributions, and evaluations of synonyms. In our view, O. megacephalus occurs in Amazonia but also extends into eastern Paraguay; its synonyms are capito Olfers (1818), cephalotes Desmarest (1819), velutinus Allen and Chapman (1893), goeldi Thomas (1897), modestus Allen (1899), and perenensis Allen (1901). Oryzomys laticeps Lund (1840) occurs in the Atlantic Forest region of eastern Brazil. We designate a lectotype for laticeps and allocate the names saltator Winge (1887) and oniscus Thomas (1904) as synonyms. 2. We provide the first comprehensive taxonomic revision of Oryzomys yunganus Thomas (1902). Its range covers tropical evergreen rainforest formations in the Guiana region and the Amazon Basin where, as documented by voucher specimens, it has been collected at the same localities as O. megacephalus, O. nitidus, and O. tern of carotid arterial circulation, occlusal patterns of second upper and lower molars, cranial proportions, and chromosomal features. Appreciable intraspecific geographic variation occurs in diploid number of chromosomes and frequency of occurrence of the hypothenar plantar pad, but sampling inadequacies obscure the significance of this variation. Large body size is characteristic of populations in the western Amazon Basin and in the tepui region of eastern Venezuela; smaller size characterizes populations in the Guianas and along the eastern margin of the Amazon Basin. No other scientific name has been correctly associated with the species. Samples from Mirador, Palmera, and Mera in the western Andean foothills of central Ecuador possess a combination of pelage, cranial, and dental traits that distinguish them from all samples of O. yunganus. These specimens are the basis for a new species we describe here, one that is more closely related to O. yunganus than to any other member of the former O. 'capito' complex. 3. We redescribe Oryzomys bolivaris (reviewed by Pine, 1971, under the name O. bombycinus), amplify its geographic range, and contrast it with O. talamancae and O. alfaroi, two sympatric congeners often confused with it. A distinctive set of morphological traits allows unambiguous identification of specimens belonging to O. bolivaris. It is a trans-Andean species recorded from very wet tropical evergreen rainforests extending from eastern Honduras and Nicaragua through Costa Rica and Panama to western Colombia and Ecuador. Allen's (1901) bolivaris is the oldest name for this species; castaneus Allen (1901), rivularis Allen (1901), bombycinus Goldman (1912), alleni Goldman (1915), and orinus Pearson (1939) are synonyms. 4. We revise the definition of Oryzomys talamancae Allen (1891) provided by Musser and Williams (1985), document additional specimens, describe karyotypes from Ecuadoran and Venezuelan samples, and contrast its morphology, chromosomes, and distribution with those of O. alfaroi and O. megacephalus. The geographic distribution of O. talamancae is also trans-Andean, but it inh

Bulletin of the American Museum of Natural History↗

Fire and aquatic ecosystems in forested biomes of North America

Synthesis of the literature suggests that physical, chemical, and biological elements of a watershed interact with long‐term climate to influence fire regime, and that these factors, in concordance with the postfire vegetation mosaic, combine with local‐scale weather to govern the trajectory and magnitude of change following a fire event. Perturbation associated with hydrological processes is probably the primary factor influencing postfire persistence of fishes, benthic macroinvertebrates, and diatoms in fluvial systems. It is apparent that salmonids have evolved strategies to survive perturbations occurring at the frequency of wildland fires (10°–10 2 years), but local populations of a species may be more ephemeral. Habitat alteration probably has the greatest impact on individual organisms and local populations that are the least mobile, and reinvasion will be most rapid by aquatic organisms with high mobility. It is becoming increasingly apparent that during the past century fire suppression has altered fire regimes in some vegetation types, and consequently, the probability of large stand‐replacing fires has increased in those areas. Current evidence suggests, however, that even in the case of extensive high‐severity fires, local extirpation of fishes is patchy, and recolonization is rapid. Lasting detrimental effects on fish populations have been limited to areas where native populations have declined and become increasingly isolated because of anthropogenic activities. A strategy of protecting robust aquatic communities and restoring aquatic habitat structure and life history complexity in degraded areas may be the most effective means for insuring the persistence of native biota where the probability of large‐scale fires has increased.

Transactions of the American Fisheries Society↗

California State Waters map series — Offshore of Aptos, California

Introduction In 2007, the California Ocean Protection Council initiated the California Seafloor Mapping Program (CSMP), designed to create a comprehensive seafloor map of high-resolution bathymetry, marine benthic habitats, and geology within California’s State Waters. The CSMP approach is to create highly detailed seafloor maps through collection, integration, interpretation, and visualization of swath sonar bathymetric data (the undersea equivalent of satellite remote-sensing data in terrestrial mapping), acoustic backscatter, seafloor video, seafloor photography, high-resolution seismic-reflection profiles, and bottom-sediment sampling data. The map products display seafloor morphology and character, identify potential marine benthic habitats, and illustrate both the surficial seafloor geology and shallow subsurface geology. The Offshore of Aptos map area is located on the Pacific Coast, on the north side of Monterey Bay, about 105 km southeast of San Francisco. The largest incorporated city in the map area, Capitola, and numerous unincorporated towns including Aptos, lie on uplifted marine terraces between the shoreline, and the northwest-trending Santa Cruz Mountains, part of California’s Coast Ranges. The map area includes the northernmost part of Santa Cruz Harbor, and Moss Landing Harbor is located about 10 km south of the map area. The offshore part of the map area is entirely within California’s State Waters and is also part of the Monterey Bay National Marine Sanctuary. In the southern part of the map area, the Soquel Canyon State Marine Conservation Area extends eastward from the limit of California’s State Waters across Soquel Canyon. The Offshore of Aptos map area is on the western margin of North American Plate—the only continental margin in the world delineated largely by transform faults. The San Andreas Fault Zone cuts through the Santa Cruz Mountains just 3.5 km northeast of the map area. The San Gregorio Fault Zone, another major plate-boundary structure, cuts through Monterey Canyon about 13 km southwest of the map area. Ongoing deformation associated with and between these major fault zones has uplifted the Santa Cruz Mountains and formed well-developed sets of marine terraces that characterize almost the entire coastal zone of the map area. The offshore part of the map area consists of relatively flat and shallow continental shelf which is underlain by variable amounts (0 to 30 m) of upper Quaternary shelf, estuarine, and fluvial sediments deposited as sea level fluctuated in the late Pleistocene. Along the southern edge of the map area, the shelf is incised by the head of Soquel Canyon, a northeast-trending tributary to the west-trending Monterey Canyon. During the last sea-level lowstand (the Last Glacial Maximum [LGM], about 21,000 years ago) Soquel Creek flowed through a paleochannel across the emergent shelf into the head of Soquel Canyon. This canyon was disconnected from its onshore watershed during the post-LGM sea-level rise of about 125 m; the abandoned paleochannel was subsequently filled with marine sediment. Coastal sediment in the Offshore of Aptos map area is supplied by coastal watersheds and bluff erosion. Sediment transport in this part of the Santa Cruz littoral cell is primarily from the northwest to the southeast and terminates in the submarine Monterey Canyon. Longshore drift is impeded by jetties at Santa Cruz Harbor, resulting in high beach erosion rates east of the harbor. Sediment dredged from the harbor mouth (estimated 300,000 yds 3 /yr) is currently being used to nourish beaches directly to the east. Farther downcoast, the rapidly eroding beach at Capitola was stabilized by construction of an about 75-m-long groin. This part of central California is exposed to large North Pacific swells from the northwest throughout the year. North Pacific swell heights range from 2 to 10 meters, with larger swells occurring from October to May. During El Niño-Southern Oscillation (ENSO) events, winter storms track farther south than they do in normal (non-ENSO) years, thereby impacting the map area more frequently and with waves of larger heights. Bedrock exposed in coastal cliffs is relatively erosion-resistant, and significant erosional events primarily are restricted to storm-wave activity that also erodes the overlying unconsolidated marine-terrace sediments. The Offshore of Aptos map area lies within the cold-temperate biogeographic zone that is called either the “Oregonian” province or the “northern California ecoregion.” This biogeographic province is maintained by the long-term stability of the southward-flowing California Current, the eastern limb of the North Pacific subtropical gyre that flows from southern British Columbia to Baja California. At its midpoint off central California, the California Current transports subarctic surface (0–500 m deep) waters southward, about 150 to 1,300 km from shore. Seasonal northwesterly winds that are, in part, responsible for the California Current, generate coastal upwelling. The south end of the Oregonian province is at Point Conception (about 310 km southeast of the map area), although its associated phylogeographic group of marine fauna may extend beyond to the area offshore of Los Angeles in southern California. The ocean off of central California has experienced a warming over the last 50 years that is driving an ecosystem shift away from the productive subarctic regime towards a depopulated subtropical environment. Seafloor habitats in the Offshore of Aptos map area lie within the “Shelf” Megahabitat class and include patchy rocky habitats, gravel-rich scour depressions, minor bedrock habitat, and predominantly sandy inner shelf. Sandy shelf habitats grade offshore to mud-dominated habitats on the midshelf in deeper water. Biological productivity resulting from coastal upwelling supports populations of Sooty Shearwater, Western Gull, Common Murre, Cassin’s Auklet, and many other less populous bird species. In addition, an observable recovery of Humpback and Blue Whales has occurred in the area; both species are dependent on coastal upwelling to provide nutrients. California sea lions and Pacific harbor seals are abundant in the map area. Common bottlenose dolphins are often observed very close to shore and in the surf zone. The large extent of exposed inner shelf bedrock supports large forests of “bull kelp,” which is well adapted for high-wave-energy environments. The kelp beds are the northernmost known habitat for the population of southern sea otters. Common fish species found in the kelp beds and rocky reefs include blue rockfish, black rockfish, olive rockfish, kelp rockfish, gopher rockfish, black-and-yellow rockfish, painted greenling, kelp greenling, and lingcod.

California↗

Global cropland-extent product at 30-m resolution (GCEP30) derived from Landsat satellite time-series data for the year 2015 using multiple machine-learning algorithms on Google Earth Engine cloud

Executive Summary Global food and water security analysis and management require precise and accurate global cropland-extent maps. Existing maps have limitations, in that they are (1) mapped using coarse-resolution remote-sensing data, resulting in the lack of precise mapping location of croplands and their accuracies; (2) derived by collecting and collating national statistical data that are often subjective, leading to substantial uncertainties in cropland-area estimates, as well as their locations; and (3) extracted from one or more classes of a land use–land cover product in which cropland classes are not the focus of mapping, leading to their mixing with other classes and creating significant errors of omission and commission. These limitations can be overcome by producing high-resolution cropland-extent maps using satellite-sensor data, such as Landsat 30-m resolution or higher. The most fundamental cropland product is the high-resolution cropland-extent map because all higher level cropland products, such as crop-watering method (that is, whether crops are irrigated or rainfed), crop types, cropping intensities, cropland fallows, crop productivity, and crop-water productivity, are dependent on a precise and accurate cropland-extent product. Given these realities, the overarching goal of this study was to produce a Landsat satellite-derived global cropland-extent product at 30-m resolution. The work, which involved a paradigm shift in how global cropland-extent maps are produced, involved the following five key steps: (1) petabyte-scale computing that involved multiyear, 8- to 16-day, time-series Landsat 30-m resolution data for the global land surface; (2) composition of analysis-ready data (ARD) cubes; (3) creation of a large global-reference data hub for machine learning; (4) use of multiple machine-learning algorithms (MLAs) by writing software and computing in the cloud; and (5) Google Earth Engine (GEE) cloud computing. The five key steps involved nine distinct phases. First, the world was segmented into 74 agroecological zones (AEZs). Second, Landsat 8- to 16-day data were used to time-composite 10-band (blue, green, red, near-infrared, short-wave infrared band 1, short-wave infrared band 2, thermal infrared, enhanced vegetation index, normalized difference water index, and normalized difference vegetation index) Landsat 30-m resolution data cubes for every 2- to 4-month time period during 3- to 4-year periods (stated as nominal-year 2015 or, simply, 2015), along with two additional 30-m resolution bands (Shuttle Radar Topography Mission elevation, and slope) in each of the 74 AEZs. Third, more than 100,000 reference-training data samples were collected using ground data (some of which were collected using a mobile application), as well as submeter- to 5-m-resolution, very high-resolution imagery sourced from other reliable sources. Fourth, reference-training data were used to create a knowledge base for separating cropland from noncropland. Fifth, MLAs such as the pixel-based supervised random forest and support-vector machines were written on the GEE using Python and JavaScript. Sixth, object-based recursive hierarchical segmentation algorithm was used, in addition to MLAs, to overcome uncertainties. Seventh, MLAs used the knowledge base to classify and separate cropland from noncropland. Eighth, accuracy assessment was conducted by generating error matrices for each of the 74 AEZs using 19,171 independent validation-data samples. Ninth, cropland areas were computed for all countries of the world and compared with United Nation’s (UN’s) Food and Agricultural Organization (FAO) and other national statistics. The outcome was a Landsat-derived global cropland-extent product at 30-m resolution (GCEP30), which has an overall accuracy of 91.7 percent. For the cropland class, producer’s accuracy was 83.4 percent, and user’s accuracy was 78.3 percent. GCEP30 calculated (using direct pixel count) the global net-cropland area (GNCA) for the year 2015 as 1.873 billion hectares (~12.6 percent of the Earth’s terrestrial area). The continental cropland distribution as a percentage of GNCA was Asia, 33 percent; Europe, 25.5 percent; Africa, 16.7 percent; North America, 14.4 percent; South America, 8.1 percent; and Australia and Oceania, 2.4 percent. The worldwide cropland areas in GCEP30 for 2015 were higher by 236 to 299 million hectares (Mha) compared to national statistics reported elsewhere for the same year (for example, in Food and Agriculture Organization’s corporate statistical database [FAOSTAT] and in the monthly irrigated and rainfed crop areas [MIRCA] database). The global cropland area reported for 2015 increased by 344 Mha (22.5 percent), compared to the year 2000. During the same period (2000–2015), the world’s population increased by 20 percent. Whereas some of these areal increases are real increases in cropland areas, others are due to the types of data, methods, and approaches used. Using the highest known resolution (compared to previous coarse-resolution global products) enabled this study to capture fragmented croplands. Coarse-resolution data compute areas on the basis of subpixels, which, for a large proportion of certain land use–land cover classes, will show only a certain percentage of the total pixel area as actual area. Subpixel areas can lead to substantial uncertainties in area computation, as determining the exact fraction of cropland areas within a coarse-resolution pixel is resource intensive and subject to errors. Other innovations in GCEP30 include reference-data hubs, machine learning, and cloud computing. Cropland areas in 214 countries, territories, departments, and regions were calculated for the year 2015 using GCEP30, on the basis of UN’s global administrative unit layers (GAUL) boundaries. The 10 leading countries in terms of cropland area (as a percentage of the GNCA) were India (9.6 percent), United States (8.95 percent), China (8.82 percent), Russia (8.32 percent), Brazil (3.42 percent), Ukraine (2.32 percent), Canada (2.29 percent), Argentina (2.05 percent), Indonesia (2 percent), and Nigeria (1.91 percent). Together, these 10 countries occupy 50 percent of the global cropland, and they have 52 percent of the global population. Their combined cropland area increased by 2 percent between 2000 and 2015, compared to the substantial increase in population of 517 million (15.5 percent). Together, India, United States, China, and Russia encompass 36 percent of the total area. In the United States and Canada, from 2000 to 2015, cropland decreased by about 2 percent, whereas their populations increased by 14 and 13 percent, respectively. The additional food requirements in these 10 countries, which are caused by increased populations, as well as increasing nutritional demands, are met by production increases in existing cropland or through virtual food trade, or both. More than 18 countries, territories, departments, or regions had 60 percent or more of their geographic area as cropland: Republic of Moldova, San Marino, and Hungary had more than 80 percent of the country’s area as cropland; Denmark, Ukraine, Ireland, and Bangladesh, 70 to 80 percent; and Uruguay, Netherlands, United Kingdom, Spain, Lithuania, Poland, Gaza Strip, Czechia, Italy, India, and Azerbaijan, 60 to 70 percent. Europe and South Asia can be considered agricultural capitals of the world, on the basis of their percentages of geographic area as cropland. United States, China, and Russia, which all have high cropland areas, are ranked second, third, and fourth in the world; India is ranked first. However, the amount of cropland as a percentage of the country’s geographic area is relatively very low for United States (18.3 percent), China (17.7 percent), and Russia (9.5 percent), whereas it is 60.5 percent for India. Most African and South American countries, territories, departments, or regions have less than 15 percent of their geographic area as cropland. China and India together house 36 percent of the world’s population; however, between 2000 and 2015, the amount of China’s cropland area fell by 18.9 percent, owing to urban expansion and the abandonment of farmlands caused by demographic changes (that is, the movement of population from villages to cities). In contrast, China’s population grew by 10 percent. The amount of India’s cropland increased by 8.5 percent, whereas its population grew by 20 percent. This study showed that, out of the 10 leading cropland countries, Ukraine, Nigeria, Russia, and Indonesia showed an 18 to 31 percent increase in cropland areas, on the basis of GCEP30 by the year 2015, compared to 2000. Nigeria’s cropland area increased by 25 percent, and its population increased by 31 percent in the same period. In these countries, food security is maintained by cropland expansion, productivity increases, and virtual food trade. Nevertheless, this trend of increasing net-cropland area and productivity will likely become difficult to maintain, owing to diminishing arable lands and plateauing of 50 years of continual yield increases, requiring policymakers to explore novel and data-supported approaches to solving future food security issues. The GCEP30 product, which can be browsed at full resolution at www.croplands.org , has been released for public download and use through U.S. Geological Survey (USGS)–National Aeronautics and Space Administration (NASA) Land Processes Distributed Active Archive Center (see https://lpdaac.usgs.gov/news/release-of-gfsad-30-meter-cropland-extent-products/ ).

Professional Paper↗

Birds of the St. Croix River valley: Minnesota and Wisconsin

The St. Croix River Valley encompasses nearly 11,550 km2 in east-central Minnesota and northwestern Wisconsin. A wide range of habitats are available for birds including upland oak, lowland deciduous, maple-basswood, lowland and upland coniferous forests, natural basin wetlands, and grasslands. Situated in the north-central region of the United States, the valley is a biological 'crossroads' for many species. Because of the mixed affinities of plant communities, the valley includes the northern and southern range limits for a number of species. Also, because the valley lies near the forest-prairie transition zone, many typical western breeding species (e.g. pintail, western meadowlark, yellow-headed blackbird) breed in proximity to typical eastern species such as tufted titmouse, eastern meadowlark, and cardinal. From 1966 to 1980, I conducted extensive surveys of avian distribution and abundance in the St. Croix River Valley. I have supplemented the results of these surveys with published and unpublished observations contributed by many ornithologists. These additional data include compilations from Christmas Bird Counts sponsored by the National Audubon Society and from the Breeding Bird Survey coordinated by the U.S. Fish and Wildlife Service. Three hundred fourteen species have been recorded in the study area; data are presented on the migration period, nesting season distribution, winter distribution, relative abundance, and habitat use of each species. Recognizing the uniqueness of the area, and its importance not only to wildlife but also to man, the U.S. Congress designated the St. Croix a National Scenic Riverway. This action provided a considerable degree of protection to lands along and directly adjacent to the river. Unfortunately, no similar legal measure exists to protect lands away from the river. With the exception of the northern quarter of the St. Croix River Valley, agricultural interests have made significant inroads into the habitat base. The continuing expansion of the nearby Minneapolis-St. Paul metropolitan region has degraded or destroyed many woodlots, upland fields, and wetlands. In numerous instances, degradation of natural habitats has influenced the abundance and distribution of bird species. Because of these changes, both the Federal government and State Departments of Natural Resources have listed several species in various categories based on their current status. In the St. Croix River Valley, seven species are endangered, eight are threatened, and 29 are watch or priority status in either or both states. Data presented in this report are of value to land managers, land use specialists, and ornithologists, in assessing current and projected habitat alterations on the avifauna of this valley. The St. Croix River bisects a large region of western Wisconsin and east central Minnesota that exhibits a wide range of habitat types. This region supports not only birds, but many mammals, fishes, reptiles and amphibians, and several thousand species of vascular and nonvascular plants. The river itself is relatively clean through most of its course, and its natural flow is interrupted by only two small dams. Because the river lies within a 1-day drive of nearly 10 million people (Waters 1977), use of the area for recreational purposes is extremely heavy. Recreational pursuits include sunbathing, boating, and wild river kayaking in the summer, and ice fishing and cross-country skiing in the winter. The large number of unique and highly fragile habitats that exist there may never be compatible with the uses and abuses of the land that go with expanding human populations. Through the efforts of a number of citizens concerned with the quality of their environment and the foresightedness of several local, State, and Federal legislators, a portion of the upper St. Croix River Valley (hereafter termed 'the Valley') was established as a National Wild and Scenic River. Through establishment of t

North American Fauna↗