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openCC (other)May 2020View details →

High-frequency temperature data from four near-shore sites, Lake Sunapee, NH, USA, 2006-2018

Onset temperature loggers were located at four near-shore sites in Lake Sunapee, New Hampshire, USA. The temperature sensors were co-located at sites where monitoring for Gloeotrichia echinulata, a large colonial cyanobacterium, occurred (see EDI data package edi.497). Temperature loggers were deployed during the summer months (approximately June through September) in 2006-2018 at Herrick Cove South (site = HerrickCoveSouth), 2007-2018 South of the Fells (site = SouthOfTheFells), Newbury (site = Newbury), North Sunapee Harbor (site = NorthSunapeeHarbor).

openCC (other)Oct 2020View details →

Ecosystem metabolism estimates from Lake Sunapee, NH, USA and meteorological driver data at the Newport, NH, USA NOAA NCDC weather station from August 2007 – December 2008

In August 2007, the Lake Sunapee Protective Association (LSPA) deployed a buoy in Lake Sunapee, NH with a meteorological station, dissolved oxygen sensor at 1 m, and a string of thermistor water temperature sensors collecting data every 10 minutes. For this dataset, the Lake Sunapee buoy was located at a location near Loon Island all year (August 2007–December 2008) including during the winter. We used high-frequency dissolved oxygen, photosynthetically active radiation (PAR), wind speed, and water temperature profile data to estimate daily rates of gross primary production, respiration, and net ecosystem production as metrics of ecosystem metabolism and carbon cycling. This dataset included under-ice data, and we compared seasonal changes in ecosystem metabolism rates for an entire lake year from the start of fall mixing in 2007 through the end of summer stratification in 2008. Under-ice and mixing periods are infrequently sampled due to logistical challenges and assumptions of low biological activity, resulting in limited understanding of the contribution of winter epilimnetic metabolism to annual carbon cycling. Using a continuous year of high-frequency dissolved oxygen data, we found that on average, under-ice net ecosystem production (NEP) was negative, in contrast to positive NEP for the spring and summer periods. Importantly, under-ice respiration was 1.2 times higher than summer respiration. Gross primary production was low but not absent under ice and increased during the last under-ice phase. Including winter metabolism estimates flipped annual NEP from autotrophy to heterotrophy, highlighting the importance of estimating metabolism year-round. Our methods for the data analysis are described in Brentrup et al. (accepted at Inland Waters) and were similar to Richardson et al. (2016) with some modifications described in the methods. This dataset also includes derived thermocline depth calculations from the water temperature thermistor data on the Lake Sunape

openCC (other)Sep 2020View details →

Physical, chemical, and metabolic leaf characteristics within sugar maple in the MELNHE study at Bartlett Experimental Forest, central NH USA, 2017

The MELNHE study looks at patterns of resource limitation through nutrient manipulations in three study sites in New Hampshire: Bartlett Experimental Forest, Hubbard Brook Experimental Forest, and Jeffers Brook, located in the White Mountain National Forest. The investigation is monitoring stem diameter, leaf area, sap flow, foliar chemistry, leaf litter production and chemistry, foliar nutrient resorption, root biomass and production, mycorrhizal associations, soil respiration, heterotrophic respiration, N and P availability, N mineralization, soil phosphatase activity, soil carbon and nitrogen, nutrient uptake capacity of roots, and mineral weathering. Applications of N and P began in June 2011 and continue at the rate of 30 kg N/ha/yr (as NH4NO3) and 10 kg P/ha/yr (as NaH2PO4). This data set includes physical, chemical, and metabolic leaf characteristics collected in a vertical transect within individual tree crowns. Because trees varied in crown depth, not all trees have the same number of samples collected. Depth from the top of the crown was measured and climbing ropes and a pole pruner were used to collect a population of leaves. These data were gathered as part of the Hubbard Brook Ecosystem Study (HBES). The HBES is a collaborative effort at the Hubbard Brook Experimental Forest, which is operated and maintained by the USDA Forest Service, Northern Research Station.

openCC (other)Sep 2023View details →

Arthropod communities in the Second College Grant, NH

Arthropods are active during the winter in temperate regions. Many use the seasonal snowpack as a buffer against harsh ambient conditions and remain active in a refugium known as the subnivium. While the use of the subnivium by insects and other arthropods is well-established, far less is known about winter community composition, abundance, biomass, and diversity and how these characteristics compare with the community in the summer. Understanding subnivean communities is especially important given observed and anticipated changes in snowpack depth and duration with changing climate. We studied winter and summer insects and other arthropods using pitfall trapping in northern New Hampshire, where snowpack is still relatively intact. We found that compositions of the subnivium and summer arthropod communities differed. The subnivium arthropod community featured moderate levels of richness and other measures of diversity that tended to be lower than in the summer community. More striking, the subnivium community was much lower in overall abundance and biomass than the summer community. Interestingly, some groups and species of arthropods were dominant in the subnivium but either rare or absent in summer collections. These putative “subnivium specialists” included one spider (order: Araneae), Cicurina brevis (Emerton, 1890), and three rove beetles (order: Coleoptera, family: Staphylinidae) Arpedium cribratum Fauvel, 1878, Lesteva pallipes LeConte, 1863, and Porrhodites inflatus (Hatch, 1957). This study provides a detailed account of the subnivium arthropod community, presents novel concepts, and establishes baseline information on arthropod communities in the North American northeastern temperate forest.

opencc-by-4.0Apr 2024View details →

High-resolution simulations of Mediterranean windstorm Adrian with the Meso-NH atmospheric model

The dataset provides numerical simulations of Mediterranean windstorm Adrian of 29 October 2018 at two horizontal resolutions and using different representations of surface turbulent fluxes at the air-sea interface. The simulations are run with the Meso-NH non-hydrostatic mesoscale atmospheric model of the French research community, version 5.4, freely available under CeCILL-C license agreement: <a href="http://mesonh.aero.obs-mip.fr/" target="_blank" rel="noopener">http://mesonh.aero.obs-mip.fr/</a> The data is formatted in Network Common Data Form (NetCDF) using the CF Metadata Conventions and standard Meso-NH names for physical variables. The data files are named as following: EXP.N.CONTENT.nc <ul> <li>EXP describes the numerical experiment (name of the parameterization of surface turbulent fluxes or their absence) </li> <li>N the horizontal resolution (1=1000m, mesoscale simulation; 2=200m, large-eddy simulation) </li> <li>CONTENT the type of data (3D zoom over the windstorm center or vertical profiles in the same area at 1530 UTC, or 2D surface fields every 6 min from 12 to 18 UTC)</li> </ul>

opencc-by-4.0Dec 2019View details →

Рис. 1. Схематическое ΑеΛение АзербайΑжана: ZQ, SH, KU, AP – БоΛьшой Кавказ; AR – Куро-Араксинская низменность; GN, KB, NH – МаΛый Кавказ; LK – ТаΛыш (вкΛючая ЗуванΑ и Αенкоранскую низменность). Fig. 1. Schematic division of Azerbaijan:ZQ, SH, KU, AP – the Greater Caucasus; AR – the Kura-Aras lowland; GN, KB, NH – the Lesser Caucasus; LK – Talysh (including Zuvand and the Lenkoran lowland). in The fauna of lamellicorn beetles (Coleoptera: Scarabaeoidea) of Azerbaijan

Рис. 1. Схематическое ΑеΛение АзербайΑжана: ZQ, SH, KU, AP – БоΛьшой Кавказ; AR – Куро-Араксинская низменность; GN, KB, NH – МаΛый Кавказ; LK – ТаΛыш (вкΛючая ЗуванΑ и Αенкоранскую низменность). Fig. 1. Schematic division of Azerbaijan:ZQ, SH, KU, AP – the Greater Caucasus; AR – the Kura-Aras lowland; GN, KB, NH – the Lesser Caucasus; LK – Talysh (including Zuvand and the Lenkoran lowland).

opencc-by-4.0Sep 2024View details →

FIG. 2 in "Bursting through all obstacles and traversing all distances" (Plin., NH 8.35.86): spatial memory of snakes in light of ancient literary accounts

FIG. 2. — Bacchus and Vesuvius. A huge snake is slithering in front of an altar. Pompeii, from the Lararium of the House of the Centenary, 55-79 AD, Naples. National Archaeological Museum,inv.112286, after Kuivalainen (2021: 117, C17).

opencc-by-4.0Sep 2024View details →

FIG. 1 in "Bursting through all obstacles and traversing all distances" (Plin., NH 8.35.86): spatial memory of snakes in light of ancient literary accounts

FIG. 1. — The Python's cave (antron). Leto escapes from Python with Apollo and Artemis in her arms. Lost Apulian red-figure neck amphora, earlier IV BC, drawing by J. H. W. Tischbein after Ogden (2013a: 39, fig. 3).

openother-openApr 2023View details →

Data_Decomposition_NH

Supplemental data for publication "Decomposing bulk signals to reveal hidden information in processive enzyme reactions: A case study in mRNA translation<code>"</code>

Fig. 8 in New species of the Madagascan genus Hovops Benoit, 1968 (Araneae: Selenopidae), with a description of the H. madagascariensis PDOH DQG DQ LGHQWL¿FDWLRQ NH\

Fig. 8. Hovops pusillus: (A) female habitus, dorsal view; (B) male, palp ventro-retrolateral view; (C) male, detail of the bulb, lateral view; (D) female, epigyne ventral view; (E) female, vulva dorsal view. Scale bars: A–C = 1 mm, D, E = 0.2 mm.

Fig. 7 in New species of the Madagascan genus Hovops Benoit, 1968 (Araneae: Selenopidae), with a description of the H. madagascariensis PDOH DQG DQ LGHQWL¿FDWLRQ NH\

Fig. 7. Hovops mariensis: (A) female habitus, dorsal view; (B) female, epigyne ventral view; (C) female, vulva dorsal view. Scale bars: A = 1 mm, B, C = 0.2 mm.

Fig. 3 in New species of the Madagascan genus Hovops Benoit, 1968 (Araneae: Selenopidae), with a description of the H. madagascariensis PDOH DQG DQ LGHQWL¿FDWLRQ NH\

Fig. 3. Hovops lidiae sp. n.: (A) female habitus, dorsal view; (B) male, palp ventral view; (C) male, palp lateral view; (D) male, detail of the tibial apophysis; (E) male, spination on the anterior tibia and metatarsi; (F) female, epigyne ventral view; (G) female, vulva dorsal view. Scale bars: A = 1 mm; B–D & F, G = 0.2 mm.

Fig. 6 in New species of the Madagascan genus Hovops Benoit, 1968 (Araneae: Selenopidae), with a description of the H. madagascariensis PDOH DQG DQ LGHQWL¿FDWLRQ NH\

Fig. 6. Hovops legrasi: (A) female habitus, dorsal view; (B) male, detail of the tibial apophysis; (C) male, palp ventral view; (D) female, epigyne ventral view; (E) female, vulva dorsal view. Scale bars: A–C = 1 mm, D, E = 0.2 mm.

Fig. 1 in New species of the Madagascan genus Hovops Benoit, 1968 (Araneae: Selenopidae), with a description of the H. madagascariensis PDOH DQG DQ LGHQWL¿FDWLRQ NH\

Fig. 1. Comparison of some somatic characters between genera of Selenopidae: (A–E) position and sizes of eyes of (A) Siamspinops, (B) Anyphops, (C) Selenops, (D) Garcorops, (E) Hovops; (F) details of the major ampullate spigots in Hovops; (G–N) number and position of ventral spines on anterior tibia and metatarsi in (G) Siamspinops, (H) Selenops, (I) Garcorops and few species of Anyphops, (J–L) other Anyphops, (M–N) Hovops.

Fig. 5 in New species of the Madagascan genus Hovops Benoit, 1968 (Araneae: Selenopidae), with a description of the H. madagascariensis PDOH DQG DQ LGHQWL¿FDWLRQ NH\

Fig. 5. Hovops merina sp. n.: (A) female habitus, dorsal view; (B) female, spination on the anterior tibiae and metatarsi; (C) details of scale-like hairs on opisthosoma; (D) female, epigyne ventral view; (E) female, vulva dorsal view. Scale bars: A = 1 mm; D, E = 0.2 mm.

Fig. 2 in New species of the Madagascan genus Hovops Benoit, 1968 (Araneae: Selenopidae), with a description of the H. madagascariensis PDOH DQG DQ LGHQWL¿FDWLRQ NH\

Fig. 2. Hovops betsileo sp. n.: (A) female habitus, dorsal view; (B) eyes arrangement; (C) female, ventral view of the prosoma; (D) female, spination of the anterior tibia and metatarsus; (E) female, epigyne ventral view; (F) female, vulva dorsal view; (G) male, palp retrolateral view; (H) male, palp ventral view. Scale bars: A–C = 1 mm; E–H = 0.2 mm.

Fig. 4 in New species of the Madagascan genus Hovops Benoit, 1968 (Araneae: Selenopidae), with a description of the H. madagascariensis PDOH DQG DQ LGHQWL¿FDWLRQ NH\

Fig. 4. Hovops madagascariensis: (A) female habitus, dorsal view; (B) female, eyes arrangement; (C) male, palp ventro-retrolateral view; (D) male, palp ventral view; (E) female, epigyne ventral view; (F) female, vulva dorsal view; (G) female, spination on the anterior tibiae and metatarsi; (H) male, spination on the anterior tibia and metatarsi. Scale bars: A, B = 1 mm, C–F = 0.2 mm.