3,352 research outputs found
High-Harmonic Generation from Subwavelength Resonators
Paper FF4N.8 f From the session Nonlinear Processes in Sub-wavelength Systems, 2D Materials, and MetasurfacesAbstract not availableAnastasia Zalogina, Luca Carletti, Aditya Tripathi, Hoo-Cheol Lee, Ilya Shadrivov, Hong-Gyu Park, Yuri Kivshar, and Sergey Krukhttps://ieeexplore.ieee.org/document/989123
An assessment of the impact of possible CAP reform scenarios on Romanian agriculture
Using a simplified model, with key-variable the prices of two different possible scenarios of CAP reform after 2013 (moderate and radical), this paper present a comparison between the price effects of implementation of each reform scenario at 2015 horizon on Romanian agriculture. This short analysis shows that, under the presented hypotheses, the net welfare effect, due to the price changes, for the selected products, is positive in both reform scenarios, yet greater in the case of the radical reform. Integrated in the large context of Romanian development, it seems that the influence of CAP reform upon agriculture and rural areas will be most likely a gradual one: an interpenetration between the two scenarios is foreseeable, starting with the moderate reform that will dominate the period around 2013, the reform measures acquiring a more radical character afterwards.CAP reform, Romania, welfare effects, Agricultural and Food Policy,
Rich, Sturmian, and trapezoidal words
In this paper we explore various interconnections between rich words, Sturmian words, and trapezoidal words. Rich words, first introduced by the second and third authors together with J. Justin and S. Widmer, constitute a new class of finite and infinite words characterized by having the maximal number of palindromic factors. Every finite Sturmian word is rich, but not conversely. Trapezoidal words were first introduced by the first author in studying the behavior of the subword complexity of finite Sturmian words. Unfortunately this property does not characterize finite Sturmian words. In this note we show that the only trapezoidal palindromes are Sturmian. More generally we show that Sturmian palindromes can be characterized either in terms of their subword complexity (the trapezoidal property) or in terms of their palindromic complexity. We also obtain a similar characterization of rich palindromes in terms of a relation between palindromic complexity and subword complexity
Oscheius onirici Torrini, Mazza, Carletti, Benvenuti, Roversi, Fanelli, Luca, Troccoli & Tarasco, 2015, sp. n.
Oscheius onirici sp. n. (Figs. 1–3, Table 1) Female: Body almost straight to slightly bent on ventral side when relaxed by gentle heat. Cuticle finely annulated. Lateral fields with basically three longitudinal ridges, delimited by four lines. In few specimens, an additional short running line could be seen in the middle part of body (Fig. 2 H). Six lips, separate, continuous with body contour; six bristle-like labial sensilla, one on each lip. Amphidial apertures elliptical (Fig. 3 E), located on lateral lips. Stoma rhabditoid type, ca four times longer than diam. Cheilostom not sclerotized, gymnostom culticularized, stegostom (pharyngeal collar) conspicuous, enveloping ca 50 % of stoma length. Glottoid apparatus well developed, isomorphic. Pharyngeal corpus cylindrical, devoid of valvate median bulb, ending in a round basal bulb. Nerve ring localized at ca 64–67 % of pharyngeal length. Excretory pore conspicuous, ventrally located at level ranging 73–100 % of pharyngeal length. Hemizonid not clearly observed. Reproductive system amphidelphic. Ovaries reflexed anteriorly. Vulva in form of a transverse slit. Vagina ca 16 % of corresponding body diameter. Rectum long, ranging 2.4–2.8 anal body diam. long, sometimes expanded proximally. Spermatheca filled with sperm. Tail conical, gradually tapering to a fine point, ca 4 anal body diam. long. Phasmids pore-like, located behind anus at 14 to 25 % of tail length. Male: Rare (only twelve, were found). Body straight to open C when heat-killed. General morphology similar to female except for smaller size and reproductive system. Testis single, anterior end reflexed ventrally. Spicules paired, of equal length, separate, with a small, rounded manubrium; lamina expanded in its proximal part, with a more or less evident velum and ending in a rounded tip. Gubernaculum slender and slightly curved, ca 46 % of spicule length. Bursa peloderan, not open; nine pairs of papillae of different lengths, arranged in a 1 + 1 + 1 / 3 + 3 pattern. Pairs 4–6 and 7–9 more closely spaced than pairs 1–3. Pairs 5 and 8 curved dorsally and not reaching rim of bursa. Tail ca 1.1 anal body diam. long. In three males, the tail protruded slightly outside the bursa (Fig. 1 I) Dauer juveniles: Body straight when heat-killed. Stoma and pharynx morphology similar to adult. Lateral fields with two longitudinal ridges. Nerve ring localized at ca 67 % of pharyngeal length. Excretory pore located at ca 83 % of pharyngeal length. Tail elongate, conical tapering to a hyaline part 11.5 ± 1.6 (9.5–16) Μm long. Type host and locality. Natural host unknown, since material was recovered by soil samples inside the karst cave “Grotta del Lago” in the Monti Pisani area: 10 ° 28 ’ 24.8 ’’E, 43 ° 44 ’ 17.7 ’’N, municipality of San Giuliano Terme, Pisa Province, Tuscany Region, Central Italy (Mazza et al. 2014). Type material. Holotype male, ten paratype females and ten dauer juveniles are mounted on glass slides and deposited at the laboratory of Nematology of the CRA-ABP of Florence (Italy). Two glass slides with two paratype males, two females and five dauer juveniles were deposited in the laboratory of Department of Soil, Plant and Food Sciences, Section of Entomology and Zoology, University of Bari “A. Moro”, Bari (Italy) and in the nematode collection at the Institute for Sustainable Plant Protection (IPSP), CNR, Bari, Italy. Additional paratypes were distributed to the United States Department of Agriculture Nematode Collection, Beltsville, MD, University of California Riverside Nematode Collection and WaNeCo, Plant Protection Service, The Netherlands, Wageningen (one glass slide with two males and two females for each Collection). Etymology. The name of the species refers to the dream [from greek őνειρον, -ου, τò (oneiron)] because one of the authors had a premonitory dream on the discovery of this new species with the indication on the precise locality of the collection. Nematode entomopathogenicity. Oscheius onirici sp. n. infected 46 % of Galleria larvae and 58 % of Tenebrio larvae, while S. carpocapsae killed 100 % of these insects in one week (LT 50: 6.8 (Galleria) and 5.2 (Tenebrio) days for O. onirici, sp. n. and 1.4 days for S. carpocapsae). IJs of both nematodes emerged from all cadavers within 72 h after host death, and from all the dissected dead larvae nematodes of different developmental stages were recovered. Galleria and Tenebrio larvae death was sufficiently rapid with a 33 % of insect larvae death within 120 hours. Diagnosis and relationships. Oscheius onirici sp. n. is characterized by a small size (mean body length of the female is 671 Μm, of the male 510 Μm and of the dauer juvenile 334 Μm), cuticle finely annulated, stoma rhabditoid type, ca three times longer than its diameter and a lateral field marked by three ridges (four longitudinal lines) in adults. Female have an amphidelphic reproductive system, a long rectum (ca 2.4 anal body diam. long), a spermatheca with sperm, and a conical tail, gradually tapering to a finely pointed terminus (ca 4 anal body diam. long). Males are characterized by a short, rounded tail, peloderan bursa with nine pairs of papillae of different lengths, arranged in a 1 + 1 + 1 / 3 + 3 pattern, spicules small and slender. The peloderan bursa, expansile rectum and the not crochet-needle-shaped spicules place O. onirici sp. n. in the Dolichura -group of Oscheius (Sudhaus & Hooper 1994, Sudhaus & Fitch 2001). Species comparisons in the Dolichura -group are presented in Table 2. 12.4 ‾ 17.1 7.7 ‾ 11.2 9.4 ± 0.7 6.1 9.7 ± 0.9 7.4 ‾ 8.3 ‾ 7.0 (8.2 ‾ 11.2) (5.4 ‾7.0) (8.6 ‾ 11.8) (6.2 ‾ 8.5) ‾ ‾ 7.0± 0.7 7.7 4.3 ± 0.4 ‾ ‾ 5.2 (5.9 ‾ 8.2) (6.9 ‾ 9.6) (3.5 ‾5.0) (4.2 ‾ 6.4) 48 ‾ 52 48.7 ‾ 55 54 ± 1.7 53 51.0 ± 1.3 45.5 ‾ 49.1 50.6 * 48.6 (51 ‾ 57) (50 ‾ 56) (47.3 ‾ 52.6) (46.4 ‾ 51.7) Max. bοdy diam. 57 ‾ 96 54 ‾ 74 ‾ 47 36 ± 5.3 46 ‾ 79 ‾ 33 (38 ‾ 61) (30 ‾ 51) (29 ‾ 42) Pharynx 197 ‾ 234 130 ‾ 197 255 ± 10.5 143 137 ± 6.2 ‾ 128 140 (231 ‾ 273) (126 ‾ 162) (126 ‾ 146) (129 ‾ 151) Excretοry pοre ‾ ‾ 207 ± 25 ‾ 108 ± 13.2 ‾ ‾ 105 (178 ‾ 225) (92 ‾ 146) (84 ‾ 120) Nerve ring ‾ ‾ ‾ ‾ 90 ± 5.0 ‾ ‾ 100 (80 ‾ 98) (81 ‾ 109) Τail length 83 ‾ 117 73 ‾ 116 144 ± 13.5 145 69 ± 5.5 ‾ 120 83 (121 ‾ 172) (116 ‾ 172) (63 ‾ 81) (70 ‾ 95) ......continued on the next page Reference Sudhaus (1974) volk (1950) Andersοn & Sudhaus & present study Korner (1954) Pοtts (1910) Sudhaus (1993) Sudhaus (1984) Hοοper (1994) Calculated After οriginal drawing (Pοtts, 1910) and repοrted by Sudhaus & Hοοper (1994) Oscheius onirici sp. n. is most closely related to O. tipulae (Sudhaus 1993), for similar body size, but can be separated by shorter body length (510 vs 676) and shorter spicules in males and shorter tail length in both adult stages. Females also differ in the value of ratio c (9.7 vs 7.0 in O. tipulae). Body length of the adult of the new species is similar to O. sechellensis, but it is clearly different for the presence of four lateral lines vs two. Oscheius onirici sp. n. can be distinguished from O. pseudodolichura (Körner 1954) by smaller size of both adult stages. They also differ in the value of ratio b (female: 4.4 –6.0 vs 6.6 –8.0; male: 3.8–4.6 vs 6.4) and females differ in the value of ratio c (8.6–11.8 vs 7.4–8.3). Oscheius onirici sp. n. differs from O. bengalensis (Sudhaus 1974), O. dolichuroides by smaller size of both adult stages and also for shorter pharynx, shorter male spicules and gubernaculum and shorter female tail (see Table 2). Based on measurements by Völk (1950), O. onirici sp. n. differs from O. dolichura (Schneider 1866) in having a shorter pharynx in males (126–146 vs 130–197) shorter tail in both adult stages, shorter male spicules and gubernaculum and four vs two lines in lateral fields. Finally, O. onirici sp. n. can be separated from O. guentheri by the shorter adults body size, by the shorter tail and by bursa arrangement, though in O. guentheri is uncertain. Adults of O. onirici sp. n. also differ in the value of ratio c (female: 8.6–11.8 vs 5.4 –7.0; male: 21.2–30.4 vs 18.4–20.8). Since different standard were used to assess classification of EPNs, according to Dillman et al. (2012) O. onirici sp. n. is an entomopathogenic nematode, because of its ability to reproduce inside the body of the insects and because Galleria and Tenebrio larvae death was sufficiently rapid that it can be distinguished from phoretic, necromenic, and other parasitic associations. This new species is the first EPN of Dolichura -group.Published as part of Torrini, Giulia, Mazza, Giuseppe, Carletti, Beatrice, Benvenuti, Claudia, Roversi, Pio Federico, Fanelli, Elena, Luca, Francesca De, Troccoli, Alberto & Tarasco, Eustachio, 2015, Oscheius onirici sp. n. (Nematoda: Rhabditidae): a new entomopathogenic nematode from an Italian cave, pp. 533-548 in Zootaxa 3937 (3) on pages 535-542, DOI: 10.11646/zootaxa.3937.3.6, http://zenodo.org/record/23950
Foreground Detection Optimization for SoCs embedded on Smart Cameras
In this paper we study the effectiveness of a set of optimizations applied on a foreground detection and background maintainance algorithm. The optimizations were specifically devised to run in real time on hardware architectures embedded on commercial smart cameras. In order to achieve these aims we focused our attention on two kinds of optimizations based on the elimination of floatingpoint operations and the adoption of SIMD instructions. The optimized version of the algorithm has been tested on two RISC architectures (CRISv32 and MIPS 32Kc) considering different stream resolutions. The results confirm the effectiveness of the proposed solutions, which allows to process in real-time up to VGA resolution
Giant Nonlinear Response at the Nanoscale Driven by Bound States in the Continuum
Being motivated by the recent prediction of high-Q modes in subwavelength dielectric resonators inspired by bound states in the continuum (BIC), we study the second-harmonic generation from isolated subwavelength AlGaAs nanoantennas. We reveal that nonlinear effects at the nanoscale can be enhanced dramatically provided the resonator parameters are tuned to the BIC regime. We predict a record-high conversion efficiency for nanoscale resonators that exceeds by 2 orders of magnitude the conversion efficiency observed at the magnetic dipole Mie resonance, thus opening the way for highly efficient nonlinear metasurfaces and metadevices
Oscheius onirici Torrini, Mazza, Carletti, Benvenuti, Roversi, Fanelli, Luca, Troccoli & Tarasco, 2015, sp. n.
Oscheius onirici sp. n. (Figs. 1–3, Table 1) Female: Body almost straight to slightly bent on ventral side when relaxed by gentle heat. Cuticle finely annulated. Lateral fields with basically three longitudinal ridges, delimited by four lines. In few specimens, an additional short running line could be seen in the middle part of body (Fig. 2 H). Six lips, separate, continuous with body contour; six bristle-like labial sensilla, one on each lip. Amphidial apertures elliptical (Fig. 3 E), located on lateral lips. Stoma rhabditoid type, ca four times longer than diam. Cheilostom not sclerotized, gymnostom culticularized, stegostom (pharyngeal collar) conspicuous, enveloping ca 50 % of stoma length. Glottoid apparatus well developed, isomorphic. Pharyngeal corpus cylindrical, devoid of valvate median bulb, ending in a round basal bulb. Nerve ring localized at ca 64–67 % of pharyngeal length. Excretory pore conspicuous, ventrally located at level ranging 73–100 % of pharyngeal length. Hemizonid not clearly observed. Reproductive system amphidelphic. Ovaries reflexed anteriorly. Vulva in form of a transverse slit. Vagina ca 16 % of corresponding body diameter. Rectum long, ranging 2.4–2.8 anal body diam. long, sometimes expanded proximally. Spermatheca filled with sperm. Tail conical, gradually tapering to a fine point, ca 4 anal body diam. long. Phasmids pore-like, located behind anus at 14 to 25 % of tail length. Male: Rare (only twelve, were found). Body straight to open C when heat-killed. General morphology similar to female except for smaller size and reproductive system. Testis single, anterior end reflexed ventrally. Spicules paired, of equal length, separate, with a small, rounded manubrium; lamina expanded in its proximal part, with a more or less evident velum and ending in a rounded tip. Gubernaculum slender and slightly curved, ca 46 % of spicule length. Bursa peloderan, not open; nine pairs of papillae of different lengths, arranged in a 1 + 1 + 1 / 3 + 3 pattern. Pairs 4–6 and 7–9 more closely spaced than pairs 1–3. Pairs 5 and 8 curved dorsally and not reaching rim of bursa. Tail ca 1.1 anal body diam. long. In three males, the tail protruded slightly outside the bursa (Fig. 1 I) Dauer juveniles: Body straight when heat-killed. Stoma and pharynx morphology similar to adult. Lateral fields with two longitudinal ridges. Nerve ring localized at ca 67 % of pharyngeal length. Excretory pore located at ca 83 % of pharyngeal length. Tail elongate, conical tapering to a hyaline part 11.5 ± 1.6 (9.5–16) Μm long. Type host and locality. Natural host unknown, since material was recovered by soil samples inside the karst cave “Grotta del Lago” in the Monti Pisani area: 10 ° 28 ’ 24.8 ’’E, 43 ° 44 ’ 17.7 ’’N, municipality of San Giuliano Terme, Pisa Province, Tuscany Region, Central Italy (Mazza et al. 2014). Type material. Holotype male, ten paratype females and ten dauer juveniles are mounted on glass slides and deposited at the laboratory of Nematology of the CRA-ABP of Florence (Italy). Two glass slides with two paratype males, two females and five dauer juveniles were deposited in the laboratory of Department of Soil, Plant and Food Sciences, Section of Entomology and Zoology, University of Bari “A. Moro”, Bari (Italy) and in the nematode collection at the Institute for Sustainable Plant Protection (IPSP), CNR, Bari, Italy. Additional paratypes were distributed to the United States Department of Agriculture Nematode Collection, Beltsville, MD, University of California Riverside Nematode Collection and WaNeCo, Plant Protection Service, The Netherlands, Wageningen (one glass slide with two males and two females for each Collection). Etymology. The name of the species refers to the dream [from greek őνειρον, -ου, τò (oneiron)] because one of the authors had a premonitory dream on the discovery of this new species with the indication on the precise locality of the collection. Nematode entomopathogenicity. Oscheius onirici sp. n. infected 46 % of Galleria larvae and 58 % of Tenebrio larvae, while S. carpocapsae killed 100 % of these insects in one week (LT 50: 6.8 (Galleria) and 5.2 (Tenebrio) days for O. onirici, sp. n. and 1.4 days for S. carpocapsae). IJs of both nematodes emerged from all cadavers within 72 h after host death, and from all the dissected dead larvae nematodes of different developmental stages were recovered. Galleria and Tenebrio larvae death was sufficiently rapid with a 33 % of insect larvae death within 120 hours. Diagnosis and relationships. Oscheius onirici sp. n. is characterized by a small size (mean body length of the female is 671 Μm, of the male 510 Μm and of the dauer juvenile 334 Μm), cuticle finely annulated, stoma rhabditoid type, ca three times longer than its diameter and a lateral field marked by three ridges (four longitudinal lines) in adults. Female have an amphidelphic reproductive system, a long rectum (ca 2.4 anal body diam. long), a spermatheca with sperm, and a conical tail, gradually tapering to a finely pointed terminus (ca 4 anal body diam. long). Males are characterized by a short, rounded tail, peloderan bursa with nine pairs of papillae of different lengths, arranged in a 1 + 1 + 1 / 3 + 3 pattern, spicules small and slender. The peloderan bursa, expansile rectum and the not crochet-needle-shaped spicules place O. onirici sp. n. in the Dolichura -group of Oscheius (Sudhaus & Hooper 1994, Sudhaus & Fitch 2001). Species comparisons in the Dolichura -group are presented in Table 2. 12.4 ‾ 17.1 7.7 ‾ 11.2 9.4 ± 0.7 6.1 9.7 ± 0.9 7.4 ‾ 8.3 ‾ 7.0 (8.2 ‾ 11.2) (5.4 ‾7.0) (8.6 ‾ 11.8) (6.2 ‾ 8.5) ‾ ‾ 7.0± 0.7 7.7 4.3 ± 0.4 ‾ ‾ 5.2 (5.9 ‾ 8.2) (6.9 ‾ 9.6) (3.5 ‾5.0) (4.2 ‾ 6.4) 48 ‾ 52 48.7 ‾ 55 54 ± 1.7 53 51.0 ± 1.3 45.5 ‾ 49.1 50.6 * 48.6 (51 ‾ 57) (50 ‾ 56) (47.3 ‾ 52.6) (46.4 ‾ 51.7) Max. bοdy diam. 57 ‾ 96 54 ‾ 74 ‾ 47 36 ± 5.3 46 ‾ 79 ‾ 33 (38 ‾ 61) (30 ‾ 51) (29 ‾ 42) Pharynx 197 ‾ 234 130 ‾ 197 255 ± 10.5 143 137 ± 6.2 ‾ 128 140 (231 ‾ 273) (126 ‾ 162) (126 ‾ 146) (129 ‾ 151) Excretοry pοre ‾ ‾ 207 ± 25 ‾ 108 ± 13.2 ‾ ‾ 105 (178 ‾ 225) (92 ‾ 146) (84 ‾ 120) Nerve ring ‾ ‾ ‾ ‾ 90 ± 5.0 ‾ ‾ 100 (80 ‾ 98) (81 ‾ 109) Τail length 83 ‾ 117 73 ‾ 116 144 ± 13.5 145 69 ± 5.5 ‾ 120 83 (121 ‾ 172) (116 ‾ 172) (63 ‾ 81) (70 ‾ 95) ......continued on the next page Reference Sudhaus (1974) volk (1950) Andersοn & Sudhaus & present study Korner (1954) Pοtts (1910) Sudhaus (1993) Sudhaus (1984) Hοοper (1994) Calculated After οriginal drawing (Pοtts, 1910) and repοrted by Sudhaus & Hοοper (1994) Oscheius onirici sp. n. is most closely related to O. tipulae (Sudhaus 1993), for similar body size, but can be separated by shorter body length (510 vs 676) and shorter spicules in males and shorter tail length in both adult stages. Females also differ in the value of ratio c (9.7 vs 7.0 in O. tipulae). Body length of the adult of the new species is similar to O. sechellensis, but it is clearly different for the presence of four lateral lines vs two. Oscheius onirici sp. n. can be distinguished from O. pseudodolichura (Körner 1954) by smaller size of both adult stages. They also differ in the value of ratio b (female: 4.4 –6.0 vs 6.6 –8.0; male: 3.8–4.6 vs 6.4) and females differ in the value of ratio c (8.6–11.8 vs 7.4–8.3). Oscheius onirici sp. n. differs from O. bengalensis (Sudhaus 1974), O. dolichuroides by smaller size of both adult stages and also for shorter pharynx, shorter male spicules and gubernaculum and shorter female tail (see Table 2). Based on measurements by Völk (1950), O. onirici sp. n. differs from O. dolichura (Schneider 1866) in having a shorter pharynx in males (126–146 vs 130–197) shorter tail in both adult stages, shorter male spicules and gubernaculum and four vs two lines in lateral fields. Finally, O. onirici sp. n. can be separated from O. guentheri by the shorter adults body size, by the shorter tail and by bursa arrangement, though in O. guentheri is uncertain. Adults of O. onirici sp. n. also differ in the value of ratio c (female: 8.6–11.8 vs 5.4 –7.0; male: 21.2–30.4 vs 18.4–20.8). Since different standard were used to assess classification of EPNs, according to Dillman et al. (2012) O. onirici sp. n. is an entomopathogenic nematode, because of its ability to reproduce inside the body of the insects and because Galleria and Tenebrio larvae death was sufficiently rapid that it can be distinguished from phoretic, necromenic, and other parasitic associations. This new species is the first EPN of Dolichura -group.Published as part of Torrini, Giulia, Mazza, Giuseppe, Carletti, Beatrice, Benvenuti, Claudia, Roversi, Pio Federico, Fanelli, Elena, Luca, Francesca De, Troccoli, Alberto & Tarasco, Eustachio, 2015, Oscheius onirici sp. n. (Nematoda: Rhabditidae): a new entomopathogenic nematode from an Italian cave, pp. 533-548 in Zootaxa 3937 (3) on pages 535-542, DOI: 10.11646/zootaxa.3937.3.6, http://zenodo.org/record/23950
Characterization Results for the Poset Based Representation of Topological Relations - I: Introduction and Models
@article{DBLP:journals/informaticaSI/ForlizziN99,
author = {Luca Forlizzi and
Enrico Nardelli},
title = {Characterization Results for the Poset Based Representation
of Topological Relations - I: Introduction and Models.},
journal = {Informatica (Slovenia)},
volume = {23},
number = {2},
year = {1999},
bibsource = {DBLP, http://dblp.uni-trier.de}
Characterization Results for the Poset Based Representation of Topological Relations - II: Intersection and Union
@article{DBLP:journals/informaticaSI/ForlizziN00,
author = {Luca Forlizzi and
Enrico Nardelli},
title = {Characterization Results for the Poset Based Representation
of Topological Relations - II: Intersection and Union.},
journal = {Informatica (Slovenia)},
volume = {24},
number = {1},
year = {2000},
bibsource = {DBLP, http://dblp.uni-trier.de}
Controlling the directivity of all-dielectric nanoantennas excited by integrated quantum emitters
We study the scattering properties of individual Al0.18Ga0.82AsAl0.18Ga0.82As nanocylinders, which support simultaneously electric and magnetic dipole resonances, excited by an integrated point dipole emitter. We show that by controlling the emitter position in the nanocylinder, it is possible to enhance directivity and the decay rate. Our findings reveal remarkable details of the emitter/antenna coupling mechanisms, opening the way to new design strategies for integrated systems used in nanosensing, quantum optics, and metamaterials
- …
