Attachment Theory: How Marvelous Mother Guided An Adoption Child

The paper focuses on analyzing a mother who guides an adoption child reflected in The Blind Side movie. The researcher applies descriptive qualitative method in analysing the problem to find the data. The research questions are 1. What problems are faced by Leigh Anne's, as a mother? 2. What are the factors cause those problems? 3. How does Leigh Anne's solve the problems? The first data consisting of texts of the movie which is related to a mother guide adoption children and the second data that support the analysis. The technique of the data analysis is carried out by applying the close of mother and children using attachment theory by John Bowlby. The result shows that Leigh Anne Tuohy creates efforts in her supporting strategy such as adopted Oher to be her family, Mrs. Tuohy’s guide Oher to be an American football player. Part of that emotional funding for Leigh Anne is that finaly Oher can find his potential as a human being and find his identity to be a happy person like everyone else.The result is the power of love a marvelous mother can make Oher to be a successful American football player.

Driving with Hemianopia VIII: Effects of a Vibro-Tactile Assistance System on Safety and Gaze Behavior in Pedestrian Crossing Situations

People with homonymous visual field defects (HVFDs), the loss of vision in the same half of the visual field in both eyes, are permitted to drive in some jurisdictions. However, the HVFD may cause difficulties in detecting hazards approaching on the side of the field loss (the blind side). An advanced driver assistance system (ADAS) could assist with hazard detection, but little research has been conducted to evaluate the potential benefits of an ADAS for visually impaired drivers. We developed a prototype vibro-tactile assistance system for drivers with HVFDs and conducted a proof-of-concept driving simulation study to evaluate the system. Given that pedestrian accidents are the second most frequent cause of death in road traffic and most of those accidents occur in urban scenarios, we evaluated the potential of the assistance system to improve responses to pedestrian hazards in a city environment. Sixteen participants, of which eight had HVFDs and eight had normal vision, took part. Our analyses evaluated the effects of the driver assistance system, crossing direction, and pedestrian behavior on the safety of pedestrian events and the participant’s gaze behavior at each of the 256 crossing situations. Generalized linear mixed effects models were used to assess binomial outcome variables. Despite the limited sample size, the results suggest that the vibro-tactile directional warnings were effective in directing the drivers’ gaze so that they were looking in the necessary direction before a potential hazard occurred. More time was spent fixating pedestrians on the blind side when the ADAS was engaged, and as a result, the safety of street crossings from the blind side improved. The effect of the ADAS was greater on responses to pedestrians from the blind than the seeing side. With an activated ADAS, crossings from the participants’ blind sides were as safe as crossings from their seeing sides, and it was as safe as the crossings when normally sighted participants were driving. The results suggest that the vibro-tactile ADAS is a promising approach to improve the safety of drivers with HVFD and surrounding traffic.

Redescription of Brachirus aspilos (Bleeker 1852), a senior synonym of four nominal species, with a note on the distribution of Dagetichthys marginatus (Boulenger 1900) (Pleuronectiformes: Soleidae)

The poorly known sole Brachirus aspilos (Bleeker 1852) is redescribed on the basis of the holotype and 48 non-type specimens from Japan, Taiwan, Philippine, Singapore, Indonesia, Papua New Guinea, and Australia. The species is characterized by the following combination of characters: dorsal-fin rays 64–76 (mode 71), anal-fin rays 51–62 (56), pored scales on straight portion of lateral line 93–126 (118); vertebrae 41–44 (43); pectoral-fin rays 4–7 (6) and 4–7 (5) on ocular and blind sides, respectively; pelvic-fin rays 4–6 (5) and 4–5 (4) on ocular and blind sides, respectively; caudal-fin rays 13–15 (14); body slightly elongate, its depth 40.0–51.0 (mean 45.5)% SL; head length 16.1–23.9 (18.6)% SL; pectoral fin on ocular side longer than that on blind side, 5.3–7.6 (6.6)% SL and 4.0–6.0 (4.8)% SL, respectively; pelvic fin on ocular side longer than that on blind side, 4.9–7.4 (6.0)% SL and 4.3–7.5 (5.8)% SL, respectively; body depth below lateral line 21.7–27.1 (23.4)% SL; lips without labial papillae; eyes separated by scaled interorbital space; cycloid or weakly ctenoid scales on blind side; body on ocular side uniformly brown or grey with dark vermiculation, some small white blotches along dorsal- and anal-fin bases, or without remarkable pattern. Brachirus dicholepis (Peters 1877), B. heterolepis (Bleeker 1856), B. marmoratus (Bleeker 1853), and B. sorsogonensis (Evermann & Seale 1907), previously regarded as valid species, are all regarded as junior synonyms of B. aspilos. In addition, specimens previously reported as Dagetichthys marginatus (Boulenger 1900) from the western Pacific Ocean are re-identified as B. aspilos, the former species being considered restricted to South African waters.

Systematic revision of the flatfish genus Peltorhamphus Günther, 1862 (Teleostei: Pleuronectiformes: Rhombosoleidae), including description of a new species from Southeastern New Zealand, with biological and ecological summaries for the species

The flatfish genus Peltorhamphus Günther, 1862 (Pleuronectiformes: Rhombosoleidae) and its constituent species are redescribed based on examination of 1885 specimens. Four species are considered valid: three previously described (P. novaezeelandiae Günther, 1862, P. latus James, 1972, and P. tenuis James, 1972) and P. kryptostomus n. sp., described herein. Peltorhamphus novaezeelandiae, P. latus, and P. tenuis have widespread distributions on soft sediments in shallow coastal and inner continental shelf waters off both islands of New Zealand. Peltorhamphus novaezeelandiae has also been reported at the Chatham Islands. Previous reports of P. novaezeelandiae from Norfolk Island are erroneous. Peltorhamphus kryptostomus n. sp. has the most restricted geographic distribution in shallow coastal waters of the Otago-Southland region along the southeastern coast of South Island. The four species of Peltorhamphus are morphologically similar and overlap in many traditional meristic and morphometric features rendering identifications difficult, especially of juveniles and earlier life-history stages. Furthermore, throughout New Zealand waters, as many as three of the species possibly occur sympatrically, while in inshore areas of southeastern South Island, all four species may occur in sympatry. Novel morphological characters discovered in this study, combined with traditional diagnostic characters were used to identify and diagnose the species. Peltorhamphus tenuis is the most distinctive of the four, differing from congeners in the following combination of characters: greater length of second ocular-side pectoral-fin ray; its higher numbers of dorsal- and anal-fin rays and total vertebrae; having a series of small scales (best developed in specimens >70 mm SL) on blind sides of dorsal- and anal-fin rays (scales absent in congeners); its elongate body; and ocular-side pigmentation. The other three species are more similar morphologically and have frequently been misidentified both in fish collections and in some previous literature on these fishes. Of these three, P. novaezeelandiae, the largest in the genus, is distinguished from congeners by the combination of: its large size (reaching 510 mm SL vs. ≤ 200 mm SL); rounded head shape; blind-side squamation; the second ocular-side pectoral-fin ray shorter than body depth; ontogenetic variation in interorbital width; greater distance (4–8 scales wide) between ventral margin of lower eye and dorsal (upper) margin of rostral hood above the mouth; and 2–6 fleshy, finger-like filaments on the inner anteroventral margin of the fleshy skinfold on the ocular-side lower jaw. Peltorhamphus latus differs from congeners by the combination of: its short (maximum 150 mm SL), relatively deep body and bluntly pointed snout; blind-side squamation; relatively long, robust gillrakers on first gill arch, with upper limb gillrakers long, but not usually overlapping tips of dorsalmost gillrakers on the lower limb; black pigment on entire roof of mouth; relatively large eyes and narrow interorbital width (without significant ontogenetic variation); short diagonal distance (usually 2–3 scales wide) between ventral margin of lower eye and dorsal (upper) margin of rostral hood above the mouth; and absence of finger-like filaments on the inner anteroventral margin of the fleshy skinfold on the ocular-side lower jaw. Peltorhamphus kryptostomus n. sp. is distinguished from congeners by the combination of: its deep body and smoothly rounded snout; blind-side squamation; long, robust gillrakers on the first gill arch, with some posterior gillrakers on the upper limb overlapping tips of the first and second dorsalmost gillrakers on the lower limb; black pigment on the entire roof of the mouth; relatively large eyes and relatively narrow interorbital width; wide distance between ventral margin of lower eye and upper margin of rostral hood (3–6, usually 4–5, scales wide); and 1–4 finger-like filaments on the inner anteroventral margin of the fleshy skinfold on the ocular-side lower jaw. Ecological and life-history information are summarized for each species, and a key to juveniles > 40 mm SL and adults is also provided. Re-assessment of the number of valid species of Peltorhamphus provides better understanding of species diversity within this genus and within the Rhombosoleidae, as well as that for the flatfish assemblage residing in New Zealand waters.

Antitrust’s Implementation Blind Side: Challenges to Major Expansion of U.S. Competition Policy

For several years, a number of commentators have expressed concern that the U.S. has a growing market power problem. Further that dysfunction in the U.S. antitrust institutions, and their failure to protect competition, has damaged the economy. This Article outlines the principal flaws that this commentary attributes to U.S. antitrust policy (the “crisis in antitrust”), and some of the proposals offered to redirect it and restore it as a central tool of economic control. The paper’s main purpose is not, however, to debate the condition of competition in the US economy or the merits of the measures proposed. Rather, its objective is to identify the magnitude of the implementation challenges that the proposals for a major expansion of the U.S. antitrust program create and the policy implementation challenges that stand between these soaring reform aspirations and their effective realisation in practice. The paper suggests that even though these “implementation” issues are significant, they have been too quickly overlooked in the commentary. In our view the failure to focus on this important matter risks creating a chasm between elevated policy commitments and the capacity of responsible public to produce expected outcomes. The paper consequently acknowledges and addresses this implementation blindside. It analyses the important impediments that are likely, if not carefully addressed, to hamper delivery of the current proposals and proposes ways to overcome them.