11,560 research outputs found
Captive Breeding and Nursery Rearing of the Indian Seahorse, Hippocampus kuda (Teleostei: Syngnathidae)
Breeding of laboratory-reared 21 pairs of broodstock Hippocampus kuda
(Bleeker 1852) and rearing of their young ones indicated that 262.00 ± 59.00 offsprings
were released during each spawning. A newly born seahorse was (mean ± SE) 7.83 ± 0.11
mm in length with a weight of 1.17 ± 0.009 mg. It could attain a mean length of 31.14 ±
0.66 mm with a mean weight of 16.13 ± 0.60 mg in 30 days when fed ad libitum with
Artemia nauplii. The mean survival per brood cycle was enhanced to 65.22 ± 1.87% from
almost less than 1.0% by improving the rearing conditions
Efficient Dynamic Approximate Distance Oracles for Vertex-Labeled Planar Graphs
Let be a graph where each vertex is associated with a label. A
Vertex-Labeled Approximate Distance Oracle is a data structure that, given a
vertex and a label , returns a -approximation of
the distance from to the closest vertex with label in . Such
an oracle is dynamic if it also supports label changes. In this paper we
present three different dynamic approximate vertex-labeled distance oracles for
planar graphs, all with polylogarithmic query and update times, and nearly
linear space requirements
Linear-Space Approximate Distance Oracles for Planar, Bounded-Genus, and Minor-Free Graphs
A (1 + eps)-approximate distance oracle for a graph is a data structure that
supports approximate point-to-point shortest-path-distance queries. The most
relevant measures for a distance-oracle construction are: space, query time,
and preprocessing time. There are strong distance-oracle constructions known
for planar graphs (Thorup, JACM'04) and, subsequently, minor-excluded graphs
(Abraham and Gavoille, PODC'06). However, these require Omega(eps^{-1} n lg n)
space for n-node graphs. We argue that a very low space requirement is
essential. Since modern computer architectures involve hierarchical memory
(caches, primary memory, secondary memory), a high memory requirement in effect
may greatly increase the actual running time. Moreover, we would like data
structures that can be deployed on small mobile devices, such as handhelds,
which have relatively small primary memory. In this paper, for planar graphs,
bounded-genus graphs, and minor-excluded graphs we give distance-oracle
constructions that require only O(n) space. The big O hides only a fixed
constant, independent of \epsilon and independent of genus or size of an
excluded minor. The preprocessing times for our distance oracle are also faster
than those for the previously known constructions. For planar graphs, the
preprocessing time is O(n lg^2 n). However, our constructions have slower query
times. For planar graphs, the query time is O(eps^{-2} lg^2 n). For our
linear-space results, we can in fact ensure, for any delta > 0, that the space
required is only 1 + delta times the space required just to represent the graph
itself
Evaluating Matrix Circuits
The circuit evaluation problem (also known as the compressed word problem)
for finitely generated linear groups is studied. The best upper bound for this
problem is , which is shown by a reduction to polynomial
identity testing. Conversely, the compressed word problem for the linear group
is equivalent to polynomial identity testing. In
the paper, it is shown that the compressed word problem for every finitely
generated nilpotent group is in . Within
the larger class of polycyclic groups we find examples where the compressed
word problem is at least as hard as polynomial identity testing for skew
arithmetic circuits
Localization Recall Precision (LRP): A New Performance Metric for Object Detection
Average precision (AP), the area under the recall-precision (RP) curve, is
the standard performance measure for object detection. Despite its wide
acceptance, it has a number of shortcomings, the most important of which are
(i) the inability to distinguish very different RP curves, and (ii) the lack of
directly measuring bounding box localization accuracy. In this paper, we
propose 'Localization Recall Precision (LRP) Error', a new metric which we
specifically designed for object detection. LRP Error is composed of three
components related to localization, false negative (FN) rate and false positive
(FP) rate. Based on LRP, we introduce the 'Optimal LRP', the minimum achievable
LRP error representing the best achievable configuration of the detector in
terms of recall-precision and the tightness of the boxes. In contrast to AP,
which considers precisions over the entire recall domain, Optimal LRP
determines the 'best' confidence score threshold for a class, which balances
the trade-off between localization and recall-precision. In our experiments, we
show that, for state-of-the-art object (SOTA) detectors, Optimal LRP provides
richer and more discriminative information than AP. We also demonstrate that
the best confidence score thresholds vary significantly among classes and
detectors. Moreover, we present LRP results of a simple online video object
detector which uses a SOTA still image object detector and show that the
class-specific optimized thresholds increase the accuracy against the common
approach of using a general threshold for all classes. At
https://github.com/cancam/LRP we provide the source code that can compute LRP
for the PASCAL VOC and MSCOCO datasets. Our source code can easily be adapted
to other datasets as well.Comment: to appear in ECCV 201
The use of an electronic computer in the estimation of sampling errors in a nutritional survey
RESP-355
Antibacterial activity of aqueous extract from selected macroalgae of southwest coast of India
Aqueous extract of seven species of marine macroalgae were screened for their antimicrobial
potency against ten pathogenic bacterial strains. Ulva fasciata, Gracilaria corticata, Sargassum
wightii and Padina tetrastromatica showed significantly higher activity against 70% of the
tested bacterial isolates. The maximum zone of inhibition was noted for the red alga G.corticata
against Proteus mirabilis (17mm) and brown alga P. tetrastromatica against the pathogens
Staphylococcus aureus and Vibrio harveyi (15mm). The general trend of inhibitory activity
was higher towards Gram negative bacteria
Convexity-Increasing Morphs of Planar Graphs
We study the problem of convexifying drawings of planar graphs. Given any
planar straight-line drawing of an internally 3-connected graph, we show how to
morph the drawing to one with strictly convex faces while maintaining planarity
at all times. Our morph is convexity-increasing, meaning that once an angle is
convex, it remains convex. We give an efficient algorithm that constructs such
a morph as a composition of a linear number of steps where each step either
moves vertices along horizontal lines or moves vertices along vertical lines.
Moreover, we show that a linear number of steps is worst-case optimal.
To obtain our result, we use a well-known technique by Hong and Nagamochi for
finding redrawings with convex faces while preserving y-coordinates. Using a
variant of Tutte's graph drawing algorithm, we obtain a new proof of Hong and
Nagamochi's result which comes with a better running time. This is of
independent interest, as Hong and Nagamochi's technique serves as a building
block in existing morphing algorithms.Comment: Preliminary version in Proc. WG 201
Polymicrobial skin lesions in the red spot emperor, Lethrinus lentjan (Lacepede 1802) during mass incursion towards shore along Kanyakumari coast, south India
Mass incursion of fishes with polymicrobial skin lesions, fin erosions and scale loss was recorded in the red spot emperor
Lethrinus lentjan (Lacepede 1802) along the Kanyakumari coast, south India during August 2009. An estimated 2.5 t of fish,
mostly the red spot emperors were found to migrate in live condition to the shore areas in a stressful state. Microbiological
analyses of tissue from sampled fishes revealed three distinct types of bacterial colonies forming 5.2 x 105 CFU g-1 of the
infected tissues. The predominant bacterial colonies were characterized as Aeromonas sp. (70.0%) followed by Flavobacterium
sp. (20%) and Vibrio sp. (10%). The Aeromonas isolate was highly susceptible to norfloxacin while the Flavobacterium and
Vibrio isolates were susceptible to chloramphenicol. The Aeromonas and Vibrio isolates exhibited protease and amylase
enzyme activities in vitro, suggesting their possible role in the progression of skin lesions and scale loss. The possibilities of
ambient unknown stressors weakening the fish and subsequent infections by these bacterial isolates are discussed
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