Abstract
CdTe quantum dots (QDs), capped with mercaptopropionic acid (MPA), were synthesized and the variation of their fluorescence properties (steady state and lifetime)with pH was assessed in solution and when immobilized in a sol-gel host Three different sizes of CdTe QDs with excited state lifetimes ranging from 42 to 48 ns and with emission maximum at 540 nm (QD(540)). 580 nm (QD(580)) and 625 nm (QD(625)) were selected The solution pH affects the maximum emission wavelength (shifts to higher wavelengths of 23, 24 and 27 nm for QD(540), QD(550) and QP(625), respectively), the excited state lifetime and the fluorescence intensity in a reversible way. Linearization of the maximum emission wavelength variation with the pH allows the estimation of an apparent ionization constant (pK(a)) for each QD: 6.5 +/- 0.1 (QD(540)), 6.1 +/- 0.5 (QD(580)) and 5.4 +/- 0.3 (QD(625)) The variation of the QDs fluorescence properties was further explored using confocal laser scanning microscopy allowing the implementation of a new calibration method for pH imaging in solution QDs were successfully immobilized on the tip of an optical fiber by dip-coating using sal-gel procedure The immobilized QDs showed a similar pH behaviour to the one observed in solution and an apparent lifetime of 80,68 and 99 ns, respectively. The proposed QDs based methodology can be successfully used to monitor pH using wavelength encoded data in imaging and fiber optic sensing applications.

Abstract
A brief review on biconical tapered fiber sensors for biosensing applications is presented. A variety of configurations and formats of this sensor have been devised for label free biosensing based on measuring small refractive index changes. The biconical nonadiabatic tapered optical fiber offers a number of favorable properties for optical sensing, which have been exploited in several biosensing applications, including cell, protein, and DNA sensors. The types of these sensors present a low-cost fiber biosensor featuring a miniature sensing probe, label-free direct detection, and high sensitivity. © The Author(s) 2012.

Abstract
The deterioration of water quality by Cyanobacteria causes outbreaks and epidemics associated with harmful diseases in Humans and animals because of the released toxins. Microcystin-LR (mcyst) is one of the most widely studied hepatotoxin and World Health Organization recommends a maximum value of 1 mu g L-1 of mcyst in drinking-water. Therefore, there is a great demand for remote, real-time sensing techniques to detect and quantify the presence of mcyst. In this work a Fabry-Perot sensing probe based on a fibre tip coated with a mcyst sensitive thin film is presented. Highly specific recognition membranes, using sol-gel based Molecular Imprinted Polymers (MIPs), were developed to quantify microcystins in water, showing great potential in the analysis of this kind of samples. The fibre Fabry-Perot MIP sensor shows a linear response to mcyst concentration with a sensitivity of -13.2 +/- 0.4 nm L mu g(-1).

Abstract
Saccharomyces cerevisiae morphology is known to be dependent on the cell physiological state and environmental conditions. On their environment, wild yeasts tend to form complex colonies architectures, such as stress response and pseudohyphal filaments morphologies, far away from the ones found inside bioreactors, where the regular cell cycle is observed under controlled conditions (e.g. budding and flocculating colonies). In this work we explore the feasibility of using micro-fiber optics spectroscopy to classify Saccharomyces cerevisiae S288C colony structures in YPD media, under different growth conditions, such as: i) no alcohol; ii) 1 % (v/v) Ethanol; iii) 1 % (v/v) 1-butanol; iv) 1 % (v/v) Isopropanol; v) 1 % (v/v) Tert-Amyl alcohol (2 Methyl-2-butanol); vi) 0,2 % (v/v) 2-Furadehyde; vii) 5 % (w/v) 5 (Hydroxymethyl)-furfural; and viii) 1 % (w/v) (-)-Adenosine3', 5'cyclic monophosphate. The microscopy system includes a hyperspectral camera apparatus and a micro fiber (sustained by micro manipulator) optics system for spectroscopy. Results show that micro fiber optics system spectroscopy has the potential for yeasts metabolic state identification once the spectral signatures of colonies differs from each others. This technique associated with other physico-chemical information can benefit the creation of an information system capable of providing extremely detailed information about yeast metabolic state that will aid both scientists and engineers to study and develop new biotechnological products.

Abstract
This paper evaluates various strategies proposed for single cell refractometry and spectroscopy using fiber optic sensors and microfluidic chips. Details concerning design, fabrication and characterization of the chips will be addressed. Preliminary results obtained with alternative on-chip configurations using combination of fiber Bragg gratings with mirrored single mode and multimode fibers will be presented indicating the possibility of performing simultaneous assessment of cellular refractive index and absorption properties.

Abstract
An intrinsic Fabry-Perot cavity for high temperature and strain measurement is presented. The in-fibre cavity is formed by a chemical etched graded index optical fiber spliced to a single mode fiber. The intrinsic sensor obtained shows high sensitivity to strain (6.2 pm/mu epsilon) and rather low sensitivity to temperature (0.9 pm/degrees C), being suitable for applications as a strain gauge at high temperature.