Biological Report Sample Clauses

Biological Report. CONSULTANT shall conduct a single reconnaissance-level field survey of the project site to document the biological conditions on the site. This information will be gathered for the purpose of characterizing the botanical resources and wildlife habitat values of the project site. The dominant biotic communities of the site, which are entirely landscaped, characterized based on dominant plants and associated wildlife, will be described. The reconnaissance-level field survey will also determine the site’s potential to support special-status plant and animal species. During the survey, CONSULTANT shall also describe the approximate boundaries of potentially sensitive or regulated habitats, such as wetlands and other waters of the U.S./State, and areas covered by the Valley Habitat Conservation Plan, on and immediately adjacent to the project site, if any. This information will be adequate to quantify approximate impacts on these habitats for CEQA assessment purposes. No additional species-specific surveys are part of the scope. Upon the completion of the field survey, CONSULTANT shall prepare a report that describes existing biological conditions, including special-status species with the potential to occur on the site and any potentially sensitive/regulated habitats that occur on the site; potential impacts on existing biological resources; and any conceptual mitigation measures necessary to mitigate potentially significant impacts to less-than- significant levels under CEQA. Based on the location of the project site relative to sensitive habitats, the biological issues addressed in the report will primarily focus on the potential for work to disturb nesting birds/bats, which are known to occur in the vicinity. Graphics to be prepared will only include site/vicinity and CNDDB maps. The report will not include preparation of a special-status species table.
Sample 1
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Related to Biological Report

  • MEDICAL REPORT The Agency/Department Head as a condition of granting sick leave with pay, may require medical evidence of sickness or injury acceptable to the Agency/Department. The acceptable medical evidence must be obtained from a medical practitioner currently treating the employee or the employee’s family member.

  • Technical Reports deliver to the Agent, and shall procure that the Manager shall deliver to the Agent, on request copies of the latest complete technical reports in respect of the Vessels.

  • Medical Reports The following applies to all employees: The Employer agrees to pay the fee for medical reports required by the Employer for Sick Leave or Weekly Indemnity provisions to a maximum of fifty dollars ($50.00).

  • Medical Records Medical records relating to Trial Subjects that are not submitted to Sponsor may include some of the same information as is included in Trial Data; however, Sponsor makes no claim of ownership to those documents or the information they contain. c.

  • Statistical Sampling Documentation a. A copy of the printout of the random numbers generated by the “Random Numbers” function of the statistical sampling software used by the IRO.

  • Statistical Analysis 31 F-tests and t-tests will be used to analyze OV and Quality Acceptance data. The F-test is a 32 comparison of variances to determine if the OV and Quality Acceptance population variances 33 are equal. The t-test is a comparison of means to determine if the OV and Quality Acceptance 34 population means are equal. In addition to these two types of analyses, independent verification 35 and observation verification will also be used to validate the Quality Acceptance test results.

  • Statistical Information Any third-party statistical and market-related data included in the Registration Statement, the Time of Sale Disclosure Package and the Prospectus are based on or derived from sources that the Company believes to be reliable and accurate in all material respects.

  • Final Report The goal of this subtask is to prepare a comprehensive Final Report that describes the original purpose, approach, results, and conclusions of the work performed under this Agreement. The CAM will review the Final Report, which will be due at least two months before the Agreement end date. When creating the Final Report Outline and the Final Report, the Recipient must use the Style Manual provided by the CAM.

  • Evaluation Report 20.5.4.1 The summary evaluation report shall be prepared by the Faculty Evaluation Committee and administrative evaluator(s) and shall include each evaluator’s individual rating. The summary evaluation report shall take into account the results of each of the evaluation components (Section 20.5.3) in order to arrive at an overall rating. When the committee and the administrative evaluator(s) cannot reach an agreement as to the overall rating, the report must include written explanation.

  • Evaluation Reports Where a formal evaluation of an employee's performance is carried out, the employee shall be provided with a copy to read and review. Provision shall be made on the evaluation form for an employee to sign it. The form shall provide for the employee's signature in two (2) places, one indicating that the employee has read and accepts the evaluation, and the other indicating that the employee disagrees with the evaluation. The employee shall sign in one of the places provided within seven (7) calendar days. No employee may initiate a grievance regarding the contents of an evaluation report unless the signature indicates disagreement with the evaluation. The employee shall receive a copy of the evaluation report at the time of signing. An evaluation report shall not be changed after an employee has signed it, without the knowledge of the employee, and any such changes shall be subject to the grievance procedure.

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