Significant historic bat declines over the last century were blamed on agricultural intensification, loss of habitat and roosts through development and exclusion from buildings. Today's main threats include land use practices, climate change, pollution, development and infrastructure, and human disturbance.
What is white-nose syndrome caused by?
White-nose syndrome is caused by a fungus, Pseudogymnoascus destructans, that infects skin of the muzzle, ears, and wings of hibernating bats.
Can humans get white-nose syndrome?
Thousands of people have visited affected caves and mines since White-nose Syndrome (WNS) was first observed, and there have been no reported human illnesses attributable to WNS. We are still learning about WNS, but we know of no risk to humans from contact with WNS-affected bats.
Is there a cure?
Not yet. Some promising interventions are being researched, such as naturally occurring bacteria that seem to limit the growth of the white-nose fungus. However, these treatments need to be carefully tested before widespread release in the environment, to make sure they'll actually be helpful, and not cause more stress to either bats or the ecosystems in which they live.
Learn more about white -nose syndrome :
brainly.com/question/14440231
#SPJ4
Answer:
c.The products of photosynthesis are the reactants of respiration.
Explanation:
Photosynthesis and Respiration can be thought of as opposites. Photosynthesis is taking in CO2 and energy and releasing O2, while Respiration is taking in O2 and energy to release CO2.
Answer:
a) There are lots of genes on chromosome 1 could be affected, and the gametes could be imbalanced (missing segments of DNA or whole chromosomes)
b) Roughly 50%
c) No. I would advise that the couple undergo preimplantation genetic diagnosis, so that a zygote carrying the normal copy of chromosome 1 could be selected.
Explanation:
Chromosome 1 is one of the largest and most gene rich chromosomes. An inversion that covers 70% of its length would cover lots of genes.
While an inversion on its own would not seem problematic (as all the genes on the chromosome are still there), when it comes to meiosis, the sister chromatids would not be able to correctly align, and crossing over would further complicate this. It could also lead to unbalanced gametes missing entire parts of the chromosome. Therefore, there are likely numerous genes that will be affected and messed up by the inversion.
This could explain the high incidence of past still births, as if lots of genes are affected, and non-functional, the pregnancy would be rendered non-viable, or highly deleterious causing premature death.
b) There is a 50% chance of a child inheriting the defective copy of chromosome 1 (and 50% of a chance of them inheriting the normal chromosome 1. Therefore, there is likely a 50% chance that future offspring would be affected by defects
c) No. I would advise that the couple undergo preimplantation genetic diagnosis. In this, the couple undergoes in vitro fertilization (IVF). When embryos are produced through IVF, they can then be tested for the presence of the abnormal chromosome. Embryos will only be implanted into the mother if the normal chromosome 1 is present.
Answer:
All living things contain carbon in some form. Carbon is the primary component of macromolecules, including proteins, lipids, nucleic acids, and carbohydrates. Carbon's molecular structure allows it to bond in many different ways and with many different elements.
Explanation: